FORMULATION AND CHARACTERIZATION OF HPMC AND HPMCAS BASED SOLID DISPERSIONS OF FENOFIBRATE: A COMPARATIVE STUDY

Authors

  • Ankit Rampal Department of Pharmaceutical Sciences, Guru Nanak Dev University, Amritsar, Punjab, India (143005)
  • Manmeet Singh Department of Pharmaceutical Sciences, Guru Nanak Dev University, Amritsar, Punjab, India (143005)
  • Shanta Mahajan Department of Pharmaceutical Sciences, Guru Nanak Dev University, Amritsar, Punjab, India (143005)
  • Neena Bedi Department of Pharmaceutical Sciences, Guru Nanak Dev University, Amritsar, Punjab, India (143005)

DOI:

https://doi.org/10.22159/ijap.2019v11i4.32592

Keywords:

Solubility, HPMC, HPMCAS, Solid dispersions, Crystallinity

Abstract

Objective: The aim of the present study was to investigate the effect of novel polymeric carriers and to develop solid dispersion formulation that could improve in vitro profile of Fenofibrate (FB).

Methods: Spray drying technique was used to fabricate solid dispersions with hydrophilic carriers, mainly hydroxypropyl methylcellulose (HPMC) and hydroxypropyl methylcellulose acetate succinate (HPMCAS). Solid dispersions in the form of spray-dried powder were characterized with respect to the pure drug and the corresponding physical mixtures by optical microscopy, x-ray diffraction (XRD), fourier transform infrared (FT-IR) spectroscopy and differential scanning calorimetry (DSC). Size and morphology of optimized solid dispersion were performed by scanning electron microscopy (SEM). Furthermore, in vitro dissolution comparisons were carried out between the optimized solid dispersion against the pure drug and the physical mixtures.

Results: Solubility studies demonstrated that the solubility of FB was not affected by pH change. The transformation of crystalline FB into an amorphous solid dispersion powder has been clearly demonstrated by optical microscopy. The molecular dispersion of drug in the dispersion matrix prepared by spray drying was confirmed in XRD and DSC studies. IR spectroscopy was observed with negligible incompatibility of the drug with polymers. Spherical morphology was observed in SEM with no evidence of FB crystals. The prepared solid dispersions exhibited dissolution improvement as compared to the pure drug and spray dried FB in 0.05 M SLS, with HPMCAS as the superior carrier over HPMC.

Conclusion: The present study vouches better in vitro profile of FB from spray-dried HPMCAS based solid dispersions.

Downloads

Download data is not yet available.

Author Biography

Neena Bedi, Department of Pharmaceutical Sciences, Guru Nanak Dev University, Amritsar, Punjab, India (143005)

Assistant Professor

References

Amidon GL, Lennernas H, Shah VP, Crison JR. A Theoretical Basis for a Biopharmaceutic Drug Classification: The Correlation of in-vitro Drug Product Dissolution and In-Vivo Bioavailability. Pharm Res 1995;12:413-20.

Pamudji JS, Wikarsa S, Tampara MH. Improvement of gliclazide’s dissolution rate by using surface solid dispersion with avicel ph 101. Int J Pharm Pharm Sci 2014;6:461-65.

Mohanty S, Pal A. Dissolution enhancement of Seroquel by solid dispersion. Asian J Pharm Clin Res 2016;9:284-87.

Nikghalb LA, Singh G, Singh G, Kahkeshan KF. Solid dispersion: methods and polymers to increase the solubility of poorly soluble drugs. J Appl Pharm Sci 2012;2:170-75.

Paudel A, Worku ZA, Meeus J, Guns S, Van den Mooter G. Manufacturing of solid dispersions of poorly water soluble drugs by spray drying: Formulation and process considerations. Int J Pharm 2013;453:253-84.

Dixit M, Rasheed A, Fijaz Rahman NC, Daniel S. Enhancing solubility and dissolution of fenofibrate by spray drying technique. Int J Pharm Pharm Sci 2015;7:173-77.

