Calliphora vicina larvae were fed on drug-laden muscle from three suic
ides involving amitriptyline, temazepam and a combination of trazodone
and trimipramine; triplicate daily harvestings were analysed. The lim
it of detection for all four drugs was 0.01 mu g drug/g larvae. Mean d
rug concentrations (mu g/g) in the initial muscle were: amitriptyline,
2.68; temazepam, 4.04; trazodone, 21.56; and trimipramine, 19.58. Lar
val rearings for days 4-8 (15 larval samples per drug) had mean and ra
nges of drug concentrations (mu g/g) of 0.10 (r, 0.02-0.24) for amitri
ptyline; 0.52 (r, 0.26-0.78) for temazepam; 0.13 (r, 0.05-0.32) for tr
azodone; and 0.28 (r, 0.10-0.59) for trimipramine. After day 8 there w
as a precipitous fall in larval drug concentrations associated with pu
pariation. At day 11 ranges of drug concentrations (mu g/g) were: amit
riptyline, < 0.01-0.01; temazepam, 0.01-0.08; trazodone, < 0.01-0.01;
and trimipramine, 0.04-0.04. Day 16 pupae had corresponding ranges (mu
g/g) of < 0.01, < 0.01-0.01, < 0.01 and < 0.01-0.02. Transfer to drug
-free food at day 5 led to similar falls in drug concentrations (mu g/
g) from day 5 to day 6: 0.08-0.03 for amitriptyline, 0.61-0.09 for tem
azepam, 0.13-0.01 for trazodone, and 0.30-0.02 for trimipramine. The r
esults show considerable variation in larval drug concentrations, both
at the same developmental stage and at different stages of the life c
ycle, under conditions which closely reflect case situations. In pract
ice, the precipitous decrease in drug concentrations in non-feeding la
rvae and at pupariation make it desirable to sample only larvae active
ly feeding on a corpse.