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替地珠单抗在奶山羊静脉内、肌内和皮下给药后在血浆、乳汁和体细胞中的药代动力学

Pharmacokinetics of Tildipirosin in Plasma, Milk, and Somatic Cells Following Intravenous, Intramuscular, and Subcutaneous Administration in Dairy Goats.

作者信息

Galecio Juan Sebastián, Marín Pedro, Hernandis Verónica, Botía María, Escudero Elisa

机构信息

Department of Pharmacology, Faculty of Veterinary Medicine, University of Murcia, 30100 Murcia, Spain.

Escuela de Medicina Veterinaria, Colegio de Ciencias de la Salud, Universidad San Francisco de Quito USFQ, Diego de Robles s/n y Vía Interoceánica, Quito 170901, Ecuador.

出版信息

Pharmaceutics. 2022 Apr 13;14(4):860. doi: 10.3390/pharmaceutics14040860.

Abstract

Tildipirosin is a macrolide currently authorized for treating respiratory diseases in cattle and swine. The disposition kinetics of tildipirosin in plasma, milk, and somatic cells were investigated in dairy goats. Tildipirosin was administered at a single dose of 2 mg/kg by intravenous (IV) and 4 mg/kg by intramuscular (IM) and subcutaneous (SC) routes. Concentrations of tildipirosin were determined by an HPLC method with UV detection. Pharmacokinetic parameters were estimated by non-compartmental analysis. Muscle damage, cardiotoxicity, and inflammation were evaluated. After IV administration, the apparent volume of distribution in the steady state was 7.2 L/kg and clearance 0.64 L/h/kg. Plasma and milk half-lives were 6.2 and 58.3 h, respectively, indicating nine times longer persistence of tildipirosin in milk than in plasma. Moreover, if somatic cells are considered, persistence and exposure measured by the area under concentration-time curve (AUC) significantly exceeded those obtained in plasma. Similarly, longer half-lives in whole milk and somatic cells compared to plasma were observed after IM and SC administration. No adverse effects were observed. In brief, tildipirosin should be reserved for cases where other suitable antibiotics have been unsuccessful, discarding milk production of treated animals for at least 45 days or treating goats at the dry-off period.

摘要

替地珠单抗是一种大环内酯类药物,目前已被批准用于治疗牛和猪的呼吸道疾病。研究了替地珠单抗在奶山羊血浆、乳汁和体细胞中的处置动力学。通过静脉注射(IV)以2 mg/kg的单剂量以及通过肌肉注射(IM)和皮下注射(SC)以4 mg/kg的单剂量给药替地珠单抗。采用带紫外检测的高效液相色谱法测定替地珠单抗的浓度。通过非房室分析估算药代动力学参数。评估了肌肉损伤、心脏毒性和炎症。静脉注射后,稳态下的表观分布容积为7.2 L/kg,清除率为0.64 L/h/kg。血浆和乳汁半衰期分别为6.2小时和58.3小时,表明替地珠单抗在乳汁中的持续时间比在血浆中长9倍。此外,如果考虑体细胞,通过浓度-时间曲线下面积(AUC)测量的持续时间和暴露量显著超过血浆中的值。同样,肌肉注射和皮下注射后,全脂牛奶和体细胞中的半衰期也比血浆中的长。未观察到不良反应。简而言之,替地珠单抗应仅用于其他合适抗生素治疗无效的情况,治疗动物的产奶量应弃用至少45天,或在干奶期对山羊进行治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a4c/9031826/548c8ccb07f0/pharmaceutics-14-00860-g001.jpg

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