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明胶微球-海藻酸钠水凝胶联合系统用于 5-氟尿嘧啶的持续和胃靶向递送。

Gelatin microsphere-alginate hydrogel combined system for sustained and gastric targeted delivery of 5-fluorouracil.

机构信息

Marmara University, Department of Chemical Engineering, Istanbul, Turkey.

Marmara University, Department of Chemical Engineering, Istanbul, Turkey.

出版信息

Int J Biol Macromol. 2024 Jan;255:128022. doi: 10.1016/j.ijbiomac.2023.128022. Epub 2023 Nov 14.

Abstract

In the current study, novel gelatin microspheres/methacrylated alginate hydrogel combined system (5-FU-GELms/Alg-MA) was developed for gastric targeted delivery of 5-fluorouracil as an anticancer agent. While water-in-oil emulsification method was used for the production of 5-FU-GELms, Alg-MA was synthesized through methacrylation reaction occurred by epoxide ring-opening mechanism. Then, 5-FU-GELms/Alg-MA hydrogel system was fabricated by the encapsulation of 5-FU-GELms into Alg-MA hydrogel network via UV-crosslinking. To evaluate applicability of fabricated 5-FU-GELms/Alg-MA as gastric targeted drug delivery vehicle, both swelling and in vitro drug release experiments were carried out at pH 1.2 medium resembling gastric fluid. Compared to drug release directly from 5-FU-GELms, 5-FU-GELms/Alg-MA hydrogel system showed more controlled and sustained drug release profile with lower amount of cumulative release starting from early stages, since hydrogel matrix created a barrier to the diffusion of 5-FU included in microspheres. Drug release kinetic results obtained by applying various kinetic models to release data showed that the mechanism of 5-FU release from 5-FU-GELms/Alg-MA hydrogel system is controlled by Fickian diffusion. All results revealed that 5-FU-GELms/Alg-MA hydrogel integrated system could be potentially utilized as gastric targeted drug carrier to enhance therapeutic efficacy and reduce systemic side effects in gastric cancer treatments for future studies.

摘要

在当前的研究中,开发了一种新型的明胶微球/甲基丙烯酰化藻酸盐水凝胶复合体系(5-FU-GELms/Alg-MA),用于将 5-氟尿嘧啶作为抗癌药物经胃靶向递送至体内。在制备 5-FU-GELms 时采用了水包油乳化法,而通过环氧化合物开环机制的甲基丙烯酰化反应合成了 Alg-MA。然后,通过将 5-FU-GELms 包封到 Alg-MA 水凝胶网络中,通过 UV 交联制备了 5-FU-GELms/Alg-MA 水凝胶体系。为了评估所制备的 5-FU-GELms/Alg-MA 作为胃靶向药物递送载体的适用性,在模拟胃液的 pH 1.2 介质中进行了溶胀和体外药物释放实验。与直接从 5-FU-GELms 释放药物相比,5-FU-GELms/Alg-MA 水凝胶体系显示出更受控和更持续的药物释放特性,从早期开始就有较低的累积释放量,因为水凝胶基质为包含在微球中的 5-FU 的扩散形成了屏障。通过将各种动力学模型应用于释放数据获得的药物释放动力学结果表明,5-FU 从 5-FU-GELms/Alg-MA 水凝胶体系中的释放机制受菲克扩散控制。所有结果表明,5-FU-GELms/Alg-MA 水凝胶集成体系可作为胃靶向药物载体用于未来的研究,以增强治疗效果并减少胃癌治疗中的全身副作用。

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