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可注射氧化还原聚合甲基纤维素水凝胶作为潜在的软组织填充材料。

Injectable redox-polymerized methylcellulose hydrogels as potential soft tissue filler materials.

作者信息

Gold Gittel T, Varma Devika M, Harbottle David, Gupta Michelle S, Stalling Simone S, Taub Peter J, Nicoll Steven B

机构信息

Department of Biomedical Engineering, The City College of New York, New York, New York.

出版信息

J Biomed Mater Res A. 2014 Dec;102(12):4536-44. doi: 10.1002/jbm.a.35132. Epub 2014 Feb 28.

Abstract

There is a significant clinical need for long-lasting, injectable materials for soft tissue reconstruction. Methylcellulose (MC) is an FDA-approved polysaccharide derivative of cellulose that is inexpensive, renewable, and biocompatible, and may serve as an alternative to existing synthetic and natural fillers. In this study, MC was modified with functional methacrylate groups and polymerized using a redox-initiation system to produce hydrogels with tunable properties. By varying the percent methacrylation and macromer concentration, the equilibrium moduli of the hydrogels were found to range between 1.29 ± 0.46 and 12.8 ± 2.94 kPa, on par with human adipose tissue, and also displayed an inverse relationship to the swelling properties. Rheological analyses determined gelation onset and completion to be in accordance with the ISO standard for injectable materials. Cellulase enzymatic treatment resulted in complete degradation of the hydrogels by 48 h, presenting the possibility of minimally invasive removal of the materials in the event of malposition or host reaction. In addition, co-culture experiments with human dermal fibroblasts showed the gels to be cytocompatible based on DNA measurements and Live/Dead staining. Taken together, these redox-polymerized MC hydrogels may be of use for a wide range of clinical indications requiring soft tissue augmentation.

摘要

对于用于软组织重建的长效可注射材料存在重大临床需求。甲基纤维素(MC)是一种经美国食品药品监督管理局(FDA)批准的纤维素多糖衍生物,价格低廉、可再生且具有生物相容性,可作为现有合成和天然填充剂的替代品。在本研究中,MC用功能性甲基丙烯酸酯基团进行修饰,并使用氧化还原引发体系进行聚合,以制备具有可调性质的水凝胶。通过改变甲基丙烯酰化百分比和大分子单体浓度,发现水凝胶的平衡模量在1.29±0.46至12.8±2.94 kPa之间,与人体脂肪组织相当,并且与溶胀性质呈反比关系。流变学分析确定凝胶化开始和完成符合可注射材料的ISO标准。纤维素酶酶处理导致水凝胶在48小时内完全降解,这表明在发生位置不当或宿主反应时,有可能以微创方式去除材料。此外,与人真皮成纤维细胞的共培养实验表明,基于DNA测量和活/死染色,该凝胶具有细胞相容性。综上所述,这些氧化还原聚合的MC水凝胶可用于广泛的需要软组织填充的临床适应症。

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