Perlik Vit, Kulasekaran Anuradha, Coutinho Graça, Votava Martin, Cardot Jean-Michel
Institute of Pharmacology, First Faculty of Medicine, Charles University, Albertov 4, 12800 Prague, Czech Republic.
Reckitt Healthcare Limited, 103-105 Bath Road, Slough, Berkshire SL1 3UH, UK.
Pharmaceutics. 2023 Jul 1;15(7):1863. doi: 10.3390/pharmaceutics15071863.
This study aimed to link pharmacokinetic (PK) data from different flurbiprofen preparations for the treatment of sore throat with published data to elucidate whether early efficacy is due to the local action of flurbiprofen or a systemic effect after absorption of the swallowed drug. Three comparative bioavailability studies conducted in healthy subjects provided data from flurbiprofen 8.75 mg formulations, including spray solution, spray gel, lozenges, and granules. A parallel interstudy comparison was made of PK parameters, including partial AUCs (pAUCs), using an ANOVA model with the calculation of 90% confidence intervals (CI) for the differences between least squares (LS) means for each of the test groups versus the respective reference groups. All three studies showed bioequivalence for the respective product comparisons. The interstudy comparison showed a slower rate of absorption for granules compared to spray solution (reference) based on T, C, and pAUCs for 1 h and 2 h. When AUC and AUC were considered, slower rates of absorption were also seen for lozenges and spray gel. The differences correlated with the reported time of onset of action, which is faster for the spray solution (20 min) compared to lozenges (26 min) and granules (30 min). These pAUCs provide useful data that allow for the discrimination between formulations. Moreover, the pAUC values represent <5% of the total AUC, suggesting that the early onset of pain relief is a response to immediate local absorption at the site of action rather than a systemic effect.
本研究旨在将不同氟比洛芬制剂治疗咽喉痛的药代动力学(PK)数据与已发表的数据相联系,以阐明早期疗效是由于氟比洛芬的局部作用还是吞咽药物吸收后的全身效应。在健康受试者中进行的三项比较生物利用度研究提供了氟比洛芬8.75 mg制剂的数据,包括喷雾溶液、喷雾凝胶、含片和颗粒剂。使用方差分析模型对PK参数(包括部分AUCs(pAUCs))进行了平行的研究间比较,并计算了每个试验组与各自参考组的最小二乘(LS)均值之间差异的90%置信区间(CI)。所有三项研究均表明各产品比较具有生物等效性。基于1小时和2小时的T、C和pAUCs,研究间比较显示颗粒剂的吸收速率比喷雾溶液(参比制剂)慢。当考虑AUC和AUC时,含片和喷雾凝胶的吸收速率也较慢。这些差异与报告的起效时间相关,喷雾溶液(20分钟)的起效时间比含片(26分钟)和颗粒剂(30分钟)快。这些pAUCs提供了有用的数据,可用于区分不同制剂。此外,pAUC值占总AUC的<5%,这表明疼痛缓解的早期起效是作用部位即时局部吸收的反应,而非全身效应。