Bioequivalence Study of Salbutamol 400 mg Tablet in Healthy Indonesian Volunteers by Liquid Chromatography Tandem with Mass Spectrometry

Priyanto P
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Abstract

This study objective was to determine the bioequivalence of Salbutamol 4 mg Tablet manufactured by PT Kimia Farma Tbk compared to Ventolin® 2x2 mg Tablet manufactured by Glaxo Wellcome Indonesia, in healthy Indonesian volunteer. The pharmacokinetic parameters calculated in this study are AUC0-24, AUC0-inf, Cmax, Tmax, and T1/2. The study was conducted in a randomized, single-dose, open-label, two-way crossover design (2 treatments, 2 periods, and 2 sequences) under fasting state with 7 (seven) days washed-out period. The number of subjects who participated in the study were 24 volunteers ((12 males and 12 females). The participants were provided with an overview of the study and signed the informed consent form. The study participants underwent a minimum 8-hour fasting period prior to receiving both the test drug and the reference drug, and blood samples were collected at 14 specified time points: 0 hours (before drug administration), minutes-20, minutes-40, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 16, and 24 hours after drug administration. Plasma concentrations of the drug were determined by LCMS/MS method. The acceptance criteria for the bioequivalence test are 80.00 - 125.00% for AUC0-t and Cmax with 90% Confidence Interval (CI) with α = 5.00%. The mean SD value of AUC0-24, AUC0-inf, Cmax, Tmax, and T1/2 respectively for test drug is 84.49 ±18.99 ng.mL-1.hour; 89.66 ±21.29 ng.mL-1.hour; 13.85 ±4.25 ng/mL; 2.00 ±0.71 hour and 5.08 ±1.27 hour. The mean SD values of AUC0-24, AUC0-inf, Cmax, Tmax, and C1/2 respectively for reference drug are 88.81 ±26.50 ng.mL-1.jam; 93.78 ±27.97 ng.mL-1.jam; 13.39 ±5.39 ng/mL; 2.63 ±1.45 hour and 5.03 ±1.16 hour. Meanwhile, the geometric mean ratio of test drug to reference drug (90% confidence interval) is 96.35% (90.55- 102.53%) for AUC0-24 and 105.39% (93.62-118.65%) for Cmax. Based on the AUC0-24 and Cmax values, Salbutamol 4 mg Tablet manufactured by PT Kimia Farma Tbk is bioequivalent to Ventolin® 2x2 mg Tablet manufactured by Glaxo Wellcome Indonesia.
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利用液相色谱-串联质谱法对印度尼西亚健康志愿者服用沙丁胺醇 400 毫克片剂进行生物等效性研究
本研究旨在确定 PT Kimia Farma Tbk 公司生产的沙丁胺醇 4 毫克片剂与印尼葛兰素威康公司生产的万托林® 2x2 毫克片剂在印尼健康志愿者中的生物等效性。本研究计算的药代动力学参数包括 AUC0-24、AUC0-inf、Cmax、Tmax 和 T1/2。该研究采用随机、单剂量、开放标签、双向交叉设计(2 个疗程、2 个时期和 2 个序列),在空腹状态下进行,并有 7 天的冲洗期。参与研究的受试者共有 24 名志愿者(12 男 12 女)。研究人员向受试者介绍了研究概况,并签署了知情同意书。受试者在接受试验药物和参照药物治疗前至少禁食 8 小时,并在 14 个指定时间点采集血液样本:在 14 个指定时间点采集血液样本:0 小时(用药前)、20 分钟、40 分钟、1 小时、1.5 小时、2 小时、2.5 小时、3 小时、4 小时、6 小时、8 小时、12 小时、16 小时和 24 小时后。血浆中的药物浓度采用 LCMS/MS 法测定。生物等效性测试的接受标准是 AUC0-t 和 Cmax 为 80.00 - 125.00%,90% 置信区间 (CI),α = 5.00%。试验药物的 AUC0-24、AUC0-inf、Cmax、Tmax 和 T1/2 的平均 SD 值分别为 84.49 ±18.99 ng.mL-1.hour; 89.66 ±21.29 ng.mL-1.hour; 13.85 ±4.25 ng/mL; 2.00 ±0.71 hour 和 5.08 ±1.27 hour。参比药物的 AUC0-24、AUC0-inf、Cmax、Tmax 和 C1/2 的平均值分别为 88.81 ±26.50 ng.mL-1.jam; 93.78 ±27.97 ng.mL-1.jam; 13.39 ±5.39 ng/mL; 2.63 ±1.45 小时和 5.03 ±1.16 小时。同时,试验药物与参照药物的几何平均比值(90% 置信区间)为:AUC0-24 为 96.35%(90.55- 102.53%),Cmax 为 105.39%(93.62-118.65%)。根据 AUC0-24 和 Cmax 值,PT Kimia Farma Tbk 生产的沙丁胺醇 4 毫克片剂与 Glaxo Wellcome Indonesia 生产的 Ventolin® 2x2 毫克片剂具有生物等效性。
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