Evaluating the sub-chronic toxicity of the BOGA -TN tablets in experimental animals
Nội dung chính của bài viết
Tóm tắt
Objective: To assess the sub-chronic toxicity of Boga-TN tablets in experimental animals to determine the effects of the drug on the hematological and biochemical indices.
Subjects and Methods: Sub-chronic toxicity experiment was carried out in compliance with the guidance of the World Health Organization. Wistar rats (160 - 200g) of both genders, provided by the Laboratory Animal Center, Dan Phuong district, Hanoi were used
Results: The study was carried out in Wistar rats for 4 consecutive weeks by oral administration at the doses of 0.77 and 2.32g/kg/day. After treatment, no significant treatment-related abnormalities were observed at both doses of Boga-TN, compared to the control group, except for the white blood cells, with lower neutrophil but higher lymphocyte values observed in the treated animals. Histopathology assessment did not show any significant variation between control and treatment groups during the study period.
Conclusions: Boga-TN with a dose equivalent to the proposed clinical dose and 3 times the clinical dose did not cause any significant toxicity resulting in death, or produce any hematological, serum chemical alteration, and histo-pathological derangements. However, significant reductions in the levels of WBC, lymphocytes and increased levels of neutrophil in treated groups were detected after 4 weeks of treatment.
Chi tiết bài viết
Từ khóa
Sub-chronic toxicity, Boga-TN tablets, experimental animals.
Tài liệu tham khảo
2. S. Sivakrishnan, M. Pharm. Liver diseases-an overview, 2019, 8(1), pp.1385-1395.
3. Gish RG, Bui TD, Nguyen CTK, et al. Liver disease in Viet Nam: Screening, surveillance, management and education: A 5-year plan and call to action. J Gastroenterol Hepatol, 2012, 27(2), pp.238-247, doi:10.1111/j.1440-1746.2011.06974.x.
4. Radha K. Dhiman MD, DM, MAMS, FACG. Herbal Medicines for Liver Diseases | SpringerLink. Digestive Diseases and Sciences, 2005, 50, pp.1807-1812.
5. Stickel F, Hellerbrand C. Herbs to treat liver diseases: More than placebo? Clinical Liver Disease, 2015, 6(6), pp.136-138.
6. Wat E, Ng CF, Wong ECW, et al. The hepatoprotective effect of the combination use of Fructus Schisandrae with statin--A preclinical evaluation. J Ethnopharmacol, 2016, 178, pp.104-114, doi:10.1016/j.jep.2015.12.004.
7. Deore A, Dhumane J, Wagh R, Sonawane R. The Stages of Drug Discovery and Development Process. Asian J Pharm Res Dev, 2019, 7, pp.62-67, doi:10.22270/ajprd.v7i6.616
8. FDA. The drug development, 2019.
9. Petterino C, Argentino-Storino A. Clinical chemistry and haematology historical data in control Sprague-Dawley rats from pre-clinical toxicity studies. Exp Toxicol Pathol, 2006, 57(3), pp.213-219, doi:10.1016/j.etp.2005.10.002.