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诺丽果提取物的药代动力学研究。

Pharmacokinetic study of Noni fruit extract.

作者信息

Issell Brian F, Franke Adrian, Fielding Robert M

机构信息

University of Hawaii's Cancer Research Center, HI, USA.

出版信息

J Diet Suppl. 2008;5(4):373-82. doi: 10.1080/19390210802519671.

Abstract

Many different products containing Noni (Morinda citrifolia) fruit extracts are sold throughout the world for health restoration and maintenance. Despite a large business enterprise fueling Noni's popularity, there is a lack of standardization of products and no scientific evidence of Noni's clinical efficacy and safety. There is also no evidence to indicate an optimal therapeutic dose or dosing interval. In an initial volunteer, scopoletin was identified as a bioactive marker of Noni exposure and a candidate for product standardization and pharmacokinetic studies. Subsequently, capsules containing the whole freeze-dried fruit of Noni were orally administered to nine healthy volunteers (3 per group) at doses of 1,500 mg (3 × 500 mg), 2,000 mg (4 × 500 mg) and 2,500 mg (5 × 500 mg). Plasma and urine samples were obtained from each subject prior to dosing and at 0.5, 1, 2, 4 and 8 h after dosing. Concentrations of scopoletin were determined by HPLC with PDA (scanning at 200-700 nm) and MS detection. Scopoletin rapidly enters the plasma after Noni ingestion, maintaining levels in the range of 0.5 to 5 ng/mL for at least 8 h after dosing. Scopoletin bioavailability appears to be low, with significant intersubject variability. We conclude that scopoletin can be used as a relatively specific marker of Noni exposure in the blood and particularly in urine when its pharmacokinetics is considered appropriately.

摘要

全球各地都在销售许多含有诺丽(海巴戟)果实提取物的不同产品,用于恢复和维持健康。尽管有大型商业企业推动诺丽的流行,但产品缺乏标准化,也没有科学证据证明诺丽的临床疗效和安全性。也没有证据表明最佳治疗剂量或给药间隔。在最初的志愿者中,东莨菪素被确定为诺丽暴露的生物活性标志物,也是产品标准化和药代动力学研究的候选物。随后,将含有诺丽全冻干果实的胶囊以1500毫克(3×500毫克)、2000毫克(4×500毫克)和2500毫克(5×500毫克)的剂量口服给予9名健康志愿者(每组3人)。在给药前以及给药后0.5、1、2、4和8小时从每个受试者采集血浆和尿液样本。采用配有PDA(在200 - 700纳米处扫描)和MS检测的HPLC测定东莨菪素的浓度。诺丽摄入后,东莨菪素迅速进入血浆,给药后至少8小时内维持在0.5至5纳克/毫升的水平。东莨菪素的生物利用度似乎较低,个体间存在显著差异。我们得出结论,当适当考虑其药代动力学时,东莨菪素可作为血液尤其是尿液中诺丽暴露的相对特异性标志物。

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