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首页> 外文期刊>Cell biochemistry and biophysics >Pharmacokinetics Study of Amoxycillin and Clavulanic acid (8:1)-A New Combination in Healthy Chinese Adult Male Volunteers Using the LC-MS/MS Method
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Pharmacokinetics Study of Amoxycillin and Clavulanic acid (8:1)-A New Combination in Healthy Chinese Adult Male Volunteers Using the LC-MS/MS Method

机译:LC-MS / MS法研究阿莫西林与克拉维酸(8:1)在中国健康成年男性志愿者中的新组合的药代动力学

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摘要

New oral granules of amoxicillin and clavulanic acid in 8:1 ratio have recently been developed and approved to conduct clinical trial in China. To date, there has been no report studying the pharmacokinetic characteristics of amoxicillin and clavulanic acid in man. Therefore, it is urgent to investigate the pharmacokinetic properties of amoxicillin and clavulanic acid in man. The aim of the study was to assess the pharmacokinetic properties of amoxicillin and clavulanic acid in 8:1 with different dosage in healthy volunteers and provide support for this drug to obtain marketing authorization in China. A liquid chromatography-tandem mass spectrometry method for determining the concentration of amoxicillin and clavulanic acid in human plasma was developed and applied to this open-label, single- and multiple-dose Pharmacokinetics study. Subjects were randomized to receive a single dose of 1, 2, and 4 pouches of the test granulation of amoxicillin and clavulanic acid in 8:1 ratio (amoxicillin is 250 mg and clavulanic acid is 31. 25 mg per pouch). In the single-dose phase, blood samples were collected before dosing and at 0. 25, 0. 5, 0. 75, 1, 1. 5, 2, 2. 5, 3, 5, 8, 12, and 24 h after drug administration. In the multiple-dose phase, samples were obtained before drug administration on days 1, 2, 3, and 4 to determine the Cmin of amoxicillin and clavulanic acid. In the 4th day, samples were collected from 0. 25 to 24 h after drug administration. Profiles of the concentration-time curves of amoxicillin and clavulanic acid were best fitted to two-compartment model. In this group of healthy Chinese subjects, the pharmacokinetics of amoxicillin fitted the linear dynamic feature at doses of 250,500 and 1,000 mg, and not obviously about clavulanic acid at doses of 31. 25, 62. 5, and 125 mg. The t1/2 of single dose and multidoses were (1. 45 ± 0. 12) and (1. 44 ± 0. 26) h of amoxicillin and (1. 24 ± 0. 23) and (1. 24 ± 0. 17) of clavulanic acid, respectively; The AUC0-24 of single dose and multidoses were (27937. 85 ± 4265. 59) and (24569. 80 ± 3663. 63) ng h mL-1 of amoxicillin and (891. 45 ± 194. 30) and (679. 61 ± 284. 05) ng h mL-1 of clavulanic acid, respectively; The Cmax of single dose and multidoses were (8414. 58 ± 1416. 78) and (7929. 17 ± 1291. 54) ng mL-1 of amoxicillin and (349. 00 ± 89. 54) and (289. 00 ± 67. 36) ng h mL-1 of clavulanic acid, respectively. t1/2, AUC0-24, and Cmax were similar after multiple-dose administration and after single-dose administration, suggesting that amoxicillin and clavulanic acid do not accumulate with multiple-dose administration of 500 and 62. 5 mg, respectively.
机译:阿莫西林和克拉维酸以8:1的比例混合的新型口服颗粒已在中国研发并获准在中国进行临床试验。迄今为止,还没有关于阿莫西林和克拉维酸在人体中药代动力学特征的研究报告。因此,迫切需要研究阿莫西林和克拉维酸在人体中的药代动力学特性。该研究的目的是评估健康志愿者中不同剂量的阿莫西林和克拉维酸8:1的药代动力学特性,并为该药物获得在中国的销售授权提供支持。建立了测定人血浆中阿莫西林和克拉维酸浓度的液相色谱-串联质谱方法,并将其应用于这项开放标签,单剂量和多剂量药代动力学研究。受试者随机接受阿莫西林和克拉维酸的8:1比例的单剂1、2和4袋测试颗粒(阿莫西林为250毫克,克拉维酸为31. 25毫克/袋)。在单剂量阶段,在给药前和0. 25、0。5、0。75、1、1、5、2、2、5、3、5、8、12和24 h时收集血液样本给药后。在多剂量阶段,在给药1、2、3和4天之前获取样品,以确定阿莫西林和克拉维酸的Cmin。在第4天,在给药后0. 25至24小时收集样品。阿莫西林和克拉维酸的浓度-时间曲线的轮廓最适合两室模型。在这组健康的中国受试者中,阿莫西林的药代动力学在剂量为250,500和1,000 mg时具有线性动态特征,而在剂量分别为31. 25、62。5和125 mg时棒酸不明显。单剂量和多剂量的t1 / 2为(1. 45±0. 12)和(1. 44±0. 26)h阿莫西林和(1. 24±0. 23)和(1. 24±0。 17)棒酸。单剂量和多剂量的AUC0-24为(27937. 85±4265. 59)和(24569. 80±3663. 63)ng h mL-1的阿莫西林和(891. 45±194. 30)和(679。 61±284. 05)ng h mL-1的棒酸。单剂量和多剂量的Cmax为(8414. 58±1416. 78)和(7929. 17±1291. 54)ng mL-1阿莫西林以及(349. 00±89. 54)和(289. 00±67) 36)ng h mL-1的棒酸。在多剂量给药后和单剂量给药后,t1 / 2,AUC0-24和Cmax相似,这表明在500和62. 5 mg的多剂量给药中阿莫西林和克拉维酸不会累积。

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