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Topic:Intramuscular Administration

Intramuscular administration in horses involves the injection of medications directly into the muscle tissue. This method is commonly used for delivering vaccines, antibiotics, and other therapeutic agents. The technique requires knowledge of equine anatomy to ensure the injection is placed in the correct location, such as the neck or hindquarters, to minimize discomfort and avoid complications. Proper intramuscular administration can facilitate the absorption of medications into the bloodstream, allowing for effective therapeutic interventions. This page compiles peer-reviewed research studies and scholarly articles that explore the techniques, benefits, and potential complications associated with intramuscular administration in equine practice.
Pharmacokinetic profile of sulphamonomethoxine-trimethoprim in horses after intravenous, intramuscular and oral administration.
Research in veterinary science    March 1, 1993   Volume 54, Issue 2 184-188 doi: 10.1016/0034-5288(93)90054-j
Carli S, Sonzogni O, Villa R, Bignazzi R, Montesissa C.The pharmacokinetic profile of a sulphamonomethoxine-trimethoprim (SMM-TMP) combination was investigated in five horses. The combination was administered intravenously, intramuscularly and orally at a constant dose of 20 mg SMM plus 4 mg TMP kg-1 bodyweight. Following intravenous administration both drugs dispersed rapidly with distribution half-lives of about 12 minutes for SMM and about 18 minutes for TMP. Elimination half-lives for intravenous, intramuscular and oral administration were closely similar, indicating that elimination was independent of administration route. Bioavailability of ...
Pharmacokinetics of ceftiofur sodium in neonatal foals after intramuscular injection.
Equine veterinary journal    November 1, 1992   Volume 24, Issue 6 485-486 doi: 10.1111/j.2042-3306.1992.tb02883.x
Meyer JC, Brown MP, Gronwall RR, Merritt K.No abstract available
Safety of ceftiofur sodium administered intramuscularly in horses.
American journal of veterinary research    November 1, 1992   Volume 53, Issue 11 2201-2205 
Mahrt CR.Ceftiofur sodium, a broad-spectrum cephalosporin antibiotic, was evaluated for safe use in horses. Male or female horses were allotted to groups and were given either saline solution (control), or 2.2, 6.6, or 11 mg of an aqueous solution of ceftiofur sodium/kg of body weight/d, IM, for 30 or 31 days. These dosages are expressed in terms of the ceftiofur free acid, and represent 1 to 5 times the proposed therapeutic dosage (2.2 mg/kg/d) administered for 3 times the maximal recommended duration of 10 days. Some of the horses were euthanatized and necropsied on day 31 or 32. The other horses wer...
Plasma concentration of furosemide versus specific gravity of urine in predicting dose of administration in race horses.
Research communications in chemical pathology and pharmacology    August 1, 1992   Volume 77, Issue 2 201-218 
Uboh CE, Soma LR, Rudy JA, Morgan E, Mengeringhausen K, Sams R.This study was undertaken to determine the applicability of plasma concentration of furosemide and specific gravity (SG) of urine in regulating the use of furosemide administered 4 hours prior to race time in Exercise-Induced Pulmonary Hemorrhage (EIPH) race horses. Nonbleeders (CTL) and certified bleeders (FUR) actively racing in Illinois (IL) and Pennsylvania (PA) were used in the study. Various doses (less than 250, 250, 300, 350, 400 and 500 mg) were administered either as a single intravenous (IV) dose or as a combination (IV-IM) of IV and intramuscular (IM) administrations 4 hours before...
The role of procaine in adverse reactions to procaine penicillin in horses.
Australian veterinary journal    June 1, 1992   Volume 69, Issue 6 129-133 doi: 10.1111/j.1751-0813.1992.tb07480.x
Chapman CB, Courage P, Nielsen IL, Sitaram BR, Huntington PJ.Procaine penicillin is a commonly used antibiotic in equine medicine but its use is associated with a substantial incidence of adverse reactions. Soluble procaine concentrations were determined by HPLC in several commercially available procaine penicillin preparations, including some that were involved in adverse reactions. The mean (+/- SEM) soluble procaine concentrations in the veterinary preparations was 20.18 +/- 5.07 mg/ml, which was higher than the concentration in the only procaine penicillin preparation for use in humans in Australia of 7.3 mg/ml. Heating the veterinary procaine penic...
