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Topic:High-performance Liquid Chromatography (HPLC)

High-performance Liquid Chromatography (HPLC) is an analytical technique used to separate, identify, and quantify components in a mixture. In equine research, HPLC is employed to analyze various biological samples from horses, such as blood, urine, and tissue, to detect and measure compounds like drugs, metabolites, and nutritional components. This technique is valued for its precision, sensitivity, and ability to handle complex matrices, making it suitable for pharmacokinetic studies, monitoring therapeutic drug levels, and assessing metabolic profiles in horses. The application of HPLC in equine studies provides insights into drug metabolism, nutritional status, and the biochemical effects of different treatments. This page compiles peer-reviewed research studies and scholarly articles that explore the applications, methodologies, and findings of HPLC in the context of equine science.
Thin-layer chromatographic screening procedure for some drugs in horse plasma.
Journal of chromatography    November 24, 1989   Volume 496, Issue 2 407-415 doi: 10.1016/s0378-4347(00)82588-8
Tanaka T, Aramaki S, Momose A.A thin-layer chromatographic screening procedure for some basic, neutral and acidic drugs was developed using 3 ml of horse plasma. Chloroform-2-propanol (95:5, v/v) was used as the extraction solvent. The drugs were identified by a high-performance thin-layer chromatographic plate and spraying successively with some detection reagents. In this study, the extraction recovery rates and the detection limits were determined at the same time.
Simultaneous analysis of furosemide and bumetanide in horse plasma using high performance liquid chromatography.
Biomedical chromatography : BMC    November 1, 1989   Volume 3, Issue 6 262-265 doi: 10.1002/bmc.1130030607
Singh AK, McArdle C, Gordon B, Ashraf M, Granley K.A high performance liquid chromatographic method is described for the simultaneous determination of furosemide and bumetanide in horse plasma. The C8 (3 microns) reversed phase column (4.8 x 150 mm) provided clear separation of furosemide and bumetanide with other components present in the horse plasma. The detection limit for both the drugs was 10 ng/mL. Both drugs were stable in plasma (at natural or acidic pH) for up to 24 h. The method is sufficiently sensitive to detect furosemide levels in plasma obtained from horses receiving a therapeutic dose of furosemide.
An improved TLC method for the detection of flunixin in equine serum.
Research in veterinary science    November 1, 1989   Volume 47, Issue 3 406-407 
Pemberton AD, Slater JS, Milne EM.A method for flunixin detection in equine serum extracts involving thin layer chromatography, spraying the chromatogram with alkaline sodium hypochlorite solution and heating with a detection limit of 50 ng ml-1 is described.
Altered sarcoplasmic reticulum function after high-intensity exercise.
Journal of applied physiology (Bethesda, Md. : 1985)    November 1, 1989   Volume 67, Issue 5 2072-2077 doi: 10.1152/jappl.1989.67.5.2072
Byrd SK, McCutcheon LJ, Hodgson DR, Gollnick PD.This study examined the effects of acute high-intensity exercise on the rate and capacity of Ca2+ uptake and Ca2+-stimulated adenosinetriphosphatase (ATPase) activity of the sarcoplasmic reticulum and the reversibility of these effects. Thoroughbred horses were run at maximal O2 uptake on a high-speed treadmill until fatigued. Muscle temperatures and biopsy samples were collected at rest, immediately after exercise, and 30 and 60 min after exercise. Blood samples were collected at rest and 5 min after exercise. Muscle and blood (lactate concentration) were three- and fivefold greater than pre-...
A new method for hydrolyzing sulfate and glucuronyl conjugates of steroids.
Analytical biochemistry    November 1, 1989   Volume 182, Issue 2 289-294 doi: 10.1016/0003-2697(89)90596-4
Tang PW, Crone DL.A new method for hydrolyzing steroid conjugates (both sulfates and glucuronides conjugates) that is efficient, effective, and inexpensive is described. This method comprises incubation of the conjugates--after salting-out into ethyl acetate or elution from a C18 cartridge--with anhydrous methanolic hydrogen chloride (methanolysis) for 10 min. It has been successfully applied to our routine radioimmunoassay screening and GC/MS confirmation studies of steroids in prerace and postrace equine urine samples. Comparative GC/MS studies on entire (male horse) urine samples showed that methanolysis gav...
Determination of leucine enkephalin and methionine enkephalin in equine cerebrospinal fluid by microbore high-performance liquid chromatography and capillary zone electrophoresis coupled to tandem mass spectrometry.
