Lipid analysis of follicular casts from cyanoacrylate strips as a new method for studying therapeutic effects of antiacne agents

Citation
A. Thielitz et al., Lipid analysis of follicular casts from cyanoacrylate strips as a new method for studying therapeutic effects of antiacne agents, BR J DERM, 145(1), 2001, pp. 19-27
Citations number
21
Categorie Soggetti
Dermatology,"da verificare
Journal title
BRITISH JOURNAL OF DERMATOLOGY
ISSN journal
00070963 → ACNP
Volume
145
Issue
1
Year of publication
2001
Pages
19 - 27
Database
ISI
SICI code
0007-0963(200107)145:1<19:LAOFCF>2.0.ZU;2-T
Abstract
Background The cyanoacrylate follicular biopsy is an established method for the examination of the horny layer and quantitative assessment of microcom edones. We have optimized the method by separating follicular casts mechani cally from the cyanoacrylate strips. Objectives To use this method to analyse topical therapy-induced changes of the lipid composition in the sebaceous follicular infundibulum. Methods Both the follicular casts and the residual skin surface strip, the last representing a mixture of stratum corneum and surface lipids, were ext racted twice with n-hexane-ethanol under ultrasonication, evaporated, redis solved in chloroform-methanol and separated by high-performance thin layer chromatography, using cholesterol sulphate, cerebroside, ceramide types 3 a nd 4, cholesterol, oleic acid, triolein, cholesterol oleate and squalene as standards. Identification was performed by computer-assisted densitometric analysis. Six patient groups receiving adapalene 0.1%, tretinoin 0.025%, c lindamycin 1%, clindamycin 1% + tretinoin 0.025%, benzoyl peroxide 5% or be nzoyl peroxide 5% + erythromycin 2% were investigated before and 12 weeks a fter application. Results A significant decrease in free fatty acid proportions combined with an increase in triglycerides was observed in the groups receiving antimicr obial therapy, supporting the hypothesis of lipolysis due to microbial colo nization. The groups treated with topical retinoids showed an additional si gnificant increase in ceramide subfractions, most probably reflecting their influence on epidermal keratinization. Conclusions Our method proved suitable for the detection of quantitative an d qualitative changes in lipid profiles of both infundibulum cast content a nd surface lipids. It enabled simple, non-invasive and objective assessment of the most relevant lipid classes in the sebaceous infundibulum, and effi cient monitoring of drug effects on the follicular infundibulum.