Protein denaturation in dosage forms measured by differential scanning calorimetry.
Ken‐ichi Izutsu, Sumie Yoshioka, Yasushi Takeda
Abstract
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Ken‐ichi Izutsu, Sumie Yoshioka, Yasushi Takeda
Abstract
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The stability of beta-galactosidase dosage forms was studied by differential scanning calorimetry (DSC). It was found that the observed enthalpy of thermal denaturation was approximately in proportion to remaining enzyme activity, and denaturation temperature was related to protein stability. These results suggest that DSC can be used to determine native proteins in dosage forms and to clarify the factors affecting protein stability. The DSC method seems to be more convenient than conventional activity assay methods, and useful to follow protein denaturation during the manufacturing process and storage of dosage forms.
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The stability of beta-galactosidase dosage forms was studied by differential scanning calorimetry (DSC). It was found that the observed enthalpy of thermal denaturation was approximately in proportion to remaining enzyme activity, and denaturation temperature was related to protein stability. These results suggest that DSC can be used to determine native proteins in dosage forms and to clarify the factors affecting protein stability. The DSC method seems to be more convenient than conventional activity assay methods, and useful to follow protein denaturation during the manufacturing process and storage of dosage forms.
Key concepts: Differential scanning calorimetry, Chemistry, Denaturation (fissile materials), Enthalpy, Dosage form, Calorimetry, Chromatography, Thermal stability