Journal of chromatography    October 27, 1989   Volume 495 41-59 doi: 10.1016/s0378-4347(00)82608-0
Mück WM, Henion JD.The performance of microbore high-performance liquid chromatography and capillary zone electrophoresis, both equipped with on-line tandem mass spectrometric detection capability, was evaluated critically for the determination of endogenous amounts of leucine enkephalin and methionine enkephalin in equine cerebrospinal fluid. Using an identical sample clean-up and enrichment procedure, capillary zone electrophoresis-mass spectrometry is limited in its concentration detection capacity owing to its much smaller injection volume. Leucine enkephalin was identified in post-mortem equine cerebrospina...
Application of high-performance liquid chromatography–inductively coupled plasma mass spectrometry to the investigation of cadmium speciation in pig kidney following cooking and in vitro gastro-intestinal digestion.
The Analyst    August 1, 1989   Volume 114, Issue 8 895-899 doi: 10.1039/an9891400895
Crews HM, Dean JR, Ebdon L, Massey RC.The speciation of cadmium in retail pig kidney has been examined by size-exclusion chromatography (SEC) coupled directly to inductively coupled plasma mass spectrometry (ICP-MS). Approximately 35% of the cadmium from uncooked kidney was soluble after aqueous extraction at pH 8 and SEC - ICP-MS revealed three discrete peaks whose retention times corresponded to estimated relative molecular masses of 1.2 x 10(6), 7.0 x 10(4) and 6 x 10(3)-9 x 10(3). In the cooked kidney, 35% of the Cd was soluble and was all associated with a peak of a relative molecular mass (Mr) of 6 x 10(3)-9 x 10(3). After s...
Screening and confirmation of drugs in horse urine by using a simple column extraction procedure.
Journal of chromatography    June 28, 1989   Volume 473, Issue 1 215-226 doi: 10.1016/s0021-9673(00)91303-7
Singh AK, Ashraf M, Granley K, Mishra U, Rao MM, Gordon B.A simple and reproducible column (Clean Screen-DAU, copolymeric bonded-phase silica column) extraction procedure has been described for the screening and confirmation of drugs in horse urine. The recovery of drugs by the column extraction was better than or comparable to the recovery by the liquid-liquid extraction, which is commonly used in the equine analytical laboratories. The column extraction provided broad coverage of drugs, separated extracts into three fractions (acidic/neutral, steroids, basic), produced a cleaner extract, and eliminated the need for special liquid-liquid extraction ...
Urinary excretion of pentoxifylline and its metabolites by standardbred mares. Kwong EC, Chen FC, Young LM.The urinary excretion of a sustained-release formulation of pentoxifylline was studied in the horse after the oral administration of 4.0 grams of Trental tablets. Urine samples were collected for 24 hours after dosing and analyzed for pentoxifylline and its metabolites using high-performance liquid chromatography coupled with an ultraviolet detector. Six metabolites of pentoxifylline were identified in horse urine in addition to less than 0.2% of unchanged drug. Concomitant use of gas chromatography/mass spectrometry allowed for the elucidation of the chemical structures of the metabolites. Me...
Analysis of N-acetyl-4-O-acetylneuraminic-acid-containing N-linked carbohydrate chains released by peptide-N4-(N-acetyl-beta-glucosaminyl)asparagine amidase F. Application to the structure determination of the carbohydrate chains of equine fibrinogen.
European journal of biochemistry    March 1, 1989   Volume 180, Issue 1 101-110 doi: 10.1111/j.1432-1033.1989.tb14620.x
Damm JB, Voshol H, Hård K, Kamerling JP, Vliegenthart JF.The carbohydrate chains of equine fibrinogen were enzymatically released by peptide-N4-(N-acetyl-beta-glucosaminyl)asparagine amidase F. The oligosaccharides obtained were fractionated by a combination of FPLC and HPLC and analyzed by 500-MHz 1H-NMR spectroscopy. Four monosialo and four disialo diantennary N-acetyllactosamine type of carbohydrate chains occur: (formula; see text)
Determination of methandrostenolone and its metabolites in equine plasma and urine by coupled-column liquid chromatography with ultraviolet detection and confirmation by tandem mass spectrometry.
