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Self-propelled particles that transport cargo through flowing blood and halt hemorrhage

Delivering therapeutics deep into damaged tissue during bleeding is challenging because of the outward flow of blood. When coagulants cannot reach and clot blood at its source, uncontrolled bleeding can occur and increase surgical complications and fatalities. Self-propelling particles have been pro...

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Autores principales: Baylis, James R., Yeon, Ju Hun, Thomson, Max H., Kazerooni, Amir, Wang, Xu, St. John, Alex E., Lim, Esther B., Chien, Diana, Lee, Anna, Zhang, Jesse Q., Piret, James M., Machan, Lindsay S., Burke, Thomas F., White, Nathan J., Kastrup, Christian J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4646796/
https://www.ncbi.nlm.nih.gov/pubmed/26601282
http://dx.doi.org/10.1126/sciadv.1500379
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author Baylis, James R.
Yeon, Ju Hun
Thomson, Max H.
Kazerooni, Amir
Wang, Xu
St. John, Alex E.
Lim, Esther B.
Chien, Diana
Lee, Anna
Zhang, Jesse Q.
Piret, James M.
Machan, Lindsay S.
Burke, Thomas F.
White, Nathan J.
Kastrup, Christian J.
author_facet Baylis, James R.
Yeon, Ju Hun
Thomson, Max H.
Kazerooni, Amir
Wang, Xu
St. John, Alex E.
Lim, Esther B.
Chien, Diana
Lee, Anna
Zhang, Jesse Q.
Piret, James M.
Machan, Lindsay S.
Burke, Thomas F.
White, Nathan J.
Kastrup, Christian J.
author_sort Baylis, James R.
collection PubMed
description Delivering therapeutics deep into damaged tissue during bleeding is challenging because of the outward flow of blood. When coagulants cannot reach and clot blood at its source, uncontrolled bleeding can occur and increase surgical complications and fatalities. Self-propelling particles have been proposed as a strategy for transporting agents upstream through blood. Many nanoparticle and microparticle systems exhibiting autonomous or collective movement have been developed, but propulsion has not been used successfully in blood or used in vivo to transport therapeutics. We show that simple gas-generating microparticles consisting of carbonate and tranexamic acid traveled through aqueous solutions at velocities of up to 1.5 cm/s and delivered therapeutics millimeters into the vasculature of wounds. The particles transported themselves through a combination of lateral propulsion, buoyant rise, and convection. When loaded with active thrombin, these particles worked effectively as a hemostatic agent and halted severe hemorrhage in multiple animal models of intraoperative and traumatic bleeding. Many medical applications have been suggested for self-propelling particles, and the findings of this study show that the active self-fueled transport of particles can function in vivo to enhance drug delivery.
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spelling pubmed-46467962015-11-23 Self-propelled particles that transport cargo through flowing blood and halt hemorrhage Baylis, James R. Yeon, Ju Hun Thomson, Max H. Kazerooni, Amir Wang, Xu St. John, Alex E. Lim, Esther B. Chien, Diana Lee, Anna Zhang, Jesse Q. Piret, James M. Machan, Lindsay S. Burke, Thomas F. White, Nathan J. Kastrup, Christian J. Sci Adv Research Articles Delivering therapeutics deep into damaged tissue during bleeding is challenging because of the outward flow of blood. When coagulants cannot reach and clot blood at its source, uncontrolled bleeding can occur and increase surgical complications and fatalities. Self-propelling particles have been proposed as a strategy for transporting agents upstream through blood. Many nanoparticle and microparticle systems exhibiting autonomous or collective movement have been developed, but propulsion has not been used successfully in blood or used in vivo to transport therapeutics. We show that simple gas-generating microparticles consisting of carbonate and tranexamic acid traveled through aqueous solutions at velocities of up to 1.5 cm/s and delivered therapeutics millimeters into the vasculature of wounds. The particles transported themselves through a combination of lateral propulsion, buoyant rise, and convection. When loaded with active thrombin, these particles worked effectively as a hemostatic agent and halted severe hemorrhage in multiple animal models of intraoperative and traumatic bleeding. Many medical applications have been suggested for self-propelling particles, and the findings of this study show that the active self-fueled transport of particles can function in vivo to enhance drug delivery. American Association for the Advancement of Science 2015-10-02 /pmc/articles/PMC4646796/ /pubmed/26601282 http://dx.doi.org/10.1126/sciadv.1500379 Text en Copyright © 2015, The Authors http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Baylis, James R.
Yeon, Ju Hun
Thomson, Max H.
Kazerooni, Amir
Wang, Xu
St. John, Alex E.
Lim, Esther B.
Chien, Diana
Lee, Anna
Zhang, Jesse Q.
Piret, James M.
Machan, Lindsay S.
Burke, Thomas F.
White, Nathan J.
Kastrup, Christian J.
Self-propelled particles that transport cargo through flowing blood and halt hemorrhage
title Self-propelled particles that transport cargo through flowing blood and halt hemorrhage
title_full Self-propelled particles that transport cargo through flowing blood and halt hemorrhage
title_fullStr Self-propelled particles that transport cargo through flowing blood and halt hemorrhage
title_full_unstemmed Self-propelled particles that transport cargo through flowing blood and halt hemorrhage
title_short Self-propelled particles that transport cargo through flowing blood and halt hemorrhage
title_sort self-propelled particles that transport cargo through flowing blood and halt hemorrhage
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4646796/
https://www.ncbi.nlm.nih.gov/pubmed/26601282
http://dx.doi.org/10.1126/sciadv.1500379
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