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Microneedle delivery of plasmid DNA to living human skin: Formulation coating, skin insertion and gene expression. | LitMetric

Microneedle delivery of plasmid DNA to living human skin: Formulation coating, skin insertion and gene expression.

J Control Release

School of Pharmacy and Pharmaceutical Sciences, Cardiff University, Redwood Building, King Edward VII Avenue, Cardiff, CF10 3NB, UK.

Published: June 2012

AI Article Synopsis

  • - Microneedle delivery of plasmid DNA (pDNA) offers a promising method for treating skin diseases and enhancing genetic immunization, with a focus on optimizing key parameters for effective delivery.
  • - The study tested human skin samples to improve microneedle pDNA loading, penetration ability, and gene expression efficiency, achieving up to 100μg of pDNA per 5-microneedle array.
  • - Although storage impacted pDNA stability, adding saccharide excipients helped maintain its biological functionality, allowing successful gene expression in living human skin.

Article Abstract

Microneedle delivery of nucleic acids, in particular plasmid DNA (pDNA), to the skin represents a potential new approach for the clinical management of genetic skin diseases and cutaneous cancers, and for intracutaneous genetic immunisation. In this study excised human skin explants were used to investigate and optimise key parameters that will determine stable and effective microneedle-facilitated pDNA delivery. These include (i) high dose-loading of pDNA onto microneedle surfaces, (ii) stability and functionality of the coated pDNA, (iii) skin penetration capability of pDNA-coated microneedles, and (iv) efficient gene expression in human skin. Optimisation of a dip-coating method enabled significant increases in the loading capacity, up to 100μg of pDNA per 5-microneedle array. Coated microneedles were able to reproducibly perforate human skin at low (<1N) insertion forces. The physical stability of the coated pDNA was partially compromised on storage, although this was improved through the addition of saccharide excipients without detriment to the biological functionality of pDNA. The pDNA-coated microneedles facilitated reporter gene expression in viable human skin. The efficiency of gene expression from coated microneedles will depend upon suitable DNA loading, efficient and reproducible skin puncture and rapid in situ dissolution of the plasmid at the site of delivery.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3390019PMC
http://dx.doi.org/10.1016/j.jconrel.2012.04.005DOI Listing

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