Preparation of a Novel Form of Gelatin With a Three-Dimensional Ordered Macroporous Structure to Regulate the Release of Poorly Water-Soluble Drugs

被引:13
作者
Xu, Jie [1 ]
Zhao, Zongzhe [1 ]
Hao, Yanna [1 ]
Zhao, Ying [1 ]
Qiu, Yang [1 ]
Jiang, Jie [1 ]
Yu, Tong [1 ]
Ji, Peng [1 ]
Liu, Ying [1 ]
Wu, Chao [1 ]
机构
[1] Liaoning Med Univ, Sch Pharm, 40 Songpo Rd, Jinzhou 121000, Liaoning Provin, Peoples R China
基金
中国国家自然科学基金;
关键词
biomaterials; polymeric drug carrier; nanotechnology; materials science; bioavailability; gelatin; three-dimensional ordered macroporous; fenofibrate; sustained release; biodegradability; MESOPOROUS SILICA NANOPARTICLES; ORAL BIOAVAILABILITY; DELIVERY-SYSTEM; CARBON; FENOFIBRATE; DISSOLUTION; POLYMER; CARRIER;
D O I
10.1016/j.xphs.2015.12.026
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
In this study, a novel three-dimensional ordered macroporous gelatin (3DOMG) was fabricated as a carrier for increasing the solubility of poorly water-soluble drugs, offering sustained release and a high oral bioavailability. Polymethyl methacrylate nanospheres (257 nm) were used as a colloidal plastic framework to synthesize 3DOMG. Fenofibrate (FNB) was selected as a model drug and loaded onto 3DOMG by the adsorption equilibrium method. Detailed characterization showed that the FNB absorbed onto 3DOMG was in a microcrystalline state. A fluorescence experiment and the prepared drug microcrystal network gave further information on the physical state of the drug. A degradation experiment proved that 3DOMG was readily biodegradable. In vitro release testing showed that 3DOMG increased the dissolution rate of FNB and produced a sustained release. An in vivo pharmacokinetic study confirmed that 3DOMG improved the oral bioavailability compared with that of commercial sustained-release capsules. These findings confirm that 3DOMG can be regarded as a promising carrier for an oral drug delivery system. (C) 2016 American Pharmacists Association (R). Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:2940 / 2948
页数:9
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