<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yeh KL</submitter><funding>Ministry of Science and Technology Taiwan</funding><pagination>1099</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9147162</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(5)</volume><pubmed_abstract>Form II paracetamol has captured the interest of researchers due to its improved compressibility. However, its low stability has made it difficult to be produced on a large scale with good reproducibility. In the present study, the selective polymorphic formation of paracetamol was carried out by cooling crystallization with four types of additives: adipic acid, fumaric acid, oxalic acid, and succinic acid. It was found that: (1) the more additives that were added, the higher the probability of forming Form II paracetamol; (2) Form II paracetamol could be induced by seeding the paracetamol aqueous solution with Form II paracetamol and fumaric acid crystals, and not the other three carboxylic acids; (3) a new solution complex of paracetamol-oxalic acid, evidenced by the solubility diagram, was responsible for the selective nucleation of Form II paracetamol in the oxalic acid aqueous solution; and (4) the range of the degree of supersaturation for nucleating Form II paracetamol was extended with the assistance of oxalic acid or fumaric acid. In large-scale crystallization, Form II paracetamol was produced by the continuous crystallization of 44 mg of paracetamol/mL in 50 wt% of fumaric acid aqueous solution with a flow rate of 150 mL/min.</pubmed_abstract><journal>Pharmaceutics</journal><pubmed_title>Crystallization of Form II Paracetamol with the Assistance of Carboxylic Acids toward Batch and Continuous Processes.</pubmed_title><pmcid>PMC9147162</pmcid><funding_grant_id>MOST 107-2221-E-008-037-MY3</funding_grant_id><pubmed_authors>Lee HL</pubmed_authors><pubmed_authors>Yeh KL</pubmed_authors><pubmed_authors>Lee T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Crystallization of Form II Paracetamol with the Assistance of Carboxylic Acids toward Batch and Continuous Processes.</name><description>Form II paracetamol has captured the interest of researchers due to its improved compressibility. However, its low stability has made it difficult to be produced on a large scale with good reproducibility. In the present study, the selective polymorphic formation of paracetamol was carried out by cooling crystallization with four types of additives: adipic acid, fumaric acid, oxalic acid, and succinic acid. It was found that: (1) the more additives that were added, the higher the probability of forming Form II paracetamol; (2) Form II paracetamol could be induced by seeding the paracetamol aqueous solution with Form II paracetamol and fumaric acid crystals, and not the other three carboxylic acids; (3) a new solution complex of paracetamol-oxalic acid, evidenced by the solubility diagram, was responsible for the selective nucleation of Form II paracetamol in the oxalic acid aqueous solution; and (4) the range of the degree of supersaturation for nucleating Form II paracetamol was extended with the assistance of oxalic acid or fumaric acid. In large-scale crystallization, Form II paracetamol was produced by the continuous crystallization of 44 mg of paracetamol/mL in 50 wt% of fumaric acid aqueous solution with a flow rate of 150 mL/min.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 May</publication><modification>2025-06-01T12:38:48.885Z</modification><creation>2025-02-19T03:22:31.637Z</creation></dates><accession>S-EPMC9147162</accession><cross_references><pubmed>35631685</pubmed><doi>10.3390/pharmaceutics14051099</doi></cross_references></HashMap>