Development of starch/chitosan expandable films as a gastroretentive carrier for ginger extract-loaded solid dispersion

被引:14
|
作者
Kaewkroek, Kanidta [1 ,2 ]
Petchsomrit, Arpa [3 ]
Septama, Abdi Wira [4 ]
Wiwattanapatapee, Ruedeekorn [1 ,5 ]
机构
[1] Prince Songkla Univ, Fac Pharmaceut Sci, Dept Pharmaceut Technol, Hat Yai 90112, Songkhla, Thailand
[2] Rajamangala Univ Technol Thanyaburi, Fac Integrat Med, Thanyaburi 12130, Pathum Thani, Thailand
[3] Burapha Univ, Fac Pharmaceut Sci, Dept Pharmaceut Technol, Muang 20131, Chonburi, Thailand
[4] Natl Res & Innovat Agcy BRIN, Kawasan Puspiptek Serpong, Res Ctr Chem, Tangerang Selatan 15314, Banten, Indonesia
[5] Prince Songkla Univ, Fac Pharmaceut Sci, Phytomed & Pharmaceut Biotechnol Excellence Res C, Hat Yai 90112, Songkhla, Thailand
关键词
Ginger extract; Solid dispersions; Starch; Chitosan; Expandable film; Gastroretentive drug delivery systems; ZINGIBER-OFFICINALE ROSCOE; STARCH; RELEASE; DRUGS; SOLUBILITY; MECHANISM; DELIVERY; INHIBIT; SYSTEM; PVP;
D O I
10.1016/j.jsps.2021.12.017
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Gastroretentive expandable films were developed to provide controlled release of ginger extract (GE) for treatment of gastric diseases. The dosage form consisted of ginger extract solid dispersion (GE-SD) loaded in a starch/chitosan composite film, which was subsequently folded and inserted into a hard gelatin capsule. GE-SD was prepared by solvent evaporation using an optimum weight ratio of 1:1 for GE and PVP K30. Expandable films containing GE-SD were prepared by solvent casting combinations of chitosan and either rice-, glutinous rice - or pregelatinized maize starch with glycerin incorporated as a plasticizer. The optimized film formulation prepared from glutinous rice starch, exhibited tensile strength of 5.4 N/cm2 and high expansion in simulated gastric fluid (SGF), resulting in a 2.8-fold increase in area. The films resulted in sustained release of up to 90% of the content of 6-gingerol during 8 h exposure to SGF. Furthermore, the 6-gingerol released from the film displayed dose-dependent cytotoxic activity against AGS human gastric adenocarcinoma cells and anti-inflammatory activity by inhibiting the production of nitric oxide (NO) in LPS-stimulated RAW264.7 cells. (c) 2021 The Author(s). Published by Elsevier B.V. on behalf of King Saud University. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:120 / 131
页数:12
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