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Stabilization of human urine doping control samples: IV. Human chorionic gonadotropin

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dc.contributor.author Tsivou, M en
dc.contributor.author Dimopoulou, HA en
dc.contributor.author Georgakopoulos, DG en
dc.contributor.author Koupparis, MA en
dc.contributor.author Atta-Politou, J en
dc.contributor.author Georgakopoulos, CG en
dc.date.accessioned 2014-06-06T06:50:43Z
dc.date.available 2014-06-06T06:50:43Z
dc.date.issued 2010 en
dc.identifier.issn 16182642 en
dc.identifier.uri http://dx.doi.org/10.1007/s00216-010-4033-9 en
dc.identifier.uri http://62.217.125.90/xmlui/handle/123456789/5133
dc.subject Doping control analysis en
dc.subject Human chorionic gonadotropin en
dc.subject Microorganisms en
dc.subject Proteases en
dc.subject Stabilization en
dc.subject Urine en
dc.subject.other Chemical mixtures en
dc.subject.other Chemical stabilization en
dc.subject.other Doping control en
dc.subject.other Doping control analysis en
dc.subject.other E. coli en
dc.subject.other Elevated temperature en
dc.subject.other Endogenous steroids en
dc.subject.other High temperature en
dc.subject.other Human chorionic gonadotropins en
dc.subject.other Human urine en
dc.subject.other Protease inhibitor en
dc.subject.other Proteases en
dc.subject.other Proteolytic enzyme en
dc.subject.other Recombinant erythropoietin (rEpo) en
dc.subject.other Urinary tract infections en
dc.subject.other Urine en
dc.subject.other Urine sample en
dc.subject.other World Anti-Doping Agency en
dc.subject.other Body fluids en
dc.subject.other Catalysts en
dc.subject.other Chemical analysis en
dc.subject.other Degradation en
dc.subject.other Doping (additives) en
dc.subject.other Enzymes en
dc.subject.other Escherichia coli en
dc.subject.other Experiments en
dc.subject.other Microorganisms en
dc.subject.other Mixtures en
dc.subject.other Stabilization en
dc.subject.other chorionic gonadotropin en
dc.subject.other conference paper en
dc.subject.other doping en
dc.subject.other enzyme immunoassay en
dc.subject.other human en
dc.subject.other standard en
dc.subject.other urine en
dc.subject.other Chorionic Gonadotropin en
dc.subject.other Doping in Sports en
dc.subject.other Humans en
dc.subject.other Immunoenzyme Techniques en
dc.subject.other Reference Standards en
dc.subject.other Escherichia coli en
dc.title Stabilization of human urine doping control samples: IV. Human chorionic gonadotropin en
heal.type conferenceItem en
heal.identifier.primary 10.1007/s00216-010-4033-9 en
heal.publicationDate 2010 en
heal.abstract The presence of proteolytic enzymes in urine samples, coming from exogenous or endogenous sources, enhances the cleavage of human chorionic gonadotropin (hCG). Moreover, elevated temperatures occurring occasionally during the delayed transportation of sport urine samples, favor the nicking of the hCG molecule. The aim of the current study, funded by the World Anti-Doping Agency (WADA), was the application of a stabilization mixture in athletes' urine samples to chemically inactivate proteolytic enzymes coming from exogenous or endogenous sources so as to prevent the degradation of hCG. The stabilization mixture applied, already tested for the stabilization of endogenous steroids and recombinant erythropoietin (rEPO), was a combination of antibiotics, antimycotic substances, and protease inhibitors. Incubation experiments were conducted in the presence or absence of the stabilization mixture in urine aliquots spiked with six proteases (first series of experiments) and one microorganism associated with urinary tract infections (UTI) (second series of experiments). Intact hCG levels were evaluated by using the EIAgen Total hCG kit. In the first series of experiments, hCG levels were reduced in the untreated aliquots following incubation at 37 °C. The addition of the chemical stabilization mixture prevented degradation of hCG induced by four of the proteases applied. In the second series of experiments, no significant difference was found in urine inoculated with E. coli, between aliquots treated with chemical mixture and the untreated aliquots. The addition of the proposed chemical stabilization mixture improves the quality of athletes' urine samples against possible deterioration due to high temperatures or attempts of proteolytic manipulation. © 2010 Springer-Verlag. en
heal.journalName Analytical and Bioanalytical Chemistry en
dc.identifier.issue 3 en
dc.identifier.volume 398 en
dc.identifier.doi 10.1007/s00216-010-4033-9 en
dc.identifier.spage 1313 en
dc.identifier.epage 1318 en


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