Influence of crystal structure on the tableting properties of sulfamerazine polymorphs

C. Sun, D. J.W. Grant

Research output: Contribution to journalArticlepeer-review

233 Scopus citations

Abstract

Purpose. To understand the influence of polymorphic structure on the tableting properties of sulfamerazine. Methods. Bulk powders of sulfamerazine polymorph I and of two batches, II(A) and II(B) of different particle size, of polymorph II were crystallized. The powders were compressed to form tablets whose porosity and tensile strength were measured. The relationships between tensile strength, porosity and compaction pressure were analyzed by the method developed by Joiris, E., et al. Pharm. Res. 15:1122-1130 (1998). Results. The sensitivity of tensile strength to compaction pressure, known as the tabletability, follows the order. I ≫ II(A) > II(B) and the porosity at the same compaction pressure, which measures the compressibility, follows the order, I ≪ II(A) < II(B). Therefore, the superior tabletability of I over II(A) or II(B) is attributed to its greater compressibility. Molecular simulation reveals slip planes in crystals of I but not in II. Slip planes provide I crystals greater plasticity and therefore greater compressibility and tabletability. Larger crystal size of II(B) than of II(A) leads to fewer contact points between crystals in the tablets and results in a slightly lower tabletability. Conclusions. Slip planes confer greater plasticity to crystals of I than II and therefore greater tabletability.

Original languageEnglish (US)
Pages (from-to)274-280
Number of pages7
JournalPharmaceutical research
Volume18
Issue number3
DOIs
StatePublished - Jul 11 2001

Keywords

  • Plasticity
  • Porosity
  • Slip planes
  • Sulfamerazine polymorphs
  • Tabletability
  • Tensile strength

Fingerprint Dive into the research topics of 'Influence of crystal structure on the tableting properties of sulfamerazine polymorphs'. Together they form a unique fingerprint.

Cite this