<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.3 20210610//EN" "JATS-journalpublishing1-3.dtd">
<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">ejols</journal-id><journal-title-group><journal-title xml:lang="en">The Eurasian Journal of Life Sciences</journal-title><trans-title-group xml:lang="ru"><trans-title>Евразийский журнал наук о жизни</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">3033-5493</issn><issn pub-type="epub">3033-6031</issn><publisher><publisher-name>Сеченовский Университет</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.47093/3033-5493.2025.1.1.4-16</article-id><article-id custom-type="elpub" pub-id-type="custom">ejols-3</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>Статьи</subject></subj-group></article-categories><title-group><article-title>Modern trends in laser  non-invasive reconstruction of biological tissues</article-title><trans-title-group xml:lang="ru"><trans-title>Современные тенденции в лазерной неинвазивной реконструкции биологических тканей</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-3207-7622</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Сучкова</surname><given-names>В. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Suchkova</surname><given-names>V. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Виктория Викторовна Сучкова, Младший научный сотрудник института бионических технологий и инжиниринга; ассистент института биомедицинских систем</p><p>119048, г. Москва, ул. Трубецкая, д. 8, стр. 2</p><p>124498, г. Зеленоград, Москва, пл. Шокина, д. 1</p></bio><bio xml:lang="en"><p>Victoria V. Suchkova, Junior Researcher, Institute for Bionic Technologies and Engineering; Assistant, Institute of Biomedical Systems</p><p>8/2, Trubetskaya str., Moscow, 119048</p><p>1, Shokin Square, Moscow, Zelenograd, 124498</p><p> </p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-1327-5690</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Рябкин</surname><given-names>Д. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Ryabkin</surname><given-names>D. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Дмитрий Игоревич Рябкин, канд. физ.-мат. наук, ассистент института бионических технологий и инжиниринга; старший преподаватель института биомедицинских систем</p><p>119048, г. Москва, ул. Трубецкая, д. 8, стр. 2</p><p>124498, г. Зеленоград, Москва, пл. Шокина, д. 1</p></bio><bio xml:lang="en"><p>Dmitry I. Ryabkin, Ph.D. (Phys.-Math.), Assistant, Institute for Bionic Technologies and Engineering; Associate Professor, Institute of Biomedical Systems</p><p>8/2, Trubetskaya str., Moscow, 119048</p><p>1, Shokin Square, Moscow, Zelenograd, 124498</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-3681-2874</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Ян</surname><given-names>Л.</given-names></name><name name-style="western" xml:lang="en"><surname>Yang</surname><given-names>L.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Лэй Ян, профессор, руководитель департамента ортопедии</p><p>150001, пров. Хэйлунцзян, г. Харбин, ул. Ючжэн, д.23</p></bio><bio xml:lang="en"><p>Lei Yang, Ph.D., Professor, Director, Department of Orthopedics</p><p>23 Youzheng Street, Harbin, Heilongjiang, 150001</p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-4221-9882</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Телышев</surname><given-names>Д. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Telyshev</surname><given-names>D. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Дмитрий Викторович Телышев, д-р техн. наук, профессор, директор института бионических технологий и инжиниринга; профессор института биомедицинских систем</p><p>119048, г. Москва, ул. Трубецкая, д. 8, стр. 2</p><p>124498, г. Зеленоград, Москва, пл. Шокина, д. 1</p></bio><bio xml:lang="en"><p>Dmitry V. Telyshev, Dr. Sc. (Engineering), Associate Professor, Director, Institute for Bionic Technologies and Engineering; Professor, Institute of Biomedical Systems</p><p>8/2, Trubetskaya str., Moscow, 119048</p><p>1, Shokin Square, Moscow, Zelenograd, 124498</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-6514-2411</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Герасименко</surname><given-names>А. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Gerasimenko</surname><given-names>A. Yu.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Александр Юрьевич Герасименко, д-р техн. наук, профессор, заведующий лабораторией биомедицинских нанотехнологий института бионических технологий и инжиниринга; руководитель научно-исследовательской лаборатории «Биомедицинские нанотехнологии» института биомедицинских систем</p><p>119048, г. Москва, ул. Трубецкая, д. 8, стр. 2</p><p>124498, г. Зеленоград, Москва, пл. Шокина, д. 1</p></bio><bio xml:lang="en"><p>Alexander Yu. Gerasimenko, Dr. Sc. (Engineering), Associate Professor, Head of Biomedical Nanotechnology Laboratory, Institute for Bionic Technologies and Engineering; Head of Biomedical Nanotechnology Laboratory, Institute of Biomedical Systems</p><p>8/2, Trubetskaya str., Moscow, 119048</p><p>1, Shokin Square, Moscow, Zelenograd, 124498</p></bio><email xlink:type="simple">gerasimenko@bms.zone</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Первый Московский государственный медицинский университет имени И.М. Сеченова (Сеченовский Университет); Национальный исследовательский университет "МИЭТ"</institution></aff><aff xml:lang="en"><institution>Sechenov First Moscow State Medical University (Sechenov University); National Research University of Electronic Technology</institution></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Первая клиническая больница Харбинского медицинского университета</institution></aff><aff xml:lang="en"><institution>The First Affiliated Hospital of Harbin Medical University</institution></aff></aff-alternatives><pub-date pub-type="collection"><year>2025</year></pub-date><pub-date pub-type="epub"><day>01</day><month>07</month><year>2025</year></pub-date><volume>1</volume><issue>1</issue><fpage>4</fpage><lpage>16</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Suchkova V.V., Ryabkin D.I., Yang L., Telyshev D.V., Gerasimenko A.Y., 2025</copyright-statement><copyright-year>2025</copyright-year><copyright-holder xml:lang="ru">Сучкова В.В., Рябкин Д.И., Ян Л., Телышев Д.В., Герасименко А.Ю.</copyright-holder><copyright-holder xml:lang="en">Suchkova V.V., Ryabkin D.I., Yang L., Telyshev D.V., Gerasimenko A.Y.</copyright-holder><license license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://www.eajls.com/jour/article/view/3">https://www.eajls.com/jour/article/view/3</self-uri><abstract><p>The article focuses on contemporary methodologies for laser-based, non-invasive reconstruction of biological tissues. It examines the mechanisms of laser-tissue interaction, including photothermal processes and the formation of new molecular bonds. A range of laser systems – neodymium-doped yttriumaluminum garnet laser (Nd:YAG laser), carbon dioxide laser (CO2 laser), diode and their applications in vascular, micro- and plastic surgery are analyzed. The analysis is further enriched by a discussion of bioorganic solders, such as albumin and indocyanine green, and nanomaterials that have been shown to enhance bond strength and reduce thermal damage. Examples of successful applications of the technology for vascular and nerve repair, wound sealing, and plastic surgery are provided. Finally, future prospects are highlighted, including temperature control systems and personalized approaches. The text emphasizes the potential of laser methods as a minimally invasive alternative to traditional surgery.</p></abstract><trans-abstract xml:lang="ru"><p>Статья посвящена современным методикам, применяемым в лазерной неинвазивной реконструкции биологических тканей. Рассмотрены механизмы взаимодействия лазера с тканями, включая фототермические процессы и образование новых молекулярных связей. Проанализировано применение различных видов лазерных систем, среди которых, неодимовый лазер на алюмоиттриевом гранате (Nd:YAG-лазер), лазер на диоксиде углерода (CO2-лазер), диодные лазеры, в различных областях медицины, включая сосудистую хирургию, микрохирургию, пластическую хирургию. Также рассмотрены вопросы применения биоорганических припоев, среди которых альбумин и индоцианин зелёный, и нанокомпозитных припоев, применение которых позволяет повысить прочность связи и снизить термическое повреждение тканей в области шва. Приведены примеры успешного применения данной технологии при реконструкции сосудов и нервов, закрытии ран и при пластических операциях. Также освещены перспективы дальнейшего развития технологии, такие как системы контроля температуры, персонализированные подходы. В статье оценивается потенциал применения лазерных технологий как малоинвазивной альтернативы для традиционной хирургии</p></trans-abstract><kwd-group xml:lang="ru"><kwd>лазерные системы</kwd><kwd>малоинвазивная хирургия</kwd><kwd>фототермические процессы</kwd><kwd>наночастицы</kwd><kwd>биоорганические припои</kwd></kwd-group><kwd-group xml:lang="en"><kwd>laser systems</kwd><kwd>non-invasive surgery</kwd><kwd>photothermal processes</kwd><kwd>nanoparticles</kwd><kwd>bioorganic solders</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Работа выполнена в рамках государственного задания Минобрнауки России (проект ФСМР-2024-0003).