POLYMERIZED LIPOSOMES AS POTENTIAL ORAL VACCINE CARRIERS - STABILITY AND BIOAVAILABILITY

Citation
Hm. Chen et al., POLYMERIZED LIPOSOMES AS POTENTIAL ORAL VACCINE CARRIERS - STABILITY AND BIOAVAILABILITY, Journal of controlled release, 42(3), 1996, pp. 263-272
Citations number
23
Categorie Soggetti
Pharmacology & Pharmacy",Chemistry
ISSN journal
01683659
Volume
42
Issue
3
Year of publication
1996
Pages
263 - 272
Database
ISI
SICI code
0168-3659(1996)42:3<263:PLAPOV>2.0.ZU;2-F
Abstract
The potential of polymerized liposomes as oral vaccine carriers is eva luated. The stability of polymerized liposomes is demonstrated in mous e gastrointestinal tracts using dual-labeled liposomes. Similar transi t kinetics displayed by the two labels of different hydrophobicity ind icate the intactness of the polymerized liposomes inside the gastroint estinal tract. Uptake of liposomes from mouse gastrointestinal tract b y Peyer's patches is quantified by measuring the amount of radiolabele d liposomes retained in the tissues following liposome oral administra tion. Bioavailability of liposomal contents is examined in macrophage cultures with calcein-containing liposomes. Liberation of calcein in c ells suggests the breakdown of liposomal membranes and the intracellul ar release of their encapsulated materials.