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日本鹌鹑单次静脉和口服给予噻苯咪唑后的药代动力学。

Pharmacokinetics of thiamphenicol in Japanese quails (Coturnix japonica) after single intravenous and oral administrations.

机构信息

Pharmacology Department, Faculty of Veterinary Medicine, Benha University, Toukh, Egypt.

Pharmacology Department, Faculty of Veterinary Medicine, Cairo University, Giza, Egypt.

出版信息

J Vet Pharmacol Ther. 2020 Sep;43(5):512-515. doi: 10.1111/jvp.12902. Epub 2020 Aug 10.

Abstract

Thiamphenicol (TP) pharmacokinetics were studied in Japanese quails (Coturnix japonica) following a single intravenous (IV) and oral (PO) administration at 30 mg/kg BW. Concentrations of TP were determined with HPLC and were analyzed by a noncompartmental method. After IV injection, elimination half-life (t ), total body clearance (Cl ) volume of distribution at steady state (V ), and mean residence time (MRT) of TP were 3.83 hr, 0.19 L/hr/kg, 0.84 L/kg, and 4.37 hr, respectively. After oral administration of TP, the peak plasma concentration (C ) was 19.81 μg/ml and was obtained at 2.00 hr (t ) postadministration. Elimination half-life (t ) and mean absorption time (MAT) were 4.01 hr and 1.56 hr, respectively. The systemic bioavailability following oral administration of TP was 78.10%. TP therapy with an oral dosage of 30 mg/kg BW is suggested for a beneficial clinical effect in quails.

摘要

研究了日本鹌鹑(Coturnix japonica)单次静脉(IV)和口服(PO)给予 30mg/kg BW 后噻苯青霉素(TP)的药代动力学。采用 HPLC 法测定 TP 浓度,并采用非房室法进行分析。静脉注射后,TP 的消除半衰期(t )、总清除率(Cl )、稳态分布容积(V )和平均驻留时间(MRT)分别为 3.83 小时、0.19 L/小时/公斤、0.84 L/公斤和 4.37 小时。口服 TP 后,血浆峰浓度(C )为 19.81μg/ml,给药后 2.00 小时(t )达到。消除半衰期(t )和平均吸收时间(MAT)分别为 4.01 小时和 1.56 小时。口服 TP 的全身生物利用度为 78.10%。建议日本鹌鹑口服 30mg/kg BW 的 TP 治疗剂量,以获得有益的临床效果。

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