Large-Scale 3D Optical Mapping and Quantitative Analysis of Nanoparticle Distribution in Tumor Vascular Microenvironment

被引:13
作者
Koo, Dong-Jun [4 ,5 ]
Choi, Jinahn [2 ]
Ahn, Minchul [2 ,3 ]
Ahn, Benjamin H. [2 ,4 ]
Min, Dal-Hee [1 ,2 ]
Kim, Sung-Yon [2 ,3 ]
机构
[1] Seoul Natl Univ, Inst Mol Biol & Genet, Program Neurosci, Seoul 08826, South Korea
[2] Seoul Natl Univ, Dept Chem, Seoul 08826, South Korea
[3] Lemonex Inc, Inst Biotherapeut Convergence Technol, Seoul 08826, South Korea
[4] Seoul Natl Univ, Inst Mol Biol & Genet, Seoul 08826, South Korea
[5] Seoul Natl Univ, Program Neurosci, Seoul 08826, South Korea
基金
新加坡国家研究基金会;
关键词
MESOPOROUS SILICA NANOPARTICLES; SINGLE-CELL RESOLUTION; WHOLE-BODY; DRUG PENETRATION; BLOOD-VESSELS; TISSUE; DELIVERY; SIZE; NANOMEDICINE; ACCUMULATION;
D O I
10.1021/acs.bioconjchem.0c00263
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Nanoparticles (NPs) are a promising carrier for cancer therapeutics. Systemically administered NPs are transported to tumor tissues via the bloodstream, extravasated from micro-vessels, and delivered to cancer cells. The distribution of NPs in the tumor vascular microenvironment critically determines the therapeutic efficacy of NP-delivered drugs, but its precise assessment in 3D across a large volume remains challenging. Here, an analytical platform-termed OMNIA (for Optical Mapping of Nanoparticles and Image Analysis)-integrating tissue clearing, high-resolution optical imaging, and semiautomated image analysis is presented, which enables accurate, unbiased, and quantitative analysis of the distribution of NPs in relation to the vasculature across a large 3D volume. Application of OMNIA to tumor tissues revealed higher accumulation and more efficient extravasation of NPs in the tumor periphery than the core. Time-course analysis demonstrated that the accumulation of NPs in tumor peaked at 24 h after injection, but the relative distribution of NPs from the vasculature remained remarkably stable over time. Comparisons between 45- and 200-nm-sized NPs showed a lower accumulation of smaller NPs in tumors relative to the liver, yet better vessel permeation. Together, our results demonstrate that OMNIA facilitates precise and reliable evaluation of NP biodistribution, and mechanistic investigations on NP delivery to tumor tissues.
引用
收藏
页码:1784 / 1794
页数:11
相关论文
共 51 条
  • [1] Angelos S, 2007, J PHYS CHEM C, V111, P6589, DOI [10.1021/jp070721l, 10.1021/jp0707211]
  • [2] Modulating Pharmacokinetics, Tumor Uptake and Biodistribution by Engineered Nanoparticles
    Arvizo, Rochelle R.
    Miranda, Oscar R.
    Moyano, Daniel F.
    Walden, Chad A.
    Giri, Karuna
    Bhattacharya, Resham
    Robertson, J. David
    Rotello, Vincent M.
    Reid, Joel M.
    Mukherjee, Priyabrata
    [J]. PLOS ONE, 2011, 6 (09):
  • [3] Matrigel: From discovery and ECM mimicry to assays and models for cancer research
    Benton, Gabriel
    Arnaoutova, Irina
    George, Jay
    Kleinman, Hynda K.
    Koblinski, Jennifer
    [J]. ADVANCED DRUG DELIVERY REVIEWS, 2014, 79-80 : 3 - 18
  • [4] Principles of nanoparticle design for overcoming biological barriers to drug delivery
    Blanco, Elvin
    Shen, Haifa
    Ferrari, Mauro
    [J]. NATURE BIOTECHNOLOGY, 2015, 33 (09) : 941 - 951
  • [5] Size-Controlled Functionalized Mesoporous Silica Nanoparticles for Tunable Drug Release and Enhanced Anti-Tumoral Activity
    Bouchoucha, Meryem
    Cote, Marie-France
    C-Gaudreault, Rene
    Fortin, Marc-Andre
    Kleitz, Freddy
    [J]. CHEMISTRY OF MATERIALS, 2016, 28 (12) : 4243 - 4258
  • [6] Structural and molecular interrogation of intact biological systems
    Chung, Kwanghun
    Wallace, Jenelle
    Kim, Sung-Yon
    Kalyanasundaram, Sandhiya
    Andalman, Aaron S.
    Davidson, Thomas J.
    Mirzabekov, Julie J.
    Zalocusky, Kelly A.
    Mattis, Joanna
    Denisin, Aleksandra K.
    Pak, Sally
    Bernstein, Hannah
    Ramakrishnan, Charu
    Grosenick, Logan
    Gradinaru, Viviana
    Deisseroth, Karl
    [J]. NATURE, 2013, 497 (7449) : 332 - +
  • [7] Heterogeneity of macrophage infiltration and therapeutic response in lung carcinoma revealed by 3D organ imaging
    Cuccarese, Michael F.
    Dubach, J. Matthew
    Pfirschke, Christina
    Engblom, Camilla
    Garris, Christopher
    Miller, Miles A.
    Pittet, Mikael J.
    Weissleder, Ralph
    [J]. NATURE COMMUNICATIONS, 2017, 8
  • [8] Computational fluid dynamics with imaging of cleared tissue and of in vivo perfusion predicts drug uptake and treatment responses in tumours
    d'Esposito, Angela
    Sweeney, Paul W.
    Ali, Morium
    Saleh, Magdy
    Ramasawmy, Rajiv
    Roberts, Thomas A.
    Agliardi, Giulia
    Desjardins, Adrien
    Lythgoe, Mark F.
    Pedley, R. Barbara
    Shipley, Rebecca
    Walker-Samuel, Simon
    [J]. NATURE BIOMEDICAL ENGINEERING, 2018, 2 (10): : 773 - 787
  • [9] Quantifying the Ligand-Coated Nanoparticle Delivery to Cancer Cells in Solid Tumors
    Dai, Qin
    Wilhelm, Stefan
    Ding, Ding
    Syed, Abdullah Muhammad
    Sindhwani, Shrey
    Zhang, Yuwei
    Chen, Yih Yang
    MacMillan, Presley
    Chan, Warren C. W.
    [J]. ACS NANO, 2018, 12 (08) : 8423 - 8435
  • [10] Transport of drugs from blood vessels to tumour tissue
    Dewhirst, Mark W.
    Secomb, Timothy W.
    [J]. NATURE REVIEWS CANCER, 2017, 17 (12) : 738 - 750