[The bioavailability of nifedipine in different solid pharmaceutical preparations for oral use].

S E Leucuta, L Vida-Simiti, A Mocan, E Făgărăşan, S Bugnariu, C Baloescu, N Olinic, R Vlaicu
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Abstract

The paper reports on the bioavailability of niphedipine in various pharmaceutic preparations administered in a single dose of 10 mg, per os, to volunteer subjects: Niphedipine dragees (Terapia, Cluj-Napoca), Adalat capsules (Bayer); Adalat coated tablets (Bayer and Birlaşik Alman Ilac Fabricalari, Istanbul) and Corinfar dragées (VEB Arzneimittelwerk, Dresden). In the blood samples collected, niphedipine was determined by a gas-chromatographic procedure. Pharmacokinetic analysis of the experimental data was made by a digital computer. Bioavailability of niphedipine was the best with Adalat capsules. The relative bioavailability of the other products was: tablets (Adalat); 93%; dragées (Niphedipine): 92%; dragées (Corinfar 86%). Absorption speed of Niphedipine decreases in the order: capsules, tablets, indigenous and imported dragées. Statistical analysis (Student test) shows that the differences in bioavailability among the preparations are not important. Efficiently therapeutic plasmatic concentrations are maintained for about 6 hours after a single dose of 10 mg administered as tablets and dragées and for 8 hours in the case of capsules. Important differences exist between the maximum concentration of niphedipine in blood, following some differences in the absorption speed, achieved after administration of capsules, on the one hand, and of tablets and dragées on the other hand. Choosing the type of tablet depends, therefore, on the nature of the affection treated. Niphedipine (Terapia) has corresponding biopharmaceutic properties and is useful in treating hypertension and for preventing and treating anginal attacks.

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硝苯地平在不同口服固体制剂中的生物利用度。
这篇论文报告了尼苯地平在各种药物制剂中的生物利用度,这些药物制剂以10mg / s的单剂量给药给志愿者:尼苯地平软糖(Terapia, Cluj-Napoca)、阿达拉胶囊(拜耳);Adalat包衣片剂(拜耳和birla Alman Ilac Fabricalari,伊斯坦布尔)和Corinfar dragsames (VEB arzneimittelworkk,德累斯顿)。在采集的血液样本中,尼苯地平采用气相色谱法测定。用数字计算机对实验数据进行药代动力学分析。阿达拉胶囊对尼苯地平的生物利用度最高。其他产品的相对生物利用度为:片剂(阿达拉特);93%;格拉西姆斯(尼苯地平):92%;(Corinfar 86%)。尼苯地平的吸收速度依次为胶囊、片剂、国产和进口药。统计分析(学生测试)表明,制剂之间的生物利用度差异并不重要。在以片剂和缓释片形式给予单剂量10mg后,有效地维持治疗性血浆浓度约6小时,在胶囊情况下维持8小时。服用胶囊和片剂和缓释片后,血液中尼苯地平的最大浓度存在重要差异,这是因为吸收速度有所不同。因此,选择何种类型的片剂取决于所治疗的情感的性质。尼苯地平(Terapia)具有相应的生物制药特性,可用于治疗高血压和预防和治疗心绞痛发作。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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