Use of spot urine sample results in physiologically based pharmacokinetic modeling of absorbed malathion doses in humans

被引:0
作者
Dong, MH [1 ]
Ross, JH [1 ]
Thongsinthusak, T [1 ]
Krieger, RI [1 ]
机构
[1] UNIV CALIF RIVERSIDE, DEPT ENTOMOL, PERSONAL EXPOSURE PROGRAM, RIVERSIDE, CA 92507 USA
来源
BIOMARKERS FOR AGROCHEMICALS AND TOXIC SUBSTANCES: APPLICATIONS AND RISK ASSESSMENT | 1996年 / 643卷
关键词
D O I
暂无
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
Recently state health and regulatory agencies in California used a PB-PK model to estimate the absorbed doses of malathion in individuals allegedly exposed to aerial sprays during an urban pesticide application. Dose simulation in that study was performed on the results of single urine samples collected within 48 h of a potential exposure, and was based on a model validated with observed values from only a single volunteer. As a continuing effort another case study is presented in this chapter to validate the model with more human literature data. Results from this validation study showed that the time courses of the serial urinary malathion (metabolites) excretion presented in the literature were consistent with those simulated by the PB-PK model. When urine results collected from the literature cases at 8 - 12 h, 12 - 24 h, and 24 - 36 h or 24 - 48 h after initial exposure were postulated as spot samples, the majority (64/85) of the individual total absorbed doses simulated were within two-fold of their measured values, with no simulation doses exceeding three-fold. This validation study further showed that the accuracy would be improved considerably, if the simulation for each literature case were performed on two or more spot samples collected at different time points preferably within the first 24 or 36 h of exposure.
引用
收藏
页码:229 / 241
页数:13
相关论文
共 50 条
  • [31] In vivo and in vitro studies of perchloroethylene metabolism for physiologically based pharmacokinetic modeling in rats, mice, and humans
    Reitz, RH
    Gargas, ML
    Mendrala, AL
    Schumann, AM
    TOXICOLOGY AND APPLIED PHARMACOLOGY, 1996, 136 (02) : 289 - 306
  • [32] Physiologically Based Pharmacokinetic Modeling to Predict Transporter-Mediated Clearance and Distribution of Pravastatin in Humans
    Watanabe, Takao
    Kusuhara, Hiroyuki
    Maeda, Kazuya
    Shitara, Yoshihisa
    Sugiyama, Yuichi
    JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2009, 328 (02) : 652 - 662
  • [33] Use of physiologically based kinetic modeling to predict neurotoxicity and genotoxicity of methylglyoxal in humans
    Zheng, Liang
    Li, Xiyu
    Widjaja, Frances
    Liu, Chen
    Rietjens, Ivonne M. C. M.
    NPJ SCIENCE OF FOOD, 2024, 8 (01)
  • [34] Physiologically based pharmacokinetic modeling of styrene and styrene oxide respiratory-tract dosimetry in rodents and humans
    Sarangapani, R
    Teeguarden, JG
    Cruzan, G
    Clewell, HJ
    Andersen, ME
    INHALATION TOXICOLOGY, 2002, 14 (08) : 789 - 834
  • [35] PHYSIOLOGICALLY BASED PHARMACOKINETIC MODELING OF SARPOGRELATE AND ITS APPLICATION FOR PREDICTION OF DRUG-DRUG INTERACTION IN HUMANS
    Min, Jee Sun
    Kim, Doyun
    Park, Jung Bae
    Heo, Hyunjin
    Bae, Soo Hyeon
    Bae, Soo Kyung
    DRUG METABOLISM AND PHARMACOKINETICS, 2017, 32 (01) : S53 - S53
  • [36] Physiologically based pharmacokinetic modeling of the disposition of octamethylcyclotetrasiloxane (D4) migration from implants in humans
    Thrall, Karla
    Soelberg, Jolen J.
    Powell, Thomas E.
    Corley, Richard A.
    Journal of Long-Term Effects of Medical Implants, 2008, 18 (02) : 133 - 144
  • [37] Application of physiologically based pharmacokinetic modeling in predicting drug-drug interactions for sarpogrelate hydrochloride in humans
    Min, Jee Sun
    Kim, Doyun
    Park, Jung Bae
    Heo, Hyunjin
    Bae, Soo Hyeon
    Seo, Jae Hong
    Oh, Euichaul
    Bae, Soo Kyung
    DRUG DESIGN DEVELOPMENT AND THERAPY, 2016, 10 : 2959 - 2972
  • [38] A Systematic Evaluation of the Use of Physiologically Based Pharmacokinetic Modeling for Cross-Species Extrapolation
    Thiel, Christoph
    Schneckener, Sebastian
    Krauss, Markus
    Ghallab, Ahmed
    Hofmann, Ute
    Kanacher, Tobias
    Zellmer, Sebastian
    Gebhardt, Rolf
    Hengstler, Jan G.
    Kuepfer, Lars
    JOURNAL OF PHARMACEUTICAL SCIENCES, 2015, 104 (01) : 191 - 206
  • [39] Use of partition coefficients in flow-limited physiologically-based pharmacokinetic modeling
    Thompson, Matthew D.
    Beard, Daniel A.
    Wu, Fan
    JOURNAL OF PHARMACOKINETICS AND PHARMACODYNAMICS, 2012, 39 (04) : 313 - 327
  • [40] Cardiac sensitization thresholds of halon replacement chemicals predicted in humans by physiologically-based pharmacokinetic modeling
    Vinegar, A
    Jepson, GW
    RISK ANALYSIS, 1996, 16 (04) : 571 - 579