ENHANCEMENT OF GLIBENCLAMIDE DISSOLUTION RATE BY SOLID DISPERSION METHOD USING HPMC AND PVP

Authors

  • ARIF BUDIMAN Department of Pharmaceutical and Technology Pharmacy, Faculty of Pharmacy, Universitas Padjadjaran
  • IYAN SOPYAN Department of Pharmaceutical and Technology Pharmacy, Faculty of Pharmacy, Universitas Padjadjaran
  • DENIA SEPTY RIYANDI Department of Pharmaceutical and Technology Pharmacy, Faculty of Pharmacy, Universitas Padjadjaran

DOI:

https://doi.org/10.22159/ijap.2019v11i5.34137

Keywords:

Dissolution Rate, Glibenclamide, Solid Dispersion, HPMC, PVP

Abstract

Objective: The aim of this study was to investigate the effects of changing in the proportions of the solid dispersion formula on the dissolution rate of glibenclamide.

Methods: Solid dispersions were prepared by solvent evaporation method by using methanol as solvent, hydroxypropyl methylcellulose (HPMC) and polyvinyl pyrrolidone (PVP) as polymers. The prepared product was evaluated by the saturated solubility test and the dissolution rate test. The prepared product was characterized by Fourier transform infrared spectroscopy (FT-IR), differential scanning calorimetry (DSC), and powder X-ray diffraction (PXRD) and Scanning Electron Microscopy (SEM).

Results: The result showed solid dispersion with a ratio of glibenclamide: PVP: HPMC (1: 3: 6) has the highest increase in solubility (20 fold) compared to pure glibenclamide. This formula also showed an improvement in dissolution rate from 19.9±1.19% (pure glibenclamide) to 99±1.60% in 60 min. Characterization of FT-IR showed that no chemical reaction occurred in solid dispersion of glibenclamide. The results of X-ray diffraction analysis showed an amorphous form in all solid dispersion formulas. The results of DSC analysis showed that endothermic peak melting point of solid dispersion occurred, and the morphology of solid dispersion was more irregular than pure glibenclamide based on SEM characterization

Conclusion: The solid dispersion of glibenclamide using PVP: HPMC as carriers can increase the solubility and dissolution rate compared to pure glibenclamide.

Downloads

Download data is not yet available.

References

Chaturvedi AK, Amita V. Solubility enhancement of poorly water soluble drugs by solid dispersion. Int J Pharm Sci Rev Res 2012;3:26-34.

Hu J, Johnston KP, Williams RO. Nanoparticle engineering processes for enhancing the dissolution rates of poorly water soluble drugs. Drug Dev Ind Pharm 2004;30:233-45.

Yalkowsky SH, Dannenfelse RM. Aquasol database of aqueous solubility. Arizona: College of Pharmacy, University of Arizona, Tucson; 1992. p. 189.

Kumar A, Bali V, Kumar M, Pathak K. Comparative evaluation of porous versus nonporous mucoadhesive films as buccal delivery system of glibenclamide. AAPS PharmSciTech 2013;14:1321-32.

Khadka P, Ro J, Kim H, Kim I, Kim JT, Kim H, et al. Pharmaceutical particle technologies: an approach to improve drug solubility, dissolution and bioavailability. Asian J Pharm Sci 2014;9:304-16.

Vojinovic T, Medarevic D, Vranic E, Potpara Z, Krstic M, Djuris J, et al. Development of ternary solid dispersions with hydrophilic polymer and surface adsorbent for improving dissolution rate of carbamazepine. Saudi Pharm J 2018;26:725-32.

Craig DQ. The mechanism of drug release from solid dispersions in water-soluble polymers. Int J Pharm 2002;231:131-44.

Sangeetha E, Rao VU, Sudhakar M, Manisha S. Enhancement of solubility and bioavailability of hydrochlorthiazide using solid dispersion technique. Am J Adv Drug Delivery 2015;3:308-16.

Suzuki H, Sunada H. Influence of water-soluble polymers on the dissolution of nifedipine solid dispersions with combined carriers. Chem Pharm Bull 1998;46:482-7.

