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Distribution of flunixin meglumine and firocoxib into aqueous humor of horses.

机译:氟尼辛葡甲胺和氟罗昔布在马房水中的分布。

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Background: Nonsteroidal anti-inflammatory drugs (NSAIDs) are commonly used systemically for the treatment of inflammatory ocular disease in horses. However, little information exists regarding the ocular penetration of this class of drugs in the horse. Objective: To determine the distribution of orally administered flunixin meglumine and firocoxib into the aqueous humor of horses. Animals: Fifteen healthy adult horses with no evidence of ophthalmic disease. Methods: Horses were randomly assigned to a control group and 2 treatment groups of equal sizes (n=5). Horses assigned to the treatment groups received an NSAID (flunixin meglumine, 1.1 mg/kg PO q24h or firocoxib, 0.1 mg/kg PO q24h for 7 days). Horses in the control group received no medications. Concentrations of flunixin meglumine and firocoxib in serum and aqueous humor and prostaglandin (PG) E2 in aqueous humor were determined on days 1, 3, and 5 and aqueous:serum ratios were calculated. Results: Firocoxib penetrated the aqueous humor to a significantly greater extent than did flunixin meglumine at days 3 and 5. Aqueous:serum ratios were 3.59+or-3.32 and 11.99+or-4.62% for flunixin meglumine and firocoxib, respectively. Ocular PGE2 concentrations showed no differences at any time point among study groups. Conclusions and Clinical Importance: Both flunixin meglumine and firocoxib penetrated into the aqueous humor of horses. This study suggests that orally administered firocoxib penetrates the aqueous humor better than orally administered flunixin meglumine at label dosages in the absence of ocular inflammation. Firocoxib should be considered for the treatment of inflammatory ophthalmic lesions in horses at risk for the development of adverse effects associated with nonselective NSAID administration.
机译:背景:非甾体类抗炎药(NSAIDs)通常系统地用于治疗马匹的炎性眼病。但是,关于这类药物在马眼中的渗透的信息很少。目的:确定口服氟尼辛葡甲胺和氟罗昔布在马房水中的分布。动物:15只健康的成年马,没有眼科疾病的迹象。方法:将马随机分为对照组和2个相同大小的治疗组(n = 5)。分配至治疗组的马接受NSAID(氟尼辛葡甲胺,1.1 mg / kg PO q24h或氟洛昔布,0.1 mg / kg PO q24h连续7天)。对照组中的马没有接受药物治疗。在第1、3和5天测定血清和房水中的氟尼辛葡甲胺和氟罗昔布的浓度以及房水中前列腺素(PG)E 2 的浓度,并计算房水与血清的比例。结果:在第3天和第5天,Firocoxib穿透房水的程度明显大于氟尼辛葡甲胺。氟尼辛葡甲胺和氟罗昔布的水:血清比率分别为3.59+或-3.32和11.99+或-4.62%。研究组之间在任何时间点的眼内PGE 2 浓度均无差异。结论和临床意义:氟尼辛葡甲胺和氟罗昔布均渗入马房水。这项研究表明,在没有眼部炎症的情况下,口服给予的费洛昔布的口服剂量比氟尼辛葡甲胺的口服剂量更好。应考虑将非诺昔布用于治疗患有非选择性NSAID给药相关​​不良反应风险的马匹中的炎性眼科病变。

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