Journal of chromatography    February 24, 1989   Volume 487, Issue 2 341-356 doi: 10.1016/s0378-4347(00)83042-x
Edlund PO, Bowers L, Henion J.Monitoring steroid use requires an understanding of the metabolism in the species in question and development of sensitive methods for screening of the steroid or its metabolites in urine. Qualitative information for confirmation of methandrostenolone and identification of its metabolites was primarily obtained by coupled-column high-performance liquid chromatography-tandem mass spectrometry. The steroids and a sulphuric acid conjugate were isolated and identified by their daughter ion mass spectra in the urine of both man and the horse following administration of methandrostenolone. Spontaneo...
Carnosine content of the middle gluteal muscle in thoroughbred horses with relation to age, sex and training.
Comparative biochemistry and physiology. A, Comparative physiology    January 1, 1989   Volume 93, Issue 3 629-632 doi: 10.1016/0300-9629(89)90023-6
Marlin DJ, Harris RC, Gash SP, Snow DH.1. Muscle biopsies were collected from 85 thoroughbred horses and analysed for carnosine content by an automated HPLC method. 2. No significant sex difference was found between colts, geldings and fillies. 3. There was a trend towards lower muscle carnosine contents with age, which was only significant between 1-year-old untrained horses and 4+ year-old horses (P less than 0.002).
Narcotic analgesics, their detection and pain measurement in the horse: a review.
Equine veterinary journal    January 1, 1989   Volume 21, Issue 1 4-12 doi: 10.1111/j.2042-3306.1989.tb02081.x
Kamerling S, Wood T, DeQuick D, Weckman TJ, Tai C, Blake JW, Tobin T.Narcotic analgesics produce pharmacological effects by interacting with specific opiate receptors. At least five major types of opiate receptors have been recognised. These include mu (morphine) and kappa (ethylketazocine) receptor types. Narcotic analgesics which interact with mu receptors produce locomotor and autonomic stimulation at doses that produce little or no analgesia. Therefore, use of these drugs as analgesics in equine medicine has not been very satisfactory. Theoretical considerations suggested that the role of kappa agonists in equine analgesia be investigated. Using a pure kapp...
Analysis of equine cisterna magna cerebrospinal fluid for the presence of some monoamine neurotransmitters and transmitter metabolites.
Veterinary research communications    January 1, 1989   Volume 13, Issue 3 237-249 doi: 10.1007/BF00142050
Vaughn DM, Smyth GB, Whitmer WL, Satjawatcharaphong C.Small volumes (0.05 ml) of cisterna magna cerebrospinal fluid (CSF) from 23 neurologically normal horses were analysed for the monoamine neurotransmitters dopamine, norepinephrine, epinephrine, serotonin and their metabolites using high pressure liquid chromatography and electrochemical detection. Two metabolites, homovanillic acid (HVA) and 5-hydroxyindoleacetic acid (5-HIAA) were present in all CSF samples. The deaminated and methylated metabolite of dopamine, HVA, was present at a mean concentration of 42.33 +/- 3.14 ng/ml of CSF. The deaminated metabolite of serotonin, 5-HIAA, was present ...
Different gradients for neurotransmitter metabolites and protein in horse cerebrospinal fluid.
Veterinary research communications    January 1, 1989   Volume 13, Issue 6 413-419 doi: 10.1007/BF00402561
Vaughn DM, Smyth GB.The serotonin metabolite, 5-hydroxyindoleacetic acid (5-HIAA) and the dopamine metabolite, homovanillic acid (HVA) in the cerebrospinal fluid (CSF) of seven clinically normal horses were evaluated with reverse phase high pressure liquid chromatography and electrochemical detection. Comparisons of the neurotransmitter metabolite concentrations were made on CSF collected simultaneously from the atlanto-occipital and lumbosacral regions. There were significantly higher amounts of 5-HIAA and HVA in atlanto-occipital CSF than in lumbosacral CSF. Mean 5-HIAA concentrations in atlanto-occipital and l...
Screening, confirmation and quantification of boldenone sulfate in equine urine after administration of boldenone undecylenate (Equipoise).
Journal of chromatography    December 9, 1988   Volume 433 9-21 doi: 10.1016/s0378-4347(00)80580-0
Weidolf LO, Chichila TM, Henion JD.Methods for screening by thin-layer chromatography, quantification by high-performance liquid chromatography with ultraviolet detection and confirmation by gas chromatography-mass spectrometry of boldenone sulfate in equine urine after administration of boldenone undecylenate (Equipoise) are presented. Sample work-up was done with C18 liquid-solid extraction followed by solvolytic cleavage of the sulfate ester. Confirmatory evidence of boldenone sulfate in equine urine was obtained from 2 h to 42 days following a therapeutic intramuscular dose of Equipoise. The use of 19-nortestosterone sulfat...
