给母马服用的两种 Altrenogest 制剂的药代动力学。

IF 2.6 3区 医学 Q2 BIOCHEMICAL RESEARCH METHODS Drug Testing and Analysis Pub Date : 2024-09-22 DOI:10.1002/dta.3796
Jaymie Loy, Adam Cawley, Kireesan Sornalingam, Colin J Scrivener, John Keledjian, Glenys K Noble
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引用次数: 0

摘要

Altrenogest 是一种合成孕激素,可抑制雌马的生殖行为并帮助维持妊娠。目前有两种配方,一种是 "每周 "肌肉注射配方,另一种是每日口服配方。使用阿孕酮后,类固醇拭子检测结果呈阳性;因此,禁止在赛马中使用注射用阿孕酮。如果在给药和比赛之间有一个晴朗的日子,则允许赛马母马口服给药。目前仅有的药代动力学数据来自骟马。因此,为了帮助兽医和分析人员确定准确的剂量和检测时间间隔,需要使用母马进行药代动力学分析。我们从 10 头母马身上采集了预处理血液样本,以获得基线浓度。给母马口服(PO;0.044 mg/kg;每天,共 15 天)或肌肉注射(IM;0.3 mg/kg;两次;第 0 天和第 7 天)阿替孕酮。在第一个和最后一个治疗日,在用药后的指定时间采集血液样本。经过 3 周的冲洗后,母马接受另一种治疗,并重复采样。初始给药时,IM 给药的平均(± SD)血浆阿替孕酮 Cmax 为 18.0 ± 6.6 纳克/毫升(7.9 ± 3.9 小时),而 PO 给药的平均(± SD)血浆 Cmax 为 13.2 ± 5.8 纳克/毫升(0.8 ± 0.8 小时)。在最后一次口服治疗后 24 小时,阿替诺孕酮的平均(± SD)血浆浓度为 1.0 ± 0.8 纳克/毫升,48 小时为 0.65 ± 0.5 纳克/毫升。血浆浓度远高于此值可能表明没有遵守 "一天一清 "的规定或剂量建议。
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Pharmacokinetics of Two Formulations of Altrenogest Administered to Mares.

Altrenogest is a synthetic progestin that suppresses reproductive behaviours and assists pregnancy maintenance in female horses. Two formulations are available, a 'weekly' intramuscular injection and a daily oral formulation. Altrenogest administration has returned positive swabs for steroids; consequently, using injectable altrenogest in racing mares is prohibited. Oral administration may be permitted in race mares if there is one clear day between dosing and racing. The only pharmacokinetic data available were generated from geldings. Therefore, to assist veterinarians and analysts in determining accurate dosing and detection intervals, pharmacokinetic analysis using mares is required. Blood samples were taken from 10 mares pretreatment to obtain baseline concentrations. Mares were administered altrenogest, either oral (PO; 0.044 mg/kg; daily for 15 days) or intramuscular (IM; 0.3 mg/kg; twice; Days 0 and 7). On the first and last treatment day, blood samples were taken at designated times post dosing. After a 3-week washout, mares received the alternative treatment with sampling repeated. At the initial dose, for IM administration mean (± SD) plasma altrenogest Cmax was 18.0 ± 6.6 ng/mL at 7.9 ± 3.9 h compared with PO dosing 13.2 ± 5.8 ng/mL at 0.8 ± 0.8 h. Plasma Cmax on the final day was significantly higher (p = 0.002 [IM]; p = 0.006 [PO]). At 24 h post final oral treatment, mean (± SD) plasma altrenogest was 1.0 ± 0.8 ng/mL and at 48 h were 0.65 ± 0.5 ng/mL. Plasma concentrations well exceeding this may indicate that the one clear day rule or dosage recommendations have not been adhered to.

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来源期刊
Drug Testing and Analysis
Drug Testing and Analysis BIOCHEMICAL RESEARCH METHODS-CHEMISTRY, ANALYTICAL
CiteScore
5.90
自引率
24.10%
发文量
191
审稿时长
2.3 months
期刊介绍: As the incidence of drugs escalates in 21st century living, their detection and analysis have become increasingly important. Sport, the workplace, crime investigation, homeland security, the pharmaceutical industry and the environment are just some of the high profile arenas in which analytical testing has provided an important investigative tool for uncovering the presence of extraneous substances. In addition to the usual publishing fare of primary research articles, case reports and letters, Drug Testing and Analysis offers a unique combination of; ‘How to’ material such as ‘Tutorials’ and ‘Reviews’, Speculative pieces (‘Commentaries’ and ‘Perspectives'', providing a broader scientific and social context to the aspects of analytical testing), ‘Annual banned substance reviews’ (delivering a critical evaluation of the methods used in the characterization of established and newly outlawed compounds). Rather than focus on the application of a single technique, Drug Testing and Analysis employs a unique multidisciplinary approach to the field of controversial compound determination. Papers discussing chromatography, mass spectrometry, immunological approaches, 1D/2D gel electrophoresis, to name just a few select methods, are welcomed where their application is related to any of the six key topics listed below.
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