Development of an acid-labile ketal linked amphiphilic block copolymer nanoparticles for pH-triggered release of paclitaxel

0542393 - ÚMCH 2022 RIV CH eng J - Journal Article
Lukáš Petrova, Svetlana - Jäger, Eliezer - Jäger, Alessandro - Höcherl, Anita - Konefal, Rafal - Zhigunov, Alexander - Pavlova, Ewa - Janoušková, Olga - Hrubý, Martin
Development of an acid-labile ketal linked amphiphilic block copolymer nanoparticles for pH-triggered release of paclitaxel.
Polymers. Roč. 13, č. 9 (2021), č. článku 1465. E-ISSN 2073-4360
R&D Projects: GA ČR(CZ) GJ20-15077Y; GA ČR(CZ) GJ20-13946Y; GA MŠMT(CZ) LTC19032
Institutional support: RVO:61389013
Keywords : MPEO-b-PCL nanoparticles * acyclic ketal group * paclitaxel
OECD category: Polymer science
Impact factor: 4.967, year: 2021
Method of publishing: Open access
https://www.mdpi.com/2073-4360/13/9/1465

Here, we report on the construction of biodegradable poly(ethylene oxide monomethyl ether) (MPEO)-b-poly(ε-caprolactone) (PCL) nanoparticles (NPs) having acid-labile (acyclic ketal group) linkage at the block junction. In the presence of acidic pH, the nanoassemblies were destabilized as a consequence of cleaving this linkage. The amphiphilic MPEO-b-PCL diblock copolymer self-assembled in PBS solution into regular spherical NPs. The structure of self-assemble and disassemble NPs were characterized in detail by dynamic (DLS), static (SLS) light scattering, small-angle X-ray scattering (SAXS), and transmission electron microscopy (TEM). The key of the obtained NPs is using them in a paclitaxel (PTX) delivery system and study their in vitro cytostatic activity in a cancer cell model. The acid-labile ketal linker enabled the disassembly of the NPs in a buffer simulating an acidic environment in endosomal (pH ~5.0 to ~6.0) and lysosomal (pH ~4.0 to ~5.0) cell compartments resulting in the release of paclitaxel (PTX) and formation of neutral degradation products. The in vitro cytotoxicity studies showed that the activity of the drug-loaded NPs was increased compared to the free PTX. The ability of the NPs to release the drug at the endosomal pH with concomitant high cytotoxicity makes them suitable candidates as a drug delivery system for cancer therapy.
Permanent Link: http://hdl.handle.net/11104/0320015