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本文引用的文献

1
Quantitative Relations in the Physiological Constitutions of Mammals.哺乳动物生理构成中的数量关系。
Science. 1949 Jun 10;109(2841):579-85. doi: 10.1126/science.109.2841.579.
2
The metabolism of acetone. I. Gross aspects of catabolism and excretion.丙酮的代谢。I. 分解代谢与排泄的总体情况。
J Biol Chem. 1950 Jul;185(1):449-59.
3
Exposure-excretion relationship of styrene and acetone in factory workers: a comparison of a lipophilic solvent and a hydrophilic solvent.工厂工人中苯乙烯和丙酮的暴露-排泄关系:亲脂性溶剂和亲水性溶剂的比较
Arch Environ Contam Toxicol. 1993 Jul;25(1):129-33. doi: 10.1007/BF00230723.
4
A physiologically based pharmacokinetic model for nasal uptake and metabolism of nonreactive vapors.一种用于非反应性蒸气经鼻摄取和代谢的基于生理学的药代动力学模型。
Toxicol Appl Pharmacol. 1993 Nov;123(1):120-9. doi: 10.1006/taap.1993.1228.
5
Effect of variation of exposure to airborne chlorobenzene on internal exposure and concentrations of urinary metabolite.空气中氯苯暴露量变化对体内暴露及尿中代谢物浓度的影响。
Occup Environ Med. 1995 Jan;52(1):65-70. doi: 10.1136/oem.52.1.65.
6
Inhalation pharmacokinetics based on gas uptake studies. II. Pharmacokinetics of acetone in rats.基于气体摄取研究的吸入药代动力学。II. 丙酮在大鼠体内的药代动力学。
Arch Toxicol. 1981 Jul;47(4):293-304. doi: 10.1007/BF00332395.
7
Exposure to acetone. Uptake and elimination in man.
Scand J Work Environ Health. 1981 Jun;7(2):84-94. doi: 10.5271/sjweh.2561.
8
A physiologically based description of the inhalation pharmacokinetics of styrene in rats and humans.基于生理学的大鼠和人体中苯乙烯吸入药代动力学描述。
Toxicol Appl Pharmacol. 1984 Mar 30;73(1):159-75. doi: 10.1016/0041-008x(84)90064-4.
9
Human styrene exposure. V. Development of a model for biological monitoring.
Int Arch Occup Environ Health. 1983;53(1):19-36. doi: 10.1007/BF00406174.
10
Uptake, distribution, metabolism, and elimination of styrene in man. A comparison between single exposure and co-exposure with acetone.人体中苯乙烯的摄取、分布、代谢及排泄:单次暴露与丙酮共同暴露的比较
Br J Ind Med. 1984 Nov;41(4):539-46. doi: 10.1136/oem.41.4.539.

丙酮的基于生理的药代动力学模型。

Physiologically based pharmacokinetic model for acetone.

作者信息

Kumagai S, Matsunaga I

机构信息

Department of Occupational Health, Osaka Prefectural Institute of Public Health, Japan.

出版信息

Occup Environ Med. 1995 May;52(5):344-52. doi: 10.1136/oem.52.5.344.

DOI:10.1136/oem.52.5.344
PMID:7795758
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1128228/
Abstract

OBJECTIVE

This study aimed to develop a physiologically based pharmacokinetic model for acetone and to predict the kinetic behaviour of acetone in the human body with that model.

METHODS

The model consists of eight tissue groups in which acetone can be distributed: the mucous layer of the inhaled air tract, the mucous layer of the exhaled air tract, a compartment for gas exchange (alveolus of the lung), a group of blood vessel rich tissues including the brain and heart, a group of tissues including muscles and skin that have low perfusion rates, a group of fatty tissues, an organ for metabolism (liver), and a compartment for urinary excretion (kidney). A mucous layer in the model is only the outermost layer of the mucus lining the wall of the air tract during inhalation and exhalation. To check the relevance of the model, the simulated results were compared with the experimental data. Next, simulation was conducted by changing the volume of the mucous layer and the respiratory rate to clarify the effect of these variables. Finally, simulation of an occupational situation was performed.

RESULTS

With an appropriate value for the volume of mucous layer, the simulated acetone concentrations in arterial blood, end exhaled air, urine, and fatty tissue were found to agree well with the experimental data. The volume of mucous layer and rate of respiration were critical for the appropriate simulation. The simulated occupational situation fitted the observed regression line in field studies quite well. The simulation also enabled predictions to be made about the characteristic kinetics for water soluble solvents.

CONCLUSION

The model is useful for understanding and explaining the kinetics of acetone.

摘要

目的

本研究旨在建立基于生理学的丙酮药代动力学模型,并利用该模型预测丙酮在人体内的动力学行为。

方法

该模型由八个可分布丙酮的组织组组成:吸入气道黏液层、呼出气道黏液层、气体交换隔室(肺泡)、一组富含血管的组织(包括脑和心脏)、一组灌注率低的组织(包括肌肉和皮肤)、一组脂肪组织、一个代谢器官(肝脏)和一个尿液排泄隔室(肾脏)。模型中的黏液层仅为吸入和呼出过程中气道壁内衬黏液的最外层。为检验模型的相关性,将模拟结果与实验数据进行了比较。接下来,通过改变黏液层体积和呼吸频率进行模拟,以阐明这些变量的影响。最后,进行了职业场景模拟。

结果

当黏液层体积取值适当时,发现模拟的动脉血、终末呼出气体、尿液和脂肪组织中丙酮浓度与实验数据吻合良好。黏液层体积和呼吸频率对适当模拟至关重要。模拟的职业场景与现场研究中观察到的回归线拟合得相当好。该模拟还能够对水溶性溶剂的特征动力学进行预测。

结论

该模型有助于理解和解释丙酮的动力学。