Physical and chemical characterization of a horse serum carboxylesterase.
Archives of biochemistry and biophysics    November 15, 1988   Volume 267, Issue 1 271-279 doi: 10.1016/0003-9861(88)90032-x
Torres JL, Rush RS, Main AR.The serine carboxylesterase from horse serum was characterized by amino acid composition, peptide mapping, molecular and subunit weights, and sequencing of the amino acids around the essential serine residue at the active site. A protocol was developed for using reversed-phase high-performance liquid chromatography as the final step to obtain homogeneous preparations of horse serum carboxylesterase. Amounts sufficient for determining the amino acid composition and for peptide maps were obtained from a partially purified starting material which contained approximately 55% carboxylesterase. The ...
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
Some applications of chromatography to steroid analysis in the horse.
The Analyst    August 1, 1988   Volume 113, Issue 8 1179-1187 doi: 10.1039/an9881301179
Houghton E, Dumasia MC, Teale P.No abstract available
Severe hypoglycemia attributable to surreptitious injection of insulin in a mare.
Journal of the American Veterinary Medical Association    July 15, 1988   Volume 193, Issue 2 224-226 
Given BD, Mostrom MS, Tully R, Ditkowsky N, Rubenstein AH.A mare with signs of hypoglycemia had high serum insulin concentrations before it was euthanatized. High pressure liquid chromatography revealed that the insulin in the mare's blood was of commercial origin. Surreptitious insulin injection has been suspected as the cause of several suspicious deaths of insured horses. The use of high-pressure liquid chromatography should help put an end to this practice.
Isolation and quantitation of cadmium-, zinc- and copper-metallothioneins by high-performance liquid chromatography-atomic absorption spectrometry.
Journal of chromatography    June 17, 1988   Volume 442 345-352 doi: 10.1016/s0021-9673(00)94482-0
Van Beek H, Baars AJ.Metallothioneins (MTs) were separated and quantitated by reversed-phase high-performance liquid chromatography (RP-HPLC), in direct combination with atomic absorption spectrometry (AAS) for quantitation of the metal contents in MTs. MTs were eluted from an RP-8 column with a gradient of Tris buffer pH 7.0 and methanol, and were detected by UV absorbance (220 nm). Commercially available purified MTs from horse kidney and rabbit liver were analyzed for purity and metal composition. One lot of horse kidney yielded only 50% of the estimated value. In some cases, the certified metal content differe...
Determination of clenbuterol and mabuterol in equine plasma by ion-pair liquid chromatography with electrochemical detection. Chromatographic and electrochemical characteristics.
Journal of chromatography    May 27, 1988   Volume 441, Issue 1 197-205 doi: 10.1016/s0021-9673(01)84666-5
Qureshi GA, Eriksson A.A method for the routine determination of the beta-adrenergic drugs clenbuterol and mabuterol in equine plasma has been developed. The drugs were isolated from alkalinized plasma by liquid-liquid extraction. The organic phase was evaporated to dryness and the residue was dissolved in the mobile phase prior to injection. The recoveries were 98% and 95% for clenbuterol and mabuterol, respectively. The drugs were separated by reversed-phase high-performance liquid chromatography and quantitated by a use of a coulometric detector set at +0.75 V vs. the internal reference electrode. The influence o...
Determination of xylazine in blood components using high-performance liquid chromatography.
Journal of chromatography    April 8, 1988   Volume 426, Issue 1 207-211 doi: 10.1016/s0378-4347(00)81945-3
Akbari A, Gordon BJ, Bush PB, Moore JN.No abstract available
Determination of boldenone sulfoconjugate and related steroid sulfates in equine urine by high-performance liquid chromatography/tandem mass spectrometry.
Biomedical & environmental mass spectrometry    March 1, 1988   Volume 15, Issue 5 283-289 doi: 10.1002/bms.1200150508
Weidolf LO, Lee ED, Henion JD.Sulfoconjugated anabolic steroids were separated by micro-bore high-performance liquid chromatography. The eluent was introduced into the atmospheric pressure ion source of the triple-quadrupole mass spectrometer via an ion spray liquid chromatograph/mass spectrometer interface operated in the negative ion mode. The limit of detection was 10 pg on-column by selected ion monitoring of the molecular ion and the response increased linearly over a concentration range of 2.4 orders of magnitude. Following work-up by a liquid-solid extraction procedure of equine urine samples, full-scan daughter ion...
