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Self-assembled chitosan-alginate polyplex nanoparticles containing temoporfin
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SYSNO ASEP 0476354 Document Type J - Journal Article R&D Document Type Journal Article Subsidiary J Článek ve WOS Title Self-assembled chitosan-alginate polyplex nanoparticles containing temoporfin Author(s) Brezaniova, I. (CZ)
Trousil, Jiří (UMCH-V) RID, ORCID
Černochová, Zulfiya (UMCH-V) RID, ORCID
Král, V. (CZ)
Hrubý, Martin (UMCH-V) RID, ORCID
Štěpánek, Petr (UMCH-V) RID, ORCID
Šlouf, Miroslav (UMCH-V) RID, ORCIDSource Title Colloid and Polymer Science - ISSN 0303-402X
Roč. 295, č. 8 (2017), s. 1259-1270Number of pages 12 s. Language eng - English Country DE - Germany Keywords chitosan ; sodium alginate ; temoporfin Subject RIV CD - Macromolecular Chemistry OECD category Polymer science R&D Projects LQ1604 GA MŠMT - Ministry of Education, Youth and Sports (MEYS) ED1.1.00/02.0109 GA MŠMT - Ministry of Education, Youth and Sports (MEYS) GA16-02870S GA ČR - Czech Science Foundation (CSF) NV15-25781A GA MZd - Ministry of Health (MZ) LO1507 GA MŠMT - Ministry of Education, Youth and Sports (MEYS) Institutional support UMCH-V - RVO:61389013 UT WOS 000406174700002 EID SCOPUS 85008514396 DOI 10.1007/s00396-016-3992-6 Annotation The aim of this study was to develop biocompatible polyplex nanoparticles with physicochemical properties suitable for the delivery of photosensitizer temoporfin. We prepared, characterized, and compared the two types of polyplex nanoformulations consisting of sodium alginate in combination with chitosan polymer or chitosan oligomer lactate. We obtained the polyplex system by multiple electrostatic interactions between cationic chitosan and anionic alginate and identified key process parameters. Particle size distribution, dispersity, and zeta potential were determined by dynamic light scattering (DLS), and the diameter and the morphology of the individual particles were visualized by a transmission electron microscopy (TEM). It was found that size distribution of the polyplex nanoparticles depends on the concentrations of chitosan and alginate stock solutions and the order and ratio of addition of stock solutions as well as on the pH of the resulting mixture. It appears that the nanoparticles are homogeneous, although micrographs indicate some (vague, indistinct) core-shell structure. The nanoparticles are stable at pH 7.4 (pH of blood plasma) and show only very little drug leak in experiment modeling conditions of blood pool transport to target tissues. Workplace Institute of Macromolecular Chemistry Contact Eva Čechová, cechova@imc.cas.cz ; Tel.: 296 809 358 Year of Publishing 2018
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