膳食补充剂的生物降解性:先进的分析方法来研究人工甜味剂和染料的环境命运。

IF 3.1 3区 医学 Q2 CHEMISTRY, ANALYTICAL Journal of pharmaceutical and biomedical analysis Pub Date : 2025-03-15 Epub Date: 2024-11-22 DOI:10.1016/j.jpba.2024.116575
Luisa Mattoli, Giada Fodaroni, Giacomo Proietti, Enrico Flamini, Bernardino Paoli, Luca Massa, Grazia Carmela Ferrara, Emiliano Giovagnoni, Mattia Gianni
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引用次数: 0

摘要

人工甜味剂和染料广泛应用于食品、饮料和制药行业,因其持久性和广泛存在性而被认为是新兴的环境污染物。这些物质通常在通过人体时保持不变,并抵抗废水处理过程,导致不断进入水生环境,并可能产生长期的环境影响。本研究首次采用经济合作与发展组织(OECD) 301 F - ready生物降解试验(RBT)(一种呼吸-压力测定法)研究了9种商业膳食补充剂的生物降解性,包括天然膳食补充剂和含有as和合成染料的膳食补充剂。虽然产物具有良好的生物降解性,但对含有ASs和染料的产物进行了进一步研究,以确定其在RBT结束时的命运。该研究涉及开发和验证一种色谱方法,用于定量测定RBT矿物介质中安赛蜜K(1)、三氯蔗糖(2)、酒黄(3)和卡麦isine(4)的存在,该方法使用超高高效液相色谱(UHPLC)和两个检测器:具有四极杆飞行时间(qToF)的高分辨率质谱仪和UV-Vis二极管阵列检测器(DAD)。结果表明,这些添加剂不易生物降解,突出了潜在的重大环境问题。这个问题超出了膳食补充剂的范畴,延伸到所有药品和个人护理产品(PPCP),包括药品和医疗器械。研究结果强调了提高持久性物质对环境影响的文化意识,鼓励医疗保健链和患者做出知情选择的重要性。从“同一个健康”的角度来看,减少环境污染可为人类健康带来积极成果。
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Biodegradability of dietary supplements: Advanced analytical methods to study the environmental fate of artificial sweeteners and dyes.

Artificial sweeteners (ASs) and dyes are widely used in foods, beverages and pharmaceutical and are recognized as emerging environmental contaminants due to their persistence and widespread occurrence. These substances often pass through the human body unchanged and resist wastewater treatment processes, leading to continuous introduction into aquatic environments and potential long-lasting term environmental effects. This study investigated, for the first time, the biodegradability of nine commercial dietary supplements, both natural and those containing ASs and synthetic dyes, using the Organisation for Economic Cooperation and Development (OECD) 301 F ready biodegradation test (RBT), which is a respirometry-manometric method. While the products showed good biodegradability, those containing ASs and dyes were further studied to determine their fate at the end of the RBT. The study involved developing and validating a chromatographic method to quantitatively determine the presence of Acesulfame K (1), Sucralose (2), Tartrazine (3) and Carmoisine (4) in the RBT mineral medium, using ultra-high performance liquid chromatography (UHPLC) coupled with two detectors: a high-resolution mass-spectrometer with quadrupole time-of-flight (qToF) and a UV-Vis diode array detector (DAD). Results indicated that these additives were not readily biodegraded, highlighting a potential significant environmental concern. This issue extends beyond dietary supplements to all Pharmaceutical and Personal Care Products (PPCP) including drugs and medical devices. The findings underscore the importance of raising cultural awareness about the environmental impact of persistent substances, encouraging the healthcare chain and patients to make informed choices. From a One Health perspective, reducing environmental contamination can lead to positive outcomes for human health.

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来源期刊
CiteScore
6.70
自引率
5.90%
发文量
588
审稿时长
37 days
期刊介绍: This journal is an international medium directed towards the needs of academic, clinical, government and industrial analysis by publishing original research reports and critical reviews on pharmaceutical and biomedical analysis. It covers the interdisciplinary aspects of analysis in the pharmaceutical, biomedical and clinical sciences, including developments in analytical methodology, instrumentation, computation and interpretation. Submissions on novel applications focusing on drug purity and stability studies, pharmacokinetics, therapeutic monitoring, metabolic profiling; drug-related aspects of analytical biochemistry and forensic toxicology; quality assurance in the pharmaceutical industry are also welcome. Studies from areas of well established and poorly selective methods, such as UV-VIS spectrophotometry (including derivative and multi-wavelength measurements), basic electroanalytical (potentiometric, polarographic and voltammetric) methods, fluorimetry, flow-injection analysis, etc. are accepted for publication in exceptional cases only, if a unique and substantial advantage over presently known systems is demonstrated. The same applies to the assay of simple drug formulations by any kind of methods and the determination of drugs in biological samples based merely on spiked samples. Drug purity/stability studies should contain information on the structure elucidation of the impurities/degradants.
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