Research Topics
| Sunita DahiyaSummaryCountry: India Publications
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Publications
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...
