Analyze Diet

Topic:Doping

Doping in horses refers to the administration of prohibited substances or methods to enhance performance or alter behavior during competitions. This practice is a concern in equestrian sports due to its potential impact on animal welfare, fair play, and the integrity of the sport. Substances used in doping can range from stimulants and painkillers to sedatives and anti-inflammatory drugs. Detection methods include blood and urine tests, designed to identify the presence of banned substances or their metabolites. This page compiles peer-reviewed research studies and scholarly articles that explore the detection methods, regulatory frameworks, and ethical considerations associated with doping in equine sports.
Morphine and etorphine: XIV. Detection by ELISA in equine urine.
Journal of analytical toxicology    November 1, 1991   Volume 15, Issue 6 305-310 doi: 10.1093/jat/15.6.305
Stanley S, Jeganathan A, Wood T, Henry P, Turner S, Woods WE, Green M, Tai HH, Watt D, Blake J.We have raised antibodies to morphine and etorphine and developed one-step enzyme-linked immunosorbent assays (ELISA) for these drugs as part of a panel of post race tests for drugs in racing horses. These tests are simple, can be completed in 2 h, and can be read by visual inspection. The morphine ELISA has an I50 for morphine of about 1.5 ng/mL, while the etorphine ELISA has an I50 for etorphine of 250 pg/mL. Cross-reactivity studies show that the antimorphine antibody cross-reacts well with levorphanol, hydromorphone, and oxycodone, while the anti-etorphine antibody showed no cross-reactivi...
The development of a gas chromatographic/mass spectrometric screening procedure to detect the administration of anabolic steroids to the horse.
Biological mass spectrometry    March 1, 1991   Volume 20, Issue 3 109-114 doi: 10.1002/bms.1200200303
Teale P, Houghton E.A screening procedure for anabolic steroid residues in horse urine has been developed based upon solid-phase extraction and gas chromatographic/mass spectrometric analysis in the selected ion mode. For moderate sample throughput the method provides a viable alternative to radioimmunoassay screening and has advantages over the latter technique due to its flexibility, specificity and ability to detect a number of steroids in a single analysis. Full automation of the gas chromatographic/mass spectrometric analysis is an additional feature of the methodology.
Interpretation of dope test results in racehorses.
The Veterinary record    February 2, 1991   Volume 128, Issue 5 114 doi: 10.1136/vr.128.5.114-a
Leadon DP.No abstract available
Interpretation of dope test results in racehorses.
The Veterinary record    January 12, 1991   Volume 128, Issue 2 41 doi: 10.1136/vr.128.2.41
Sanford J.No abstract available
GC/MS/MS detection of detomidine carboxylic acid in horse urine.
Biological mass spectrometry    January 1, 1991   Volume 20, Issue 1 41-43 doi: 10.1002/bms.1200200110
Seymour MA, Teale P, Horner MW.No abstract available
[Ethical and analytical problems in man and greater mammals].
Annales pharmaceutiques francaises    January 1, 1991   Volume 49, Issue 2 67-75 
Bourdon R.Toxicomania and doping give rise to an increasing number of drug measurements in the body fluids. Consequently the analysts have to face, at one and the same time, ethical and analytical problems. Should the analyst participate to investigations organised in order to disclose a toxicomania in a working place? The author suggests a positive answer as long as the adduct person benefits to a social and medical care. What is the analytical meaning of a positive test? Taking into account the increasing sensitivity of the methods used, thresholds have to be established, at least for the blood concen...
Interpretation of dope test results in racehorses.
The Veterinary record    December 15, 1990   Volume 127, Issue 24 602 
Rossdale PD.No abstract available
Rapid extraction and detection of mazindol in horse urine.
Journal of pharmaceutical and biomedical analysis    January 1, 1990   Volume 8, Issue 5 445-448 doi: 10.1016/0731-7085(90)80073-x
Moore CM, Tebbett IR, Kalita S, Artememko M.No abstract available
Rapid determination of methandrostenolone in equine urine by isotope dilution liquid chromatography-tandem mass spectrometry.
