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Transport of organochlorine residues in the rat and human blood.

作者信息

Gómez-Catalán J, To-Figueras J, Rodamilans M, Corbella J

机构信息

Unitat de Medicina Legal, Facultat de Medicina, Hospital Clinic i Provincial, Universitat de Barcelona, Spain.

出版信息

Arch Environ Contam Toxicol. 1991 Jan;20(1):61-6. doi: 10.1007/BF01065329.

Abstract

Organochlorine residues (OCR)2 are poorly soluble in water and are transported in the organism bound by the blood components. The distribution among blood fractions (cells/plasma, lipoproteins/rest of plasma proteins) were variable depending on the residue (HCB, p p'-DDE, HCH, Aroclor 1260, PCP) and on the species (rat, man). Differences were not found between in vivo (after oral single dosing) and in vitro (blood incubation) experiments. Results indicated a high affinity of organochlorine residues for lipoproteins; however, binding to blood carriers was very weak as demonstrated by the rapid release of residues by elution through a reverse phase column. The effects of residue binding to blood components on the distribution kinetics to tissues are discussed.

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