Wiseman Clare L S
School of the Environment, Earth Sciences, University of Toronto, 33 Willcocks Street, Toronto, Ontario, Canada.
Anal Chim Acta. 2015 Jun 2;877:9-18. doi: 10.1016/j.aca.2015.01.024. Epub 2015 Jan 27.
In contrast to the existence of standardized methods to assess metal bioaccessibility via the gastrointestinal route, there are no widely-accepted, established in vitro testing protocols to measure elemental solubility in the human lung. This may be attributed, in part, to the difficulty associated with simulating the lung's complex in vivo conditions. The purpose of this review is two-fold: (1) to determine how the bioaccessibility of metals associated with ambient particulate matter (PM) in the human lung has been assessed in the literature, and (2) examine the suitability and biological relevance of applied methods for the measurement of metal bioaccessibility employed to date. The review revealed that limited attention has been paid to the development and application of biologically-relevant in vitro methods to measure elemental solubility in ambient PM as a proxy for bioaccessibility in the human lung. Few studies (n=14) used synthetic lung fluids to simulate in vivo conditions, with only half extracting samples at a biologically-relevant temperature of 37°C. There was limited evidence suggesting that the use of water is less effective as a leaching agent compared to simulated lung fluids. In sum, this scoping review highlights a critical need to develop standardized methods for the systematic assessment of elemental bioaccessibility via the respiratory route. Priority should be placed on the validation of biologically-relevant methods, including the use of leaching agents and extraction parameters used, which allow for testing to be conducted in a reliable, yet cost efficient, manner.
与通过胃肠道途径评估金属生物可及性的标准化方法的存在形成对比的是,目前尚无广泛接受的、既定的体外测试方案来测量人体肺部中元素的溶解度。这可能部分归因于模拟肺部复杂的体内条件所存在的困难。本综述的目的有两个:(1)确定文献中是如何评估与环境颗粒物(PM)相关的金属在人体肺部的生物可及性的,以及(2)检验迄今为止用于测量金属生物可及性的应用方法的适用性和生物学相关性。该综述表明,对于开发和应用生物学相关的体外方法来测量环境PM中的元素溶解度以作为人体肺部生物可及性的替代指标,人们关注有限。很少有研究(n = 14)使用合成肺液来模拟体内条件,只有一半的研究在37°C这个具有生物学相关性的温度下提取样本。仅有有限的证据表明,与模拟肺液相比,用水作为浸出剂的效果较差。总之,这项范围综述突出表明迫切需要开发用于系统评估通过呼吸道途径的元素生物可及性的标准化方法。应优先对生物学相关方法进行验证,包括所使用的浸出剂和提取参数,这使得测试能够以可靠且具有成本效益的方式进行。