Pharmacopoeial and physicochemical properties of α-cellulose and microcrystalline cellulose powders derived from cornstalks

Authors

  • Chukwuemeka P. Azubuike
  • Boladale O. Silva
  • Augustine O. Okhamafe

DOI:

https://doi.org/10.22377/ijgp.v6i3.260

Abstract

Background: Suitable α-cellulose and microcrystalline cellulose powders for use in the pharmaceutical industry can be derived
from agricultural wastes. Aims: The pharmacopoeial and physicochemical properties of cornstalk α-cellulose (CCC) and cornstalk microcrystalline cellulose powders (MCCC) were compared to a commercial brand of microcrystalline cellulose (Avicel PH101) to evaluate their usefulness as pharmaceutical excipients. Settings and Design: Physicochemical properties of an excipient play a very crucial role in the functions of the excipient; hence, these properties were evaluated and compared with a commercial brand. Materials and Methods: α-cellulose was extracted from cornstalks. Modification of this α-cellulose powder was carried out by its partial hydrolysis with hydrochloric acid (HCl) to obtain a microcrystalline cellulose powder. Their pharmacopoeial, physicochemical and microbiological properties were evaluated using standard methods. Statistical Analysis: OriginPro 8 SR2 v. 0891 (B891) software (OriginLab Corporation USA) was used for statistical evaluation. One-way analysis of variance was used to differentiate between samples and decide where significant differences were established. Results: The yield of α–cellulose from the cornstalks was 32.5%w/w
and that of microcrystalline cellulose 26%w/w. All the cellulose samples met all the pharmacopoeial parameters that were carried out. The comparison of physicochemical properties of the CCC, MCCC and Avicel PH101 suggests that the microcrystalline celluloses might have better flow and compression properties than the CCC sample. The three cellulose powders were of high microbial excipient quality. For almost all parameters evaluated, it was generally observed that the MCCC has similar characteristics to Avicel PH101. Conclusions: MCCC can be a suitable alternative to the expensive Avicel PH101as pharmaceutical excipients.
Key words: Cornstalk, microcrystalline cellulose, pharmacopoeial properties, physicochemical properties, α-cellulose

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References

Krässig HA. Cellulose structure, accessibility and reactivity.

Yverdon: Gordon and Breach Science Publishers; 1993.

Wen LF, Chang KC, Gallaher DD. Isolation and characterization

of hemicellulose and cellulose from sugar beet pulp. J Food Sci

;53:826-9.

Zhu S, Wu Y, Cheng Q, Yu Z, Wang C, Jen S. et al. Can cellulose

rival petroleum? Green Chem 2006;8:325-7.

Paralikar KM, Bhatawdekar SP. Microcrystalline cellulose from

bagasse pulp. Biol Wastes 1988;24:75-7.

Uesu NY, Pineda EA, Hechenleitner AA. Microcrystalline cellulose

from soybean husk: Effects of solvent treatments on its properties

as acetylsalicylic acid carrier. Int J Pharm 2000;206:85-96.

Azubuike CP, Okhamafe AO, Falodun A. Some pharmacopoeial

and diluent-binder properties of cellulose derived from maize cob

in selected tablet formulations. J Chem Pharm Res 2011;3:481-8.

Ohwoavworhua FO, Adelakun TA, Okhamafe AO. Processing

pharmaceutical grade microcrystalline cellulose from groundnut

husk: Extraction methods and characterization. Int J Green Pharm

;3:97-104.

Landin M, Martinez-Pacheco R, Gomez-Amoza JL, Souto C,

Concheiro A, Rowe RC. Effects of batch variation and source of

pulp on the properties of microcrystalline cellulose. Int J Pharm

;91:133-41.

Ganjyal GM, Reddy N, Yang YQ, Hanna MA. Biodegradable

packaging foams of starch acetate blended with corn stalk fibers.

J Appl Polym Sci 2004;93:2627-33.

Reddy N, Yang Y. Structure and properties of high quality natural

cellulose fibers from cornstalks. Polymers 2005;46:5494-500.

Reddy N, Yang Y. Biofibres from agricultural byproducts for

industrial applications. Trends Biotechnol 2005;23:22-7.

Okhamafe AO, Azubuike CP. Direct compression studies on lowcost

cellulose derived from maize cob. J Pharm Sci Pharm Prac

;2:26-9.

Browning BL. Methods of wood chemistry. Vol. 2. New York:

Interscience; 1967. p. 387-882.

British Pharmacopoeia (B. P). London: Her Majesty’s Stationery

Office; 2003.

Ejikeme PM. Investigation of the physicochemical properties

of microcrystalline cellulose from agricultural wastes I: Orange

mesocarp. Cellulose 2008;15:141-7.

Azubuike CP, Rodrı´guez H, Okhamafe AO, Rogers RD.

Physicochemical properties of maize cob cellulose powders

reconstituted from ionic liquid solution. Cellulose 2012;

:425-33.

Carr RL Jr. Evaluating flow properties of solids. Chem Eng

;72:163-8.

Hausner HH. Friction conditions in a mass of metal powders. Int

J Powd Metall 1967;3:7-13.

Ozolua RI, Omogbai EK, Akerele JO, Okhamafe AO. Microbiological

and toxicological studies on cellulose generated from agricultural

wastes. Afr J Biotechnol 2005;4:1147-51.

Ohwoavworhua FO, Adelakun TA. Non-wood fibre production of

microcrystalline cellulose from Sorghum caudatum: Characterization

and tableting properties. Indian J Pharm Sci 2010;72:295-301.

Lv G, Wu S, Lou R. Characteristics of cornstalk hemicelluloses

pyrolysis in a tubular reactor. BioRes 2010;5:2051-62.

United States Pharmacopeial Convention, United States

Pharmacopeia and National Formulary (USP 27-NF 22), Rockville,

MD. 2004 p. 2845-6.

Evans WC. Trease and evans pharmacognosy. 13th ed. Bailliere

Tinall Ltd., London 1989. p. 133-41

Peck GE, Bailey GJ, McCurdy VE, Banker GS. Tablet formulation

and design. In: Lieberman HA, Lachman L, Schwarz JB, editors.

Pharmaceutical dosage forms: Tablets, Vol 1, 2nd ed. New York:

Marcel Dekker; 1989.

Korhonen O, Pohja S, Peltonen S, Suihko E, Vidgren M, Paronen P,

et.al. Effects of physical properties for starch acetate powders on

tabletting. AAPS PharmSciTech 2002;3:E34.

Bhimte NA, Tayade PT. Evaluation of microcrystalline cellulose

prepared from sisal fibres as a tablet excipient. AAPS PharmSciTech

;8:8.

Wells JI. Pharmaceutical preformulation: The physicochemical

properties of drug substances. New York: Wiley; 1988.

Fowler HW. Powder flow and compaction. In: Carter SJ, editor.

Cooper and Gunn’s tutorial pharmacy. 6th ed. Delhi: CBS

Publishers; 2000.

British Pharmacopoeia Commission. British pharmacopoeia. Vol 1.

London: HMSO Press; 1993. p. 53.

Bos CE, Vari Doorme H, Lerk CF. Microbiological stability of drugs

stored under tropical conditions. Int J Pharm 1989;55:175-83.

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