盐酸达吡拉唑角膜内皮毒性研究。

Lens and eye toxicity research Pub Date : 1992-01-01
L Cheeks, J M Chapman, K Green
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引用次数: 0

摘要

研究了一种新的肾上腺素能拮抗剂对兔离体角膜内皮的直接毒性作用。在镜面显微镜下,以1.25 ~ 1000微克/毫升的浓度灌注盐酸达吡拉唑。在3小时的灌注期间,通过角膜厚度测定,没有观察到毒性,直到浓度大于125微克/毫升。250微克/毫升时溶胀率为17.8微米/小时,500微克/毫升时溶胀率为17.1微米/小时;1000微克/毫升诱导溶胀率为23.3微米/小时。很明显,外用后到达内皮的药物浓度对角膜没有毒性作用,药物只能在指导下使用,而不能用作前房灌注剂。
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Corneal endothelial toxicity of dapiprazole hydrochloride.

A new adrenergic antagonist designed for topical use to induce pupillary miosis has been tested for direct toxicity on isolated rabbit corneal endothelium. Dapiprazole hydrochloride was perfused across endothelia in the specular microscope at concentrations from 1.25 micrograms/ml to 1000 micrograms/ml. No toxicity was observed, as determined by corneal thickness determinations over a 3 hour perfusion period, until concentrations greater than 125 micrograms/ml were reached. At 250 micrograms/ml a swelling rate of 17.8 microns/hour occurred, and at 500 micrograms/ml the swelling rate was 17.1 microns/hour; with 1000 micrograms/ml inducing a swelling rate of 23.3 microns/hour. It is evident that the drug concentration that reaches the endothelium after topical application has no toxic effect on the cornea, and that the drug should only be used as directed and not used as an anterior chamber perfusate.

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