单次宫内输注后未怀孕母马子宫液中青霉素和庆大霉素的浓度。

IF 1.5 4区 农林科学 Q3 PHARMACOLOGY & PHARMACY
C Scott Bailey, Theresa M Beachler, Jonathan P Mochel, Larry W Wulf, Michael Yaeger, Debosmita Kundu, Kate Withowski, Mark G Papich
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引用次数: 0

摘要

尽管临床上广泛使用,但许多马宫内抗菌剂的药代动力学数据有限。本研究的目的是测量庆大霉素和青霉素的浓度在母马子宫液后输注标准(PPGent)或长效(LA-PPGent)复方制剂。我们假设两种配方都会产生治疗浓度,使用长效配方总浓度持续时间更长。母马给予24000mg普鲁卡因青霉素和200mg庆大霉素单次宫内输注标准制剂(n = 6)或悬浮在缓释基质中的冻干制剂(n = 6)。采集72h的宫内液,采用高效液相色谱、超高效液相色谱和串联质谱分析抗生素浓度。PPGent组平均最高浓度出现在0.5 h(青霉素:10123.0±4298.0 μg/mL,庆大霉素:3397.3±1338.5 μg/mL),超过相关生物MIC 72 h(青霉素:2.59±6.34 μg/mL,庆大霉素:2.14±2.4 μg/mL)。有趣的是,LA-PPG组最大浓度较低(青霉素:2213.8±967.8 μg/mL-p)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Penicillin and Gentamicin Concentrations in the Uterine Fluid of Non-Pregnant Mares Following a Single Intrauterine Infusion.

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.

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来源期刊
CiteScore
3.10
自引率
15.40%
发文量
69
审稿时长
8-16 weeks
期刊介绍: The Journal of Veterinary Pharmacology and Therapeutics (JVPT) is an international journal devoted to the publication of scientific papers in the basic and clinical aspects of veterinary pharmacology and toxicology, whether the study is in vitro, in vivo, ex vivo or in silico. The Journal is a forum for recent scientific information and developments in the discipline of veterinary pharmacology, including toxicology and therapeutics. Studies that are entirely in vitro will not be considered within the scope of JVPT unless the study has direct relevance to the use of the drug (including toxicants and feed additives) in veterinary species, or that it can be clearly demonstrated that a similar outcome would be expected in vivo. These studies should consider approved or widely used veterinary drugs and/or drugs with broad applicability to veterinary species.
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