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用于生物医学应用的静电纺丝果胶纳米纤维的预测性设计框架

https://doi.org/10.47093/3033-5493.2025.1.2.3-24

摘要

果胶是一种结构多样的植物源性多糖,正逐渐成为构建生物指导性纳米纤维支架的独特平台。与静电纺丝中常用的其他天然聚合物(如海藻酸盐、透明质酸或胶原蛋白)相比,果胶具有独特的粘附性、免疫调节潜力,以及由同型半乳糖醛酸聚糖和鼠李糖半乳糖醛酸聚糖结构域平衡所决定的、可精细调控的分子架构。然而,其固有的聚电解质行为、较低的链缠结度和高水溶性历来限制了其在纳米纤维制造中的应用。近期在化学改性、溶剂工程和纺后稳定化方面的进展,使得制备形态可控、机械性能稳定且降解动力学可调的静电纺丝果胶纤维成为可能。本综述引入了一个预测性"结构-性能-功能"框架,用于指导静电纺丝果胶纳米纤维在生物医学应用中的理性设计。我们将分子策略分为三类(共价、物理和复合策略),并评估了每种策略如何影响纤维形成及后续的生物学性能,特别关注其免疫相互作用、生物活性物质负载和支架重塑。同时,我们指出了转化应用的瓶颈,包括材料的变异性、对灭菌的敏感性以及交联化学与法规要求的不匹配。通过将这些因素整合到以设计为依据的支架逻辑中,本综述为推动静电纺丝果胶材料从实验室原型走向再生医学、伤口愈合和局部治疗递送等临床可行平台提供了路线图。

关于作者

G. K. Tugaeva
谢切诺夫第一莫斯科国立医科大学(谢切诺夫大学)
俄罗斯联邦

Gilyana K. Tugaeva,研究员助理,再生医学研究所

地址:8/2, Trubetskaya str., Moscow, 119048



M. M. Bashkatova
谢切诺夫第一莫斯科国立医科大学(谢切诺夫大学)
俄罗斯联邦

Margarita M. Bashkatova,实习研究员,再生医学研究所

地址:8/2, Trubetskaya str., Moscow, 119048



Yu. M. Efremov
谢切诺夫第一莫斯科国立医科大学(谢切诺夫大学)
俄罗斯联邦

Yuri M. Efremov,哲学博士(PhD),副教授,先进生物材料部主任,再生医学研究所

地址:8/2, Trubetskaya str., Moscow, 119048



S. L. Kotova
谢切诺夫第一莫斯科国立医科大学(谢切诺夫大学)
俄罗斯联邦

Svetlana L. Kotova,哲学博士(PhD),首席研究员,高分子设计实验室, 再生医学研究所

地址:8/2, Trubetskaya str., Moscow, 119048



Peifeng Li
青岛大学医学部附属医院,转化医学研究院
中国

李培峰,医学博士,院长,特聘教授

地址:青岛,266021



A. I. Shpichka
谢切诺夫第一莫斯科国立医科大学(谢切诺夫大学)
俄罗斯联邦

Anastasia I. Shpichka,哲学博士(PhD),副教授,应用微流控实验室主任,再生医学研究所

地址:8/2, Trubetskaya str., Moscow, 119048



P. S. Timashev
谢切诺夫第一莫斯科国立医科大学(谢切诺夫大学)
俄罗斯联邦

Peter S. Timashev,化学科学博士,教授,生物医学科技园学术主任

地址:8/2, Trubetskaya str., Moscow, 119048



参考

1. Li N, Xue F, Zhang H, et al. Fabrication and Characterization of Pectin Hydrogel Nanofiber Scaffolds for Differentiation of Mesenchymal Stem Cells into Vascular Cells. ACS Biomater Sci Eng. 2019;5(12):6511-6519. https://doi.org/10.1021/acsbiomaterials.9b01178.

2. Chan SY, Chan BQY, Liu Z, et al. Electrospun Pectin-Polyhydroxybutyrate Nanofibers for Retinal Tissue Engineering. ACS Omega. 2017;2(12):8959-8968. https://doi.org/10.1021/acsomega.7b01604.

3. Fiorentini F, Suarato G, Summa M, et al. Plant-Based, Hydrogel-like Microfibers as an Antioxidant Platform for Skin Burn Healing. ACS Appl Bio Mater. 2023;6(8):3103-3116. https://doi.org/10.1021/acsabm.3c00214.