Friesen DT, Shanker R, Crew M, Smithey DT, Curatolo WJ, Nightingale JA. Hydroxypropyl methylcellulose acetate succinate-based spray-dried dispersions: an overview. Mol Pharm 2008;5:1003-19.

Tanno F, Nishiyama Y, Kokubo H, Obara S. Evaluation of hypromellose acetate succinate (HPMCAS) as a carrier in solid dispersions. Drug Dev Ind Pharm 2004;30:9-17.

Jamzad S, Fassihi R. Role of surfactant and pH on dissolution properties of fenofibrate and glipizide-A technical note. AAPS Pharm Sci Tech 2006;7:E1-E6

Khan KA, Rhodes CT. Effect of compaction pressure on the dissolution efficiency of some direct compression systems. Pharm Acta Helv 1972;47:594-607.

Costa P, Sousa Lobo JM. Modeling and comparison of dissolution profiles. Eur J Pharm Sci 2001;13:123-33.

Xie Y, Li G, Yuan Y, Cai Z, Rong R. Preparation and In Vitro Evaluation of Solid Dispersions of Total Flavones of Hippophae rhamnoides L. AAPS Pharm Sci Tech 2012;10:631-40.

Mura P, Faucci MT, Manderioli A, Bramanti G, Parrini P. Thermal behaviour and dissolution properties of naproxen from binary and ternary solid dispersions. Drug Dev Ind Pharm 1999;25:257-64.

Ghosh I, Snyder J, Vippagunta R, Alvine M, Vakil R, Tong WQ, et al. Comparison of HPMC based polymers performance as carriers for manufacture of solid dispersions using the melt extruder. Int J Pharm 2011;419:12-19.

Curatolo W, Nightingale JA, Herbig SM. Utility of hydroxypropylmethylcellulose acetate succinate (HPMCAS) for initiation and maintenance of drug supersaturation in the GI milieu. Pharm Res 2009;26:1419-31

Betageri GV, Makarla KR. Enhancement of dissolution of glyburide by solid dispersion and lyophilization techniques. Int J Pharm 1995;126:155-60.

Matsuda Y, Otsuka M, Onoe M, Tatsumi E. Amorphism and physicochemical stability of spray-dried furosemide. J Pharm Pharmacol 1992;44:627-33.

Nandiyanto ABD, Okuyama K. Progress in developing spray-drying methods for the production of controlled morphology particles: from the nanometer to submicrometer size ranges. Adv Powder Technol 2011;22:1-19.

Shah TJ, Amin AF, Parikh JR, Parikh RH. Process optimization and characterization of poloxamer solid dispersions of a poorly water soluble drug. AAPS PharmSciTech 2006;8:18-24.

Tanno F, Nishiyama Y, Kokubo H, Obara S. Evaluation of hypromellose acetate succinate (HPMCAS) as a carrier in solid dispersions. Drug Dev Ind Pharm 2004;30:9-17.

Tashtoush BM, Al-Qashi ZS, Najib NM. In vitro and in vivo evaluation of glibenclamide in solid dispersion systems. Drug Dev Ind Pharm 2004;30:601-17.

Surikutchi BT, Patil SP, Shete G, Patel S, Bansal AK. Drug-excipient behavior in polymeric amorphous solid dispersions. Journal Excip and Food Chem 2013;4:70-94

Published

07-07-2019

How to Cite

Rampal, A., Singh, M., Mahajan, S., & Bedi, N. (2019). FORMULATION AND CHARACTERIZATION OF HPMC AND HPMCAS BASED SOLID DISPERSIONS OF FENOFIBRATE: A COMPARATIVE STUDY. International Journal of Applied Pharmaceutics, 11(4), 41–48. https://doi.org/10.22159/ijap.2019v11i4.32592

Issue

Section

Original Article(s)