Complete separation of nine equine oestrogens by high-performance liquid chromatography.
Journal of chromatography    January 8, 1988   Volume 435, Issue 2 385-390 doi: 10.1016/s0021-9673(01)82201-9
Desta B.No abstract available
Pigment types of various color genotypes of horses.
Pigment cell research    January 1, 1988   Volume 1, Issue 6 410-413 doi: 10.1111/j.1600-0749.1988.tb00144.x
Sponenberg DP, Ito S, Eng LA, Schwink K.Hair samples of various colors of horses were analyzed for content of both eumelanin and pheomelanin by a procedure using high performance liquid chromatography. The results are in accord with generally accepted genetic hypotheses accounting for the various colors. However, the results support the hypothesis that the chestnut/sorrel group of colors is conditioned by the extension locus, not the brown locus. The results also indicate that the brown locus is a likely contributor to some rare color phenotypes.
Diurnal and episodic variations of plasma hydrocortisone concentrations in horses.
Domestic animal endocrinology    January 1, 1988   Volume 5, Issue 1 55-59 doi: 10.1016/0739-7240(88)90026-4
Toutain PL, Oukessou M, Autefage A, Alvinerie M.Using a specific high-performance liquid chromatographic technique, plasma hydrocortisone values were measured hourly in 6 horses and every 10 minutes in 4 horses over 24 hours. Both circadian and episodic variation was observed. The mean plasma hydrocortisone concentration was a maximum of 58.8 +/- 9.54 ng/ml at 9.19 +/- 0.59 hr and a minimum of 27.85 +/- 6.85 g/ml at 21.19 +/- 0.59 hr. The number of episodes of secretion was 10.0 +/- 1.41; the mean amplitude and duration of peak were 26.21 +/- 3.71 ng/ml and 105.25 +/- 21.24 min respectively.
Structural, histochemical and biochemical observations on horse milk-fat-globule membranes and casein micelles.
Histochemistry    January 1, 1988   Volume 88, Issue 3-6 357-365 doi: 10.1007/BF00570295
Welsch U, Buchheim W, Schumacher U, Schinko I, Patton S.Horse milk fat globules (MFGs) and casein micelles were studied using freeze fracturing, freeze etching and thin-section electron microscopy, as well as lectin histochemistry, gel electrophoresis, and Western blotting. Horse MFGs were found to be relatively small, their average volume-surface diameter being about 2.75 microns. The MFG membrane is composed of three layers: an inner proteinaceous coat occasionally having a paracrystalline substructure, a unit membrane, and a prominent filamentous glycocalyx. The last is rich in glycoconjugates, as revealed by its binding of various lectins. In a...
Characterization of a homogeneous paraprotein from a horse with spontaneous multiple myeloma syndrome.
Veterinary immunology and immunopathology    December 1, 1987   Volume 17, Issue 1-4 69-77 doi: 10.1016/0165-2427(87)90128-0
Seide RK, Jacobs RM, Dobblestein TN, Kehoe JM.A novel myeloma paraprotein has been isolated from a horse with a lymphoid tumor. The protein was a euglobulin and consequently was readily isolated from serum in pure form and high yield by simple dilution in distilled water. The purified intact protein had a molecular weight of 150,000 and was composed of heavy and light chains, both of which had blocked amino-termini and were thus not susceptible to amino-terminal sequence analysis. The amino acid compositions of these respective chains corresponded to those of comparable chains from immunoglobulins of other species. Peptide maps of parapro...
The major protamine from stallion sperm. Isolation and amino-acid sequence.
Biological chemistry Hoppe-Seyler    December 1, 1987   Volume 368, Issue 12 1619-1626 doi: 10.1515/bchm3.1987.368.2.1619
Ammer H, Henschen A.The major stallion protamine was isolated from sperm cell nuclei by extraction with 6M guanidine/5% mercaptoethanol, alkylation with 4-vinylpyridine and subsequent reversed-phase high-performance liquid chromatography. The primary structure of stallion protamine was determined by N-terminal sequencing of the intact protein and of the fragments obtained from thermolysin cleavage of the S-pyridylethylated and from endoproteinase Lys-C cleavage of the S-aminoethylated protein. Stallion protamine consists of 49 amino-acid residues and shows 49% identity with all other sequenced mammalian type 1 pr...
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