Lipid nanoparticles as vehicles for topical psoralen delivery: Solid lipid nanoparticles (SLN) versus nanostructured lipid carriers (NLC)

Jia You Fang, Chia Lang Fang, Chi Hsien Liu, Yu Han Su

Research output: Contribution to journalArticle

281 Citations (Scopus)

Abstract

Solid lipid nanoparticles (SLN) were developed by using Precirol ATO 5 as the solid core of the particles for topical psoralen delivery. Nanostructured lipid carriers (NLC) consisting of Precirol and squalene, a liquid lipid, were also prepared for comparison. SLN and NLC showed respective mean particle sizes of ∼300 and 200 nm, respectively. Viscosity, polarity, and differential scanning calorimetry (DSC) studies were performed to characterize the physicochemical properties of the SLN and NLC. The viscosity of all nanoparticulate systems exhibited Newtonian behavior except the NLC with Tween 80 and soybean phospholipids as the emulsifiers (NLC-Tw). According to the DSC thermograms, the melting peak of Precirol shifted from 58 to 55 °C after incorporating squalene into the solid lipid cores (of NLC), which suggests defects in the crystalline lattice of the lipid cores and smaller particle sizes. Three psoralen derivatives for psoriasis treatments were loaded in SLN and NLC to examine their ability to permeate skin. The permeability of psoralens increased in the order of 8-methoxypsoralen (8-MOP) > 5-methoxypsoralen (5-MOP) > 4,5,8-trimethylpsoralen (TMP). Enhanced permeation and controlled release of psoralen delivery were both achieved using the NLC. The in vitro permeation results showed that NLC-Tw increased the 8-MOP flux 2.8 times over that of a conventional emulsion. Hyperproliferative or psoriasis-like skin produced by repeated strippings in the dorsal skin of nude mouse was also used as a permeation barrier. The results showed that the entrapment of 8-MOP in nanoparticulate systems could minimize the permeation differentiation between normal and hyperproliferative skin compared to the free drug in an aqueous control.

Original languageEnglish
Pages (from-to)633-640
Number of pages8
JournalEuropean Journal of Pharmaceutics and Biopharmaceutics
Volume70
Issue number2
DOIs
Publication statusPublished - Oct 2008

Fingerprint

Ficusin
Nanoparticles
Lipids
Methoxsalen
Squalene
Skin
Differential Scanning Calorimetry
Psoriasis
Particle Size
Viscosity
Trioxsalen
Aptitude
Polysorbates

Keywords

  • Nanostructured lipid carriers
  • Psoralen
  • Psoriasis
  • Solid lipid nanoparticles
  • Topical delivery

ASJC Scopus subject areas

  • Biotechnology
  • Pharmaceutical Science

Cite this

Lipid nanoparticles as vehicles for topical psoralen delivery : Solid lipid nanoparticles (SLN) versus nanostructured lipid carriers (NLC). / Fang, Jia You; Fang, Chia Lang; Liu, Chi Hsien; Su, Yu Han.

In: European Journal of Pharmaceutics and Biopharmaceutics, Vol. 70, No. 2, 10.2008, p. 633-640.

Research output: Contribution to journalArticle

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