Journal of chromatography    December 29, 1989   Volume 497 49-57 doi: 10.1016/0378-4347(89)80004-0
Edlund O, Bowers L, Henion J, Covey TR.Urine samples were spiked with [17-methyl-2H3]methandrostenolone as internal standard and extracted with a mixture of dichloromethane and cyclohexane. The organic phase was concentrated and injected onto a short octyl-silica column (30 mm x 4.6 mm I.D.) for separation of methandrostenolone and 17-epimethandrostenolone. The effluent from the column was connected to a Sciex TAGA 6000E triple quadrupole mass spectrometer equipped with an atmospheric pressure ion source for sampling of ions generated by a heated pneumatic nebulizer with corona discharge ionization. This ion source produced abundan...
Equine drug use: protecting your license.
Journal of the American Veterinary Medical Association    March 15, 1989   Volume 194, Issue 6 748-749 
Gloyd JS.No abstract available
Doping in race horses.
Journal of the South African Veterinary Association    March 1, 1989   Volume 60, Issue 1 4-6 
Debackere M.No abstract available
Immunoassay detection of drugs in racing horses. IX. Detection of detomidine in equine blood and urine by radioimmunoassay.
Research communications in chemical pathology and pharmacology    February 1, 1989   Volume 63, Issue 2 263-279 
Wood T, Tai CL, Taylor DG, Woods WE, Wang CJ, Houtz PK, Tai HH, Weckman TJ, Yang JM, Sturma L.Detomidine is a potent non-narcotic sedative agent which is currently in the process of being approved for veterinary clinical use in the United States. Since no effective screening method in horses is available for detomidine, we have developed an 125I radioimmunoassay for detomidine in equine blood and urine as part of a panel of tests for illegal drugs in performance horses. Our 125I radioimmunoassay has an I-50 for detomidine of approximately 2 ng/ml. Our assay shows limited cross-reactivity with the pharmacodynamically similar xylazine, but does not cross-react with acepromazine, epinephr...
Immunoassay detection of drugs in racing horses. VII. Detection of acepromazine in equine urine and blood by ELISA and PCFIA.
Research communications in chemical pathology and pharmacology    September 1, 1988   Volume 61, Issue 3 391-412 
Kwiatkowski S, Sturma L, Dai MR, Tai HH, Watt DS, Tai CL, Woods WE, Weckman TJ, Yang JM, Wood T.We have developed and evaluated a one step enzyme-linked immunosorbent assay (ELISA) test and a particle concentration fluorescence immunoassay (PCFIA) test for acepromazine as part of a panel of pre- and post-race tests for illegal medications in racing horses. These tests are rapid, sensitive and economical and development of the tests occurred in less than seven months. The ELISA test detects acepromazine with an I-50 of about 150 pg/ml. In vivo, it readily detects the presence of acepromazine or its metabolites in equine blood and urine from 8 to 72 hours or longer, respectively, after adm...
Identification of doping agents by chromatographic techniques and UV spectrophotometry.
The Analyst    August 1, 1988   Volume 113, Issue 8 1189-1195 doi: 10.1039/an9881301189
Salvadori MC, Velletri ME, Camargo MM, Araújo AC.No abstract available
Gas chromatographic analysis of flunixin in equine urine after extractive methylation.
Journal of chromatography    May 13, 1988   Volume 427, Issue 1 55-66 doi: 10.1016/0378-4347(88)80104-x
Johansson M, Anlér EL.A quantitative method for the analysis of flunixin, 2-(2-methyl-3-trifluoromethylanilino) nicotinic acid, in equine urine by gas chromatography with nitrogen-phosphorus detection has been developed. Flunixin and the internal standard, mefenamic acid, N-(2,3-xylyl) anthranilic acid, were analysed after extractive methylation of the carboxylic acid group using methyl iodide. The extraction and alkylation conditions of flunixin and mefenamic acid have been studied. The detection limit of the method was 0.25 mumol/l flunixin in urine (74 ng/ml). Flunixin was found to be conjugated to 96.5% in equi...
