<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>15(2)</volume><submitter>Guinet Y</submitter><pubmed_abstract>Designing co-amorphous formulations is now recognized as a relevant strategy for improving the bioavailability of low-molecular-weight drugs. In order to determine the most suitable low-molecular-weight excipients for stabilizing the drug in the amorphous state, screening methods were developed mostly using amino acids as co-formers. The present study focused on the analysis of the thermal stability of co-amorphous blends prepared by cryo-milling indomethacin with several amino acids in order to understand the stabilization mechanism of the drug in the amorphous state. Combining low- and mid-frequency Raman investigations has provided information on the relation between the physical properties of the blends and those of the H-bond network of the amorphous drug. This study revealed the surp</pubmed_abstract><journal>Pharmaceutics</journal><pagination>337</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9964172</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Mechanism for Stabilizing an Amorphous Drug Using Amino Acids within Co-Amorphous Blends.</pubmed_title><pmcid>PMC9964172</pmcid><pubmed_authors>Paccou L</pubmed_authors><pubmed_authors>Guinet Y</pubmed_authors><pubmed_authors>Hedoux A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Mechanism for Stabilizing an Amorphous Drug Using Amino Acids within Co-Amorphous Blends.</name><description>Designing co-amorphous formulations is now recognized as a relevant strategy for improving the bioavailability of low-molecular-weight drugs. In order to determine the most suitable low-molecular-weight excipients for stabilizing the drug in the amorphous state, screening methods were developed mostly using amino acids as co-formers. The present study focused on the analysis of the thermal stability of co-amorphous blends prepared by cryo-milling indomethacin with several amino acids in order to understand the stabilization mechanism of the drug in the amorphous state. Combining low- and mid-frequency Raman investigations has provided information on the relation between the physical properties of the blends and those of the H-bond network of the amorphous drug. This study revealed the surp</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2025-04-04T08:52:39.076Z</modification><creation>2025-04-04T08:52:39.076Z</creation></dates><accession>S-EPMC9964172</accession><cross_references><pubmed>36839663</pubmed><doi>10.3390/pharmaceutics15020337</doi></cross_references></HashMap>