Synthesis of F127-GA@ZnO nanogel as a cisplatin drug delivery pH-sensitive system

被引:1
|
作者
Son, Nguyen Ngoc [1 ]
Thanh, Vu Minh [1 ]
Huong, Nguyen Thi [1 ]
机构
[1] Inst Chem & Mat, 17 Hoang Sam, Hanoi, Vietnam
关键词
ZINC-OXIDE NANOPARTICLES; ZNO NANOPARTICLES; GALLIC ACID; MOLECULAR-MECHANISMS; TARGETED DELIVERY; INDUCE APOPTOSIS; IFOSFAMIDE; PACLITAXEL; RESISTANCE; POLOXAMER;
D O I
10.1039/d4ra06514j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this study, a novel drug delivery system based on zinc oxide nanoparticles (ZnO NPs) was developed for the enhanced delivery of cisplatin (CPT) to improve cancer treatment. The ZnO NPs were synthesized from guava leaf extract and then surface-functionalized with gallic acid (GA) to improve their biocompatibility and drug loading capacity. Pluronic F127, a biocompatible polymer, was then conjugated to the GA-modified ZnO NPs to further enhance their stability and cellular uptake. The resulting NPs were characterized by various techniques, including FT-IR, UV-Vis, SEM, TEM, 1H NMR, and DLS. The drug loading and release profiles of CPT from the NPs were investigated, showing high CPT loading capacity and pH-dependent release behavior. The in vitro cytotoxicity of the NPs was evaluated against various cancer cell lines, demonstrating enhanced cytotoxicity compared to free CPT. Overall, this study highlights the potential of GA and Pluronic-modified ZnO NPs as a promising drug delivery system for enhanced CPT delivery and improved cancer therapy.
引用
收藏
页码:35005 / 35020
页数:16
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