1. An in vitro and in vivo comparison of solid and liquid-oil cores in transdermal aconitine nanocarriers.
- Author
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Zhang YT, Wu ZH, Zhang K, Zhao JH, Ye BN, and Feng NP
- Subjects
- Aconitine chemistry, Aconitine metabolism, Aconitine toxicity, Administration, Cutaneous, Analgesics chemistry, Analgesics metabolism, Analgesics toxicity, Animals, Anti-Inflammatory Agents chemistry, Anti-Inflammatory Agents metabolism, Anti-Inflammatory Agents toxicity, Cell Line, Chemistry, Pharmaceutical, Delayed-Action Preparations, Emulsions, Humans, Hydrogen-Ion Concentration, Keratinocytes metabolism, Male, Mice, Hairless, Permeability, Rats, Sprague-Dawley, Skin metabolism, Skin Absorption, Surface-Active Agents chemistry, Technology, Pharmaceutical, Time Factors, Water chemistry, Aconitine administration & dosage, Analgesics administration & dosage, Anti-Inflammatory Agents administration & dosage, Drug Carriers, Fatty Acids chemistry, Nanoparticles, Oleic Acids chemistry, Transdermal Patch
- Abstract
This study compared transdermal aconitine delivery using solid lipid nanoparticles (SLN) and microemulsion (ME) vehicles. Aconitine-loaded SLN and ME were formulated with the same surfactant, cosurfactant, and water content, with an equal amount of oil matrix (ATO 888 for SLN and ethyl oleate for ME). These nanosized formulations (70-90 nm) showed suitable pH values and satisfactory skin tissue biocompatibility. SLN contained a higher concentration of smaller nanoparticles, compared with that in ME. Neither of the nanocarriers penetrated across excised skin in their intact form. In vitro transdermal delivery studies found that transdermal aconitine flux was lower from SLN than from ME (p < 0.05), but skin aconitine deposition was higher using SLN (p < 0.05). Fluorescence-activated cell sorting indicated that in vitro uptake of fluorescently labeled SLN by human immortalized keratinocyte (HaCaT) cells was greater than that of ME, indicating that a transcellular pathway may contribute to cutaneous drug absorption more effectively from SLN. In vivo studies found that these formulations could loosen stratum corneum layers and increase skin surface crannies, which may also enhance transdermal aconitine delivery. SLN produced a more sustained aconitine release, indicating that compared with ME, this transdermal delivery vehicle may reduce the toxicity of this drug., (© 2014 Wiley Periodicals, Inc. and the American Pharmacists Association.)
- Published
- 2014
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