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