Renally Excretable and Size-Tunable Silver Sulfide Nanoparticles for Dual-Energy Mammography or Computed Tomography
Significant effort has been focused on developing renally clearable nanoparticle agents since efficient renal clearance is important for eventual clinical translation. Silver sulfide nanoparticles (Ag2S-NP) have recently been identified as contrast agents for dual-energy mammography, computed tomogr...
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Published in: | Chemistry of materials Vol. 31; no. 19; pp. 7845 - 7854 |
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Main Authors: | , , , , , , |
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American Chemical Society
08-10-2019
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Abstract | Significant effort has been focused on developing renally clearable nanoparticle agents since efficient renal clearance is important for eventual clinical translation. Silver sulfide nanoparticles (Ag2S-NP) have recently been identified as contrast agents for dual-energy mammography, computed tomography (CT), and fluorescence imaging and probes for drug delivery and photothermal therapy with good biocompatibility. However, most Ag2S-NP reported to date are not renally excretable and are observed in vivo to accumulate and remain in the reticuloendothelial system (RES) organs, i.e., liver and spleen, for a long time, which could negatively impact their likelihood for translation. Herein, we present renally clearable, 3.1 nm Ag2S-NP with 85% of the injected dose (ID) being excreted within 24 h of intravenous injection, which is among the best clearance of similarly sized nanoparticles reported thus far (mostly between 20 and 75% of ID). The urinary excretion and low RES accumulation of these nanoparticles in mice were indicated by in vivo CT imaging and biodistribution analysis. In summary, these ultrasmall Ag2S-NP can be effectively eliminated via urine and have high translational potential for various biomedical applications. |
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AbstractList | Significant effort has been focused on developing renally clearable nanoparticle agents since efficient renal clearance is important for eventual clinical translation. Silver sulfide nanoparticles (Ag2S-NP) have recently been identified as contrast agents for dual-energy mammography, computed tomography (CT), and fluorescence imaging and probes for drug delivery and photothermal therapy with good biocompatibility. However, most Ag2S-NP reported to date are not renally excretable and are observed in vivo to accumulate and remain in the reticuloendothelial system (RES) organs, i.e., liver and spleen, for a long time, which could negatively impact their likelihood for translation. Herein, we present renally clearable, 3.1 nm Ag2S-NP with 85% of the injected dose (ID) being excreted within 24 h of intravenous injection, which is among the best clearance of similarly sized nanoparticles reported thus far (mostly between 20 and 75% of ID). The urinary excretion and low RES accumulation of these nanoparticles in mice were indicated by in vivo CT imaging and biodistribution analysis. In summary, these ultrasmall Ag2S-NP can be effectively eliminated via urine and have high translational potential for various biomedical applications. Significant effort has been focused on developing renally-clearable nanoparticle agents since efficient renal clearance is important for eventual clinical translation. Silver sulfide nanoparticles (Ag 2 S-NP) have recently been identified as contrast agents for dual energy mammography, computed tomography (CT) and fluorescence imaging and probes for drug delivery and photothermal therapy with good biocompatibility. However, most Ag 2 S-NP reported to date are not renally excretable and are observed in vivo to accumulate and remain in the reticuloendothelial system (RES) organs, i.e. liver and spleen, for a long time, which could negatively impact their likelihood for translation. Herein, we present renally-clearable, 3.1 nm Ag 2 S-NP with 85% of the injected dose (ID) being excreted within 24 hours of intravenous injection, which is amongst the best clearance of similarly sized nanoparticles reported thus far (mostly between 20-75% of ID). The urinary excretion and low RES accumulation of these nanoparticles in mice were indicated by in vivo CT imaging and biodistribution analysis. In summary, these ultrasmall Ag 2 S-NP can be effectively eliminated via urine and have high translational potential for various biomedical applications. |
Author | Lau, Kristen C Maidment, Andrew D. A Cruz, Emma D Hsu, Jessica C Cormode, David P Bouché, Mathilde Kim, Johoon |
AuthorAffiliation | Department of Bioengineering University of Pennsylvania Department of Radiology |
AuthorAffiliation_xml | – name: University of Pennsylvania – name: Department of Bioengineering – name: Department of Radiology – name: 1 Department of Radiology, University of Pennsylvania 3400 Spruce St, 1 Silverstein, Philadelphia, PA 19104, USA – name: 2 Department of Bioengineering, University of Pennsylvania, Philadelphia, PA, USA |
Author_xml | – sequence: 1 givenname: Jessica C orcidid: 0000-0002-3599-2834 surname: Hsu fullname: Hsu, Jessica C organization: University of Pennsylvania – sequence: 2 givenname: Emma D surname: Cruz fullname: Cruz, Emma D organization: Department of Radiology – sequence: 3 givenname: Kristen C surname: Lau fullname: Lau, Kristen C organization: University of Pennsylvania – sequence: 4 givenname: Mathilde orcidid: 0000-0003-2707-1290 surname: Bouché fullname: Bouché, Mathilde organization: Department of Radiology – sequence: 5 givenname: Johoon orcidid: 0000-0002-1138-5984 surname: Kim fullname: Kim, Johoon organization: University of Pennsylvania – sequence: 6 givenname: Andrew D. A surname: Maidment fullname: Maidment, Andrew D. A organization: Department of Radiology – sequence: 7 givenname: David P orcidid: 0000-0002-8391-9500 surname: Cormode fullname: Cormode, David P email: david.cormode@uphs.upenn.edu organization: University of Pennsylvania |
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Title | Renally Excretable and Size-Tunable Silver Sulfide Nanoparticles for Dual-Energy Mammography or Computed Tomography |
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