A common sense change in ‘doping’ rules.
Equine veterinary journal    March 1, 1988   Volume 20, Issue 2 84 doi: 10.1111/j.2042-3306.1988.tb01463.x
Moss MS.No abstract available
[The doping problem from an animal welfare view].
DTW. Deutsche tierarztliche Wochenschrift    February 1, 1988   Volume 95, Issue 2 46-47 
Grahwit G.No abstract available
Identification of a flunixin metabolite in the horse by gas chromatography-mass spectrometry.
Journal of chromatography    December 25, 1987   Volume 423 123-130 doi: 10.1016/0378-4347(87)80334-1
Jaussaud P, Courtot D, Guyot JL, Paris J.The main metabolite of flunixin, a hydroxylated product, has been identified by gas chromatography-mass spectrometry and 1H NMR spectroscopy in equine urine and plasma. The method also permits the qualitative monitoring of the urinary elimination of the drug and its metabolite. The two products are detected up to 175 and 54 h, respectively, after a single intravenous administration at the dose of 1 mg/kg. Simultaneous detection of the two compounds increases the reliability of anti-doping control analysis.
Screening of amphetamines by gradient microbore liquid chromatography and pre-column technology.
Journal of chromatography    April 22, 1987   Volume 393, Issue 1 57-68 doi: 10.1016/s0021-9673(01)94204-9
Slais K, Nielen MW, Brinkman UA, Frei RW.Amphetamine-type drugs with a wide polarity range have been screened in both human and horse urine using on-line pre-concentration on pre-columns packed with hydrophobic and cation-exchange sorbents in series and gradient microbore high-performance liquid chromatography. The underivatized amphetamines were identified by UV detection at 210 nm. The method has potential for the automated liquid chromatographic screening of amphetamines in urine, e.g., for doping control.
Detection of the administration of anabolic preparations of nandrolone to the entire male horse.
Equine veterinary journal    November 1, 1986   Volume 18, Issue 6 491-493 doi: 10.1111/j.2042-3306.1986.tb03701.x
Houghton E, Ginn A, Teale P, Dumasia MC, Moss MS.No abstract available
Determination of nefopam in equine plasma by gas chromatography-mass spectrometry with chemical ionization.
Journal of chromatography    April 25, 1986   Volume 377 379-383 doi: 10.1016/s0378-4347(00)80797-5
Bondesson U, Johansson IM.This study demonstrates the development of a method using gas chromatography-mass spectrometry for determining nefopam, a non-narcotic pain reliever that is sometimes abused in horse doping, in equine plasma. Background […]
[Flunixin and its use in horses].
Annales de recherches veterinaires. Annals of veterinary research    January 1, 1986   Volume 17, Issue 4 353-362 
Jaussaud P.Flunixin is a non-steroidal anti-inflammatory agent, with a potent analgesic activity and a slight toxicity. It is largely used in horses, in the form of meglumine salt, for the treatment of inflammatory diseases or colics, and often identified in dopage cases. Physical and chemical properties of the drug, its pharmacological and toxicological properties, and its use in equine species are depicted.
Efficacy of testing for illegal medication in horses.
Journal of the American Veterinary Medical Association    November 1, 1985   Volume 187, Issue 9 927-930 
Woods WE, Chay S, Houston T, Blake JW, Tobin T.The efficacy of testing for illegal drugs in race horses was surveyed by evaluating 27 questionnaires received from 28 racing jurisdictions polled. Large variations in the number of samples tested and drugs detected were reported. Some jurisdictions reported only illegal medications, whereas others also reported permitted medications. To facilitate comparison, stimulants, depressants, local anesthetics, narcotic analgesics, and tranquilizers were classified as hard drugs. Other drugs, which are legal in some jurisdictions, were classified as soft. To evaluate the efficacy of testing, positive ...
Effects of phenylbutazone and oxyphenbutazone on basic drug detection in high performance thin layer chromatographic systems.
