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溶剂法制备阿司匹林缓释固体分散体中载体对药物溶出度的影响 被引量:2

The Effect of Dissolution Rate for the Carriers in the Sustained Release Solid Dispersion of Aspirin Prepared by Solvent Method
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摘要 目的:采用溶剂法制备阿司匹林缓释固体分散体,并考查载体对药物体外溶出速度的影响.方法:分别选用乙基纤维素(EC)、羟丙甲基纤维素(HPMC)及甲基纤维素(MC)为辅料,通过测定阿司匹林在各种辅料水溶液的溶解度及固体分散体在水中的溶出度选择最优载体,来制备阿司匹林缓释固体分散体.结果:当选择EC和HPMC为共同载体,且药物:EC:HPMC的比例为1 7 0.7时,药物在2、6、12 h分别能溶出至30%、50%、80%左右,对药物可起到很好的缓释效果. Objective: Solvent method is used to prepare the sustained release solid dispersions of aspirin and the effect of carriers for dissolution rate of the drug is checked. Methods : Sustained release solid dispersions of aspirin have been prepared with EC, HPMC, MC, respectively. Then the optimal materials and the ratio from the solubility and dissolution test are chosen. Conclusion: The dissolution rate of drug was 30% ,50% ,80% at 2,6,12 h,when chosing the EC and HPMC as the cocarriers and the ratio of the drug: EC: HPMC was 1:7 : 0.7. The solid dispersion has a better sustained release effect for the drug.
出处 《吉林化工学院学报》 CAS 2014年第9期28-30,共3页 Journal of Jilin Institute of Chemical Technology
关键词 固体分散体 缓释 阿司匹林 体外溶出度 solid dispersion sustained release aspirin in vitro dissolution
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  • 1王玉,王东凯,张晓君,韩晓,刘相男,孙念.复方阿司匹林/硫酸氢氯吡格雷双层缓释片的制备[J].中国药剂学杂志(网络版),2010(3):81-88. 被引量:4
  • 2魏传梅,王滨,刘学红,刘呈华.固体分散技术在缓控释制剂中的应用[J].中国药师,2004,7(11):899-900. 被引量:2
  • 3崔福德.药剂学[M].北京:人民卫生出版社,2011:96.
  • 4Vo CL, Park C, Lee BJ. Current trends and future perspectives of sol- id dispersions containing poorly water-soluble drugs [ J ]. Eur J Pharm Biopharm, 2013, 85(3 Pt B) : 799-813.
  • 5Patel BB, Patel JK, Chakraborty S; Solubility enhancement using poly (meth) acrylate based solid dispersions [ J ]. Powder Technology" 2015, 270(A) : 27-38.
  • 6Liu X, Wang S, Chai L, et al. A two-step strategy to design high bio- available controlled-release nimodipine tablets: the push-pull osmotic pump in combination with the micronization/ solid dispersion tech- niques[ J]. lnt J Pharm, 2014, 461 (1-2) : 529-539.
  • 7Mahmah O, Tabbakh R, Kelly A, et al. A comparative study of the effect of spray drying and hot-melt extrusion on the properties of amor- phous solid dispersions contailfing felodipine[J]. J Pharm Pharmacol, 2014, 66(2) : 275-284.
  • 8EI Maghraby GM, Elsergany RN. Fast disintegrating tablets of nisol- dipine for iutra-oral administration [ J ]. Pharm Din; Technol, 2014, 19 (6) :641-650.
  • 9Hirasawa N, lshise S, Miyata H, et al. Physieochemical characteriza- tion and drug release studies of nilvadipine solid dispersions using wa- ter-insoluble polymer as a carrier[J]. Drug Dev Ind Pharm, 2003, 29 (3) : 339-344.
  • 10Jang DJ, Sire T, Oh E. Formulation and optimization of spray-dried arrdodipine solid dispersion for enhanced oral absorption [J]. Drug Dev Ind Pharm, 2013, 39(7) : 1133-1141.

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