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Toxicology of Industrial Compounds

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this allows a realistic evaluation <strong>of</strong> the risk when these compounds are<br />

used.<br />

Due to their economic importance, most studies have been carried out<br />

with anionic surfactants. Fewer studies exist for the other classes <strong>of</strong><br />

surfactants. In vitro measurements <strong>of</strong> the percutaneous absorption <strong>of</strong><br />

sodium dodecyl sulphate indicated a low absorption value for rat skin as<br />

well as for human skin (Blank and Gould, 1961; Embery and Dugard,<br />

1969; Howes, 1975). The low cutaneous absorption <strong>of</strong> sodium dodecyl<br />

sulphate could also be confirmed in experiments with rats (Greb, 1980).<br />

After application <strong>of</strong> a 0.7 per cent aqueous solution <strong>of</strong> sodium dodecyl<br />

sulphate (contact time 15 min), a cutaneous absorption <strong>of</strong> 0.26 µg cm −2<br />

within 24 h was measured (Howes,1975).<br />

In summarizing the results <strong>of</strong> the available studies, one can conclude that<br />

only small amounts <strong>of</strong> surfactants are resorbed through the intact skin.<br />

Since human skin in general is less permeable to chemicals (Rice, 1977;<br />

Wester and Maibach, 1982), the amounts <strong>of</strong> surfactants absorbed<br />

cutaneously in everyday use are probably even smaller. If the epidermis is<br />

removed completely or partially, e.g. damaged skin, the degree <strong>of</strong><br />

absorption can increase substantially (Scala et al., 1968). In vitro studies<br />

demonstrated that cationic surfactants are absorbed by the skin to a much<br />

lesser extent than anionic surfactants (Scala et al., 1968; Geisler, 1976;<br />

Faucher et al., 1979).<br />

The degree <strong>of</strong> percutaneous absorption is generally larger for nonionic<br />

surfactants than for anionic or cationic surfactants. Studies on the<br />

percutaneous absorption <strong>of</strong> alkyl polyethyleneglycol ethers <strong>of</strong> the structure<br />

C 12-(CH 2-CH 2-O) 3H, C 12-(CH 2-CH 2-O) 6H , C 12-(CH 2-CH 2-O) 10H, and<br />

C 15-(CH 2-CH 2-O) 3H were performed under conditions <strong>of</strong> use (Black and<br />

Howes, 1979). The aqueous solutions <strong>of</strong> the applied surfactants were<br />

washed <strong>of</strong>f after a contact time with the skin <strong>of</strong> 15 min. Under these<br />

conditions, the penetration <strong>of</strong> the alkyl polyethyleneglycol ethers was<br />

greater than the penetration <strong>of</strong> the analogous alcohol sulphates or alcohol<br />

ether sulphates. The penetration increased with increasing length <strong>of</strong> the<br />

carbon chain. Percutaneous absorption decreases for an ethylene oxide<br />

content <strong>of</strong> 6 moles or more in the ethoxylate moiety.<br />

Intestinal absorption, metabolism and excretion<br />

W.STERZEL 347<br />

The ingestion <strong>of</strong> surfactants is possible e.g. through the use <strong>of</strong><br />

surfactantcontaining toothpaste, through residues from dishwashing<br />

detergents and through traces <strong>of</strong> surfactants in potable water. Anionic<br />

surfactants are resorbed well in the intestine (Michael, 1968; Black and<br />

Howes, 1980; Bartnik and Künstler, 1987). After absorption, a part <strong>of</strong> this<br />

is excreted together with bile in the faeces and is subject to a enterohepatic<br />

cycle. The majority <strong>of</strong> the absorbed surfactant is metabolized in the liver

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