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Biological Properties of the Aggregated Form of Chitosan Magnetic Nanoparticle
- Source :
- In Vivo
- Publication Year :
- 2020
-
Abstract
- Background/Aim: Chitosan-coated iron oxide nanoparticles (Chi-NP) have gained attention because of their biocompatibility, biodegradability, low toxicity and targetability under magnetic field. In this study, we investigated various biological properties of Chi-NP. Materials and Methods: Chi-NP was prepared by mixing magnetic NP with chitosan FL-80. Particle size was determined by scanning and transmission electron microscopes, cell viability by MTT assay, cell cycle distribution by cell sorter, synergism with anticancer drugs by combination index, PGE(2) production in human gingival fibroblast was assayed by ELISA. Results: The synthetic process of Chi-NP from FL-80 and magnetic NP increased the affinity to cells, up to the level attained by nanofibers. Upon contact with the culture medium, Chi-NP instantly formed aggregates and interfered with intracellular uptake. Aggregated Chi-NP did not show cytotoxicity, synergism with anticancer drugs, induce apoptosis (accumulation of subG1 cell population), protect the cells from X-ray-induced damage, nor affected both basal and IL-1β-induced PGE(2) production. Conclusion: Chi-NP is biologically inert and shows high affinity to cells, further confirming its superiority as a scaffold for drug delivery.
- Subjects :
- Cancer Research
Biocompatibility
Population
General Biochemistry, Genetics and Molecular Biology
Chitosan
03 medical and health sciences
chemistry.chemical_compound
0302 clinical medicine
Drug Delivery Systems
Humans
MTT assay
Viability assay
Particle Size
Cytotoxicity
education
Magnetite Nanoparticles
Pharmacology
education.field_of_study
Drug Carriers
Chemistry
030220 oncology & carcinogenesis
Drug delivery
Biophysics
Nanoparticles
Iron oxide nanoparticles
Research Article
Subjects
Details
- ISSN :
- 17917549
- Volume :
- 34
- Issue :
- 4
- Database :
- OpenAIRE
- Journal :
- In vivo (Athens, Greece)
- Accession number :
- edsair.doi.dedup.....9db365879bd8e1227aa20d1a9a3a5f8a