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   <subfield code="a">10.1016/j.jpba.2014.09.020</subfield>
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   <subfield code="a">Langó Péter</subfield>
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   <subfield code="a">Analysis of the polymorph changes of a drug candidate</subfield>
   <subfield code="h">[elektronikus dokumentum] /</subfield>
   <subfield code="c"> Langó Péter</subfield>
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   <subfield code="a">229-235</subfield>
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   <subfield code="a">JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS</subfield>
   <subfield code="v">102</subfield>
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   <subfield code="a">The effects of solvents, temperature and humidity on the stability of a former drug candidate obtained from Sanofi (Hungary) were examined by a slurry equilibration method, variable temperature and humidity X-ray powder diffractometry (VT/VH-XRPD) and differential scanning calorimetry (DSC). The VH-XRPD study showed that all 8 polymorphic forms of this material were stable in the interval 20-80 RH%. The VT-XRPD measurements indicated that all the polymorphs except Form II underwent changes in the range 30-200 degrees C. The stable form was Form II, though Form IVb had almost the same stability. The investigation demonstrated that VT-XRPD is a very useful in situ method for relative stability studies.</subfield>
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   <subfield code="a">Várkonyi E.</subfield>
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   <subfield code="a">Ulrich Joachim</subfield>
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   <subfield code="a">Révész Piroska</subfield>
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   <subfield code="a">Aigner Zoltán</subfield>
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   <subfield code="u">http://publicatio.bibl.u-szeged.hu/11099/1/Lang__JPBA_u.pdf</subfield>
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