Evaluation of a New Cellulose Material as Binding Agent for Direct Compression of Tablets
- 1 January 1986
- journal article
- research article
- Published by Taylor & Francis in Drug Development and Industrial Pharmacy
- Vol. 12 (11-13) , 2091-2111
- https://doi.org/10.3109/03639048609042625
Abstract
The properties of a new microcrystalline cellulose product EmcocelR, was compared with those of fine grade of other commercial microcrystalline cellulose, AvicelR PH 101. The crystal structure of Avicel was noticed to be some more amorphous than that of Emcocel. Both materials were similarly composed of irregularly shaped fibrous cellulose particles. The particle size distribution was clearly larger for Emcocel than for Avicel. Emcocel contained more both very small and very large particles. The loose density was also slightly smaller for Emcocel. There was practically no difference in spesific: surface area, water content and effective density of these materials. The behaviour of both microcrystalline cellulose powders during flow and binding processes was similar. Emcocel and Emcocel were rather cohesive and only fairly flowing materials. Tablets with very advantageous strength/pressure profiles were possible to produce using plain materials and also using tablet masses containing high concentrations of acetaminophenone. According to the results of this evaluation the physical and tableting properties of a new microcrystalline cellulose material, Emcocel, resemble very closely those of Avicel PH 101. Thus neither advantage nor disadvantage is derived using Emcocel instead of Avicel PH 101 as a binding component in tablet masses.Keywords
This publication has 4 references indexed in Scilit:
- An experimental study on the relationships between compressibility, fluidity and cohesion of powder solids at small tapping numbersPowder Technology, 1983
- Further Studies of the Potential of Recording Powder Flow MetersDrug Development and Industrial Pharmacy, 1980
- The properties of tablets containing microcrystalline celluloseJournal of Pharmacy and Pharmacology, 1977
- Some considerations on powder compression equationsPowder Technology, 1971