Development of a solid-supported light-triggered nitric oxide donor

Nitric Oxide (NO) photocleavable donors are useful tools for interrogating nitric oxide signalling and have potential use in photopharmacological applications. There is currently intensive research into newer methods to improve NO release and kinetic profiles. Herein, we report the design and synthe...

Ausführliche Beschreibung

Bibliographische Detailangaben
Veröffentlicht in:Journal of photochemistry and photobiology. A, Chemistry. - 1998. - 450(2024) vom: 01. Feb.
1. Verfasser: Cabello, Maidileyvis Castro (VerfasserIn)
Weitere Verfasser: Lippert, Alexander R
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2024
Zugriff auf das übergeordnete Werk:Journal of photochemistry and photobiology. A, Chemistry
Schlagworte:Journal Article cellular delivery nitric oxide photocleavable donors solid-phase chemistry
LEADER 01000naa a22002652 4500
001 NLM368953386
003 DE-627
005 20240229171135.0
007 cr uuu---uuuuu
008 240229s2024 xx |||||o 00| ||eng c
024 7 |a 10.1016/j.jphotochem.2024.115466  |2 doi 
028 5 2 |a pubmed24n1310.xml 
035 |a (DE-627)NLM368953386 
035 |a (NLM)38405370 
035 |a (PII)115466 
040 |a DE-627  |b ger  |c DE-627  |e rakwb 
041 |a eng 
100 1 |a Cabello, Maidileyvis Castro  |e verfasserin  |4 aut 
245 1 0 |a Development of a solid-supported light-triggered nitric oxide donor 
264 1 |c 2024 
336 |a Text  |b txt  |2 rdacontent 
337 |a ƒaComputermedien  |b c  |2 rdamedia 
338 |a ƒa Online-Ressource  |b cr  |2 rdacarrier 
500 |a Date Revised 28.02.2024 
500 |a published: Print-Electronic 
500 |a Citation Status PubMed-not-MEDLINE 
520 |a Nitric Oxide (NO) photocleavable donors are useful tools for interrogating nitric oxide signalling and have potential use in photopharmacological applications. There is currently intensive research into newer methods to improve NO release and kinetic profiles. Herein, we report the design and synthesis of a solid-supported photocleavable NO donor synthesized by ligating an N-nitroso photocleavable nitric oxide derivative to a TentaGel® polymer resin bead. Illumination with 365 nm light released nitric oxide that could be tracked via a turn-on fluorescence response (λex = 450 nm, λem = 545 nm) and measured using the Griess assay and diaminorhodamine derivatives. These beads were further shown to be compatible with living A549 cells and had the ability to deliver greater concentrations of nitric oxide to cells proximal to a bead versus cells at more distal locations within the same well 
650 4 |a Journal Article 
650 4 |a cellular delivery 
650 4 |a nitric oxide 
650 4 |a photocleavable donors 
650 4 |a solid-phase chemistry 
700 1 |a Lippert, Alexander R  |e verfasserin  |4 aut 
773 0 8 |i Enthalten in  |t Journal of photochemistry and photobiology. A, Chemistry  |d 1998  |g 450(2024) vom: 01. Feb.  |w (DE-627)NLM098186027  |x 1010-6030  |7 nnns 
773 1 8 |g volume:450  |g year:2024  |g day:01  |g month:02 
856 4 0 |u http://dx.doi.org/10.1016/j.jphotochem.2024.115466  |3 Volltext 
912 |a GBV_USEFLAG_A 
912 |a SYSFLAG_A 
912 |a GBV_NLM 
912 |a GBV_ILN_350 
951 |a AR 
952 |d 450  |j 2024  |b 01  |c 02