Toward Predicting Nanoparticle Distribution in Heterogeneous Tumor Tissues. MacMillan, P., Syed, A. M., Kingston, B. R., Ngai, J., Sindhwani, S., Lin, Z. P., Nguyen, L. N. M., Ngo, W., Mladjenovic, S. M., Ji, Q., Blackadar, C., & Chan, W. C. W. Nano Letters, 23(15):7197-7205, 2023. PMID: 37506224
Toward Predicting Nanoparticle Distribution in Heterogeneous Tumor Tissues [link]Paper  doi  abstract   bibtex   2 downloads  
Nanobio interaction studies have generated a significant amount of data. An important next step is to organize the data and design computational techniques to analyze the nanobio interactions. Here we developed a computational technique to correlate the nanoparticle spatial distribution within heterogeneous solid tumors. This approach led to greater than 88% predictive accuracy of nanoparticle location within a tumor tissue. This proof-of-concept study shows that tumor heterogeneity might be defined computationally by the patterns of biological structures within the tissue, enabling the identification of tumor patterns for nanoparticle accumulation.
@article{doi:10.1021/acs.nanolett.3c02186,
author = {MacMillan, Presley and Syed, Abdullah M. and Kingston, Benjamin R. and Ngai, Jessica and Sindhwani, Shrey and Lin, Zachary P. and Nguyen, Luan N. M. and Ngo, Wayne and Mladjenovic, Stefan M. and Ji, Qin and Blackadar, Colin and Chan, Warren C. W.},
title = {Toward Predicting Nanoparticle Distribution in Heterogeneous Tumor Tissues},
journal = {Nano Letters},
volume = {23},
number = {15},
pages = {7197-7205},
year = {2023},
doi = {10.1021/acs.nanolett.3c02186},
    note ={PMID: 37506224},

URL = { 
        https://doi.org/10.1021/acs.nanolett.3c02186
    
},
eprint = { 
        https://doi.org/10.1021/acs.nanolett.3c02186
    
}
,
    abstract = { Nanobio interaction studies have generated a significant amount of data. An important next step is to organize the data and design computational techniques to analyze the nanobio interactions. Here we developed a computational technique to correlate the nanoparticle spatial distribution within heterogeneous solid tumors. This approach led to greater than 88\% predictive accuracy of nanoparticle location within a tumor tissue. This proof-of-concept study shows that tumor heterogeneity might be defined computationally by the patterns of biological structures within the tissue, enabling the identification of tumor patterns for nanoparticle accumulation. }
}

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