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Polyethylenimine-Coated Ultrasmall Holmium Oxide Nanoparticles: Synthesis, Characterization, Cytotoxicities, and Water Proton Spin Relaxivities

Water proton spin relaxivities, colloidal stability, and biocompatibility of nanoparticle magnetic resonance imaging (MRI) contrast agents depend on surface-coating ligands. In this study, hydrophilic and biocompatible polyethylenimines (PEIs) of different sizes (M(n) = 1200 and 60,000 amu) were use...

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Detalles Bibliográficos
Autores principales: Liu, Shuwen, Yue, Huan, Ho, Son Long, Kim, Soyeon, Park, Ji Ae, Tegafaw, Tirusew, Ahmad, Mohammad Yaseen, Kim, Seungho, Saidi, Abdullah Khamis Ali Al, Zhao, Dejun, Liu, Ying, Nam, Sung-Wook, Chae, Kwon Seok, Chang, Yongmin, Lee, Gang Ho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9101814/
https://www.ncbi.nlm.nih.gov/pubmed/35564300
http://dx.doi.org/10.3390/nano12091588
Descripción
Sumario:Water proton spin relaxivities, colloidal stability, and biocompatibility of nanoparticle magnetic resonance imaging (MRI) contrast agents depend on surface-coating ligands. In this study, hydrophilic and biocompatible polyethylenimines (PEIs) of different sizes (M(n) = 1200 and 60,000 amu) were used as surface-coating ligands for ultrasmall holmium oxide (Ho(2)O(3)) nanoparticles. The synthesized PEI1200- and PEI60000-coated ultrasmall Ho(2)O(3) nanoparticles, with an average particle diameter of 2.05 and 1.90 nm, respectively, demonstrated low cellular cytotoxicities, good colloidal stability, and appreciable transverse water proton spin relaxivities (r(2)) of 13.1 and 9.9 s(−1)mM(−1), respectively, in a 3.0 T MR field with negligible longitudinal water proton spin relaxivities (r(1)) (i.e., 0.1 s(−1)mM(−1)) for both samples. Consequently, for both samples, the dose-dependent contrast changes in the longitudinal (R(1)) and transverse (R(2)) relaxation rate map images were negligible and appreciable, respectively, indicating their potential as efficient transverse T(2) MRI contrast agents in vitro.