Pregled bibliografske jedinice broj: 558329
Mucoadhesive liposomal delivery systems: the choice of coating material
Mucoadhesive liposomal delivery systems: the choice of coating material // Drug development and industrial pharmacy, 37 (2011), 4; 482-488 doi:10.3109/03639045.2010.523425 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 558329 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Mucoadhesive liposomal delivery systems: the choice of coating material
Autori
Karn, Pankaj Ranjan ; Pepić, Ivan ; Vanić, Željka ; Škalko Basnet, Nataša
Izvornik
Drug development and industrial pharmacy (0363-9045) 37
(2011), 4;
482-488
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
atenolol; carbopol; chitosan; eudragit; liposomes; mucoadhesion; polymer-coating
Sažetak
Objective was to development of liposomal mucoadhesive drug delivery system, which is able to improve the bioavailability of poorly absorbed oral drugs by prolonging their gastric and intestinal residence time, through facilitating the intimate contact of the delivery system with the absorption membrane. Liposomes containing model drug atenolol were prepared by the modified ethanol injection method. Liposomes containing atenolol were coated by different mucoadhesive polymers, for example, chitosan, Carbopol 974P, Eudragit L100, and Eudragit S100, to optimize the choice of coating material. The delivery systems were tested for their in vitro mucoadhesiveness. Liposomes prepared by the ethanol injection method were of satisfactory size (around 100 nm, before coating). Through the coating of liposomes in the presence of unentrapped material, the entrapment efficiency for drug was increased. In vitro mucoadhesive test confirmed the mucoadhesive properties of the coated layer for all tested polymers ; however, Eudragit S100-coated liposomes were superior to other coating materials. Discussion: Eudragit coating appeared to be an optimal polymer choice. These preliminary data indicate that polymer-coated mucoadhesive liposomes are able to carry sufficient amount of drug and to remain attached to the intestinal mucosa for a sufficient period of time to enable prolonged absorption of entrapped drug. Conclusion: While keeping in mind that the in vivo conditions may vary with the in vitro ones, we may recommend the system described in our work for possible oral delivery of peptides and phytochemicals.
Izvorni jezik
Engleski
Znanstvena područja
Farmacija
POVEZANOST RADA
Projekti:
006-0061117-1244 - Terapijski nanosustavi (Filipović-Grčić, Jelena, MZOS ) ( CroRIS)
Ustanove:
Farmaceutsko-biokemijski fakultet, Zagreb
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE