Literature DB >> 16297487

Lipid nanoparticles for skin penetration enhancement-correlation to drug localization within the particle matrix as determined by fluorescence and parelectric spectroscopy.

S Lombardi Borgia1, M Regehly, R Sivaramakrishnan, W Mehnert, H C Korting, K Danker, B Röder, K D Kramer, M Schäfer-Korting.   

Abstract

With topical treatment of skin diseases, the requirement of a high and reproducible drug uptake often still is not met. Moreover, drug targeting to specific skin strata may improve the use of agents which are prone to cause local unwanted effects. Recent investigations have indicated that improved uptake and skin targeting may become feasible by means of nanoparticular systems such as solid lipid nanoparticles (SLN), nanostructured lipid carriers (NLC) and nanoemulsions (NE). Here we describe techniques to characterize drug loading to carrier systems and skin penetration profiles by using the lipophilic dye nile red as a model agent. Since the mode of drug association with the particle matrix may strongly influence the efficiency of skin targeting, parelectric spectroscopy (PS) was used to differentiate between matrix incorporation and attachment to the particle surface and fluorescence spectroscopy (FS) to solve dye distribution within NLC particles. Nile red was incorporated into the lipid matrix or the covering tensed shell, respectively, of SLN and NLC with all the lipids studied (Compritol, Precirol, oleic acid, Miglyol). In NLC, the dye was enriched in the liquid phase. Next, nile red concentrations were followed by image analysis of vertical sections of pigskin treated with dye-loaded nanoparticular dispersions and an oil-in-water cream for 4 and 8 h in vitro. Following the SLN dispersions, dye penetration increased about fourfold over the uptake obtained following the cream. NLC turned out less potent (<threefold increase) and penetration appeared even reduced when applying a NE. In contrast to previous studies with glucocorticoids attached to the surface of SLN, a targeting effect was not detected here. Therefore, drug targeting appears to be more strictly related to the mode of interaction of drug and particle than penetration enhancement.

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Year:  2005        PMID: 16297487     DOI: 10.1016/j.jconrel.2005.09.045

Source DB:  PubMed          Journal:  J Control Release        ISSN: 0168-3659            Impact factor:   9.776


  21 in total

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Journal:  Nanoscale Res Lett       Date:  2010-07-20       Impact factor: 4.703

7.  Squalene-containing nanostructured lipid carriers promote percutaneous absorption and hair follicle targeting of diphencyprone for treating alopecia areata.

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8.  Nanoparticle coated submicron emulsions: sustained in-vitro release and improved dermal delivery of all-trans-retinol.

Authors:  Nasrin Ghouchi Eskandar; Spomenka Simovic; Clive A Prestidge
Journal:  Pharm Res       Date:  2009-04-22       Impact factor: 4.200

Review 9.  Interaction of nanoparticles and cell-penetrating peptides with skin for transdermal drug delivery.

Authors:  Pinaki Desai; Ram R Patlolla; Mandip Singh
Journal:  Mol Membr Biol       Date:  2010-10       Impact factor: 2.857

10.  Squarticles as a lipid nanocarrier for delivering diphencyprone and minoxidil to hair follicles and human dermal papilla cells.

Authors:  Ibrahim A Aljuffali; Calvin T Sung; Feng-Ming Shen; Chi-Ting Huang; Jia-You Fang
Journal:  AAPS J       Date:  2013-12-04       Impact factor: 4.009

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