首页> 外文期刊>Journal of Veterinary Pharmacology and Therapeutics >Pharmacokinetics and pharmacodynamics of gamithromycin in pulmonary epithelial lining fluid in naturally occurring bovine respiratory disease in multisource commingled feedlot cattle
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Pharmacokinetics and pharmacodynamics of gamithromycin in pulmonary epithelial lining fluid in naturally occurring bovine respiratory disease in multisource commingled feedlot cattle

机译:加源霉素在多源混合饲养场牛自然发生的牛呼吸道疾病中肺上皮衬里液中的药代动力学和药效学

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The objectives of this study were to determine (i) whether an association exists between individual pharmacokinetic parameters and treatment outcome when feeder cattle were diagnosed with bovine respiratory disease (BRD) and treated with gamithromycin (Zactran((R))) at the label dose and (ii) whether there was a stronger association between treatment outcome and gamithromycin concentration in plasma or in the pulmonary epithelial lining fluid (PELF) effect compartment. The study design was a prospective, blinded, randomized clinical trial utilizing three groups of 60 (362-592lb) steers/bulls randomly allocated within origin to sham injection or gamithromycin mass medication. Cattle were evaluated daily for signs of BRD by a veterinarian blinded to treatment. Animals meeting the BRD case definition were enrolled and allocated to a sample collection scheme consisting of samples for bacterial isolation (bronchoalveolar lavage fluid and nasopharyngeal swabs) and gamithromycin concentration determination (PELF and plasma). Gamithromycin susceptibility of M.haemolytica (n=287) and P.multocida (n=257) were determined using broth microdilution with frozen panels containing gamithromycin at concentrations from 0.03 to 16g/mL. A two-compartment plasma pharmacokinetic model with an additional compartment for gamithromycin in PELF was developed using rich data sets from published and unpublished studies. The sparse data from our study were then fit to this model using nonlinear mixed effects modeling to estimate individual parameter values. The resulting parameter estimates were used to simulate full time-concentration profiles for each animal in this study. These profiles were analyzed using noncompartmental methods so that PK/PD indices (AUC(24)/MIC, AUC/MIC, C-MAX/MIC) could be calculated for plasma and PELF (also T>MIC) for each individual. The calculated PK/PD indices were indicative that for both M.haemolytica and P.multocida a higher drug exposure in terms of concentration, and duration of exposure relative to the MIC of the target pathogen, was favorable to a successful case outcome. Asignificant association was found between treatment success and PELF AUC(0-24)/MIC for P.multocida. The calves in this study demonstrated an increased clearance and volume of distribution in plasma as compared to the healthy calves in two previously published reports. Ultimately, the findings from this study indicate that higher PK/PD indices were predictive of positive treatment outcomes.
机译:这项研究的目的是确定(i)当饲喂牛被诊断出患有牛呼吸道疾病(BRD)并用标记剂量的阿霉素(Zactran(R))治疗时,个体药代动力学参数与治疗结果之间是否存在关联(ii)血浆或肺上皮内衬液(PELF)效应隔室中治疗结果与丙种霉素浓度之间是否存在更强的联系。该研究设计是一项前瞻性,盲法,随机临床试验,使用三组共60个(362-592lb)ers牛/公牛,在产地内随机分配给假注射或加霉素霉素大剂量药物。每天对不知情的兽医评估牛的BRD征象。招募符合BRD病例定义的动物,并将其分配到一个样品收集方案中,该方案包括用于细菌分离(支气管肺泡灌洗液和鼻咽拭子)和伽马霉素浓度测定(PELF和血浆)的样品。使用肉汤微稀释,用浓度为0.03至16g / mL的加米霉素的冷冻板,测定溶血支原体(n = 287)和多杀梭菌(n = 257)对加米霉素的敏感性。使用来自已发表和未发表研究的丰富数据集,开发了一个两室血浆药代动力学模型,并在PELF中添加了一个额外的丙种霉素室。然后,使用非线性混合效应模型来估计单个参数值,将来自我们研究的稀疏数据拟合到该模型。所得参数估计值用于模拟本研究中每只动物的完整时间浓度曲线。使用非房室方法分析这些分布图,以便可以计算每个人的血浆和PELF(以及T> MIC)的PK / PD指数(AUC(24)/ MIC,AUC / MIC,C-MAX / MIC)。计算得出的PK / PD指数表明,对于溶血支原体和腐烂支原体而言,相对于目标病原体的MIC而言,相对于目标病原体的MIC浓度和暴露持续时间而言,较高的药物暴露量是有利于成功病例的。发现治疗成功与多杀性疟原虫的PELF AUC(0-24)/ MIC之间存在显着关联。在两项先前发表的报告中,与健康牛犊相比,这项研究中的牛犊表现出血浆中的清除率和分布体积增加。最终,这项研究的结果表明较高的PK / PD指数可预示积极的治疗结果。

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