</funding-statement><funding-statement xml:lang="en">The work was carried out within the framework of the state assignment of the Ministry of Education and Science of Russia (Project FSMR-2024-0003).</funding-statement></funding-group></article-meta></front><body><sec><title>Introduction</title><p>Contemporary medicine is actively developing minimally invasive surgical methods, which are not only comparable in effectiveness to traditional approaches, but also provide less traumatic, reduced blood loss, minimal scarring, and shorter hospitalization and rehabilitation of patients. Thanks to the introduction of robotic systems, high-precision imaging, such interventions are becoming increasingly precise and safe, opening up new possibilities in the treatment of complex diseases. One of the most promising methods meeting these requirements is laser-assisted biological tissue reconstruction. This technology, based on the use of laser radiation in combination with biomaterials, demonstrates significant advantages over traditional surgical methods, such as suturing or stapling [<xref ref-type="bibr" rid="cit1">1</xref>][<xref ref-type="bibr" rid="cit2">2</xref>].</p><p>The aim of this article is to summarize current advancements in laser-assisted tissue repair, assess its benefits and limitations, and outline future research directions that could establish this technology as a standard in surgical practice.</p></sec><sec><title>Mechanism of interaction of laser radiation with biological tissues</title><p>When the process is exclusively laser-driven (laser tissue welding), it operates through a photothermal mechanism: laser energy induces structural rearrangements in the extracellular matrix components of connective tissue, leading to the formation of fusion bonds between opposing wound margins [<xref ref-type="bibr" rid="cit3">3</xref>].</p><p>Thermal exposure induces unwinding of collagen’s triple helices through hydrogen bond cleavage, resulting in denaturation and tissue contraction. Temperatures exceeding 60°C provoke covalent bond dissociation, disrupting the collagen fibers and modifying tissue characteristics, with complete relaxation achieved above 75°C [<xref ref-type="bibr" rid="cit4">4</xref>][<xref ref-type="bibr" rid="cit5">5</xref>].</p><p>The most common interpretation of the mechanism of operation of laser welding is the unravelling of collagen fibers at the cut ends, followed by intertwining of the fibers (interdigitation) across the cut under the action of laser radiation. As a result, fusion occurs either between the cut ends of collagen fibers or between their parallel edges. Also, new chemical bonds are formed during laser irradiation: formation of new covalent cross-links at the welding site and non-covalent interactions between unwound collagen filaments on both sides of the seam [<xref ref-type="bibr" rid="cit6">6</xref>][<xref ref-type="bibr" rid="cit7">7</xref>]. The operating temperature of laser welding is usually in the range of 60-65 °C.</p><p>Another effect occurring during laser welding of tissues is complete homogenization of the tissue (also called hyalinosis), in which the loose structure of collagen fibers is completely destroyed. In these cases, the temperature in the weld zone exceeds 75 °C. Denatured collagen and intracellular proteins photocoagulate, acting as endogenous glue (microsoldering) and forming new molecular bonds on cooling [<xref ref-type="bibr" rid="cit8">8</xref>].</p><p>Photothermal soldering is based on the coagulation of protein solder due to a laser-induced temperature rise in the tissue. After cooling, non-covalent interactions between the solder and the collagen matrix in the tissue are responsible for the strength of the weld [<xref ref-type="bibr" rid="cit9">9</xref>].</p><p>The higher the tissue’s absorption coefficient, the more pronounced the photothermal effect. However, this also limits the penetration depth of laser radiation, making welding of deeper tissue layers considerably more challenging. Conversely, when tissues have low absorption coefficients, laser radiation can penetrate deeper, but the resulting photothermal effect is weaker, leading to lower tensile strength of the weld.</p></sec><sec><title>Laser systems for tissue reconstruction</title><p>One of the first lasers to be widely used in surgery is the Neodymium-doped yttrium-aluminum garnet laser (Nd:YAG laser) with a wavelength of λ=1064 nm. This wavelength coincides with the absorption peak of melanin and hemoglobin, giving it a hemostatic effect on soft tissue. At the same time, Nd:YAG laser radiation is poorly absorbed by water, allowing it to penetrate tissue to a depth of more than 5 mm. The benefits of the Nd:YAG laser also include its bactericidal and biostimulating properties. The positive effect of the Nd:YAG laser on cell proliferation and differentiation has also been demonstrated [<xref ref-type="bibr" rid="cit10">10</xref>][<xref ref-type="bibr" rid="cit11">11</xref>].</p><p>To study Nd:YAG laser tissue welding modes, Li et al. compared three techniques on porcine skin: continuous linear, zigzag, and segmented welding. The segmented method demonstrated superior outcomes, reducing thermal damage through intermittent exposure while preserving tissue regenerative potential. This approach achieved a weld strength of 0.37 MPa, outperforming linear (0.32 MPa) and zigzag methods, which exhibited energy concentration and heterogeneous joint strength, respectively [<xref ref-type="bibr" rid="cit12">12</xref>].</p><p>The study of the effect of the Nd:YAG laser suture temperature on the tensile strength of the suture and the degree of denaturation of the reconstructed tissue showed that the strength of the sutures is maximum at a suture formation temperature close to 55 °C. At a temperature of 65 °C, the degree of protein denaturation becomes too great and the tensile strength of the sutures decreases [<xref ref-type="bibr" rid="cit13">13</xref>].</p><p>The primary advantage of Nd:YAG lasers lies in their ability to penetrate deep into biological tissues. However, excessive energy density may cause uncontrolled thermal damage to surrounding tissues at depth. Consequently, the application of Nd:YAG lasers remains significantly limited in microsurgery and vascular surgery [<xref ref-type="bibr" rid="cit14">14</xref>].</p><p>In contrast, the carbon dioxide laser (CO₂ laser) with a wavelength of λ=10,600 nm has found predominant application in microsurgery fields. This wavelength corresponds to water’s peak absorption spectrum. Since water constitutes the primary component of most biological tissues, the laser energy gets predominantly absorbed in superficial tissue layers, with only exponentially diminishing energy available for deeper tissue heating [<xref ref-type="bibr" rid="cit15">15</xref>].</p><p>A CO2 laser system equipped with a fiber optic radiometer can be used for corneal integrity. Laser light is delivered via an optical fiber located directly over the treatment area. The system incorporates an infrared radiometer to monitor corneal temperature in real time, with the detector capturing thermal radiation from the tissue and transmitting the data to a computer. The laser targets only the superficial layers (less than 0.1 mm), thus avoiding damage to the deeper structures of the eye [<xref ref-type="bibr" rid="cit16">16</xref>].</p><p>The most widely used lasers for soldering biological tissues are diode lasers with various wavelengths. Typically, semiconductor systems are more compact and consume significantly less energy than other laser technologies. The radiation from diode lasers is easily transmitted through fiber-optic delivery systems, which is crucial for applications in endoscopic surgery. However, the use of diode lasers has certain limitations, as their peak output power is significantly lower than that of CO₂ and Nd:YAG lasers. This drawback is minimized through the use of bioorganic solders and dyes that enhance tissue absorption [<xref ref-type="bibr" rid="cit17">17</xref>].</p><p>In vascular surgery, an effective approach is the combination of a diode laser equipped with an optical fiber and a surgical microscope. One of the most commonly used wavelengths is λ = 810 ± 10 nm. This wavelength interacts efficiently with indocyanine green (ICG), a cyanine dye incorporated into a chitosan patch. Initially, single pulses (100 J cm²) were delivered to the tissue, with the fiber pressed firmly against the chitosan patch. Then, the patch was subjected to non-contact continuous-wave irradiation at an intensity of 20 W/cm² to ensure full adhesion of the patch to the outer vascular walls [<xref ref-type="bibr" rid="cit18">18</xref>].