Chemotherapy control by breath profile with application of SPME-GC/MS method

被引:29
作者
Ulanowska, Agnieszka [1 ]
Trawinska, Ewa [2 ]
Sawrycki, Piotr [3 ]
Buszewski, Boguslaw [1 ]
机构
[1] Nicholas Copernicus Univ, Chair Environm Chem & Bioanalyt, Fac Chem, PL-87100 Torun, Poland
[2] Nicholas Copernicus Univ, Dept Lung Dis, Coll Med, PL-87100 Torun, Poland
[3] Nicholas Copernicus Univ, Dept Canc Chemotherapy, Coll Med, PL-87100 Torun, Poland
关键词
Breath analysis; Chemotherapy; Lung cancer; Solid-phase microextraction (SPME); Volatile organic compounds (VOCs); SOLID-PHASE MICROEXTRACTION; HIGH-DOSE CHEMOTHERAPY; GAS-CHROMATOGRAPHY; ISOPRENE; TOXICITY; ALKANES;
D O I
10.1002/jssc.201200333
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Chemotherapy used as a treatment against lung cancer has influence on metabolic processes occurring in healthy cells. The changes of biochemical pathways proceeded inside cells might be observed in expired air. In the experiment, breath analysis was carried out before and after anticancer therapy. Expired air samples were collected from 22 patients with a biopsy confirmed lung cancer. Volatile organic compounds present in breath were analyzed by gas chromatography/mass spectrometry. For enrichment of analytes solid-phase microextraction technique was applied. Eight fibers covered by different sorbents were tested. Carboxen-polydimethylsiloxane fiber revealed the highest extraction efficiency in relation to analytes in breath. The data showed that cytostatic drugs increase the concentration of acetone and isoprene in the breath collected after chemotherapy. Volatile metabolites of administrated drugs were not identified in expired air.
引用
收藏
页码:2908 / 2913
页数:6
相关论文
共 17 条
[1]   Breath alkanes as a marker of oxidative stress in different clinical conditions [J].
Aghdassi, E ;
Allard, JP .
FREE RADICAL BIOLOGY AND MEDICINE, 2000, 28 (06) :880-886
[2]   DNA methylation-based biomarkers for early detection of non-small cell lung cancer: an update [J].
Anglim, Paul P. ;
Alonzo, Todd A. ;
Laird-Offringa, Ite A. .
MOLECULAR CANCER, 2008, 7 (1)
[3]  
BERG JM, 2009, BIOCHEMISTRY
[4]   BLOOD ISOPRENE CONCENTRATIONS IN HUMANS AND IN SOME ANIMAL SPECIES [J].
CAILLEUX, A ;
COGNY, M ;
ALLAIN, P .
BIOCHEMICAL MEDICINE AND METABOLIC BIOLOGY, 1992, 47 (02) :157-160
[5]  
Edelman M. J, 2009, LUNG CANCER, P169
[6]  
Hyspler R, 2000, J CHROMATOGR B, V739, P183
[7]   DETERMINATION OF ISOPRENE IN HUMAN BREATH BY THERMAL-DESORPTION GAS-CHROMATOGRAPHY WITH ULTRAVIOLET DETECTION [J].
JONES, AW ;
LAGESSON, V ;
TAGESSON, C .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 1995, 672 (01) :1-6
[8]   Tumoral drug metabolism: Overview and its implications for cancer therapy [J].
Michael, M ;
Doherty, MM .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (01) :205-229
[9]   Diagnostic potential of breath analysis - focus on volatile organic compounds [J].
Miekisch, W ;
Schubert, JK ;
Noeldge-Schomburg, GFE .
CLINICA CHIMICA ACTA, 2004, 347 (1-2) :25-39
[10]   Ozone-induced increase in exhaled 8-isoprostane in healthy subjects is resistant to inhaled budesonide [J].
Montuschi, P ;
Nightingale, JA ;
Kharitonov, SA ;
Barnes, PJ .
FREE RADICAL BIOLOGY AND MEDICINE, 2002, 33 (10) :1403-1408