Ashwagandha (Withania somnifera)根提取物缓释胶囊的比较药代动力学研究:开放标签、随机、两治疗、两顺序、两周期、单剂量交叉临床研究

V. Alluri, S. Thanawala, V. Upadhyay
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引用次数: 2

摘要

背景:在这项开放标签、随机、平衡、两处理、两顺序、两期、交叉、单剂量口服比较药代动力学研究中,试验产品“ashwagandha (Withania somnifera)”根提取物缓释胶囊300mg (Prolanza™)的药代动力学、安全性和耐受性,每个含有15mg的withanolides(给药剂量:2×15 mg)与参考产品(有机KSM-66 ashwagandha提取物[素食]胶囊,每个含有15 mg的withanolides[给药剂量:2×15 mg])进行比较。方法:共有14名健康男性随机接受试验产品或参考产品,分别为单剂量2粒胶囊,在禁食条件下服用。采用高效液相色谱-质谱/质谱法测定血浆中总戊内酯、戊内酯A和12-脱氧戊内酯的浓度。结果:与参比制剂相比,该制剂具有较高的相对吸收度、较好的相对生物利用度和较长的消除半衰期,具有较好的缓释特性。具体而言,试验制剂的总戊内酯、戊内酯A和12-脱氧戊内酯的相对生物利用度分别是前者的12倍、44倍和11倍。研究期间无不良事件报告。结论:与参考产品相比,试验产品的缓释特性将提供更持久的每日单剂量治疗效果(回顾性应用于印度临床试验登记处[CTRI])。申请参考号:REF/2020/03/032408)。本研究报道了苦参根提取物的独特缓释配方。药动学研究也首次成功测定了ashwagandha中主要植物活性成分withanolide A和12- deoxywithastraonolide的血浆含量。
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A comparative pharmacokinetics study of Ashwagandha (Withania somnifera) Root Extract sustained-release capsules: an open-label, randomized, two treatment, two-sequence, two period, single-dose crossover clinical study
Background: In this open-label, randomized, balanced, two-treatment, two-sequence, two-period, crossover, single-dose oral comparative pharmacokinetics study, the pharmacokinetics, safety, and tolerability of test product ‘ashwagandha (Withania somnifera)’ root extract sustained release capsule 300 mg (Prolanza™), each containing 15 mg withanolides (administered dose: 2×15 mg) was compared with that of a reference product (organic KSM-66 ashwagandha extract [vegan] capsule, each containing 15 mg withanolides [administered dose: 2×15 mg]).Methods: Total 14 healthy men were randomized to receive either the test or the reference product as a single dose of 2 capsules in sequence, administered under fasting conditions. Plasma concentrations of total withanolides, withanolide A and 12-deoxywithastramonolide were measured using validated liquid chromatography–mass spectroscopy/mass spectroscopy.Results: The test product had higher relative absorption, better relative bioavailability, and longer elimination half-life indicating a sustained-release profile compared to reference. Specifically, the relative bioavailability of the test formulation was 12, 44, and 11 times higher for total withanolides, withanolide A and 12-deoxywithastramonolide, respectively. No adverse events were reported during the study.Conclusions: The sustained-release profile of the test product, compared to reference product, will provide more long-lasting therapeutic effects from a single daily dose (Retrospectively applied on Clinical Trials Registry - India [CTRI]. Application reference number: REF/2020/03/032408). The study reports the unique sustained release formulation of Withania somnifera (Ashwagandha) root extract. The pharmacokinetic study also reports for first time, the successful plasma estimation of withanolide A and 12-deoxywithastraamonolide, the major phytoactives of ashwagandha.
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