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多西环素牙周缓释凝胶的配方筛选研究

Formula Screening Study on Periodontal Sustained-release Gel with Doxycycline
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摘要 目的探索一种牙周缓释凝胶的最佳配方。方法将聚乳酸-乙醇酸共聚物(PLGA)浓度、溶剂配比和多西环素浓度按三个水平作正交设计,进行体外释放度试验,以第6天的释放百分率和凝结时间的综合分为指标,计算极差。结果按极差大小,PLGA浓度>溶剂配比>多西环素浓度,最佳配方为PLGA浓度15%,1MP:GTA=7:3,多西环素浓度为6%。结论用正交设计进行配方筛选是一种较好的试验方法。 OBJECTIVE To explore a best formula of sustained-released gel. METHODS Made an orthogonal design at 3 levels of 3 factors ( concentration of PLGA, portion of solvent and concentration of doxycycline) to measure the concentration of doxycycline in vitro, caculated the range using the releasing rate on the sixth day and score of coagulate time as parameter. RESULTS According to the range, PLGA's concentration 〉 solvent's portion 〉 doxycycline's concentration,the best formula was:the concentration of PLGA80 : 20 = 15 % (w/w) , 1MP: GTA = 7:3 and doxycycline concentration = 6 % (w/w). CONCLUSION It is a good screening method to find out the best formula by orthogonal design.
出处 《中国现代应用药学》 CAS CSCD 北大核心 2007年第6期484-486,共3页 Chinese Journal of Modern Applied Pharmacy
关键词 缓释凝胶 聚乳酸-乙醇酸共聚物 多西环素 正交设计 sustained-released gel PLGA doxycycline orthogonal design
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  • 1KIM T S,BURKLIN T,SCHACHER B,et al.Pharmacokinetic profile of a locally administered doxycycline gel in crevicular fluid,blood,and saliva[J].J Periodontol,2002,73(11):1285-1291.
  • 2JOHNSON L R,STOLLER N H,POLSON A,et al.The effects of subgingival calculus on the clinical outcomes of locally-delivered controlled-release doxycycline compared to scaling and root planing[J].J Clin Periodontol,2002,29(2):87-91.
  • 3张国栋,杨纪元,冯新德,顾忠伟.聚乳酸的研究进展[J].化学进展,2000,12(1):89-102. 被引量:137
  • 4张蜀,谭载友,陈济民,李帼姬,陈绍斌.盐酸多西环素注入用缓释凝胶的体外释放度研究[J].中国新药杂志,2003,12(9):731-734. 被引量:15
  • 5NIYX.Discuss between Multiindex test formula and integrate compare.应用概率统计,1988,4(1):85-88.
  • 6GONG Z,ZHOU S C,MA Y L,et al.Clinical usage of antibiotics(抗生素的临床应用)[M].Hangzhou:Zhejiang Science and Technology Publishing House,1985:3,125.
  • 7GRAYSON A C,VOSKERICIAN G,LYNN A,et al.Differential degradation rates in vivo and in vitro of biocompatible poly(lactic acid) and poly(glycolic acid) homo-and co-polymers for a polymeric drug-delivery microchip[J].J Biomater Sci Polym Ed,2004,15(10):1281-304.
  • 8TRACY M A,WARD K L,FIROUZABADIAN L,et al.Factors affecting the degradation rate of poly(lactide-co-glycolide) microspheres in vivo and in vitro[J].Biomaterials,1999,20(11):1057-1062.

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