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A short PEG linker alters the in vivo pharmacokinetics of trastuzumab to yield high-contrast immuno-PET images

Authors
Lee, WoongheeBobba, Kondapa NaiduKim, Jung YoungPark, HyunBhise, AbhinavKim, WanookLee, KiwoongRajkumar, SubramaniNam, BoraLee, Kyo ChulLee, Sang HyukKo, SanghwanLee, Hye JinJung, Sang TaekYoo, Jeongsoo
Issue Date
7-4월-2021
Publisher
ROYAL SOC CHEMISTRY
Citation
JOURNAL OF MATERIALS CHEMISTRY B, v.9, no.13, pp.2993 - 2997
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF MATERIALS CHEMISTRY B
Volume
9
Number
13
Start Page
2993
End Page
2997
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/128253
DOI
10.1039/d0tb02911d
ISSN
2050-7518
Abstract
The prolonged blood circulation of the radiolabeled antibody conjugates is problematic when using immuno-PET imaging due to the increased radiation exposure and longer hospitalization required until sufficient contrast develops. In contrast to the prevailing belief that PEGylation prolongs blood retention time, we observed that a PEGylated antibody with a short PEG(8) linker cleared much faster from the blood while maintaining tumor uptake compared to its non-PEGylated counterpart. Breast tumors were clearly visualized with a very high tumor-to-background ratio as early as 24 h after injection in immuno-positron emission tomography (PET) imaging.
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