ArticlePhotochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology2026
TPE-based cationic AIEgen with large stokes shift enables detection of blood anti-coagulator heparin with high selectivity.
Article in Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
Abstract
In this present study, a thiazolium based tetraphenyl ethylene derivative (TPET) was developed for the sensitive and selective detection of heparin (Hp), exploiting the aggregation-induced emission (AIE) feature of TPE. The probe, TPET remains weakly emissive in its dispersed monomeric form but exhibits a pronounced fluorescence "turn-on" response upon interaction with Hp. The probe, TPET due to its inherent cationic nature, experiences a strong electrostatic interaction at the vicinity of polyanionic Hp, which eventually helps TPE derivative to form aggregated species, leading to fluorescence light up response via aggregation-induced emission (AIE). This strategy allows for reliable detection of Hp down to 20.2 nM in aqueous solution. Furthermore, ruggedness of the dye-Hp complex across a broad pH range, showcasing the excellent stability and environmental robustness of the TPE-based system. Importantly, the probe demonstrates excellent preferential response towards heparin compared to other glucosamines and bio-analytes, encouraging its utilization for Hp detection even in complex biomedia. The system achieved a low limit of detection (LOD) of 614.9 nM and 78.4 nM in 25% artificial urine and 0.5% human serum, respectively. Additionally, the dye-Hp complex can also be applied for the detection of Hp antidote, protamine (Pr) as low as 0.15 μM. Overall, this work demonstrates a promising, facile, and non-invasive method for Hp detection, which can be extended to biomedical and clinical diagnostics.
Indexed as
Identifiers
41697628What OpenQuestion holds
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.