- Physicochemical characterization and dissolution enhancement of aceclofenac-hydroxypropyl beta-cyclodextrin binary systemsSunita Dahiya
Department of Pharmaceutics, Rajiv Academy for Pharmacy, Mathura 281 001, India
PDA J Pharm Sci Technol 60:378-88. 2006..Hence, it was suggested that complexation of aceclofenac with HPbetaCD may be used as an approach to change the drug from Biopharmaceutics Classification System BCS Class II to BCS Class I without changing its intrinsic permeability...
- Influence of amorphous cyclodextrin derivatives on aceclofenac release from directly compressible tabletsS Dahiya
Department of Pharmaceutics, Rajiv Academy for Pharmacy, Mathura, Uttar Pradesh, India
Pharmazie 62:278-83. 2007..The dissolution data were characterized by different model independent parameters such as dissolution efficiency (DE), difference factor (f1) and similarity factor (f2)...
- Development of extended release coevaporates and coprecipitates of promethazine HCl with acrylic polymers: formulation considerationsSunita Dahiya
Department of Pharmaceutics, Rajiv Academy for Pharmacy, Mathura, India
Chem Pharm Bull (Tokyo) 56:504-8. 2008..90% drug release for 12 h. Among different formulations, tablets prepared by Eudragit RLPO coevaporates (1 : 5) displayed extended release of drug for 12 h with 90.87% release followed by zero order kinetics (r(2)=0.9808)...
- Solid dispersion of meloxicam: factorially designed dosage form for geriatric populationDeepa Pathak
Department of Pharmaceutics, Rajiv Academy for Pharmacy, Mathura, U P 281001, India
Acta Pharm 58:99-110. 2008..Formulations containing higher levels of methyl cellulose and higher levels of either sodium citrate or Tween 80 exhibited the highest drug release...
- Preparation and evaluation of oxytetracycline hydrochloride microbeads for delayed releaseSunita Dahiya
Department of Pharmaceutics, Rajiv Academy for Pharmacy, Mathura 281 001 UP, India
Pak J Pharm Sci 21:103-8. 2008..Selected formulation was coated using enteric polymer cellulose acetate phthalate to minimize burst drug release along with delayed drug release in intestinal medium...