4.5 Article

Crystalline to amorphous transition of disodium hydrogen phosphate during primary drying

Journal

PHARMACEUTICAL RESEARCH
Volume 20, Issue 5, Pages 802-803

Publisher

KLUWER ACADEMIC/PLENUM PUBL
DOI: 10.1023/A:1023445905372

Keywords

sodium phosphate buffers; freeze-drying; crystallization; dehydration

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Purpose. To monitor the phase transitions during freeze-drying of disodium hydrogen phosphate. Methods. The variable temperature sample stage of the X-ray diffractometer (XRD) was attached to a vacuum pump, which enabled the entire freeze-drying process to be carried out in the sample chamber. The phase transitions during the freeze-drying cycle were monitored in real time by XRD. Aqueous buffer solution ( containing disodium hydrogen phosphate and sodium dihydrogen phosphate) was cooled at 2degreesC/min from room temperature to -70degreesC. It was then heated to -25degreesC and subjected to primary drying for 2 h at a chamber pressure of similar to100 mTorr, followed by secondary drying at -10degreesC. Results. In the frozen solution, disodium hydrogen phosphate had crystallized as the dodecahydrate (Na2HPO4.12H(2)O) as was evident from its characteristic lines at similar to5.37, 4.27, and 2.81 Angstrom. Primary drying for 2 h resulted in ice sublimation, and the complete disappearance of the dodecahydrate peaks. Conclusion. The dehydration of the crystalline dodecahydrate resulted in an amorphous anhydrate. Thus the amorphous nature of the end product is a result of phase transitions during the process and do not reflect the solid-state of the ingredients during the entire process.

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