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用于递送姜黄素的多孔微凝胶:基于微流控技术的制备及细胞毒性评估

Porous Microgels for Delivery of Curcumin: Microfluidics-Based Fabrication and Cytotoxicity Evaluation.

作者信息

Orbay Sinem, Sanyal Rana, Sanyal Amitav

机构信息

Institute of Biomedical Engineering, Bogazici University, Istanbul 34684, Türkiye.

Biomedical Engineering Department, Erzincan Binali Yildirim University, Erzincan 24002, Türkiye.

出版信息

Micromachines (Basel). 2023 Oct 22;14(10):1969. doi: 10.3390/mi14101969.

Abstract

Polymeric microgels, fabricated via microfluidic techniques, have garnered significant interest as versatile drug delivery carriers. Despite the advances, the loading and release of hydrophobic drugs such as curcumin from polymeric microgels is not trivial. Herein, we report that effective drug loading can be achieved by the design of porous particles and the use of supramolecular cyclodextrin-based curcumin complexes. The fabrication of porous microgels through the judicious choice of chemical precursors under flow conditions was established. The evaluation of the curcumin loading dependence on the porosity of the microgels was performed. Microgels with higher porosity exhibited better curcumin loading compared to those with lower porosity. Curcumin-loaded microgels released the drug, which, upon internalization by U87 MG human glioma cancer cells, induced cytotoxicity. The findings reported here provide valuable insights for the development of tailored drug delivery systems using a microfluidics-based platform and outline a strategy for the effective delivery of hydrophobic therapeutic agents such as curcumin through supramolecular complexation.

摘要

通过微流控技术制备的聚合物微凝胶作为多功能药物递送载体已引起了广泛关注。尽管取得了这些进展,但从聚合物微凝胶中负载和释放姜黄素等疏水药物并非易事。在此,我们报告通过设计多孔颗粒和使用基于超分子环糊精的姜黄素复合物可以实现有效的药物负载。通过在流动条件下明智地选择化学前体建立了多孔微凝胶的制备方法。进行了姜黄素负载量对微凝胶孔隙率依赖性的评估。与孔隙率较低的微凝胶相比,孔隙率较高的微凝胶表现出更好的姜黄素负载量。负载姜黄素的微凝胶释放药物,该药物在被U87 MG人胶质瘤癌细胞内化后诱导细胞毒性。本文报道的研究结果为使用基于微流控的平台开发定制药物递送系统提供了有价值的见解,并概述了通过超分子络合有效递送姜黄素等疏水治疗剂的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e3b/10609253/03b7c1b3fdb4/micromachines-14-01969-g001.jpg

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