Evidence map›Paper›PMID 37699547›Full record

ArticleACS applied materials & interfaces2023

Formation of Highly Emissive Anthracene Excimers for Aggregation-Induced Emission/Self-Assembly Directed (Bio)imaging.

Pedro J Pacheco-Liñán, Carlos Alonso-Moreno, Alberto Ocaña, Consuelo Ripoll, Elena García-Gil, Andrés Garzón-Ruíz, Diego Herrera-Ochoa, Sofía Blas-Gómez, Boiko Cohen, Iván Bravo

Open access · hybridAbstract read
In one paragraph

Article in ACS applied materials & interfaces, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.7field-weighted citation impact, top 16% of its field
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

3 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
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

10 authors at 4 institutions in 1 country.

Pedro J Pacheco-LiñánUnidad nanoDrug. Facultad de Farmacia de Albacete, Universidad de Castilla-La Mancha, 02008 Albacete, Spain.ORCID 0000-0002-8591-0147
Carlos Alonso-MorenoUnidad nanoDrug. Facultad de Farmacia de Albacete, Universidad de Castilla-La Mancha, 02008 Albacete, Spain.ORCID 0000-0002-7588-0781
Alberto OcañaExperimental Therapeutics Unit, Hospital clínico San Carlos, IdISSC and CIBERONC, 28040 Madrid, Spain.
Consuelo RipollUnidad nanoDrug. Facultad de Farmacia de Albacete, Universidad de Castilla-La Mancha, 02008 Albacete, Spain.
Elena García-GilUnidad de Investigación del Complejo Hospitalario Universitario de Albacete. Oncología Traslacional, 02008 Albacete, Spain.
Andrés Garzón-RuízUnidad nanoDrug. Facultad de Farmacia de Albacete, Universidad de Castilla-La Mancha, 02008 Albacete, Spain.ORCID 0000-0002-0077-4562
Diego Herrera-OchoaUnidad nanoDrug. Facultad de Farmacia de Albacete, Universidad de Castilla-La Mancha, 02008 Albacete, Spain.ORCID 0000-0002-3870-4113
Sofía Blas-GómezUnidad nanoDrug. Facultad de Farmacia de Albacete, Universidad de Castilla-La Mancha, 02008 Albacete, Spain.
Boiko CohenDepartamento de Química Física, Facultad de Ciencias Ambientales y Bioquímica, and Instituto de Nanociencia, Nanotecnología y Materiales Moleculares (INAMOL), Universidad de Castilla-La Mancha, Avenida Carlos III, S/N, 45071 Toledo, Spain.ORCID 0000-0002-5400-4678
Iván BravoUnidad nanoDrug. Facultad de Farmacia de Albacete, Universidad de Castilla-La Mancha, 02008 Albacete, Spain.ORCID 0000-0003-1589-5399
University of Castilla-La Mancha · ESComplejo Hospitalario Universitario de Albacete · ESHospital Clínico San Carlos · ESORFEO-CINQA Research Network · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

AIEgens have emerged as a promising alternative to molecular rotors in bioimaging applications. However, transferring the concept of aggregation-induced emission (AIE) from solution to living systems remains a challenge. Given the highly heterogeneous nature and the compartmentalization of the cell, different approaches are needed to control the self-assembly within the crowded intricate cellular environment. Herein, we report for the first time the self-assembly mechanism of an anthracene-guanidine derivative (AG) forming the rare and highly emissive T-shaped dimer in breast cancer cell lines as a proof of concept. This process is highly sensitive to the local environment in terms of polarity, viscosity, and/or water quantity that should enable the use of the AG as a fluorescence lifetime imaging biosensor for intracellular imaging of cellular structures and the monitoring of intracellular state parameters. Different populations of the monomer and T-shaped and π-π dimers were observed in the cell membrane, cytoplasm, and nucleoplasm, related to the local viscosity and presence of water. The T-shaped dimer is formed preferentially in the nucleus because of the higher density and viscosity compared to the cytoplasm. The present results should serve as a precursor for the development of new design strategies for molecular systems for a wide range of applications such as cell viscosity, density, or temperature sensing and imaging.

Indexed as

AnthracenesOptical ImagingCell MembraneCytoplasmPolymersWateranthraceneAnthracenesPolymersWateraggregation-induced emissionAIEgensbreast cancerFLIMfluorescence lifetime imaging microscopyliving systemsmolecular rotorsT-shaped anthracene dimers

Identifiers

PMID37699547
PMCPMC11165449
OpenAlexW4386646693

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.