4. Wang JH, Tsai CW, Tsai NY, et al. An injectable, dual crosslinkable hybrid pectin methacrylate (PECMA)/gelatin methacryloyl (GelMA) hydrogel for skin hemostasis applications. Int J Biol Macromols. 2021;185:441-450. https://doi.org/10.1016/j.ijbiomac.2021.06.162.

5. Schulte-Werning LV, Singh B, Johannessen M, Engstad RE, Holsæter AM. Antimicrobial liposomes-in-nanofiber wound dressings prepared by a green and sustainable wire-electrospinning set-up. Int J Pharm. 2024;657:124136. https://doi.org/10.1016/j.ijpharm.2024.124136.

6. Mirhaj M, Varshosaz J, Labbaf S, et al. Mupirocin loaded core-shell pluronic-pectinkeratin nanofibers improve human keratinocytes behavior, angiogenic activity and wound healing. Int J Biol Macromol. 2023;253:126700. https://doi.org/10.1016/j.ijbiomac.2023.126700.

7. Guo H, Ran W, Jin X, et al. Development of pectin/chitosan-based electrospun biomimetic nanofiber membranes loaded with dihydromyricetin inclusion complexes for wound healing application. Int J Biol Macromol. 2024;278:134526. https://doi.org/10.1016/j.ijbiomac.2024.134526.

8. Martău GA, Mihai M, Vodnar DC. The Use of Chitosan, Alginate, and Pectin in the Biomedical and Food Sector-Biocompatibility, Bioadhesiveness, and Biodegradability. Polymers (Basel). 2019;11(11):1837. https://doi.org/10.3390/polym11111837.

9. Mohammadinejad R, Maleki H, Larrañeta E, et al. Status and future scope of plant-based green hydrogels in biomedical engineering. Appl Mater Today. 2019;16:213-246. https://doi.org/10.1016/j.apmt.2019.04.010.

10. Zheng J, Yang Q, Shi X, Xie Z, Hu J, Liu Y. Effects of preparation parameters on the properties of the crosslinked pectin nanofiber mats. Carbohydr Polym. 2021;269:118314. https://doi.org/10.1016/j.carbpol.2021.118314.

11. Feng S, Yi J, Ma Y, Bi J. Study on the ice crystals growth under pectin gels with different crosslinking strengths by modulating the degree of amidation in HG domain. Food Chem. 2023;428:136758. https://doi.org/10.1016/j.foodchem.2023.136758.

12. Dong Y, Li H, Zou F, Baniasadi H, Budtova T, Vapaavuori J. Structure-properties correlations in low-methylated pectin hydrogels and aerogels crosslinked by divalent ions. Int J Biol Macromol. 2025;285:137980. https://doi.org/10.1016/j.ijbiomac.2024.137980.

13. McCune D, Guo X, Shi T, et al. Electrospinning pectin-based nanofibers: a parametric and cross-linker study. Appl Nanosci. 2018;8(1-2):33-40. https://doi.org/10.1007/s13204-018-0649-4.

14. Yang M, Zhang M, Zhuang Y, Li Y, Fei P. Amidation pectin with high viscosity and enhanced gelation properties: Preparation, characterization and viscoelastic behaviors. Int J Biol Macromol. 2025;318:145108. https://doi.org/10.1016/j.ijbiomac.2025.145108.

15. Shao F, Xu J, Zhang J, et al. Study on the influencing factors of natural pectin’s flocculation: Their sources, modification, and optimization. Water Environ Res. 2021;93(10):2261-2273. https://doi.org/10.1002/wer.1598.

16. Cui S, Yao B, Gao M, et al. Effects of pectin structure and crosslinking method on the properties of crosslinked pectin nanofibers. Carbohydr Polym. 2017;157:766-774. https://doi.org/10.1016/j.carbpol.2016.10.052.

17. Muñoz-Almagro N, Wilde PJ, Montilla A, Villamiel M. Development of low-calorie gels from sunflower pectin extracted by the assistance of ultrasound. LWT. 2025;222:117609. https://doi.org/10.1016/j.lwt.2025.117609.

