Sultana Humaira, Aamir Muhammad Naeem, Madni Asadullah, Rehman Masood Ur, Shafiq Afifa, Shirazi Jafir Hussain, Hassan Sidra
Department of Pharmaceutics, Faculty of Pharmacy, The Islamia University of Bahawalpur, 63100, Bahawalpur, Pakistan.
School of Pharmacy, Newcastle University, Newcastle Upon Tyne, NE1 7RU, UK.
AAPS PharmSciTech. 2023 Jan 26;24(1):43. doi: 10.1208/s12249-023-02499-7.
Nanogel has attracted considerable attention as one of the most versatile drug delivery systems, especially for site-specific and/or time-controlled delivery of the chemotherapeutic agent. The main objective of this study was to prepare the polymeric nanogel characterized by Fourier transform infrared spectroscopy, x-ray diffraction, thermogravimetric analysis, differential scanning, and oral acute toxicity. Free radical polymerization was done for the fabrication of polymeric nanogel. Fourier transform infrared spectroscopy was used to confirm the successful free radical polymerization. Various techniques such as x-ray diffraction, differential scanning calorimetric, and thermogravimetric analysis measurement were used to investigate the thermal behavior and crystallinity of developed nanogel. Parameters such as swelling, drug loading, and in vitro drug release is enhanced as polymers and monomers concentrations increase while these parameters decrease in case of increasing crosslinker concentration. The oral biocompatibility results of developed nanogel exhibited no toxicity in rabbits. Histopathological changes were observed between empty and loaded group. The nanosized gel offers a specific surface area which increases the stability of loaded drug (oxaliplatin) and bioavailability of the drug (oxaliplatin) as compared to the conventional drug delivery systems.
纳米凝胶作为最通用的药物递送系统之一,尤其是用于化疗药物的位点特异性和/或时间控制递送,已经引起了相当大的关注。本研究的主要目的是制备通过傅里叶变换红外光谱、X射线衍射、热重分析、差示扫描和口服急性毒性表征的聚合物纳米凝胶。采用自由基聚合制备聚合物纳米凝胶。傅里叶变换红外光谱用于确认成功的自由基聚合。使用各种技术,如X射线衍射、差示扫描量热法和热重分析测量,来研究所制备纳米凝胶的热行为和结晶度。随着聚合物和单体浓度的增加,诸如溶胀、载药量和体外药物释放等参数会提高,而在交联剂浓度增加的情况下这些参数会降低。所制备纳米凝胶的口服生物相容性结果表明在兔子中无毒性。在空白组和载药组之间观察到组织病理学变化。与传统药物递送系统相比,纳米尺寸的凝胶提供了一个比表面积,增加了载药(奥沙利铂)稳定性和药物(奥沙利铂)的生物利用度。