Bioavailability and bioequivalence of veterinary drug dosage forms, with particular reference to horses: an overview.
Journal of veterinary pharmacology and therapeutics    June 1, 1992   Volume 15, Issue 2 160-173 doi: 10.1111/j.1365-2885.1992.tb01003.x
Baggot JD.The route of administration and formulation of the dosage form affect the bioavailability (rate and extent of absorption) of a drug and may thereby influence the intensity and duration of the pharmacological effect. Location of injection site may affect the plasma concentration profile of drugs administered as aqueous suspensions or sustained release parenteral preparations (procaine penicillin G). When absorption influences the rate of elimination ('flip-flop' phenomenon), the apparent half-life of the drug will be increased (cefazolin sodium, i.m.; meclofenamic acid, p.o.). Absorption genera...
Superovulation of cattle with equine pituitary extract and porcine ESH.
Theriogenology    May 1, 1992   Volume 37, Issue 5 1091-1099 doi: 10.1016/0093-691x(92)90107-3
Staigmiller RB, Bellows RA, Anderson GB, Seidel GE, Foote WD, Menino AR, Wright RW.Superovulation has been practiced in cattle for more than 50 years but the results have been highly variable. Scientists at six locations compared a horse pituitary extract (HAP) with a single batch of porcine FSH (pFSH) to determine the efficacy of these hormones to induce superovulation and to test for variability in the superovulatory response. Acetone-dried equine pituitaries were suspended in 40% ethanol containing 6% ammonium acetate, and the supernatant was mixed with 2.5 volumes of cold ethanol. The resulting precipitate was washed with cold ether and dried. Total doses of 18 mg of HAP...
Critical and controlled tests of activity of moxidectin (CL 301,423) against natural infections of internal parasites of equids.
Veterinary parasitology    March 1, 1992   Volume 41, Issue 3-4 255-284 doi: 10.1016/0304-4017(92)90086-o
Lyons ET, Tolliver SC, Drudge JH, Granstrom DE, Collins SS, Stamper S.The activity of moxidectin was evaluated in 1988 and 1989 against natural infections of internal parasites in 20 critical tests (n = 20 equids) and three controlled tests (n = 20 equids). Two formulations, injectable administered intramuscularly (i.m.) or intraorally (i.o.) and gel i.o., were given at dose rates of 0.2, 0.3 or 0.4 mg kg-1 body weight. For the critical tests (all three dose rates evaluated), removals of second instar Gasterophilus intestinalis were 93-100%, except (89%) for the injectable formulation (i.m.) at 0.2 mg kg-1. Removals of third instar G. intestinalis were 88-100% f...
Plasma elimination and urinary excretion of procaine after administration of different products to standardbred mares.
Equine veterinary journal    March 1, 1992   Volume 24, Issue 2 118-124 doi: 10.1111/j.2042-3306.1992.tb02795.x
Stevenson AJ, Weber MP, Todi F, Young L, Beaumier P, Kacew S.Plasma and urinary concentrations of procaine were examined in Standardbred mares after subcutaneous administration of various doses (80 mg to 1600 mg) of procaine hydrochloride. Regardless of dose, peak plasma procaine values occurred within 1 h, but remained detectable in a dose-dependent manner, with procaine present at 1 h with the 80 mg dose and 6 h at the 1600 mg dose. Similarly, peak urinary procaine concentrations were attained within 1.5 to 3 h, irrespective of dose, while detection time was dose-dependent, being 23 h for 80-200 mg doses but as long as 30-54 h with the 1600 mg dose. W...
Nonsurgical treatment of cubital subchondral cyst-like lesions in horses: seven cases (1983-1987).
Journal of the American Veterinary Medical Association    February 15, 1992   Volume 200, Issue 4 527-530 
Hopen LA, Colahan PT, Turner TA, Nixon AJ.Subchondral cyst-like lesions of the cubital joint were diagnosed in 7 horses at the teaching hospital between 1983 and 1987. Diagnosis of the lesions was made by administration of intra-articular local anesthesia and/or radiographically. Initial treatment for all horses consisted of stall rest for 60 to 90 days. In addition, 2 horses were administered sodium hyaluronate intra-articularly, 1 horse was given injections of polysulfated glycosaminoglycans IM, and 1 horse was given phenylbutazone orally. Follow-up information was compiled 6 weeks to 4 years after initial examination. At the time o...
Testosterone disposition after intramuscular injection in castrated thoroughbred race horses.
Journal of veterinary pharmacology and therapeutics    December 1, 1991   Volume 14, Issue 4 430-434 doi: 10.1111/j.1365-2885.1991.tb00859.x
Martinez R, Urquieta B, Altieri E, Garzón L, Cid E.No abstract available
Pharmacokinetics of caffeine and its metabolites in horses after intravenous, intramuscular or oral administration.
Chemical & pharmaceutical bulletin    November 1, 1991   Volume 39, Issue 11 2999-3002 doi: 10.1248/cpb.39.2999
Aramaki S, Suzuki E, Ishidaka O, Momose A, Umemura K.The pharmacokinetics of caffeine (CAF) and its metabolites, dimethylxanthines, were examined in horses administered 2.5 mg/kg of CAF intravenously (i.v.), intramusculary (i.m.), or orally (p.o.). The plasma samples were extracted by Extrelut and the concentrations of CAF and metabolites were determined by high performance liquid chromatography (HPLC) with a short column. The pharmacokinetics of CAF after bolus i.v. injection were described by the assumption of a two-compartment model, and those of CAF after i.m. or p.o. administration were done by the assumption of a one-compartment model. The...
[The effect of the sedative and analgesic detomidine for laryngoscopy of adult horses and foals].
Berliner und Munchener tierarztliche Wochenschrift    October 1, 1991   Volume 104, Issue 10 340-346 
Ohnesorge VB, Deegen E, Jöchle W.Detomidine was used in this field trial effectively as a sedative and analgesic for laryngoscopic examinations in a total of 193 foals and 806 mature horses (Hanoverians). Detomidine was given either i.v. in foals 3 to 11 months old (20 micrograms/kg) and in mature horses (15 micrograms/kg), or i.m. in foals below 6 months of age (35 micrograms/kg). After i.v. administration, laryngoscopy was tolerated in more than 90% of all animals without additional use of a twitch, while in foals treated i.m. more than 70% required a twitch in order to enable this procedure. The effectiveness of detomidine...
Detection of reserpine in horses by high-performance liquid chromatography.
Australian veterinary journal    September 1, 1991   Volume 68, Issue 9 296-298 doi: 10.1111/j.1751-0813.1991.tb03259.x
Chapman CB, Courage P, Huntington PJ.A high-performance liquid chromatography (HPLC) assay was developed for the detection of reserpine. The assay was used to monitor the plasma concentrations of the drug given intramuscularly on one or two occasions to five horses. The blood concentrations of reserpine varied quite considerably between horses given the same dose of the drug. However, on average, reserpine could be detected consistently, and quantified, for 48 h after a single dose of 2.5 mg, and for a similar period after the second of two 2.5 mg doses given 13 d apart. Because of the apparently large variability in the pharmaco...
Pharmacokinetic, biochemical and tolerance studies on carprofen in the horse.
Equine veterinary journal    July 1, 1991   Volume 23, Issue 4 280-284 doi: 10.1111/j.2042-3306.1991.tb03718.x
McKellar QA, Bogan JA, von Fellenberg RL, Ludwig B, Cawley GD.Carprofen, a non-steroidal anti-inflammatory drug (NSAID) was administered to three Thoroughbred geldings and three Shetland ponies to determine its plasma disposition and tolerance. The main pharmacokinetic characteristics of carprofen in horses and ponies were a volume of distribution of 0.08 to 0.32 litres/kg (mean +/- se = 0.23 +/- 0.04) a systemic clearance of 26.4 to 78.5 ml/min (mean +/- se = 44.9 +/- 8.0) and a plasma elimination half-life of 14.5 to 31.4 h (mean +/- se = 21.9 +/- 2.3). There was no evidence of any accumulation of carprofen in plasma when the drug was given orally at a...
Cardiovascular effects of xylazine and detomidine in horses.
American journal of veterinary research    May 1, 1991   Volume 52, Issue 5 651-657 
Wagner AE, Muir WW, Hinchcliff KW.The cardiovascular effects of xylazine and detomidine in horses were studied. Six horses were given each of the following 5 treatments, at 1-week intervals: xylazine, 1.1 mg/kg, IV; xylazine, 2.2 mg/kg, IM; detomidine, 0.01 mg/kg, IV; detomidine, 0.02 mg/kg, IV; and detomidine, 0.04 mg/kg, IM. All treatments resulted in significantly decreased heart rate, increased incidence of atrioventricular block, and decreased cardiac output and cardiac index; cardiac output and cardiac index were lowest following IV administration of 0.02 mg of detomidine/kg. Mean arterial pressure was significantly redu...
Pharmacokinetics and bioavailability of ticarcillin and clavulanate in foals after intravenous and intramuscular administration.
Journal of veterinary pharmacology and therapeutics    March 1, 1991   Volume 14, Issue 1 78-89 doi: 10.1111/j.1365-2885.1991.tb00807.x
Wilson WD, Spensley MS, Baggot JD, Hietala SK, Pryor P.The pharmacokinetics and bioavailability of ticarcillin and clavulanate were determined after intravenous (i.v.) or intramuscular (i.m.) administration of ticarcillin disodium (50 mg/kg) combined with clavulanate potassium (1.67 mg/kg) to groups of healthy foals at 3 days and 28 days of age. After i.v. administration of the combination to five foals, the disposition kinetics of ticarcillin and clavulanate were best described using a two-compartment open model. Mean plasma elimination-rate constant (beta) and clearance (ClB) for ticarcillin were significantly less (P less than 0.01), and volume...
Ototoxic potential of gentamicin in ponies.
American journal of veterinary research    March 1, 1991   Volume 52, Issue 3 494-498 
Nostrandt AC, Pedersoli WM, Marshall AE, Ravis WR, Robertson BT.Ototoxicosis was evaluated in 6 healthy ponies given 5 mg of gentamicin/kg of body weight, q 8 h, IM. Ponies 1, 2, and 3 were dosed for 7 days and ponies 4, 5, and 6 were dosed for 14 days. Serum peak and trough concentrations of gentamicin were measured by radioimmunoassay at regular intervals. Brain stem auditory-evoked responses were recorded every 5 days up to 60 days after the first dose to monitor auditory function. Although serum gentamicin concentrations were within or above the accepted clinical therapeutic range, loss of auditory function was not observed at the frequency range (1 to...
Triglyceride, insulin, and cortisol responses of ponies to fasting and dexamethasone administration.
Journal of veterinary internal medicine    January 1, 1991   Volume 5, Issue 1 15-22 doi: 10.1111/j.1939-1676.1991.tb00925.x
Freestone JF, Wolfsheimer KJ, Ford RB, Church G, Bessin R.Ponies were evaluated for their response to feed withholding and exogenous administration of corticosteroids (dexamethasone 0.04 mg/kg intramuscular [IM]) in an attempt to reproduce the hyperlipemia syndrome. Because insulin resistance has been associated with hyperlipemia, all ponies were initially evaluated for insulin response to an oral glucose load and normal dexamethasone suppression of serum cortisol. Four ponies were identified as hyperinsulinemic reflecting insulin resistance. All ponies had suppressed cortisol concentrations following dexamethasone administration. Feed withdrawal res...
Prolactin secretion in lactating mares before and after treatment with bromocriptine.
