Nanoparticle elasticity directs tumor uptake

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Nanoparticle elasticity directs tumor uptake

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Title: Nanoparticle elasticity directs tumor uptake
Author: Guo, Peng; Liu, Daxing; Subramanyam, Kriti; Wang, Biran; Yang, Jiang; Huang, Jing; Auguste, Debra T.; Moses, Marsha A.

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Citation: Guo, Peng, Daxing Liu, Kriti Subramanyam, Biran Wang, Jiang Yang, Jing Huang, Debra T. Auguste, and Marsha A. Moses. 2018. “Nanoparticle elasticity directs tumor uptake.” Nature Communications 9 (1): 130. doi:10.1038/s41467-017-02588-9. http://dx.doi.org/10.1038/s41467-017-02588-9.
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Abstract: To date, the role of elasticity in drug delivery remains elusive due to the inability to measure microscale mechanics and alter rheology without affecting chemistry. Herein, we describe the in vitro cellular uptake and in vivo tumor uptake of nanolipogels (NLGs). NLGs are composed of identical lipid bilayers encapsulating an alginate core, with tunable elasticity. The elasticity of NLGs was evaluated by atomic force microscopy, which demonstrated that they exhibit Young’s moduli ranging from 45 ± 9 to 19,000 ± 5 kPa. Neoplastic and non-neoplastic cells exhibited significantly greater uptake of soft NLGs (Young’s modulus <1.6 MPa) relative to their elastic counterparts (Young’s modulus >13.8 MPa). In an orthotopic breast tumor model, soft NLGs accumulated significantly more in tumors, whereas elastic NLGs preferentially accumulated in the liver. Our findings demonstrate that particle elasticity directs tumor accumulation, suggesting that it may be a design parameter to enhance tumor delivery efficiency.
Published Version: doi:10.1038/s41467-017-02588-9
Other Sources: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5760638/pdf/
Terms of Use: This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#LAA
Citable link to this page: http://nrs.harvard.edu/urn-3:HUL.InstRepos:34868904
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