The work is focused on the development of microspheres based on the combination of two polysaccharides; chitosan and alginic acid with the aim to allocate, hold, release and protect environmentally sensible molecules. The microspheres were prepared using a solvent-free, low cost and scalable approach and two enzymes; trypsin and protease from Aspergillus Oryzae have been used as a model to evaluate the microspheres peculiarities. The proteins were encapsulated during the microspheres preparation. The relationship between the polysaccharides weight ratio and the morphology, stability and ability of the carrier to allocate the enzymes has been evaluated. The enzymatic activity and the release kinetics were assessed in different conditions to assess the impact of the external environment. Obtained results demonstrate the efficacy of the prepared microspheres to preserve the activity of relevant bioactive compounds which are highly relevant in food, cosmetic and pharmaceutic, but the application is limited due to their high sensibility.
- MeSH
- Aspergillus oryzae enzymologie MeSH
- buňky NIH 3T3 MeSH
- chitosan chemie toxicita MeSH
- enzymy imobilizované chemie metabolismus MeSH
- koncentrace vodíkových iontů MeSH
- kyselina alginová chemie toxicita MeSH
- lidé MeSH
- mikrosféry * MeSH
- myši MeSH
- testování materiálů MeSH
- tobolky MeSH
- trypsin chemie metabolismus MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
In this work, nanocomplexes based on chitosan grafted by carboxy-modified polylactic acid (SPLA) were prepared with the aim of loading simultaneously two anticancer drugs - doxorubicin and 5-fluorouracil, as well as to control their release, reduce the initial burst and boost cytotoxicity. The SPLA was prepared by a polycondensation reaction, using pentetic acid as the core molecule, and linked to the chitosan backbone through a coupling reaction. Nanocomplexes loaded with both drugs were formulated by the polyelectrolyte complexation method. The structure of the SPLA was characterized by1H NMR, while the product CS-SPLA was analyzed by FTIR-ATR to prove the occurrence of the reaction. Results showed that the diameters and ζ-potential of the nanocomplexes fall in the range 120-200nm and 20-37mV, respectively. SEM and TEM analysis confirmed the spherical shape and dimensions of the nanocomplexes. The presence of hydrophobic side chain SPLA did not influence the encapsulation efficiency of the drugs but strongly reduced the initial burst and prolonged release over time compared to unmodified chitosan. MS analysis showed that no degradation or interactions between the drugs and carrier were exhibited after loading or 24h of release had taken place, confirming the protective role of the nanocomplexes. In vitro tests demonstrated an increase in the cytotoxicity of the drugs when loaded in the prepared carriers.
- MeSH
- buňky NIH 3T3 MeSH
- chitosan chemie toxicita MeSH
- doxorubicin chemie MeSH
- fluorouracil chemie MeSH
- léky s prodlouženým účinkem MeSH
- myši MeSH
- nanostruktury chemie toxicita MeSH
- nosiče léků chemie MeSH
- polyestery chemie MeSH
- viabilita buněk účinky léků MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
BACKGROUND: Plasma treatment enables effective binding of chitosan film to textile fibres. Heavy metal ions such as Ag(+) adsorbed onto the chitosan coating are known to enhance toxicity to microorganisms. The acaricidal effect of chitosan and chitosan/metal adducts with Ag(+) , Zn(2+) and Cu(2+) was tested in laboratory experiments. Tested species Acarus siro, Dermatophagoides farinae, D. pteronyssinus and Tyrophagus putrescentiae are allergen producers and important pests in house dust, stored food and feed. The mortality was compared after 24 h of exposure of mites to plasma-treated textiles. RESULTS: Chitosan/Ag(+) textile caused at least 80% mortality of all species tested. Chitosan/Zn(2+) and chitosan/Cu(2+) textiles had a smaller effect on mite mortality than chitosan/Ag(+) . The conversion of chitosan/Ag(+) finishing to chitosan/Ag2 O did not influence the mortality of mites in biotests, except that of Tyrophagus putrescentiae, where the mortality decreased from 86 to 64%. CONCLUSION: The results support a great potential of chitosan/Ag(+) fibres in acaricidal materials and/or mite protective food packages.
- MeSH
- akaricidy chemie farmakologie MeSH
- chitosan chemie toxicita MeSH
- měď chemie farmakologie MeSH
- roztoči účinky léků fyziologie MeSH
- stříbro chemie farmakologie MeSH
- textilie analýza MeSH
- zinek chemie farmakologie MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
