ZHANG Xu-hui, SUN Yong-hai, ZHANG Hong. Preparation of polyactic-coglycolic acid morphine microspheres and establishment of its in vitro releasing modelJ. ACADEMIC JOURNAL OF CHINESE PLA MEDICAL SCHOOL, 2009, 30(2): 128-129.
Citation: ZHANG Xu-hui, SUN Yong-hai, ZHANG Hong. Preparation of polyactic-coglycolic acid morphine microspheres and establishment of its in vitro releasing modelJ. ACADEMIC JOURNAL OF CHINESE PLA MEDICAL SCHOOL, 2009, 30(2): 128-129.

Preparation of polyactic-coglycolic acid morphine microspheres and establishment of its in vitro releasing model

  • Objective: To study the preparation of polyactic-coglycolic acid(PLGA)morphine microspheres and establish its in vitro releasing model. Methods: PLGA morphine microspheres were prepared using the emulsify-solvent evaporation method and observed under a super-microscope.Drug content in morphine microspheres was detected by high performance liquid chromatography(HPLC).Dialysis method was used to examine the in vitro drug release.The release data fit three model equations. Results: The drug content in morphine microspheres accounted for 11.86%,and the ratio of drug envelopment was 33%.The releasing test in vitro showed that the releasing time of morphine microspheres could last over 10 days and fit the zero-model. Conclusion: PLGA morphine microspheres can obviously prolong the releasing time of morphine.
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