Development, optimization and evaluation of solid dosage form of Thiocolchicoside by using absorption enhancers
نویسندگان
چکیده
Thiocolchicoside has a selective affinity for g-amino-butyric acid (GABA) receptors and acts on themuscular contracture by activating the GABA-nergicinhibitory pathways thereby acting as a potent muscle relaxant Thiocolchicoside (Muscoril, Myoril, Neoflax) is a muscle relaxant with anti-inflammatory and analgesic effects. It is used for the treatment of orthopedic, traumatic and rheumatologic disorders.This drug can not be absorbed oraly owing to its very less permeation through GI epithelia. The physico chemical properties of thiocolchicoside are not favorable for its permeation across the skin. Thiocolchicoside has a relatively high molecular weight (563), relatively high water solubility (16.1mg/ml) and low octanol/water partition coefficient (log P=-0.34). The present study attempts to increase the intestinal permeability of BCS class III drug Thiocolchicoside by using certain intestinal absorption enhancers. To enhance the permeation, intestinal permeation enhancers were used in various molar ratios with the drug. The liphophilicity of Thiocolchicoside was determined by means of the n-octanol/water syatem to check the effect of absorption enhancers. The changes in partition coefficient by the octanol/water system were confirmed using an invitro transport model with the excised animal tissue membrane. The Data Expert software is applied for the 3 factorial designand the ANOVA study of the linear regression model, response surface plot as well as contour plot confirms the predicted batch with the desirability of 0.982.Result of R and T-test confirmed that predicted and observed responses showed no significant difference. The result indicated that there is significant improvement in the permeability of the drug and the extent of enhancement was highly dependent on the type of absorption enhancers used. Thus the study indicated that Thiocolchicoside could be successfully delivered orally when formulated with permeation enhancers.
منابع مشابه
Solubility enhancement of glimperide: Development of solid dispersion by solvent melt method, characterization and dosage form development
The aim of the present work was to develop immediate release dosage form of the solid dispersion of glimperide (GLIM) for potential enhancement in the bioavailability. The solid dispersions of GLIM were prepared with PEG6000, PVP K30 and Poloxamer 188, in 1:1, 1:3 and 1:5 %w/w ratio by using solvent wetting and solvent melt method. The in vitro dissolution parameters (%DE10min, %DE30min, %DE60m...
متن کاملThe Enhancing Effect of Sodium Glycocholate and Sodium Salicylate on Rats Gastro-intestinal Permeability to Insulin
There have been numerous efforts to formulate insulin into an oral dosage form. The major problems involved with the oral administration of insulin are acidic and enzymatic decomposition by the gastric medium, and poor absorption in the small intestine due to its macromolecular structure. This study attempted to test the enhancing ability of two absorption enhancers, sodium glycocholate (Na-G...
متن کاملDevelopment and Optimization of Transdermal System of Lisinopril dehydrate: Employing Permeation Enhancers
Lisinopril dihydrate (angiotensin converting enzyme inhibitor) is a lysine derivative of enalaprilat and does not require hydrolysis to exert pharmacological activity. It has an extensive hepatic first pass metabolism resulting in a bioavailabil-ity of 6-60%. To overcome the poor bioavailability of the drug, transdermal patches have been prepared. The present study also aims at optimizati...
متن کاملThe Enhancing Effect of Sodium Glycocholate and Sodium Salicylate on Rats Gastro-intestinal Permeability to Insulin
There have been numerous efforts to formulate insulin into an oral dosage form. The major problems involved with the oral administration of insulin are acidic and enzymatic decomposition by the gastric medium, and poor absorption in the small intestine due to its macromolecular structure. This study attempted to test the enhancing ability of two absorption enhancers, sodium glycocholate (Na-G...
متن کاملFormulation & Evaluation of Oral Disintegrating Tablets of Lamotrigine Solid Dispersions
Lamotrigine is used in the treatment of CNS disorders, particularly epilepsy; pain; oedema; multiple sclerosis and psychiatric indications including bipolar disorder. Lamotrigine belongs to biopharmaceutical classification systems, BCS class II (Low solubility & High permeability). In addition, it requires immediate therapeutic action hence the main objective of this study is to improve the sol...
متن کامل