结冷胶
自愈水凝胶
壳聚糖
药物输送
化学
控制释放
生物相容性材料
化学工程
高分子化学
纳米技术
材料科学
有机化学
生物医学工程
医学
食品科学
工程类
作者
Henrique Carrêlo,Mercedes Jiménez‐Rosado,Tânia Vieira,Rafaela R. da Rosa,Víctor Manuel Pérez Puyana,Jorge Silva,Alberto Romero,João Paulo Borges,Paula I. P. Soares
标识
DOI:10.1016/j.ijbiomac.2024.131981
摘要
The development of new Drug Delivery Systems (DDS) by incorporating microparticles within hydrogels can prolong the release rate of drugs and/or other bioactive agents. In this study, we combined gellan gum/alginate microparticles within a thermoresponsive chitosan (Ch) hydrogel with β-Glycerophosphate (β-GP), designing the system to be in the sol state at 21 °C and in the gel state at 37 °C to enable the injectability of the system. The system was in the sol state between 10 °C and 21 °C. Higher concentrations of β-GP (0, 2, 3, 4, 5 w/v%) and microparticles (0, 2 and 5 w/v%) allowed a faster sol-gel transition with higher mechanical strength at 37 °C. However, the sol-gel transition was not instantaneous. The release profile of methylene blue (MB) from the microparticles was significantly affected by their incorporation in Ch/β-GP hydrogels, only allowing the release of 60–70 % of MB for 6 days, while the microparticles alone released all the MB in 48 h. The proposed system did not present cytotoxicity to VERO cell lines as a preliminary assay, with the Ch/β-GP/GG:Alg having >90 % of cellular viability. The proposed Ch/β-GP system proved to have a delaying effect on drug release and biocompatible properties, being a promising future DDS.
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