</p><p>In the medical laser field, 970 nm radiation is widely used, especially for vascular repair. These units are equipped with a diode laser and a precision positioning system including a moving table with coordinate control (x, y, z) and a focusing lens with a fixed working distance of 18 mm, which ensures a stable laser spot diameter of 1.0 mm. The control mechanism is facilitated by a foot switch that incorporates a timer, while the integrated video system, equipped with a zoom function and an IR sensor, enables precise real-time control of the beam position, thereby mitigating the impact of human error. This configuration ensures a high degree of precision with minimal risk of damage to surrounding tissues [<xref ref-type="bibr" rid="cit19">19</xref>].</p><p>To address the limited penetration depth of diode lasers, an intravascular approach was developed, utilizing a quartz fiber with a conical silver mirror to generate 360° ring radiation, delivered via a catheter to the anastomotic site. The procedure involved two sequential irradiation phases: primary soldering (0.41 W, 30 s, 1.52–4.1 W/cm²) followed by reinforced treatment with additional solder application (0.55 W, 45 s, 2.04–5.5 W/cm²). This method ensured uniform thermal diffusion across the vessel wall, achieving sutureless anastomotic integrity, as confirmed by histomorphological analysis demonstrating precise coaptation of vascular edges and controlled collagen denaturation within the irradiated zone [<xref ref-type="bibr" rid="cit20">20</xref>].</p><p>Diode lasers with wavelengths in the 1900–1950 nm range are increasingly used in microsurgery because their penetration depth closely matches the thickness of microvessel walls (about 150 μm), enabling precise, solder- and dye-free vascular welding. This wavelength is strongly absorbed by water, resulting in shallow tissue penetration and highly localized thermal effects, which minimizes collateral damage and allows for effective vessel sealing-making it ideal for delicate procedures like microanastomoses in hand surgery [<xref ref-type="bibr" rid="cit21">21</xref>][<xref ref-type="bibr" rid="cit22">22</xref>].</p><p>One of the most promising laser soldering technologies is the integration of temperature feedback into laser systems. Temperature feedback allows a preset temperature to be maintained in the weld area, preventing overheating and necrosis of the surrounding tissue. The basis of such systems is an infrared bolometric matrix sensor that scans the laser weld area and determines the temperature at the most heated point. The data received is transmitted to a microcontroller which, using a proportional-integral-differential controller, corrects the laser power to maintain the set temperature with high accuracy (up to 0.5°C). This avoids overheating the tissue and minimizes the thermal damage zone, providing optimal conditions for the formation of a strong and biocompatible joint. This technology is particularly effective in combination with biopolymer nanocomposite solders, as the feedback ensures uniform heating and stable transformation of the liquid dispersion into a solid framework material [<xref ref-type="bibr" rid="cit23">23</xref>].</p><p>A comparison of the main types of laser radiation used in laser reconstruction of biological tissues is presented in Table 1.</p><table-wrap id="table-1"><caption><p>Table 1. Comparison of laser systems for tissue reconstruction</p><p>Notes: Nd:YAG, neodymium-doped yttrium-aluminum garnet laser; CO₂, carbon dioxide laser</p></caption><table><tbody><tr><td>Laser type</td><td>Wavelength, nm</td><td>Penetration depth, mm</td><td>Main advantages</td><td>Restrictions</td><td>Application</td></tr><tr><td>Nd:YAG [10-14]</td><td>1064</td><td>&gt;5</td><td>Deep penetration, bactericidal properties</td><td>Risk of thermal damage</td><td>Dermatology</td></tr><tr><td>CO₂ [15][16]</td><td>10600</td><td>&lt;0.1</td><td>High precision, minimal damage to surrounding tissues</td><td>Limited depth of penetration</td><td>Microsurgery, ophthalmology</td></tr><tr><td>Diode (near infrared) [17-20][23]</td><td>810-970</td><td>1-3</td><td>Compactness, safety, low cost</td><td>Low capacity</td><td>Plastic surgery, nerve repair</td></tr><tr><td>Diode [21-22]</td><td>1900</td><td>0.15</td><td>Spot treatment, no solder required</td><td>Narrow therapeutic window</td><td>Vascular microsurgery</td></tr></tbody></table></table-wrap></sec><sec><title>Materials for optimizing laser tissue reconstruction</title><p>The use of bioorganic solders in laser tissue repair significantly increased the strength of welds, reduced thermal necrosis of tissues and accelerated the repair process [<xref ref-type="bibr" rid="cit23">23</xref>][<xref ref-type="bibr" rid="cit24">24</xref>].</p><p>Blood protein serum albumin is the most widely used as a base for bioorganic solders. In experiments, bovine serum albumin (BSA) [<xref ref-type="bibr" rid="cit13">13</xref>][<xref ref-type="bibr" rid="cit25">25</xref>][<xref ref-type="bibr" rid="cit26">26</xref>] and human serum albumin [<xref ref-type="bibr" rid="cit24">24</xref>] are most commonly used. Albumin is a class of water-soluble proteins that have a globular structure. Albumin is found in the tissues of almost all animals and plants. Albumin acts as a bacteriostatic coating that simultaneously promotes attachment and proliferation of eukaryotic cells. These properties make albumin a major component of bioorganic solders [<xref ref-type="bibr" rid="cit27">27</xref>].</p><p>In order to focus the laser impact in the incision zone and prevent thermal necrosis of the surrounding non-target tissues, a chromophore that absorbs the wavelength of laser radiation is added to the solder composition. The incorporation of chromophores enables the utilization of a more compact laser apparatus with reduced power, consequently reducing operational and financial expenditures while enhancing safety for the operating surgeon [<xref ref-type="bibr" rid="cit28">28</xref>].</p><p>The most successful combination in laser soldering of biological tissues involves the use of ICG aired with an 810 nm diode laser ICG is a non-toxic fluorescent iodide dye characterized by rapid hepatic clearance. This pairing has gained widespread adoption because the peak absorption wavelength of ICG (800 nm) closely aligns with the laser’s emission wavelength (810 nm), ensuring optimal energy absorption and efficient tissue bonding [28-30].</p><p>Another effective exogenous chromophore is methylene blue, which exhibits a peak absorption at 670 nm. methylene blue has found extensive use in oncology as a photosensitizer—when activated by laser irradiation, it promotes the destruction of cancer cells [<xref ref-type="bibr" rid="cit31">31</xref>].</p><p>However, chromophores have several limitations: low stability in aqueous solutions, tendency to migrate into surrounding tissues (increasing necrosis risk), and absorption dependency on concentration, pH, and temperature [<xref ref-type="bibr" rid="cit32">32</xref>]. To enhance stability, they are incorporated into biopolymer matrices such as chitosan. Chitosan films not only immobilize the dye but also promote healing by providing mechanical strength and electrical conductivity. Chitosan is a high-molecular-weight glucose polymer that is water-insoluble. Current research is actively exploring its applications in tissue engineering, gene therapy, and targeted drug delivery. ICG-doped chitosan films are used in laser-assisted end-to-end anastomosis. The anastomosis site is fully wrapped with a chitosan patch, which is then irradiated with a near-infrared laser [<xref ref-type="bibr" rid="cit33">33</xref>].</p><p>An alternative technology to prevent chromophore run off into the surrounding tissue walls is the creation of frameworks based on polycaprolactone (PCL) and ICG by electrospinning. Electrospinning represents a method for the production of fibers in the nano- and micrometer range that is undergoing active development. Electrospinning frameworks find application in targeted drug delivery [<xref ref-type="bibr" rid="cit34">34</xref>], tissue and cell engineering [<xref ref-type="bibr" rid="cit35">35</xref>], supporting cell adhesion and the delivery of growth factors, and promoting wound healing [<xref ref-type="bibr" rid="cit36">36</xref>].</p><p>To fabricate the PCL scaffold, PCL was first dissolved in chloroform while ICG was dissolved in methanol. Each solution was stirred for 24 hours to achieve homogeneity. The solutions were then combined to obtain a final ICG concentration of 0.1 wt.%. The soldering scaffolds were produced via electrospinning. A high voltage was applied to the polymer solution to generate a fluid jet, resulting in the formation of long, thin fibers. During deposition, the solvent evaporated, causing the fiber diameter to significantly decrease from 100 μm to 3-9 μm. The jet was ultimately deposited onto a grounded collector, forming a random non-woven fibrous scaffold. Prior to laser soldering, the fabricated scaffold was soaked in a 40 wt.% BSA solution and air-dried for 15 minutes. The resulting scaffolds were flexible and moderately adhesive, making them suitable for use around vascular anastomoses [<xref ref-type="bibr" rid="cit36">36</xref>].</p><p>Although polymer frameworks have greatly improved the efficiency of laser soldering, when PCL melts under laser irradiation, a significant portion of the chromophore penetrates into healthy tissue, leading to thermal necrosis [<xref ref-type="bibr" rid="cit37">37</xref>].