Abstract
The purpose of the present study was to develop a reverse-phase high performance liquid chromatographic (HPLC) assay for quantifying 5-aminolevulinic acid (ALA). The assay was applied to study the skin permeation of ALA and the influence of a novel skin penetration enhancement technology. Separation was achieved utilizing a Phenomenex Jupiter C18 column following fluorescence derivatization with fluorescamine. The assay was linear (r2 > 0.99) with a minimum limit of quantitation of 400 ng/mL. The inter- and intraday variation was 1.6 and 0.9% at the lower end of the linear range and 1.5 and 1.9% at the upper end, respectively. The HPLC assay and fluorescence derivatization procedure is sensitive, simple, rapid, accurate and reproducible and offers advantages with regard to stability of ALA in comparison to other fluorescence derivatization methods. Results from the preliminary skin permeation study demonstrated substantial skin penetration of ALA only when applied with Dermaportation as a skin penetration enhancement device. © 2007 Elsevier B.V. All rights reserved.
Author supplied keywords
Cite
CITATION STYLE
Namjoshi, S., Caccetta, R., Edwards, J., & Benson, H. A. E. (2007). Liquid chromatography assay for 5-aminolevulinic acid: Application to in vitro assessment of skin penetration via Dermaportation. Journal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciences, 852(1–2), 49–55. https://doi.org/10.1016/j.jchromb.2006.12.040
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.