Formulation and Evaluation of Aspirin Nanosuspension Using Probe Sonication Method

A. Krishna Sailaja
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Abstract

Aspirin inhibit the activity of the enzyme now called cyclooxygenase (COX) which leads to the formation of prostaglandins (PGs) that cause inflammation, swelling, pain and fever. Aspirin having various function like anti-inflammatory, analgesic, antipyretic etc. Aspirin loaded nanosuspension was prepared to enhance the bioavailability of the drug. Nanosuspension is defined as a finely dispersed solid particle dissolved in aqueous and organic medium for oral, tropical, parenteral or pulmonary administration. The size ranges about 200nm to 600nm.Aspirin loaded nanosuspension was prepared by probe sonication method. The probe sonication method is used to reduce the particle size and to increase the solubility of the drug. Total 5 Nano formulations were prepared in which NS1 shows 100% of drug content. Invitro Drug release was performed using Franz diffusion cell in which NS5 formulation shows 94.7% drug release in a time period of two hours and 30 minutes. Entrapment efficiency was performed using Ultracentrifugation method kept for 40 minutes at 17,000 rpm speed. Among all NS5 shows 71.9% of entrapment efficiency.
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探针超声法制备阿司匹林纳米混悬液及评价
阿司匹林抑制了一种叫做环氧合酶(COX)的酶的活性,这种酶会导致前列腺素(pg)的形成,而前列腺素会引起炎症、肿胀、疼痛和发烧。阿司匹林具有抗炎、镇痛、解热等多种作用。制备了载阿司匹林纳米混悬液,以提高药物的生物利用度。纳米悬浮液被定义为一种精细分散的固体颗粒,溶解在水和有机介质中,用于口服、热带、肠外或肺部给药。尺寸范围在200nm ~ 600nm之间。采用探针超声法制备了阿司匹林负载纳米混悬液。探针超声法用于减小颗粒大小和增加药物的溶解度。共制备了5个纳米制剂,其中NS1的药物含量为100%。体外释药采用Franz扩散池,NS5制剂在2小时30分钟内释药率为94.7%。采用17000 rpm转速下保持40分钟的超离心法测定包封效率。其中,NS5的捕集效率为71.9%。
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