Abstract
Using cocrystals has emerged as a promising strategy to improve the physicochemical properties of active pharmaceutical ingredients (APIs) by forming a new crystalline phase from two or more components. Particle size and morphology control are key quality attributes for cocrystal medicinal products. The needle-shaped morphology is often considered high-risk and complex in the manufacture of solid dosage forms. Cocrystal particle engineering requires advanced methodologies to ensure high-purity cocrystals with improved solubility and bioavailability and with optimal crystal habit for industrial manufacturing. In this study, 3D-printed microfluidic chips were used to control the cocrystal habit and polymorphism of the sulfadimidine (SDM): 4-aminosalicylic acid (4ASA) cocrystal. The addition of PVP in the aqueous phase during mixing resulted in a high-purity cocrystal (with no traces of the individual components), while it also inhibited the growth of needle-shaped crystals. When mixtures were prepared at the macroscale, PVP was not able to control the crystal habit and impurities of individual mixture components remained, indicating that the microfluidic device allowed for a more homogenous and rapid mixing process controlled by the flow rate and the high surface-to-volume ratios of the microchannels. Continuous manufacturing of SDM:4ASA cocrystals coated on beads was successfully implemented when the microfluidic chip was connected in line to a fluidized bed, allowing cocrystal formulation generation by mixing, coating, and drying in a single step.
Original language | English |
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Article number | 1064 |
Number of pages | 15 |
Journal | Pharmaceuticals |
Volume | 16 |
Issue number | 8 |
DOIs | |
Publication status | Published - 27 Jul 2023 |
Funding
This study was partially supported by the Complutense University of Madrid (910,939, Formulación y biodisponibilidad de nuevos medicamentos), by the Science Foundation Ireland grants co-funded under the European Regional Development Fund (SFI/12/RC/2275 and SFI/12/RC/2275_P2) awarded to A. M. Healy, and by the Ministry of Science and Innovation (PID2021-126310OA-I00) grant to D. Serrano. This study has been partially funded by a Research Grant [year 2021, ID: 16,306] from the European Society of Clinical Microbiology and Infectious Diseases (ESCMID) to Dolores Serrano.
Keywords
- microfluidics
- crystal habit
- continuous manufacturing
- 4-aminosalicylic acid
- sulfadimidine
- fluidised bed
- spray coating
- 3D printing
- chips