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用于生物医学应用的交联羧甲基壳聚糖多孔膜支架的制备及性能表征。

Preparation and characterization of cross-linked carboxymethyl chitin porous membrane scaffold for biomedical applications.

机构信息

College of Chemistry and Chemical Engineering, Shenzhen University, Shenzhen, Guangdong 518060, China.

College of Chemistry and Chemical Engineering, Shenzhen University, Shenzhen, Guangdong 518060, China.

出版信息

Carbohydr Polym. 2015 Aug 1;126:150-5. doi: 10.1016/j.carbpol.2015.02.050. Epub 2015 Mar 5.

Abstract

Porous dermal scaffold membrane (PDSM) was successfully prepared by using a so-called sol-gel freeze-drying method. In this method, the carboxymethyl chitin (CMC) hydrosol was first cross-linked by 1-ethyl-3-[3-dimethylaminopropyl] carbodiimide hydrochloride (EDC) and N-hydroxysuccinimide (NHS), and then lyophilized to form the PDSM. For the first time, this research focused on the cross-linked CMC as the only component for three-dimensional PDSM. The effects of cross-linking conditions on the performance of the PDSM were investigated. And PDSM with optimal performance was obtained through 4-h cross-linking at 4 wt% of CMC concentration in the hydrosol, where the mass ratio of EDC to NHS to CMC was 5:3:10. The porosity of the optimized PDSM was more than 90% and the water swelling rate was above 4000%. The pore size was well distributed and was between 100 μm and 200 μm. And the tensile strength was above 0.09 MPa. The as-made PDSM could be degraded above 80% in 12 days in the presence of a 0.2mg/mL lysozyme solution. Very importantly, the PDSM had no cytotoxicity and good biocompatibility from MTT assays. Our results showed the application possibility of the as-prepared PDSM as dermal scaffold for skin tissue engineering.

摘要

多孔真皮支架膜(PDSM)是通过所谓的溶胶-凝胶冷冻干燥方法成功制备的。在该方法中,首先通过 1-乙基-3-[3-二甲基氨基丙基]碳化二亚胺盐酸盐(EDC)和 N-羟基琥珀酰亚胺(NHS)使羧甲基壳聚糖(CMC)水溶胶交联,然后冻干形成 PDSM。本研究首次将交联 CMC 作为唯一成分用于三维 PDSM。研究了交联条件对 PDSM 性能的影响。通过在水溶胶中 CMC 浓度为 4wt%、交联 4h 的条件下,获得了性能最佳的 PDSM,其中 EDC 与 NHS 与 CMC 的质量比为 5:3:10。优化后的 PDSM 的孔隙率超过 90%,水膨胀率超过 4000%。孔径分布均匀,在 100μm 到 200μm 之间。拉伸强度大于 0.09MPa。在含有 0.2mg/mL 溶菌酶溶液的条件下,制备的 PDSM 在 12 天内可降解超过 80%。非常重要的是,从 MTT 测定结果来看,PDSM 无细胞毒性,具有良好的生物相容性。我们的结果表明,所制备的 PDSM 作为皮肤组织工程的真皮支架具有应用潜力。

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