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磷酸川芎嗪犬一日一次控释微丸的制备与药代动力学研究。

Preparation and pharmacokinetics in beagle dogs of once-a-day tetramethylpyrazine phosphate sustained-release pellets.

机构信息

Department of Pharmacy, China Pharmaceutical University, Nanjing, China.

出版信息

Drug Dev Ind Pharm. 2012 Mar;38(3):301-6. doi: 10.3109/03639045.2011.602408. Epub 2011 Aug 19.

Abstract

In this study, once-a-day tetramethylpyrazine phosphate (TMPP) sustained-release pellets were successfully prepared. The pellets cores were carried out in extrusion-spheronization machine and then coated in fluidized-bed. To optimize cumulative release profile, two different coating systems with the same the TMPP pellets cores were employed. The first coating system consisted of surlease, containing HPMC E5 (0.1% w/w), i.e., P1. The second coating system only consisted of surlease, i.e., P2. The two kinds of coating systems were both given coating levels in terms of weight gain of 10%. The resulted once-a-day TMPP sustained-release pellets (OTSP), the mixture of P1 and P2 with the weight proportion of 1:1, were filled in a capsule (150 mg TMPP/capsule). The relative bioavailability of OTSP was studied in six beagle dogs after oral administration using a commercial TMPP tablets as a reference. The C(max) and T(max) for OTSP and TMPP tablets were 213.06 ng/mL, 2.50 h and 3402.13 ng/mL, 0.33 h, respectively and the relative bioavailability of P3 was 97.18% compared with TMPP tablets. Based on the results, it was indicated that TMPP sustained-release pellets and TMPP conventional tablets were bioequivalent.

摘要

在这项研究中,成功制备了每日一次的磷酸川芎嗪(TMPP)缓释微丸。微丸核芯采用挤出滚圆机制备,然后在流化床中包衣。为了优化累积释放曲线,采用两种不同的包衣系统对相同的 TMPP 微丸核芯进行包衣。第一种包衣系统由包含 HPMC E5(0.1%w/w)的 surlease 组成,即 P1。第二种包衣系统仅由 surlease 组成,即 P2。两种包衣系统的包衣增重均为 10%。得到的每日一次 TMPP 缓释微丸(OTSP),即 P1 和 P2 以 1:1 的重量比例混合,填充在胶囊中(150mgTMPP/胶囊)。将 OTSP 和 TMPP 片剂作为参比制剂,在 6 只比格犬中进行了口服给药后的相对生物利用度研究。OTSP 和 TMPP 片剂的 Cmax 和 Tmax 分别为 213.06ng/mL 和 2.50h,3402.13ng/mL 和 0.33h,P3 与 TMPP 片剂的相对生物利用度为 97.18%。基于这些结果,表明 TMPP 缓释微丸和 TMPP 普通片剂具有生物等效性。

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