首页|二氧化硅载药微球的制备及其缓释性能

二氧化硅载药微球的制备及其缓释性能

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以水包油型的Pickering乳液为模板,以阿司匹林为药物模型,分别通过一步合成法和后负载法制备二氧化硅载药微球。采用光学显微镜,傅里叶变换红外(FTIR)光谱对制备的阿司匹林载药微球进行形貌及结构的表征。结果表明,微球为均匀的球形,阿司匹林存在于微球中。探究了 2种载药微球在模拟肠液和模拟胃液中的缓释性能,通过一步合成法得到的二氧化硅载药微球在模拟肠液和模拟胃液中均表现出缓慢的药物释放速率。
Preparation and release performance of drug loaded silica microspheres
In this paper,using an oil-in-water Pickering emulsion as template and aspirin as drug model,SiO2 drug-loaded microspheres were prepared by one-step synthesis and post-loading method.The morphology and structure of drug-loaded microspheres were characterized by Fourier transform infrared(FTIR)spectroscopy and optical microscope.The results of optical microscopy showed that the microspheres were uniform and the FTIR analysis showed that aspirin existed in the microsphere.And then the release performances of the above two kinds of drug-loaded microspheres were investigated.The results showed that the drug-loaded microspheres through one-step synthesis method showed slow drug release rate in simulated intestinal fluid and gastric fluid.

Pickering emulsionTemplate methodSilicaAspirinSustained-release

魏丽娟、张婉雪、赵维

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咸阳师范学院化学与化工学院,陕西咸阳 712000

Pickering乳液 模板法 二氧化硅 阿司匹林 缓释

陕西省自然科学基础研究计划陕西省教育厅科研项目咸阳师范学院科研计划

2022JQ-13523JK0717XSYK21033

2024

化工科技
中国石油天然气股份有限公司吉林石化分公司

化工科技

CSTPCD
影响因子:0.386
ISSN:1008-0511
年,卷(期):2024.32(2)