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体外和体内评价生物相容性聚合物微凝胶用于 pH 驱动的酮咯酸氨丁三醇递送。

In-vitro and in-vivo evaluation of biocompatible polymeric microgels for pH- driven delivery of Ketorolac tromethamine.

机构信息

School of Pharmacy, Kaohsiung Medical University, 100 Shih-Chuan 1st Road, Kaohsiung City 80708, Taiwan.

School of Pharmacy, Kaohsiung Medical University, 100 Shih-Chuan 1st Road, Kaohsiung City 80708, Taiwan.

出版信息

Int J Pharm. 2022 Oct 15;626:122194. doi: 10.1016/j.ijpharm.2022.122194. Epub 2022 Sep 14.

Abstract

The aim of the current study was to prepare glutamic acid crosslinked poly(itaconic acid/methacrylic acid) microgels for pH-responsive delivery of ketorolac tromethamine, using aqueous free radical polymerization technique. The polymerization of polymer with monomers was carried out by a crosslinking agent N', N'-methylene bisacrylamide in the presence of initiator ammonium persulfate. The prepared microgels were characterized for structure, surface morphology, thermal stability, and crystallinity. Similarly, studies such as sol-gel analysis, drug loading, and polymer volume fraction were performed for the fabricated microgels. The pH-sensitivity of the developed microgels was investigated at three different pH values i.e., pH 1.2, 4.6, and 7.4 by swelling and in-vitro drug release studies. Maximum swelling and drug release were found at pH 7.4 as compared to pH 1.2 and 4.6, which indicated the pH-sensitive nature of the prepared microgels. The toxicity of the prepared microgels was evaluated by cell line and HET-CAM test, which demonstrated no toxic effect of the prepared microgels. In-vivo study was carried out on rabbits and high plasma concentration was reported for the drug loaded microgels as compared to drug solution and commercial product Keten. Hence, the prepared microgel system could be employed as an excellent carrier for the controlled drug delivery system.

摘要

本研究旨在通过水溶液自由基聚合技术,制备谷氨酸交联的聚(衣康酸/甲基丙烯酸)微凝胶,用于酮咯酸氨丁三醇的 pH 响应型递送。聚合过程中,单体在引发剂过硫酸铵和交联剂 N',N'-亚甲基双丙烯酰胺的存在下进行聚合。对所制备的微凝胶进行结构、表面形貌、热稳定性和结晶度的表征。同样,对所制备的微凝胶进行溶胶-凝胶分析、药物负载和聚合物体积分数等研究。通过溶胀和体外药物释放研究,在三种不同的 pH 值(即 pH 1.2、4.6 和 7.4)下研究了所开发的微凝胶的 pH 敏感性。与 pH 1.2 和 4.6 相比,在 pH 7.4 时,微凝胶的最大溶胀和药物释放,表明所制备的微凝胶具有 pH 敏感性。通过细胞系和 HET-CAM 测试评估了所制备的微凝胶的毒性,结果表明所制备的微凝胶没有毒性。在兔子体内进行了研究,与药物溶液和商业产品 Ketorolac 相比,载药微凝胶的血浆浓度较高。因此,所制备的微凝胶系统可用作控制药物递送系统的优良载体。

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