Department of Pharmaceutical Sciences, R. T. M. Nagpur, University, Amravati Road, Nagpur, Maharashtra,India.
Nagpur college of Pharmacy, DBATU, Wanadongri, Hingna road, Nagpur,India.
Antiinflamm Antiallergy Agents Med Chem. 2021;20(4):333-343. doi: 10.2174/1871523020666210203103433.
Pain is an immunological response to an infection or inflammation and long-term use of pain management therapy includes the use of Nonsteroidal anti-inflammatory drugs, which is associated with the occurrence of toxicity as well as gastrointestinal bleeding. Therefore, the investigation of new analgesic and anti-inflammatory agents remains a major challenge.
The objective of this research study is to undergo the pharmacological evaluation of newly synthesized benzoxazole derivatives. These novel derivatives were evaluated for anti-nociceptive, anti-inflammatory and cytotoxic activity using various in-vivo and ex-vivo methods Methods: The study was carried out using swiss mice (adult male) weighing between 20gm to 30gm and were divided into groups containing (n=6) six animals in each group for treatment. The anti-nociceptive activity was performed by using 0.1ml of 0.6% v/v acetic acid as nociception inducer and evaluated by the diminished number of abdominal writhes. The anti-inflammatory activity was done using 0.1 ml of 2% w/v Carrageenan induced paw edema method was observed which was evaluated by calculating the percent maximum possible effect. Histopathological evaluation and cytotoxic activity of the compounds were carried out.
The results of this research study revealed that synthesized derivatives (a, b, c, d and e) showed promising anti-nociceptive and anti-inflammatory effects along significantly higher cytotoxic activity in MCF-7 cell lines.
It can be concluded that synthesized derivatives (a, b, c, d and e) have potential anti- nociceptive and anti-inflammatory effects along with cytotoxic activity and certain modification in structure may result in the potent activity.
疼痛是对感染或炎症的免疫反应,长期使用疼痛管理疗法包括使用非甾体抗炎药,这与毒性和胃肠道出血的发生有关。因此,研究新的镇痛和抗炎药物仍然是一个主要挑战。
本研究旨在对新合成的苯并恶唑衍生物进行药理学评价。这些新型衍生物通过各种体内和体外方法评估其抗伤害感受、抗炎和细胞毒性活性。
本研究使用体重在 20 克至 30 克之间的成年雄性瑞士小鼠进行,将其分为每组含有 6 只动物的 6 组进行治疗。通过使用 0.6%v/v 的 0.1ml 乙酸作为伤害感受诱导物来进行抗伤害感受活性,通过减少的腹部扭动次数来评估。通过计算最大可能效果的百分比来进行抗炎活性。进行化合物的组织病理学评价和细胞毒性活性。
本研究的结果表明,合成的衍生物(a、b、c、d 和 e)表现出有希望的抗伤害感受和抗炎作用,同时在 MCF-7 细胞系中表现出显著更高的细胞毒性活性。
可以得出结论,合成的衍生物(a、b、c、d 和 e)具有潜在的抗伤害感受和抗炎作用以及细胞毒性活性,并且结构的某些修饰可能导致活性增强。