Hyaluronic-acid-based β-cyclodextrin grafted copolymers as biocompatible supramolecular hosts to enhance the water solubility of tocopherol

被引:22
|
作者
Singh, Parbeen [1 ,2 ]
Wu, Li [2 ]
Ren, Xiaohong [2 ]
Zhang, Wei [2 ]
Tang, Yan [2 ]
Chen, Yongli [1 ]
Carrier, Andrew [3 ,4 ]
Zhang, Xu [1 ,3 ,4 ]
Zhang, Jiwen [2 ,5 ]
机构
[1] Shenzhen Polytech, Postdoctoral Innovat Practice Base, Shenzhen 518055, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Mat Med, Ctr Drug Delivery Syst, 501 Haike Rd, Shanghai 201203, Peoples R China
[3] Cape Breton Univ, Dept Chem, 1250 Grand Lake Rd, Sydney, NS B1P 6L2, Canada
[4] Cape Breton Univ, Dept Hlth Sci, 1250 Grand Lake Rd, Sydney, NS B1P 6L2, Canada
[5] Natl Inst Food & Drug Control, NMPA Key Lab Qual Res & Evaluat Pharmaceut Excipi, 2 Tiantan Xili, Beijing 100050, Peoples R China
基金
国家重点研发计划; 中国博士后科学基金;
关键词
Solubility enhancement; Hyaluronic acid-beta-cyclodextrin grafted copolymer; alpha-Tocopherol; Inclusion complex; VITAMIN-E; INCLUSION COMPLEX; IN-VITRO; PHOTOSTABILITY; POLYMERS; MATS;
D O I
10.1016/j.ijpharm.2020.119542
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Hyaluronic acid (HA), a common biopolymer found in the extracellular fluid, was grafted with beta-cyclodextrin (beta-CD) to form a composite polymer that could form inclusion complexes with tocopherol (VE), enhancing its water-solubility and serving as a model drug delivery system. Herein, different copolymers were prepared with varying HA:beta-CD ratios and characterized. VE loading capacity was directly correlated with increased beta-CD composition in the polymers and morphological changes were observed upon VE binding. The host materials and their VE inclusion complexes are not cytotoxic, and are thus useful for VE and drug delivery.
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页数:7
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