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决定散瞳药物对人体药效的因素。

Factors determining the potency of mydriatic drugs in man.

作者信息

Smith S A

出版信息

Br J Clin Pharmacol. 1976 Jun;3(3):503-7. doi: 10.1111/j.1365-2125.1976.tb00628.x.

Abstract

1 The mydriasis resulting from topical application of five atropine-like drugs was measured photographically in man. Drug potency was obtained from log dose-response curves. 2 The in vitro potency of eight cholinoceptor blocking drugs, including those studied in man, was obtained by measuring their affinity constants for binding to the receptors of an isolated preparation of the rabbit sphincter pupillae. Values agreed closely with those obtained for the muscarinic receptors of guinea-pig ileum. 3 In vitro and in vivo potency was compared to obtain a quantitative measure of the relative ease with which drugs gain access to the receptors after topical application. 4 The large differences that occur in the intensity and duration of the mydriatic response to atropine-like drugs is primarily the result of differences in their ability to blcok the receptors. Only with tropicamide does its relatively high accessibility affect its potency in man.

摘要
  1. 通过摄影测量了人体局部应用五种阿托品样药物引起的瞳孔散大情况。药物效价由对数剂量-反应曲线得出。2. 包括在人体中研究的药物在内的八种胆碱受体阻断药物的体外效价,是通过测量它们与兔瞳孔括约肌分离制剂受体结合的亲和常数获得的。这些值与豚鼠回肠毒蕈碱受体的值非常接近。3. 比较了体外和体内效价,以定量衡量局部应用后药物进入受体的相对难易程度。4. 对阿托品样药物瞳孔散大反应的强度和持续时间出现的巨大差异,主要是由于它们阻断受体能力的差异。只有托吡卡胺因其相对较高的可及性影响其在人体中的效价。

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Factors determining the potency of mydriatic drugs in man.决定散瞳药物对人体药效的因素。
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本文引用的文献

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Proc Natl Acad Sci U S A. 1967 Feb;57(2):335-41. doi: 10.1073/pnas.57.2.335.
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Mydriatic effect of four drugs determined with pupillograph.
Arch Ophthalmol. 1967 Jun;77(6):740-6. doi: 10.1001/archopht.1967.00980020742005.
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