硫酸镁与阿司匹林、扑热息痛、萘普生配合物镇痛活性的研究

S. Kundu, Md. Zakir Sultan, Asma Rahman, S. Paul, S. Shikder, Shampa Kundu, Md. Shah Amran, Md. Amjad Hossain
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引用次数: 3

摘要

药物分子与其他药物和各种金属离子的相互作用和络合作用的研究是化学、生化、医学和药理学的一个重要研究领域。药物-金属配合物的生物作用可能通过改变药代动力学和药效学性质来影响药物的稳定性和常规活性。采用小鼠醋酸扭体实验评价其镇痛作用。在本实验中,阿司匹林与硫酸镁的剂量分别为300mg、600mg和1.5 g/ 60kg体重,扑热息痛与硫酸镁的剂量分别为500mg、1g和2.5 g/ 60kg体重,萘普生与硫酸镁的剂量分别为500mg、1g和2.5 g/ 60kg体重,比例分别为1:1、1:2和2:1。观察到不同配比的硫酸镁对阿司匹林、扑热息痛和萘普生复合药物扭体试验的抑制率均小于主药,即镇痛活性均低于主药。结果表明,硫酸镁在与阿司匹林、扑热息痛和萘普生以不同比例配伍时均能抑制主药的镇痛活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Study of Analgesic Activity of Complexes of Magnesium Sulfate with Aspirin, Paracetamol and Naproxen
The study on interaction and complexation of drug molecules with other drugs and various metal ions is an important field of research in the chemical, biochemical, medicinal and pharmacological point of views. The biological action of the drug-metal complexes may affect stability and usual activities of drugs through changing pharmacokinetic and pharmacodynamic properties. The analgesic activity was evaluated by acetic acid induced writhing test in mice. In this experiment, aspirin with magnesium sulfate at the dose of 300 mg, 600 mg and 1.5 g/60 kg body weight, Paracetamol with magnesium sulfate at the dose of 500 mg, at the dose of 1 g and of 2.5 g /60 kg body weight and Naproxen with magnesium sulfate at the dose of 500 mg, at the dose of 1 g and at the dose of 2.5 g/60 kg body weight at a ratio of 1:1, 1:2 and 2:1. It was observed that % inhibition of writhing test of all complex drug of aspirin, paracetamol and naproxen with magnesium sulfate at different ratio were less than the main drug i.e. analgesic activity were lower than the main drug. It is concluded that magnesium sulfate while formed complex as well as mixed with aspirin, paracetamol and naproxen at different ratio suppress the analgesic activity of main drug.
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