Abstract

A comparative analysis of the molecular process of nanostructured zinc oxide of different shape (rod and spherical particle) and zinc chloride as a source of free ions on human lymphocytes was carried out. Our data indicated that ZnO nanostructures induced a decrease in the lymphocyte viability and an increase in the intracellular labile Zn 2+ pool in a concentration-dependent manner after 20 and 40 h incubation with cells. It was found that ZnO NRs have the lowest cytotoxicity, but ZnCl 2 - the highest. The Zn-mediated activation of free radical processes - ROS accumulation in the cells -is a possible mechanism of the cytotoxic action of these agents. Thus, the shape of ZnO nanomaterial and its ability “to shed” zinc ions make the main contribution to the detected molecular and membrane process on human lymphocytes in vitro .

Highlights

  • A comparative analysis of the molecular process of nanostructured zinc oxide of different shape and zinc chloride as a source of free ions on human lymphocytes was carried out

  • Our data indicated that ZnO nanostructures induced a decrease in the lymphocyte viability and an increase in the intracellular labile Zn2+ pool in a concentration-dependent manner after 20 and 40 h incubation with cells

  • It was found that ZnO NRs have the lowest cytotoxicity, but ZnCl2 – the highest

Read more

Summary

Introduction

A comparative analysis of the molecular process of nanostructured zinc oxide of different shape (rod and spherical particle) and zinc chloride as a source of free ions on human lymphocytes was carried out. Для оценки жизнеспособности лимфоцитов после воздействия исследуемых форм наноструктурированного оксида цинка – сферических частиц и стержней, а также хлорида цинка как источника свободных ионов Zn2+, был выбран тест FITCанексин-V / 7-AAD [5].

Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.