2019
DOI: 10.1007/s00216-019-02169-3
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Analysis of endogenous steroids in urine by means of multi-immunoaffinity chromatography and isotope ratio mass spectrometry for sports drug testing

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Cited by 7 publications
(3 citation statements)
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“…e peak values of hip extension moment (P � 0.023), knee extension moment (P � 0.003), ankle plantar flexion moment (P < 0.001), and knee valgus moment (P � 0.028) have significant differences between the two different squats (Table 3). Except that the peak value of hip extension moment of restricted squat is greater than that of unrestricted squat [17], the peak value of knee extension moment, ankle plantar flexion moment, and knee valgus moment are greater than that of unrestricted squat.…”
Section: Results Analysismentioning
confidence: 74%
“…e peak values of hip extension moment (P � 0.023), knee extension moment (P � 0.003), ankle plantar flexion moment (P < 0.001), and knee valgus moment (P � 0.028) have significant differences between the two different squats (Table 3). Except that the peak value of hip extension moment of restricted squat is greater than that of unrestricted squat [17], the peak value of knee extension moment, ankle plantar flexion moment, and knee valgus moment are greater than that of unrestricted squat.…”
Section: Results Analysismentioning
confidence: 74%
“…While increasing sample throughput by optimizing sample preparation protocols and/or analytical turnaround times is not necessarily critical in research projects, fast reporting times for doping control analyses are desirable during major national and international sporting competitions. Consequently, options to enhance the laboratory's efficiency have been further explored regarding IRMS in particular and in that context, the GC/C/IRMS strategy employed at the Games of the XXXI Olympiad (2016) was recently discussed by de Oliveira et al 85 Putz et al presented an approach employing immunoaffinity purification of TCs and ERCs instead of frequently utilized HPLC fraction collection in order to expedite the overall analysis time 86 . A volume of 2–3 ml of urine was preconcentrated by SPE and retained unconjugated steroidal analytes were removed by subsequent LLE prior to an enzymatic hydrolysis of glucurono‐conjugated TCs and ERCs.…”
Section: Anabolic Agentsmentioning
confidence: 99%
“…Several purification strategies are at the analyst’s disposal to separate target analytes from sample interferences, also referred to as a matrix, in carbon-CSIA sample preparation. These strategies range from offline chromatographic techniques using conventional solid-phase extraction (SPE) materials, , molecularly imprinted polymers (MIPs), cyclodextrin polymers, immunoaffinity chromatography, silica gel chromatography, , or ion-exchange chromatography to different types of online chromatographic purification techniques including size-exclusion chromatography or the most widely used reversed-phase (RP) high-performance liquid chromatography (HPLC). , While the target analytes are monitored in most of these works, this is not necessarily the case for all interferences. For example, consider 13 C/ 12 C measurement of atrazine in a groundwater extract containing interfering NOM, where chromatographic cleanup is warranted prior to GC-c-IRMS.…”
Section: Introductionmentioning
confidence: 99%