journal article·2015-01

Short-term effects of ultrahigh concentration cationic silica nanoparticles on cell internalization, cytotoxicity, and cell integrity with human breast cancer cell line (MCF-7)

Ji Hyun Seog, Bokyung Kong, Dongheun Kim, Lauren M. Graham, Joon Sig Choi, Sang Bok Lee

Journal of Nanoparticle Research· Volume 17· Issue 1
Publisher page

Abstract

High concentrations of cationic colloidal silica nanoparticles (CCS-NPs) have been widely used for the enrichment of plasma membrane proteins. However, the interaction between the CCS-NPs and cells under the required concentration for the isolation of plasma membrane are rarely investigated. We evaluated the internalization and toxicity of the 15 nm CCS-NPs which were exposed at high concentrations with short time in human breast cancer cells (MCF-7) with transmission electron microscopy, energy dispersive X-ray spectroscopy, inductively coupled plasma atomic emission spectroscopy, and colorimetric assays. The NPs were observed throughout the cells, particularly in the cytoplasm and the nucleus, after short incubation periods. Additionally, the NPs significantly influenced the membrane integrity of the MCF-7 cells.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Advanced biosensing and bioanalysis techniques · Nanoparticle-Based Drug Delivery · Nanoparticles: synthesis and applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (31)

Show source-provided references
1. Aillon KL, Xie Y, El-Gendy N, Berkland CJ, Forrest ML (2009) Effects of nanomaterial physicochemical properties on in vivo toxicity. Adv Drug Deliv Rev 61:457–46610.1016/j.addr.2009.03.010 ↗
2. Alkilany AM, Murphy CJ (2010) Toxicity and cellular uptake of gold nanoparticles: what we have learned so far? J Nanopart Res 12:2313–233310.1007/s11051-010-9911-8 ↗
3. Arvizo RR, Miranad OR, Thompson MA, Pabelick CM, Bhattacharya R, Robertson JD, Rotello VM, Prakash YS, Mukherjee P (2010) Effect of nanoparticle surface charge at the plasma membrane and beyond. Nano Lett 10:2543–254810.1021/nl101140t ↗
4. Bouwmeester H, Dekkers S, Noordam MY, Hagens WI, Bulder AS, de Heer C, ten Voorde SE, Wijnhoven SW, Marvin HJ, Sips AJ (2009) Review of health safety aspects of nanotechnologies in food production. Regul Toxicol Pharmacol 53:52–5610.1016/j.yrtph.2008.10.008 ↗
5. Chaney LK, Jacobson BS (1983) Coating cells with colloidal silica for high yield isolation of plasma membrane sheets and identification of transmembrane proteins. J Biol Chem 258:10062–1007210.1016/S0021-9258(17)44606-0 ↗
6. Chang JS, Chang KL, Hwang DF, Kong ZL (2007) In vitro cytotoxicitiy of silica nanoparticles at high concentrations strongly depends on the metabolic activity type of the cell line. Environ Sci Technol 41:2064–206810.1021/es062347t ↗
7. Durr E, Yu J, Krasinska KM, Carver LA, Yates JR, Testa JE, Oh P, Schnitzer JE (2004) Direct proteomic mapping of the lung microvascular endothelial cell surface in vivo and in cell culture. Nat Biotechnol 22:985–99210.1038/nbt993 ↗
8. Halas NJ (2008) Nanoscience under glass: the versatile chemistry of silica nanostructures. ACS Nano 2:179–18310.1021/nn800052e ↗
9. Kim YJ, Yu MR, Park HO, Yang SI (2010) Comparative study of cytotoxicity, oxidative stress and genotoxicity induced by silica nanomaterials in human neuronal cell line. Mol Cell Toxicol 6:337–344
10. Kong B, Seog JH, Graham LM, Lee SB (2011) Experimental considerations on the cytotoxicity of nanoparticles. Nanomedicine 6:929–94110.2217/nnm.11.77 ↗
11. Kovalenko GA, Shitova NB, Sokolovskii VD (1981) Immobilization of oxyreductases on inorganic supports based on alumina. Immobilization of lactate dehydrogenase on alumina by adsorption. Biotechnol Bioeng 23:1721–173410.1002/bit.260230805 ↗
12. Kuhlbusch TAJ, Asbach C, Fissan H, Goehler D, Stintz M (2011) Nanoparticle exposure at nanotechnology workplaces: a review. Part Fibre Toxicol 8:2210.1186/1743-8977-8-22 ↗
13. Kumar P, Pirjola L, Ketzel M, Harrison RM (2013) Nanoparticle emissions from 11 non-vehicle exhaust sources—a review. Atmos Environ 67:252–27710.1016/j.atmosenv.2012.11.011 ↗
14. Lee H, Larson RG (2009) Multiscale modeling of dendrimers and their interactions with bilayers and polyelectrolytes. Molecules 14:423–43810.3390/molecules14010423 ↗
15. Leroueil PR, Berry SA, Duthie K, Han G, Rotello VM, McNerny DQ, Baker JR, Orr BG, Holl MM (2008) Wide varieties of cationic nanoparticles induce defects in supported lipid bilayers. Nano Lett 8:420–42410.1021/nl0722929 ↗
16. Lin J, Alexander-Katz A (2013) Cell membranes open “doors” for cationic nanoparticles/biomolecules: insights into uptake kinetics. ACS Nano 7:10799–1080810.1021/nn4040553 ↗
17. Lu J, Liong M, Li Z, Zink JI, Tamanoi F (2010) Biocompatibility, biodistribution, and drug-delivery efficiency of mesoporous silica nanoparticles for cancer therapy in animals. Small 6:1794–180510.1002/smll.201000538 ↗
18. Madani F, Lindberg S, Langel U, Futaki S, Gräslund A (2011) Mechanisms of cellular uptake of cell-penetrating peptides. J Biophys 2011:41472910.1155/2011/414729 ↗
19. Mathias RA, Chen YS, Goode RJ, Kapp EA, Mathivanan S, Moritz RL, Zhu HJ, Simpson RJ (2011) Tandem application of cationic colloidal silica and Triton X-114 for plasma membrane protein isolation and purification: towards developing an MDCK protein database. Proteomics 11:1238–125310.1002/pmic.201000591 ↗
20. Nel A, Xia T, Madler L, Li N (2006) Toxic potential of materials at the nanolevel. Science 311:622–62710.1126/science.1114397 ↗
21. Niemeyer CM (2001) Nanoparticles, proteins, and nucleic acids: biotechnology meets materials science. Angew Chem Int Ed 40:4128–415810.1002/1521-3773(20011119)40:22<4128::AID-ANIE4128>3.0.CO;2-S ↗
22. Qhobosheane M, Santra S, Zhang P, Tan W (2001) Biochemically functionalized silica nanoparticles. Analyst 126:1274–127810.1039/b101489g ↗
23. Rahbar AM, Fenselau C (2004) Integration of Jacobson’s Pellicle Method into proteomic strategies for plasma membrane proteins. J Proteome Res 3:1267–127710.1021/pr040004t ↗
24. Ranjan S, Dasgupta N, Chakraborty AR, Samuel SM, Ramalingam C, Shanker R, Kumar A (2014) Nanoscience and nanotechnologies in food industries: opportunities and research trends. J Nanopart Res 16:246410.1007/s11051-014-2464-5 ↗
25. Robinson JM, Ackerman WET, Tewari AK, Kniss DA, Vandre DD (2009) Isolation of highly enriched apical plasma membranes of the placental syncytiotrophoblast. Anal Biochem 387:87–9410.1016/j.ab.2009.01.012 ↗
26. Shinkai M (2002) Functional magnetic particles for medical application. J Biosci Bioeng 94:606–61310.1016/S1389-1723(02)80202-X ↗
27. Sozer N, Kokini JL (2009) Nanotechnology and its applications in the food sector. Trends Biotechnol 27:82–8910.1016/j.tibtech.2008.10.010 ↗
28. Stepnik M, Arkusz J, Smok-Pieniążek A, Bratek-Skicki A, Salvati A, Lynch I, Dawso KA, Gromadzińska J, De Jong WH, Rydzynski K (2012) Cytotoxic effects in 3T3-L1 mouse and WI-38 human fibroblasts following 72 hour and 7 day exposures to commercial silica nanoparticles. Toxicol Appl Pharmacol 263:89–10110.1016/j.taap.2012.06.002 ↗
29. Wang L, Zhao W, Tan W (2008) Bioconjugated silica nano particles: development and applications. Nano Res 1:99–11510.1007/s12274-008-8018-3 ↗
30. Wang J, Asbach C, Fissan H, Hulser T, Kaminski H, Kuhlbusch TAJ, Pui DYH (2012) Emission measurement and safety assessment for the production process of silicon nanoparticles in a pilotscale facility. J Nanopart Res 14:759–76710.1007/s11051-012-0759-y ↗
31. Yoon D, Woo D, Kim JH, Kim MK, Kim T, Hwang ES, Baik S (2011) Agglomeration, sedimentation, and cellular toxicity of alumina nanoparticles in cell culture medium. J Nanopart Res 13:2543–255110.1007/s11051-010-0147-4 ↗