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Modified cellulose II powder: preparation, characterization, and tableting properties.
Maria de la Luz Reus Medina1, Vijay Kumar
1Division of Pharmaceutics, College of Pharmacy, The University of Iowa, Iowa City, Iowa 52242, USA.
Glutaraldehyde treatment of cellulose II powder (UICEL-A/102) created UICEL-XL, enhancing binder properties without compromising rapid disintegration. This modified cellulose serves as an effective disintegrant with superior binding capabilities.
Area of Science:
- Materials Science
- Pharmaceutical Technology
Background:
- Cellulose II powder (UICEL-A/102) derived from Avicel PH-102 exhibits desirable disintegration properties.
- Improving binder characteristics of cellulose materials is crucial for pharmaceutical formulations.
Purpose of the Study:
- To investigate the reaction of UICEL-A/102 with glutaraldehyde to enhance binder properties.
- To assess if binder improvements adversely affect the rapid disintegration characteristic of the cellulose powder.
Main Methods:
- UICEL-A/102 was reacted with glutaraldehyde in 0.01 N HCl at a 1:0.6 weight ratio and 100°C for 8.5 hours.
- Characterization included degree of polymerization, crystallinity, density, porosity, yield pressure, crushing strength, tensile strength, and Heckel analysis.
- Moisture sorption isotherms and disintegration times were evaluated.
Main Results:
- The resulting product, UICEL-XL, exhibited lower polymerization, higher crystallinity, lower densities, and higher porosity compared to UICEL-A/102.
- UICEL-XL demonstrated increased compressibility and compactability, indicated by lower yield pressure and higher strengths.
- Elasticity was reduced in UICEL-XL, while moisture sorption and disintegration remained comparable to UICEL-A/102.
Conclusions:
- Glutaraldehyde treatment successfully improved the binder properties of cellulose II powder.
- UICEL-XL functions as an effective disintegrant while possessing enhanced binder capabilities.
- The modified cellulose powder offers a dual benefit for pharmaceutical applications.
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