Evaluation of Anti-Inflammatory and Analgesic Activity of Synthesized Substituted Isoxazole Derivatives

G. Kaur, Bhavneet Singh, A. Chopra, Navpreet Kaur, Divneet Kaur
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引用次数: 0

Abstract

Inflammation is the body’s response to harmful stimuli, such as pathogens, damaged cells, or irritants. Inflammation is a protective attempt by the organism to remove the injurious stimuli and initiate the healing process. Inflammations are of two types: acute and chronic. The signs of acute inflammation are warmth, redness, pain, swelling and loss of function. Chronic inflammation is characterized by long lasting pain, redness and swelling. Non steroidal anti-inflammatory drugs (NSAIDS) are used to treat pain and inflammation but is often accomplished by side effects such as gastric ulceration, bleeding, and renal function suppression. The aim of this research was to synthesize substituted isoxazole derivatives and to evaluate anti-inflammatory and analgesic activity of synthesized derivatives. In the present study, the chemicals o-hydroxyacetophenone and 1H-indole-3-carbaldehyde were reacted to synthesize 2’’-[5’-(1Hindol-3-yl)isoxazole-3’-yl]phenol. For pharmacological activity, rats were randomly divided into five groups. Group I animals served as control and received vehicle (CMC 0.5% solution) intraperitoneally. Group II (Diseased controlled vehicle group) animals were injected with 0.1ml of 1% carrageenan in planter of left hind limb. Group III (Standard control group) animals were treated with standard drug Diclofenac sodium (20mg/kg) intraperitoneally. Group IV animals were treated with test drug at a dose of 100mg/kg body weight, intraperiotneally as a suspension in CMC (0.5% solution). This study suggests that the isoxazole derivatives have significant anti-inflammatory and analgesic effect compared to standard (diclofenac). © 2019 iGlobal Research and Publishing Foundation. All rights reserved. Cite this article as: Kaur, G.; Singh, B.; Chopra, A.; Kaur, N.; Kaur, D. Evaluation of Anti-Inflammatory and Analgesic Activity of Synthesized Substituted Isoxazole Derivatives. Indo Global J. Pharm. Sci., 2019; 9(2Suppl.): 118. DOI: http://doi.org/10.35652/IGJPS.2019.92S16 . Indo Global Journal of Pharmaceutical Sciences( ISSN 2249 1023; CODENIGJPAI; NLM ID: 101610675) indexed and abstracted in CrossRef (DOI Enabling), UGC CARE Journal List, EMBASE(Elsevier), National Library of Medicine (NLM) Catalog, ResearchGate, Publons, CAS (ACS), Index Copernicus, Google Scholar and many more. For further details, visit http://iglobaljournal.com This is a special issue as an outcome of ‘RAPSCON-2019’ sponsored by APTI and organized by Sri Sai College of Pharmacy, Manawala, Amritsar, Punjab, India. Relaxation offered in journal format.
合成取代异恶唑衍生物的抗炎镇痛活性评价
炎症是身体对有害刺激的反应,如病原体、受损细胞或刺激物。炎症是机体消除有害刺激并启动愈合过程的一种保护性尝试。炎症有两种类型:急性和慢性。急性炎症的症状是发热、发红、疼痛、肿胀和功能丧失。慢性炎症的特征是持续的疼痛、红肿。非甾体抗炎药(NSAIDS)用于治疗疼痛和炎症,但往往伴随着胃溃疡、出血和肾功能抑制等副作用。本研究的目的是合成取代异恶唑衍生物,并评价其抗炎和镇痛活性。本研究以邻羟基苯乙酮和1h -吲哚-3-醛为原料,合成了2′-[5′-(1吲哚-3-基)异恶唑-3′-基]苯酚。药理活性方面,将大鼠随机分为5组。ⅰ组为对照,腹腔注射CMC 0.5%溶液。第二组(病鼠对照组)左后肢种植体注射1%卡拉胶0.1ml。第三组(标准对照组)采用标准药物双氯芬酸钠(20mg/kg)腹腔注射。IV组动物以试验药物100mg/kg体重作为混悬液,经肠内注射于CMC(0.5%溶液)中。本研究提示异恶唑衍生物与标准双氯芬酸相比具有显著的抗炎镇痛作用。©2019 igglobal研究与出版基金会。版权所有。引用本文如下:Kaur, G.;辛格,b;Chopra, a;考尔:;合成取代异恶唑衍生物抗炎和镇痛活性的评价。印度国际制药公司。科学。, 2019;9(2生理):118。DOI: http://doi.org/10.35652/IGJPS.2019.92S16。印度全球药物科学杂志(ISSN 2249 1023;CODENIGJPAI;NLM ID: 101610675)在CrossRef (DOI Enabling), UGC CARE Journal List, EMBASE(Elsevier), National Library of Medicine (NLM) Catalog, ResearchGate, Publons, CAS (ACS), Index哥白尼,Google Scholar等中索引和摘要。欲了解更多详情,请访问http://iglobaljournal.com这是由APTI赞助,印度旁遮普阿姆利则马纳瓦拉斯里赛药学院组织的“RAPSCON-2019”的特刊。以日志形式提供放松。
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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