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Porous Silicon and Polymer Nanocomposites for Delivery of Peptide Nucleic Acids as Anti-MicroRNA Therapies.


ABSTRACT: Self-assembled polymer/porous silicon nanocomposites overcome intracellular and systemic barriers for in vivo application of peptide nucleic acid (PNA) anti-microRNA therapeutics. Porous silicon (PSi) is leveraged as a biodegradable scaffold with high drug-cargo-loading capacity. Functionalization with a diblock polymer improves PSi nanoparticle colloidal stability, in vivo pharmacokinetics, and intracellular bioavailability through endosomal escape, enabling PNA to inhibit miR-122 in vivo.

SUBMITTER: Beavers KR 

PROVIDER: S-EPMC5152671 | biostudies-literature | 2016 Sep

REPOSITORIES: biostudies-literature

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Porous Silicon and Polymer Nanocomposites for Delivery of Peptide Nucleic Acids as Anti-MicroRNA Therapies.

Beavers Kelsey R KR   Werfel Thomas A TA   Shen Tianwei T   Kavanaugh Taylor E TE   Kilchrist Kameron V KV   Mares Jeremy W JW   Fain Joshua S JS   Wiese Carrie B CB   Vickers Kasey C KC   Weiss Sharon M SM   Duvall Craig L CL  

Advanced materials (Deerfield Beach, Fla.) 20160706 36


Self-assembled polymer/porous silicon nanocomposites overcome intracellular and systemic barriers for in vivo application of peptide nucleic acid (PNA) anti-microRNA therapeutics. Porous silicon (PSi) is leveraged as a biodegradable scaffold with high drug-cargo-loading capacity. Functionalization with a diblock polymer improves PSi nanoparticle colloidal stability, in vivo pharmacokinetics, and intracellular bioavailability through endosomal escape, enabling PNA to inhibit miR-122 in vivo. ...[more]

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