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Aptamer-displaying peptide amphiphile micelles as a cell-targeted delivery vehicle of peptide cargoes.
Smith, Josiah D; Cardwell, Leah N; Porciani, David; Nguyen, Julie A; Zhang, Rui; Gallazzi, Fabio; Tata, Rama Rao; Burke, Donald H; Daniels, Mark A; Ulery, Bret D.
Afiliação
  • Smith JD; Department of Biomedical, Biological and Chemical Engineering, University of Missouri, Columbia, MO, United States of America.
Phys Biol ; 15(6): 065006, 2018 10 22.
Article em En | MEDLINE | ID: mdl-30124431
Peptide amphiphile micelles (PAMs) are attractive vehicles for the delivery of a variety of therapeutic and prophylactic peptides. However, a key limitation of PAMs is their lack of preferential targeting ability. In this paper, we describe our design of a PAM system that incorporates a DNA oligonucleotide amphiphile (antitail amphiphile-AA) to form A/PAMs. A cell-targeting DNA aptamer with a 3' extension sequence (tail) complementary to the AA is annealed to the surface to form aptamer-displaying PAMs (Aptamer~A/PAMs). Aptamer~A/PAMs are small, anionic, stable nanoparticles capable of delivering a large mass percentage peptide amphiphile (PA) compared to targeting DNA components. Aptamer~A/PAMs are stable for over 4 h in the presence of biological fluids. Additionally, the aptamer retains its cell-targeting properties when annealed to the A/PAM, thus leading to enhanced delivery to a specifically-targeted B-cell leukemia cell line. This exciting modular technology can be readily used with a library of different targeting aptamers and PAs, capable of improving the bioavailability and potency of the peptide cargo.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Peptídeos / Sistemas de Liberação de Medicamentos / Aptâmeros de Nucleotídeos / Micelas Limite: Animals / Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Peptídeos / Sistemas de Liberação de Medicamentos / Aptâmeros de Nucleotídeos / Micelas Limite: Animals / Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article