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具有双pH响应药物释放功能的核壳结构微胶囊。

Core-shell structure microcapsules with dual pH-responsive drug release function.

作者信息

Yang Chih-Hui, Wang Chih-Yu, Grumezescu Alexandru Mihai, Wang Andrew H-J, Hsiao Ching-Ju, Chen Zu-Yu, Huang Keng-Shiang

机构信息

Department of Biological Science and Technology, I-Shou University, Kaohsiung, Taiwan.

出版信息

Electrophoresis. 2014 Sep;35(18):2673-80. doi: 10.1002/elps.201400210. Epub 2014 Jul 29.

Abstract

We report dual pH-responsive microcapsules manufactured by combining electrostatic droplets (ESD) and microfluidic droplets (MFD) techniques to produce monodisperse core (alginate)-shell (chitosan) structure with dual pH-responsive drug release function. The fabricated core-shell microcapsules were size controllable by tuning the synthesis parameters of the ESD and MFD systems, and were responsive in both acidic and alkaline environment, We used two model drugs (ampicillin loaded in the chitosan shell and diclofenac loaded in the alginate core) for drug delivery study. The results show that core-shell structure microcapsules have better drug release efficiency than respective core or shell particles. A biocompatibility test showed that the core-shell structure microcapsules presented positive cell viability (above 80%) when evaluated by the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. The results indicate that the synthesized core-shell microcapsules were a potential candidate of dual-drug carriers.

摘要

我们报道了通过结合静电液滴(ESD)和微流控液滴(MFD)技术制造的双pH响应微胶囊,以生产具有双pH响应药物释放功能的单分散核(海藻酸盐)-壳(壳聚糖)结构。通过调整ESD和MFD系统的合成参数,制备的核壳微胶囊尺寸可控,并且在酸性和碱性环境中均有响应。我们使用两种模型药物(壳聚糖壳中负载的氨苄青霉素和海藻酸盐核中负载的双氯芬酸)进行药物递送研究。结果表明,核壳结构微胶囊比各自的核或壳颗粒具有更好的药物释放效率。生物相容性测试表明,通过3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)测定法评估时,核壳结构微胶囊呈现出阳性细胞活力(高于80%)。结果表明,合成的核壳微胶囊是双药载体的潜在候选者。

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