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Polymer-Directed Crystallization of Luteolin, Quercetin, and Myricetin
for active pharmaceutical ingredients, the bioavailability, stability, and processability critically depend on crystal habit and size. The presence of polymers in a crystallization solution can engineer broader ranges of crystal habit and size, but only in certain cases. To elucidate the underlying...
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Published in: | Macromolecular research 2020, 28(13), , pp.1276-1281 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | for active pharmaceutical ingredients, the bioavailability, stability, and processability critically depend on crystal habit and size. The presence of polymers in a crystallization solution can engineer broader ranges of crystal habit and size, but only in certain cases. To elucidate the underlying mechanism of this selectivity, polymer-directed crystallization was systematically investigated here for a series of natural polyphenols, namely luteolin, quercetin, and myricetin. Significant changes in crystal habit and size were observed in the cases of quercetin and myricetin. Peak broadening in X-ray diffraction profiles and significant amounts of polymer within the crystallized particles suggested possible composite structure formation
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a non-classical crystallization mechanism. Polyethyleneimine and poly(vinyl alcohol) showed relatively stronger crystal engineering effects than poly(ethylene glycol). The results facilitate understanding of the specific interactions important for crystal engineering and thus preparing polyphenols to attain wide ranges of habit and particle size for various applications. |
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ISSN: | 1598-5032 2092-7673 |
DOI: | 10.1007/s13233-020-8163-4 |