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骆驼体内某些抗生素的药代动力学解释

Pharmacokinetic interpretation of some antibiotics in camels.

作者信息

El-Gendi A Y, El-Sayed M G, Atef M, Hussin A Z

出版信息

Arch Int Pharmacodyn Ther. 1983 Feb;261(2):186-95.

PMID:6838280
Abstract

Evaluation of the pharmacokinetic properties of 4 antibiotics: penicillin-G (P), streptomycin (S), chloramphenicol (C) and oxytetracycline (O) was performed in groups of camels following a single i.m. injection of therapeutic doses, i.e. 6000 IU, 10, 4 and 3 mg/kg b.wt., respectively. The concentrations of these antibiotics in serum were determined by microbiological assay methods. The highest serum concentrations were reached after 0.42, 1.44, 4.02 and 0.94 hr for P, S, C, and O respectively with corresponding t 1/2 alpha values of 0.12, 0.28, 1.48 and 0.17 hr and t 1/2 beta values of 1.09, 8.28, 6.20 and 7.00 hr.

摘要

在骆驼群体中,对4种抗生素:青霉素G(P)、链霉素(S)、氯霉素(C)和土霉素(O)进行了药代动力学特性评估。单次肌肉注射治疗剂量后,即分别为6000国际单位、10、4和3毫克/千克体重。通过微生物测定法测定这些抗生素在血清中的浓度。P、S、C和O分别在0.42、1.44、4.02和0.94小时后达到最高血清浓度,相应的t 1/2α值分别为0.12、0.28、1.48和0.17小时,t 1/2β值分别为1.09、8.28、6.20和7.00小时。

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