4.1 Article

Design, Synthesis, and Preparation of Ultrasound-Responsive Curcumin-Loaded Chitosan Nanocarriers

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RUSSIAN JOURNAL OF GENERAL CHEMISTRY
卷 93, 期 1, 页码 108-115

出版社

MAIK NAUKA/INTERPERIODICA/SPRINGER
DOI: 10.1134/S1070363223010152

关键词

curcumin; chitosan; nanoparticles; ultrasonic stimulation; controllable drug release

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In this study, functional materials with liver-targeting and ultrasound-responsive properties were prepared by alkylating chitosan with o-nitrobenzyl. Curcumin-loaded Chitosan nanoparticles were then prepared using the ion-crosslinking method. The nanoparticles exhibited high encapsulation efficiency (89%) and a particle size of approximately 520 nm. The release of curcumin from the nanoparticles was slow under ultrasound-free conditions, but increased significantly when stimulated by ultrasound, suggesting the potential application of on-demand released drug delivery systems.
In this study, chitosan was alkylated by o-nitrobenzyl to obtain liver-targeting and ultrasound-responsive functional materials. The Curcumin-loaded Chitosan nanoparticles were prepared by ion-crosslinking method. The encapsulation efficiency of the nanoparticles was about 89%, and the particle size of Curcumin-loaded Chitosan nanoparticles was about 520 nm. The in vitro drug release of curcumin from Curcumin-loaded Chitosan nanoparticles under ultrasound-free condition was very slow within 0-48 h, while the release of curcumin was very quick when the Curcumin-loaded Chitosan nanoparticles were stimulated by the ultrasound within 1-45 h. The ultrasound stimulation could cause a significant effect in promoting drug release from nanocarriers, indicating the broad application prospects of the on-demand released drug delivery systems.

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