Literature DB >> 9795044

Dependence between dissolution rate and porosity of compressed erythromycin acistrate tablets.

M Riippi1, J Yliruusi, T Niskanen, J Kiesvaara.   

Abstract

The correlation between dissolution rate and porosity of compressed erythromycin acistrate tablets was studied. The total porosity of the tablets, the pore size distribution and the specific surface area of the pores were determined using high-pressure mercury porosimetry. The particle size and specific surface area of the raw material and of the dry granulated mass of the tablets were also determined. The results show that the pore size distribution, showing the differences in pore structure, is more informative than total intruded volume of mercury. However, it is very difficult to explain the dissolution behaviour of erythromycin acistrate tablets only by porosity results of the tablets, and more work is still needed in this field.

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Year:  1998        PMID: 9795044     DOI: 10.1016/s0939-6411(98)00003-4

Source DB:  PubMed          Journal:  Eur J Pharm Biopharm        ISSN: 0939-6411            Impact factor:   5.571


  3 in total

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2.  Drug-Polymers Composite Matrix Tablets: Effect of Hydroxypropyl Methylcellulose (HPMC) K-Series on Porosity, Compatibility, and Release Behavior of the Tablet Containing a BCS Class I Drug.

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Journal:  Polymers (Basel)       Date:  2022-08-19       Impact factor: 4.967

3.  Influence of Formulation Factors and Compression Force on Release Profile of Sustained Release Metoprolol Tablets using Compritol(®) 888ATO as Lipid Excipient.

Authors:  Shilpa N Patere; Chhanda J Kapadia; Mangal S Nagarsenker
Journal:  Indian J Pharm Sci       Date:  2015 Sep-Oct       Impact factor: 0.975

  3 in total

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