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一种可调节时间的酮洛芬脉冲释放系统:在药代动力学研究和 IVIVC 评价中的体外和体内研究。

A time-adjustable pulsatile release system for ketoprofen: In vitro and in vivo investigation in a pharmacokinetic study and an IVIVC evaluation.

机构信息

Department of Pharmaceutics, School of Pharmacy, Shenyang Pharmaceutical University, 103 Wenhua Road, 110016 Shenyang, China.

Department of Pharmacy, Shanxi Medical College for Continuing Education, Jinzhong 030619, China.

出版信息

Eur J Pharm Biopharm. 2017 Oct;119:192-200. doi: 10.1016/j.ejpb.2017.06.015. Epub 2017 Jun 17.

DOI:10.1016/j.ejpb.2017.06.015
PMID:28633956
Abstract

A time-adjustable pulsatile release system (TAPS) containing ketoprofen (KF) as an active pharmaceutical agent was developed having been designed for bedtime dosing and releasing drug in the early morning to control the symptoms of rheumatoid arthritis (RA). The formulation involved a tablet core (KF) and a control-release layer, and the coating membrane was composed of EC and Eudragit L100. A single-factor study, a central composite design and a response surface method were selected to optimize the formula and the optimum prescription was as follows: tablet core (KF 50mg, MCC 70mg, lactose 40mg, L-HPC 38mg), and film (EC 7.8g, Eudragit L100 4.2g, PEG 6000 1.8g in 95% alcohol each 200ml). The in vivo release behavior of the tablets was evaluated in Beagle dogs after a parallel oral administration of KF TAPS tablets and commercial KF capsules, when it was found that the KF TAPS tablets released the drug after a lag-time of 3.458h and the T was 5.833h. The relative bioavailability was 85.01%, and the two formulations were bioequivalent in terms of C and AUC and the in vitro- in vivo correlations indicated that test formulation had a good in vivo-in vitro correlation (r=0.9703). These results show that the novel drug delivery system (TAPS) has the potential to be used as a KF preparation with chronophamacokinetics characteristics.

摘要

一种含有酮洛芬(KF)作为活性药物成分的时间可调脉冲释放系统(TAPS)被开发出来,旨在睡前给药,并在清晨释放药物,以控制类风湿关节炎(RA)的症状。该制剂包括片剂芯(KF)和控释层,包衣膜由 EC 和 Eudragit L100 组成。选择单因素研究、中心组合设计和响应面法来优化配方,最佳处方如下:片剂芯(KF 50mg、MCC 70mg、乳糖 40mg、L-HPC 38mg)和薄膜(EC 7.8g、Eudragit L100 4.2g、PEG 6000 1.8g,各用 95%乙醇 200ml)。在 Beagle 犬中进行平行口服 KF TAPS 片剂和商业 KF 胶囊后,评估了片剂的体内释放行为,结果发现 KF TAPS 片剂在滞后时间 3.458h 后释放药物,T 为 5.833h。相对生物利用度为 85.01%,两种制剂在 C 和 AUC 方面具有生物等效性,体外-体内相关性表明试验制剂具有良好的体内-体外相关性(r=0.9703)。这些结果表明,新型药物递送系统(TAPS)具有作为具有时间药效学特征的 KF 制剂的潜力。

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