Yataba Ikuko, Otsuka Noboru, Matsushita Isao, Kamezawa Miho, Yamada Ichimaro, Sasaki Sigeru, Uebaba Kazuo, Matsumoto Hideo, Hoshino Yuichi
Development Headquarters, Taisho Pharmaceutical Co. Ltd, 3-24-1 Takada, Toshima-ku, Tokyo, 170-8633, Japan.
Mitsubishi Tanabe Pharma Corporation, Tokyo, Japan.
Eur J Clin Pharmacol. 2016 Jan;72(1):53-9. doi: 10.1007/s00228-015-1960-6. Epub 2015 Oct 6.
The purpose of this study is to investigate the pharmacokinetics and deep tissue penetration capability of the newly developed S-flurbiprofen plaster (SFPP) in humans.
Study 1: SFPP tape-type patch (2-60 mg) was applied to the lower back for 24 h in healthy adult volunteers. S-flurbiprofen (SFP) plasma concentration was measured over time to examine SFP pharmacokinetics. Study 2: SFPP (20 mg) was applied for 12 h to the affected knee of osteoarthritis (OA) patients who were scheduled for total knee arthroplasty. Deep tissues (synovial tissue and synovial fluid) were collected during surgery to compare SFP concentrations after application of SFPP or a commercially available flurbiprofen (FP) gel-type patch.
Study 1: The plasma concentration of SFP was sustained during 24-h topical application of the SFPP, showing a high percutaneous absorption ratio of 51.4-72.2 %. Cmax and AUC0-∞ were dose-proportional. Study 2: After application of the SFPP for 12 h, SFP concentrations in the synovial tissue and synovial fluid were 14.8-fold (p = 0.002) and 32.7-fold (p < 0.001) higher, respectively, than those achieved by the FP patch.
Sustained plasma concentration of SFP and high percutaneous absorption ratio was observed after 24-h topical application of the SFPP. Compared to the FP patch, the SFPP showed superior percutaneous absorption and greater tissue penetration of SFP into the synovial tissue. Greater tissue penetration of the SFPP seemed to be primarily due to its formulation. Thus, SFPP is expected to show higher efficacy for the treatment of knee OA.
本研究旨在探讨新开发的S-氟比洛芬贴剂(SFPP)在人体中的药代动力学及深部组织渗透能力。
研究1:在健康成年志愿者的下背部应用SFPP带状贴剂(2 - 60毫克)24小时。随时间测量S-氟比洛芬(SFP)血浆浓度,以研究SFP的药代动力学。研究2:将SFPP(20毫克)应用于计划进行全膝关节置换术的骨关节炎(OA)患者的患膝12小时。在手术期间收集深部组织(滑膜组织和滑液),以比较应用SFPP或市售氟比洛芬(FP)凝胶型贴剂后SFP的浓度。
研究1:在SFPP 24小时局部应用期间,SFP的血浆浓度保持稳定,经皮吸收比率高达51.4 - 72.2%。Cmax和AUC0-∞与剂量成正比。研究2:应用SFPP 12小时后,滑膜组织和滑液中SFP的浓度分别比FP贴剂高14.8倍(p = 0.002)和32.7倍(p < 0.001)。
SFPP局部应用24小时后,观察到SFP血浆浓度持续稳定且经皮吸收比率高。与FP贴剂相比,SFPP显示出更好的经皮吸收以及SFP向滑膜组织的更强组织渗透能力。SFPP更强的组织渗透能力似乎主要归因于其剂型。因此,预计SFPP在治疗膝骨关节炎方面具有更高的疗效。