TY - JOUR
T1 - Determination of N,N',N''-triethylenethiophosphoramide and its active metabolite N,N',N''-triethylenephosphoramide in plasma and urine using capillary gas chromatography
AU - Van Maanen, Rianne J.
AU - Van Ooijen, Ronald D.
AU - Zwikker, Jan W.
AU - Huitema, Alwin D.r.
AU - Rodenhuis, Sjoerd
AU - Beijnen, Jos H.
PY - 1998/11/20
Y1 - 1998/11/20
N2 - A sensitive assay for the determination of N,N',N''-triethylenethiophosphoramide (thioTEPA) and its metabolite N,N',N''-triethylenephosphoramide (TEPA) in micro-volumes human plasma and urine has been developed. ThioTEPA and TEPA were analysed using gas chromatography with selective nitrogen-phosphorus detection or mass spectrometry after extraction with a mixture of 1-propanol-chloroform from the biological matrix. Diphenylamine was used as internal standard. The limit of detection was 1.5 ng/ml for thioTEPA and 2.5 ng/ml for TEPA, using 100 μl of biological sample; recoveries ranged between 70 and 90% and both accuracy and precision were less than 10%. Linearity was accomplished in the range of 10-1000 ng/ml for plasma and 100-10 000 ng/ml for urine using thermionic nitrogen-phosphorus detection. With mass spectrometry a linear range of 100-25 000 ng/ml TEPA in plasma or urine was obtained. For thioTEPA a second-order polynomial function describes the relationship between the analyte concentration in the range of 500-25 000 ng/ml and detection response. TEPA proved to be stable in plasma and urine for at least 10 weeks at -80°C. ThioTEPA and TEPA plasma concentrations of two patients treated with thioTEPA are presented demonstrating the applicability of the assay for clinical samples. Copyright (C) 1998 Elsevier Science B.V.
AB - A sensitive assay for the determination of N,N',N''-triethylenethiophosphoramide (thioTEPA) and its metabolite N,N',N''-triethylenephosphoramide (TEPA) in micro-volumes human plasma and urine has been developed. ThioTEPA and TEPA were analysed using gas chromatography with selective nitrogen-phosphorus detection or mass spectrometry after extraction with a mixture of 1-propanol-chloroform from the biological matrix. Diphenylamine was used as internal standard. The limit of detection was 1.5 ng/ml for thioTEPA and 2.5 ng/ml for TEPA, using 100 μl of biological sample; recoveries ranged between 70 and 90% and both accuracy and precision were less than 10%. Linearity was accomplished in the range of 10-1000 ng/ml for plasma and 100-10 000 ng/ml for urine using thermionic nitrogen-phosphorus detection. With mass spectrometry a linear range of 100-25 000 ng/ml TEPA in plasma or urine was obtained. For thioTEPA a second-order polynomial function describes the relationship between the analyte concentration in the range of 500-25 000 ng/ml and detection response. TEPA proved to be stable in plasma and urine for at least 10 weeks at -80°C. ThioTEPA and TEPA plasma concentrations of two patients treated with thioTEPA are presented demonstrating the applicability of the assay for clinical samples. Copyright (C) 1998 Elsevier Science B.V.
KW - N,N',N''-Triethylenephosphoramide
KW - N,N',N''-Triethylenethiophosphoramide
UR - http://www.scopus.com/inward/record.url?scp=0005220796&partnerID=8YFLogxK
U2 - 10.1016/S0378-4347(98)00381-8
DO - 10.1016/S0378-4347(98)00381-8
M3 - Article
C2 - 9869370
AN - SCOPUS:0005220796
SN - 1572-6495
VL - 719
SP - 103
EP - 112
JO - Journal of Chromatography B: Biomedical Applications
JF - Journal of Chromatography B: Biomedical Applications
IS - 1-2
ER -