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以药物酒石黄为模型,设计、制备并评价羟丙甲纤维素(HPMC)和尤特奇 L100 肠溶性包衣配方在羧甲基琼脂糖水凝胶上的应用。

Design, Preparation, and Evaluation of Enteric Coating Formulation of HPMC and Eudragit L100 on Carboxylated Agarose Hydrogel by Using Drug Tartrazine.

机构信息

College of Food Science and Engineering, Ocean University of China, Qingdao 266003, China.

Department of Pharmaceutics, Faculty of Pharmacy, Gomal University, Dera Ismail Khan 29050, Pakistan.

出版信息

Biomed Res Int. 2022 Jan 28;2022:1042253. doi: 10.1155/2022/1042253. eCollection 2022.

Abstract

Enteric-coated application on drug is used to prevent the drug from inactivation which are degraded by gastric enzyme. The present study is aimed at achieving controlled drug delivery in acidic medium of gastrointestinal tract (GIT) by enteric coating of hydroxy propyl methylcellulose (HPMC) and Eudragit L100 on carboxylated agarose hydrogel, creating a pH-dependent delivery system. Fourier-transformed infrared spectroscopy (FTIR) was for the detection of carboxylic group on agarose hydrogel, and scanning electron microscope (SEM) was used for the determination surface of prepared formulation. To check the pH sensitivity of enteric-coated formulation, different pH solution was used. It was found that the formulation was not dissolved in 1.2 but dissolve in pH 6.8 similarly; hydrogels lacking coating showed that tartrazine was more dissolved in pH 1.2, and less dissolved at pH 6.8. The release of tartrazine from the hydrogels was measured by using spectrophotometer and using a scanning electron microscope to examine the morphology and surface appearance of hydrogel capsules. This study revealed cracks on coated samples, while noncoated samples showed clear appearance with no cracks. Our findings revealed that this method could be useful for the development of an enteric coating drug delivery system.

摘要

将肠溶应用于药物可防止药物因被胃酶降解而失活。本研究旨在通过在羧基化琼脂糖水凝胶上对羟丙基甲基纤维素 (HPMC) 和 Eudragit L100 进行肠溶包衣,在胃肠道 (GIT) 的酸性介质中实现控释药物,从而构建 pH 依赖性给药系统。傅里叶变换红外光谱 (FTIR) 用于检测琼脂糖水凝胶上的羧基,扫描电子显微镜 (SEM) 用于确定制剂的表面。为了检查肠溶制剂的 pH 敏感性,使用了不同的 pH 溶液。结果发现,该制剂在 1.2 下不溶解,但在 pH 6.8 下溶解;缺乏涂层的水凝胶表明,酒石黄在 pH 1.2 下溶解更多,在 pH 6.8 下溶解更少。使用分光光度计测量酒石黄从水凝胶中的释放,并使用扫描电子显微镜检查水凝胶胶囊的形态和表面外观。该研究揭示了涂层样品上的裂缝,而未涂层的样品则显示出清晰的外观,没有裂缝。我们的研究结果表明,该方法可用于开发肠溶性药物传递系统。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e61/8816555/84a6fe889264/BMRI2022-1042253.001.jpg

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