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The quinoline photoremovable group (PPG) platform - a medicinal chemist's approach for photocage development and applications
ID
Kontra, Bence
(
Author
),
ID
Mucsi, Zoltán
(
Author
),
ID
Ilaš, Janez
(
Author
),
ID
Dunkel, Petra
(
Author
)
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MD5: 7EA4321C53F42554E78EFDF7D9011BC3
URL - Source URL, Visit
https://onlinelibrary.wiley.com/doi/10.1002/med.22111
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Abstract
Photoremovable protecting groups (PPGs) offer a straightforward solution for the temporary inactivation of biologically active substrates and their subsequent controlled release by light irradiation. Their relatively easy design and mode of application have made them useful tools for studying dynamic biological processes in vitro and in vivo. Recently, there has been a growing body of data investigating their potential application in the development of drug delivery systems. Of the various PPG scaffolds in use, quinoline photocages have a history of about 20 years. The structure-property relationships of quinoline PPGs, as well as alternative multibranch designs based on quinoline monomers have been thoroughly studied both experimentally and theoretically. Therefore, quinoline PPGs serve as a representative study of PPG development, showing how the various applications of quinoline photocages followed the chemical optimization or how the applications drove the chemical design. Since the raison d’être of PPGs lies in their application for light-activated release of various substrates or performing light-activated structural changes in materials, it is crucial to understand how PPGs are selected and utilized by their end-users, who are often not chemists themselves. Therefore, we discuss whether the conclusions drawn from the selected quinoline PPG family could lead to more general insights for the field as whole. As PPG-related applications still rely heavily on a limited number of chemical scaffolds, it is worth considering, what could be the reasons for the slow uptake of novel chemical scaffolds.
Language:
English
Keywords:
drug delivery systems
,
neuronal signaling
,
photoremovable protecting groups
,
quinoline photocages
,
structure‐property relationships
,
two‐photon absorption
,
two‐photon uncaging
Work type:
Article
Typology:
1.02 - Review Article
Organization:
FFA - Faculty of Pharmacy
Publication status:
Published
Publication version:
Version of Record
Year:
2024
Number of pages:
Str. 1423-1451
Numbering:
Vol. 45, iss. 5
PID:
20.500.12556/RUL-175591
UDC:
615.015.14
ISSN on article:
1098-1128
COBISS.SI-ID:
245245955
Publication date in RUL:
05.11.2025
Views:
88
Downloads:
60
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Record is a part of a journal
Title:
Medicinal research reviews
Shortened title:
Med. res. rev.
Publisher:
Wiley
ISSN:
1098-1128
COBISS.SI-ID:
512824089
Licences
License:
CC BY 4.0, Creative Commons Attribution 4.0 International
Link:
http://creativecommons.org/licenses/by/4.0/
Description:
This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.
Secondary language
Language:
Slovenian
Keywords:
nevronska signalizacija
,
fotoodstranljive zaščitne skupine
,
kinolinske fotokletke
,
razmerja med strukturo in lastnostmi
,
dvofotonska absorpcija
,
dvofotonsko odstranjevanje iz škatle
,
dostavni sistemi
Projects
Funder:
Other - Other funder or multiple funders
Funding programme:
Hungary, National Research, Development and Innovation Office (NKFIH)
Project number:
SNN 135825
Funder:
Other - Other funder or multiple funders
Funding programme:
Hungary, National Research, Development and Innovation Office (NKFIH)
Project number:
TKP2021‐NVA‐14
Funder:
Other - Other funder or multiple funders
Funding programme:
Hungary, National Research, Development and Innovation Office (NKFIH)
Project number:
ED‐2022‐00208
Funder:
ARIS - Slovenian Research and Innovation Agency
Project number:
P1-0208
Name:
Farmacevtska kemija: načrtovanje, sinteza in vrednotenje učinkovin
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