Development of a protective dermal drug delivery system for therapeutic DNAzymes

Abstract

RNA-cleaving DNAzymes are a potential novel class of nucleic acid-based active pharmaceutical ingredients (API). However, developing an appropriate drug delivery system (DDS) that achieves high bioavailability is challenging. Especially in a dermal application, DNAzymes have to overcome physiological barriers composed of penetration barriers and degrading enzymes. The focus of the present study was the development of a protective and penetration-enhanced dermal DDS that was tailor made for DNAzymes. DNAzyme Dz13 was used as a potential API for topical therapy against actinic keratosis. In the progress of development and selection, different preservatives, submicron emulsions (SMEs) and the physiological pH range were validated with respect to the API's integrity. A physicochemical stable SME of a pharmaceutical grade along with a high API integrity was achieved. Additionally, two developed protective systems, consisting of a liposomal formulation or chitosan-polyplexes, reduced the degradation of Dz13 in vitro. A combination of SME and polyplexes was finally validated at the skin and cellular level by in vitro model systems. Properties of penetration, degradation and distribution were determined. The result was enhanced skin penetration efficiency and increased cellular uptake with a high protective efficiency for DNAzymes due to the developed protective DDS.

Keywords: Benzoic acid (PubChem CID: 243); Benzyl alcohol (PubChem CID: 244); Chitosan; Chitosan (PubChem CID: 21896651); DNAzyme; DNase; Drug delivery system; Methylparaben (PubChem CID: 7456); Oleyl oleate (PubChem CID: 543844); Phenoxy ethanol (PubChem CID: 31236); Phosphatidylcholin (PubChem CID: 45266626); Polyplex; Propylene glycol (PubChem CID: 1030); Propylparaben (PubChem CID: 7175); Submicron emulsion.