Solvent-mediated morphology selection of the active pharmaceutical ingredient isoniazid: Experimental and simulation studies


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<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Han, Dandan</dc:creator>
  <dc:creator>Karmakar, Tarak</dc:creator>
  <dc:creator>Bjelobrk, Zoran</dc:creator>
  <dc:creator>Gong, Junbo</dc:creator>
  <dc:creator>Parrinello, Michele</dc:creator>
  <dc:date>2020-01-28</dc:date>
  <dc:description>In solution crystallization, solvent has a profound effect on controlling crystal morphology. However, the role played by solvents in affecting crystal morphology remains elusive. Here, we accompany experiments with molecular dynamics simulations to investigate crystallization of an anti-tuberculosis drug, isoniazid, in different solvents. Experiments show that isoniazid grows as needle-like crystals in water, while in alcohols such as methanol, ethanol and isopropanol, it exhibits a rod-like crystal habit. The aspect ratio of isoniazid crystals decreases with the decrease in the relative solvent polarity. We modeled these experiments by performing molecular dynamics simulations of isoniazid crystallization in different solvents at constant chemical potential thus keeping the solution concentration constant. The simulation results reveal a rough growth mechanism for the fast growing (1 1 0) surface, and bulk transport of the solute from solution to the growing surface is the limiting-step. In accordance with experiments, the relative growth rate of this surface decreases from methanol, ethanol to isopropanol. On the other hand, the slow growing (0 0 2) surface appears to follow a stepwise growth mechanism, with a surface integration step chiefly controlling the growth. The relative growth rate of this surface increases from methanol to ethanol and isopropanol.</dc:description>
  <dc:identifier>https://archive.materialscloud.org/record/2020.0014/v1</dc:identifier>
  <dc:identifier>doi:10.24435/materialscloud:2020.0014/v1</dc:identifier>
  <dc:identifier>mcid:2020.0014/v1</dc:identifier>
  <dc:identifier>oai:materialscloud.org:316</dc:identifier>
  <dc:language>en</dc:language>
  <dc:publisher>Materials Cloud</dc:publisher>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>Creative Commons Attribution 4.0 International https://creativecommons.org/licenses/by/4.0/legalcode</dc:rights>
  <dc:subject>ERC</dc:subject>
  <dc:subject>MARVEL</dc:subject>
  <dc:subject>MARVEL/DD1</dc:subject>
  <dc:subject>Solution crystallization</dc:subject>
  <dc:subject>Crystal growth</dc:subject>
  <dc:subject>Morphology</dc:subject>
  <dc:subject>solvent effect on crystal shape</dc:subject>
  <dc:title>Solvent-mediated morphology selection of the active pharmaceutical ingredient isoniazid: Experimental and simulation studies</dc:title>
  <dc:type>Dataset</dc:type>
</oai_dc:dc>