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Guiding Drug Through Interrupted Bloodstream for Potentiated Thrombolysis by C‐Shaped Magnetic Actuation System In Vivo

Fast and effective thrombolysis using tissue plasminogen activator (tPA) is limited by the poor delivery efficiency of thrombolytic drugs, which is induced by an interrupted bloodstream and delayed recanalization. Existing magnetic micro/nanodrug‐loaded robots used for targeted thrombotic therapy ar...

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Published in:Advanced materials (Weinheim) 2021-12, Vol.33 (51), p.e2105351-n/a
Main Authors: Wang, Longchen, Wang, Jienan, Hao, Junnian, Dong, Ziliang, Wu, Jianrong, Shen, Guofeng, Ying, Tao, Feng, Liangzhu, Cai, Xiaojun, Liu, Zhuang, Zheng, Yuanyi
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creator Wang, Longchen
Wang, Jienan
Hao, Junnian
Dong, Ziliang
Wu, Jianrong
Shen, Guofeng
Ying, Tao
Feng, Liangzhu
Cai, Xiaojun
Liu, Zhuang
Zheng, Yuanyi
description Fast and effective thrombolysis using tissue plasminogen activator (tPA) is limited by the poor delivery efficiency of thrombolytic drugs, which is induced by an interrupted bloodstream and delayed recanalization. Existing magnetic micro/nanodrug‐loaded robots used for targeted thrombotic therapy are limited by the complexity of the clinical verification of nanodrugs and the limited space of magnetic actuation systems. Herein, a general drug delivery strategy based on mass transportation theory for thrombolysis is presented, and an open space C‐shaped magnetic actuation system with laser location and ultrasound imaging navigation for in vivo evaluation is developed. tPA can be guided through an interrupted bloodstream to the thrombi by the locomotion of magnetic nanoparticle swarms (MNSs), thereby improving the thrombolysis efficacy. Notably, this strategy is able to quickly establish a life channel to achieve time‐critical recanalization, which is typically inaccessible using native tPA. Both in vitro and in vivo thrombolysis experiments demonstrate that the thrombus lysis efficacy significantly increases after the application of the MNS under a rotating magnetic field. This study provides an anticipated C‐shaped magnetic actuation system for in vivo validation and also presents a clinically feasible drug delivery strategy for targeted thrombolytic therapy with minimal systemic tPA exposure. Manipulation of magnetic nanoparticle swarms (MNSs) for thrombolysis is validated in in vivo experiments with an autonomously developed C‐shaped magnetic actuation system. Accompanied by the locomotion of MNSs, a tissue plasminogen activator (tPA) can be transported along with the swarms through the interrupted bloodstream to the clots, thus improving the thrombolysis efficacy and quickly opening a channel for achieving time‐critical recanalization.
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Existing magnetic micro/nanodrug‐loaded robots used for targeted thrombotic therapy are limited by the complexity of the clinical verification of nanodrugs and the limited space of magnetic actuation systems. Herein, a general drug delivery strategy based on mass transportation theory for thrombolysis is presented, and an open space C‐shaped magnetic actuation system with laser location and ultrasound imaging navigation for in vivo evaluation is developed. tPA can be guided through an interrupted bloodstream to the thrombi by the locomotion of magnetic nanoparticle swarms (MNSs), thereby improving the thrombolysis efficacy. Notably, this strategy is able to quickly establish a life channel to achieve time‐critical recanalization, which is typically inaccessible using native tPA. Both in vitro and in vivo thrombolysis experiments demonstrate that the thrombus lysis efficacy significantly increases after the application of the MNS under a rotating magnetic field. 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This study provides an anticipated C‐shaped magnetic actuation system for in vivo validation and also presents a clinically feasible drug delivery strategy for targeted thrombolytic therapy with minimal systemic tPA exposure. Manipulation of magnetic nanoparticle swarms (MNSs) for thrombolysis is validated in in vivo experiments with an autonomously developed C‐shaped magnetic actuation system. Accompanied by the locomotion of MNSs, a tissue plasminogen activator (tPA) can be transported along with the swarms through the interrupted bloodstream to the clots, thus improving the thrombolysis efficacy and quickly opening a channel for achieving time‐critical recanalization.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>34647345</pmid><doi>10.1002/adma.202105351</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0001-5964-3746</orcidid><orcidid>https://orcid.org/0000-0002-1629-1039</orcidid><orcidid>https://orcid.org/0000-0002-1328-0641</orcidid></addata></record>
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subjects Actuation
Animals
C‐shaped magnetic actuation systems
drug delivery
Drug Delivery Systems - instrumentation
Fibrinolytic Agents - chemistry
Fibrinolytic Agents - pharmacology
Fibrinolytic Agents - therapeutic use
Humans
In vivo methods and tests
Locomotion
Magnetic Fields
magnetic micro/nanorobots
magnetic nanoparticle swarms
Magnetite Nanoparticles - chemistry
Materials science
Mice
Nanoparticles
thrombolysis
Thrombolytic Therapy - methods
Thrombosis - drug therapy
Tissue Plasminogen Activator
title Guiding Drug Through Interrupted Bloodstream for Potentiated Thrombolysis by C‐Shaped Magnetic Actuation System In Vivo
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