Biocompatible Ionic Liquid Enhances Transdermal Antigen Peptide Delivery and Preventive Vaccination Effect.
Administration, Cutaneous
Animals
Antigens, Neoplasm
/ administration & dosage
Cancer Vaccines
/ administration & dosage
Cell Line, Tumor
/ transplantation
Choline
/ chemistry
Disease Models, Animal
Drug Carriers
/ chemistry
Fatty Acids
/ chemistry
Humans
Hydrophobic and Hydrophilic Interactions
Ionic Liquids
/ chemistry
Mice
Neoplasms
/ immunology
Permeability
Skin
Skin Absorption
Solvents
/ chemistry
Vaccination
/ methods
Vaccines, Subunit
/ administration & dosage
biocompatible
ionic liquid
peptide
transdermal delivery
vaccine
Journal
Molecular pharmaceutics
ISSN: 1543-8392
Titre abrégé: Mol Pharm
Pays: United States
ID NLM: 101197791
Informations de publication
Date de publication:
05 10 2020
05 10 2020
Historique:
pubmed:
10
9
2020
medline:
3
8
2021
entrez:
9
9
2020
Statut:
ppublish
Résumé
Ionic liquids (ILs) attract significant attention as novel solvents for drug delivery systems because of their ability to solubilize poorly soluble drugs and tune the physiological properties of active pharmaceutical ingredients. For the next generation of IL-based drug delivery systems, biocompatibility is a high priority. In the current study, choline-fatty acids ([Cho][FA]) were used as a biocompatible IL to mediate the dissolution of a water-soluble antigen peptide in an oil-based skin penetration enhancer. Among the candidate fatty acids (C8, C10, C12, C14, C16, C18:0, and C18:1), C18:1 was selected because of its low cytotoxicity and mediation of skin permeability for an antigen peptide. Using IL[Cho][C18:1] and an oil-based penetration enhancer, the flux of transdermal delivery of the peptide increased 28-fold compared with delivery using an aqueous vehicle. Furthermore, the IL-mediated transcutaneous vaccination succeeded in suppressing tumor growth in vivo compared to injection. The skin irritation produced by this formulation was tested using an in vitro 3D constructed skin tissue model and an in vivo histological study, which concluded that the formulation did not cause skin irritation. The results suggest that biocompatible IL-mediated dissolution in an oil-based skin penetration enhancer is a promising strategy for transdermal drug delivery.
Identifiants
pubmed: 32902989
doi: 10.1021/acs.molpharmaceut.0c00598
doi:
Substances chimiques
Antigens, Neoplasm
0
Cancer Vaccines
0
Drug Carriers
0
Fatty Acids
0
Ionic Liquids
0
Solvents
0
Vaccines, Subunit
0
Choline
N91BDP6H0X
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM