ArticleMicrosystems & nanoengineering2025
One-step generation of luminescent core-shell microspheres for cell encapsulation via pulsed operation in centrifugal microfluidics.
Article in Microsystems & nanoengineering, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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
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.
Who cites it
2 citing papers in PubMed.
- Collagen-Based Microspheres for Biomedical Applications in Drug Delivery and Tissue Engineering.Biomimetics (Basel, Switzerland) · 2026Review
- Research Progress of Sodium Alginate-Based Hydrogels in Biomedical Engineering.Gels (Basel, Switzerland) · 2025Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
9 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Biopolymer core-shell microspheres play a crucial role in various biomedical applications, including drug delivery, tissue engineering, and diagnostics. These applications require microparticles with consistent, well-controlled size and precise shape fidelity. However, achieving high-throughput synthesis of size and shape-controlled core-shell biopolymer microgels remains a significant challenge. Herein, we present a one-step process for the high-throughput generation of monodisperse, luminescent, chitosan alginate core-shell microspheres by a novel manipulation of a centrifugal microfluidic device. We utilized the pH sensitivity of chitosan and the ionic gelation properties of alginate to create well-defined core-shell morphologies. To address particle merging issues and promote uniform particle size generation, we introduced an innovative pulsed mode operation in our centrifugal microfluidics device. We also incorporated fluorescent, nitrogen-functionalized graphene quantum dots into the core-shell structures, thereby rendering them useful for real-time imaging, which is necessary for diagnostic and therapeutic applications. To enhance biocompatibility, the alginate solution was supplemented with fish gelatin (FG). The resulting microspheres exhibited excellent structural integrity maintaining their core-shell structure after 15 days. Biocompatibility was demonstrated by C2C12 cell viability exceeding 88% after 15 days and by bacterial viability reaching the same percentage after 2 days. The system demonstrates considerable scalability, allowing for the consistent production of large quantities of microspheres without compromising functionality. The streamlined and efficient methodology simplifies the production process while unlocking new possibilities in targeted therapies, tissue regeneration, and diagnostics.
Identifiers
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Registered trials
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.