Detailed Information on Publication Record
2024
Long circulating liposomal platform utilizing hydrophilic polymer-based surface modification: preparation, characterisation, and biological evaluation
TURANEK, Jaroslav, Petr KOSZTYU, Pavlina TURANEK KNOTIGOVA, Eliska BARTHELDYOVA, Frantisek HUBATKA et. al.Basic information
Original name
Long circulating liposomal platform utilizing hydrophilic polymer-based surface modification: preparation, characterisation, and biological evaluation
Authors
TURANEK, Jaroslav (203 Czech Republic), Petr KOSZTYU (203 Czech Republic), Pavlina TURANEK KNOTIGOVA (203 Czech Republic), Eliska BARTHELDYOVA (203 Czech Republic), Frantisek HUBATKA (203 Czech Republic), Nikola ODEHNALOVA (203 Czech Republic), Robert MIKULÍK (203 Czech Republic), Naděžda VAŠKOVICOVÁ (203 Czech Republic, belonging to the institution), Hana ČELECHOVSKÁ (203 Czech Republic, belonging to the institution), Irena KRATOCHVILOVA (203 Czech Republic), Ladislav FEKETE (203 Czech Republic), Marina R. TAVARES (203 Czech Republic), Petr CHYTIL (203 Czech Republic), Milan RASKA (203 Czech Republic) and Tomas ETRYCH (203 Czech Republic)
Edition
International Journal of Pharmaceutics, AMSTERDAM, ELSEVIER, 2024, 0378-5173
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10608 Biochemistry and molecular biology
Country of publisher
Netherlands
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 5.800 in 2022
Organization unit
Faculty of Medicine
UT WoS
001273994500001
Keywords in English
Stealth liposomes; HPMA copolymer; Complement activation; Drug delivery system; Long-circulating liposomes
Tags
International impact, Reviewed
Změněno: 5/8/2024 08:51, Mgr. Tereza Miškechová
Abstract
V originále
Liposomes are one of the most important drug delivery vectors, nowadays used in clinics. In general, polyethylene glycol (PEG) is used to ensure the stealth properties of the liposomes. Here, we have employed hydrophilic, biocompatible and highly non-fouling N-(2-hydroxypropyl) methacrylamide (HPMA)-based copolymers containing hydrophobic cholesterol anchors for the surface modification of liposomes, which were prepared by the method of lipid film hydration and extrusion through 100 nm polycarbonate filters. Efficient surface modification of liposomes was confirmed by transmission electron microscopy, atomic force microscopy, and gradient ultracentrifugation. The ability of long-term circulation in the vascular bed was demonstrated in rabbits after i.v. application of fluorescently labelled liposomes. Compared to PEGylated liposomes, HPMA-based copolymer-modified liposomes did not induce specific antibody formation and did not activate murine and human complement. Compared with PEGylated liposomes, HPMA-based copolymer-modified liposomes showed a better long-circulating effect after repeated administration. HPMA-based copolymer-modified liposomes thus represent suitable new candidates for a generation of safer and improved liposomal drug delivery platforms.
Links
EH22_008/0004596, research and development project |
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NU21-08-00510, research and development project |
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