BROWSE

Related Researcher

Author's Photo

Kim, Byeong-Su
Soft and Hybrid Nanomaterials Lab
Research Interests
  • Carbon materials, polymer, Layer-by-Layer (LbL) assembly, hyperbranched polymer, polyglycerol (PG), bio-applications

ITEM VIEW & DOWNLOAD

Hydrogen-bonding layer-by-layer assembled biodegradable polymeric micelles as drug delivery vehicles from surfaces

DC Field Value Language
dc.contributor.author Kim, Byeong-Su ko
dc.contributor.author Park, Sang Wook ko
dc.contributor.author Hammond, Paula T. ko
dc.date.available 2014-11-10T01:40:03Z -
dc.date.created 2014-11-07 ko
dc.date.issued 2008-02 -
dc.identifier.citation ACS NANO, v.2, no.2, pp.386 - 392 ko
dc.identifier.issn 1936-0851 ko
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/8457 -
dc.identifier.uri http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=42549132351 ko
dc.description.abstract We present the integration of amphiphilic block copolymer micelles as nanometer-sized vehicles for hydrophobic drugs within layer-by-layer (LbL) films using alternating hydrogen bond interactions as the driving force for assembly for the first time, thus enabling the incorporation of drugs and pH-sensitive release. The film was constructed based on the hydrogen banding between poly(acrylic acid) (PAA) as an H-bond donor and biodegradable poly(ethylene oxide)-block-poly(E-caprolactone) (PEO-b-KL) micelles as the H-bond acceptor when assembled under acidic conditions. By taking advantage of the weak interactions of the hydrogen-bonded film on hydrophobic surfaces, it is possible to generate flexible free-standing films of these materials. A free-standing micelle LbL film of (PEG-b-PCL/PAA)60 with a thickness of 3.1 μm was isolated, allowing further characterization of the bulk film properties, including morphology and phase transitions, using transmission electron microscopy and differential scanning calorimetry. Because of the sensitive nature of the hydrogen bonding employed to build the multilayers, the film can be rapidly deconstructed to release micelles upon exposure to physiological conditions. However, we could also successfully control the rate of film deconstruction by cross-linking carboxylic acid groups in PAA through thermally induced anhydride linkages, which retard the drug release to the surrounding medium to enable sustained release over multiple days. To demonstrate efficacy in delivering active therapeutics, in vitro Kirby-Bauer assays against Staphylococcus aureus were used to illustrate that the drug-loaded micelle LbL film can release significant amounts of an active antibacterial drug, triclosan, to inhibit the growth of bacteria. Because the micellar encapsulation of hydrophobic therapeutics does not require specific chemical interactions, we believe this noncovalent approach provides a new route to integrating active small, uncharged, and hydrophobic therapeutics into LbL thin films for biological and biomedical coatings. ko
dc.description.statementofresponsibility close -
dc.language ENG ko
dc.publisher AMER CHEMICAL SOC ko
dc.subject Biodegradable ko
dc.subject Block copolymer micelle hydrogen bond ko
dc.subject Drug delivery ko
dc.subject Layer-by-layer ko
dc.subject Polymer assembly ko
dc.title Hydrogen-bonding layer-by-layer assembled biodegradable polymeric micelles as drug delivery vehicles from surfaces ko
dc.type ARTICLE ko
dc.identifier.scopusid 2-s2.0-42549132351 ko
dc.identifier.wosid 000253503300030 ko
dc.type.rims ART ko
dc.description.wostc 139 *
dc.description.scopustc 175 *
dc.date.tcdate 2015-05-06 *
dc.date.scptcdate 2014-11-08 *
dc.identifier.doi 10.1021/nn700408z ko
Appears in Collections:
PHY_Journal Papers

find_unist can give you direct access to the published full text of this article. (UNISTARs only)

Show simple item record

qrcode

  • mendeley

    citeulike

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

MENU