</p><p>The development of research in the field of nanoscale particles has made a significant contribution to the improvement of modern medicine in general, and surgery in particular. Addition of nanoparticles to solder leads to increased absorption of laser radiation by solder, localization of irradiation in the area of weld formation and prevention of thermal damage to surrounding tissues</p><p>Encapsulating ICG silicon dioxide (SiO₂) nanoparticles prevented chromophore migration from the repair site into surrounding tissues and increased the tensile strength of welded joints [<xref ref-type="bibr" rid="cit33">33</xref>]. The porous nanoshells were created by polymerizing silicon around cetyltrimethylammonium bromide micelles. To counteract electrostatic repulsion between negatively charged ICG molecules and the SiO₂ nanoparticle framework, the nanoshells were coated with polyallylamine hydrochloride. The positively charged polyallylamine hydrochloride retains ICG within the pores through electrostatic attraction [<xref ref-type="bibr" rid="cit38">38</xref>].</p><p>Gold nanoparticles are widely used in tissue engineering due to their high absorption capacity, stability in physiological environments, and biochemical versatility[<xref ref-type="bibr" rid="cit33">33</xref>].Gold nanoparticles were employed to create a nanocomposite solder. Polyethylene glycol-modified gold nanorods were centrifuged in phosphate buffer. Hyaluronic acid was then added to the resulting suspension to achieve a final concentration of 3 wt.%. The solder mixture was continuously stirred for 48 hours to obtain a homogeneous burgundy paste. The gold nanorod-based solder demonstrated low diffusion through the tissue matrix and highly localized laser energy absorption at the weld site. But it should be taken into account that gold nanoparticles can aggregate in biological fluids, which reduces their photothermal efficiency and consistency of tissue repair [39-42].</p><p>The addition of carbon nanotubes (CNT) to solder not only addresses the issue of laser radiation localization in the welding zone but also significantly enhances the tensile strength of welded seams [<xref ref-type="bibr" rid="cit43">43</xref>]. Carbon nanotubes are actively used in regenerative medicine and diagnostics due to their size, which matches the main components of the cellular matrix, and their properties, which are comparable to protein structures [<xref ref-type="bibr" rid="cit44">44</xref>]. CNT-based biopolymers exhibit low cytotoxicity and have a positive effect on cell differentiation and proliferation [45-46].</p><p>A three-dimensional nanocomposite for tissue integrity restoration was obtained by irradiating a biopolymer dispersion based on BSA and CNT with a pulsed femtosecond laser at a wavelength of λ = 810 nm. To create the nanocomposite, single-walled carbon nanotubes (SWCNT) with an average diameter of 1.4–1.6 nm and a length of 0.3–0.8 μm were used. An aqueous dispersion of SWCNT with a concentration of 0.001 wt.% was mixed with BSA powder until a protein concentration of 25 wt.% was achieved. The mixture was then sonicated in an ultrasonic bath until complete homogenization (for 40–60 minutes). The dispersion was irradiated with an unfocused laser beam. The pulse duration was 140 fs, with a frequency of 80 MHz. The laser output power was set to 2 W [<xref ref-type="bibr" rid="cit47">47</xref>]. When using laser soldering technology for biological tissues in combination with this nanocomposite dispersion, the restoration strength achieved was 10 times higher than the tensile strength of sutures soldered using a solder based solely on BSA and ICG [<xref ref-type="bibr" rid="cit23">23</xref>].</p><p>A description of the main components of solders used in laser reconstruction of biological tissues is presented in Table 2.</p><table-wrap id="table-2"><caption><p>Table 2. Main compounds used in laser tissue reconstruction</p><p>Notes: BSA, bovine serum albumin; ICG, indocyanine green</p></caption><table><tbody><tr><td>Material</td><td>Purpose</td><td>Advantages</td><td>Disadvantages</td><td>Examples of applications</td></tr><tr><td>BSA [25-27]</td><td>Solder base, regeneration promoter</td><td>Biocompatibility, accessibility, promotion of cell proliferation</td><td>Low strength without additives</td><td>Vascular anastomoses, nerve repair</td></tr><tr><td>Chitosan [32][33]</td><td>Biopolymer matrix for solders</td><td>Biodegradability, antibacterial properties, healing promotion</td><td>Insoluble in water, requires modification</td><td>Anastomosis patches, drug delivery</td></tr><tr><td>ICG [28-30]</td><td>Chromophore for focusing the laser</td><td>High absorption at 800 nm, non-toxic, rapid clearance from the body</td><td>Migration into surrounding tissues, low stability</td><td>Plastic surgery, wound sealing</td></tr><tr><td>Carbon nanotubes [23][43-47]</td><td>Enhancing weld strength</td><td>High mechanical strength, biocompatibility, regeneration stimulation</td><td>Potential cytotoxicity at high doses</td><td>Reconstructing connective tissues</td></tr><tr><td>Gold nanoparticles [39-42]</td><td>Localization of laser action</td><td>Stability, high absorption capacity, biological inertness</td><td>Aggregation in physiological fluids</td><td>Skin reconstruction</td></tr><tr><td>Silicon nanoparticles [38]</td><td>Carrier for chromophores</td><td>Prevent dye migration, increase seam stability and strength</td><td>Complexity of synthesis, potential toxicity in case of improper functionalization</td><td>Vascular surgery, deep tissue soldering</td></tr></tbody></table></table-wrap></sec><sec><title>Practical application of laser tissue reconstruction technology</title><p>The gold standard in vascular anastomosis is the classic suture method, but this method of tissue repair is time-consuming and in many cases is associated with hypoxia and tissue damage, as the supply of oxygenated blood to the operated and surrounding vessels is cut off during suturing. In addition, the effectiveness of microsurgical sutures depends on the skills of the surgeon. Laser methods of vascular repair have an advantage over suturing because they reduce the risk of stenosis, foreign body reaction and inflammation, require less surgical time, are less traumatic to surrounding tissues and limit the thrombogenicity of the anastomosis. Laser soldering provides immediate watertight wound closure [<xref ref-type="bibr" rid="cit23">23</xref>][<xref ref-type="bibr" rid="cit48">48</xref>].</p><p>Studies on laser-assisted tissue repair were conducted on porcine aortas. The vessels were divided into identical rectangular samples with an area of 3 cm² and cleaned of excess connective tissue to achieve a sample thickness of approximately 1 mm. For vascular anastomosis, two samples were pressed firmly together, and a polyetherimide membrane soaked in a solution of BSA (2 wt.%) and ICG (0.002 wt.%) was applied. The membrane was positioned to overlap approximately 10% of the surrounding healthy tissue. The weld was then treated with a diode laser at a wavelength of λ = 810 nm and a temperature of 80°C for 30 seconds [<xref ref-type="bibr" rid="cit49">49</xref>].</p><p>The potential application of laser technologies for gum and oral mucosa restoration is being actively studied. For ex vivo experiments, pig gum tissue and oral soft tissues were used. The tissues were divided into samples with an area of 6 cm², and the average sample thickness was 1 mm. A 2 cm long incision was made in the center of each sample. ICG was applied to the incision, followed by exposure to laser radiation at a wavelength of λ = 808 nm. The results demonstrate that the use of an 808 nm diode laser in combination with ICG enables effective laser welding of oral soft tissues. The optimal bonding strength was achieved at an ICG concentration of 9% and a laser power of 4.5 W (10 Hz), with the weld strength comparable to that of conventional suturing. The average surface temperature reached 74 ± 5.4 °C, while the thermal damage zone remained within 333 μm. Histological analysis confirmed the localized thermal effect, indicating minimal collateral tissue damage [<xref ref-type="bibr" rid="cit50">50</xref>].</p><p>Peripheral nerve injuries are one of the most common consequences of motor vehicle accidents and work-related injuries, resulting in sensory and motor impairment. Despite the advances made in neurosurgery over the last 10 years, effective reconstruction of peripheral nerve injuries is still a major challenge in regenerative medicine. A comparison of sciatic nerve repair using traditional needle-and-thread sutures versus an 810 nm diode laser (500 mW) with a protein solder based on 25 wt.% ICG and 62 wt.% BSA showed that the average operation time was significantly shorter in the laser repair group compared to the suture group. Electromyography revealed no differences between the experimental groups. However, the sciatic nerve function index was significantly better in the laser-repaired nerves compared to sutured nerves after 12 weeks. Histological evaluation showed no difference in inflammatory processes between the groups but demonstrated faster and more effective restoration of the peripheral nerve outer layer (epineurium) following laser repair compared to the suture method [<xref ref-type="bibr" rid="cit51">51</xref>].