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生物溶解性对亲脂性化学物质气体和蒸气的肺部摄取及分布的影响。

Effects of biosolubility on pulmonary uptake and disposition of gases and vapors of lipophilic chemicals.

作者信息

Fiserova-Bergerova V, Tichy M, Di Carlo F J

出版信息

Drug Metab Rev. 1984;15(5-6):1033-70. doi: 10.3109/03602538409033557.

Abstract

Since statistical analysis proved the intercorrelation of tissue-gas partition coefficients of chemicals with similar chemical structures, bioavailability is controlled by one parameter dependent on the physicochemical properties of the chemicals and two constants distinguishing the tissues. Oil-gas partition coefficients are suggested to describe the biosolubility of volatile halogenated aliphatic chemicals. Tissue-gas partition coefficients derived from oil-gas partition coefficients were substituted in a pharmacokinetic model in order to study the effect of biosolubility on uptake, distribution, and elimination of inhaled chemicals. The simulation was focused on occupational exposures (8 h/day, 5 days/wk). Desaturation curves for all tissues show three exponential decays. The analysis of the simulation data indicates three patterns in behavior of inhaled vapors and gases in the body. Tissue uptake of poorly soluble chemicals (oil-gas partition coefficient less than 10) is flow limited at the beginning of exposure, but the partial pressures of such chemicals in the body equilibrate very rapidly with ambient air. Increased pulmonary uptake compensates for metabolic clearance. The rapid response of tissue concentrations to changes in exposure concentrations indicates that the toxic effect can easily be induced by short-term increase of exposure concentration, and that emergence from the reversible effect is rapid when exposure ceases. Tissue uptake of chemicals with oil-gas partition coefficients between 10 and 10(4) is flow limited during the entire 8-h exposure. Tissue concentrations increase slowly. Pulmonary uptake, being restricted by alveolar ventilation, compensates at steady state only for the amount of chemical removed by metabolic clearance. Therefore, tissue concentrations at steady state are lower than biosolubility. Accumulation during occupational exposure is obvious. Dumping of inhaled chemicals in adipose tissue protects the target organ from the occasional short-term increases in the exposure concentration. Tissue uptake of highly soluble chemicals (oil-gas partition coefficients greater than 10(4)) is limited by alveolar ventilation and exposure concentration. The rising and declining of tissue concentrations is very slow, half-times being in the magnitude of months and years. Metabolism reduces the half-time significantly. A lagging acute toxic effect can develop as the chemical accumulates in the body; the effect is most likely to persist long after the termination of the exposure.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

由于统计分析证明,化学结构相似的化学物质的组织 - 气体分配系数之间存在相互关联,生物利用度由一个取决于化学物质物理化学性质的参数和两个区分不同组织的常数控制。建议用油气分配系数来描述挥发性卤代脂肪族化学物质的生物溶解度。为了研究生物溶解度对吸入化学物质的摄取、分布和消除的影响,将由油气分配系数推导得出的组织 - 气体分配系数代入药代动力学模型。模拟研究聚焦于职业暴露(每天8小时,每周5天)。所有组织的去饱和曲线呈现出三个指数衰减阶段。对模拟数据的分析表明,吸入的蒸汽和气体在体内的行为存在三种模式。难溶性化学物质(油气分配系数小于10)在暴露开始时组织摄取受流量限制,但此类化学物质在体内的分压与环境空气能很快达到平衡。肺部摄取增加可补偿代谢清除。组织浓度对暴露浓度变化的快速响应表明,短期暴露浓度增加很容易诱发毒性作用,且暴露停止后可逆效应迅速消失。油气分配系数在10至10⁴之间的化学物质在整个8小时暴露期间组织摄取受流量限制。组织浓度缓慢增加。肺部摄取受肺泡通气限制,仅在稳态时补偿代谢清除所去除的化学物质数量。因此,稳态时的组织浓度低于生物溶解度。职业暴露期间会出现蓄积现象。吸入的化学物质在脂肪组织中的蓄积可保护靶器官免受偶尔的短期暴露浓度增加的影响。高溶性化学物质(油气分配系数大于10⁴)的组织摄取受肺泡通气和暴露浓度限制。组织浓度的上升和下降非常缓慢,半衰期在数月至数年的量级。代谢可显著缩短半衰期。随着化学物质在体内蓄积,可能会出现滞后的急性毒性作用;这种作用很可能在暴露终止后持续很长时间。(摘要截取自400字)

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