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新型冠状病毒有机物(马达加斯加抗新冠草药茶)在动物模型中的急、亚急性经口毒性特征及安全性评价。

Acute and subacute oral toxicity characterization and safety assessment of COVID organics (Madagascar's Anti-COVID Herbal Tea) in animal models.

机构信息

Department of Biochemistry and Nutrition, Centre for Research in Traditional, Complementary and Alternative Medicine, Nigerian Institute of Medical Research, Yaba, Lagos, Nigeria.

Department of Pathology, College of Medicine, University of Ibadan, University College Hospital, Ibadan, Oyo State, Nigeria.

出版信息

Ann Afr Med. 2023 Oct-Dec;22(4):481-488. doi: 10.4103/aam.aam_112_21.

DOI:10.4103/aam.aam_112_21
PMID:38358149
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10775938/
Abstract

INTRODUCTION

Coronavirus disease 2019 (COVID-19) is an infectious disease caused by severe acute respiratory syndrome coronavirus 2. No drug has been generally approved as safe and effective for the treatment of COVID-19. Several therapeutic agents such as COVID Organics (CVO) have been explored as treatment options. CVO is an herbal tea composed of 62% of Artemisia annua and 38% of other plants. There is presently no existing scientific report and data on the safety and efficacy of CVO herbal drug. Thus, acute and subacute toxicity studies were undertaken to evaluate the safety and toxicity of CVO on short- and long-term usage in animal models.

MATERIALS AND METHODS

Phytochemical and nutritional compositions of CVO were determined using standard methods. Acute oral toxicity was investigated using female Swiss albino mice (three per group). While subacute oral toxicity was done using female and male Swiss albino rats (five per group). The animals were administered 2000 mg/kg, 5000 mg/kg, therapeutic dose; 5500 mg/kg and supratherapeutic dose; 11,000 mg/kg of CVO herbal product. The control group received water ad libitum. The oral toxicity studies were done in accordance with Organization for Economic Corporation and Development guidelines. The experimental protocol was approved by the Institutional Animal Care and Use Committee, Nigerian Institute of Medical Research (Ethics No. IRB/17/043).

RESULTS

CVO is rich in antioxidants: flavonoids (10.3%), tannins (29.1%), and phenolics (434.4 mg). It contains proteins (33.8%), carbohydrates (34.5%), fat (6.8%), and fiber (0.5%). In the acute toxicity study, no mortality was recorded in all the treated and untreated groups. The lethal dose of CVO is >5000 mg/kg body weight. The hematological, biochemical, lipid profile, and histologic parameters were all normal at therapeutic doses when compared to the control group.

CONCLUSION

The acute and subacute oral toxicity studies revealed that CVO is not toxic. The specific organ toxicity evaluations also indicated that CVO has no toxic effects on blood parameters and vital organs structure and function at therapeutic dose. Thus, CVO is safe for short- and long-term usage. We recommend that CVO should be subjected to efficacy studies to investigate whether it is effective for COVID-19 treatment as claimed by the manufacturer.

摘要

简介

新型冠状病毒病(COVID-19)是由严重急性呼吸系统综合征冠状病毒 2 引起的传染病。目前尚无药物被普遍批准为 COVID-19 的安全有效治疗药物。一些治疗药物,如 COVID 有机化合物(CVO),已被探索为治疗选择。CVO 是一种由 62%青蒿和 38%其他植物组成的草药茶。目前尚无关于 CVO 草药药物安全性和疗效的现有科学报告和数据。因此,进行了急性和亚急性毒性研究,以评估 CVO 在动物模型中长期和短期使用的安全性和毒性。

材料和方法

使用标准方法确定 CVO 的植物化学和营养成分。使用雌性瑞士白化病小鼠(每组 3 只)进行急性口服毒性研究。而使用雌性和雄性瑞士白化病大鼠(每组 5 只)进行亚急性口服毒性研究。给动物服用 2000mg/kg、5000mg/kg、治疗剂量;5500mg/kg 和超治疗剂量;11000mg/kg 的 CVO 草药产品。对照组给予自由饮水。口服毒性研究按照经济合作与发展组织的指导方针进行。实验方案得到了尼日利亚医学研究所机构动物护理和使用委员会的批准(伦理编号 IRB/17/043)。

结果

CVO 富含抗氧化剂:类黄酮(10.3%)、单宁(29.1%)和酚类(434.4mg)。它含有蛋白质(33.8%)、碳水化合物(34.5%)、脂肪(6.8%)和纤维(0.5%)。在急性毒性研究中,所有治疗组和未治疗组均未记录死亡。CVO 的致死剂量>5000mg/kg 体重。与对照组相比,在治疗剂量下,血液学、生化学、脂质谱和组织学参数均正常。

结论

急性和亚急性口服毒性研究表明 CVO 无毒。特定的器官毒性评估还表明,CVO 在治疗剂量下对血液参数和重要器官的结构和功能没有毒性作用。因此,CVO 可安全短期和长期使用。我们建议对 CVO 进行疗效研究,以调查其是否如制造商声称的那样对 COVID-19 治疗有效。

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