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1.
Drug Test Anal ; 7(10): 967-70, 2015 Oct.
Article in English | MEDLINE | ID: mdl-26112364

ABSTRACT

Glycerol is a naturally occurring polyol in the human body, essential for several metabolic processes. It is widely used in the food, pharmaceutical, and medical industries and in clinical practice as a plasma volume expander (PVE). Athletes, however, may use glycerol to mask the presence of forbidden substances or to enhance performance, inclusively through hyperhydration achieved by glycerol ingestion with added fluid. These practices are considered doping, and are prohibited by the World Anti-Doping Agency (WADA). Therefore, glycerol was introduced in the prohibited list. Doping through glycerol ingestion can readily be identified by detection of elevated glycerol concentrations in urine. In this paper, a protocol for the fast detection of glycerol in urine is proposed. It consists of a previous visual colourimetric screening, followed by a quantitative/qualitative confirmation analysis by mass spectrometry. The screening procedure involves a reaction in which polyhydric alcohols are oxidized by periodate to formic acid and formaldehyde, which is detected by the addition of a fuchsin solution. For the subsequent qualitative/quantitative confirmation analysis, a gas chromatography-mass spectrometry based approach with a non-deuterated internal standard and a drying step of only 10 min is proposed. The linear correlation was demonstrated within WADA´s threshold range. The calculated RSD were 2.1% for within-day precision and 2.8% for between-day precision. The uncertainty estimation was calculated, and a value of 2.7% was obtained. The procedure may also be used for the analysis of other polyols in urine, as for example the PVE mannitol.


Subject(s)
Colorimetry/methods , Gas Chromatography-Mass Spectrometry/methods , Glycerol/urine , Substance Abuse Detection/methods , Athletes , Doping in Sports , Humans , Limit of Detection
2.
Bioanalysis ; 3(2): 215-26, 2011 Jan.
Article in English | MEDLINE | ID: mdl-21250849

ABSTRACT

Plasma volume expanders comprise a heterogeneous group of substances used in medicine that are intravenously administered in cases of great blood loss owing to surgery or medical emergency. These substances, however, can also be used to artificially enhance performance of healthy athletes in sport activities, and to mask the presence of others substances. These practices are considered doping, and are therefore prohibited by the International Olympic Committee and the World Antidoping Agency. Consequently, drug testing procedures are essential. The present work provides an overview of plasma volume expanders, assembling pertinent data such as chemical characteristics, physiological aspects, adverse effects, doping and analytical detection methods, which are currently dispersed in the literature.


Subject(s)
Doping in Sports , Pharmaceutical Preparations/analysis , Plasma Substitutes/analysis , Substance Abuse Detection/methods , Humans
3.
J Inherit Metab Dis ; 33(4): 411-9, 2010 Aug.
Article in English | MEDLINE | ID: mdl-20549362

ABSTRACT

Fumaric aciduria is a rare metabolic disease, with 40 cases reported so far. Fumarase deficiency leads mainly to brain abnormalities, developmental delay, and great accumulation of fumaric acid in urine. This work presents the first case of fumaric aciduria described in Brazil, which presented with some interesting clinical and biochemical findings such as colpocephaly, hepatic alterations, and marked metabolic acidosis since birth. Common findings were ventriculomegaly, hypotonia, and microcephaly. Biochemically, besides the high urinary fumaric acid excretion, atypical elevation of plasma citrulline, tyrosine and methionine levels were also observed. In order to show all features and variants of fumaric aciduria, literature data of 40 patients was reviewed and compared with the case reported here. Findings in all these patients demonstrate that this disorder does not yet have its phenotype completely defined; it is important that more patients be described.


Subject(s)
Fumarate Hydratase/metabolism , Fumarates/urine , Metabolism, Inborn Errors/diagnosis , Metabolism, Inborn Errors/urine , Brazil , Family Health , Female , Fumarate Hydratase/genetics , Humans , Infant , Metabolism, Inborn Errors/genetics
4.
J Sci Med Sport ; 13(1): 13-5, 2010 Jan.
Article in English | MEDLINE | ID: mdl-18768354

ABSTRACT

The artificial colloid hydroxyethyl starch (HES) is among the most frequently used plasma volume expanders in the medical field. However, in 1998, its misuse by the athletic community was officially reported and since 2000, HES is prohibited by the International Olympic Committee (IOC). Therefore, several methods enabling the detection of HES in urine were developed, most based on gas chromatography-mass spectrometry (GC-MS). In the present work, a simple and low-cost screening method, intended to reduce the number of samples to be analysed by GC-MS, was developed. The method is based on the acid hydrolysis of HES and detection of the resulting glucose and hydroxyethyl glucose derivatives by Benedict's reaction (reduction of copper sulfate to brick-red cuprous oxide by glucose and/or derivatives). Samples considered suspect were submitted to GC-MS analysis for identification of HES. The method was successfully applied for screening of HES in 2627 urine samples from 1346 Brazilian soccer players and 1281 athletes from the Pan-American Games (Rio de Janeiro, 2007); 71 (2.7%) samples, considered suspect, were submitted to GC-MS, but no positive results were found. Moreover, a thin layer chromatography (TLC) method was adapted for visualisation of the characteristic band pattern of HES hydrolysis products. The results indicate that the methods are efficient and useful for the screening of HES in urine.


Subject(s)
Doping in Sports , Gas Chromatography-Mass Spectrometry/methods , Hydroxyethyl Starch Derivatives/urine , Plasma Substitutes/analysis , Brazil , Humans , Soccer , Sports
5.
Rev. bras. genét ; 16(1): 237-44, mar. 1993. tab, ilus
Article in English | LILACS | ID: lil-135326

ABSTRACT

Apresentamos um caso típico de hiperglicinemia näo-cetótica neonatal (McKusick 23830) detectado em um programa de triagem para erros inatos do metabolismo realizado no Rio de Janeiro e confirmado por análises que caracterizam os sintomas específicos desse distúrbio. Dados clínicos e características bioquímicas säo descritos e comparados com casos previamente relatados


Subject(s)
Humans , Male , Infant, Newborn , Infant , Child , Amino Acids , Chromatography, Paper , Genetic Testing , Glycine/metabolism , Metabolism, Inborn Errors , Brazil , Signs and Symptoms
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