18. Wang S, Han H, Zhang X, et al. Efficient extraction of pectin from spaghetti squash (Cucurbita pepo L. subsp. pepo) peel by electron beam irradiation combined with ultrasound: Structural characterization and functional properties. Food Chem. 2025;485:144492. https://doi.org/10.1016/j.foodchem.2025.144492.

19. Würfel H, Heinze T. Acidic dimethyl sulfoxide: A solvent system for the fast dissolution of pectin derivatives suitable for subsequent modification. Carbohydr Polym. 2025;348:122872. https://doi.org/10.1016/j.carbpol.2024.122872.

20. Shi X, Cui S, Song X, et al. Gelatin-crosslinked pectin nanofiber mats allowing cell infiltration. Mater Sci Eng C Mater Biol Appl: C. 2020;112:110941. https://doi.org/10.1016/j.msec.2020.110941.

21. Liu SC, Li R, Tomasula PM, Sousa AMM, Liu L. Electrospun Food-Grade Ultrafine Fibers from Pectin and Pullulan Blends. Food and Nutrition Sciences. 2016;7(7):636-646. https://doi.org/10.4236/fns.2016.77065.

22. Popov S, Paderin N, Chistiakova E, et al. Swelling, Protein Adsorption, and Biocompatibility of Pectin–Chitosan Hydrogels. Gels. 2024;10(7):472. https://doi.org/10.3390/gels10070472.

23. Zirak Hassan Kiadeh S, Ghaee A, Farokhi M, Nourmohammadi J, Bahi A, Ko FK. Electrospun pectin/modified copper-based metal–organic framework (MOF) nanofibers as a drug delivery system. Int J Biol Macromol. 2021;173:351-365. https://doi.org/10.1016/j.ijbiomac.2021.01.058.

24. Pallavicini P, Arciola CR, Bertoglio F, et al. Silver nanoparticles synthesized and coated with pectin: An ideal compromise for anti-bacterial and anti-biofilm action combined with wound-healing properties. J Colloid Interface Sci. 2017;498:271-281. https://doi.org/10.1016/j.jcis.2017.03.062.

25. Alipour R, Khorshidi A, Shojaei AF, Mashayekhi F, Moghaddam MJM. Skin wound healing acceleration by Ag nanoparticles embedded in PVA/PVP/Pectin/Mafenide acetate composite nanofibers. Polym Test. 2019;79:106022. https://doi.org/10.1016/j.polymertesting.2019.106022.

26. Zarandona I, Correia DM, Moreira J, et al. Magnetically responsive chitosan-pectin films incorporating Fe3O4 nanoparticles with enhanced antimicrobial activity. Int J Biol Macromol. 2023;227:1070-1077. https://doi.org/10.1016/j.ijbiomac.2022.11.286.

27. Kolgesiz S, Ozcelik N, Erdemir NE, Unal H. Hybrid Pectin/Polydopamine Hydrogels with Photothermal Properties. ACS Omega. 2025;10(21):21994-22004. https://doi.org/10.1021/acsomega.5c02084.

28. Balakrishnan B, Subramanian S, Mallia MB, et al. Multifunctional Core–Shell Glyconanoparticles for Galectin-3-Targeted, Trigger-Responsive Combination Chemotherapy. Biomacromolecules. 2020;21(7):2645-2660. https://doi.org/10.1021/acs.biomac.0c00358.

29. Mehrali M, Thakur A, Kadumudi FB, et al. Pectin Methacrylate (PEMA) and Gelatin Based Hydrogels for Cell Delivery: Converting Waste Materials into Biomaterials. ACS Appl Mater Interfaces. 2019;11(13):12283-12297. https://doi.org/10.1021/acsami.9b00154.

30. Türkkan S, Atila D, Akdağ A, Tezcaner A. Fabrication of functionalized citrus pectin/silk fibroin scaffolds for skin tissue engineering. J Biomed Mater Res B Appl Biomater. 2018;106(7):2625-2635. https://doi.org/10.1002/jbm.b.34079.

31. Zannini D, Monteforte M, Gargiulo L, et al. Citrus Wastes as Source of Pectin and Bioactive Compounds Extracted via One-Pot Microwave Process: An In Situ Path to Modulated Property Control. Polymers (Basel). 2025;17(5):659. https://doi.org/10.3390/polym17050659.

