Acta Pharmaceutica Sinica B · 2014 · 77 citations · 19 references
PharmacyBioengineeringPharmaceuticsDrug DeliveryNanoparticle Drug DeliveryTransdermal Drug DeliveryDrug Delivery EngineeringMicroneedle-based DeliveryPeptide DeliveryPermeation EnhancersProtein DeliveryTransdermal Delivery Of PeptidesMacromolecule Skin PermeationMicroneedle Delivery SystemsPeptide Permeability EnhancementPeptide Permeation EnhancementPeptide Skin PermeationPermeation StudiesTransdermal Delivery SystemsTransdermal Drug Delivery Systems
The aims of this study were to investigate the utility of solid microneedle arrays (150 µm in length) in enhancing transdermal delivery of peptides and to examine the relationship between peptide permeation rates and D2O flux. Four model peptides were used (Gly-Gln-Pro-Arg [tetrapeptide-3, 456.6 Da], Val-Gly-Val-Ala-Pro-Gly [hexapeptide, 498.6 Da], AC-Glu-Glu-Met-Gln-Arg-Arg-NH2 [acetyl hexapeptide-3, 889 Da] and Cys-Tyr-Ile-Gln-Asn-Cys-Pro-Leu-Gly-NH2 [oxytocin, 1007.2 Da]). The influence of microneedle pretreatment on skin permeation was evaluated using porcine ear skin with Franze diffusion cell. Peptide permeation across the skin was significantly enhanced by microneedle pretreatment, and permeation rates were dependent on peptide molecular weights. A positive correlation between D2O flux and acetyl hexapeptide-3 clearances suggests that convective solvent flow contributes to the enhanced transdermal peptide delivery. It is concluded that solid microneedle arrays are effective devices to enhance skin delivery of peptides.
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