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Echogenic exosomes as ultrasound contrast agents

Exosomes are naturally secreted extracellular bilayer vesicles (diameter 40–130 nm), which have recently been found to play a critical role in cell-to-cell communication and biomolecule delivery. Their unique characteristics—stability, permeability, biocompatibility and low immunogenicity—have made...

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Autores principales: Osborn, Jenna, Pullan, Jessica E., Froberg, James, Shreffler, Jacob, Gange, Kara N., Molden, Todd, Choi, Yongki, Brooks, Amanda, Mallik, Sanku, Sarkar, Kausik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: RSC 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9410358/
https://www.ncbi.nlm.nih.gov/pubmed/36034734
http://dx.doi.org/10.1039/d0na00339e
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author Osborn, Jenna
Pullan, Jessica E.
Froberg, James
Shreffler, Jacob
Gange, Kara N.
Molden, Todd
Choi, Yongki
Brooks, Amanda
Mallik, Sanku
Sarkar, Kausik
author_facet Osborn, Jenna
Pullan, Jessica E.
Froberg, James
Shreffler, Jacob
Gange, Kara N.
Molden, Todd
Choi, Yongki
Brooks, Amanda
Mallik, Sanku
Sarkar, Kausik
author_sort Osborn, Jenna
collection PubMed
description Exosomes are naturally secreted extracellular bilayer vesicles (diameter 40–130 nm), which have recently been found to play a critical role in cell-to-cell communication and biomolecule delivery. Their unique characteristics—stability, permeability, biocompatibility and low immunogenicity—have made them a prime candidate for use in delivering cancer therapeutics and other natural products. Here we present the first ever report of echogenic exosomes, which combine the benefits of the acoustic responsiveness of traditional microbubbles with the non-immunogenic and small-size morphology of exosomes. Microbubbles, although effective as ultrasound contrast agents, are restricted to intravascular usage due to their large size. In the current study, we have rendered bovine milk-derived exosomes echogenic by freeze drying them in the presence of mannitol. Ultrasound imaging and direct measurement of linear and nonlinear scattered responses were used to investigate the echogenicity and stability of the prepared exosomes. A commercial scanner registered enhancement (28.9% at 40 MHz) in the brightness of ultrasound images in presence of echogenic exosomes at 5 mg mL(−1). The exosomes also showed significant linear and nonlinear scattered responses—11 dB enhancement in fundamental, 8.5 dB in subharmonic and 3.5 dB in second harmonic all at 40 μg mL(−1) concentration. Echogenic exosomes injected into the tail vein of mice and the synovial fluid of rats resulted in significantly higher brightness—as much as 300%—of the ultrasound images, showing their promise in a variety of in vivo applications. The echogenic exosomes, with their large-scale extractability from bovine milk, lack of toxicity and minimal immunogenic response, successfully served as ultrasound contrast agents in this study and offer an exciting possibility to act as an effective ultrasound responsive drug delivery system.
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spelling pubmed-94103582022-08-25 Echogenic exosomes as ultrasound contrast agents Osborn, Jenna Pullan, Jessica E. Froberg, James Shreffler, Jacob Gange, Kara N. Molden, Todd Choi, Yongki Brooks, Amanda Mallik, Sanku Sarkar, Kausik Nanoscale Adv Chemistry Exosomes are naturally secreted extracellular bilayer vesicles (diameter 40–130 nm), which have recently been found to play a critical role in cell-to-cell communication and biomolecule delivery. Their unique characteristics—stability, permeability, biocompatibility and low immunogenicity—have made them a prime candidate for use in delivering cancer therapeutics and other natural products. Here we present the first ever report of echogenic exosomes, which combine the benefits of the acoustic responsiveness of traditional microbubbles with the non-immunogenic and small-size morphology of exosomes. Microbubbles, although effective as ultrasound contrast agents, are restricted to intravascular usage due to their large size. In the current study, we have rendered bovine milk-derived exosomes echogenic by freeze drying them in the presence of mannitol. Ultrasound imaging and direct measurement of linear and nonlinear scattered responses were used to investigate the echogenicity and stability of the prepared exosomes. A commercial scanner registered enhancement (28.9% at 40 MHz) in the brightness of ultrasound images in presence of echogenic exosomes at 5 mg mL(−1). The exosomes also showed significant linear and nonlinear scattered responses—11 dB enhancement in fundamental, 8.5 dB in subharmonic and 3.5 dB in second harmonic all at 40 μg mL(−1) concentration. Echogenic exosomes injected into the tail vein of mice and the synovial fluid of rats resulted in significantly higher brightness—as much as 300%—of the ultrasound images, showing their promise in a variety of in vivo applications. The echogenic exosomes, with their large-scale extractability from bovine milk, lack of toxicity and minimal immunogenic response, successfully served as ultrasound contrast agents in this study and offer an exciting possibility to act as an effective ultrasound responsive drug delivery system. RSC 2020-06-18 /pmc/articles/PMC9410358/ /pubmed/36034734 http://dx.doi.org/10.1039/d0na00339e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Osborn, Jenna
Pullan, Jessica E.
Froberg, James
Shreffler, Jacob
Gange, Kara N.
Molden, Todd
Choi, Yongki
Brooks, Amanda
Mallik, Sanku
Sarkar, Kausik
Echogenic exosomes as ultrasound contrast agents
title Echogenic exosomes as ultrasound contrast agents
title_full Echogenic exosomes as ultrasound contrast agents
title_fullStr Echogenic exosomes as ultrasound contrast agents
title_full_unstemmed Echogenic exosomes as ultrasound contrast agents
title_short Echogenic exosomes as ultrasound contrast agents
title_sort echogenic exosomes as ultrasound contrast agents
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9410358/
https://www.ncbi.nlm.nih.gov/pubmed/36034734
http://dx.doi.org/10.1039/d0na00339e
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