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[维拉帕米口服缓释制剂在清醒犬体内的长期作用演示]

[Demonstration of the long term action of an oral retard preparation of verapamil in the conscious dog].

作者信息

Raschack M

出版信息

Arzneimittelforschung. 1975 Aug;25(8):1275-8.

PMID:1242358
Abstract
  1. In the conscious dog the duration of action of verapamil, usual galenic preparation (Isoptin, Cordilox), and of verapamil retard (Isoptin retard: verapamil mixed and pressed with the swelling agent sodium alginate) was tested by measuring the blood pressure decrease occurring with higher dosage. Furthermore lead II of the ECG was recorded. 2. Already 2 h after oral application of verapamil retard a significant action is observed. As had been expected verapamil retard shows a slightly protracted onset of action compared to verapamil. 3. At the end of the test period, 12 h after administration, the effect of verapamil retard is still significant. In equipotent dosage its duration of action is clearly superior to that of conventional verapamil dragées. 4. During the period of 2 h to 12 h the intensity of action of verapamil retard shows only slight variations; significant differences could not be detected. 5. Verapamil mixed and pressed with sodium alginate, used as swelling substance and food additive, is an adequate preparation which allows the oral administration of verapamil with very long duration and almost constant intensity of action.
摘要
  1. 在清醒犬中,通过测量较高剂量时出现的血压下降情况,对维拉帕米普通制剂(异搏定、合心爽)以及维拉帕米缓释制剂(缓释异搏定:维拉帕米与膨胀剂海藻酸钠混合压制而成)的作用持续时间进行了测试。此外,还记录了心电图的II导联。2. 口服维拉帕米缓释制剂2小时后就已观察到明显作用。正如预期的那样,与维拉帕米相比,维拉帕米缓释制剂的起效时间稍有延长。3. 在给药12小时后的试验期末,维拉帕米缓释制剂的作用仍然显著。在等效剂量下,其作用持续时间明显优于传统维拉帕米糖衣片。4. 在2小时至12小时期间,维拉帕米缓释制剂的作用强度仅有轻微变化;未检测到显著差异。5. 维拉帕米与用作膨胀物质和食品添加剂的海藻酸钠混合压制而成的制剂,是一种合适的制剂,它使得口服维拉帕米具有很长的作用持续时间和几乎恒定的作用强度。

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[Demonstration of the long term action of an oral retard preparation of verapamil in the conscious dog].[维拉帕米口服缓释制剂在清醒犬体内的长期作用演示]
Arzneimittelforschung. 1975 Aug;25(8):1275-8.
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