Drug Development and Analysis Laboratory, School of Pharmaceutical Sciences, Siksha O Anusandhan Deemed to be University, Kalinga Nagar, Bhubaneswar, 751003, Odisha, India.
Infectious Disease Biology Lab, Institute of Life Sciences, Bhubaneswar, 751023, Odisha, India.
Mol Divers. 2024 Jun;28(3):1261-1272. doi: 10.1007/s11030-023-10654-2. Epub 2023 Apr 21.
Chikungunya virus infection has become a global health concern because of its high rates of morbidity and mortality in patients with preexisting conditions. Inflammation and arthritis are the major symptoms of CHIKV that persist even after clearance of CHIKV. To develop an antiviral that can reduce infection and manage inflammation independent of the CHIKV infection, ibuprofen (IBU) conjugates with sulfonamide and thiosemicarbazide were synthesized. The conjugates, IBU-SULFA, IBU-ISS and IBU-IBT significantly inhibited CHIKV infection in vitro with a selectivity index (CC/IC) of > 11.9, > 25.1 and > 21, respectively. The reduction in infection was attributed to the interference of the conjugates in the early stages of CHIKV life cycle. With no acute oral toxicity, these compounds significantly reduced inflammation and arthritis in rats. Unlike IBU, the conjugates were not ulcerogenic. In conclusion, the conjugation imparted anti-CHIKV properties while retaining the anti-inflammatory properties of IBU. These findings can encourage further validation and research to develop an antiviral for CHIKV to manage both infection and arthritis.
基孔肯雅热病毒感染因其在有基础疾病的患者中发病率和死亡率高而成为全球健康关注的问题。炎症和关节炎是 CHIKV 的主要症状,即使在 CHIKV 清除后仍持续存在。为了开发一种能够降低感染并独立于 CHIKV 感染来控制炎症的抗病毒药物,合成了与磺胺和硫代氨基脲结合的布洛芬(IBU)缀合物。缀合物 IBU-SULFA、IBU-ISS 和 IBU-IBT 分别以选择性指数(CC/IC)>11.9、>25.1 和>21 显著抑制了体外 CHIKV 感染。感染的减少归因于这些缀合物在 CHIKV 生命周期的早期阶段的干扰。这些化合物没有急性口服毒性,可显著减轻大鼠的炎症和关节炎。与 IBU 不同,这些缀合物没有致溃疡作用。总之,缀合赋予了抗 CHIKV 特性,同时保留了 IBU 的抗炎特性。这些发现可以鼓励进一步验证和研究,以开发一种用于 CHIKV 的抗病毒药物来管理感染和关节炎。