Design of fast dissolving tablet of Atenolol using novel co-processed superdisintegrant

Asian Journal of Pharmaceutical and Clinical Research

Volumn 6, Issue 3, 2013, Pages 81-85

  Kumare, Mangesh M ^a   Marathe, Rajendra P ^a   Kawade, Rajendra M ^b   Ghante, Mahavir H ^b   Shendarkar, Giridhar R ^b  

^a GOVERNMENT COLLEGE OF PHARMACY   (India)

^b Nanded Pharmacy College   (India)

Author keywords

Atenolol; Co processed Superdisintegrants; Croscarmellose sodium; Crospovidone; Fast dissolving tablet

Indexed keywords

ATENOLOL; CO PROCESSED DISINTEGRANT; CROSCARMELLOSE SODIUM; CROSPOVIDONE; DISINTEGRATING AGENT; UNCLASSIFIED DRUG;

ANGLE OF REPOSE; ARTICLE; CARR INDEX; CHEMICAL PARAMETERS; CONTROLLED STUDY; COST EFFECTIVENESS ANALYSIS; DISPERSION; DOSAGE SCHEDULE COMPARISON; DRUG DESIGN; DRUG RELEASE; DRUG SOLUBILITY; FAST DISSOLVING TABLET; HAUSNER RATIO; TABLET; TABLET COMPRESSION; TABLET DISINTEGRATION TIME; TABLET DRUG CONTENT; TABLET FORMULATION; TABLET FRIABILITY; TABLET HARDNESS; TABLET PROPERTY; TABLET THICKNESS; TABLET WATER ABSORPTION RATIO; TABLET WEIGHT VARIATION; TABLET WETTING TIME;

EID: 84879931462     PISSN: 09742441     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (25)

1. Government of India Ministry of Health and Family Weifare. The Pharmacopoeia of India. Delhi: India: Controller of Publication; 1996.
2. Roden DM. Antiarrhythmic Drugs, In: Goodman and Gilman's The Pharmacology Basis of Therapeutics. 10th ed., Mc Graw Hill Medical Publishing Division; New York; 2006. p. 949-950.
3. Ranch KM, Koli AR, Vyas BA, Parikh RK, Vyas RB, Maniyar N. International Journal of PharmTech Research. 2009; 1:4: p.1559-1563.
4. The United States Pharmacopoeial Convention Inc., USP; 27-NF; 2002: p.177-180.
5. Alfred Martin. Physical Pharmacy. 4th ed. Philadelphia: Lippincott Williams and Wilkins: 1993.
6. York P. Crystal engineering and particle design for the powder compaction process. Drug Dev Ind Pharm. 1992; 18: 6, 7: p. 677-721.
7. Block LH et al. Co-processed excipients. Pharmacopeial forum. 2009; 35:4: p.1026-1028.
8. Avachat A, Ahire VJ. Characterization and evaluation of spray dried co-processed Excipients and their application in solid dosage forms. Indian J Pharm Sci. 2007; 69:1: p. 85-90.
9. Reimerdes D. The near future of tablet excipients. Manuf chem. 1993; 64: p.14-5.
10. Michoel P, Rombaut A. Verhoye. Comparative evaluation of co-processed lactose and microcrystalline cellulose with their physical mixtures in the formulation of folic acid tablets. Pharm. Dev. Technol. 2002; 7: p.79-87.
11. Rowe RC, Sheskey PJ, Weller PJ. Handbook of pharmaceutical excipients, 4th Edn. Washington, DC: American Pharmaceutical Association, London. Pharmaceutical Press. 2003; p.184-185.
12. Takao M, Yoshinori M, Muneo F. Intrabuccally dissolving compressed mouldings and production process thereof. US patent. 1996; 5: 576: 014.
13. Bankar GS, Anderson NR. Tablets. In: Lachman L, Lieberman HA, Kanig JL, editor. The theory and practice of industrial pharmacy. 3rded. Mumbai: Varghese Publishing House; 1987.p.293-99.
14. Indian Pharmcopoeia: New Delhi: Controller of Publication, Government of India; 1996. p. 735-736.
15. United States of Pharmacopeia-National Formulary, USP 30-NF 25. MD: The Unit States Pharmacopeial Convention Rockville.2007; 1: p.644,242, 645, 731 and 634.
16. Debjit B, Chiranjib B, Krishnakant, Pankaj, Margret RC. Fast dissolving tablet: An overview. J chem and pharma Res. 2009; 1:1: p.163-177.
17. Azharuddin M, Kamath K, Panneerselvam T, Pillai SS, Shabaraya AR. Formulation and evaluation of controlled release matrix tablets of antihypertensive drug using natural and synthetic Hydrophilic polymers. Res in Biotech. 2011; 2:4: p. 26-32.
18. Manivannan R. Oral disintegrating tablets: A future compaction. Drug Invention Today 2009; 1:1: p. 61-65.
19. Liberman, HA, Lachman L, Schwartz JB. Pharmaceutical dosage forms: Tablets volume-2. Marcel dekker: New York: 2005: p.165-7.
20. Gun CJ, Carter SJ. Powder Flow and Compaction. CBS publication; New Delhi: 1986: p.211-33.
21. Sinko PJ. Martin's Physical pharmacy and pharmaceutical sciences; Lippincott Williams and Wilkins: New York: 2006: p.557.
22. Shirsand SB, Ramani RG, Swami PV. Novel co-processed superdisintegrants in the design of fast dissolving tablets. Int J pharm & Bio Sci. 2010; 1:1: p.1-12.
23. Kumar M, Visth S, Sazid A, Agarwal S, Bhola A. Preparation and evaluation of fast dissolving drug delivery system Containing levocetrizine HCl. Int J Pharm & Pharm Sci. 2010; 2:3: p.109-111.
24. Patel B, Patel C, Serasiya T, Sanja SD. Development and in vitro evaluation of fastdissolving tablets of glipizide. Int J Pharm & Pharm Sci. 2009; 1:1: p.145-150.
25. Chandile GK, Kumar JA, Kakde SM, Rajasekar S, Jadhav RT. Development and evaluation of haloperidol orally disintegrating tablet using novel coprocessed superdisintegrants. Int J Pharm & Pharm Sci. 2011; 2:3: p.348-352.