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RYR食品补充剂的风险评估:认知与现实

Risk Assessment of RYR Food Supplements: Perception vs. Reality.

作者信息

Righetti Laura, Dall'Asta Chiara, Bruni Renato

机构信息

Department of Food and Drug, University of Parma, Parma, Italy.

出版信息

Front Nutr. 2021 Dec 7;8:792529. doi: 10.3389/fnut.2021.792529. eCollection 2021.

Abstract

Thirty-seven red yeast rice (RYR) food supplements were screened for their mycotoxin and natural statin content. Products included pure RYR capsules and multi-ingredient formulations with standardized amounts of monacolin K (MK), marketed both online and retail in the European Union. In terms of mycotoxins, citrinin (CIT) was found in all the monitored products. As CIT content ranged from 100 to 25100 μg/kg, only four products were compliant with maximum EU levels in force until April 2020, while a single product was compliant with the limit of 100 μg/kg introduced after that date. Four contaminated products were labeled as "citrinin free". In terms of natural statins, nine products had a lower content vs. label statements (from -30 to -83%), while for 24 a larger MK amount (from 10 to 266%) was noticed. Three products had a negligible MK content and only 19 offered a daily dosage exceeding 10 mg as dictated by the health claim granted by EFSA in the EU. No sample had label values compliant with pharmaceutical Good Manufacturing Practices requirements (95-105% content of active constituent). Variable, but small amounts of simvastatin (0.1-7.5 μg per daily dose) were found in 30 samples. These results suggest that limited efficacy and reported safety issues may stem from an under-regulated and undercontrolled market, weakening both effectiveness and risk assessment evaluations.

摘要

对37种红曲米(RYR)食品补充剂进行了霉菌毒素和天然他汀类药物含量筛查。产品包括纯红曲米胶囊以及含有标准化莫纳可林K(MK)含量的多成分制剂,在欧盟的线上和零售渠道均有销售。在霉菌毒素方面,所有受监测产品中均检测出桔青霉素(CIT)。由于CIT含量在100至25100μg/kg之间,截至2020年4月,只有4种产品符合当时有效的欧盟最高限量,而只有1种产品符合该日期之后引入的100μg/kg的限量。有4种受污染产品标注为“无桔青霉素”。在天然他汀类药物方面,9种产品的含量低于标签声明(相差-30%至-83%),而24种产品的MK含量更高(相差10%至266%)。3种产品的MK含量可忽略不计,只有19种产品提供的每日剂量超过了欧盟食品安全局(EFSA)批准的健康声明所规定的10mg。没有样品的标签值符合药品生产质量管理规范要求(活性成分含量为95%-105%)。在30个样品中发现了含量各异但数量较少的辛伐他汀(每日剂量0.1-7.5μg)。这些结果表明,疗效有限和报告的安全问题可能源于监管不足和控制不力的市场,削弱了有效性和风险评估。

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