External‐Radiation‐Induced Local Hydroxylation Enables Remote Release of Functional Molecules in Tumors
Abstract Radiation‐induced cleavage for controlled release in vivo is yet to be established. We demonstrate the use of 3,5‐dihydroxybenzyl carbamate (DHBC) as a masking group that is selectively and efficiently removed by external radiation in vitro and in vivo. DHBC reacts mainly with hydroxyl radicals produced by radiation to afford hydroxylation at para/ ortho positions, followed by 1,4‐ or 1,6‐elimination to rescue the functionality of the client molecule. The reaction is rapid and can liberate functional molecules under physiological conditions. This controlled‐release platform is compatible with living systems, as demonstrated by the release of a rhodol fluorophore derivative in cells and tumor xenografts. The combined benefits of the robust caging group, the good release yield, and the independence of penetration depth make DHBC derivatives attractive chemical caging moieties for use in chemical biology and prodrug activation..
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2020 |
---|---|
Erschienen: |
2020 |
Enthalten in: |
Zur Gesamtaufnahme - volume:132 |
---|---|
Enthalten in: |
Angewandte Chemie - 132(2020), 48, Seite 21730-21736 |
Beteiligte Personen: |
Fu, Qunfeng [VerfasserIn] |
---|
BKL: |
---|
Anmerkungen: |
© 2020 Wiley‐VCH GmbH |
---|
Umfang: |
7 |
---|
doi: |
10.1002/ange.202005612 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
WLY001829912 |
---|
LEADER | 01000caa a22002652 4500 | ||
---|---|---|---|
001 | WLY001829912 | ||
003 | DE-627 | ||
005 | 20230307111102.0 | ||
007 | cr uuu---uuuuu | ||
008 | 230210s2020 xx |||||o 00| ||und c | ||
024 | 7 | |a 10.1002/ange.202005612 |2 doi | |
028 | 5 | 2 | |a ANGE_ANGE202005612.xml |
035 | |a (DE-627)WLY001829912 | ||
035 | |a (WILEY)ANGE202005612 | ||
040 | |a DE-627 |b ger |c DE-627 |e rda | ||
082 | 0 | 4 | |a 540 |a 660 |q ASE |
084 | |a 35.00 |2 bkl | ||
100 | 1 | |a Fu, Qunfeng |e verfasserin |4 aut | |
245 | 1 | 0 | |a External‐Radiation‐Induced Local Hydroxylation Enables Remote Release of Functional Molecules in Tumors |
264 | 1 | |c 2020 | |
300 | |a 7 | ||
336 | |a Text |b txt |2 rdacontent | ||
337 | |a Computermedien |b c |2 rdamedia | ||
338 | |a Online-Ressource |b cr |2 rdacarrier | ||
500 | |a © 2020 Wiley‐VCH GmbH | ||
520 | |a Abstract Radiation‐induced cleavage for controlled release in vivo is yet to be established. We demonstrate the use of 3,5‐dihydroxybenzyl carbamate (DHBC) as a masking group that is selectively and efficiently removed by external radiation in vitro and in vivo. DHBC reacts mainly with hydroxyl radicals produced by radiation to afford hydroxylation at para/ ortho positions, followed by 1,4‐ or 1,6‐elimination to rescue the functionality of the client molecule. The reaction is rapid and can liberate functional molecules under physiological conditions. This controlled‐release platform is compatible with living systems, as demonstrated by the release of a rhodol fluorophore derivative in cells and tumor xenografts. The combined benefits of the robust caging group, the good release yield, and the independence of penetration depth make DHBC derivatives attractive chemical caging moieties for use in chemical biology and prodrug activation. | ||
700 | 1 | |a Li, Hongyu |4 aut | |
700 | 1 | |a Duan, Dongban |4 aut | |
700 | 1 | |a Wang, Changlun |4 aut | |
700 | 1 | |a Shen, Siyong |4 aut | |
700 | 1 | |a Ma, Huimin |4 aut | |
700 | 1 | |a Liu, Zhibo |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Angewandte Chemie |g 132(2020), 48, Seite 21730-21736 |w (DE-627)WLY001751093 |x 15213757 |7 nnns |
773 | 1 | 8 | |g volume:132 |g year:2020 |g number:48 |g pages:21730-21736 |g extent:7 |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_WLY | ||
936 | b | k | |a 35.00 |q ASE |
951 | |a AR | ||
952 | |d 132 |j 2020 |e 48 |h 21730-21736 |g 7 |