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Quantification

Quantization methods are validated in order to quantify specific crystal forms or amorphous content in API mixtures and tablets (formulated compounds). Depending on the physical-chemical API characteristics, one of the following techniques is chosen to obtain high accuracy, specificity and sensitivity:

  • X-ray powder diffraction
  • Thermal analysis (DSC)
  • Spectroscopic analysis (FT-IR, FT-RAMAN)
  • s.s. N.M.R.

The methods are built following GLP compliances and validated according to ICH guidelines.

In addition, for multiphase mixtures, such analysis reveals quantitative composition. 

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Amorphous versus crystallinity determination
XRPD is used in the determination of percent crystallinity where the volume concentration of, for example, amorphous filler to crystalline active matrix, is measured within the dose form of a drug. Percent crystallinity is an important parameter as...
Date: 21/02/2011


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Amorphous versus crystallinity determination
21/02/2011
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