Biological matrices for the evaluation of in utero exposure to drugs of abuse

被引:134
作者
Lozano, Jaime
Garcia-Algar, Oscar
Vall, Oriol
de la Torre, Rafael
Scaravelli, Giulia
Pichini, Simona
机构
[1] Ist Super Sanita, Dept Therapeut Res & Med Evaluat, I-00161 Rome, Italy
[2] Univ Autonoma Barcelona, Hosp Mar, Dept Pediat Ginecol & Obstet & Med Prevent, Paediat Serv, Barcelona, Spain
[3] Univ Pompeu Fabra, Hosp del Mar, Inst Municipal Invest Med, Dept Ciencies Expt Salut, Barcelona, Spain
[4] Ist Super Sanita, Natl Ctr Epidemiol Surveilliance & Hlth Promot, Rome, Italy
[5] Ist Super Sanita, Dept Therapeut Res & Med Evaluat, Rome, Italy
关键词
drugs of abuse; exposure; fetus; biological matrices;
D O I
10.1097/FTD.0b013e31815c14ce
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
In recent years, the evaluation of in utero exposure to drugs of abuse has been achieved by testing biological matrices coming from the fetus or newborn (eg, meconium, fetal hair, cord blood, neonatal urine), the pregnant or nursing mother (eg, hair, blood, oral fluid, sweat, urine, breast milk), or from both the fetus and the mother (placenta, amniotic fluid). Overall, these matrices have the advantage of noninvasive collection (with the exception of amniotic fluid) and early detection of exposure from different gestational periods. Matrices such as amniotic fluid, meconium, fetal hair, and maternal hair provide a long historical record of prenatal exposure to certain drugs and can account for different periods of gestation: amniotic fluid from the early pregnancy, meconium for the second and third trimester of gestation, fetal hair for the third, and finally maternal hair (when long enough) for the whole pregnancy. Placenta may reveal the passage of a substance from the mother to the fetus. Cord blood and neonatal urine are useful for determining acute exposure to drugs of abuse in the period immediately previous to delivery. Drug detection in maternal blood, oral fluid, and sweat accounts only for acute consumption that occurred in the hours previous to collection and gives poor information concerning fetal exposure. Different immunoassays were used as screening methods for drug testing in the above-reported matrices or as unique analytical investigation tools when chromatographic techniques coupled to mass spectrometry were not commonly available. However, in the last decade, both liquid and gas chromatography-mass spectrometric methodologies have been routinely applied after appropriate extraction of drugs and their metabolites from these biological matrices.
引用
收藏
页码:711 / 734
页数:24
相关论文
共 111 条
[1]  
ARESES R, 2002, PROTOCOLOS NEFROLOGI
[2]   Methamphetamine and other substance use during pregnancy: Preliminary estimates from the infant development, environment, and lifestyle (IDEAL) study [J].
Arria, Amelia M. ;
Derauf, Chris ;
LaGasse, Linda L. ;
Grant, Penny ;
Shah, Rizwan ;
Smith, Lynne ;
Haning, William ;
Huestis, Marilyn ;
Strauss, Arthur ;
Della Grotta, Sheri ;
Liu, Jing ;
Lester, Barry .
MATERNAL AND CHILD HEALTH JOURNAL, 2006, 10 (03) :293-302
[3]   Gestational cocaine exposure and intrauterine growth: Maternal lifestyle study [J].
Bada, HS ;
Das, A ;
Bauer, CR ;
Shankaran, S ;
Lester, B ;
Wright, LL ;
Verter, J ;
Smeriglio, VL ;
Finnegan, LP ;
Maza, PL .
OBSTETRICS AND GYNECOLOGY, 2002, 100 (05) :916-924
[4]   Noninvasive methods for drug measurement in pediatrics [J].
Bailey, B ;
Klein, J ;
Koren, G .
PEDIATRIC CLINICS OF NORTH AMERICA, 1997, 44 (01) :15-&
[5]   Comparison of meconium and neonatal hair analysis for detection of gestational exposure to drugs of abuse [J].
Bar-Oz, B ;
Klein, J ;
Karaskov, T ;
Koren, G .
ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION, 2003, 88 (02) :F98-F100
[6]   The Maternal Lifestyle Study: Drug exposure during pregnancy and short-term maternal outcomes [J].
Bauer, CR ;
Shankaran, S ;
Bada, HS ;
Lester, B ;
Wright, LL ;
Krause-Steinrauf, H ;
Smeriglio, VL ;
Finnegan, LP ;
Maza, PL ;
Verter, J .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2002, 186 (03) :487-495
[7]   Fatty acid ethyl esters: Quantitative biomarkers for maternal alcohol consumption [J].
Bearer, CF ;
Santiago, LM ;
O'Riordan, MA ;
Buck, K ;
Lei, SC ;
Singer, LT .
JOURNAL OF PEDIATRICS, 2005, 146 (06) :824-830
[8]   Validation of a new biomarker of fetal exposure to alcohol [J].
Bearer, CF ;
Jacobson, JL ;
Jacobson, SW ;
Barr, D ;
Croxford, J ;
Molteno, CD ;
Viljoen, DL ;
Marais, AS ;
Chiodo, LM ;
Cwik, AS .
JOURNAL OF PEDIATRICS, 2003, 143 (04) :463-469
[9]   Ethyl linoleate in meconium: A biomarker for prenatal ethanol exposure [J].
Bearer, CF ;
Lee, S ;
Salvator, AE ;
Minnes, S ;
Swick, A ;
Yamashita, T ;
Singer, LT .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1999, 23 (03) :487-493
[10]  
Bibb K W, 1995, J Perinatol, V15, P199