FORMULATION AND EVALUATION OF DILTIAZEM HYDROCHLORIDE TRANSDERMAL PATCH
Journal Title: Indo American Journal of Pharmaceutical Research - Year 2012, Vol 2, Issue 4
Abstract
Transdermal drug delivery systems (TDDS) are dosage forms designed to deliver a therapeutically effective amount of drug across a patient’s skin. In the current research Diltiazem hydrochloride was loaded in transdermal patch and they are prepared by solvent casting method using aluminum foil as the backing membrane. Eudragit RS100 and HPMC were weighed in requisite ratios and they were then dissolved in methanol as solvent using magnetic stirrer.Four optimized transdermal patches were formulated with different drug-polymer ratios. Diltiazem Hcl (20mg) was added into homogenous dispersion under slow stirring with a magnetic stirrer. Dibutyl phthalate 30%w/w of polymer composition was used as plasticizer, added to the above dispersion under continuous stirring. Invitro and physico-chemical evaluation methods were performed. Finally F3 formulation showed higher drug release (83.4 %),thickness (0.45±0.04), weight (532.6±0.36), folding endurance(5),drug content(86.23±0.08)%MC (4.66±0.04),%MA (8.24±0.75),%ML (3.97±0.02),WVTR(2.07±0.01) and drug permeation (1173 μg/ml) than the remaining formulations. Hence, F3 can be selected as best formulation among the four optimized formulations.
Authors and Affiliations
C. SUMATHI, RAJESH CHATAKONDA, G. ARCHANA, PRASANTH KUMAR PUTTI, V. P. V. LAKSHMI
CORRELATION BETWEEN SERUM ZINC, INSULIN AND C-PEPTIDE IN PATIENTS OF TYPE 2 DM IN A TERTIARY HOSPITAL IN NORTH INDIA
Zinc has been reported to be involved in the synthesis and release of insulin and C-peptide from the beta cells of pancreas. The possibility of a correlation between these parameters needs to be explored, specially with...
IN-VITRO DISSOLUTION AND SOME PHYSICAL PROPERTIES OF TWO GENERICS OF LEVAMISOLE BLOUS FORMULATIONS FOR LARGE ANIMALS
Abstract Physical and dissolution properties of solid oral dosage formulations significantly affect therapeutic outcomes following their use in veterinary medicine. Therapeutic failure of most levamisole boluses for the...
DEVELOPMENT AND VALIDATION OF A STABILITY INDICATING RP-UPLC METHOD FOR THE SIMULTANEOUS QUANTIFICATION OF SOFOSBUVIR AND VELPATASVIR IN FINISHED DOSAGE FORM
A simple, rapid, accurate, precise and economical reverse phase Ultra performance liquid chromatographic method was developed for simultaneous quantification of two anti-viral drugs, viz., Sofosbuvir and Velpatasvir. The...
EVALUATION OF PHYSICAL AND CHEMICAL STABILITY OF DOCETAXEL INCORPORATED NANO STRUCTURED LIPID CARRIER SYSTEM
Abstract Poor physical and chemical stability associated with NLC formulation has been a concern and has taken away the initial attraction in formulating them. Recently it has been reported that the process of lyophiliza...
KINETICS OF OXIDATION OF FAST GREEN FCF DYE WITH 1-CHLOROBENZOTRIAZOLE IN ALKALINE MEDIUM: MECHANISTIC AND SPECTROPHOTOMETRIC STUDY
Abstract Fast Green FCF (FGF) is a synthetic food dye. The kinetics of oxidation of Fast Green FCF with 1-chlorobenzotriazole in NaOH medium has been spectrophotometrically investigated at ƛmax 625 nm at the temperature...