2022
DOI: 10.1039/d2tb00765g
|View full text |Cite
|
Sign up to set email alerts
|

Hypochlorous acid triggered fluorescent probes forin situimaging of a psoriasis model

Abstract: Psoriasis is a common skin disease with complex pathogenesis that lacks of diagnostic methods. Typically, psoriasis is an inflammation-related disease accompanied by high expression of reactive oxygen species (ROS) in...

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
4
0

Year Published

2023
2023
2024
2024

Publication Types

Select...
7

Relationship

0
7

Authors

Journals

citations
Cited by 10 publications
(4 citation statements)
references
References 63 publications
(76 reference statements)
0
4
0
Order By: Relevance
“…Furthermore, after addition of HOCl, an absorption peak at around 665 nm and an emission peak at around 688 nm occurred, which corresponded with the absorption peak (665 nm) and emission peak (692 nm) of methylene blue, demonstrating that methylene blue is released when the probes interact with HOCl. We hypothesize that the mechanism of probes reacting to HOCl is depicted in Figure b based on relevant literature studies. , HOCl nucleophilically attacks the electron-deficient carbon atom in the amide carbon group and then further oxidizes it to separate the amide moiety from the methylene blue moiety. This process releases the fluorophore methylene blue and the unstable carbamic acid structure, which is then rapidly hydrolyzed in aqueous solution to form the amino group.…”
Section: Results and Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Furthermore, after addition of HOCl, an absorption peak at around 665 nm and an emission peak at around 688 nm occurred, which corresponded with the absorption peak (665 nm) and emission peak (692 nm) of methylene blue, demonstrating that methylene blue is released when the probes interact with HOCl. We hypothesize that the mechanism of probes reacting to HOCl is depicted in Figure b based on relevant literature studies. , HOCl nucleophilically attacks the electron-deficient carbon atom in the amide carbon group and then further oxidizes it to separate the amide moiety from the methylene blue moiety. This process releases the fluorophore methylene blue and the unstable carbamic acid structure, which is then rapidly hydrolyzed in aqueous solution to form the amino group.…”
Section: Results and Discussionmentioning
confidence: 99%
“…We hypothesize that the mechanism of probes reacting to HOCl is depicted in Figure 2b based on relevant literature studies. 59,60 HOCl nucleophilically attacks the electron-deficient carbon atom in the amide carbon group and then further oxidizes it to separate the amide moiety from the methylene blue moiety. This process releases the fluorophore methylene blue and the unstable carbamic acid structure, which is then rapidly hydrolyzed in aqueous solution to form the amino group.…”
Section: S20 S29 and S31) The Above Results Indicate That The Probesmentioning
confidence: 99%
“…In recent years, several other articles (probes 15 and 17) have reported the use of such phenazine derivatives similar to probe 13 in the detection of arthritis. [164][165][166] Due to the sensitivity of phenazine derivatives in detecting HClO, these phenazine compounds could be further developed for in-depth arthritis studies.…”
Section: Fl Imaging Of Arthritismentioning
confidence: 99%
“…In our previous studies, we have successfully developed a series of HOCl-specific fluorescent probes using methylene blue (MB) structure and utilized them to investigate the presence of HOCl in diverse conditions such as the arthritis 36 , tumor microenvironment 37 - 39 , psoriasis 40 , and other diseases 41 - 43 . Herein, we designed and synthesized a fluorescent probe DHU-CBA1 by attachment of IBP (ibuprofen, a nonsteroidal anti-inflammatory drug) and MB.…”
Section: Introductionmentioning
confidence: 99%