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新型唑类化合物在眼部的渗透及对实验性念珠菌性眼内炎的疗效

Penetration of new azole compounds into the eye and efficacy in experimental Candida endophthalmitis.

作者信息

Savani D V, Perfect J R, Cobo L M, Durack D T

出版信息

Antimicrob Agents Chemother. 1987 Jan;31(1):6-10. doi: 10.1128/AAC.31.1.6.

Abstract

We studied the penetration of three azole compounds, ketoconazole, itraconazole, and fluconazole, into the ocular tissues and fluids of rabbits in the presence and absence of ocular inflammation. Drug concentrations were compared with those found in serum and cerebrospinal fluid. The rank order of penetration into eye tissue was fluconazole greater than ketoconazole greater than itraconazole. Fluconazole penetrated freely into both inflamed and uninflamed eyes. The presence of inflammation improved penetration of all three compounds into ocular fluids and tissues. Penetration of these azoles into the anterior chamber of uninflamed eyes and into the cerebrospinal fluid was similar. All three azole compounds reduced the number of yeasts found in the eye in hematogenous Candida albicans endophthalmitis in rabbits when therapy was initiated within 24 h of inoculation. However, only ketoconazole significantly reduced yeast counts in the eye when therapy was postponed for 7 days.

摘要

我们研究了三种唑类化合物——酮康唑、伊曲康唑和氟康唑,在有和没有眼部炎症的情况下,在兔眼组织和眼内液中的渗透情况。将药物浓度与血清和脑脊液中的浓度进行了比较。眼组织渗透的排序为氟康唑大于酮康唑大于伊曲康唑。氟康唑可自由渗透到炎症和非炎症眼中。炎症的存在提高了所有三种化合物在眼内液和组织中的渗透。这些唑类化合物在非炎症眼的前房和脑脊液中的渗透情况相似。当在接种后24小时内开始治疗时,所有三种唑类化合物都减少了兔血源性白色念珠菌眼内炎眼中发现的酵母菌数量。然而,当治疗推迟7天时,只有酮康唑显著减少了眼中的酵母菌数量。

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