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A PEG-assisted membrane coating to prepare biomimetic mesoporous silicon for PET/CT imaging of triple-negative breast cancer

Wen, Huang; Martínez, María Gómez; Happonen, Emilia; Qian, Jing; Vallejo, Vanessa Gómez; Mendazona, Helena Jorge; Jokivarsi, Kimmo; Scaravilli, Mauro; Latonen, Leena; Llop, Jordi; Lehto, Vesa Pekka; Xu, Wujun (2024-03-05)

 
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Wen, Huang
Martínez, María Gómez
Happonen, Emilia
Qian, Jing
Vallejo, Vanessa Gómez
Mendazona, Helena Jorge
Jokivarsi, Kimmo
Scaravilli, Mauro
Latonen, Leena
Llop, Jordi
Lehto, Vesa Pekka
Xu, Wujun
05.03.2024

International Journal of Pharmaceutics
123764
doi:10.1016/j.ijpharm.2023.123764
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Julkaisun pysyvä osoite on
https://urn.fi/URN:NBN:fi:tuni-202403213009

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Peer reviewed
Tiivistelmä
Triple-negative breast cancer (TNBC) diagnosis remains challenging without expressing critical receptors. Cancer cell membrane (CCm) coating has been extensively studied for targeted cancer diagnostics due to attractive features such as good biocompatibility and homotypic tumor-targeting. However, the present study found that widely used CCm coating approaches, such as extrusion, were not applicable for functionalizing irregularly shaped nanoparticles (NPs), such as porous silicon (PSi). To tackle this challenge, we proposed a novel approach that employs polyethylene glycol (PEG)-assisted membrane coating, wherein PEG and CCm are respectively functionalized on PSi NPs through chemical conjugation and physical absorption. Meanwhile, the PSi NPs were grafted with the bisphosphonate (BP) molecules for radiolabeling. Thanks to the good chelating ability of BP and homotypic tumor targeting of cancer CCm coating, a novel PSi-based contrast agent (CCm-PEG-89Zr-BP-PSi) was developed for targeted positron emission tomography (PET)/computed tomography (CT) imaging of TNBC. The novel imaging agent showed good radiochemical purity (∼99 %) and stability (∼95 % in PBS and ∼99 % in cell medium after 48 h). Furthermore, the CCm-PEG-89Zr-BP-PSi NPs had efficient homotypic targeting ability in vitro and in vivo for TNBC. These findings demonstrate a versatile biomimetic coating method to prepare novel NPs for tumor-targeted diagnosis.
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Kalevantie 5
PL 617
33014 Tampereen yliopisto
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Kalevantie 5
PL 617
33014 Tampereen yliopisto
oa[@]tuni.fi | Tietosuoja | Saavutettavuusseloste