Tacsi, Kornélia and Galata, Dorián László and Domokos, András and Pusztai, Éva and Nagy, Brigitta and Stoffán, György Nimród and Nagy, Zsombor Kristóf and Pataki, Hajnalka (2024) Development and integration of a continuous horizontal belt filter into drug production procedure. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 666. No.-124729. ISSN 0378-5173
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Abstract
In the pharmaceutical industry, filtration is traditionally carried out in batch mode. However, with the spread of continuous technologies, there is an increasing demand for robust continuous filtration strategies suitable for processing suspensions produced in continuous crystallizers. Accordingly, this study aimed to investigate a lab-scale horizontal conveyor belt filtration approach for pharmaceutical separation purposes for the first time. The newly developed continuous horizontal belt filter (CHBF) was tested under different systems (microcrystalline cellulose (MCC)/water, lactose/ethanol and acetylsalicylic acid (ASA)/water) and diverse conditions. Filtration was robust using a well-defined unimodal particle size distribution MCC in water system, where the residual moisture content varied within narrow limits of 45–52% independently from the process conditions. Besides, the residual moisture content highly depended on the applied solvent and particle size. It could be reduced to below 2% by processing the suspensions of either a volatile solvent (lactose in ethanol) or an aqueous slurry of a large particle size ASA. Finally, the CHBF was connected to a mixed suspension mixed product removal (MSMPR) or a plug flow crystallizer (PFC). The residual moisture content of the CHBF-filtered ASA product and operation characteristics (onset of steady-state) were evaluated in both continuous crystallizer-filter systems. The MSMPR-CHBF system operated with a longer startup period. The size of the in situ-produced crystals was of a similar order magnitude in both systems, resulting in a similar residual moisture content (around 20%). Overall, the tested continuous filter was robust, did not modify the crystal morphology in the examined experimental range, and could be effectively integrated with continuous crystallizers. © 2024 The Author(s)
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| Additional Information: | Funding Agency and Grant Number: New National Excellence Program of the Ministry for Culture and Innovation from the source of the National Research, Development and Innovation Fund Funding text: The authors are grateful to the H-ION Chemistry Team for providing the filter equipment and supporting this work. This work was financially supported by the National Research Development and Innovation Office of Hungary (FK-143019, PD-142970) . Project no. RRF-2.3.1-21-2022-00015 has been implemented with the support provided by the European Union. Brigitta Nagy is thankful for the Janos Bolyai Research Scholarship of the Hungarian Academy of Sciences. The research was also supported by the UNKP-22-4-I-BME-257 and UNKP-23-5-BME-443 New National Excellence Program of the Ministry for Culture and Innovation from the source of the National Research, Development and Innovation Fund.r New National Excellence Program of the Ministry for Culture and Innovation from the source of the National Research, Development and Innovation Fund. |
| Uncontrolled Keywords: | Continuous filtration, Horizontal belt filter, Mixed suspension mixed product removal, Plug flow crystallizer, Acetylsalicylic acid, Design of experiments |
| Subjects: | Q Science / természettudomány > QD Chemistry / kémia Q Science / természettudomány > QH Natural history / természetrajz > QH301 Biology / biológia > QH3015 Molecular biology / molekuláris biológia |
| SWORD Depositor: | MTMT SWORD |
| Depositing User: | MTMT SWORD |
| Date Deposited: | 23 Sep 2025 14:03 |
| Last Modified: | 23 Sep 2025 14:03 |
| URI: | https://real.mtak.hu/id/eprint/225045 |
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