Bioconjugate Chemistry · 2004 · 1.6K citations · 25 references
PharmacyChemistryToxicologyMechanisms Of ToxicityNanobiotechnologyNanomaterialsCell-nanoparticle InteractionsInorganic NanoparticlesNanomedicineNanoparticle CharacterizationNanoparticle DesignNanotoxicologyCell Viability AssaysLipid VesiclesNanomaterial ToxicityNanoparticle CytotoxicityNanoparticle ToxicityNanoparticlesSurface-functionalized NanoparticlesViability Assays
Gold nanoparticles are valuable for diverse biological applications, but high concentrations can cause toxicity. The authors employed MTT, hemolysis, and bacterial viability assays on 2‑nm gold nanoparticles, and dye‑release studies with lipid vesicles revealed concentration‑dependent lysis driven by electrostatic binding as the likely mechanism of cationic particle toxicity. Cationic gold nanoparticles exhibit moderate toxicity while anionic ones are largely nontoxic, with concentration‑dependent lysis via electrostatic binding explaining the observed toxicity.
The structure and properties of gold nanoparticles make them useful for a wide array of biological application. Toxicity, however, has been observed at high concentrations using these systems. MTT, hemolysis, and bacterial viability assays were used to explore differential toxicity among the cell types used, using 2 nm core particles. These studies show that cationic particles are moderately toxic, whereas anionic particles are quite nontoxic. Concentration-dependent lysis mediated by initial electrostatic binding was observed in dye release studies using lipid vesicles, providing the probable mechanism for observed toxicity with the cationic MMPCs.
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