ASSESSMENT OF SELF-EXTRACTED CELLULOSE FROM ORYZA SATIVA FOR DESIGN OF CONTROLLED DRUG DELIVERY SYSTEM OF DALFAMPRIDINE

Authors

  • JEEVANA JYOTHI B Department of Institute of Pharmaceutical Technology, Sri PadmavatiMahilaVisvavidyalayam (Women’s University), Tirupati, Andhra Pradesh, India.
  • MOUNIKA M Department of Institute of Pharmaceutical Technology, Sri PadmavatiMahilaVisvavidyalayam (Women’s University), Tirupati, Andhra Pradesh, India.

DOI:

https://doi.org/10.22159/ajpcr.2019.v12i2.29785

Keywords:

Cellulose from Oryza sativa, Soxhlation method, Fourier-transform infrared, Compatibility, Dalfampridine, Controlled delivery

Abstract

Objectives: The main objective of the present work includes extraction of cellulose from Oryza sativa (OS), characterization of cellulose, development of controlled release tablet dalfampridine using cellulose of OS, and in vitro evaluation.

Methods: Dry powdered OS husk sample was extracted with a mixture of hexane and methanol (2:1, v/v) using soxhlation method and was characterized by solubility, melting point determination, differential scanning calorimetry (DSC), and Fourier-transform infrared (FTIR) analysis. Compatibility between dalfampridine and the mixture of cellulose with dalfampridine was confirmed by FTIR and DSC analysis. Then, controlled drug delivery system of dalfampridine were prepared as directly compressed tablets using various compositions containing OS cellulose, hydroxypropyl methylcellulose (HPMC), dicalcium phosphate, and magnesium stearate (8 nos. F1 to f8) and were evaluated.

Results: Cellulose was extracted from OS extract to possess its ideal characteristics. Dalfampridine and its mixture with cellulose were compatible according to FTIR and DSC analysis. Directly compressed tablets made with 10 mg of dalfampridine and OS cellulose, HPMC, dicalcium phosphate, and magnesium stearate evidenced prolonged and controlled drug delivery of dalfampridine for 12 h. Formulation made with OS cellulose 250 mg, HPMC 20 mg, dicalcium phosphate 40 mg, and magnesium stearate 5 mg was ideal without burst release.

Conclusion: Cellulose extracted from OS is used successfully for the production of directly compressed tablets of dalfampridine to elicit optimum characteristics including controlled drug delivery for 12 h.

Downloads

Download data is not yet available.

Author Biography

JEEVANA JYOTHI B, Department of Institute of Pharmaceutical Technology, Sri PadmavatiMahilaVisvavidyalayam (Women’s University), Tirupati, Andhra Pradesh, India.

professor

References

Sahraian MA, Maghzi AH, Etemadifar M, Minagar A. Dalfampridine: Review of its efficacy in improving gait in patients with multiple sclerosis. J Cent Nerv Syst Dis 2011;3:87-93.

Jorfi EM, Foster J. Recent advances in nanocellulose for biomedical applications. J Appl Biopolym Sci 2014;24:1-19.

Das AM, Ali AA, Hazarika MP. Synthesis and characterization of cellulose acetate from Oryza sativa: Eco-friendly condition. Carbohydr Polym 2014;112:342-9.

Ahmad Z, Rozyanty AR, Nawawi WI. Isolation and characterization of microcrystalline cellulose (MCC) from Oryza sativa (RH). EDP Sci 2016;2:22-45.

Moran JI, Alvarez VA, Cyras VP, Vazquez A. Extraction of cellulose and preparation of nanocellulose from sisal fibers. Cellulose 2008;15:149-59.

Kihlman M, Medronho BF, Romano AL, Germgard U, Lindman B. Cellulose dissolution in an alkali-basedsolvent: Influence of additives and pretreatments. J Braz Chem Soc 2013;24:295-303.

Venugopal V. Formulation and optimization of sustained release tablets of tramadol and dalfampridine by factorial design model. Asian Med Sci Technol 2015;2:1-243.

Haritha B. A review on the evaluation of tablets. J Formul Sci Bioavailab 2017;1:1-5.

Naveen Goyal, Anil Kumar. Formulation and in vitro evaluation of salbutamol sulphate and theophylline extended-release tablets using modified polymers. Int J Pharm Pharm Sci 2018;10:67-71.

Srikanthreddy P, Bose PS, Saritha D, Sruthi V. Formulation and evaluation of colon targeted matrix tablet usinf natural tree gums. Int J Pharm Pharm Sci 2018;10:92-7.

Rosa SM, Rehman N, De Miranda MI, Nachtigall SM, Bica CI. Chlorine-free extraction of cellulose from Oryza sativa and whisker isolation. Carbohydr Polym 2012;87:1131-8.

Krumm C, Pfaendtner J, Dauenhauer PJ. Millisecond pulsed films unify the mechanisms of cellulose fragmentation. Chem Mater 2016;28:2-12.

Reddy CS, Reddy YR, Devanna N. formulation and optimization of the extended-release tablets of dalfampridine by 23 factorial design. J Pharm Sci Innov 2016;5:27-37.

Ceballos A, Cirri M, Maestrelli F, Corti G, Mura P. Influence of formulation and process variables on in vitro release of theophylline from directly-compressed Eudragit matrix tablets. II Farmaco 2005;60:913-8

Published

07-02-2019

How to Cite

JYOTHI B, J., and M. M. “ASSESSMENT OF SELF-EXTRACTED CELLULOSE FROM ORYZA SATIVA FOR DESIGN OF CONTROLLED DRUG DELIVERY SYSTEM OF DALFAMPRIDINE”. Asian Journal of Pharmaceutical and Clinical Research, vol. 12, no. 2, Feb. 2019, pp. 338-45, doi:10.22159/ajpcr.2019.v12i2.29785.

Issue

Section

Original Article(s)