Tang Dan-Dan, Zhang Jiao, Wang Ji-Rui, Zhang Ji-Fen, Xu Xiao-Yu
College of Pharmaceutical Sciences, Southwest University, Chongqing 400716, China.
Chongqing Engineering Research Center for Pharmacological Evaluation, Chongqing 400716, China.
Zhongguo Zhong Yao Za Zhi. 2016 Mar;41(5):940-947. doi: 10.4268/cjcmm20160529.
To compare the effects of different preparation technologies on the concentrations of puerarin and catalpol in plasma and brain of rats after oral administration, in order to lay an experimental basis for developing new oral Zige preparations. The nanocrystal, self-microemulsions (tween-80 and Cremophor RH-40 as emulsifiers) and inclusion complex of HP-β-CD containing puerarin and catalpol were prepared. The concentrations of puerarin and catalpol in plasma and brain of rats after oral administration were determined by HPLC-MS/MS method. The pharmacokinetic parameters and brain target index were compared. The results showed that preparation technologies had different influences on the concentrations of puerarin and catalpol in plasma and brain. The self-microemulsion (tween-80) could significantly increase the oral absorption of puerarin than other technologies(P<0.05), and inclusion complex could remarkably increase the oral absorption of catalpol than nanocrystal(P<0.01). For puerarin, the brain targeting index of inclusion complex was the highest (P<0.05); but for catalpol, the brain targeting index of inclusion complex and self-microemulsions were both higher than nanocrystal (P<0.05). The self-microemulsion(tween-80) had the highest AUCbrain of puerarin than other groups (P<0.01); the inclusion complex had the highest AUCbrain for catalpol, but there was no significant difference compared with self-microemulsions. In conclusion, the self-microemulsion (tween-80) technology could increase the amount of puerarin and catalpol in brain, and was expected to be used in new oral Zige preparations.
为比较不同制剂技术对大鼠口服给药后血浆及脑组织中葛根素和梓醇浓度的影响,为开发新的紫葛口服制剂奠定实验基础。制备了葛根素和梓醇的纳米晶、自微乳(以吐温-80和聚氧乙烯蓖麻油RH-40为乳化剂)及HP-β-CD包合物。采用HPLC-MS/MS法测定大鼠口服给药后血浆及脑组织中葛根素和梓醇的浓度。比较了药代动力学参数和脑靶向指数。结果表明,制剂技术对血浆及脑组织中葛根素和梓醇的浓度有不同影响。自微乳(吐温-80)能比其他技术显著提高葛根素的口服吸收量(P<0.05),包合物能比纳米晶显著提高梓醇的口服吸收量(P<0.01)。对于葛根素,包合物的脑靶向指数最高(P<0.05);但对于梓醇,包合物和自微乳的脑靶向指数均高于纳米晶(P<0.05)。自微乳(吐温-80)组葛根素的AUCbrain最高,高于其他组(P<0.01);包合物组梓醇的AUCbrain最高,但与自微乳组相比无显著差异。综上所述,自微乳(吐温-80)技术可提高葛根素和梓醇在脑中的含量,有望用于新的紫葛口服制剂。