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用于生物医学应用的可注射、原位成型、可调谐、生物相容性明胶水凝胶。

Injectable, in-situ forming, tunable, biocompatible gelatin hydrogels for biomedical applications.

作者信息

Chauhan Meenakshi, Roopmani Purandhi, Rajendran Jayakumar, Narayan Kumar Pranav, Giri Jyotsnendu

机构信息

Department of Biomedical Engineering, Indian Institute of Technology Hyderabad, Kandi, Telangana, India.

Department of Biological Sciences, Birla Institute of Technology & Science, Pilani, Hyderabad Campus, Telangana, India.

出版信息

Int J Biol Macromol. 2025 Jan;285:138200. doi: 10.1016/j.ijbiomac.2024.138200. Epub 2024 Nov 29.

Abstract

Gelatin hydrogels have drawn attention for their diverse biomedical applications due to their flexible physiochemical properties. However, such gelatin hydrogels are made of toxic crosslinkers and photoinitiators, restricting their non-invasive deep tissue application. The in-situ forming chemical crosslinked without such toxic crosslinker and UV light has not been explored under physiological conditions. This study establishes a simple method to fabricate an injectable click-chemistry-based in-situ forming gelatin hydrogel in a physiological environment (without toxic UV or photoinitiator) with tunable physiochemical properties to modulate cellular response. Using Divinyl Sulfone (DVS) modification, gelatin hydrogel (GelVS) is optimized with tunable degradation properties, moduli (100 Pa -1000 Pa), gelation time, swelling, degradation, and viscoelastic behaviour. The in-vitro results using fibroblast and stem cells show that the hydrogel and its precursors were cytocompatible with diverging feedback of cells as the modulus varies. The in-vivo analysis for injectability, degradation, and biocompatibility of the GelVS hydrogel displays their biocompatible nature and lasts up to 30 days at the injecting site. Overall results indicate that DVS-modified GelVS hydrogel will be a great system with tunable physicochemical properties to modulate favorable cellular response for tissue regeneration and non-invasive deep tissue application.

摘要

明胶水凝胶因其灵活的物理化学性质在多种生物医学应用中受到关注。然而,此类明胶水凝胶由有毒的交联剂和光引发剂制成,限制了它们在非侵入性深层组织中的应用。在生理条件下,尚未探索过无需此类有毒交联剂和紫外线的原位形成化学交联方法。本研究建立了一种简单的方法,可在生理环境(无有毒紫外线或光引发剂)中制备基于点击化学的可注射原位形成明胶水凝胶,其物理化学性质可调,以调节细胞反应。通过二乙烯砜(DVS)改性,优化了明胶水凝胶(GelVS)的降解性能、模量(100帕 - 1000帕)、凝胶化时间、溶胀、降解和粘弹性行为。使用成纤维细胞和干细胞的体外结果表明,随着模量变化,水凝胶及其前体与细胞的不同反馈具有细胞相容性。对GelVS水凝胶的可注射性、降解和生物相容性的体内分析显示了它们的生物相容性,并且在注射部位可持续长达30天。总体结果表明,DVS改性的GelVS水凝胶将是一个具有可调物理化学性质的优秀体系,可调节有利于组织再生和非侵入性深层组织应用的细胞反应。

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