Pegylated polyelectrolyte nanoparticles containing paclitaxel as a promising candidate for drug carriers for passive targeting

• Published in: Colloids and surfaces, B, Biointerfaces B, Biointerfaces, 2016-07, Vol.143, p.463-471
• Main Authors: Szczepanowicz, Krzysztof, Bzowska, Monika, Kruk, Tomasz, Karabasz, Alicja, Bereta, Joanna, Warszynski, Piotr
• Format: Article
• Language: English
• Subjects: Animals; Antineoplastic Agents, Phytogenic - chemistry; Antineoplastic Agents, Phytogenic - pharmacology; Biocompatibility; Biotechnology; Cancer; Cell Line, Tumor; Cell Survival - drug effects; Dioctyl Sulfosuccinic Acid - chemistry; Droplets; Drug Carriers; Drug Compounding; Drug delivery; Emulsions; Encapsulation; Mice; Molecular Targeted Therapy; Nanoparticles; Nanoparticles - chemistry; Paclitaxel; Paclitaxel - chemistry; Paclitaxel - pharmacology; Particle Size; Passive targeting; Polyelectrolytes; Polyelectrolytes - chemistry; Polyethylene Glycols - chemistry; Polyglutamic Acid - analogs & derivatives; Polyglutamic Acid - chemistry; Polylysine - chemistry; Surface chemistry
• ISSN: 0927-7765; 1873-4367
• DOI: 10.1016/j.colsurfb.2016.03.064

[Display omitted] •Polyelectrolyte nanocapsules with pegylated external layer were prepared.•The empty nanocapsules did not affect the viability of the tested cells.•Encapsulated paclitaxel retained its strong cytotoxic/cytostatic activity. Targeted drug delivery systems are of special importance in cancer therapies, since serious side effects resulting from unspecific accumulation of highly toxic chemotherapeutics in healthy tissues can restrict effectiveness of the therapy. In this work we present the method of preparing biocompatible, polyelectrolyte nanoparticles containing the anticancer drug that may serve as a vehicle for passive tumor targeting. The nanoparticles were prepared via direct encapsulation of emulsion droplets in a polyelectrolyte multilayer shell. The oil cores that contained paclitaxel were stabilized by docusate sodium salt/poly-l-lysine surface complex (AOT/PLL) and were encapsulated in shells formed by the LbL adsorption of biocompatible polyelectrolytes, poly-L-glutamic acid (PGA) and PLL up to 5 or 6 layers. The surface of the nanoparticles was pegylated through the adsorption of the pegylated polyelectrolyte (PGA-g-PEG) as the outer layer to prolong the persistence of the nanocarriers in the circulation. The synthesized nanoparticles were stable in cell culture medium containing serum and their average size was 100nm, which makes them promising candidates for passive targeted drug delivery. This notion was further confirmed by the results of studying the biological effects of nanoformulations on two tumor cell lines: mouse colon carcinoma cell line CT26-CEA and the mouse mammary carcinoma cell line 4T1. The empty polyelectrolyte nanoparticles did not affect the viability of the tested cells, whereas encapsulated paclitaxel retained its strong cytotoxic/cytostatic activity.