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1000 Titel
  • Repurposing Antiviral Protease Inhibitors Using Extracellular Vesicles for Potential Therapy of COVID-19
1000 Autor/in
  1. Kumar, Santosh |
  2. Zhi, Kaining |
  3. Mukherji, Ahona |
  4. Gerth, Kelli |
1000 Erscheinungsjahr 2020
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2020-04-26
1000 Erschienen in
1000 Quellenangabe
  • 12(5):486
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1000 Verlagsversion
  • https://doi.org/10.3390/v12050486 |
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1000 Begutachtungsstatus
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1000 Abstract/Summary
  • zoom_out_map search menu Journals Viruses Volume 12 Issue 5 10.3390/v12050486 viruses-logo Submit to this Journal Review for this Journal Edit a Special Issue ► Article Menu This is an early access version, the complete PDF, HTML, and XML versions will be available soon. Open AccessReview Repurposing Antiviral Protease Inhibitors Using Extracellular Vesicles for Potential Therapy of COVID-19 by Santosh Kumar 1,*,Kaining Zhi 2,Ahona Mukherji 1 andKelli Gerth 1 1 Department of Pharmaceutical Sciences, University of Tennessee Health Science Center, 881 Madison Ave, Memphis, TN 38163, USA 2 Plough Center for Sterile Drug Delivery Solutions, University of Tennessee Health Science Center, 208 South Dudley Street, Memphis, TN 38163, USA * Author to whom correspondence should be addressed. Viruses 2020, 12(5), 486; https://doi.org/10.3390/v12050486 (registering DOI) Received: 6 April 2020 / Revised: 16 April 2020 / Accepted: 24 April 2020 / Published: 26 April 2020 (This article belongs to the Special Issue Drug-Repositioning Opportunities for Antiviral Therapy) Download PDF Cite This Paper Abstract In January 2020, Chinese health agencies reported an outbreak of a novel coronavirus-2 (CoV-2) which can lead to severe acute respiratory syndrome (SARS). The virus, which belongs to the coronavirus family (SARS-CoV-2), was named coronavirus disease 2019 (COVID-19) and declared a pandemic by the World Health Organization (WHO). Full-length genome sequences of SARS-CoV-2 showed 79.6% sequence identity to SARS-CoV, with 96% identity to a bat coronavirus at the whole-genome level. COVID-19 has caused over 133,000 deaths and there are over 2 million total confirmed cases as of April 15th, 2020. Current treatment plans are still under investigation due to a lack of understanding of COVID-19. One potential mechanism to slow disease progression is the use of antiviral drugs to either block the entry of the virus or interfere with viral replication and maturation. Currently, antiviral drugs, including chloroquine/hydroxychloroquine, remdesivir, and lopinavir/ritonavir, have shown effective inhibition of SARS-CoV-2 in vitro. Due to the high dose needed and narrow therapeutic window, many patients are experiencing severe side effects with the above drugs. Hence, repurposing these drugs with a proper formulation is needed to improve the safety and efficacy for COVID-19 treatment. Extracellular vesicles (EVs) are a family of natural carriers in the human body. They play a critical role in cell-to-cell communications. EVs can be used as unique drug carriers to deliver protease inhibitors to treat COVID-19. EVs may provide targeted delivery of protease inhibitors, with fewer systemic side effects. More importantly, EVs are eligible for major aseptic processing and can be upscaled for mass production. Currently, the FDA is facilitating applications to treat COVID-19, which provides a very good chance to use EVs to contribute in this combat.
1000 Sacherschließung
gnd 1206347392 COVID-19
lokal antiviral drugs
lokal HIV
lokal extracellular vesicles
lokal Coronaviruses
lokal protease inhibitors
1000 Fächerklassifikation (DDC)
1000 Liste der Beteiligten
  1. https://orcid.org/0000-0001-7846-5674|https://orcid.org/0000-0003-1413-9399|https://frl.publisso.de/adhoc/uri/TXVraGVyamksIEFob25h|https://frl.publisso.de/adhoc/uri/R2VydGgsIEtlbGxp
1000 Label
1000 Förderer
  1. National Institutes of Health |
  2. Health Science Center, University of Tennessee |
1000 Fördernummer
  1. DA047178
  2. -
1000 Förderprogramm
  1. -
  2. -
1000 Dateien
1000 Förderung
  1. 1000 joinedFunding-child
    1000 Förderer National Institutes of Health |
    1000 Förderprogramm -
    1000 Fördernummer DA047178
  2. 1000 joinedFunding-child
    1000 Förderer Health Science Center, University of Tennessee |
    1000 Förderprogramm -
    1000 Fördernummer -
1000 Objektart article
1000 Beschrieben durch
1000 @id frl:6420463.rdf
1000 Erstellt am 2020-04-27T12:02:44.673+0200
1000 Erstellt von 122
1000 beschreibt frl:6420463
1000 Bearbeitet von 122
1000 Zuletzt bearbeitet Mon Apr 27 12:03:47 CEST 2020
1000 Objekt bearb. Mon Apr 27 12:03:32 CEST 2020
1000 Vgl. frl:6420463
1000 Oai Id
  1. oai:frl.publisso.de:frl:6420463 |
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