Efficacy assessment of self-assembled PLGA-PEG-PLGA nanoparticles: Correlation of nano-bio interface interactions, biodistribution, internalization and gene expression studies
Autor: | Nikola Geskovski, Boguslaw Szczupak, Rozafa Koliqi, Jordi Llop, Aleksandar Dimovski, Sonja Ugarkovic, Katerina Goracinova, Delyan R. Hristov, Gjorgji Petruševski, Eneko San Sebastián, Nadica Matevska-Geskovska, Vanessa Gómez Vallejo, Marco P. Monopoli, Simona Dimchevska |
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Rok vydání: | 2017 |
Předmět: |
Biodistribution
Biocompatibility Surface Properties media_common.quotation_subject Fibroblast Growth Factor 3 Muscle Proteins Pharmaceutical Science Nanoparticle Cell Cycle Proteins Nerve Tissue Proteins Nanotechnology 02 engineering and technology Irinotecan 010402 general chemistry 01 natural sciences Polyethylene Glycols Histones Cell Line Tumor Zeta potential Copolymer Animals Humans Tissue Distribution Particle Size Rats Wistar Internalization Polyglactin 910 Ubiquitins media_common Chemistry technology industry and agriculture Serum Albumin Bovine 021001 nanoscience & nanotechnology Antineoplastic Agents Phytogenic 0104 chemical sciences Gene Expression Regulation Neoplastic Molecular Weight Biophysics Nanoparticles Camptothecin Adsorption Nanocarriers 0210 nano-technology Protein adsorption |
Zdroj: | International Journal of Pharmaceutics. 533:389-401 |
ISSN: | 0378-5173 |
Popis: | The aim of our study was to develop and compare the biological performance of two types of biodegradable SN-38 loaded nanoparticles (NPs) with various surface properties, composed of low and high Mw triblock PLGA-PEG-PLGA copolymers, applying rational quality and safety by design approach. Therefore, along with the optimization of crucial physico-chemical properties and in order to evaluate the therapeutical potential and biocompatibility of prepared polymeric nanoparticles, analysis of nano-bio interactions, cell internalization, gene expression and biodistribution studies were performed. The optimized formulations, one of low Mw and one composed of high Mw PLGA-PEG-PLGA copolymer, exhibited different characteristics in terms of surface properties, particle size, zeta potential, drug loading, protein adsorption and biodistribution, which may be attributed to the variations in nano–bio interface interactions due to different NP building blocks length and Mw. On the contrary to protein adsorption and biodistribution studies, both types of NPs exhibited similar results during cell internalization and gene expression studies performed in cell culture medium containing serum proteins. This pool of useful data for internalization and efficacy as well as the notable advance in the circulation time of low Mw NPs may be further employed for shaping the potential of the designed nanocarriers. |
Databáze: | OpenAIRE |
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