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用于药物递送的新型pH敏感型戊二醛交联果胶纳米凝胶的制备

Fabrication of a novel pH-sensitive glutaraldehyde cross-linked pectin nanogel for drug delivery.

作者信息

Chang Cong, Wang Zong-Chun, Quan Chang-Yun, Cheng Han, Cheng Si-Xue, Zhang Xian-Zheng, Zhuo Ren-Xi

机构信息

Department of Pharmacy, Renmin Hospital of Wuhan University, Wuhan 430072, PR China.

出版信息

J Biomater Sci Polym Ed. 2007;18(12):1591-9.

Abstract

A novel pH-sensitive nanogel based on pectin cross-linked with glutaraldehyde (PT-GA) was designed and synthesized for drug delivery. Transmission electron microscope observation shows that the nano-sized gel particles exhibit a spherical morphology. The optical absorbance study of nanogel suspension reveals its pH sensitivity. Cytotoxicity study shows that the nanogel has no apparent inhibitory effect on cells. The in vitro drug-release behavior of the drug-loaded nanogel particles in three kinds of media, i.e., simulated gastric fluid, simulated intestine fluid and simulated colon fluid, was studied. PT-GA nanogel exhibits a faster release at a high pH, and the release could be further accelerated in the presence of pectinolytic enzyme, indicating that the nanogel may be used for colon-specific drug delivery.

摘要

设计并合成了一种基于果胶与戊二醛交联的新型pH敏感纳米凝胶(PT-GA)用于药物递送。透射电子显微镜观察表明,纳米尺寸的凝胶颗粒呈现球形形态。纳米凝胶悬浮液的吸光度研究揭示了其pH敏感性。细胞毒性研究表明,纳米凝胶对细胞没有明显的抑制作用。研究了载药纳米凝胶颗粒在三种介质(即模拟胃液、模拟肠液和模拟结肠液)中的体外药物释放行为。PT-GA纳米凝胶在高pH值下释放更快,并且在果胶酶存在的情况下释放可以进一步加速,这表明该纳米凝胶可用于结肠特异性药物递送。

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