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Preparation of pH-responsive Polymeric Micelles based on Sodium Alginate and Its Drug Release Property |
Received:May 20, 2020 |
DOI:10.11981/j.issn.1000-6842.2021.02.18 |
Key Words:sodium alginate;polymeric micelles;pH-responsiveness;biomass material;drug release |
Fund Project:湖南省自然科学基金项目(2015JJ2008)。 |
Author Name | Affiliation | Postcode | HAN Junyuan* | School of Chemistry and Food Engineering, Changsha University of Science and Technology, Changsha, Hu'nan Province, 410114 | 410114 | WANG Yulong | School of Chemistry and Food Engineering, Changsha University of Science and Technology, Changsha, Hu'nan Province, 410114 | 410114 | LIU Qingjian | School of Chemistry and Food Engineering, Changsha University of Science and Technology, Changsha, Hu'nan Province, 410114 | 410114 | LIU Yanxin | School of Chemistry and Food Engineering, Changsha University of Science and Technology, Changsha, Hu'nan Province, 410114 | 410114 |
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Abstract: |
In this study sodium alginate (SA) was modified with 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride (EDC) and N-hydroxysuccinimide (NHS), then the sodium alginate-based pH-responsive polymer micelles were prepared. The Fourier transform infrared spectroscopy (FT-IR), critical micelle concentration (CMC), particle size, and Zeta potential were analyzed for SA before and after modified by EDC/NHS. The genistein was then encapsulated in polymeric micelles based on anti-solvent recrystallization method, and the drug loading efficiency, drug loading capacity, and pH responsiveness of the polymer micelles were studied. The results showed that EDC/NHS-modified SA could form polymer micelles in water, and its CMC was 0.041 mg/mL. The loading efficiency and drug loading capacity of polymeric micelles were 74.4% and 8.6%, respectively when the mass ratio of polymeric micelles to genistein was 10∶1. The in vitro release study showed that the polymeric micelles loaded with drug were pH-responsive and relatively stable under acidic conditions (pH value=2.0), and would release drugs under neutral conditions (pH value =7.4), enabling it to be used as a carrier for oral drugs absorbing by intestinal tract, so as to achieve controlled release and sustained release of drugs. |
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