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用于控释给药的载马来酸噻吗洛尔的泊洛沙姆-共-聚(丙烯酸)基水凝胶的研制

Development of Timolol Maleate-Loaded Poloxamer-co-Poly (acrylic acid) based hydrogel for controlled drug delivery.

作者信息

Mansoor Raneem, Barkat Kashif, Anjum Irfan, Aamir Muhammad, Badshah Syed Faisal, Ullah Riaz, Iqbal Zafar, Raza Muhammad Ahmer

机构信息

Faculty of Pharmacy, The University of Lahore, Lahore, Pakistan.

Faculty of Health Sciences, Equator University of Science and Technology, Masaka, Uganda.

出版信息

PLoS One. 2024 Dec 20;19(12):e0309101. doi: 10.1371/journal.pone.0309101. eCollection 2024.

Abstract

Free radical polymerization technique was used to formulate Poloxamer-188 based hydrogels for controlled delivery. A total of seven formulations were formulated with varying concentrations of polymer, monomer ad cross linker. In order to assess the structural properties of the formulated hydrogels, Fourier Transform Infrared Spectroscopy (FTIR), Thermogravimetric analysis (TGA), Differential Scanning Calorimetry (DSC), Scanning electron microscopy (SEM), and X-ray diffraction (XRD) were carried out. To assess the effect of pH on the release of the drug from the polymeric system, drug release studies were carried in pH 1.2 and 7.4 and it was found that release of the drug was significant in pH 7.4 as compared to that of pH 1.2 which confirmed the pH responsiveness of the system. Different kinetic models were also applied to the drug release to evaluate the mechanism of the drug release from the system. To determine the safety and biocompatibility of the system, toxicity study was also carried out for which healthy rabbits were selected and formulated hydrogels were orally administered to the rabbits. The results obtained suggested that the formulated poloxamer-188 hydrogels are biocompatible with biological system and have the potential to serve as controlled drug delivery vehicles.

摘要

采用自由基聚合技术制备基于泊洛沙姆-188的水凝胶用于控释。共制备了七种配方,其中聚合物、单体和交联剂的浓度各不相同。为了评估所制备水凝胶的结构性质,进行了傅里叶变换红外光谱(FTIR)、热重分析(TGA)、差示扫描量热法(DSC)、扫描电子显微镜(SEM)和X射线衍射(XRD)分析。为了评估pH对药物从聚合物体系中释放的影响,在pH 1.2和7.4条件下进行了药物释放研究,结果发现与pH 1.2相比,药物在pH 7.4条件下的释放显著,这证实了该体系的pH响应性。还将不同的动力学模型应用于药物释放,以评估药物从体系中释放的机制。为了确定该体系的安全性和生物相容性,还进行了毒性研究,为此选择了健康的兔子,并将制备的水凝胶口服给予兔子。所得结果表明,所制备的泊洛沙姆-188水凝胶与生物体系具有生物相容性,并且有潜力用作控释药物载体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68fa/11661597/9a49dc04996c/pone.0309101.g001.jpg

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