Subacute Oral Toxicity Studies of Pankajakasthuri Orthoherb Tablets Formulated for Managing Pain and Inflammation of Joints

Hareendran Nair J, Kasthuri Nair A, Sithara Ms, Shan Sasidharan
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Abstract

Objectives: The objective of this investigation was to assess the subacute oral toxicity of the Pankajakasthuri Orthoherb Tablets, a polyherbal formulation used to manage pain and inflammation due to various pathological reasons, including osteoarthrosis, polyarthritis, rheumatoid arthritis, and other chronic degenerative disorders. Materials and Methods: The subacute toxicity studies of Pankajakasthuri Orthoherb Tablets were conducted using Wistar albino rats of both sexes, according to Organization for Economic Cooperation and Development-approved procedures. In this study, rats were orally administered Pankajakasthuri Orthoherb Tablets daily at doses of 250, 500, and 1000 mg/kg body weight for 28 days. Throughout the study period, general behavior, mortality, and adverse effects were recorded. Body weight, selected hematological and clinical chemistry parameters were determined at the end of the investigation period. Finally, histopathological analysis was performed to determine whether the study drug was inducing any alternations in the vital organs. Results: Daily administration of Pankajakasthuri Orthoherb Tablets for a continuous 28 days did not record any major toxicity indications. Additionally, no significant variation in food and water consumption, body weight, relative organs and hematology and clinical chemistry parameters was recorded in both sexes compared to the control. Histopathological investigation of the vital organs also revealed normal architecture, which suggests no morphological alterations after the administration of Pankajakasthuri Orthoherb Tablets. Conclusion: The outcomes of this investigation confirmed that Pankajakasthuri Orthoherb Tablets did not have the potential to induce toxicity signs in the experimental rats. The No observed Adverse Effect Level (NOAEL) for female and male rats of Pankajakasthuri Orthoherb Tablets under these experimental conditions was 500 mg/kg body weight. Based on the NOAEL, the human equivalent dose of the Pankajakasthuri Orthoherb Tablet was calculated at 5.195 g/day.
用于治疗关节疼痛和炎症的 Pankajakasthuri Orthoherb 片剂亚急性期口服毒性研究
研究目的本研究旨在评估 Pankajakasthuri Orthoherb 片的亚急性口服毒性,这是一种多草药制剂,用于控制各种病理原因引起的疼痛和炎症,包括骨关节炎、多关节炎、类风湿性关节炎和其他慢性退行性疾病。材料和方法:按照经济合作与发展组织批准的程序,使用 Wistar 白化雌雄大鼠进行了 Pankajakasthuri Orthoherb 片的亚急性毒性研究。在这项研究中,每天按 250、500 和 1000 毫克/千克体重的剂量给大鼠口服 Pankajakasthuri Orthoherb 片剂,持续 28 天。在整个研究期间,记录了大鼠的一般行为、死亡率和不良反应。研究结束时,测定体重、选定的血液学和临床化学参数。最后,还进行了组织病理学分析,以确定研究药物是否会导致重要器官发生变化。研究结果连续 28 天每天服用 Pankajakasthuri Orthoherb 片,未发现任何重大毒性迹象。此外,与对照组相比,雌雄动物的食物和水消耗量、体重、相对器官、血液学和临床化学指标均无明显变化。重要器官的组织病理学调查也显示结构正常,这表明服用 Pankajakasthuri Orthoherb 片剂后没有发生形态改变。结论调查结果表明,Pankajakasthuri Orthoherb 片不会诱发实验大鼠出现毒性症状。在这些实验条件下,Pankajakasthuri Orthoherb 片对雌性和雄性大鼠的无观测不良效应水平(NOAEL)为 500 毫克/千克体重。根据无观测不良效应水平,计算出 Pankajakasthuri Orthoherb 片剂的人体等效剂量为 5.195 克/天。
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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