Singh D, Dua JS, Prasad DN. Formulation and evaluation of glibenclamide tablet using solid dispersion with various polymer. Asian J Pharm Res Dev 2018;6:81-6.

Sharma A, Jain CP. Preparation and characterization of solid dispersions of carvedilol with PVP K30. Res Pharm Sci 2010;5:49-56.

Bari A, Chella N, Sanka K, Shastri NR, Diwan PV. Improved anti-diabetic activity of glibenclamide using oral self nano emulsifying powder. J Microencapsul 2015;32:54-60.

Dora CP, Singh SK, Kumar S, Datusalia AK, Deep A. Development and characterization of nanoparticles of glibenclamide by solvent displacement method. Acta Pol Pharm Drug Res 2010;67:283-90.

Budiman A, Megantara S, Raraswati P, Tazyinul QA. Solid dosage form development of glibenclamide with increasing the solubility and dissolution rate using cocrystallization. Int J Appl Pharm 2018;10:181-6.

Ohyagi N, Ueda K, Higashi K, Yamamoto K, Kawakami K, Moribe K. Synergetic role of hypromellose and methacrylic acid copolymer in the dissolution improvement of amorphous solid dispersions. J Pharm Sci 2017;106:1042-50.

Vinesha V, Sevukarajan M, Rajalakshmi R, Chowdary GT, Haritha K. Enhancement of solubility of tadalafil by cocrystal approach. Int Res J Pharm 2016;4:218-23.

Fitriani L, Haqi A, Zaini E. Preparation and characterization of solid dispersion freeze-dried efavirenz–polyvinylpyrrolidone K-30. J Adv Pharm Technol Res 2016;7:105-9.

Budiman A, Khoerunnisa R, Tazyinul QA. Wound-healing test of piper betle leaf extract and aloe vera in gel preparation. Int J Appl Pharm 2018;10:86-91.

Tachibana T, Nakamura A. Method for preparing an aqueous colloidal dispersion of organic materials by using water-soluble polymers: dispersion of beta-carotene by polyvinylpyrrolidone. Colloid Polym Sci 1965;203:130-3.

Singh S, Baghel RS, Yadav L. A review on solid dispersion. Int J Pharm Life Sci 2011;2:1078-95.

Chiou W, Riegelman S. Pharmaceutical applications of solid dispersion systems. J Pharm Sci 1971;60:1281–302.

Douroumis D, Bouropoulos N, Fahr A. Physicochemical characterization of solid dispersions of three antiepileptic drugs prepared by solvent evaporation method. J Pharm Pharm 2007;59:645-53.

Mishra MK, Ray D, Barik BB. Microcapsules and transdermal patch: a comparative approach for improved delivery of antidiabetic drug. AAPS PharmSciTech 2009;10:928-34.

Gracin S, Rasmuson AC. Solubility of phenylacetic acid, p-hydroxyphenylacetic acid, p-aminophenylacetic acid, p-hydroxy-benzoic acid, and ibuprofen in pure solvents. J Chem Eng 2002;47:1379-83.

Augustjins P, Brewster ME. Biotechnology: pharmaceutical aspect solvent systems and their selection in biopharmaceutics. 6th ed. New York: AAPS Press; 2007.

El Maghraby GM, Elsergany RN. Fast disintegrating tablets of nisoldipine for intra-oral administration. Pharm Dev Technol 2014;19:641-50.

Elbary AA, Salem HF, Maher ME. In vitro and in vivo evaluation of glibenclamide using surface solid dispersion (SSD) approach. Br J Pharm Toxic 2011;2:51-62.

Published

07-09-2019

How to Cite

BUDIMAN, A., SOPYAN, I. ., & RIYANDI, D. S. . (2019). ENHANCEMENT OF GLIBENCLAMIDE DISSOLUTION RATE BY SOLID DISPERSION METHOD USING HPMC AND PVP. International Journal of Applied Pharmaceutics, 11(5), 19–24. https://doi.org/10.22159/ijap.2019v11i5.34137

Issue

Section

Original Article(s)

Most read articles by the same author(s)

1 2 3 4 > >>