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局部治疗单纯疱疹病毒感染的疗效:基于体外药物特性指数的预测

Efficacy of topical treatment for herpes simplex virus infections: predictions from an index of drug characteristics in vitro.

作者信息

Freeman D J, Spruance S L

出版信息

J Infect Dis. 1986 Jan;153(1):64-70. doi: 10.1093/infdis/153.1.64.

Abstract

Topical antiviral treatments for recurrent infection with herpes simplex virus in immunocompetent patients have been generally ineffective. We investigated whether in vitro drug measures could predict in vivo efficacy. Twelve topical antiviral formulations were evaluated in vitro by measuring inhibition of viral plaque formation in cell culture (ID50) and drug penetration through excised guinea pig skin. In vivo efficacy for each treatment was determined in an experimental cutaneous infection with herpes simplex virus type 1 in guinea pigs and expressed as the percent reduction in lesion number, lesion area, and virus titer in the lesions. The in vitro findings were correlated with the results in the animal model. ID50 was a poor predictor of in vivo efficacy, whereas stronger correlations were found between the degree of skin penetration and in vivo activity. The best correlation was noted by using a summary expression of the in vitro results as follows: the ratio of drug penetration through skin at 37 C to ID50 (r = .95, .94, and .92 for lesion number, area, and virus titer, respectively, P less than .0005). Determination of this in vitro index should be included in the preclinical evaluation of new topical antiviral formulations.

摘要

对于免疫功能正常的复发性单纯疱疹病毒感染患者,局部抗病毒治疗通常无效。我们研究了体外药物检测指标能否预测体内疗效。通过测量细胞培养中病毒蚀斑形成的抑制作用(半数抑制浓度,ID50)以及药物透过切除的豚鼠皮肤的渗透情况,对12种局部抗病毒制剂进行了体外评估。在豚鼠1型单纯疱疹病毒实验性皮肤感染中确定了每种治疗的体内疗效,并表示为病变数量、病变面积和病变中病毒滴度的减少百分比。将体外研究结果与动物模型中的结果进行了相关性分析。ID50对体内疗效的预测能力较差,而皮肤渗透程度与体内活性之间的相关性更强。通过使用体外结果的汇总表达式得出了最佳相关性:37℃时药物透过皮肤的渗透率与ID50的比值(病变数量、面积和病毒滴度的r值分别为0.95、0.94和0.92,P<0.0005)。新的局部抗病毒制剂的临床前评估应包括该体外指标的测定。

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