麝香保心pH依赖型梯度释药微丸的研究  被引量:45

STUDIES ON HEART-PROTECTING MUSK pH-DEPENDENT GRADIENT-RELEASE PELLETS

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作  者:宋洪涛[1] 郭涛[1] 张汝华[2] 马燕[2] 李铣[2] 毕开顺[2] 

机构地区:[1]沈阳军区总医院药剂科,辽宁沈阳110016 [2]沈阳药科大学,辽宁沈阳110016

出  处:《药学学报》2002年第10期812-817,共6页Acta Pharmaceutica Sinica

基  金:辽宁省博士启动基金项目 (2 0 0 110 2 0 42 )

摘  要:目的 制备麝香保心pH依赖型梯度释药微丸并进行体内外考察。方法 分别以HPMC ,EudragitL 30D 5 5和EudragitL10 0 EudragitS10 0 (1∶5 )为包衣材料制备pH依赖型梯度释药微丸 ,并进行体外释放度、胃肠道转运和体内药代动力学研究。结果 冰片和人参总皂苷体外释放度的f2 值为 79 6 ,3种包衣微丸分别在胃、十二指肠和空回肠部崩解 ,由 3种微丸组成的缓释胶囊中冰片的Tmax与原丸剂相近 ,而Cmax明显降低 ,相对生物利用度为 96 %。结论缓释胶囊中的冰片和人参总皂苷在体外可同步缓释 ,在体内具有pH依赖性崩解溶散的特征 ,冰片作为指标性成分具有梯度缓释的药代动力学特点。AIM To prepare heart protecting musk pH dependent gradient release pellets and investigate the drug release in vitro and in vivo . METHODS The pH dependent gradient release pellet system was prepared by using HPMC, Eudragit L 30D 55 and Eudragit L100 Eudragit S100 ( 1∶5 ) combinations as coater. The release of borneol and total ginsenoside from pH dependent gradient release pellets were determined according to the method of Pharmacopoeia of the People's Republic of China (2000) in the simulated gastrointestinal pH conditions. The gastrointestinal transit and disintegration of pellets was investigated by using γ scintigraphic trace in volunteers. The pharmacokinetics of borneol of heart protecting musk pH dependent gradient release pellets was studied in 6 healthy volunteers by GC methods. RESULTS The f 2 value of release data of borneol and total ginsenoside of the heart protecting musk pH dependent gradient release pellets was 79 6 in the simulated gastrointestinal pH conditions. The γ scintigraphic trace evaluation demonstrated that the pellets coated with HPMC, Eudragit L 30D 55 or Eudragit L100 Eudragit S100 ( 1∶5 ) combinations can disintegrate in stomach, duodenum and jejunum or ileum. The gastrointestinal transit time of pellets was about 5 hours in fasted state and about 6 hours in fed state. The concentration time curves of borneol of heart protecting musk pills fit in two compartment model. The pharmacokinetics data showed that borneol had a short time of absorption and elimination. The mean residence time (MRT) of borneol of heart protecting musk pills was 2 61 hours. The plasma concentration of borneol of heart protecting musk sustained release capsule which consisted of three kinds of pellets coated with HPMC, Eudragit L 30D 55 or Eudragit L100 Eudragit S100 ( 1∶5 ) combinations was steadier than those of heart protecting musk pills, its C max was lower than and T max was near to those of heart protecting musk pills, its

关 键 词:复方中药 麝香保心微丸 pH依赖型梯度释药系统 胃肠道转运 药代动力学 

分 类 号:R285.1[医药卫生—中药学]

 

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