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抗疟药α/β-蒿甲醚与磺胺多辛-乙胺嘧啶的临床药代动力学药物相互作用评估。

Assessment of Clinical Pharmacokinetic Drug-Drug Interaction of Antimalarial Drugs α/β-Arteether and Sulfadoxine-Pyrimethamine.

机构信息

Pharmacokinetics & Metabolism Division, CSIR-Central Drug Research Institute, Lucknow, India.

Academy of Scientific and Innovative Research, New Delhi, India.

出版信息

Antimicrob Agents Chemother. 2017 Aug 24;61(9). doi: 10.1128/AAC.02177-16. Print 2017 Sep.

Abstract

Antimalarial drug combination therapy is now being widely used for the treatment of uncomplicated malaria. The objective of the present study was to investigate the effects of coadministration of intramuscular α/β-arteether (α/β-AE) and oral sulfadoxine-pyrimethamine (SP) on the pharmacokinetic properties of each drug as a drug-drug interaction study to support the development of a fixed-dose combination therapy. A single-dose, open-label, crossover clinical trial was conducted in healthy adult Indian male volunteers (18 to 45 years, = 13) who received a single dose of AE or SP or a combination dose of AE and SP. Blood samples were collected up to 21 days postadministration, and concentrations of α-AE, β-AE, sulfadoxine, and pyrimethamine were determined by using a validated liquid chromatography-tandem mass spectrometry method. Pharmacokinetic parameters were calculated and statistically analyzed to calculate the geometric mean ratio and confidence interval. Following single-dose coadministration of intramuscular AE and oral SP, the pharmacokinetic properties of α/β-AE were not significantly affected, and α/β-AE had no significant effect on the pharmacokinetic properties of SP in these selected groups of healthy volunteers. However, more investigations are needed to explore this further. (This study has been registered in the clinical trial registry of India under approval no. CTRI/2011/11/002155.).

摘要

抗疟药物联合疗法目前被广泛用于治疗不复杂的疟疾。本研究的目的是研究肌内α/β-青蒿素(α/β-AE)和口服磺胺多辛-乙胺嘧啶(SP)联合给药对每种药物药代动力学特性的影响,作为药物相互作用研究,以支持固定剂量联合疗法的开发。在健康的成年印度男性志愿者(18 至 45 岁,n = 13)中进行了一项单次、开放标签、交叉临床试验,他们接受了单次 AE 或 SP 或 AE 和 SP 联合剂量的给药。在给药后 21 天内采集血样,并使用经过验证的液相色谱-串联质谱法测定 α-AE、β-AE、磺胺多辛和乙胺嘧啶的浓度。计算药代动力学参数并进行统计学分析,以计算几何均数比和置信区间。在肌内 AE 和口服 SP 单次联合给药后,α/β-AE 的药代动力学特性没有受到显著影响,并且 α/β-AE 对这些选定的健康志愿者群体中 SP 的药代动力学特性没有显著影响。然而,需要进一步的研究来探讨这一点。(本研究已在印度临床试验注册处注册,注册号为 CTRI/2011/11/002155。)。

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