Exploring the potential for rosacea therapeutics of siRNA dispersion in topical emulsions.
Animals
Computer Simulation
Disease Models, Animal
Drug Delivery Systems
Emulsions
Excipients
/ chemistry
Female
Gene Silencing
Glycerol
/ chemistry
Humans
Mice
Mice, Inbred BALB C
RNA Interference
RNA, Double-Stranded
/ metabolism
RNA, Small Interfering
/ pharmacology
Rosacea
/ drug therapy
Skin
/ metabolism
Toll-Like Receptor 2
/ metabolism
Urea
/ chemistry
TLR2
drug delivery
skin inflammation
small interference RNA
topical formulation
Journal
Experimental dermatology
ISSN: 1600-0625
Titre abrégé: Exp Dermatol
Pays: Denmark
ID NLM: 9301549
Informations de publication
Date de publication:
03 2019
03 2019
Historique:
received:
11
07
2018
revised:
10
12
2018
accepted:
11
01
2019
pubmed:
17
1
2019
medline:
30
7
2020
entrez:
17
1
2019
Statut:
ppublish
Résumé
Rosacea is a prevalent skin condition dependent on the individual genetic profile. The current pharmacological management of this condition is mostly based on small molecule drugs predominately effective in ameliorating the inflammatory condition. Emerging molecular approaches could present an opportunity for managing rosacea conditions at transcriptomic level, and in the future allow personalized approaches. RNA medicines, such as small RNA interference (siRNA), could provide a flexible and applicable tool reaching this aim. However, the topical siRNA delivery by dermatological emulsions, commonly used in the daily management of rosacea, is still largely unexplored. Consequently, RNA interference application to rosacea was defined on molecular bases by genetic expression meta-data analysis. Based on this, a siRNA directed against TLR2 was designed and validated in vitro on murine macrophages and fibroblasts. Next, siRNA was dispersed in the continuous phase of emulsions and was characterized for commonly used dermatologic bases. Finally, the potential delivery performance of the topical emulsions was tested in vivo on healthy Balb/c mice. It was found that the interaction of siRNA with combination of excipients, such as urea and glycerol, is likely to favour the siRNA delivery, inducing genetic silencing of TLR2. These findings provide a foundation for the future development of topical RNA-based dispersions for topical molecular medicines, by emphasizing on the formulation and therapeutic-based opportunities with dermatological treatments.
Substances chimiques
Emulsions
0
Excipients
0
RNA, Double-Stranded
0
RNA, Small Interfering
0
Tlr2 protein, mouse
0
Toll-Like Receptor 2
0
Urea
8W8T17847W
Glycerol
PDC6A3C0OX
Banques de données
GENBANK
['NM_011905.3']
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
261-269Subventions
Organisme : Innovation Fund Denmark
ID : 5179-00660B
Pays : International
Organisme : Lundbeckfonden
ID : R218-2016-1323
Pays : International
Informations de copyright
© 2019 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.