Bailey C Scott, Beachler Theresa M, Mochel Jonathan P, Wulf Larry W, Yaeger Michael, Kundu Debosmita, Withowski Kate, Papich Mark G
Department of Clinical Sciences, College of Veterinary Medicine, North Carolina State University, Raleigh, North Carolina, USA.
Department of Veterinary Diagnostic and Production Animal Medicine, College of Veterinary Medicine, Iowa State University, Ames, Iowa, USA.
J Vet Pharmacol Ther. 2025 Sep;48(5):389-396. doi: 10.1111/jvp.13518. Epub 2025 May 14.
Despite their widespread clinical use, there is limited pharmacokinetic data for many equine intrauterine antimicrobials. This study aimed to measure the concentration of gentamicin and penicillin in the uterine fluid of mares following infusion of either a standard (PPGent) or long-acting (LA-PPGent) compounded formulation. We hypothesized that both formulations would result in therapeutic concentrations, with total concentrations sustained for longer using the long-acting formulation. Mares were administered 2400 mg of procaine penicillin and 200 mg of gentamicin via a single intrauterine infusion in either a standard (n = 6) or a lyophilized formulation suspended in a slow-release matrix (n = 6). Intrauterine fluid was collected over a 72-h period and analyzed for antibiotic concentrations using high-performance liquid chromatography and ultra-high-performance liquid chromatography and tandem mass spectrometry. Mean maximal concentrations were seen at 0.5 h in group PPGent (Penicillin: 10,123.0 ± 4298.0 μg/mL, Gentamicin: 3397.3 ± 1338.5 μg/mL) and exceeded MIC for relevant organisms for 72 h (Penicillin: 2.59 ± 6.34 μg/mL, Gentamicin: 2.14 ± 2.4 μg/mL). Interestingly, maximal concentrations were lower in group LA-PPG (Penicillin: 2213.8 ± 967.8 μg/mL-p < 0.05, Gentamicin: 1859 ± 2413 μg/mL) and exceeded MIC for a shorter period of time than the unmodified mixture of commonly used FDA-approved antibiotics.
尽管马用子宫内抗菌药物在临床上广泛使用,但许多此类药物的药代动力学数据有限。本研究旨在测量母马在输注标准(PPGent)或长效(LA-PPGent)复合制剂后子宫液中庆大霉素和青霉素的浓度。我们假设两种制剂都能产生治疗浓度,且长效制剂能使总浓度维持更长时间。通过单次子宫内输注,给母马分别施用2400毫克普鲁卡因青霉素和200毫克庆大霉素,分为标准制剂组(n = 6)或悬浮于缓释基质中的冻干制剂组(n = 6)。在72小时内收集子宫液,并使用高效液相色谱法、超高效液相色谱法和串联质谱法分析抗生素浓度。PPGent组在0.5小时时出现平均最大浓度(青霉素:10123.0±4298.0μg/mL,庆大霉素:3397.3±1338.5μg/mL),且相关微生物的最低抑菌浓度在72小时内均被超过(青霉素:2.59±6.34μg/mL,庆大霉素:2.14±2.4μg/mL)。有趣的是,LA-PPG组的最大浓度较低(青霉素:2213.8±967.8μg/mL - p<0.05,庆大霉素:1859±2413μg/mL),且超过最低抑菌浓度的时间比常用的FDA批准抗生素的未改良混合物短。