32. Karbuz P, Tugrul N. Microwave and ultrasound assisted extraction of pectin from various fruits peel. J Food Sci Technol. 2021;58(2):641-650. https://doi.org/10.1007/s13197-020-04578-0.

33. Hamed R, Magamseh KH, Al-Shalabi E, et al. Green Hydrogels Prepared from Pectin Extracted from Orange Peels as a Potential Carrier for Dermal Delivery Systems. ACS Omega. 2025;10(17):17182-17200. https://doi.org/10.1021/acsomega.4c08449.

34. Douglas TEL, Dziadek M, Schietse J, et al. Pectin-bioactive glass self-gelling, injectable composites with high antibacterial activity. Carbohydr Polym. 2019;205:427-436. https://doi.org/10.1016/j.carbpol.2018.10.061.

35. Akinalan Balik B, Argin S, Lagaron JM, Torres-Giner S. Preparation and Characterization of Electrospun Pectin-Based Films and Their Application in Sustainable Aroma Barrier Multilayer Packaging. Appl Sci (Basel). 2019;9(23):5136. https://doi.org/10.3390/app9235136.

36. Rockwell PL, Kiechel MA, Atchison JS, Toth LJ, Schauer CL. Various-sourced pectin and polyethylene oxide electrospun fibers. Carbohydr Polym. 2014;107:110-118. https://doi.org/10.1016/j.carbpol.2014.02.026.

37. Zhang W, Sun J, Li Q, et al. Effects of different extraction solvents on the compositions, primary structures, and anti-inflammatory activity of pectin from sweet potato processing by-products. Carbohydr Polym. 2025;347:122766. https://doi.org/10.1016/j.carbpol.2024.122766.

38. Ahadi F, Khorshidi S, Karkhaneh A. A hydrogel/fiber scaffold based on silk fibroin/oxidized pectin with sustainable release of vancomycin hydrochloride. Eur Polym J. 2019;118:265-274. https://doi.org/10.1016/j.eurpolymj.2019.06.001.

39. Belousov A, Titov S, Shved N, et al. Hydrogels based on modified pectins capable of modulating neural cell behavior as prospective biomaterials in glioblastoma treatment. Int Rev Neurobiol. 2020;151:111-138. https://doi.org/10.1016/bs.irn.2020.03.025.

40. Elsherbini AM, Shalaby TI, Abdelmonsif DA, Rashed SA, Haroun M, Sabra SA. Tadalafil-loaded zein nanoparticles incorporated into pectin/PVA nanofibers as a diabetic wound dressing with enhanced angiogenic and healing properties. J Drug Deliv Sci Technol 2023;89:105019. https://doi.org/10.1016/j.jddst.2023.105019.

41. Hosseini SA, Javad Hoseini S, Askari VR, et al. Pectin-reinforced electrospun nanofibers: Fabrication and characterization of highly biocompatible mats for wound healing applications. J Drug Deliv Sci Technol. 2022;77:103916. https://doi.org/10.1016/j.jddst.2022.103916.

42. Kocaaga B, Kurkcuoglu O, Tatlier M, Batirel S, Guner FS. Low-methoxyl pectin–zeolite hydrogels controlling drug release promote in vitro wound healing. J Appl Polym Sci. 2019;136(24):47640. https://doi.org/10.1002/app.47640.

43. Archana D, Dutta J, Dutta PK. Evaluation of chitosan nano dressing for wound healing: characterization, in vitro and in vivo studies. Int J Biol Macromol. 2013;57:193-203. https://doi.org/10.1016/j.ijbiomac.2013.03.002.

44. Giusto G, Vercelli C, Comino F, Caramello V, Tursi M, Gandini M. A new, easy-to-make pectin-honey hydrogel enhances wound healing in rats. BMC Complement Altern Med. 2017;17(1):266. https://doi.org/10.1186/s12906-017-1769-1.

45. Gan D, Xing W, Jiang L, et al. Plant-inspired adhesive and tough hydrogel based on Ag-Lignin nanoparticles-triggered dynamic redox catechol chemistry. Nat Commun. 2019;10(1):1487. https://doi.org/10.1038/s41467-019-09351-2.

46. Lee J, Hlaing SP, Cao J, et al. In Situ Hydrogel-Forming/Nitric Oxide-Releasing Wound Dressing for Enhanced Antibacterial Activity and Healing in Mice with Infected Wounds. Pharmaceutics. 2019;11(10):496. https://doi.org/10.3390/pharmaceutics11100496.