</p><p>The most dangerous postoperative complication in thoracic surgery is alveolar air leaks. However, there is still no optimal method for eliminating leaks. Laser soldering enables the formation of airtight seams, overcoming the limitations of traditional suturing. For lung sealing, a semiconductor pulsed diode laser with a wavelength of 808 nm was used in combination with a semi-solid solder based on 50 wt.% BSA and 0.1 wt.% ICG. In vivo studies were conducted on 14 pigs, where two types of lung injuries were created: a linear incision and a circular incision. The protein solder was applied to the incision site and irradiated with the laser. In all cases of laser repair (except for two requiring repeat closure), no postoperative air leaks were detected. By the seventh day, all animals showed complete healing of the lung lesions with fibrous scar formation and only minor inflammatory reaction in the adjacent lung tissue [<xref ref-type="bibr" rid="cit52">52</xref>].</p><p>Due to its ability to rapidly provide tight wound closure, laser soldering is suitable for leak prevention in gastrointestinal surgical treatment. A gold-based nanocomposite solder (Au nanorods) and collagen at a wavelength of 800 nm was used for laser soldering. The pulsed mode of laser sealing with a pulse duration of 130 fs and an interval of 12.5 ns ensures minimal heating of adjacent tissues, which prevents thermal damage. As a result, the suture strength reaches 42% of the natural tissue strength, and the tightness is 64% of the physiologic norm [<xref ref-type="bibr" rid="cit53">53</xref>].</p><p>One of the most promising applications of laser-assisted tissue repair is in plastic surgery, as laser soldering enables precise suture formation without scar formation. Studies, including experimental work on rats, have demonstrated that laser-assisted edge joining using solder composed of BSA, ICG, and SWCNT results in significantly less noticeable scarring. For instance, Scar assessment scale evaluation on postoperative day 21 showed only 1 point for the laser method compared to 4 points for conventional sutures. Laser treatment stimulates healing processes, as confirmed by histological data: experimental groups exhibited earlier appearance of hair follicles and reduced inflammatory infiltration compared to control groups [<xref ref-type="bibr" rid="cit54">54</xref>].</p></sec><sec><title>Discussion</title><p>Improvement of laser systems, aimed at the introduction of temperature feedback, providing precise control of tissue heating (up to 0.5 °C) and minimizing thermal damage. Integration of Proportional–integral–derivative controller and infrared sensors allows to optimize the soldering process safety and efficiency of the technique.</p><p>To increase the strength of laser repair and enhance the proliferative properties of repaired tissues, new generation biocomposite solders include albumin, collagen, carbon nanotubes and nanoparticles (gold, SiO₂). These materials not only increase connection strength (up to 4±0.4 MPa), but also stimulate tissue regeneration, shortening healing time. Innovative approaches, such as encapsulation of dyes in nanoparticles or polymer matrices, solve the problem of chromophore migration and reduce the risk of necrosis of surrounding tissues.</p><p>At this stage of development, laser reconstruction is moving towards personalized solutions, including the selection of laser parameters and solder composition for different tissue types. This trend is supported by the development of machine learning to predict weld strength and optimize exposure modes [<xref ref-type="bibr" rid="cit55">55</xref>].</p><p>Despite the successes, challenges remain, such as standardization of techniques, ensuring long-term stability of compounds, and scaling of technologies for mass clinical application. Further research should focus on: in-depth study of molecular mechanisms of regeneration under laser exposure, development of universal biosimilars with programmable properties, and multicenter clinical trials.</p></sec><sec><title>Conclusion</title><p>Contemporary technologies of laser restoration of biological tissues demonstrate rapid development, opening new perspectives for reconstructive and plastic surgery.</p><p>Laser reconstruction of tissue is bringing the era of sutureless surgery closer, where precision, minimal invasiveness and aesthetics are becoming the standard. Already transforming approaches to wound care and reconstructive surgery, this technology may become the gold standard in plastic and microsurgery in the near future.</p></sec></body><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Basov S, Milstein A, Sulimani E, Platkov M, Peretz E, Rattunde M, Wagner J. Netz. U, Katzir A, Nisky I. Robot-assisted laser tissue soldering system. Biomed. Opt. Express. 2018;9(12):5635-5644. https://doi.org/10.1364/BOE.9.005635.</mixed-citation><mixed-citation xml:lang="en">Basov S, Milstein A, Sulimani E, Platkov M, Peretz E, Rattunde M, Wagner J. Netz. U, Katzir A, Nisky I. Robot-assisted laser tissue soldering system. Biomed. Opt. Express. 2018;9(12):5635-5644. https://doi.org/10.1364/BOE.9.005635.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Legres LG, Chamot C, Varna M, Janin A. The Laser Technology: New Trends in Biology and Medicine. J. Mod. Phys. 2014;5(5):330-337. https://doi.org/10.4236/jmp.2014.55037</mixed-citation><mixed-citation xml:lang="en">Legres LG, Chamot C, Varna M, Janin A. The Laser Technology: New Trends in Biology and Medicine. J. Mod. Phys. 2014;5(5):330-337. https://doi.org/10.4236/jmp.2014.55037</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Prahl SA, Pearson SD. Rate process models for thermal welding. Laser-Tissue Interaction VIII. 1997;2975:245-252. https://doi.org/10.1117/12.275486.</mixed-citation><mixed-citation xml:lang="en">Prahl SA, Pearson SD. Rate process models for thermal welding. Laser-Tissue Interaction VIII. 1997;2975:245-252. https://doi.org/10.1117/12.275486.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Le Lous M, Flandin F, Herbage D, Allain JC. Influence of collagen denaturation on the chemorheological properties of skin, assessed by differential scanning calorimetry and hydrothermal isometric tension measurement. Biochim Biophys Acta Gen Subj. 1982;717(2):295-300. https://doi.org/10.1016/0304-4165(82)90182-9.</mixed-citation><mixed-citation xml:lang="en">Le Lous M, Flandin F, Herbage D, Allain JC. Influence of collagen denaturation on the chemorheological properties of skin, assessed by differential scanning calorimetry and hydrothermal isometric tension measurement. Biochim Biophys Acta Gen Subj. 1982;717(2):295-300. https://doi.org/10.1016/0304-4165(82)90182-9.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Bianchi L, Cavarzan F, Ciampitti L, Cremonesi M, Grilli F, Saccomandi P. Thermophysical and mechanical properties of biological tissues as a function of temperature: a systematic literature review. Int J Hyperthermia. 2022;39(1):297-340. https://doi.org/10.1080/02656736.2022.2028908.</mixed-citation><mixed-citation xml:lang="en">Bianchi L, Cavarzan F, Ciampitti L, Cremonesi M, Grilli F, Saccomandi P. Thermophysical and mechanical properties of biological tissues as a function of temperature: a systematic literature review. Int J Hyperthermia. 2022;39(1):297-340. https://doi.org/10.1080/02656736.2022.2028908.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Bass LS, Moazami N, Pocsidio J, Oz MC, Logerfo P, Treat MR. Changes in type I collagen following laser welding. Lasers Surg Med. 1992;12(5):500-505. https://doi.org/10.1002/lsm.1900120508.</mixed-citation><mixed-citation xml:lang="en">Bass LS, Moazami N, Pocsidio J, Oz MC, Logerfo P, Treat MR. Changes in type I collagen following laser welding. Lasers Surg Med. 1992;12(5):500-505. https://doi.org/10.1002/lsm.1900120508.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Small IV W, Celliers P, Kopchok G. Temperature feedback and collagen crosslinking in argon laser vascular welding. Lasers Med Sci. 1998;13:98-105. https://doi.org/10.1007/s101030050061.</mixed-citation><mixed-citation xml:lang="en">Small IV W, Celliers P, Kopchok G. Temperature feedback and collagen crosslinking in argon laser vascular welding. Lasers Med Sci. 1998;13:98-105. https://doi.org/10.1007/s101030050061.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Schober R, Ulrich F, Sander T, Dürselen H, Hessel S. Laser-induced alteration of collagen substructure allows microsurgical tissue welding. Science. 1986;232(4756):1421-1422. https://doi.org/10.1126/science.3715454.</mixed-citation><mixed-citation xml:lang="en">Schober R, Ulrich F, Sander T, Dürselen H, Hessel S. Laser-induced alteration of collagen substructure allows microsurgical tissue welding. Science. 1986;232(4756):1421-1422. https://doi.org/10.1126/science.3715454.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Mushaben M, Urie R, Flake T, Jaffe M, Rege K, Heys J. Spatiotemporal modeling of laser tissue soldering using photothermal nanocomposites. Lasers Surg. Med. 2018;50(2):143-152. https://doi.org/10.1002/lsm.22746.</mixed-citation><mixed-citation xml:lang="en">Mushaben M, Urie R, Flake T, Jaffe M, Rege K, Heys J. Spatiotemporal modeling of laser tissue soldering using photothermal nanocomposites. Lasers Surg. Med. 2018;50(2):143-152. https://doi.org/10.1002/lsm.22746.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Vescovi P, Merigo E, Fornaini C, Rocca J, Nammour S. Thermal increase in the oral mucosa and in the jawbone during Nd:YAG laser applications: ex vivo study. Med Oral Patol Oral Cir Bucal. 2012;17(4):e697-e704. https://doi.org/10.4317/medoral.17726.</mixed-citation><mixed-citation xml:lang="en">Vescovi P, Merigo E, Fornaini C, Rocca J, Nammour S. Thermal increase in the oral mucosa and in the jawbone during Nd:YAG laser applications: ex vivo study. Med Oral Patol Oral Cir Bucal. 2012;17(4):e697-e704. https://doi.org/10.4317/medoral.17726.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Pirnat S, Lukac M, Ihan A. Study of the direct bactericidal effect of Nd:YAG and diode laser parameters used in endodontics on pigmented and nonpigmented bacteria. Lasers Med Sci. 2011;26:755-761. https://doi.org/10.1007/s10103-010-0808-7.</mixed-citation><mixed-citation xml:lang="en">Pirnat S, Lukac M, Ihan A. Study of the direct bactericidal effect of Nd:YAG and diode laser parameters used in endodontics on pigmented and nonpigmented bacteria. Lasers Med Sci. 2011;26:755-761. https://doi.org/10.1007/s10103-010-0808-7.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Li C, Wang K, Huang J. Effect of scanning modes on the tensile strength and stability in laser skin welding in vitro. Optik. 2019;179:408-412. https://doi.org/10.1016/j.ijleo.2018.10.037.</mixed-citation><mixed-citation xml:lang="en">Li C, Wang K, Huang J. Effect of scanning modes on the tensile strength and stability in laser skin welding in vitro. Optik. 2019;179:408-412. https://doi.org/10.1016/j.ijleo.2018.10.037.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Li C, Wang K. Effect of welding temperature and protein denaturation on strength of laser biological tissue welding. Opt Laser Technol. 2021;138:106862. https://doi.org/10.1016/j.optlastec.2020.106862.</mixed-citation><mixed-citation xml:lang="en">Li C, Wang K. Effect of welding temperature and protein denaturation on strength of laser biological tissue welding. Opt Laser Technol. 2021;138:106862. https://doi.org/10.1016/j.optlastec.2020.106862.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Gomes DF, Galvão I, Loja MAR. Overview on the evolution of laser welding of vascular and nervous tissues. Appl Sci. 2019;9(10):2157. https://doi.org/10.3390/app9102157.</mixed-citation><mixed-citation xml:lang="en">Gomes DF, Galvão I, Loja MAR. Overview on the evolution of laser welding of vascular and nervous tissues. Appl Sci. 2019;9(10):2157. https://doi.org/10.3390/app9102157.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Gil Z, Shaham A, Vasilyev T, Brosh T, Forer B, Katzir A, &amp; Fliss DM. Novel laser tissue-soldering technique for dural reconstruction. J Neurosurg. 2005;103(1):87-91. https://doi.org/10.3171/jns.2005.103.1.0087.</mixed-citation><mixed-citation xml:lang="en">Gil Z, Shaham A, Vasilyev T, Brosh T, Forer B, Katzir A, &amp; Fliss DM. Novel laser tissue-soldering technique for dural reconstruction. J Neurosurg. 2005;103(1):87-91. https://doi.org/10.3171/jns.2005.103.1.0087.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Strassmann E, Livny E, Loy N, Kariv N, Ravid A, Katzir A, Gaton DD. CO2 laser welding of corneal cuts with albumin solder using radiometric temperature control. Ophthalmic Res. 2013;50:174-179. https://doi.org/10.1159/000353436.</mixed-citation><mixed-citation xml:lang="en">Strassmann E, Livny E, Loy N, Kariv N, Ravid A, Katzir A, Gaton DD. CO2 laser welding of corneal cuts with albumin solder using radiometric temperature control. Ophthalmic Res. 2013;50:174-179. https://doi.org/10.1159/000353436.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Ashbell I, Agam N, Katzir A, Basov S, Platkov M, Avital I, Netz U. Laser tissue soldering of the gastrointestinal tract: A systematic review. Heliyon. 2023;9(5):e16018. https://doi.org/10.1016/j.heliyon.2023.e16018.</mixed-citation><mixed-citation xml:lang="en">Ashbell I, Agam N, Katzir A, Basov S, Platkov M, Avital I, Netz U. Laser tissue soldering of the gastrointestinal tract: A systematic review. Heliyon. 2023;9(5):e16018. https://doi.org/10.1016/j.heliyon.2023.e16018.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Rossi F, Matteini P, Ratto F, Pini R, Esposito G, Albanese A, et al. Experimental study on laser assisted vascular repair and anastomosis with ICG-infused chitosan films. In: 2011 International Workshop on Biophotonics; June 2011; 1-3. https://doi.org/10.1109/IWBP.2011.5954804.</mixed-citation><mixed-citation xml:lang="en">Rossi F, Matteini P, Ratto F, Pini R, Esposito G, Albanese A, et al. Experimental study on laser assisted vascular repair and anastomosis with ICG-infused chitosan films. In: 2011 International Workshop on Biophotonics; June 2011; 1-3. https://doi.org/10.1109/IWBP.2011.5954804.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Nakadate R, Omori S, Ikeda T, Akahoshi T, Oguri S, Arata J, et al. Improving the strength of sutureless laser-assisted vessel repair using preloaded longitudinal compression on tissue edge. Lasers Surg Med. 2017;49(5):533-538. https://doi.org/10.1002/lsm.22621.</mixed-citation><mixed-citation xml:lang="en">Nakadate R, Omori S, Ikeda T, Akahoshi T, Oguri S, Arata J, et al. Improving the strength of sutureless laser-assisted vessel repair using preloaded longitudinal compression on tissue edge. Lasers Surg Med. 2017;49(5):533-538. https://doi.org/10.1002/lsm.22621.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Ott B, Constantinescu MA, Erni D, Banic A, Schaffner T, Frenz M. Intraluminal laser light source and external solder: in vivo evaluation of a new technique for microvascular anastomosis. Lasers Surg Med. 2004;35(4):312-316. https://doi.org/10.1002/lsm.20096.</mixed-citation><mixed-citation xml:lang="en">Ott B, Constantinescu MA, Erni D, Banic A, Schaffner T, Frenz M. Intraluminal laser light source and external solder: in vivo evaluation of a new technique for microvascular anastomosis. Lasers Surg Med. 2004;35(4):312-316. https://doi.org/10.1002/lsm.20096.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Leclère FM, Schoofs M, Vogt P, Mordon S. 1950-nm diode laser-assisted microanastomoses (LAMA): an innovative surgical tool for hand surgery emergencies. Lasers Med Sci. 2015;30(4): 1269-1273. https://doi.org/10.1007/s10103-015-1711-z.</mixed-citation><mixed-citation xml:lang="en">Leclère FM, Schoofs M, Vogt P, Mordon S. 1950-nm diode laser-assisted microanastomoses (LAMA): an innovative surgical tool for hand surgery emergencies. Lasers Med Sci. 2015;30(4): 1269-1273. https://doi.org/10.1007/s10103-015-1711-z.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Leclère FM, Vogt P, Schoofs M, Delattre M, Mordon S. Current laser applications in reconstructive microsurgery: a review of the literature. J Cosmet Laser Ther. 2016;18(3):130-133. https://doi.org/10.3109/14764172.2015.1114640.</mixed-citation><mixed-citation xml:lang="en">Leclère FM, Vogt P, Schoofs M, Delattre M, Mordon S. Current laser applications in reconstructive microsurgery: a review of the literature. J Cosmet Laser Ther. 2016;18(3):130-133. https://doi.org/10.3109/14764172.2015.1114640.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Gerasimenko AY, Morozova EA, Ryabkin DI, Fayzullin A, Tarasenko SV, Molodykh VV, et al. Reconstruction of soft biological tissues using laser soldering technology with temperature control and biopolymer nanocomposites. Bioengineering (Basel). 2022;9(6):238. https://doi.org/10.3390/bioengineering9060238.</mixed-citation><mixed-citation xml:lang="en">Gerasimenko AY, Morozova EA, Ryabkin DI, Fayzullin A, Tarasenko SV, Molodykh VV, et al. Reconstruction of soft biological tissues using laser soldering technology with temperature control and biopolymer nanocomposites. Bioengineering (Basel). 2022;9(6):238. https://doi.org/10.3390/bioengineering9060238.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Mistry YA, Natarajan SS, Ahuja SA. Evaluation of Laser Tissue Welding and LaserTissue Soldering for Mucosal and Vascular Repair. Annals of Maxillofacial Surgery. 2018;8(1):35-41. https://doi.org/10.4103/ams.ams_147_17.</mixed-citation><mixed-citation xml:lang="en">Mistry YA, Natarajan SS, Ahuja SA. Evaluation of Laser Tissue Welding and LaserTissue Soldering for Mucosal and Vascular Repair. Annals of Maxillofacial Surgery. 2018;8(1):35-41. https://doi.org/10.4103/ams.ams_147_17.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Ryabkin DI, Rimshan IB, Gerasimenko AY, Pyankov ES, Zar VV. Research of dependence of the laser weld tensile strength on the protein denaturation temperature, which is part of the solder. In: 2017 IEEE Conference of Russian Young Researchers in Electrical and Electronic Engineering (EIConRus); February 2017; St. Petersburg, Russia. p68-70. https://doi.org/10.1109/EIConRus.2017.7910494.