Formulation development and optimization of fast dissolving film containing carvedilol nanocrystals for improved bioavailability
Journal Title: Journal of Drug Delivery and Therapeutics - Year 2018, Vol 8, Issue 6
Abstract
In this work, fast dissolving films (FDF) were prepared using nanocrystal formulations in order to optimise dissolution properties of lipophilic, poorly soluble drug Cavedilol. Drug nanocrystals are crystals with a size in the nanometer range, meaning that they are nanoparticles with a crystalline character. Carvedilol nanosuspensions were prepared using a high-pressure homogenizer, and then encapsulated in to films by solvent casting method using polymers such as maltodextrin and PVA in different concentrations. Propylene glycol used as a plasticizer. This study aimed to develop and evaluate the formulation of FDF containing Carvedilol nanocrystals for enhanced bioavailability and better compliance. The formulation of FDF was optimized by Box-Behnken Design (BBD) (design expert 11.03).In this design, 13 formulas were performed. One of the formula were suggested by design expert desirability = 1.
VALIDATED RP HPLC METHOD DEVELOPMENT FOR EXEMESTANE IN TABLET DOSAGE FORM
The aim of this present work was to develop stability indicating LC method, which is selective, accurate, simple, precise, reliable, cost effective and rapid for the quantification of all possible degradants and determin...
FORMULATION OPTIMIZATION AND EVALUATION OF GASTRORETENTIVE TABLETS OF ONDANSETRON HCL
The aim of the work is to design Gastroretentive tablets of Ondansetron HCl for gastric retention by using 32 factorial designs. Floating tablets of Ondansetron HCl were prepared by direct compression method using polyme...
FORMULATION AND EVALUATION OF EFFERVECENT FLOATING TABLETS OF ANTIDIABETIC DRUG
The aim present investigation is Formulation and Evaluation of Effervescent Floating Tablets of antidiabetic drug. Gastric retention are such systems, which increase the gastric retention time of the dosage forms at the...
STABILITY TESTING GUIDELINES OF PHARMACEUTICAL PRODUCTS
Stability studies of pharmaceutical products ensuring the maintenance of product quality, safety and efficacy throughout the shelf life are considered as pre-requisite for the acceptance and approval of any pharmaceutica...
Study on Drug Prescribing Pattern in Dengue Patients in a Tertiary Care Hospital – A tool to teach Clinical Pharmacology
Introduction and Aim: Dengue fever (DF) is the most common arboviral infection of mankind gaining global attention. Data about drug usage patterns in DF in India are lacking.The present study was undertaken to analyze dr...