Nanoparticles Mimicking Viral Cell Recognition Strategies Are Superior Transporters into Mesangial Cells.

mesangial cells multivalent nanoparticles renal targeting stepwise cell recognition virus‐mimetic

Journal

Advanced science (Weinheim, Baden-Wurttemberg, Germany)
ISSN: 2198-3844
Titre abrégé: Adv Sci (Weinh)
Pays: Germany
ID NLM: 101664569

Informations de publication

Date de publication:
Jun 2020
Historique:
received: 11 11 2019
revised: 12 03 2020
accepted: 17 03 2020
entrez: 16 6 2020
pubmed: 17 6 2020
medline: 17 6 2020
Statut: epublish

Résumé

Poor drug availability in the tissue of interest is a frequent cause of therapy failure. While nanotechnology has developed a plethora of nanocarriers for drug transport, their ability to unequivocally identify cells of interest remains moderate. Viruses are the ideal nanosized carriers as they are able to address their embedded nucleic acids with high specificity to their host cells. Here, it is reported that particles endowed with a virus-like ability to identify cells by three consecutive checks have a superior ability to recognize mesangial cells (MCs) in vivo compared to conventional nanoparticles. Mimicking the initial viral attachment followed by a stepwise target cell recognition process leads to a 5- to 15-fold higher accumulation in the kidney mesangium and extensive cell uptake compared to particles lacking one or both of the viral traits. These results highlight the relevance that the viral cell identification process has on specificity and its application on the targeting strategies of nanomaterials. More so, these findings pave the way for transporting drugs into the mesangium, a tissue that is pivotal in the development of diabetic nephropathy and for which currently no efficient pharmacotherapy exists.

Identifiants

pubmed: 32537398
doi: 10.1002/advs.201903204
pii: ADVS1704
pmc: PMC7284201
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1903204

Informations de copyright

© 2020 The Authors. Advanced Science published by Wiley‐VCH Verlag GmbH & Co. KGaA.

Déclaration de conflit d'intérêts

The authors declare no conflict of interest.

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Auteurs

Sara Maslanka Figueroa (S)

Department of Pharmaceutical Technology University of Regensburg Regensburg 93053 Germany.

Daniel Fleischmann (D)

Department of Pharmaceutical Technology University of Regensburg Regensburg 93053 Germany.

Sebastian Beck (S)

Department of Pharmaceutical Technology University of Regensburg Regensburg 93053 Germany.

Philipp Tauber (P)

Department of Physiology II University of Regensburg Regensburg 93053 Germany.

Ralph Witzgall (R)

Department of Molecular and Cellular Anatomy University of Regensburg Regensburg 93053 Germany.

Frank Schweda (F)

Department of Physiology II University of Regensburg Regensburg 93053 Germany.

Achim Goepferich (A)

Department of Pharmaceutical Technology University of Regensburg Regensburg 93053 Germany.

Classifications MeSH