Ullmann U, Oberwittle H, Grossmann M, Riegger C
DSM Nutritional Products Ltd, R&D Human Nutrition & Health, 4303 Kaiseraugst, Switzerland.
Planta Med. 2005 Oct;71(10):891-6. doi: 10.1055/s-2005-864186.
Bonistein is a new product consisting of > 99.5 % synthetic genistein, an isoflavone with phyto-oestrogenic properties, which might be a safe and efficacious alternative for the prevention of post-menopausal bone loss to the traditional hormone replacement therapy. A randomised, open-labelled and sequential-group phase I study was performed to assess safety, tolerability and pharmacokinetic characteristics of oral administrations of Bonistein. Thirty healthy volunteers received in three subsequent groups 30, 60 or 120 mg once daily for 14 days. For the pharmacokinetic profiles of Bonistein, blood samples were taken on study Days 1 (after first dose) and 14 (steady state). Repeated intake of Bonistein was well tolerated. A total of 33 adverse events were reported, mainly of mild intensity. No relevant changes in clinical laboratory or vital signs were observed. The pharmacokinetic characteristics of Bonistein revealed comparable results for extent and rate of absorption on Days 1 and 14. Both AUC and C (max) values of Bonistein increased in proportion with the dose.
博尼斯坦是一种新产品,其合成染料木黄酮含量超过99.5%,染料木黄酮是一种具有植物雌激素特性的异黄酮,对于预防绝经后骨质流失而言,它可能是传统激素替代疗法的一种安全有效的替代方法。进行了一项随机、开放标签和序贯组的I期研究,以评估口服博尼斯坦的安全性、耐受性和药代动力学特征。30名健康志愿者分三组,连续14天每天一次分别服用30毫克、60毫克或120毫克。为了获取博尼斯坦的药代动力学曲线,在研究第1天(首剂后)和第14天(稳态)采集血样。重复服用博尼斯坦耐受性良好。共报告了33起不良事件,主要为轻度。未观察到临床实验室指标或生命体征有相关变化。博尼斯坦的药代动力学特征显示,第1天和第14天在吸收程度和吸收速率方面结果相当。博尼斯坦的AUC和C(max)值均随剂量成比例增加。