</mixed-citation><mixed-citation xml:lang="en">Ryabkin DI, Rimshan IB, Gerasimenko AY, Pyankov ES, Zar VV. Research of dependence of the laser weld tensile strength on the protein denaturation temperature, which is part of the solder. In: 2017 IEEE Conference of Russian Young Researchers in Electrical and Electronic Engineering (EIConRus); February 2017; St. Petersburg, Russia. p68-70. https://doi.org/10.1109/EIConRus.2017.7910494.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Jawale SA. Suture-less circumcision by glutaraldehyde albumin glue enhanced laser tissue welding-a comparative study. Open J Urol. 2019;9(7):107. https://doi.org/10.4236/oju.2019.97013.</mixed-citation><mixed-citation xml:lang="en">Jawale SA. Suture-less circumcision by glutaraldehyde albumin glue enhanced laser tissue welding-a comparative study. Open J Urol. 2019;9(7):107. https://doi.org/10.4236/oju.2019.97013.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Tal K, Strassmann E, Loya N, Ravid A, Kariv N, Weinberger D, et al. Corneal cut closure using temperature-controlled CO2 laser soldering system. Lasers Med Sci. 2015;30:1367-1371. https://doi.org/10.1007/s10103-015-1737-2.</mixed-citation><mixed-citation xml:lang="en">Tal K, Strassmann E, Loya N, Ravid A, Kariv N, Weinberger D, et al. Corneal cut closure using temperature-controlled CO2 laser soldering system. Lasers Med Sci. 2015;30:1367-1371. https://doi.org/10.1007/s10103-015-1737-2.</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Gerasimenko AY, Ichkitidze LP, Piyankov ES, Pyanov IV, Rimshan IB, Ryabkin DI, et al. Use of indocyanine green in nanocomposite solders to increase strength and homogeneity in laser welding of tendons. Biomed Eng. 2017;50:310-313. https://doi.org/10.1007/s10527-017-9644-4.</mixed-citation><mixed-citation xml:lang="en">Gerasimenko AY, Ichkitidze LP, Piyankov ES, Pyanov IV, Rimshan IB, Ryabkin DI, et al. Use of indocyanine green in nanocomposite solders to increase strength and homogeneity in laser welding of tendons. Biomed Eng. 2017;50:310-313. https://doi.org/10.1007/s10527-017-9644-4.</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Wu T, Li H, Xue J, Mo X, Xia Y. Photothermal welding, melting, and patterned expansion of nonwoven mats of polymer nanofibers for biomedical and printing applications. Angew Chem Int Ed Engl. 2019;58(46):16416-16421. https://doi.org/10.1002/anie.201907876.</mixed-citation><mixed-citation xml:lang="en">Wu T, Li H, Xue J, Mo X, Xia Y. Photothermal welding, melting, and patterned expansion of nonwoven mats of polymer nanofibers for biomedical and printing applications. Angew Chem Int Ed Engl. 2019;58(46):16416-16421. https://doi.org/10.1002/anie.201907876.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Lim ZY, Mohan S, Balasubramaniam S, Ahmed S, Siew CCH, Shelat VG. Indocyanine green dye and its application in gastrointestinal surgery: the future is bright green. World J Gastrointest Surg. 2023;15(9):1841-1857. https://doi.org/10.4240/wjgs.v15.i9.1841.</mixed-citation><mixed-citation xml:lang="en">Lim ZY, Mohan S, Balasubramaniam S, Ahmed S, Siew CCH, Shelat VG. Indocyanine green dye and its application in gastrointestinal surgery: the future is bright green. World J Gastrointest Surg. 2023;15(9):1841-1857. https://doi.org/10.4240/wjgs.v15.i9.1841.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Khan I, Saeed K, Zekker I, Zhang B, Hendi AH., Ahmad A, et al. Review on methylene blue: its properties, uses, toxicity and photodegradation. Water (Basel). 2022;14(2):242. https://doi.org/10.3390/w14020242.</mixed-citation><mixed-citation xml:lang="en">Khan I, Saeed K, Zekker I, Zhang B, Hendi AH., Ahmad A, et al. Review on methylene blue: its properties, uses, toxicity and photodegradation. Water (Basel). 2022;14(2):242. https://doi.org/10.3390/w14020242.</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Rau I, Tane A, Zgarian R, Meghea A, Grote JG, et al. Stability of Selected Chromophores in Biopolymer Matrix. Molecular Crystals and Liquid Crystals. 2012;554(1):43- 55. https://doi.org/10.1080/15421406.2012.633025.</mixed-citation><mixed-citation xml:lang="en">Rau I, Tane A, Zgarian R, Meghea A, Grote JG, et al. Stability of Selected Chromophores in Biopolymer Matrix. Molecular Crystals and Liquid Crystals. 2012;554(1):43- 55. https://doi.org/10.1080/15421406.2012.633025.</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Esposito G, Rossi F, Matteini P, Scerrati A, Puca A, Albanese A, et al. In vivo laser assisted microvascular repair and end-to-end anastomosis by means of indocyanine green-infused chitosan patches: a pilot study. Lasers Surg Med. 2013;45(5):318-325. https://doi.org/10.1002/lsm.22145.</mixed-citation><mixed-citation xml:lang="en">Esposito G, Rossi F, Matteini P, Scerrati A, Puca A, Albanese A, et al. In vivo laser assisted microvascular repair and end-to-end anastomosis by means of indocyanine green-infused chitosan patches: a pilot study. Lasers Surg Med. 2013;45(5):318-325. https://doi.org/10.1002/lsm.22145.</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Torres-Martínez E.J, Cornejo Bravo JM, Serrano Medina A, Pérez González GL, Villarreal Gómez LJ. A summary of electrospun nanofibers as drug delivery system: drugs loaded and biopolymers used as matrices. Curr Drug Deliv. 2018;15(10):1360- 1374. https://doi.org/10.2174/1567201815666180723114326.</mixed-citation><mixed-citation xml:lang="en">Torres-Martínez E.J, Cornejo Bravo JM, Serrano Medina A, Pérez González GL, Villarreal Gómez LJ. A summary of electrospun nanofibers as drug delivery system: drugs loaded and biopolymers used as matrices. Curr Drug Deliv. 2018;15(10):1360- 1374. https://doi.org/10.2174/1567201815666180723114326.</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Ivanov D. Methods and challenges in the fabrication of biopolymer-based scaffolds for tissue engineering application. In: Functional Biomaterials: Design and Development for Biotechnology, Pharmacology, and Biomedicine. 1st ed. Wiley-VCH; 2023:335-370. https://doi.org/10.1002/9783527827657.ch11.</mixed-citation><mixed-citation xml:lang="en">Ivanov D. Methods and challenges in the fabrication of biopolymer-based scaffolds for tissue engineering application. In: Functional Biomaterials: Design and Development for Biotechnology, Pharmacology, and Biomedicine. 1st ed. Wiley-VCH; 2023:335-370. https://doi.org/10.1002/9783527827657.ch11.</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Hu Z, Qin Z, Qu Y, Wang F, Huang B, Chen G, et al. Cell electrospinning and its application in wound healing: principles, techniques and prospects. Burns Trauma. 2023;11:tkad028. https://doi.org/10.1093/burnst/tkad028.</mixed-citation><mixed-citation xml:lang="en">Hu Z, Qin Z, Qu Y, Wang F, Huang B, Chen G, et al. Cell electrospinning and its application in wound healing: principles, techniques and prospects. Burns Trauma. 2023;11:tkad028. https://doi.org/10.1093/burnst/tkad028.</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Bregy A, Bogni S, Bernau VJ, Vajtai I, Vollbach F, Petri-Fink A, et al. Solder doped polycaprolactone scaffold enables reproducible laser tissue soldering. Lasers in Surgery and Medicine. 2008;40(10):716-725. https://doi.org/10.1002/lsm.20710.</mixed-citation><mixed-citation xml:lang="en">Bregy A, Bogni S, Bernau VJ, Vajtai I, Vollbach F, Petri-Fink A, et al. Solder doped polycaprolactone scaffold enables reproducible laser tissue soldering. Lasers in Surgery and Medicine. 2008;40(10):716-725. https://doi.org/10.1002/lsm.20710.</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Schöni DS, Bogni S, Bregy A, Wirth A, Raabe A, Vajtai I, et al. Nanoshell assisted laser soldering of vascular tissue. Lasers in Surgery and Medicine. 2011;43(10):975- 983. https://doi.org/10.1002/lsm.21140.</mixed-citation><mixed-citation xml:lang="en">Schöni DS, Bogni S, Bregy A, Wirth A, Raabe A, Vajtai I, et al. Nanoshell assisted laser soldering of vascular tissue. Lasers in Surgery and Medicine. 2011;43(10):975- 983. https://doi.org/10.1002/lsm.21140.</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Matteini P, Ratto F, Rossi F, Pini R. Laser-activated nano-biomaterials for tissue repair and controlled drug release. Quantum Electronics. 2014;44(7):675. https://doi.org/10.1070/QE2014v044n07ABEH015484.</mixed-citation><mixed-citation xml:lang="en">Matteini P, Ratto F, Rossi F, Pini R. Laser-activated nano-biomaterials for tissue repair and controlled drug release. Quantum Electronics. 2014;44(7):675. https://doi.org/10.1070/QE2014v044n07ABEH015484.</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Frost SJ, Mawad D, Hook J, Lauto A. Micro- and nanostructured biomaterials for sutureless tissue repair. Adv Healthc Mater. 2016;5(4):401-414. https://doi.org/10.1002/adhm.201500589.</mixed-citation><mixed-citation xml:lang="en">Frost SJ, Mawad D, Hook J, Lauto A. Micro- and nanostructured biomaterials for sutureless tissue repair. Adv Healthc Mater. 2016;5(4):401-414. https://doi.org/10.1002/adhm.201500589.