Journal of reproduction and fertility. Supplement    January 1, 1991   Volume 44 551-559 
Neuschaefer A, Bracher V, Allen WR.The effect of treating lactating mares with the dopamine agonist bromocriptine was investigated. Seven pony and 4 Thoroughbred lactating mares were given a single intramuscular (i.m.) injection of 100 mg bromocriptine between Days 18 and 28 after foaling when the secretion rate of prolactin was elevated. Prolactin and luteinizing hormone (LH) concentrations were measured in serial peripheral plasma samples taken before and after the treatment and, in 5 of the pony mares, levels of these hormones were also measured in pituitary venous effluent obtained by cannulation of the cavernous sinus. In ...
Control of onset of breeding season in the mare and its artificial regulation by progesterone treatment.
Journal of reproduction and fertility. Supplement    January 1, 1991   Volume 44 307-318 
Alexander SL, Irvine CH.Mean plasma luteinizing hormone (LH) and follicle-stimulating hormone (FSH) levels and their pulse frequencies and the size of the largest ovarian follicle increased during spring in 12 mares studied twice monthly from deep anoestrus to the occurrence of the first ovulation of the breeding season. Mean FSH levels were reduced significantly in deep anoestrus and when a pre-ovulatory follicle was present, whereas mean LH levels were highest close to ovulation. Five of these 12 research mares and 20 of 40 maiden or barren Standardbred mares at a commercial studfarm were given daily intramuscular ...
Ovarian response in mares to prolonged treatment with exogenous equine pituitary gonadotrophins.
Journal of reproduction and fertility. Supplement    January 1, 1991   Volume 44 341-349 
Hofferer S, Duchamp G, Palmer E.Twelve anoestrous mares were treated with an intravaginal sponge containing 0.5 g allyl trembolone (Regumate; Roussel UCLAF, Paris) and 50 mg oestradiol benzoate for 7 days, followed by daily intramuscular (i.m.) injections of 25 mg crude equine pituitary extract (CEG), with (n = 6) or without (n = 6) 0.25 mg porcine growth hormone (pGH). No difference in ovarian response to this superovulation treatment was observed between the 2 groups (2.2 +/- 0.4 vs 2.3 +/- 0.4 ovulations per mare, respectively). CEG treatment was then combined with allyl trembolone (40 mg per os per day) and prolonged in ...
Bioavailability of ascorbic acid in horses.
Journal of veterinary pharmacology and therapeutics    December 1, 1990   Volume 13, Issue 4 393-403 doi: 10.1111/j.1365-2885.1990.tb00794.x
Snow DH, Frigg M.The bioavailability of ascorbic acid administered to thoroughbreds by intramuscular injection was investigated. For intramuscular injection two preparations were studied, and the percentage bioavailability up to 24 h of 10 g of ascorbic acid was 95% +/- 22 in four horses and 60% in two horses with preparations A and B, respectively. Bioavailability at 24 h in three horses injected subcutaneously with 10 g of preparation B was 82%. Intramuscular injection of both preparations was apparently well tolerated while subcutaneous injection of preparation B (pH 6.0) was associated with marked irritanc...
Endoscopic diagnosis of unilateral ectopic ureter in a yearling filly.
Journal of the American Veterinary Medical Association    September 1, 1990   Volume 197, Issue 5 617-618 
MacAllister CG, Perdue BD.Unilateral ectopic ureter was diagnosed by endoscopic examination in an 18-month-old filly examined because of chronic urine dribbling. Intramuscular administration of azosulfamide discolored the urine and enhanced visualization of the ectopic ureter. Endoscopy proved valuable in determining that only one ureter entered the urinary bladder and in locating the ectopic ureter in the ventral portion of the vagina.
The changes of antioxidative enzyme activities in equine erythrocytes following exercise.
Nihon juigaku zasshi. The Japanese journal of veterinary science    August 1, 1990   Volume 52, Issue 4 759-765 doi: 10.1292/jvms1939.52.759
Ono K, Inui K, Hasegawa T, Matsuki N, Watanabe H, Takagi S, Hasegawa A, Tomoda I.The change in activities of 3 major antioxidative enzymes in equine erythrocytes, superoxide dismutase (SOD), glutathione peroxidase (GSHpx), and catalase, was investigated in order to evaluate the effect of exercise. Blood samples were obtained from 11 thoroughbred horses before and immediately after vigorous exercise which induced the increase of plasma lipid peroxide (Lpx) concentration from 1.16 +/- 0.40 nmol/ml to 1.29 +/- 0.34 nmol/ml. Following the exercise, the GSHpx activity in erythrocytes was significantly reduced from 69 +/- 10 IU/gHb to 65 +/- 8 IU/gHb, whereas SOD and catalase ac...
