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非洲灰鹦鹉单次和多次口服氟康唑后的药代动力学

Pharmacokinetics of fluconazole after oral administration of single and multiple doses in African grey parrots.

作者信息

Flammer Keven, Papich Mark

机构信息

Department of Clinical Sciences, College of Veterinary Medicine, North Carolina State University, Raleigh, 27606, USA.

出版信息

Am J Vet Res. 2006 Mar;67(3):417-22. doi: 10.2460/ajvr.67.3.417.

Abstract

OBJECTIVE

To determine the pharmacokinetics and effects of orally administered fluconazole in African grey parrots.

ANIMALS

40 clinically normal Timneh African grey parrots (Psittacus erithacus timneh).

PROCEDURE

In single-dose trials, parrots were placed into groups of 4 to 5 birds each and fluconazole was administered orally at 10 and 20 mg/kg. Blood samples for determination of plasma fluconazole concentrations were collected from each group at 2 or 3 of the following time points: 1, 3, 6, 9, 12, 24, 31, 48, and 72 hours. In multiple-dose trials, fluconazole was administered orally to groups of 5 birds each at doses of 10 and 20 mg/kg every 48 hours for 12 days. Trough plasma concentrations were measured 3 times during treatment. Groups receiving 20 mg/kg were monitored for changes in plasma biochemical analytes, and blood samples were collected on days 1 and 13 of treatment to allow comparison of terminal half-life.

RESULTS

Peak plasma concentrations of fluconazole were 7.45 and 18.59 microg/mL, and elimination half-lives were 9.22 and 10.19 hours for oral administration of 10 and 20 mg/kg, respectively. Oral administration of fluconazole for 12 days at 10 or 20 mg/kg every 48 hours did not cause identifiable adverse effects or change the disposition of fluconazole.

CONCLUSIONS AND CLINICAL RELEVANCE

Oral administration of fluconazole to parrots at 10 to 20 mg/kg every 24 to 48 hours maintains plasma concentrations above the minimum inhibitory concentration for several common yeast species. The prolonged dosing interval is an advantage of this treatment regimen.

摘要

目的

确定口服氟康唑在非洲灰鹦鹉体内的药代动力学及效果。

动物

40只临床健康的提姆neh非洲灰鹦鹉(Psittacus erithacus timneh)。

程序

在单剂量试验中,将鹦鹉分成每组4至5只的小组,分别以10毫克/千克和20毫克/千克的剂量口服氟康唑。在以下时间点中的2个或3个时间点从每组采集血样以测定血浆氟康唑浓度:1、3、6、9、12、24、31、48和72小时。在多剂量试验中,每组5只鸟,每48小时口服10毫克/千克和20毫克/千克的氟康唑,持续12天。在治疗期间测量3次谷血浆浓度。对接受20毫克/千克剂量的组监测血浆生化分析物的变化,并在治疗的第1天和第13天采集血样以比较终末半衰期。

结果

口服10毫克/千克和20毫克/千克氟康唑时,血浆氟康唑峰值浓度分别为7.45和18.59微克/毫升,消除半衰期分别为9.22和10.19小时。每48小时口服10毫克/千克或20毫克/千克氟康唑12天未引起可识别的不良反应,也未改变氟康唑的处置。

结论及临床意义

每24至48小时以10至20毫克/千克的剂量给鹦鹉口服氟康唑可使血浆浓度维持在高于几种常见酵母菌种的最低抑菌浓度水平。延长给药间隔是该治疗方案的一个优点。

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