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Breaking the Barrier

  • Topical administration permits targeted, sustained delivery of therapeutics to human skin. Delivery to the skin, however, is typically limited to lipophilic molecules with molecular weight of < 500 Da, capable of crossing the stratum corneum. Nevertheless, there are indications protein delivery may be possible in barrier deficient skin, a condition found in several inflammatory skin diseases such as psoriasis, using novel nanocarrier systems. Methods: Water in water thermo-nanoprecipitation; dynamic light scattering; zeta potential measurement; nanoparticle tracking analysis; atomic force microscopy; cryogenic transmission electron microscopy; UV absorption; centrifugal separation membranes; bicinchoninic acid assay; circular dichroism; TNF alpha binding ELISA; inflammatory skin equivalent construction; human skin biopsies; immunohistochemistry; fluorescence microscopy; western blot; monocyte derived Langerhans cells; ELISA Results: Here, we report the novel synthesis of thermoresponsive nanogels (tNG) and the stable encapsulation ofTopical administration permits targeted, sustained delivery of therapeutics to human skin. Delivery to the skin, however, is typically limited to lipophilic molecules with molecular weight of < 500 Da, capable of crossing the stratum corneum. Nevertheless, there are indications protein delivery may be possible in barrier deficient skin, a condition found in several inflammatory skin diseases such as psoriasis, using novel nanocarrier systems. Methods: Water in water thermo-nanoprecipitation; dynamic light scattering; zeta potential measurement; nanoparticle tracking analysis; atomic force microscopy; cryogenic transmission electron microscopy; UV absorption; centrifugal separation membranes; bicinchoninic acid assay; circular dichroism; TNF alpha binding ELISA; inflammatory skin equivalent construction; human skin biopsies; immunohistochemistry; fluorescence microscopy; western blot; monocyte derived Langerhans cells; ELISA Results: Here, we report the novel synthesis of thermoresponsive nanogels (tNG) and the stable encapsulation of the anti-TNFa fusion protein etanercept (ETR) (similar to 150 kDa) without alteration to its structure, as well as temperature triggered release from the tNGs. Novel tNG synthesis without the use of organic solvents was conducted, permitting in situ encapsulation of protein during assembly, something that holds great promise for easy manufacture and storage. Topical application of ETR loaded tNGs to inflammatory skin equivalents or tape striped human skin resulted in efficient ETR delivery throughout the SC and into the viable epidermis that correlated with clear anti-inflammatory effects. Notably, effective ETR delivery depended on temperature triggered release following topical application. Conclusion: Together these results indicate tNGs hold promise as a biocompatible and easy to manufacture vehicle for stable protein encapsulation and topical delivery into barrier-deficient skin.show moreshow less

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Author details:Michael GiulbudagianORCiDGND, Guy YeallandORCiD, S. Hönzke, A. Edlich, Birte Geisendörfer, Burkhard KleuserORCiDGND, Sarah HedtrichORCiD, Marcelo CalderonORCiD
DOI:https://doi.org/10.7150/thno.21668
ISSN:1838-7640
Pubmed ID:https://pubmed.ncbi.nlm.nih.gov/29290820
Title of parent work (English):Theranostics
Subtitle (English):potent anti-inflammatory activity following efficient topical delivery of etanercept using thermoresponsive nanogels
Publisher:Ivyspring International Publisher
Place of publishing:Lake haven
Publication type:Article
Language:English
Date of first publication:2018/01/01
Publication year:2018
Release date:2022/03/14
Tag:anti-inflammatory therapy; etanercept; skin equivalents; thermoresponsive-nanogel; topical
Volume:8
Issue:2
Number of pages:14
First page:450
Last Page:463
Funding institution:project A04 [Sonderforschungsbereich 1112]; Deutsche Forschungsgemeinschaft (DFG)German Research Foundation (DFG) [HE 7440/4-1]; Berlin-Brandenburg Forschungsplattform BB3R; Bundesministerium fur Bildung und Forschung (BMBF) through the NanoMatFutur awardFederal Ministry of Education & Research (BMBF) [13N12561]; project C02 [Sonderforschungsbereich 1112]; project Z01 [Sonderforschungsbereich 1112]
Organizational units:Mathematisch-Naturwissenschaftliche Fakultät / Institut für Chemie
DDC classification:5 Naturwissenschaften und Mathematik / 54 Chemie
Peer review:Referiert
Publishing method:Open Access / Gold Open-Access
DOAJ gelistet
License (German):License LogoCC-BY-NC - Namensnennung, nicht kommerziell 4.0 International
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