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Photoacoustic Imaging of Embryonic Stem Cell-Derived Cardiomyocytes in Living Hearts with Ultrasensitive Semiconducting Polymer Nanoparticles.
Qin, Xulei; Chen, Haodong; Yang, Huaxiao; Wu, Haodi; Zhao, Xin; Wang, Huiyuan; Chour, Tony; Neofytou, Evgenios; Ding, Dan; Daldrup-Link, Heike; Heilshorn, Sarah C; Li, Kai; Wu, Joseph C.
Afiliação
  • Qin X; Stanford Cardiovascular Institute, Stanford, CA, 94305, United States.
  • Chen H; Stanford Cardiovascular Institute, Stanford, CA, 94305, United States.
  • Yang H; Stanford Cardiovascular Institute, Stanford, CA, 94305, United States.
  • Wu H; Stanford Cardiovascular Institute, Stanford, CA, 94305, United States.
  • Zhao X; Stanford Cardiovascular Institute, Stanford, CA, 94305, United States.
  • Wang H; Department of Materials Science and Engineering, Stanford, CA, 94305, United States.
  • Chour T; Stanford Cardiovascular Institute, Stanford, CA, 94305, United States.
  • Neofytou E; Stanford Cardiovascular Institute, Stanford, CA, 94305, United States.
  • Ding D; State Key Laboratory of Medicinal Chemical Biology, College of Life Sciences, Nankai University, China, 300071.
  • Daldrup-Link H; Department of Radiology, Stanford, CA, 94305, United States.
  • Heilshorn SC; Department of Materials Science and Engineering, Stanford, CA, 94305, United States.
  • Li K; Department of Radiology, Stanford, CA, 94305, United States.
  • Wu JC; Stanford Cardiovascular Institute, Stanford, CA, 94305, United States.
Adv Funct Mater ; 28(1)2018 Jan 04.
Article em En | MEDLINE | ID: mdl-30473658
ABSTRACT
The last decade has seen impressive progress in human embryonic stem cell-derived cardiomyocytes (hESC-CMs) that makes them ideal tools to repair injured hearts. To achieve an optimal outcome, advanced molecular imaging methods are essential to accurately track these transplanted cells in the heart. Herein, we demonstrate for the first time that a class of photoacoustic nanoparticles (PANPs) incorporating semiconducting polymers (SPs) as contrast agents can be used in the photoacoustic imaging (PAI) of transplanted hESC-CMs in living mouse hearts. This is achieved by virtue of two benefits of PANPs. First, strong PA signals and specific spectral features of SPs allow PAI to sensitively detect and distinguish a small number of PANP-labeled cells (2,000) from background tissues in vivo. Second, the PANPs show a high efficiency for hESC-CM labeling without adverse effects on cell structure, function, and gene expression. Assisted by ultrasound imaging, the delivery and engraftment of hESC-CMs in living mouse hearts can be assessed by PANP-based PAI with high spatial resolution (~100 µm). In summary, this study explores and validates a novel application of SPs as a PA contrast agent to track labeled cells with high sensitivity and accuracy in vivo, highlighting the advantages of integrating PAI and PANPs to advance cardiac regenerative therapies.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article