Cephalexin in ponies: a preliminary investigation.
The Veterinary record    June 30, 1990   Volume 126, Issue 26 635-637 
Lees P, May SA, Hooke RE, Silley P.The administration of a single dose of the antibacterial agent cephalexin intramuscularly to six ponies at a dose rate of 7 mg/kg was well tolerated. No reactions at the injection site were apparent. It was absorbed rapidly and reached a mean peak plasma concentration of 6.77 micrograms/ml after a mean of 1.41 hours; plasma concentrations above 2.0 and 0.5 micrograms/ml were maintained for 3.8 and 9.8 hours, respectively.
The effect of phenylbutazone on the plasma disposition of penicillin G in the horse.
Journal of veterinary pharmacology and therapeutics    June 1, 1990   Volume 13, Issue 2 179-185 doi: 10.1111/j.1365-2885.1990.tb00766.x
Firth EC, Nouws JF, Klein WR, Driessens F.A pilot study in two ponies showed that the plasma concentrations of intramuscularly administered procaine penicillin were higher if phenylbutazone was administered concurrently. In two other trials, each involving five horses, intravenous sodium penicillin was administered with and without concurrent intravenously injected phenylbutazone, and procaine penicillin was injected intramuscularly with and without oral phenylbutazone. In both cases the plasma concentrations of penicillin were higher when phenylbutazone was given. The pharmacokinetic parameters indicated that the effect was probably ...
The use of long-acting neuroleptics, perphenazine enanthate and pipothiazine palmitate in two horses.
Journal of the South African Veterinary Association    December 1, 1989   Volume 60, Issue 4 208-209 
McCrindle CM, Ebedes H, Swan GE.Two Arabian horse stallions with behavioural problems were treated with long-acting neuroleptics in order to facilitate corrective training. Perphenazine enanthate, administered intramuscularly at a dose of 0.5 mg kg-1 had an effect for 30 d. Pipothiazine palmitate (1 mg kg-1) induced tranquilization of 30 d duration as well as extra-pyramidal clinical signs, ataxia and aphagia. Neither horse showed prolapse of the penis or haemolysis.
Efficacy of ivermectin against experimental and natural infections of Gasterophilus spp in ponies.
American journal of veterinary research    December 1, 1989   Volume 50, Issue 12 2120-2123 
Bello TR.Antiparasitic efficacy of ivermectin against migrating Gasterophilus intestinalis was evaluated in 36 treated and 24 nontreated (n = 12) or vehicle-treated (n = 12) ponies experimentally and naturally infected with G intestinalis and naturally infected with G nasalis. Each pony was experimentally infected with 500 G intestinalis 1st instars in 2 divided doses on days -14 and -7 before treatment. On day 0, ivermectin was administered at the rate of 200 micrograms/kg of body weight by IV (n = 12) or IM injection (n = 12) or given as an oral paste (n = 12). Ponies were euthanatized and necropsied...
Effect of probenecid administration on cephapirin pharmacokinetics and concentrations in mares.
American journal of veterinary research    October 1, 1989   Volume 50, Issue 10 1742-1747 
Juzwiak JS, Brown MP, Gronwall R, Houston AE.Cephapirin (20 mg/kg of body weight, IV) was administered before and after 3 doses of probenecid (25, 50, or 75 mg/kg, intragastrically, at 12-hour intervals) to 2 mares. Clearance and apparent volume of distribution, based on area under the curve, were negatively correlated with probenecid dose. Clearance of cephapirin was decreased by approximately 50% by administration of 50 mg of probenecid/kg. Serum, synovial fluid, peritoneal fluid, CSF, urinary, and endometrial concentrations of cephapirin were determined after 5 doses of cephapirin (20 mg/kg, IM, at 12-hour intervals) without and with ...
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