Comparative evaluation of the use of dry binders in a physical mixture or as a coprocessed dry binder in matrix tablets with extended drug release
Language English Country Poland Media print
Document type Comparative Study, Journal Article
PubMed
31259696
DOI
10.2478/acph-2018-0030
PII: /j/acph.2018.68.issue-3/acph-2018-0030/acph-2018-0030.xml
Knihovny.cz E-resources
- Keywords
- coprocessed dry binder, dissolution testing, energy profile of compression, matrix tablets, polyvinyl alcohol, tensile strength of tablets,
- MeSH
- Cellulose chemistry MeSH
- Chemistry, Pharmaceutical methods MeSH
- Technology, Pharmaceutical methods MeSH
- Salicylic Acid administration & dosage chemistry MeSH
- Lactose chemistry MeSH
- Nonlinear Dynamics MeSH
- Tensile Strength MeSH
- Polyvinyl Alcohol chemistry MeSH
- Excipients chemistry MeSH
- Solubility MeSH
- Tablets MeSH
- Drug Liberation MeSH
- Publication type
- Journal Article MeSH
- Comparative Study MeSH
- Names of Substances
- Cellulose MeSH
- Salicylic Acid MeSH
- Lactose MeSH
- microcrystalline cellulose MeSH Browser
- Polyvinyl Alcohol MeSH
- Excipients MeSH
- Tablets MeSH
This paper evaluates and compares the properties of directly compressible tabletting materials and matrix tablets containing a combination of α-lactose monohydrate and microcrystalline cellulose in the 3:1 ratio in a physical mixture and in a coprocessed dry binder. Tested parameters include flow properties, compressibility, compactibility and the rate of drug release from tablets. Compressibility is evaluated by means of the energy profile of the compression process. Compactibility is evaluated by means of the tensile strength of the tablets. Dissolution testing is done using the rotating basket method. Dissolution profiles are evaluated by non-linear regression analysis. Total energy of compression and plasticity values were higher in tabletting materials with the coprocessed dry binder. Increasing additions of polyvinyl alcohol decreased the values of total energy of compression, plasticity, tensile strength of tablets and drug release rate. Dissolution behaviour of tablets, which contained the physical mixture or coprocessed dry binder and the same amount of polyvinyl alcohol, was comparable.
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