Deependra Jain, Nishiprakash Jain, SK Jain, Nitin Jonwal, Shashank Mishra, Deepak Bhatt, Soham Shukla
Deependra Jain1*, Nishiprakash Jain1, Dr. SK Jain1, Nitin Jonwal2, Shashank Mishra2,
Deepak Bhatt2, Soham Shukla3
1Sagar Institute of Research & Technology-Pharmacy, Bhopal, India
2 Cadila Pharmaceuticals Ltd., Ahmadabad, India
3B. S. Patel Pharmacy College, Mehsana, India
Volume - 6,
Issue - 3,
Year - 2013
The main goal of this study was to develop a stable formulation of antihypertensive drugs amlodipine and hydrochlorothiazide (HCTZ) as an immediate release tablet and to evaluate the dissolution profile. The formulation development work was initiated with wet granulation. Lactose monohydrate and microcrystalline cellulose were used as diluents. Starch paste is prepared in purified water and was used as the binder. Sodium starch glycollate is added as a disintegrating agent. Magnesium stearate was used as the lubricant. Disintegration time and drug release were taken as the basis to optimize the formulation. The prepared granules were compressed into a single layer compression machine. Capping was observed in the formulation F1. However, in the remaining four formulations no capping was observed. The tablets thus formulated with higher proportion of sodium starch glycollate showed satisfactory physical parameters, and it was found to be stable and in vitro release studies showed that formulation F5 was 101.03% for amlodipine and 99.14% for hydrochlorothiazide respectively. The results suggest the feasibility of developing immediate release tablets consisting of amlodipine and hydrochlorothiazide for the convenience of patients with hypertension.
Cite this article:
Deependra Jain, Nishiprakash Jain, SK Jain, Nitin Jonwal, Shashank Mishra, Deepak Bhatt, Soham Shukla. Preparation, Physicochemical Characterization, Dissolution and Formulation Studies of Immediate release tablets of Amlodipine Besylate and Hydrochlorothiazide. Research J. Pharm. and Tech. 6(3): March 2013; Page 247-250.