Near-Infrared Bodipy-Based Molecular Rotors for β-Amyloid Imaging In Vivo.

biological imaging central nervous system fluorescent probes rodent models β-amyloid

Journal

Advanced healthcare materials
ISSN: 2192-2659
Titre abrégé: Adv Healthc Mater
Pays: Germany
ID NLM: 101581613

Informations de publication

Date de publication:
Oct 2023
Historique:
revised: 12 07 2023
received: 09 03 2023
pubmed: 31 7 2023
medline: 31 7 2023
entrez: 31 7 2023
Statut: ppublish

Résumé

β-amyloid (Aβ) is one of the important biomarkers for diagnosing Alzheimer's disease (AD). Many near-infrared probes based on the donor-π-acceptor structure have been developed to detect Aβ. Most reported Aβ probes are based on the N,N-dimethylamino group as the ideal donor, which is a widely accepted binding unit. As such, the development of fluorescent probes with improved binding units to detect Aβ is urgently required. Therefore, with this research three anchoring molecular rotor electron donors consisting of cyclic amines of different ring sizes are developed, namely five-membered ring (TPyr), six-membered ring (TPip), and seven-membered ring (THAI). These new anchored molecular rotors are connected to a 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) and named TPyrBDP, TPipBDP, and THAIBDP. These probes exhibit high affinities (from 28 to 54 nm) for Aβ

Identifiants

pubmed: 37523149
doi: 10.1002/adhm.202300733
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2300733

Subventions

Organisme : Academy of Medical Sciences Newton Advanced Fellowship
ID : NAFR13∖1015
Organisme : National Key Research and Development Program of China
ID : 2021YFC2101500
Organisme : China Scholarship Council
Organisme : Beijing Natural Science Foundation
ID : 7232342;8222074
Organisme : Open Research Fund of the School of Chemistry and Chemical Engineering, Henan Normal University
ID : 2020ZD01

Informations de copyright

© 2023 The Authors. Advanced Healthcare Materials published by Wiley-VCH GmbH.

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Auteurs

Lijun Ma (L)

State Key Laboratory of Chemical Resource Engineering, College of Chemistry, Beijing Advanced Innovation Center for Soft Matter Science and Engineering, Beijing University of Chemical Technology, Beijing, 100029, China.

Yujie Geng (Y)

State Key Laboratory of Chemical Resource Engineering, College of Chemistry, Beijing Advanced Innovation Center for Soft Matter Science and Engineering, Beijing University of Chemical Technology, Beijing, 100029, China.

Guoyang Zhang (G)

State Key Laboratory of Chemical Resource Engineering, College of Chemistry, Beijing Advanced Innovation Center for Soft Matter Science and Engineering, Beijing University of Chemical Technology, Beijing, 100029, China.

Ziwei Hu (Z)

State Key Laboratory of Chemical Resource Engineering, College of Chemistry, Beijing Advanced Innovation Center for Soft Matter Science and Engineering, Beijing University of Chemical Technology, Beijing, 100029, China.

Tony D James (TD)

Department of Chemistry, University of Bath, Bath, BA2 7AY, UK.
School of Chemistry and Chemical Engineering, Henan Normal University, Xinxiang, 453007, China.

Xuefei Wang (X)

School of Chemistry and Chemical Engineering, University of Chinese Academy of Sciences, Beijing, 100049, China.

Zhuo Wang (Z)

State Key Laboratory of Chemical Resource Engineering, College of Chemistry, Beijing Advanced Innovation Center for Soft Matter Science and Engineering, Beijing University of Chemical Technology, Beijing, 100029, China.
Department of Chemistry, University of Bath, Bath, BA2 7AY, UK.

Classifications MeSH