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两种喹硫平缓释片在中国健康志愿者空腹及进食条件下的生物等效性以及食物对药代动力学特征的影响。

Bioequivalence of two quetiapine extended release tablets in Chinese healthy volunteers under fasting and fed conditions and effects of food on pharmacokinetic profiles.

作者信息

Huang Xiaomei, Zhang Suhua, Ma Yanxia, Yang Heng, He Chuan, Tian Rufang, Mei Han, Liu Lipeng, Zhang Bikui

机构信息

Department of National Drug Clinical Trial Research Center, Xiangya Boai Rehabilitation Hospital, Changsha, People's Republic of China,

Department of Pharmacy, The Second Xiangya Hospital of Central South University, Changsha, People's Republic of China,

出版信息

Drug Des Devel Ther. 2018 Dec 31;13:255-264. doi: 10.2147/DDDT.S182965. eCollection 2019.

Abstract

OBJECTIVE

The objectives of this study were to evaluate the bioequivalence of Quesero extended release (Quesero XR) tablets and Seroquel extended release (Seroquel XR) tablets under fasting and fed conditions and to determine the effect of food on the pharmacokinetic (PK) properties of Quesero XR or Seroquel XR in Chinese healthy volunteers.

METHODS

A single-site, randomized, open-label, two-period crossover design with a 10-day washout period was conducted in 20 subjects under the fed and fasting studies. A single oral dose of 200 mg Quesero XR or Seroquel XR was given to the subjects after an overnight fast of 10 hours. Blood samples were taken at scheduled time spots from 0 hour pre dose to 36 hours post dose. Plasma concentrations of quetiapine were measured by a validated ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method. The PK parameters were calculated by non-compartment analysis using Phoenix WinNonlin software.

RESULTS

On both conditions, no significant differences were found among the main PK parameters of the two preparations by analysis of variance (>0.05); the Wilcoxon test of maximum peak plasma concentration (T) showed no significant differences (>0.05); the 90% confidence limit (CL) of lnC, lnAUC, and lnAUC fell within the acceptable range of 80%-125%. As compared with the fasting state, the T was advanced and the mean maximum plasma concentration (C), AUC, and AUC were also increased in the fed state; the geometric mean ratio and 90% CI of the main PK parameters fell outside the range of the CIs; analysis of variance showed significant differences in the other PK parameters except for apparent total clearance after oral administration (clearance rate; <0.05).

CONCLUSION

The two formulations of Quesero XR and Seroquel XR are bioequivalent under both fasting and fed conditions, and food may affect the PK profiles by increasing the rate and extent of absorption of Quesero XR or Seroquel XR in Chinese healthy volunteers.

摘要

目的

本研究旨在评估喹塞罗缓释(Quesero XR)片与喹硫平缓释(Seroquel XR)片在禁食和进食条件下的生物等效性,并确定食物对中国健康志愿者中Quesero XR或Seroquel XR药代动力学(PK)特性的影响。

方法

在进食和禁食研究中,对20名受试者采用单中心、随机、开放标签、两周期交叉设计,洗脱期为10天。在10小时过夜禁食后,给受试者单次口服200 mg Quesero XR或Seroquel XR。在给药前0小时至给药后36小时的预定时间点采集血样。采用经过验证的超高效液相色谱 - 串联质谱(UPLC-MS/MS)法测定喹硫平的血浆浓度。使用Phoenix WinNonlin软件通过非房室分析计算PK参数。

结果

在两种条件下,通过方差分析,两种制剂的主要PK参数之间均未发现显著差异(>0.05);最大血浆浓度(T)的Wilcoxon检验显示无显著差异(>0.05);lnC、lnAUC和lnAUC的90%置信区间(CL)落在80% - 125%的可接受范围内。与禁食状态相比,进食状态下T提前,平均最大血浆浓度(C)、AUC和AUC也增加;主要PK参数的几何平均比值和90%CI超出CI范围;方差分析显示,除口服给药后的表观总清除率外,其他PK参数存在显著差异(清除率;<0.05)。

结论

Quesero XR和Seroquel XR的两种制剂在禁食和进食条件下均具有生物等效性,食物可能通过增加中国健康志愿者中Quesero XR或Seroquel XR的吸收速率和程度来影响PK曲线。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dad/6319427/a86cf2642dd1/dddt-13-255Fig1.jpg

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