Evaluation of in vivo efficacy and toxicity of prednisolone- loaded hydrogel-based drug delivery device
Amit Kumar De1★, Plaban Bhattacharya1, Sriparna Datta1, Arup Mukherjee1★ Corresponding author
- 1Department of Chemical Technology, Division of Pharmaceutical and Fine Chemical Technology, University College of Science and Technology, University of Calcutta, Kolkata, West Bengal, INDIA.
CORRESPONDENCE
Amit Kumar De
Department of Chemical Technology, Division of Pharmaceutical and Fine Chemical Technology, University College of Science and Technology, University of Calcutta, Kolkata, West Bengal, INDIA.
Volume 3, Issue 4 · pp. 225–233 · PUBLISHED · DOI: 10.4103/2230-973X.121308
ABSTRACT
Drugs prescribed for the treatment of moderate to severe inflammatory bowel disease (IBD) are associated with number of side effects. Targeted drug delivery is essential for the treatment of inflammatory bowel disease in order to increase efficacy and reduce toxicity. The established delivery system is designed on enzyme and time-based release of poorly soluble prednisolone, a drug of choice for the treatment of moderate to severe inflammatory bowel disease. Their pharmacological evaluation was done in 2,4,6-trinitrobenzene sulphonic acid (TNBS)-induced model of colitis in rat. The drug was administered once daily for 3 consecutive days. Visible severity of colitis, tissue to bodyweight ratio, tissue histology along with nitric oxide (NO), malondialdehyde (MDA) and myeloperoxidase (MPO) activity of colonic tissue were studied to estimate the efficacy of the drug-loaded delivery system. The highest efficacy was observed for formulation in which Eudragit RS100 (EU) was used along with guar gum (GG) in a ratio 2:5 for the preparation of delivery device. An effective recovery was observed from the study of tissue histology of animals treated with the drug-loaded optimized formulation and the biochemical parameters supported it. The toxicity of prednisolone (PD) was reduced significantly as predicted from thymus to body weight ratio of treated animals. GG and EU RS100 provided a newer bipolymer combination for the colon-targeted delivery of PD which increased its efficacy and reduced the toxic side effects. The in vivo experiments presented effective amelioration from colitis in TNBS-induced animal model of colitis.
KEYWORDS
REFERENCES
As publishedShowing references and in-text citations exactly as published.
Cite this article
SELECT FORMAT
De, A. K., Bhattacharya, P., Datta, S., & Mukherjee, A. (). Evaluation of in vivo efficacy and toxicity of prednisolone- loaded hydrogel-based drug delivery device. International Journal of Pharmaceutical Investigation, 3(4), 225–233. https://doi.org/10.4103/2230-973X.121308