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Appendix D Food Codes for NHANES - OEHHA

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Scientific Review Panel Draft February, 2012<br />

was absorbed, a dose of 14 C-DEHP was given intramuscularly to a group of<br />

animals (n=5) and radioactivity was measured in urine and feces <strong>for</strong> up to seven<br />

days.<br />

After 24 hours, 3% (7% after correction) of the dermally applied dose was<br />

eliminated in urine and feces. After seven days, approximately 21% (53% after<br />

correction) of the dose had been absorbed by the skin and eliminated, while<br />

another 11.3% of the dose had been skin stripped from the dose area. An<br />

additional group (n=6) of animals was given DEHP (53 µg) dermally to estimate<br />

the dose remaining in the tissues. After 7 days, 14 C content (% of applied dose)<br />

was as follows: urine, 18 ± 4; feces, 4 ± 1; skin wash after 24 hrs, 32 ± 10; skin<br />

patch, 13 ± 5; skin (dosed area), 5 ± 3; other tissues (liver, fat, muscle, skin), 4 ±<br />

3%. An additional 10% was estimated to be lost to volatilization.<br />

In the in vitro study, Ng et al. (1992) examined absorption of DEHP through<br />

viable and non-viable dermatomed guinea pig skin (200 µm sections) with 24-hr<br />

exposure. Radiolabeled DEHP was applied in 10 µl acetone at concentrations of<br />

35.6, 153, or 313 nmol/cm 2 . The percentage of dose that permeated the viable<br />

skin into the receptor fluid was 6, 2.4, and 2.5% <strong>for</strong> the low-, medium-, and highdose<br />

groups, respectively. The percentage of dose that remained in the skin disc<br />

was 41.0, 37.5, and 36.2% <strong>for</strong> the low-, medium-, and high-dose groups,<br />

respectively. Use of nonviable skin resulted in a slightly decreased penetration<br />

of 5.0% at the applied dose of 35.6 nmol/cm 2 , likely due to decreased<br />

metabolism of DEHP. There was a dose-related increase in metabolism but the<br />

total metabolites were between 0.5 and 1% of the applied dose <strong>for</strong> each dose<br />

group.<br />

Chu et al. (1996) examined the skin reservoir effects of 14 C-labelled DEHP (119-<br />

529 µg/cm 2 ) applied on hairless guinea pigs <strong>for</strong> 24 hrs, followed by washing of<br />

the skin to remove DEHP and analysis of DEHP distribution up to 14 days posttreatment.<br />

As DEHP in the dosed skin decreased from 11.1% to 0.66% from 24hrs<br />

to 7 days post-treatment, excreted DEHP gradually increased from 0.74 to<br />

17.3%.<br />

This finding provided evidence that DEHP stored in skin enters the systemic<br />

circulation, although the considerable intraspecies variation <strong>for</strong> percent of<br />

absorbed dose precluded a specific estimate of DEHP absorbed systemically<br />

after 24 hrs post-treatment. DEHP in the carcass was 1.01 and 0.92% of applied<br />

dose at 24 hrs and 7 days, respectively. By 14 days post-treatment, essentially<br />

no DEHP remained in dosed skin. Autoradiographic analysis of the dosed skin at<br />

24 hrs revealed dense radiolabel accumulation in the epidermis and along the<br />

hair follicles, which indicated hair follicles may be a penetration pathway <strong>for</strong><br />

DEHP.<br />

The authors also reported that the percent absorbed at 24 hours by Ng et al.<br />

(1992) was higher than that found in this study, with nearly identical experimental<br />

F-64

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