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环糊精接枝聚合物作为灯盏花乙素的高效药物载体。

Cyclodextrin pendant polymer as an efficient drug carrier for scutellarin.

机构信息

Pharmacy Department, Chongqing Emergency Medical Center, Chongqing University Central Hospital, Chongqing, P.R. China.

Industrial Crop Research Institute, Yunnan Academy of Agricultural Sciences, Kunming, P.R. China.

出版信息

Drug Deliv. 2020 Nov 26;27(1):1741-1749. doi: 10.1080/10717544.2020.1856223.

Abstract

A novel β-cyclodextrin pendant polymer (ε-PL-CD), composed of poly(ε-lysine) (ε-PL) main chain and glycine-β-cyclodextrin (Gly-CD) side chains, was prepared by a simple two-step procedure. The ε-PL-CD was investigated as a drug carrier of hydrophobic drug scutellarin (SCU). The characterization and complexation mode of the SCU:ε-PL-CD were researched in both solution and solid state by means of photoluminescence spectroscopy, H and 2D NMR, X-Ray powder diffraction (XRPD), thermal gravimetric analysis, Particle size and Zeta potential. The solubility test indicated that the solubilizing ability of SCU:ε-PL-CD was significantly improved compared with SCU:β-CD and free SCU. Besides, in cell experiment, it was found that SCU:ε-PL-CD has a strong inhibitory effect on the growth and invasion of tumor cells. The present study provides useful information for ε-PL-CD as a drug carrier material.

摘要

一种新型的β-环糊精接枝聚合物(ε-PL-CD),由聚(ε-赖氨酸)(ε-PL)主链和甘氨酸-β-环糊精(Gly-CD)侧链组成,通过简单的两步法制备。将 ε-PL-CD 作为疏水性药物灯盏乙素(SCU)的药物载体进行了研究。通过荧光光谱法、氢谱和二维核磁(H and 2D NMR)、X 射线粉末衍射(XRPD)、热重分析(thermal gravimetric analysis)、粒径和 Zeta 电位等手段,研究了 SCU:ε-PL-CD 在溶液和固态中的结构特征和包合模式。溶解度测试表明,与 SCU:β-CD 和游离 SCU 相比,SCU:ε-PL-CD 的增溶能力显著提高。此外,在细胞实验中发现,SCU:ε-PL-CD 对肿瘤细胞的生长和侵袭具有很强的抑制作用。本研究为 ε-PL-CD 作为药物载体材料提供了有用的信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e335/7738300/4dddd3d8182c/IDRD_A_1856223_F0001_C.jpg

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