Polyphenol-Functionalized Cubosomes as Thrombolytic Drug Carriers.


Journal

Advanced healthcare materials
ISSN: 2192-2659
Titre abrégé: Adv Healthc Mater
Pays: Germany
ID NLM: 101581613

Informations de publication

Date de publication:
11 2022
Historique:
revised: 03 08 2022
received: 15 05 2022
pubmed: 30 8 2022
medline: 4 11 2022
entrez: 29 8 2022
Statut: ppublish

Résumé

The safe administration of thrombolytic agents is a challenge for the treatment of acute thrombosis. Lipid-based nanoparticle drug delivery technologies present opportunities to overcome the existing clinical limitations and deliver thrombolytic therapy with enhanced therapeutic outcomes and safety. Herein, lipid cubosomes are examined as nanocarriers for the encapsulation of thrombolytic drugs. The lipid cubosomes are loaded with the thrombolytic drug urokinase-type plasminogen activator (uPA) and coated with a low-fouling peptide that is incorporated within a metal-phenolic network (MPN). The peptide-containing MPN (pep-MPN) coating inhibits the direct contact of uPA with the surrounding environment, as assessed by an in vitro plasminogen activation assay and an ex vivo whole blood clot degradation assay. The pep-MPN-coated cubosomes prepared with 22 wt% peptide demonstrate a cell membrane-dependent thrombolytic activity, which is attributed to their fusogenic lipid behavior. Moreover, compared with the uncoated lipid cubosomes, the uPA-loaded pep-MPN-coated cubosomes demonstrate significantly reduced nonspecific cell association (<10% of the uncoated cubosomes) in the whole blood assay, a prolonged circulating half-life, and reduced splenic uPA accumulation in mice. These studies confirm the preserved bioactivity and cell membrane-dependent release of uPA within pep-MPN-coated lipid cubosomes, highlighting their potential as a delivery vehicle for thrombolytic drugs.

Identifiants

pubmed: 36037807
doi: 10.1002/adhm.202201151
doi:

Substances chimiques

Fibrinolytic Agents 0
Drug Carriers 0
Polyphenols 0
Urokinase-Type Plasminogen Activator EC 3.4.21.73
Lipids 0
Peptides 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2201151

Informations de copyright

© 2022 Wiley-VCH GmbH.

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Auteurs

Haitao Yu (H)

Department of Chemical Engineering, The University of Melbourne, Parkville, Victoria, 3010, Australia.

Jason S Palazzolo (JS)

NanoBiotechnology Laboratory, Australian Centre for Blood Diseases, Central Clinical School, Monash University, Melbourne, Victoria, 3004, Australia.

Yi Ju (Y)

Department of Chemical Engineering, The University of Melbourne, Parkville, Victoria, 3010, Australia.
School of Health and Biomedical Sciences, RMIT University, Bundoora, Victoria, 3083, Australia.

Be'eri Niego (B)

NanoBiotechnology Laboratory, Australian Centre for Blood Diseases, Central Clinical School, Monash University, Melbourne, Victoria, 3004, Australia.

Shuaijun Pan (S)

Department of Chemical Engineering, The University of Melbourne, Parkville, Victoria, 3010, Australia.

Christoph E Hagemeyer (CE)

NanoBiotechnology Laboratory, Australian Centre for Blood Diseases, Central Clinical School, Monash University, Melbourne, Victoria, 3004, Australia.

Frank Caruso (F)

Department of Chemical Engineering, The University of Melbourne, Parkville, Victoria, 3010, Australia.

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