白藜芦醇增强地尔硫卓在健康人体内的口服生物利用度:一项开放标签、两期序贯研究

Q3 Biochemistry, Genetics and Molecular Biology Journal of Natural Science, Biology, and Medicine Pub Date : 2020-07-01 DOI:10.4103/jnsbm.JNSBM_163_19
Bharagavi Athukuri, P. Neerati
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引用次数: 4

摘要

背景:本研究的目的是探讨白藜芦醇(RSV)对地尔硫卓(DLT)治疗的生物利用度提高潜力。材料和方法:在12名健康男性志愿者中进行了一项开放标签、两期序贯研究。在治疗期间,每天给药单剂量RSV 500 mg,持续10天。在禁食条件下,在对照阶段和治疗后阶段给予单剂量DLT 30mg。在DLT给药后,以预定的时间间隔采集血样,并使用高效液相色谱法进行分析。结果:RSV治疗显著提高了最大血药浓度和曲线下面积,DLT分布体积和表观清除率(CL/F)显著低于对照组。结论:DLT生物利用度的提高可能是通过抑制P-gp和CYP3A4来生物增强RSV的潜能。此外,当DLT与RSV补充剂或含有RSV的食物同时使用时,应重新调整剂量。
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Enhanced oral bioavailability of diltiazem by resveratrol in healthy human subjects: An open-label, two-period, sequential study
Background: The purpose of this study was to investigate the bioavailability enhancing potential of resveratrol (RSV) on diltiazem (DLT) treatment in healthy human volunteers. Materials and Methods: An open-label, two-period, sequential study was conducted in 12 healthy human male volunteers. A single dose of RSV 500 mg was administered daily for 10 days during the treatment phase. A single dose of DLT 30 mg was administered during the control phase and after treatment phases under fasting conditions. The blood samples were collected at predetermined time intervals after DLT dosing and analyzed using high-performance liquid chromatography. Results: Treatment with RSV significantly enhanced maximum plasma concentration, area under the curve, whereas the volume of distribution and apparent clearance (CL/F) of DLT was significantly decreased when compared to control. Conclusions: The results suggested that enhanced bioavailability of DLT might be attributed by bio enhancing the potential of RSV resulted by inhibition of P-gp and CYP3A4. Further, the dosage of DLT should be readjusted when it is used concomitantly with RSV supplements or food containing RSV.
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来源期刊
Journal of Natural Science, Biology, and Medicine
Journal of Natural Science, Biology, and Medicine Biochemistry, Genetics and Molecular Biology-Biochemistry, Genetics and Molecular Biology (all)
CiteScore
2.40
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0.00%
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0
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