Design of Gadoteridol-Loaded Cationic Liposomal Adjuvant CAF01 for MRI of Lung Deposition of Intrapulmonary Administered Particles.
Adjuvants, Immunologic
/ chemistry
Adjuvants, Pharmaceutic
Animals
Cations
/ chemistry
Chemistry, Pharmaceutical
/ methods
Female
Gadolinium
/ administration & dosage
Heterocyclic Compounds
/ administration & dosage
Lipids
/ chemistry
Liposomes
/ chemistry
Lung
/ drug effects
Magnetic Resonance Imaging
/ methods
Mice
Mice, Inbred BALB C
Nanoparticles
/ chemistry
Organometallic Compounds
/ administration & dosage
Tuberculosis
/ drug therapy
Tuberculosis Vaccines
/ chemistry
Vaccines, Subunit
/ chemistry
adjuvant
drug delivery
gadoteridol
liposomes
lung proton MRI
quality-by-design
Journal
Molecular pharmaceutics
ISSN: 1543-8392
Titre abrégé: Mol Pharm
Pays: United States
ID NLM: 101197791
Informations de publication
Date de publication:
04 11 2019
04 11 2019
Historique:
pubmed:
21
9
2019
medline:
3
6
2020
entrez:
21
9
2019
Statut:
ppublish
Résumé
Designing effective and safe tuberculosis (TB) subunit vaccines for inhalation requires identification of appropriate antigens and adjuvants and definition of the specific areas to target in the lungs. Magnetic resonance imaging (MRI) enables high spatial resolution, but real-time anatomical and functional MRI of lungs is challenging. Here, we describe the design of a novel gadoteridol-loaded cationic adjuvant formulation 01 (CAF01) for MRI-guided vaccine delivery of the clinically tested TB subunit vaccine candidate H56/CAF01. Gadoteridol-loaded CAF01 liposomes were engineered by using a quality-by-design approach to (i) increase the mechanistic understanding of formulation factors governing the loading of gadoteridol and (ii) maximize the loading of gadoteridol in CAF01, which was confirmed by cryotransmission electron microscopy. The encapsulation efficiency and loading of gadoteridol were highly dependent on the buffer pH due to strong attractive electrostatic interactions between gadoteridol and the cationic lipid component. Optimal gadoteridol loading of CAF01 liposomes showed good in vivo stability and safety upon intrapulmonary administration into mice while generating 1.5-fold MRI signal enhancement associated with approximately 30%
Identifiants
pubmed: 31539263
doi: 10.1021/acs.molpharmaceut.9b00908
doi:
Substances chimiques
Adjuvants, Immunologic
0
Adjuvants, Pharmaceutic
0
Cations
0
Heterocyclic Compounds
0
Lipids
0
Liposomes
0
Organometallic Compounds
0
Tuberculosis Vaccines
0
Vaccines, Subunit
0
gadoteridol
0199MV609F
Gadolinium
AU0V1LM3JT
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM