Evidence map›Paper›PMID 41820683›Full record

ReviewAdvances in biochemical engineering/biotechnology2026

Continuous Crystallization Platforms to Crystallize Biomolecules.

Siyu Pu, Kunn Hadinoto

Abstract readReview
PubMed Publisher
In one paragraph

Review in Advances in biochemical engineering/biotechnology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Siyu PuSchool of Chemistry, Chemical Engineering and Biotechnology, Nanyang Technological University, Singapore, Singapore.
Kunn HadinotoSchool of Chemistry, Chemical Engineering and Biotechnology, Nanyang Technological University, Singapore, Singapore. kunnong@ntu.edu.sg.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the realm of industrial crystallization for biomolecules, batch crystallizers have been the predominant platform, although continuous crystallizers with clearly superior performances have been actively investigated in recent years. Among them, mixed-suspension-mixed-product-removal crystallizer (MSMPRC), plug flow crystallizer (PFC), slug flow crystallizer (SFC), oscillatory flow baffled crystallizer (OFBC), and other innovative continuous platforms such as membrane crystallizer and Couette-Taylor (CT) crystallizer are introduced in this chapter. These crystallizers have been utilized in continuous crystallization of biomolecules including globular proteins such as lysozyme and insulin. Their key design variables encompassing variables affecting kinetics (residence time distribution (RTD), mixing strategy, etc.) and variables affecting thermodynamics (driving force of crystallization) are discussed. As a promising alternative to conventional chromatography method, continuous crystallization shows great potential for downstream processing of biomolecules.

Indexed as

InsulinMuramidaseProteinsContinuous Flow ChemistryCrystallizationInsulinMuramidaseProteinsBiomolecule crystallizationContinuous crystallizationDownstream processingMSMPR crystallizerOscillatory flow baffled crystallizer (OFBC)Plug-flow crystallizer (PFC)Protein crystallizationSlug-flow crystallizer (SFC)

Identifiers

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.