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Preparation and In Vitro Release of Ramose Chitosan-Based-5-Fluorouracil Microspheres
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  • Preparation and In Vitro Release of Ramose Chitosan-Based-5-Fluorouracil Microspheres
  • Preparation and In Vitro Release of Ramose Chitosan-Based-5-Fluorouracil Microspheres
저자명
Li. He-Ping,Li. Hui,Wang. Zhou-Dong,Zhang. Juan-Juan,Deng. Man-Feng,Chen. San-Long
간행물명
대한화학회지
권/호정보
2013년|57권 1호|pp.88-93 (6 pages)
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대한화학회
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정기간행물|ENG|
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
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기타언어초록

In order to construct a controlled release system of drugs and to reduce toxic side effects of 5-fluorouracil, the novel ramose chitosan-based-5-fluorouracil microspheres (CS-FU-MS) were prepared. Firstly, using chitosan (CS) as carriers and 5-fluorouracil (5-FU) as a model drug, ramose chitosan-based-5-fluorouracil (CS-FU) was efciently synthesized by chemical crosslinking method through microwave irradiation, drug loading was 10.6%; Secondly, CS-FU-MS were prepared by CS-FU self-assembled under the dialysis conditions and the free 5-FU was encapsulated further at the same time. The size dispersivity of particles is uniform, and the average diameter of the CS-FU-MS was $4{mu}m$. The drug encapsulation efficiency was 76.1%, and the drug loading was increased to 26.22%. CS-FU-MS maintain the zero-order release time in PBS (pH = 7.4) and HCl/KCl (pH = 1.2) dialysis medium was 40h and 34h respectively, and the cumulative release were 58.89% and 79.33% in 182 h. The results showed that CS-FU-MS have excellent sustained release properties.