Open Access Open Access  Restricted Access Subscription Access
Open Access Open Access Open Access  Restricted Access Restricted Access Subscription Access

Formulation and Assessment of Quick Dissolving Tablet of Candesartan Cilexetil Arranged from Their Circular Agglomerates


Affiliations
1 Assistant Professor, Annasaheb Dange College of B. Pharmacy, Ashta. 416301, Maharashtra., India
2 Head of Department, Annasaheb Dange College of B. Pharmacy Ashta. Ashta: 416301, Maharashtra., India
     

   Subscribe/Renew Journal


Candesartan cilexetil is water insoluble drug which comes under BCS class second category. Drug was used in the treatment of acute and chronic hypertension. The research workgenerally focuses on the solubility enhancement, increasing dissolution behavior, flowability and compressibility of the drug. Tablets and capsule are the solid dosage form mostly used. Spherical agglomerates of Candesartan cilexetil were prepared. Candesartan cilexetil water insoluble drug was used. With the incorporation of polymer, Agglomerates of such drug was prepared. Fast dissolving tablet was prepared and evaluated. Evaluation parameter like FTIR, DSC was carried out. Precompression parameters like bulk density, tap density, angle of repose, compressibility index was carried out. Post compression parameters like friability, hardness, thickness, disintegration time, wetting time was carried out and evaluated. Effect of different disintegrant like Crospovidone, cross carmellose sodium was studied. From in vitro study it was found that cross carmellose sodium containing batch F3 shows better drug release so it shows enhanced dissolution rate while if cross carmellose sodium level increases thus decreasing their dissolution rate.

Keywords

FTIR, DSC, Disintegrates, Dissolution rate etc.
Subscription Login to verify subscription
User
Notifications
Font Size


  • Nikam SP, A Review: Increasing Solubility Of Poorly Soluble Drugs, By Solid Dispersion Technique. Research Journal Of Pharmacy And Technology, 2011; 4(12), 1933-1940.
  • Chauhan NN, Patel NV, Suthar SJ, Patel JK, Patel MP. Micronization Of BCS-II Drugs By Various Approaches For Solubility Enhancement-A Review. Research Journal Of Pharmacy And Technology, 2012; 5(8), 999-1005
  • Pardhi D, Shivhare U, Suruse P, Chabra G. Lquisolid Technique For Solubility Enhancement Of Poorly Water Soluble Drugs. Research Journal Pharmaceutical Dosage Forms And Technology, 2010; 2(5), 314-322.
  • Janika Garg, Sadhna Khatry, Sandeep Arora, Spherical Crystallization: An Overview, International Journal of Pharmacy and Technology, 2012; 4 (1), 1909-1928.
  • Panchal Hardik K, Mrs. Kinjal Sanghvi, A Review On Spherical Agglomeration For Improvement Of Micromeritic Properties And Solubility, International Journal of Pharmaceutical Research And Bio-Science , 2014; 3(2), 570-579.
  • E. Hari Krishna, V. Rama Mohan Gupta, N. SoubiaSamreen And S. Jyothi, Modification Of Drug Particle Morphology By Spherical Crystallization Technique To Obtain Directly Compressible Material, Pelagia Research Library, Der Pharmacia Sinica, 2013; 4 (1),77-87.
  • Pradnya Patil, Gupta V.R.M., Udupi R.H., Spherical Agglomeration Direct Tabletting Technique, International Research Journal of Pharmacy, 2011; 2 (11), 30-35.
  • Mudit Dixit, P. K. Kulkarni, Ashwini G. Kini and Akash Johri,Spherical agglomerates of mefenamic acid by Solvent change method, An International Journal of Pharmaceutical Sciences, 2011; 2(2), 111-125
  • P. K. Kulkarni, Mudit Dixit, Ashwini G Kini And M.Karthik, Preparation And Characterization Of Spherical Agglomerates Of Ibuprofen By Solvent Change Method, Scholars Research Library, Der Pharmacia Letter, 2010; 2 (5), 289-301.
  • E. Hari Krishna, V. Rama. Mohan Gupta, Mohan Krishna, Preparation and evaluation of sodium CMC zaltoprofen spherical agglomerates for direct compression, Journal of Pharmacy Research, 2013; 6, 61-67.
  • C.P. Jain And P.S. Naruka, Formulation And Evaluation Of Fast Dissolving Tablet Of Valsartan, International Journal Of Pharmacy and Pharmaceutical Sciences, 2009; 1(1), 219-226.
  • Manish R. Bhise, Sandip B. Sapkal, Mahesh B. Narkhede. Formulation And Evaluation Of Intraorally Fast Dissolving Tablet Of Olmesartan Medoxomil. Scholars Research Library Der Pharmacia Lettre,2013; 5 (1):232-237.
  • Vishal Dhiman, Gaurav Jain, Vaibhav Jagtap, R.V.Sheorey. Formulation and In-Vitro evaluation of fast dissolving tablets of Telmisartan. International Journal Of Pharmacy and Life Sciences. 2012; 3(11), 2159-2164
  • K. Kranthi Kumar, L. Srinivas, V. Sai Kishore, S. Naseeb Basha, Formulation and evaluation of poorly soluble Febuxostat orodispersible tablet, American Journal of Advanced Drug Deliver, 2014; 2(2), 191-202.
  • Rahul Dass, Sandhya Jaiswal, G.D Gupta. Formulation and evaluation of Febuxostat fast disintegrating tablet. Indo American Journal of Pharmaceutical Research, 2014; 4(6), 2928-2936.

Abstract Views: 119

PDF Views: 0




  • Formulation and Assessment of Quick Dissolving Tablet of Candesartan Cilexetil Arranged from Their Circular Agglomerates

Abstract Views: 119  |  PDF Views: 0

Authors

Swapnil Shankar Patil
Assistant Professor, Annasaheb Dange College of B. Pharmacy, Ashta. 416301, Maharashtra., India
Shashikant Sudarshan Upadhye
Head of Department, Annasaheb Dange College of B. Pharmacy Ashta. Ashta: 416301, Maharashtra., India

Abstract


Candesartan cilexetil is water insoluble drug which comes under BCS class second category. Drug was used in the treatment of acute and chronic hypertension. The research workgenerally focuses on the solubility enhancement, increasing dissolution behavior, flowability and compressibility of the drug. Tablets and capsule are the solid dosage form mostly used. Spherical agglomerates of Candesartan cilexetil were prepared. Candesartan cilexetil water insoluble drug was used. With the incorporation of polymer, Agglomerates of such drug was prepared. Fast dissolving tablet was prepared and evaluated. Evaluation parameter like FTIR, DSC was carried out. Precompression parameters like bulk density, tap density, angle of repose, compressibility index was carried out. Post compression parameters like friability, hardness, thickness, disintegration time, wetting time was carried out and evaluated. Effect of different disintegrant like Crospovidone, cross carmellose sodium was studied. From in vitro study it was found that cross carmellose sodium containing batch F3 shows better drug release so it shows enhanced dissolution rate while if cross carmellose sodium level increases thus decreasing their dissolution rate.

Keywords


FTIR, DSC, Disintegrates, Dissolution rate etc.

References