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Electrochemical Methodology for NSAID's Determination and its Interaction with Steroid Dexamethasone

机译:NSAID的电化学方法及其与类固醇地塞米松的相互作用

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The new generations of Non-Steroidal Anti-inflammatory Drugs (NSAIDS) are COX-2 selectivecyclooxygenase-2 inhibitors (analgesic and anti-inflammatory) capable to cause adverse gastrointestinalevents due to drug interactions between one or more co-administered medicines. This causes alterationof the efficacy or toxicity of the co-administered drug. This study presents an electrochemical method(CV) evaluation to study the interactions of Naproxen Sodium and Piroxicam with Dexamethasone(Steroid) under optimized conditions. The proposed method is electrochemically diffusion controlled asboth drugs showed different diffusion coefficients (Piroxicam: 2.188×10 -7 ; Naproxen Sodium:3.755×10 -5 ). The method has good reproducibility and validated according to ICH guide lines (R 2 =0.9994 for Naproxen Sodium and 0.9991 for Piroxicam). The interactions were confirmed by the FTIRstudies indicated the variation of wave number and intensity of significant peaks thereby revealedpossible interaction sites.
机译:新一代的非甾体抗炎药(NSAIDS)是COX-2选择性环氧化酶2抑制剂(镇痛和抗炎药),由于一种或多种共同给药药物之间的药物相互作用,它们能够引起不良的胃肠道事件。这引起了共同给药药物的功效或毒性的改变。本研究提出了一种电化学方法(CV)评价,以研究萘普生钠和吡罗昔康与地塞米松(甾体)在最佳条件下的相互作用。所提出的方法是电化学扩散控制的,因为两种药物均显示出不同的扩散系数(吡罗昔康:2.188×10 -7;萘普生钠:3.755×10 -5)。该方法具有良好的重现性,并根据ICH指南进行了验证(萘普生钠的R 2 = 0.9994,吡罗昔康的0.9991)。 FTIR证实了相互作用,研究表明波数和重要峰强度的变化,从而揭示了可能的相互作用位点。

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