Amino functionalized chiral mesoporous silica nanoparticles for improved loading and release of poorly water-soluble drug

被引:24
|
作者
Wang, Xin [1 ]
Li, Chang [1 ]
Fan, Na [1 ]
Li, Jing [1 ]
Zhang, Haotian [3 ]
Shang, Lei [2 ]
He, Zhonggui [1 ]
Sun, Jin [1 ,4 ]
机构
[1] Shenyang Pharmaceut Univ, Wuya Coll Innovat, 103 Wenhua Rd, Shenyang 110016, Liaoning, Peoples R China
[2] Shenyang Med Coll, Coll Basic Med Sci, 146 Huanghe North St, Shenyang 110034, Liaoning, Peoples R China
[3] Shenyang Pharmaceut Univ, Sch Life Sci & Biopharmaceut, 103 Wenhua Rd, Shenyang 110016, Liaoning, Peoples R China
[4] Shenyang Pharmaceut Univ, Municipal Key Lab Biopharmaceut, Sch Pharm, 103 Wenhua Rd, Shenyang 110016, Liaoning, Peoples R China
关键词
Chiral mesoporous silica; Amino functionalization; Curled drug loading; Curled drug release; HELICAL MESOSTRUCTURED SILICA; IMPROVED DELIVERY; DISSOLUTION; SBA-15; NANOCRYSTALS; MICROSPHERE; DENDRIMERS; CARRIERS;
D O I
10.1016/j.ajps.2018.04.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In the present paper, chiral mesoporous silica nano-cocoon (A-CMSN) functionalized with amino group was synthesized, and its loading and release of indomethacin (IMC), a poorly soluble drug, was studied. Due to the use of chiral anionic surfactants as a template, A-CMSN possessed 2D hexagonal nano-cocoon morphology with curled channels on its surface, which was quite different from another 2D hexagonal mesoporous silica nanoparticles (MCM-41) with straightway channels. After being loaded into the two silica carriers by hydrogen bond, crystalline IMC converted to amorphous form, leading to the improved drug dissolution. And IMC loading capacity of A-CMSN was higher than MCM-41 because curled loading process originating from curvature chiral channels can hold more drug molecules. Compared with IMC, IMC loaded A-CMSN presented obviously fast release throughout the in vitro release experiment, while IMC loaded MCM-41 released faster than IMC at the initial 5 h then showed controlled slow release afterwards, which was closely related to the mesoporous silica nanoparticles and different channel mesostructures of these two carriers. A-CMSN possessed nano-cocoon morphology with curled 2D hexagonal channel and its channel length was shorter than MCM-41, therefore IMC molecules can easily get rid of the constraint of A-CMSN then to be surrounded by dissolution medium. (C) 2018 Published by Elsevier B.V. on behalf of Shenyang Pharmaceutical University.
引用
收藏
页码:405 / 412
页数:8
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