Toxicity Studies of Triazolo-Thiadiazoles in Ehrlich Ascitic Carcinoma Cells

Sunil, Dhanya and Isloor, Arun M and Shetty, Prakash and Pai, KSR (2013) Toxicity Studies of Triazolo-Thiadiazoles in Ehrlich Ascitic Carcinoma Cells. Research Journal of Pharmaceutical Sciences, 2 (6). pp. 1-6. ISSN 2319 – 555X

[img] PDF
Dr. Dhanya Sunil. Res J. Pharma. Sci..pdf - Published Version
Restricted to Registered users only

Download (719kB) | Request a copy
Official URL: http://www.isca.in/

Abstract

Novel treatment approaches are urgently needed for cancer management due to high systemic toxicity and drug resistance in cancer chemotherapy. Three triazolo-thiadiazoles, 6-[3-(4-chlorophenyl)-1H-pyrazol-4-yl]-3-[(2-naphthoxy)methyl] [1,2,4] triazolo [3,4-b] [1,3,4] thiadiazole (CPNT), 6-[3-(4-fluorophenyl)-1H-pyrazol-4-yl]-3-[(2-naphthoxy)methyl] [1,2,4] triazolo [3,4-b] [1,3,4] thiadiazole (FPNT) and 6-[3-(4-chlororophenyl)-1H-pyrazol-4-yl]-3-[phenoxymethyl] [1,2,4] triazolo [3,4-b][1,3,4]thiadiazole (CPPT) were tested for their anti-tumor activity in ehrlich ascites carcinoma (EAC) bearing Swiss albino mice. The effect of thiadiazoles in the mean survival time, body weight, hematological and biochemical parameters in cancer induced mice was studied. The inner peritoneal lining of mice was checked for angiogenesis. Histopathology studies of liver, kidney and spleen to assess the toxicity of thiadiazoles were performed. Statistical analyses were performed by one-way ANOVA, followed by Tukey’s post hoc test using Graph Pad Prism 5.02. An increase in mean survival time was observed in mice treated with CPNT, 50 mg/kg body weight over control and standard mice. The rise in body weight associated with progression of cancer was controlled on treatment with CPNT. Differed hematological and biochemical parameters in EAC bearing mice were restored towards normal after CPNT treatment. Histopathology studies exhibited only mild hepatic and nephrotoxicity on CPNT treatment. CPNT at an optimal dose of 50 mg/kg body weight inhibited angiogenesis and exhibited excellent anticancer activity with minimal toxic effects in vivo against EAC cells when compared to the standard drug cisplatin.

Item Type: Article
Uncontrolled Keywords: Thiadiazole, hematology, angiogenesis, histopathology
Subjects: Engineering > MIT Manipal > Chemistry
Pharmacy > MCOPS Manipal > Pharmacology
Engineering > MIT Manipal > Printing and Media
Depositing User: MIT Library
Date Deposited: 01 Aug 2013 10:57
Last Modified: 01 Aug 2013 10:57
URI: http://eprints.manipal.edu/id/eprint/136718

Actions (login required)

View Item View Item