Determination of Morphine and 6-Acetylmorphine in Blood With Use of Dried Blood Spots

被引:85
作者
Boy, Regine Garcia [1 ]
Henseler, Joerg [2 ]
Mattern, Rainer [1 ]
Skopp, Gisela [1 ]
机构
[1] Univ Hosp, Inst Legal Med & Forens Med, D-69115 Heidelberg, Germany
[2] Radboud Univ Nijmegen, NL-6525 ED Nijmegen, Netherlands
关键词
dried blood spots (DBS); opiates; LC-MS/MS; extraction efficiency; comparison of whole blood to DBS;
D O I
10.1097/FTD.0b013e31818d9fdb
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
The use of dried blood spots (DBS) which has successfully been introduced in neonatal metabolic screening is an appropriate method to reduce virus infection risk to a minimum, facilitating regular mailing and handling of samples in the laboratory. Injection diacetylmorphine use is notably associated with a prevalence of infection and a risk of transmission of blood-borne Viruses. The aim or the present Study was to establish a method to determine morphine and 6-acetylmorphine (6-AM) as accurately and sensitively from DBS as from whole blood. Analysis by liquid chromatography/tandem mass spectrometry was checked for carryover, ion suppression/enhancement, linearity of response, lower limits of detection and quantification, and the within-run and between-run assay imprecision for both whole blood and DBS after liquid/liquid extraction. DBS drying time and elution were optimized, and extraction efficiency from DBS was compared with that of blood and of a solution of the pure compounds. Short-term stability of morphine and 6-AM was determined at -20 degrees C, 4 degrees C, and 40 degrees C up to 7 clays from both whole blood and DBS. Furthermore, it was tested whether analysis of DBS may be as reliable as that of whole blood investigating 50 authentic samples. The lower limit of detection was 0.4 ng of morphine per spot and 0.8 ng of 6-AM per Spot using a DBS blood volume of 100 mu L and was 0.3 and 0.7 ng/100 mu L whole blood for morphine and 6-AM, respectively Recovery rates of the analytes from DBS did not differ from those from whole blood and were >= 55% for 6-AM and >= 25% for morphine, and the within- and between-run coefficients of variation were always <= 9%. 6-AM degraded rapidly at both 4 degrees C and 40 degrees C in whole blood; however, it seemed to be much more stable in DBS. Significant correlations between real whole-blood samples and DBS were obtained. The DBS assay has potential as a precise and inexpensive option for the determination of morphine and 6-AM in small blood samples. Further, the DBS matrix proved to excellently stabilize 6-AM.
引用
收藏
页码:733 / 739
页数:7
相关论文
共 14 条
[1]  
ARBUCKLE JL, 2003, AMOS 5
[2]   STATISTICAL METHODS FOR ASSESSING AGREEMENT BETWEEN TWO METHODS OF CLINICAL MEASUREMENT [J].
BLAND, JM ;
ALTMAN, DG .
LANCET, 1986, 1 (8476) :307-310
[3]  
Bollen K. A., 1989, Structural equations with latent variables, DOI DOI 10.1002/9781118619179
[4]   Multicenter evaluation of use of dried blood and plasma spot specimens in quantitative assays for human immunodeficiency virus RNA: Measurement, precision, and RNA stability [J].
Brambilla, D ;
Jennings, C ;
Aldrovandi, G ;
Bremer, J ;
Comeau, AM ;
Cassol, SA ;
Dickover, R ;
Jackson, JB ;
Pitt, J ;
Sullivan, JL ;
Butcher, A ;
Grosso, L ;
Reichelderfer, P ;
Fiscus, SA .
JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (05) :1888-1893
[5]  
*DTSCH I NORM, 1994, 32465 DIN
[6]   REVERSED-PHASE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY DETERMINATION OF QUININE IN PLASMA, WHOLE-BLOOD, URINE, AND SAMPLES DRIED ON FILTER-PAPER [J].
ERICSSON, O ;
FRIDEN, M ;
HELLGREN, U ;
GUSTAFSSON, LL .
THERAPEUTIC DRUG MONITORING, 1993, 15 (04) :334-337
[7]   A GENERAL METHOD FOR ANALYSIS OF COVARIANCE STRUCTURES [J].
JORESKOG, KG .
BIOMETRIKA, 1970, 57 (02) :239-&
[8]  
KLEESIEK K, 1995, LEHRBUCH KLIN CHEM P, P825
[9]   Quantification of antiretroviral drugs in dried blood spot samples by means of liquid chromatography/tandem mass spectrometry [J].
Koal, T ;
Burhenne, H ;
Römling, R ;
Svoboda, M ;
Resch, K ;
Kaever, V .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2005, 19 (21) :2995-3001
[10]   Use of filter paper for the collection and analysis of human whole blood specimens [J].
Mei, JV ;
Alexander, JR ;
Adam, BW ;
Hannon, WH .
JOURNAL OF NUTRITION, 2001, 131 (05) :1631S-1636S