Evidence map›Paper›PMID 42857226›Full record

ArticleRSC advances2026

Simulation-guided design of a 3D flow focusing chip for the uniform production of polymer dots.

Reynaldo Carlos K Montalbo, Yung-Teng Chiu, Aishwarya Satpathy, Yang-Hsiang Chan, Hsiung-Lin Tu

Abstract read
In one paragraph

Article in RSC advances, 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

5 authors.

Reynaldo Carlos K MontalboDepartment of Engineering and System Science, National Tsing-Hua University Hsinchu 300044 Taiwan.
Yung-Teng ChiuInstitute of Chemistry, Academia Sinica Taipei 11529 Taiwan hltu@as.edu.tw.
Aishwarya SatpathyInstitute of Chemistry, Academia Sinica Taipei 11529 Taiwan hltu@as.edu.tw.
Yang-Hsiang ChanDepartment of Applied Chemistry, National Yang Ming Chiao Tung University Hsinchu 300 Taiwan.ORCID https://orcid.org/0000-0002-9007-3910
Hsiung-Lin TuInstitute of Chemistry, Academia Sinica Taipei 11529 Taiwan hltu@as.edu.tw.ORCID https://orcid.org/0000-0003-1125-1879

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Semiconducting polymer dots (Pdots) are fluorescent conjugated polymer nanoparticles that exhibit high photoluminescence and biocompatibility, making them promising for high photoluminescence and biocompatibility, giving them high potential in biomedical applications such as bioimaging, drug delivery, and phototherapy. Accordingly, the size of the Pdots has become a critical factor in determining their bioavailability, biodistribution, and clearance. Towards this goal, microfluidic technologies have gained attention for the precise control of their size. However, the limitations of conventional glass capillary systems still inhibit the production of uniform and small nanoparticles. Here, computational fluid dynamics (CFD) simulations were used to guide the design of a 3D printed master for the fabrication of a solvent resistant 3D flow focusing microfluidic chip. Compared to glass capillary microfluidics, the developed chip offers more flexibility towards optimization of the design. Small and homogeneous Pdots (<50 nm) from commercially available MEH-PPV, CN-PPV, F8BT, and custom synthesized Pttc-4O-TTQ were produced. Large red shifts in the emission spectra of some Pdots suggest an efficient and tight packing of the polymers within the particles. Coprecipitation of the polymers with chitosan or PMSA enhanced their cell uptake, with complete cell uptake achieved in less than an hour in some cases. Furthermore, the spectral properties of both aggregation-induced quenching-prone and aggregation-induced emission-prone Pdots were observed, highlighting the chip's flexibility with different types of Pdots. The 3D flow focusing chip offers an accessible and cost-effective alternative to traditional microfluidic systems for the production of smaller Pdots.

Identifiers

PMID42857226
PMCPMC13651805

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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.