ArticleAnalytical sciences : the international journal of the Japan Society for Analytical Chemistry2026
Biosensing device based on optical waveguide spectrometry with fluorescent solvatochromic beads for label-free tracking of avidin-biotin interaction.
Article in Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 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
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
A biosensing device based on optical waveguide spectrometry was developed using fluorescent solvatochromic beads as a sensor material. This device facilitated the analysis of the avidin-biotin interaction without labeling avidin. The fluorescent solvatochromic beads were synthesized from the 4-iodobenzoic-acid-substituted Wang resin, 2-bromothiophene, and N-tert-butyloxycarbonyl (Boc)-protected phenylpiperazine boronic ester through Suzuki-Miyaura cross-coupling, followed by condensation with NHS-biotin after the deprotection of the Boc-protected piperazine. The fluorescence spectrum of the beads showed a blue shift, and the fluorescence intensity rapidly increased with the addition of the neutravidin-dissolved phosphate-buffered saline (PBS) solution. This phenomenon indicated that the fluorescent solvatochromic dye on the beads was incorporated into neutravidin. Additionally, the kinetic and equilibrium properties of the interaction were analyzed by measuring the fluorescence intensity of the beads and comparing it with that of bovine serum albumin (BSA). The observed binding rate constants were found to be 2.7 × 10
Indexed as
Identifiers
41593291What 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.