ijddr

International Journal of Drug Development and Research

ISSN - 0975-9344

- (2011) Volume 3, Issue 2

A NEW BINARY POLYMERIC MATRIX SYSTEM FOR SUSTAINED RESEASE DRUG DELIVERY OF HIGHLY SOLUBLE DRUG: DILTIAZEM HYDROCHLORIDE

 

Author info »

Abstract

The major objective of this study was to use pectin (high methoxylated) in combination with guar gum to control the burst effect by promoting gelation and also to examine the release pattern of guar-pectin matrices. Guar gum has long been used to prepare matrix tablets. But its uncontrolled rate of hydration and initial slow gelling results into undesirable burst effect. Various combination of drug: polymer ratios were tried, out of which the ratio 1:2 yielded best results. The ratio of gaur: pectin in the polymer blend which gave best results was found to be 1:1.The effects of various diluents on the drug release were also determined at the same polymer level. The matrix tablet were prepared by wet granulation method using distilled water, were subjected to physical characterization and in vitro release studies. Release kinetics was evaluated by using USP apparatus type II at 100 rpm in 900 ml of acidic dissolution medium ( pH 1.2) for two hours, followed by 900 ml phosphate buffer dissolution medium (pH 6.8).The in-vitro drug release study revealed that (batch F3) combining pectin with guar gum sustained the drug release for 10 hours (87.54±2.36% release). Fitting the in-vitro drug release data to Korsmeyer-Peppas equation indicated that diffusion along with erosion could be the mechanism of drug release. At the same polymer level the order of release fell in the following manner lactose, avicel pH 101, starch and Emcompress®. It was concluded from the study that guar-pectin binary polymeric matrix system is an interesting alternative for preparing sustained release tablets.

References

  1. Gambhire MN, Ambade KW, Kurmi SD, Kadam VJ, Jadhav KR. Development and in vitro evaluation of an oral floating matrix tablets formulation of diltiazem hydrochloride. AAPS Pharm Sci Tech., 2007; 8(3): E1-E9.
  2. Kim H, Fassihi RA. A new ternary polymeric matrix system for controlled drug delivery of highly soluble drug: diltazem hydrochloride. Pharm.Res., 1997; 29: 1415-1421.
  3. Smith MS, Vergese CP, Shand DG, Pritchett EL. Pharmacokinetic and pharmacodynamic effects of diltazem. Am. J. Cardiol., 1983; 51: 1369-1374.
  4. Tiwari SB, Murthy SK, Pai MR, Mehta PR, Chowdary PB. Controlled release formulation of tramadol hydrochloride using hydrophilic and hydrophobic matrix system. AAPS Pharm Sci Tech., 2003, 4(3): Article 31.
  5. Heller J, helwing RW, Baker RW, Tuttle ME. Controlled release of water soluble macromolecules from bioerodible hydrogel. Biomaterials 1983; 4: 262-266.
  6. Graham NB, Mcneill ME. Hydrogels for controlled drug delivery. Biomaterials 1984; 5: 27-36.
  7. Bhardwaj TR, Kanwar M, Lal R, Gupta A. Natural gums and modified natural gums as sustained release carriers. Drug Dev Ind Pharm. 2000; 26(10): 1025-1038.
  8. Sungthongjeen S, Pitaksuteepong T, Somsiri A, Sriamornsak P. Studies on pectins as potential hydrogel matrices for controlled release drug delivery. Drug Dev Ind Pharm. 1999; 25(12): 1271- 1276.
  9. Nakano M, Ogata A. Examination of natural gums as matrices for sustained release of theophyline. Chem. Pharm. Bull., 1984; 32: 782785.
  10. Mishra AN, Baweja JM. Modified guar gum as hydrophilic matrix for controlled release tablets. Indian Drugs 1997; 34: 216-223.
  11. Duru C, Colombo P, Gaudy D, Massimo G, Barthelemy P. Comparative study of the disintegrating efficiency of polysaccharides in a directly tabletable formulation. Pharmaceut Technol Int 1992; 4:15-16, 20, 22-23.
  12. Baweja JM, Misra AN. Modified guar gum as a tablet disintegrant. Pharmazie 1997; 52:856-859.
  13. Indian pharmacopoeia, Vol. II, 4th edition, the controller of publication, New Delhi, 1996:734-736.
  14. Chang R, Robinson JR. Sustained release from tablets and particles through coatin. In: Libreman HA, Lachman L, Schwartz JB (Eds). Pharmaceuticals dosage form tablets. 2nd Edn, Vol.3, Marcel Dekker; 1990: 199-302.
  15. Nokano M, Ogata A. In vitro release characteristics of matrix tablets: Study of karaya gum and guar gum as release modulators. Ind J Pharm Sci., 2006; 68(6): 824-826.
  16. Sharma YR. Elementary Organic Spectroscopy Principles and Chemical applications, S, Chand and Co., New Delhi. 2005; 65-133.
  17. Korsemeyer RW, Gurny R, Doelker E, Buri P, Peppas NA. Mechanism of solute release from porous hydrophilic polymers. Int J Pharm. 1983; 15: 25-35.
  18. Siemann J, Peppas NA. Modeling of drug release from delivery system based on hydroxylpropyl methylcellulose (HPMC). Adv Drug Deli Rev. 2001; 48: 139-157.
  19. Mathews BR. Regulatory aspects of stability testing in Europe. Drug Dev Ind Pharm.1999; 25: 831-856.

Author Info

 

Copyright:This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.