Formulation of sustained-release matrix tablets using cross-linked karaya gum

Tropical Journal of Pharmaceutical Research

Volumn 11, Issue 2, 2012, Pages 185-192

  Reddy, Mahesh M ^a   Reddy, Jagadeeswara D ^a   Moin, Afrasim ^a   Shivakumar, H G ^a  

^a JSS COLLEGE OF PHARMACY   (India)

Author keywords

Diltiazem hydrochloride; Karaya gum; Matrix tablets sustained release; Tri sodium tri metaphosphate

Indexed keywords

CROSS LINKING REAGENT; DILTIAZEM; KARAYA GUM; TRISODIUM TRIMETAPHOSPHATE; UNCLASSIFIED DRUG;

ARTICLE; CONTROLLED DRUG RELEASE; CONTROLLED STUDY; CROSS LINKING; DEGRADATION KINETICS; DIFFERENTIAL SCANNING CALORIMETRY; DIFFUSION; DRUG DOSAGE FORM COMPARISON; DRUG SOLUBILITY; EXCIPIENT COMPATIBILITY; IN VITRO STUDY; INFRARED SPECTROSCOPY; MATRIX TABLET; MEAN DISSOLUTION TIME; SCANNING ELECTRON MICROSCOPY; SURFACE PROPERTY; SUSTAINED RELEASE FORMULATION; TABLET COMPRESSION; TABLET EROSION; TABLET PROPERTY; WATER TRANSPORT;

EID: 84859994942     PISSN: 15965996     EISSN: 15969827     Source Type: Journal    
DOI: 10.4314/tjpr.v11i2.3     Document Type: Article

References (20)

1. Viriden A, Wittgren B, Larsson A. Investigation of critical polymer properties for polymer release and water uptake of HPMC matrix tablets. Eur J Pharm Sci 2009; 36: 297-309.
2. Hiremath PS, Saha RN. Controlled Release Hydrophilic Matrix Tablet Formulations of Isoniazid: Design and In Vitro Studies. AAPS PharmSciTech 2008; 9(4): 1171-1178.
3. Bhardwaj TR, Kanwar M, Lal R, Gupta A. Natural gums and modified natural gums as sustainedrelease carriers. Drug Dev Ind Pharm 2000; 26(10): 1025-1038.
4. Coviello T, Matricardi P, Marianecci C, Alhaique F. Polysaccharide hydrogels for modified release formulations. J Control Release 2007; 119: 5-24.
5. Weiping W. Tragacanth and karaya, in: Philips GO, Williams PA (Eds.). Handbook of Hydrocolloids. Woodhead, Cambridge; 2000; p 155.
6. Meier P, Seiler WO, Stahelin HB. Bulk-forming agents as laxatives in geriatric patients. Schweiz Med. Wochenschr. 1990; 120(9): 314-321.
7. Park CR, Munday DL. Evaluation of selected polysaccharide excipients in buccoadhesive tablets for sustained release of nicotine. Drug Dev. Ind. Pharm. 2004; 30(6): 609.
8. Verbeken D, Dierckx S, Dewettinck K. Exudate gums: occurrence, production, and applications. Appl Microbiol Biotechnol 2003; 63(1): 10-21.
9. Wurzburg OB, in: Wurzburg OB (Eds.). Modified Starches: Properties and Uses. CRC Press Boca Raton, Florida; 1986; pp 42-52.
10. Gliko-Kabir I, Yagen B, Penhasi A, Rubinstein A. Phosphated crosslinked guar for colon-specific drug delivery: I. Preparation and physicochemical character. J Control Release 2000; 63: 121-129.
11. Dulong V, Lack S, Le Cerf D, Picton L, Vannier JP, Muller G. Hyaluronan-based hydrogels particles prepared by crosslinking with trisodium trimetaphosphate. Synthesis and characterization. Carbohydr Polym, 2004; 57: 1-8.
12. Gambhire MN, Ambade KW, Kurmi SD, Kadam VJ, Jadhav KR. Development and in vitro evaluation of an oral floating matrix tablet formulation of diltiazem hydrochloride. AAPS PharmSciTech 2007; 8(3): E1-E9.
13. Afrasim Moin, HG Shivakumar. Formulation of Sustained-Release Diltiazem Matrix tablets Using Hydrophilic Gum Blends. Trop J Pharm Res, 2010; 9 (3): 283-291.
14. Government of India Ministry of Health and Family Welfare; The Pharmacopoeia of India 1996, Volume II; New Delhi; Controller of Publication; p. 734-736.
15. Varshosaz J, Tavakoli N, Kheirolahi F. Use of hydrophilic natural gums in formulation of sustained-release matrix tablets of tramadol hydrochloride. AAPS PharmSciTech 2006; 7(1): E1-E7.
16. Durig T, Fassihi R. Guar-based monolithic matrix systems: effect of ionizable and non-ionizable substances and excipients on gel dynamics and release kinetics. J Control Release 2002; 80: 45-56.
17. Kuksal A, Tiwary AK, Jain NK, Jain S. Formulation and in vitro, in vivo evaluation of extendedrelease matrix tablet of zidovudine: influence of combination of hydrophilic and hydrophobic matrix formers. AAPS PharmSciTech 2006; 7(1): E1-E9.
18. Costa P, Sousa Lobo JM, Gohel MC, Panchal MK. Modeling and comparison of dissolution profiles. Eur J Pharm Sci 2001; 13(2): 123-133.
19. Chandran S, Ravi R, Saha RN. Development and In vitro Evaluation of Oral Controlled Release Formulations of Celecoxib Using Optimization Techniques. Yakugaku zasshi 2006; 126(7): 505-515.
20. Sujja-areevath J, Munday DL, Cox PJ, Khan KA. Relationship between water uptake, erosion and drug release in hydrophillic natural gum mini-matrix formulations. Eur J Pharm Sci 1998; 6: 207-217.