<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>22(10)</volume><submitter>Hugo Silva M</submitter><pubmed_abstract>Long-acting injectables are a unique drug formulation strategy, providing a slow and sustained release of active pharmaceutical ingredients (APIs). In this study, a novel approach that combines liquid antisolvent precipitation with seeding to obtain a stable form of the API indomethacin while achieving the desired particle size distribution is described. It was proven that when a metastable form of indomethacin was initially nucleated, the rate of its transformation to the stable form was influenced by the presence of excipients and seeds (17.10 ± 0.20 μm), decreasing from 48 to 4 h. The final particle size (D50) of the indomethacin suspension produced without seeding was 7.33 ± 0.38 μm, and with seeding, it was 5.61 ± 0.14 μm. Additionally, it was shown that the particle size distribution</pubmed_abstract><journal>Crystal growth &amp; design</journal><pagination>6056-6069</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9542716</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Impact of Excipients and Seeding on the Solid-State Form Transformation of Indomethacin during Liquid Antisolvent Precipitation.</pubmed_title><pmcid>PMC9542716</pmcid><pubmed_authors>Holm R</pubmed_authors><pubmed_authors>Hudson SP</pubmed_authors><pubmed_authors>Hugo Silva M</pubmed_authors><pubmed_authors>Tajber L</pubmed_authors><pubmed_authors>Kumar A</pubmed_authors><pubmed_authors>Hodnett BK</pubmed_authors></additional><is_claimable>false</is_claimable><name>Impact of Excipients and Seeding on the Solid-State Form Transformation of Indomethacin during Liquid Antisolvent Precipitation.</name><description>Long-acting injectables are a unique drug formulation strategy, providing a slow and sustained release of active pharmaceutical ingredients (APIs). In this study, a novel approach that combines liquid antisolvent precipitation with seeding to obtain a stable form of the API indomethacin while achieving the desired particle size distribution is described. It was proven that when a metastable form of indomethacin was initially nucleated, the rate of its transformation to the stable form was influenced by the presence of excipients and seeds (17.10 ± 0.20 μm), decreasing from 48 to 4 h. The final particle size (D50) of the indomethacin suspension produced without seeding was 7.33 ± 0.38 μm, and with seeding, it was 5.61 ± 0.14 μm. Additionally, it was shown that the particle size distribution</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Oct</publication><modification>2025-04-29T11:01:30.138Z</modification><creation>2025-04-06T19:47:23.765Z</creation></dates><accession>S-EPMC9542716</accession><cross_references><pubmed>36217420</pubmed><doi>10.1021/acs.cgd.2c00678</doi></cross_references></HashMap>