Evaluation of various natural gums as release modifiers in tablet formulations

Pharmacognosy Journal

Volumn 2, Issue 13, 2010, Pages 525-529

  Srivastava, Pranati ^a   Malviya, Rishabha ^a   Gupta, Sumedha ^a   Sharma, Pramod Kumar ^a  

^a MEERUT INSTITUTE OF ENGINEERING AND TECHNOLOGY   (India)

Author keywords

Diclofenac sodium; Guar gum; Gum acacia; Sustained release matrix tablets

Indexed keywords

DICLOFENAC; GUAR GUM; GUM ARABIC; MICROCRYSTALLINE CELLULOSE; POLYMER;

ARTICLE; CONTROLLED DRUG RELEASE; DRUG CONTENT; DRUG DOSAGE FORM COMPARISON; MATRIX TABLET; PH; SUSTAINED RELEASE FORMULATION; TABLET FORMULATION; TABLET FRIABILITY; TABLET HARDNESS; TABLET PROPERTY; TABLET THICKNESS; TABLET WEIGHT;

EID: 78650668862     PISSN: 09753575     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0975-3575(10)80055-0     Document Type: Article

References (26)

1. Mishra B, Seena J, Singh S, Sankar C. Development and characterization of matrix tablets of ketorolac tromethamine. Indian Pharm. 2003; 2: 86-9.
2. Ansel HC, Loyyd VA. Pharmaceutical dosage forms and drug delivery systems. Lippincott's Williams and Wilking, Hong Kong.1999; 8: 275-80.
3. Malviya R, Srivastava P, Bansal M, Sharma PK. Formulation and optimization of sustained release tablets of diclofenac sodium using guar gum as release modifier. Int J Pharm Sci Res. 2010; 1(6): 82-8.
4. Langer RS, Peppas NA. Present and future application of biomaterials in controlled drug delivery systems. Biomaterials. 1981; 2(10): 201-13.
5. Arthur HK. Handbook of Pharmaceutical Excipients. 3rd ed. American Pharmaceutical Association, London. 2000; 271, 297, 463-4.
6. Malviya R, Srivastava P, Bansal M, Sharma PK. Formulation, evaluation and comparision of sustained release matrix and tablets of diclofenac sodium using tamarind gum as release modifier. Asian J Pharm Clin Res. 2010; 3(3).
7. Nandi RC. A Process for preparation of polyose from the seeds of Tamarindus indica. Indian Patent 1975; 142092.
8. Kulkarni D, Ddwivedi DK, Sarin JPS, Singh S. Tamarind seed polyose: A potential polysaccharide for sustained release of verapamil hydrochloride as a model drug. Indian J Pharm Sci. 1997; 59(1): 1-7.
9. Indian Pharmacopoeia. Ministry of Health. The Controller of Publications, New Delhi, 1996; 4 ed: 432.
10. Harland RS, Gazzaniga A, Sanagalli ME, et al. Drug/polymer matrix swelling and dissolution. Pharm. Res. 1988; 5: 488-94.
11. Peppas NA, Sahlin JJ. A simple equation for the description of sustained release. III Coupling of diffusion and relaxation. Int. J. Pharm. 1989; 57: 169-72.
12. Lee PL, Kim CJ. Probing the mechanism of drug release from hydrogels. J. Control. Release. 1991; 16: 229-36.
13. Reynolds TD, Gehrke SH, Hussain AS, et al. Polymer erosion and drug release characterization of hydroxypr opylmethylcellulose matrices. J. Pharm. Sci. 1998; 87: 1115-23.
14. Sujja-areevath J, Munday DL, Cox PJ, Khan KA. Release characteristics of diclofenac sodium from encapsulated natural gum mini-matrix formulations. Int J Pharm. 1996; 139: 53-62.
15. Nokano M, Ogata A. In vitro release characteristics of matrix tablets: Study of Karaya gum and Guar gum as release modulators. Indian J Pharm Sci. 2006; 68(6): 824-26.
16. Gwen MJ, Joseph RR, Rhodes CT. Modern Pharmaceutics, Marcel Dekker, Inc, New York. 1996; 72(3): 581.
17. USP30-NF25, The official compendium of standards. The United States Pharmacopoeial Convention, 2007.
18. Malviya R, Srivastava P, Bansal V, Sharma PK. Formulation, Evaluation and Comparison of Sustained Release Matrix Tablets of Diclofenac Sodium Using Natural Polymers as Release Modifiers. Int J Pharm Biosci. 2010; 1(2): 1-8.
19. Malviya R, Srivastava P, Bansal M, Sharma PK. Preparation and Evaluation of Disintegrating Properties of Cucurbita Maxima Pulp Powder. Int J Pharm Sci. 2010; 2(1): 395-9.
20. Krishnaiah YSR, Rama Rao T, Ushasree M, Satyanarayana S. A study on the in vitro evaluation of guar gum as a carrier for oral controlled drug delivery. Saudi Pharm J. 2001; 9: 91-8.
21. Sujja-areevath J, Munday DL, Cox PJ, Khan KA. Relationship between swelling, erosion and drug release in hydrophilic natural gum mini-matrix formulations. Eur J Pharm Sci. 1998; 6: 207-17.
22. Abrahamsson B, Alpsten M, Bake B, Larsson A, Sjogren J. In vitro and in vivo erosion of two different hydrophilic gel matrix tablets. Eur J Pharm Biopharm. 1998; 46: 69-75.
23. Yeole PG, Galgatte UC. Design & evaluation of xanthan gum based sustained release matrix tablets of diclofenac sodium, Indian J Pharm Sci. 2006; 185-89.
24. Ei-Arini SK, Leuenberger H. Modelling of drug release from polymer matrices: Effect of drug loading. Int J Phar. 1995; 121: 141-48.
25. Ritger PL, Peppas NA. A simple equation for description of solute release II Fickian and anomalous from swellable devices. J Control Release.1987; 5: 37-42.
26. Munday DL, Cox PJ. Compressed xanthan and karya gum matrices: hydration, erosion and drug release mechanisms. Int J Pharm. 2000; 203: 179-82.