Organic compounds percutaneous penetration in vivo in man: Relationship to mathematical predictive model

被引:5
作者
Burli, Anuk [1 ,2 ]
Law, Rebecca M. [1 ,3 ]
Rodriguez, Jocelyn [1 ,4 ]
Maibach, Howard I. [1 ]
机构
[1] Univ Calif San Francisco, Dept Dermatol, 2340 Sutter St N461, San Francisco, CA 94115 USA
[2] Univ Rochester, Sch Med & Dent, 601 Elmwood Ave, Rochester, NY 14642 USA
[3] Mem Univ Newfoundland, Sch Pharm, H3440,300 Prince Phillip Dr, St John, NF A1B 3V6, Canada
[4] Washington Univ, Sch Med, 660 S Euclid Ave, St Louis, MO 63110 USA
关键词
Percutaneous penetration; Potts and Guy model; In vivo; Organic compounds; Pesticides; Human Hydrogen bonds; Permeability constant; Octanol water partition coefficient; Aqueous solubility; ESTIMATING DERMAL ABSORPTION; CHEMICAL-EXPOSURE; SKIN; PERMEABILITY; PESTICIDES;
D O I
10.1016/j.yrtph.2020.104614
中图分类号
DF [法律]; D9 [法律]; R [医药、卫生];
学科分类号
0301 ; 10 ;
摘要
Human skin is a common pathway through which chemicals in our environment enter the body. To aid with risk management of environmental chemicals, the US EPA utilizes mathematical models to estimate percutaneous penetration when experimental data is not available. Here, the accuracy of predicted flux by the Potts and Guy model based on in vitro penetration is compared to human in vivo data of percutaneous absorption of various organic compounds. For most chemicals, the flux was over- or underestimated by a factor 10-100. In vitro flux was significantly correlated to experimental human in vivo flux; however, the physiochemical parameters used in the Potts and Guy equation, Kp, Koctanol, and molecular weight, did not correlate significantly with in vivo flux. We discuss possible explanations for why the computer model did not accurately predict in vivo flux. Further research is needed with different types of chemicals encountered in the environment, and/or as used in clinical practice. This manuscript discusses limitations to the mathematical models currently used, and why the models should be further refined for use.
引用
收藏
页数:6
相关论文
共 27 条
[1]   Skin tolerability associated with transdermal drug delivery systems: an overview [J].
Ale, Iris ;
Lachapelle, Jean-Marie ;
Maibach, Howard I. .
ADVANCES IN THERAPY, 2009, 26 (10) :920-935
[2]   Mathematical and pharmacokinetic modelling of epidermal and dermal transport processes [J].
Anissimov, Yuri G. ;
Jepps, Owen G. ;
Dancik, Yuri ;
Roberts, Michael S. .
ADVANCED DRUG DELIVERY REVIEWS, 2013, 65 (02) :169-190
[3]  
[Anonymous], [No title captured]
[4]  
[Anonymous], [No title captured]
[5]  
[Anonymous], [No title captured]
[6]  
Blickenstaff Nicholas R., 2014, Reviews on Environmental Health, V29, P145, DOI 10.1515/reveh-2014-0052
[7]   A NEW METHOD FOR ESTIMATING DERMAL ABSORPTION FROM CHEMICAL-EXPOSURE .2. EFFECT OF MOLECULAR-WEIGHT AND OCTANOL WATER PARTITIONING [J].
BUNGE, AL ;
CLEEK, RL .
PHARMACEUTICAL RESEARCH, 1995, 12 (01) :88-95
[8]   Evaluating Molecular Properties Involved in Transport of Small Molecules in Stratum Corneum: A Quantitative Structure-Activity Relationship for Skin Permeability [J].
Chen, Chen-Peng ;
Chen, Chan-Cheng ;
Huang, Chia-Wen ;
Chang, Yen-Ching .
MOLECULES, 2018, 23 (04)
[9]   A NEW METHOD FOR ESTIMATING DERMAL ABSORPTION FROM CHEMICAL-EXPOSURE .1. GENERAL-APPROACH [J].
CLEEK, RL ;
BUNGE, AL .
PHARMACEUTICAL RESEARCH, 1993, 10 (04) :497-506
[10]   ABSORPTION OF SOME ORGANIC COMPOUNDS THROUGH SKIN IN MAN [J].
FELDMANN, RJ ;
MAIBACH, HI .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1970, 54 (05) :399-&