DETERMINATION OF SOLVENT THINNER COMPONENTS IN HUMAN-BODY FLUIDS BY CAPILLARY GAS-CHROMATOGRAPHY WITH TRAPPING AT LOW OVEN TEMPERATURE FOR HEADSPACE SAMPLES
Xp. Lee et al., DETERMINATION OF SOLVENT THINNER COMPONENTS IN HUMAN-BODY FLUIDS BY CAPILLARY GAS-CHROMATOGRAPHY WITH TRAPPING AT LOW OVEN TEMPERATURE FOR HEADSPACE SAMPLES, Analyst, 123(1), 1998, pp. 147-150
A simple and sensitive method is presented for determination of solven
t thinner components in human body fluids by capillary gas chromatogra
phy (GC) with a low oven temperature for trapping headspace vapor comp
onents, After heating a blood or urine sample containing ethyl acetate
, benzene, butan-1-ol, toluene, butyl acetate, isoamyl acetate and eth
ylbenzene (internal standard) in a 7.5 ml vial at 90 degrees C for 30
min, 5 ml of headspace vapor were drawn into a glass syringe, All vapo
r was introduced through an injection port in the splitless mode into
a DB-624 medium-bore capillary column at a 5 degrees C oven temperatur
e for trapping the volatile compounds, and the oven temperature was pr
ogrammed up to 110 degrees C for their detection by GC, These conditio
ns gave sharp peaks, a good separation of each peak and low background
noise for both whole blood and urine samples, As much as 3.58-55.1 an
d 3.52-57.9% of the six compounds, which had been added to vials, coul
d be introduced to the GC instrument for whole blood and urine, respec
tively, The intra-day RSD values in terms of the introduction rate (ne
t recovery) of the six compounds in whole blood and urine samples were
less than or equal to 8.1%. The calibration curves showed linearity i
n the range 0.78-400 ng per 0.5 ml whole blood or urine, The detection
limits were 0.5-5 ng per 0.5 ml. The data on toluene in post mortem b
lood in an actual case are also presented.