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溶胶-凝胶包埋阿昔洛韦与二氧化硅基质的相互作用。

Interactions of sol-gel encapsulated acyclovir with silica matrix.

机构信息

G.A. Krestov Institute of Solution Chemistry of Russian Academy of Sciences, 1 Academicheskaya Str., Ivanovo, 153045, Russian Federation.

G.A. Krestov Institute of Solution Chemistry of Russian Academy of Sciences, 1 Academicheskaya Str., Ivanovo, 153045, Russian Federation.

出版信息

Colloids Surf B Biointerfaces. 2019 Jun 1;178:103-110. doi: 10.1016/j.colsurfb.2019.02.052. Epub 2019 Feb 27.

Abstract

Encapsulation of drugs is promising strategy to improve their pharmacological and consumer properties. The functional properties of the encapsulated drug depend on interactions between the drug and capsule material. Antiviral drug acyclovir (ACV) was encapsulated in silica matrixes using sol-gel technology. The effects of synthesis pH and the silica matrix functionalization by organic groups on the drug - silica matrix interaction were studied. The interactions were investigated using UV/VIS spectroscopy and Fourier-transform infrared (FTIR) spectroscopy. The nature of the interactions in the obtained composites was discussed. It was found that the drug self-association in some composites can be provoked by electrostatic repulsion between the drug and the silica matrix.

摘要

药物包封是改善其药理和消费性能的有前途的策略。被包封药物的功能性质取决于药物与胶囊材料之间的相互作用。使用溶胶-凝胶技术将抗病毒药物阿昔洛韦(ACV)包封在二氧化硅基质中。研究了合成 pH 值以及有机基团对二氧化硅基质功能化对药物-二氧化硅基质相互作用的影响。使用紫外/可见光谱法和傅里叶变换红外(FTIR)光谱法研究了相互作用。讨论了所得复合材料中的相互作用性质。结果发现,在某些复合材料中,药物与二氧化硅基质之间的静电排斥作用可能会引起药物的自组装。

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