O. Nygren et C. Lundgren, DETERMINATION OF PLATINUM IN WORKROOM AIR AND IN BLOOD AND URINE FROMNURSING STAFF ATTENDING PATIENTS RECEIVING CISPLATIN CHEMOTHERAPY, International archives of occupational and environmental health, 70(3), 1997, pp. 209-214
Objectives: The use of anti-neoplastic drugs is increasing and nursing
staff are evidently concerned about the risk of hazardous exposure. G
eneral methods are available for measuring exposure to carcinogens. Th
ese methods, however, lack specificity. One group of antineoplastic dr
ugs, based on cisplatin derivatives, contain platinum, which can be an
alysed at low concentrations with the use of adsorptive voltammetry. T
he aim of this study was to employ this technique for assessment of oc
cupational exposure by selective determination of platinum in workroom
air and in blood and urine samples from medical staff nursing cancer
patients. Methods: The voltammetric method for determination of platin
um has been further developed for analysis of blood, urine and air sam
ples. The effects of different materials in crucibles and different ac
ids for sample pre-treatment, and of the ashing temperature programme
were investigated for optimum conditions for analysis of blood, urine
and filter samples. Occupational exposure to cisplatin derivatives was
also investigated among medical staff. Air sampling in the workroom,
as well as analysis of blood and urine samples from the exposed subjec
ts, was carried out during the process of drug preparation and adminis
tration and when attending treated patients. Results: After developmen
t of the experimental method by the introduction of synthetic quartz c
rucibles and the optimization of acid composition, and of the temperat
ure programme for sample pre-treatment, the recovery has been improved
and the method has proved to be adequate for determination of platinu
m (Pt) in blood, urine and air-filter samples. Increased Pt blood leve
ls were found in both graduate (2.2 +/- 1.7 ng ml(-1)) and staff nurse
s (3.8 +/- 4.0 ng ml(-1)), but not in pharmacists (0.47 +/- 0.31 ng ml
(-1)), in comparison with unexposed subjects (1.2 +/- 0.69 ng ml(-1)).
The variation was, however, high with CV > 50% for all groups. From t
he median values it can be seen that a few subjects with high values h
ad a large impact on the mean values. The mean Pt level in urine sampl
es was 126 +/- 92 ng l(-1), which was found to be close to the pooled
reference urine (110 ng l(-1)). No increased Pt air levels were found
in any of the measurements. Moreover, the results showed difference in
mean Pt blood level between staff at the investigated hospitals. The
staff at hospital A had 1.2 +/- 0.53 ng ml(-1), at hospital B 3.8 +/-
4.3 ng ml(-1) and at hospital C 2.0 +/- 2.1 ng ml(-1). Conclusions: Th
e method has proved to be adequate for determination of platinum in bl
ood, urine and air-filter samples. No increased airborne Pt levels wer
e found. However, increased Pt blood levels were found. Staff nurses h
ad a higher mean level than graduate nurses, which indicates that poss
ible exposure occurs while attending treated patients rather than duri
ng the preparation and administration of drugs. There was a noticeable
variations in the mean blood level for the investigated groups as a w
hole. This variation might reflect an actual difference in the exposur
e situation, but more probably depends on differences in skill and exp
erience between the subjects. Routines and facilities for handling ant
i-neoplastic drugs vary between the clinics and this also probably has
an impact on exposure.