Stability studies of hydralazine hydrochloride orodispersible formulations

Muthukumar S (1) , Sundaraganapathy R (2) , Sankar C (3) , Sundaramoorthy C (4) , Yuvaraja K R (5)
(1) Research Scholar, Karpagam Academy of Higher education, Coimbatore, Tamil Nadu, India, India ,
(2) Faculty of Pharmacy, Karpagam Academy of Higher Education, Coimbatore-21, Tamil Nadu, India, India ,
(3) Department of Pharmaceutics, KMCH College of Pharmacy, Coimbatore, Tamilnadu, India, India ,
(4) Department of Pharmaceutics, KMCH College of Pharmacy, Coimbatore, Tamilnadu, India, India ,
(5) Department of Pharmaceutical chemistry, KMCH College of Pharmacy, Coimbatore, Tamilnadu, India, India

Abstract

Solid dosage forms also have a impervious difficulties in patients especially for geriatric and paediatric patients.Dysphagia is common among all age groups. Orodispersible formulations (Fast dissolving tablets & Fast dissolving oral thin films) constitute an inventive dosage form that overcome the problems swallowing and provides speedy onset of action. The objective of present study was to formulate orodispersible formulations of Hydralazine HCL by different methods (Direct compression method, Sublimation method and solvent casting method). Based on physiochemical evaluations F9 (Direct compression method),SF9 (Sublimation method) for Fast dissolving tablets and H2 formulations (Solvent casting method) for Fast dissolving oral thin films were found optimized formula. The optimized formula were kept for stability under long term, accelerated and intermediate conditions for the study period of six months as per ICH guidelines.Based on stability reports the H2 formulations (Fast dissolving oral thin films) got a better drug release than Fast dissolving tablets.

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Authors

Muthukumar S
pharmmuthu@gmail.com (Primary Contact)
Sundaraganapathy R
Sankar C
Sundaramoorthy C
Yuvaraja K R
Muthukumar S, Sundaraganapathy R, Sankar C, Sundaramoorthy C, & Yuvaraja K R. (2020). Stability studies of hydralazine hydrochloride orodispersible formulations. International Journal of Research in Pharmaceutical Sciences, 11(1), 75–86. Retrieved from https://ijrps.com/home/article/view/390

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