Multifunctional Nanodelivery Platform for Maximizing Nucleic Acids Combination Therapy.


Journal

Methods in molecular biology (Clifton, N.J.)
ISSN: 1940-6029
Titre abrégé: Methods Mol Biol
Pays: United States
ID NLM: 9214969

Informations de publication

Date de publication:
2020
Historique:
entrez: 2 2 2020
pubmed: 2 2 2020
medline: 2 2 2021
Statut: ppublish

Résumé

The silencing of an oncogene with a small interfering RNA (siRNA) is a promising way for cancer therapy. Its efficacy can be further enhanced by integrating with other therapeutics; however, transporting siRNA and other active ingredients to the same location at the same time is challenging. Here, we report a novel multifunctional nanodelivery platform by sequentially layering several functional ingredients, such as siRNAs, microRNAs, peptides, and targeting ligands, onto a core through charge-charge interaction. The prepared nanovectors effectively and programmably delivered multiple active components to maximize therapeutic combination with minimal off-targeting effects.

Identifiants

pubmed: 32006395
doi: 10.1007/978-1-0716-0290-4_4
doi:

Substances chimiques

Drug Carriers 0
Peptides 0
RNA, Small Interfering 0
Gold 7440-57-5
Hyaluronic Acid 9004-61-9

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

79-90

Auteurs

Seung Koo Lee (SK)

Department of Radiology, Weill Cornell Medicine, Molecular Imaging Innovations Institute, New York, NY, USA.

Benedict Law (B)

Department of Radiology, Weill Cornell Medicine, Molecular Imaging Innovations Institute, New York, NY, USA.

Ching-Hsuan Tung (CH)

Department of Radiology, Weill Cornell Medicine, Molecular Imaging Innovations Institute, New York, NY, USA. cht2018@med.cornell.edu.

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Classifications MeSH