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Independent effect of polymeric nanoparticle zeta potential/surface charge, on their cytotoxicity and affinity to cells.
- Source :
-
Cell proliferation [Cell Prolif] 2015 Aug; Vol. 48 (4), pp. 465-74. Date of Electronic Publication: 2015 May 27. - Publication Year :
- 2015
-
Abstract
- Objectives: Up to now, little research has been focussed on discovering how zeta potential independently affects polymeric nanoparticle (NP) cytotoxicity.<br />Methods: Polymeric nanoparticles of gradient zeta potential ranging from -30 mv to +40 mv were fabricated using the same poly-3-hydroxybutyrate-co-3-hydroxyhexanoate (PHBHHx) biopolymer. Interaction forces between nanoparticles and cells were measured by atomic force microscopy (AFM). Cytotoxicity of the nanoparticles to cells was investigated by using MTT (3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2-H-tetrazolium bromide) assay.<br />Results: Four kinds of nanoparticle with similar sizes and gradient zeta potentials, were fabricated. Those with positive surface charges were found to be more toxic than those with negative surface charges. Positively charged nanoparticles or nanoparticles with higher 'like' charges, offered higher interaction force with cells.<br />Conclusion: This work proposes a novel approach for investigating interaction between NPs and cells, and discloses the importance of controlling zeta potential in developing NPs-based formulations in the future.<br /> (© 2015 John Wiley & Sons Ltd.)
- Subjects :
- Animals
Caproates toxicity
Cell Line
Cell Survival drug effects
Drug Carriers toxicity
Hydroxybutyrates toxicity
Mice
Nanoparticles toxicity
Nanoparticles ultrastructure
Particle Size
Polyesters toxicity
Static Electricity
Caproates chemistry
Drug Carriers chemistry
Hydroxybutyrates chemistry
Nanoparticles chemistry
Polyesters chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1365-2184
- Volume :
- 48
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Cell proliferation
- Publication Type :
- Academic Journal
- Accession number :
- 26017818
- Full Text :
- https://doi.org/10.1111/cpr.12192