ArticleIndustrial & engineering chemistry research2025
Hydrodynamic Cavitation-induced Breakage of Carbamazepine Dihydrate Crystals: Experimental Insights and Modeling.
Article in Industrial & engineering chemistry research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
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Who cites it
1 citing paper in PubMed.
- Flow of Non-Newtonian Fluids through a Vortex-Based Hydrodynamic Cavitation Device.ACS engineering Au · 2026Article
Corrections and comments
- Erratum issued
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Downstream milling is often employed to control the particle size distribution (PSD) of crystalline products. Recently, hydrodynamic cavitation (HC) was shown to be quite effective for particle breakage compared to traditional wet milling and acoustic cavitation. In this work, we investigated the use of HC for tailoring the size and shape of carbamazepine dihydrate (CBZ-DH) crystals. A vortex-based HC device (VD) was used. An endoscopic optical probe (SOPAT GmbH, Germany) was used to measure the PSD during the breakage experiments. The variation in mean length, width, and aspect ratio (AR) of CBZ-DH crystals as a function of the number of passes through the VD was quantified. The breakage of CBZ-DH crystals exhibited two regimesinitially fast breakage up to a certain number of passes, followed by a significantly slower breakage. An empirical correlation for estimating the reduction in the mean length and width of the crystals was developed. The HC-induced breakage was modeled using the population balance model (PBM). The model successfully simulated the experimental PSD across all operating conditions with an appropriate selection of breakage model parameters. The data and models presented in this work provide a useful basis for tailoring pharmaceutical crystals by using VD.
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Registered trials
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