Pharmaceutical Manufacturing Continuous Crystallization Procedures: A Review

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Sunita N. Vaidya


This academic publication provides an overview of constant crystallization of solutions in the pharmaceutical
industry. The comparison of continuous versus batch crystallizers, their construction benefits and drawbacks, and
the addition of solid form framing to create a constantly focused interaction between digital advanced process
technology technologies and chemical manufacturing functionalities were all covered in detail because of the
broad key knowledge spectrum of precipitation. In-depth discussion was also given to mechanistic multiscale
modeling, whose comprehension is crucial for the creation of future control applications. Process simulation and
crystallizer optimization are also covered in the multiscale modeling section describes the model-based provided,
which also addresses the intensifying method. Techniques the last section, is taken into consideration. The reader
can become familiar with research pieces and their outcomes, which have thus far created different emerging
viewpoints, by reading the unique articles on a particular theme that is gathered, talked about, and contrasted in
the aforementioned primary categories. The pharmaceutical sector places a lot of emphasis on crystallization,
and readers may already discover literature on continuous crystallization. However, due to the increasing trend
towards the synthesis of items with special features that cannot be produced using conventional methodologies,
the current study has placed a greater emphasis on the construction of automatic control for the generation of
certain fine chemicals. Continuous crystallization may also allow for intensification techniques, modeling for
optimization, “on-demand” production, and MPC. A classification study examines the literature.


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How to Cite
N. Vaidya, S. . (2023). Pharmaceutical Manufacturing Continuous Crystallization Procedures: A Review. Asian Journal of Pharmaceutics (AJP), 17(03).