M. Vandenberg et al., INDIVIDUAL PCBS AS PREDICTORS FOR CONCENTRATIONS OF NON AND MONO-ORTHO PCBS IN HUMAN-MILK, Environmental science and pollution research international, 2(2), 1995, pp. 73-82
32 Dutch human milk samples were analyzed for PCBs with either HRGC-EC
D or HRGC-LRMS in the NCI mode. Samples were collected from three diff
erent locations in The Netherlands: Amsterdam, Rotterdam and Groningen
. Quantitatively, no differences could be observed between the three l
ocalities, while in addition the congener specific pattern showed a st
riking similarity for all individual samples. Only principal component
analysis revealed slight individual differences. Based on similaritie
s in the PCB profiles, linear relationships were calculated between 2,
3'4,4',5-PnCB (#118) or 2,2'4,4'5,5'-HxCB (#153) and the most relevant
non and mono-ortho PCBs exhibiting dioxinlike activity. These PCBs in
cluded 2,3,3',4,4'-PnCB (#105), 3,3',4,4'5-PnCB (#126) 2,3,3',4,4',5-H
xCB (#156), 2,3,3',4,4',5'-HxCB (#157), 2,3',4,4',5,5'-HxCB (#167) and
3,3',4,4',5'5-HxCB (#169). Good linear relationships were observed be
tween individual PCBs. Based on the results of this study, PCB #118 ca
n be used to predict concentrations of the PCBs #105 and #126. PCB #15
3 can be used as a predictor for the PCBs #156, #157, #167 and #169, b
ut also for the total toxic equivalencies (TEQs) of non and mono-ortho
PCBs present in human milk. This method using certain PCBs as predict
ors for other toxicological relevant congeners, can be useful and cost
effective, e.g. for epidemiological studies. However, before applied
a number of conditions should be met. These are: 1) A stable compositi
on of the PCB matrix should be established. 2) A possible time depende
nt change in composition of the matrix should first be excluded when u
sed over different time periods.