Ultrasound-Responsive Smart Drug Delivery System of Lipid Coated Mesoporous Silica Nanoparticles.

cellular uptake lipid coating mechanical index mesoporous silica nanoparticles ultrasound triggered release

Journal

Pharmaceutics
ISSN: 1999-4923
Titre abrégé: Pharmaceutics
Pays: Switzerland
ID NLM: 101534003

Informations de publication

Date de publication:
03 Sep 2021
Historique:
received: 09 08 2021
revised: 27 08 2021
accepted: 31 08 2021
entrez: 28 9 2021
pubmed: 29 9 2021
medline: 29 9 2021
Statut: epublish

Résumé

The immediate release of chemotherapeutics at the target site, along with no premature release in circulation is always challenging. The purpose of this study was to develop a stimuli responsive drug delivery system, composed of lipid supported mesoporous silica nanoparticles (MSNPs) for triggered drug release at the target site and simultaneously avoiding the premature release. MSNPs with a higher drug loading capacity and very slow release were designed so as to enhance release by FDA approved US-irradiation. Doxorubicin, as a model drug, and perfluoropentane (PFP) as a US responsive material, were entrapped in the porous structure of MSNPs. Lipid coating enhanced the cellular uptake and in addition provided a gatekeeping effect at the pore opening to reduce premature release. The mechanical and thermal effects of US induced the conversion of liquid PFP to a gaseous form that was able to rupture the lipid layer, resulting in triggered drug release. The prolonged stability profile and non-toxic behavior made them suitable candidate for the delivery of anticancer drugs. This smart system, with the abilities of better cellular uptake and higher cytotoxic effects on US-irradiation, would be a good addition to the applied side of chemotherapeutic advanced drug delivery systems.

Identifiants

pubmed: 34575472
pii: pharmaceutics13091396
doi: 10.3390/pharmaceutics13091396
pmc: PMC8468042
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Muhammad Umair Amin (MU)

Department of Pharmaceutics and Biopharmaceutics, University of Marburg, Robert-Koch-Str. 4, 35037 Marburg, Germany.

Sajid Ali (S)

Department of Pharmaceutics and Biopharmaceutics, University of Marburg, Robert-Koch-Str. 4, 35037 Marburg, Germany.
Angström Laboratory, Department of Chemistry, Uppsala University, 75123 Uppsala, Sweden.

Imran Tariq (I)

Department of Pharmaceutics and Biopharmaceutics, University of Marburg, Robert-Koch-Str. 4, 35037 Marburg, Germany.
Punjab University College of Pharmacy, University of Punjab, Lahore 54000, Pakistan.

Muhammad Yasir Ali (MY)

Department of Pharmaceutics and Biopharmaceutics, University of Marburg, Robert-Koch-Str. 4, 35037 Marburg, Germany.
Faculty of Pharmaceutical Sciences, GC University Faisalabad, Faisalabad 38000, Pakistan.

Shashank Reddy Pinnapreddy (SR)

Department of Pharmaceutics and Biopharmaceutics, University of Marburg, Robert-Koch-Str. 4, 35037 Marburg, Germany.

Eduard Preis (E)

Department of Pharmaceutics and Biopharmaceutics, University of Marburg, Robert-Koch-Str. 4, 35037 Marburg, Germany.

Christian Wölk (C)

Institute of Pharmacy, Pharmaceutical Technology, Faculty of Medicine, Leipzig University, Eilenburger Straße 15a, 04317 Leipzig, Germany.

Richard D Harvey (RD)

Department of Pharmaceutical Chemistry, University of Vienna, Althanstraße 14, A-1090 Vienna, Austria.

Gerd Hause (G)

Biocenter, Martin Luther University Halle-Wittenberg, Weinbergweg 22, 06120 Halle, Germany.

Jana Brüßler (J)

Department of Pharmaceutics and Biopharmaceutics, University of Marburg, Robert-Koch-Str. 4, 35037 Marburg, Germany.

Udo Bakowsky (U)

Department of Pharmaceutics and Biopharmaceutics, University of Marburg, Robert-Koch-Str. 4, 35037 Marburg, Germany.

Classifications MeSH