</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Matteini P, Ratto F, Rossi F, Pini R. Emerging concepts of laser-activated nanoparticles for tissue bonding. J Biomed Opt. 2012;17(1):010701. https://doi.org/10.1117/1.JBO.17.1.010701.</mixed-citation><mixed-citation xml:lang="en">Matteini P, Ratto F, Rossi F, Pini R. Emerging concepts of laser-activated nanoparticles for tissue bonding. J Biomed Opt. 2012;17(1):010701. https://doi.org/10.1117/1.JBO.17.1.010701.</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Cai Z, Zhang H, Wei Y, Cong F. Hyaluronan-inorganic nanohybrid materials for biomedical applications. Biomacromolecules. 2017;18(6):1677-1696. https://doi.org/10.1021/acs.biomac.7b00424.</mixed-citation><mixed-citation xml:lang="en">Cai Z, Zhang H, Wei Y, Cong F. Hyaluronan-inorganic nanohybrid materials for biomedical applications. Biomacromolecules. 2017;18(6):1677-1696. https://doi.org/10.1021/acs.biomac.7b00424.</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Gerasimenko AY, Gubar’kov OV, Ichkitidze LP, Podgaetskii VM, Selishchev SV, Ponomareva OV. Nanocomposite solder for laser welding of biological tissues. Semiconductors. 2011;45:1713-1718. https://doi.org/10.1134/S1063782611130112.</mixed-citation><mixed-citation xml:lang="en">Gerasimenko AY, Gubar’kov OV, Ichkitidze LP, Podgaetskii VM, Selishchev SV, Ponomareva OV. Nanocomposite solder for laser welding of biological tissues. Semiconductors. 2011;45:1713-1718. https://doi.org/10.1134/S1063782611130112.</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Gerasimenko AY, Ichkitidze LP, Podgaetsky VM, Selishchev SV. Biomedical applications of promising nanomaterials with carbon nanotubes. Biomed Eng. 2015;48(6):310-314. https://doi.org/0006-3398/15/4806-0310.</mixed-citation><mixed-citation xml:lang="en">Gerasimenko AY, Ichkitidze LP, Podgaetsky VM, Selishchev SV. Biomedical applications of promising nanomaterials with carbon nanotubes. Biomed Eng. 2015;48(6):310-314. https://doi.org/0006-3398/15/4806-0310.</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Sun Y, Liu X, George MN, Park S, Gaihre B, Terzic A, Lu L. Enhanced nerve cell proliferation and differentiation on electrically conductive scaffolds embedded with graphene and carbon nanotubes. J Biomed Mater Res A. 2021;109(2):193-206. https://doi.org/10.1002/jbm.a.37016.</mixed-citation><mixed-citation xml:lang="en">Sun Y, Liu X, George MN, Park S, Gaihre B, Terzic A, Lu L. Enhanced nerve cell proliferation and differentiation on electrically conductive scaffolds embedded with graphene and carbon nanotubes. J Biomed Mater Res A. 2021;109(2):193-206. https://doi.org/10.1002/jbm.a.37016.</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Ye L, Ji H, Liu J, Tu CH, Kappl M, Koynov K, et al. Carbon nanotube-hydrogel composites facilitate neuronal differentiation while maintaining homeostasis of network activity. Adv Mater. 2021;33(41):2102981. https://doi.org/10.1002/adma.202102981.</mixed-citation><mixed-citation xml:lang="en">Ye L, Ji H, Liu J, Tu CH, Kappl M, Koynov K, et al. Carbon nanotube-hydrogel composites facilitate neuronal differentiation while maintaining homeostasis of network activity. Adv Mater. 2021;33(41):2102981. https://doi.org/10.1002/adma.202102981.</mixed-citation></citation-alternatives></ref><ref id="cit47"><label>47</label><citation-alternatives><mixed-citation xml:lang="ru">Gerasimenko AY, Glukhova OE, Savostyanov GV, Podgaetsky VM. Laser structuring of carbon nanotubes in the albumin matrix for the creation of composite biostructures. J Biomed Opt. 2017;22(6):065003. https://doi.org/10.1117/1.JBO.22.6.065003.</mixed-citation><mixed-citation xml:lang="en">Gerasimenko AY, Glukhova OE, Savostyanov GV, Podgaetsky VM. Laser structuring of carbon nanotubes in the albumin matrix for the creation of composite biostructures. J Biomed Opt. 2017;22(6):065003. https://doi.org/10.1117/1.JBO.22.6.065003.</mixed-citation></citation-alternatives></ref><ref id="cit48"><label>48</label><citation-alternatives><mixed-citation xml:lang="ru">Wang M, Guo H, Zhang G, Ruan P, Zhi K. Development and Innovation of Modern Microvascular Anastomoses. Journal of Biosciences and Medicines. 2024;12:105- 118. https://doi.org/10.4236/jbm.2024.1210011.</mixed-citation><mixed-citation xml:lang="en">Wang M, Guo H, Zhang G, Ruan P, Zhi K. Development and Innovation of Modern Microvascular Anastomoses. Journal of Biosciences and Medicines. 2024;12:105- 118. https://doi.org/10.4236/jbm.2024.1210011.</mixed-citation></citation-alternatives></ref><ref id="cit49"><label>49</label><citation-alternatives><mixed-citation xml:lang="ru">Hiebl B, Ascher L, Luetzow K, Kratz K, Gruber C, Mrowietz C, et al. Albumin solder covalently bound to a polymer membrane: new approach to improve binding strength in laser tissue soldering in-vitro. Clin Hemorheol Microcirc. 2018;69(12):317-326. https://doi.org/10.3233/CH-189108.</mixed-citation><mixed-citation xml:lang="en">Hiebl B, Ascher L, Luetzow K, Kratz K, Gruber C, Mrowietz C, et al. Albumin solder covalently bound to a polymer membrane: new approach to improve binding strength in laser tissue soldering in-vitro. Clin Hemorheol Microcirc. 2018;69(12):317-326. https://doi.org/10.3233/CH-189108.</mixed-citation></citation-alternatives></ref><ref id="cit50"><label>50</label><citation-alternatives><mixed-citation xml:lang="ru">Rasca E, Nyssen-Behets C, Tielemans M, Peremans A, Hendaoui N, Heysselaer D, et al. Gingiva laser welding: preliminary study on an ex vivo porcine model. Photomed Laser Surg. 2014;32(8):437-443. https://doi.org/10.1089/pho.2013.3662.</mixed-citation><mixed-citation xml:lang="en">Rasca E, Nyssen-Behets C, Tielemans M, Peremans A, Hendaoui N, Heysselaer D, et al. Gingiva laser welding: preliminary study on an ex vivo porcine model. Photomed Laser Surg. 2014;32(8):437-443. https://doi.org/10.1089/pho.2013.3662.</mixed-citation></citation-alternatives></ref><ref id="cit51"><label>51</label><citation-alternatives><mixed-citation xml:lang="ru">Fekrazad R, Mortezai O, Pedram M, Kalhori KA, Joharchi K, Mansoori K, et al. Transected sciatic nerve repair by diode laser protein soldering. J Photochem Photobiol B. 2017;173:441-447. https://doi.org/10.1016/j.jphotobiol.2017.06.008.</mixed-citation><mixed-citation xml:lang="en">Fekrazad R, Mortezai O, Pedram M, Kalhori KA, Joharchi K, Mansoori K, et al. Transected sciatic nerve repair by diode laser protein soldering. J Photochem Photobiol B. 2017;173:441-447. https://doi.org/10.1016/j.jphotobiol.2017.06.008.</mixed-citation></citation-alternatives></ref><ref id="cit52"><label>52</label><citation-alternatives><mixed-citation xml:lang="ru">Schiavon M, Marulli G, Zuin A, Lunardi F, Villoresi P, Bonora S., et al. Experimental evaluation of a new system for laser tissue welding applied on damaged lungs. Interact Cardiovasc Thorac Surg. 2013;16(5):577-582. https://doi.org/10.1093/icvts/ivt029.</mixed-citation><mixed-citation xml:lang="en">Schiavon M, Marulli G, Zuin A, Lunardi F, Villoresi P, Bonora S., et al. Experimental evaluation of a new system for laser tissue welding applied on damaged lungs. Interact Cardiovasc Thorac Surg. 2013;16(5):577-582. https://doi.org/10.1093/icvts/ivt029.</mixed-citation></citation-alternatives></ref><ref id="cit53"><label>53</label><citation-alternatives><mixed-citation xml:lang="ru">Urie R, Quraishi S, Jaffe M, Rege K. Gold nanorod-collagen nanocomposites as photothermal nanosolders for laser welding of ruptured porcine intestines. ACS Biomater Sci Eng. 2018;4(9):805-815. https://doi.org/10.1021/acsbiomaterials.5b00174.</mixed-citation><mixed-citation xml:lang="en">Urie R, Quraishi S, Jaffe M, Rege K. Gold nanorod-collagen nanocomposites as photothermal nanosolders for laser welding of ruptured porcine intestines. ACS Biomater Sci Eng. 2018;4(9):805-815. https://doi.org/10.1021/acsbiomaterials.5b00174.</mixed-citation></citation-alternatives></ref><ref id="cit54"><label>54</label><citation-alternatives><mixed-citation xml:lang="ru">Galichenko KA, Ryabkin DI, Suchkova VV, Blinov KD, Dydykin SS, Istranov AL, et al. Comparative evaluation of tissue fusion efficacy in laser-assisted flap plasty (experimental study). Russ J Oper Surg Clin Anat. 2024;8(2):5-11. https://doi.org/10.17116/OPERHIRURG202480215.</mixed-citation><mixed-citation xml:lang="en">Galichenko KA, Ryabkin DI, Suchkova VV, Blinov KD, Dydykin SS, Istranov AL, et al. Comparative evaluation of tissue fusion efficacy in laser-assisted flap plasty (experimental study). Russ J Oper Surg Clin Anat. 2024;8(2):5-11. https://doi.org/10.17116/OPERHIRURG202480215.</mixed-citation></citation-alternatives></ref><ref id="cit55"><label>55</label><citation-alternatives><mixed-citation xml:lang="ru">Ryabkin DI, Suchkova VV, Gerasimenko AY. Prediction of tensile strength of biotissue laser welds by machine learning methods. Biomed Eng. 2023;57:112-115. https://doi.org/10.1007/s10527-023-10280-0.</mixed-citation><mixed-citation xml:lang="en">Ryabkin DI, Suchkova VV, Gerasimenko AY. Prediction of tensile strength of biotissue laser welds by machine learning methods. Biomed Eng. 2023;57:112-115. https://doi.org/10.1007/s10527-023-10280-0.</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
