Size‐Dependent Penetration of Nanoparticles in Tumor Spheroids: A Multidimensional and Quantitative Study of Transcellular and Paracellular Pathways

Author:

Chen Wenjing12,Wang Wenqian1ORCID,Xie Zhouzun1ORCID,Centurion Franco12ORCID,Sun Bin1ORCID,Paterson David J.3ORCID,Tsao Simon Chang‐Hao45ORCID,Chu Dewei6ORCID,Shen Yansong1ORCID,Mao Guangzhao1ORCID,Gu Zi127ORCID

Affiliation:

1. School of Chemical Engineering University of New South Wales Sydney NSW 2052 Australia

2. Australian Centre for NanoMedicine University of New South Wales Sydney NSW 2052 Australia

3. Australian Synchrotron ANSTO Clayton VIC 3168 Australia

4. School of Natural Sciences Macquarie University Sydney NSW 2109 Australia

5. Department of Surgery Austin Hospital University of Melbourne Melbourne VIC 3084 Australia

6. School of Materials Science and Engineering University of New South Wales Sydney NSW 2052 Australia

7. UNSW RNA Institute University of New South Wales Sydney NSW 2052 Australia

Abstract

AbstractTumor penetration of nanoparticles is crucial in nanomedicine, but the mechanisms of tumor penetration are poorly understood. This work presents a multidimensional, quantitative approach to investigate the tissue penetration behavior of nanoparticles, with focuses on the particle size effect on penetration pathways, in an MDA‐MB‐231 tumor spheroid model using a combination of spectrometry, microscopy, and synchrotron beamline techniques. Quasi‐spherical gold nanoparticles of different sizes are synthesized and incubated with 2D and 3D MDA‐MB‐231 cells and spheroids with or without an energy‐dependent cell uptake inhibitor. The distribution and penetration pathways of nanoparticles in spheroids are visualized and quantified by inductively coupled plasma mass spectrometry, two‐photon microscopy, and synchrotron X‐ray fluorescence microscopy. The results reveal that 15 nm nanoparticles penetrate spheroids mainly through an energy‐independent transcellular pathway, while 60 nm nanoparticles penetrate primarily through an energy‐dependent transcellular pathway. Meanwhile, 22 nm nanoparticles penetrate through both transcellular and paracellular pathways and they demonstrate the greatest penetration ability in comparison to other two sizes. The multidimensional analytical methodology developed through this work offers a generalizable approach to quantitatively study the tissue penetration of nanoparticles, and the results provide important insights into the designs of nanoparticles with high accumulation at a target site.

Funder

Australian Synchrotron

Publisher

Wiley

Subject

Biomaterials,Biotechnology,General Materials Science,General Chemistry

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