Safety profile of Ayurvedic poly‑herbomineral formulation - Bacnil capsule in albino rats.

Ayu Pub Date : 2019-07-01 Epub Date: 2020-08-08 DOI:10.4103/ayu.AYU_64_18
Balaji Panigrahi, Swati Sharma, Bhakti Sitapara, Subrata De, Mukesh Nariya
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引用次数: 2

Abstract

Introduction: Bacnil capsule is a poly‑herbomineral formulation used to treat gastroenteritis. It contains many potential drugs derived from plant sources and Bhasma (calcined fine powder) preparations.

Aims: The study was designed to ascertain the safety of bacnil capsule orally in Charle's Foster albino rats.

Materials and methods: As per the Organization for Economic Cooperation and Development (OECD) 425 protocol oral acute toxicity study, bacnil capsule was administered orally once only at the dose of 2000 mg/kg in rats. For repeated dose toxicity study, AYUSH 170 and OECD 407, it was administered at three dose levels, Therapeutic doses (TED) (196.2), TED × 5 (981) and TED × 10 (1962) mg/kg/day orally for 28 days in albino rats followed by a 15‑day recovery period only on TED × 10 dose level.

Observation and results: Bacnil at the oral dose of 2000 mg/kg did not produce any toxicity or mortality in albino rats. Repeated dose 28‑day oral toxicity revealed that test formulation did not produce any significant change in serum biochemical, hematological, and histopathological parameters at therapeutic dose level. Mild‑to‑moderate pathological changes were observed in the various serum biochemical and cytoarchitecture of the liver, heart, kidney, and stomach at a dose of 10 TEDs; however, the same was reversed after discontinuation in the recovery test.

Conclusion: Bacnil at 196.2 mg/kg/day is safe at the therapeutic dose level in albino rats.

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阿育吠陀多草药制剂Bacnil胶囊在白化病大鼠中的安全性。
Bacnil胶囊是一种多草药制剂,用于治疗胃肠炎。它含有许多从植物来源和Bhasma(煅烧细粉)制剂中提取的潜在药物。目的:探讨口服巴肯胶囊对白化大鼠的安全性。材料与方法:根据经济合作与发展组织(OECD) 425方案口服急性毒性研究,大鼠只口服一次巴肯胶囊,剂量为2000 mg/kg。在重复给药毒性研究中,AYUSH 170和OECD 407分别以治疗剂量(TED)(196.2)、TED × 5(981)和TED × 10(1962) 3个剂量水平给药,白化病大鼠口服剂量(TED × 10) mg/kg/天,持续28天,随后仅以TED × 10剂量水平给予15天的恢复期。观察和结果:白化病大鼠口服剂量2000 mg/kg巴肯无毒性,无死亡。重复给药28天口服毒性试验显示,试验制剂在治疗剂量水平下未对血清生化、血液学和组织病理学参数产生任何显著变化。在10 TEDs剂量下,肝脏、心脏、肾脏和胃的各种血清生化和细胞结构发生轻至中度病理改变;然而,在恢复测试中,同样的情况在停药后发生逆转。结论:白化病大鼠治疗剂量196.2 mg/kg/d的巴克尼是安全的。
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