Journal of veterinary pharmacology and therapeutics    June 1, 1985   Volume 8, Issue 2 181-189 doi: 10.1111/j.1365-2885.1985.tb00942.x
Woods WE, Chay S, Houston T, Blake JW, Tobin T.Interference or 'masking' in thin layer chromatography occurs when the presence of one drug on a thin layer plate physically obscures or interferes with the detection of another drug. We investigated the ability of phenylbutazone and oxyphenbutazone to mask or interfere with the detection by high performance thin layer chromatography (HPTLC) of basic drugs used illegally in horse racing. Of fifty-five basic drugs called 'positive' since 1981 by laboratories affiliated with the Association of Official Racing Chemists (AORC), forty did not comigrate with phenylbutazone or oxyphenbutazone and cou...
[Chronopharmacokinetics of phenylbutazone in the horse. Application to antidoping control].
Annales de recherches veterinaires. Annals of veterinary research    January 1, 1985   Volume 16, Issue 4 385-391 
Jaussaud P, Courtot D, Doron P, Guyot JL.Chronopharmacokinetics of intravenous phenylbutazone in the horse was studied with the aim of antidoping control. Among parameters studied, the single one which seemed to depend on circadian rhythm was the elapsed time between the injection and the plasmatic peak. There was no relationship between the injection time and the both parameters: half-life and time required to reach the forensic level of 4 micrograms/ml. This later, and oxyphenbutazone/phenylbutazone ratio, should depend on individual factors. Therefore, the injection time should not be a main parameter for the phenylbutazone evalua...
[Doping control in race horses].
Tierarztliche Praxis    January 1, 1985   Volume 13, Issue 1 35-53 
Ungemach FR.Doping in performance horses is defined as the "illegal application of any substance, except normal diet, that might modify the natural and present capacities of the horse at the time of the race." The prohibition of doping is mainly based on the protection of animals. Doping can be performed with various aims: "doping to win" can be regarded as the classical method by mobilization of overphysiological capacities. Such positive doping may be classified as an acute form using psychomotoric stimulants, as a chronic form using anabolic hormones, and as a paradoxical form using small doses of neur...
[Veterinary treatment of race horses: doping problems].
Schweizer Archiv fur Tierheilkunde    June 1, 1984   Volume 126, Issue 6 287-291 
Gerber H.No abstract available
Analysis of propionylpromazine and its metabolites in horse urine.
The Cornell veterinarian    January 1, 1984   Volume 74, Issue 1 38-49 
Dewey EA, Maylin GA.The metabolism of propionylpromazine in the horse was studied. Although propionylpromazine is not currently approved or recommended for use in horses, it has been used illegally to alter their performance. Propionylpromazine hydrochloride was administered intramuscularly at clinical and subclinical doses. Three metabolites were detected in urine. The major metabolite was identified as 2-(1-hydroxypropyl) promazine sulfoxide. The detection of this metabolite in routine drug testing has been described.
Survey of positive results from racecourse antidoping samples received at Racecourse Security Services’ Laboratories.
Equine veterinary journal    January 1, 1984   Volume 16, Issue 1 39-42 doi: 10.1111/j.2042-3306.1984.tb01846.x
Moss M S..A review of positive Jockey Club "dope tests" during the 12 years from 1970 to 1981 inclusive is presented and a comparison made with certain overseas racing authorities for varying periods between 1975 and 1981. Urinary pH of post race urine samples is predominantly acidic (although varying in a significant manner throughout the year) and thus favours excretion of the generally more potent basic drugs. The proportion of positive results was about the same in winners and non-winners, ie, one in 400 horses sampled. Drugs found fell mainly into four categories: methylxanthines; non-steroidal ant...
[Method for detection of doping drugs in the horse urine containing polyethylene glycol by high performance liquid chromatography].
Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan    July 1, 1983   Volume 103, Issue 7 800-804 doi: 10.1248/yakushi1947.103.7_800
Ohtake I, Matsui Y, Matsumoto T, Momose A.No abstract available