含PTX定向治疗乳腺癌的肝素-波洛沙姆p407纳米凝胶的合成

Q2 Engineering
Ngoc The Nguyen
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引用次数: 0

摘要

摘要本研究成功合成了不同接枝率的肝素-波洛沙姆P407 (HR-P407)缀合纳米凝胶。采用傅里叶变换红外光谱(FT-IR)和质子核磁共振(1h - nmr)对产物的结构性质进行了表征。采用动态光散射(DLS)方法对纳米颗粒的形貌和粒径进行了表征,结果表明纳米颗粒的粒径分布范围在144 ~ 214 nm之间。HR-P407纳米凝胶系统具有生物相容性,对健康细胞无毒。虽然游离PTX表现出快速和有效的细胞毒性作用,但HR-P407 (1:10)/PTX释放的PTX表现出逐渐和持续的细胞毒性。这种控制释放机制允许延长药物暴露时间,降低急性毒性并随着时间的推移增强细胞毒性。结果表明,所合成的纳米凝胶可作为一种有效的疏水抗癌药物载体体系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis of heparin-and-poloxamer P407-based nanogel carrying PTX for orientating in treatment of breast cancer
Abstract In this study, nanogels based on the conjugation of heparin and poloxamer P407 (HR-P407) with different grafting ratios were successfully synthesised. The structural properties of products were evaluated by Fourier-transform infrared spectroscopy (FT-IR) and proton nuclear magnetic resonance ( 1 H-NMR). The morphology and size of nanoparticles were assessed by dynamic light scattering (DLS) method, which showed that particle size distribution was from 144 nm to 214 nm. The HR-P407 nanogel systems were biocompatible and non-toxic to healthy cells. While free PTX displayed rapid and potent cytotoxic effects, PTX released from HR-P407 (1:10)/PTX demonstrated a gradual and sustained cytotoxicity. This controlled release mechanism allowed prolonged drug exposure, reducing acute toxicity and enhancing cytotoxicity over time. The results suggest that the synthesised nanogels can be used as an effective hydrophobic anticancer drug carrier system.
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来源期刊
Advances in Natural Sciences: Nanoscience and Nanotechnology
Advances in Natural Sciences: Nanoscience and Nanotechnology Engineering-Industrial and Manufacturing Engineering
CiteScore
3.80
自引率
0.00%
发文量
60
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