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正常实验猫经皮给予昂丹司琼的吸收评估。

Assessment of absorption of transdermal ondansetron in normal research cats.

作者信息

Zajic Lara B, Herndon Andrea K, Sieberg Liberty G, Caress Amber L, Morgan Paula K, Hansen Ryan J, Wittenburg Luke A, Gustafson Daniel L, Quimby Jessica M

机构信息

Department of Clinical Sciences, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Fort Collins, CO, USA.

出版信息

J Feline Med Surg. 2017 Dec;19(12):1245-1248. doi: 10.1177/1098612X16688807. Epub 2017 Jan 23.

Abstract

Objectives The objective of this study was to assess the absorption of transdermal ondansetron in healthy cats. Methods Five research cats with unremarkable complete blood count, biochemistry and urinalysis were used for both single- and multiple-dose application studies. For single-dose application, 4 mg ondansetron in 0.1 ml Lipoderm gel was applied once to the internal ear pinna. Blood samples were collected via jugular catheter over a 48 h period following administration (0, 15 mins, 30 mins, 1 h, 2 h, 4 h, 8 h, 12 h, 24 h and 48 h). For multiple-dose application, 4 mg ondansetron in 0.1 ml Lipoderm gel was applied for five consecutive days before blood samples were obtained in the same manner. Serum was separated and frozen prior to analysis. Ondansetron was measured via liquid chromatography coupled to tandem mass spectrometry. Results Analysis revealed no clinically relevant drug levels in serum after either single- or multiple-dose administration of 4 mg transdermal ondansetron. Conclusions and relevance Transdermal application of 4 mg ondansetron does not result in clinically relevant serum concentrations of drug. Despite characteristics of the drug that imply suitability for transdermal application, this does not appear to be an acceptable method of drug delivery for this medication at this dose. This study highlights the importance of assessing the suitability of each medication for transdermal administration.

摘要

目的 本研究的目的是评估透皮应用昂丹司琼在健康猫体内的吸收情况。方法 选用5只全血细胞计数、生化指标及尿液分析均无异常的研究用猫进行单剂量和多剂量应用研究。单剂量应用时,将含4 mg昂丹司琼的0.1 ml Lipoderm凝胶一次涂于耳廓内侧。给药后48小时内(0、15分钟、30分钟、1小时、2小时、4小时、8小时、12小时、24小时和48小时)通过颈静脉导管采集血样。多剂量应用时,在以相同方式采集血样前,连续5天应用含4 mg昂丹司琼的0.1 ml Lipoderm凝胶。血清在分析前分离并冷冻。通过液相色谱 - 串联质谱法测定昂丹司琼。结果 分析显示,单剂量或多剂量给予4 mg透皮昂丹司琼后,血清中均未出现具有临床意义的药物水平。结论及相关性 4 mg昂丹司琼透皮应用不会导致血清中出现具有临床意义的药物浓度。尽管该药物的特性表明其适合透皮应用,但在该剂量下,这似乎不是一种可接受的给药方式。本研究强调了评估每种药物透皮给药适用性的重要性。

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