47. Rezvanian M, Ng SF, Alavi T, Ahmad W. In-vivo evaluation of Alginate-Pectin hydrogel film loaded with Simvastatin for diabetic wound healing in Streptozotocin-induced diabetic rats. Int J Biol Macromol. 2021;171:308-319. https://doi.org/10.1016/j.ijbiomac.2020.12.221.

48. Hasan N, Cao J, Lee J, Kim H, Yoo JW. Development of clindamycin-loaded alginate/pectin/hyaluronic acid composite hydrogel film for the treatment of MRSA-infected wounds. J Pharm Investig. 2021;51(5):597-610. https://doi.org/10.1007/s40005-021-00541-z.

49. Chang L, Chang R, Liu X, et al. Self-healing hydrogel based on polyphosphate conjugated pectin with hemostatic property for wound healing applications. Biomater Adv. 2022;139:212974. https://doi.org/10.1016/j.bioadv.2022.212974.

50. Chetouani A, Elkolli M, Haffar H, et al. Multifunctional hydrogels based on oxidized pectin and gelatin for wound healing improvement. Int J Biol Macromol. 2022;212:248-256. https://doi.org/10.1016/j.ijbiomac.2022.05.082.

51. Bernardi B, Malafatti JOD, Moreira AJ, et al. Antimicrobial membranes based on polycaprolactone: pectin blends reinforced with zeolite faujasite for cloxacillin controlled release. Discover Nano. 2025;20(1):8. https://doi.org/10.1186/s11671-024-04161-y.

52. Wei YS, Feng K, Wu H. Regulation of the colon-targeted release rate of lactoferrin by constructing hydrophobic ethyl cellulose/pectin composite nanofibrous carrier and its effect on anti-colon cancer activity. Int J Biol Macromol. 2024;261:129466. https://doi.org/10.1016/j.ijbiomac.2024.129466.

53. Nawaz A, Irshad S, Walayat N, Khan MR, Iqbal MW, Luo X. Fabrication and Characterization of Apple-Pectin–PVA-Based Nanofibers for Improved Viability of Probiotics. Foods. 2023;12(17):3194. https://doi.org/10.3390/foods12173194.

54. Lin HY, Chen HH, Chang SH, Ni TS. Pectin-chitosan-PVA nanofibrous scaffold made by electrospinning and its potential use as a skin tissue scaffold. J Biomater Sci Polym Ed. 2013;24(4):470-484. https://doi.org/10.1080/09205063.2012.693047.

55. Tavakoli M, Al-Musawi MH, Kalali A, et al. Platelet rich fibrin and simvastatin-loaded pectin-based 3D printed-electrospun bilayer scaffold for skin tissue regeneration. Int J Biol Macromol. 2024;265(Pt 1):130954. https://doi.org/10.1016/j.ijbiomac.2024.130954.

56. Dai Z, Ronholm J, Tian Y, Sethi B, Cao X. Sterilization techniques for biodegradable scaffolds in tissue engineering applications. J Tissue Eng. 2016;7:2041731416648810. https://doi.org/10.1177/2041731416648810.

57. Yoganarasimha S, Best A, Madurantakam PA. Peracetic Acid Sterilization Induces Divergent Biological Response in Polymeric Tissue Engineering Scaffolds. Appl Sci (Basel). 2019;9(18):3682. https://doi.org/10.3390/app9183682.


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供引用:


Tugaeva G.K., Bashkatova M.M., Efremov Yu.M., Kotova S.L., Li P., Shpichka A.I., Timashev P.S. 用于生物医学应用的静电纺丝果胶纳米纤维的预测性设计框架. 欧亚生命科学杂志. 2025;1(2):3-24. https://doi.org/10.47093/3033-5493.2025.1.2.3-24

For citation:


Tugaeva G.K., Bashkatova M.M., Efremov Yu.M., Kotova S.L., Li P., Shpichka A.I., Timashev P.S. Predictive design framework for electrospun pectin nanofibers in biomedical applications. The Eurasian Journal of Life Sciences. 2025;1(2):3-24. https://doi.org/10.47093/3033-5493.2025.1.2.3-24

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