A method for measuring octanol:water partition coefficients of highly toxic organophosphorus compounds

被引:0
作者
Czerwinski, SE [1 ]
Maxwell, DM [1 ]
Lenz, DE [1 ]
机构
[1] USA, Med Res Inst Chem Def, Div Pharmacol, Biochem Pharmacol Branch, Aberdeen Proving Ground, MD 21010 USA
来源
TOXICOLOGY METHODS | 1998年 / 8卷 / 02期
关键词
chemical warfare agents; gas chromatograph; octanol : water; organophosphates; organophosphonates; organophosphorus compounds; partition coefficient;
D O I
暂无
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Octanol:water partition coefficients (logP) can be used to provide invaluable information for the overall understanding of the up take distribution, biotransformation, and elimination of a wide variety of chemicals. This is especially important in the study of certain. classes of organophosphorus compounds, e.g., chemical warfare agents. Although several analytical methods currently exist for providing the necessary data for determination of logP values, their use in the study of chemical warfare agents has been limited due to the rapid hydrolysis and biolethality of this class of compounds. To overcome those limitations a rapid, convenient, and safe method for generating the required data was developed using a computer-controlled gas chromatograph (GC) equipped with a nitrogen phosphorus detector. For method development four organophosphorus compounds were used: diisopropyl methyl phosphonate (DIMP), diethyl p-nitrophenyl phosphate (paraoxon), diisopropyl fluorophosphate (DFP), and pinacolyl methylphosphonofluoridate (soman). The method was capable of determining the concentration of DIMP in. hexane over the concentration range of 1 to I x 10(-4) mg/mL by comparing the GC peak areas to analytic standards (r(2) = 0. 999). The latter concentration was found to be the limiting concentration for qualitative analysis. A concentration of analyte of 10(-2) mg/mL was found to provide excellent quantitative results. The intra- and interanalysis coefficient of variation. (CV) for DIMP, over the concentration range 10(-1) to 10(-2) mg/mL in octanol subsequently diluted 1:100 in, hexane or in. water subsequently extracted with art equal volume of octanol followed by a 1:100 dilution in hexane, were 7.3 and 3.5%, respectively. The intra- and interanalysis CV for paraoxon, DFP or soman, each at a fixed concentration of 10-2 mg/mL in the same two solvents and treated in the same manner as DIMP, were 4. 0 and 5. 6% for paraoxon, 3.3 and 3. 6% for DFP, and 0. 7 and 1.1% for soman, respectively. Log P values were determined and found to be 0.478 for DIMP, 1. 600 for paraoxon, 1.173 for DFP, and 1.824 for soman. All results were in excellent agreement with previously determined theoretical or experimental values. Based on the logP determined for DFP and soman it was possible to estimate the fluorophosphate and fluorophosphonate fragment values to be -2.14 and -1. 97, respectively. Using this method toxic organophosphorus compounds at a concentration of 10(-2) mg/mL could be analyzed directly in octanol, the organic solvent used for log P determinations. This analytical method was reproducible, safe, and sensitive where determination of the presence of organophosphorus compounds is a desired endpoint for comparative in vitro analytical studies.
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页码:139 / 149
页数:11
相关论文
共 12 条
[1]  
*BIOB CORP, 1996, MAC LOG P SOFTW VERS
[3]  
HANSCH C, 1979, SUBSTITUENT CONSTANT, P256
[4]  
Hansch C., 1971, DRUG DESIGN, V1
[5]   PHYSICAL AND CHEMICAL BASIS FOR SYSTEMIC MOVEMENT OF ORGANOPHOSPHORUS ESTERS IN COTTON PLANT [J].
HUSSAIN, M ;
FUKUTO, TR ;
REYNOLDS, HT .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1974, 22 (02) :225-230
[6]   DETERMINATION OF PARTITIONING VALUES OF PARATHION-METHYL AND RELATED COMPOUNDS [J].
JAGLAN, PS ;
GUTHER, FA .
ANALYST, 1970, 95 (1133) :763-&
[7]  
KIRKORIAN S, 1987, QUANT STRUCT-ACT REL, V6, P65
[8]  
LEO AJ, 1977, DATA BASE PARAMETER
[9]  
LOGAN TP, 1996, STANDARD OPERATING P
[10]   QUANTITATIVE STRUCTURE ACTIVITY STUDY OF A SERIES OF SUBSTITUTED 0,0-DIMETHYL 0-(PARA-NITROPHENYL) PHOSPHOROTHIOATES AND 0-ANALOGS [J].
MUNDY, RL ;
BOWMAN, MC ;
FARMER, JH ;
HALEY, TJ .
ARCHIVES OF TOXICOLOGY, 1978, 41 (02) :111-123