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Safety of Intravitreal Ketorolac and Diclofenac: An Electroretinographic and Histopathologic Study.

机译:玻璃体内酮咯酸和双氯芬酸的安全性:视网膜电图和组织病理学研究。

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OBJECTIVE:: To determine the clinical, histologic, and electroretinographic effects in the rabbit retina of escalating doses of two intravitreally delivered nonsteroidal anti-inflammatory drugs (NSAIDs): ketorolac and diclofenac. METHODS:: Right eyes received a single 0.1 mL injection of either ketorolac (500-6000 mug/0.1 mL) or diclofenac (300-1500 mug/0.1 mL) prepared in balanced salt solution (BSS). Left eyes served as controls and received BSS. Dark- and light-adapted electroretinograms (ERG) were obtained at baseline and 4 and 8 weeks postinjection. Enucleated eyes were examined histologically. RESULTS:: Ophthalmic examinations demonstrated no signs of intraocular inflammation or retinal toxicity. Intraocular pressure measurements remained similar between NSAID injected and control eyes. Histologic and ERG studies of eyes injected with 6000 mug ketorolac and >/=500 mug diclofenac demonstrated toxicity. In contrast, doses up to 3000 mug ketorolac demonstrated enhanced b-wave amplitude responses. Delayed drug toxicity was observed for the highest doses of both NSAIDs. CONCLUSIONS:: Intravitreal 3000 mug ketorolac and 300 mug diclofenac were nontoxic in this animal study, and may offer an effective and safer alternative to intravitreal corticosteroids.
机译:目的:为了确定逐步增加剂量的两种玻璃体内非甾体抗炎药(酮咯酸和双氯芬酸)对兔子视网膜的临床,组织学和视网膜电图影响。方法:右眼在平衡盐溶液(BSS)中制备单次0.1 mL注射的酮咯酸(500-6000杯/0.1 mL)或双氯芬酸(300-1500杯/0.1 mL)。左眼作为对照并接受BSS。在基线,注射后4周和8周获得暗适应和亮适应的视网膜电图(ERG)。有组织的眼睛进行了组织学检查。结果:眼科检查显示没有眼内炎症或视网膜毒性的迹象。 NSAID注射和对照眼之间的眼压测量值仍然相似。注射6000马克酮酮和> / = 500马克双氯芬酸的眼睛的组织学和ERG研究显示毒性。相反,剂量高达3000杯的酮咯酸显示出增强的b波振幅响应。对于两种NSAID的最高剂量,观察到延迟的药物毒性。结论:玻璃体内3000杯酮咯酸和300杯双氯芬酸在该动物研究中无毒,可能为玻璃体内皮质类固醇提供一种有效且安全的替代方法。

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