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Author

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

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Layer-by-Layer-Assembled Multilayer Films for Transcutaneous Drug and Vaccine Delivery

Cited 61 times inthomson ciCited 66 times inthomson ci
Title
Layer-by-Layer-Assembled Multilayer Films for Transcutaneous Drug and Vaccine Delivery
Author
Su, XingfangKim, Byeong-SuKim, Sara R.Hammond, Paula T.Irvine, Darrell J.
Keywords
Amino esters; Antigen presenting cells; Assembled multilayer films; Bi-layer; Confocal fluorescence microscopy; Degradable polymers; Diesters; DNA oligonucleotides; Dual release; Electrostatic interactions; Immunotherapeutics; In-vivo; Langerhans cells; Layer-by-layers; Linear growth; Lymph node; Model proteins; Nano layers; Nano scale; Ovalbumins; Polymer assemblies; Polymer assembly; Saline solutions; Skin model; Skin patch; Transcutaneous; Transcutaneous delivery; Vaccine delivery
Issue Date
200911
Publisher
AMER CHEMICAL SOC
Citation
ACS NANO, v.3, no.11, pp.3719 - 3729
Abstract
We describe protein- and oligonuclecitide-loaded layer-by-layer (LbL)-assembled multilayer films incorporating a hydrolytically degradable polymer for transcutaneous drug or vaccine delivery. Films were constructed based on electrostatic interactions between a cationic poly(beta-amino ester) (denoted Poly-1) with a model protein antigen, ovalbumin (ova), and/or immunostimulatory CpG (cytosine-phosphate diester-guanine-rich) DNA oligonucleotide adjuvant molecules. Linear growth of nanoscale Poly-1/ova bilayers was observed. Dried ova protein-loaded films rapidly deconstructed when rehydrated in saline solutions, releasing ova as nonaggregated/nondegraded protein, suggesting that the structure of biomolecules integrated into these multilayer films is preserved during release. Using confocal fluorescence microscopy and an in vivo murine ear skin model, we demonstrated delivery of ova from LbL films Into barrier-disrupted skin, uptake of the protein by skin-resident antigen-presenting cells (Langerhans cells), and transport of the antigen to the skin-draining lymph nodes. Dual incorporation of ova and CpG oligonucleotides into the nanolayers of LbL films enabled dual release of the antigen and adjuvant with distinct kinetics for each component; ova was rapidly released, while CpG was released in a relatively sustained manner. Applied as skin patches, these films delivered ova and CpG to Langerhans cells in the skin. To our knowledge, this is the first demonstration of LbL films applied for the delivery of biomolecules into skin. This approach provides a new route for storage of vaccines and other immunotherapeutics in a solid-state thin film for subsequent delivery into the immunologically rich milieu of the skin.
URI
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DOI
http://dx.doi.org/10.1021/nn900928u
ISSN
1936-0851
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