Physicochemical and biological characterization of single-walled and double-walled carbon nanotubes in biological media

Journal of Hazardous Materials

Volumn 280, Issue , 2014, Pages 216-225

  Liu, Wen Te ^a,b   Bien, Mauo Ying ^a,c   Chuang, Kai Jen ^d,e   Chang, Ta Yuan ^f   Jones, Tim ^g   BéruBé, Kelly ^h   Lalev, Georgi ^g   Tsai, Dai Hua ⁱ   Chuang, Hsiao Chi ^a,b   Cheng, Tsun Jen ^j  

^a TAIPEI MEDICAL UNIVERSITY   (Taiwan)

^b TAIPEI MEDICAL UNIVERSITY   (Taiwan)

^c TAIPEI MEDICAL UNIVERSITY HOSPITAL   (Taiwan)

^d TAIPEI MEDICAL UNIVERSITY   (Taiwan)

^e TAIPEI MEDICAL UNIVERSITY   (Taiwan)

^f CHINA MEDICAL UNIVERSITY   (Taiwan)

^g CARDIFF UNIVERSITY   (United Kingdom)

^h CARDIFF UNIVERSITY   (United Kingdom)

ⁱ UNIVERSITY OF LAUSANNE   (Switzerland)

^j NATIONAL TAIWAN UNIVERSITY   (Taiwan)

more..

Author keywords

Carbon nanotube; Inflammation; Nanomaterials; Nanotoxicology; Proteomics

Indexed keywords

BIOCHEMISTRY; CARBON NANOTUBES; CELL DEATH; MAMMALS; NANOPARTICLES; NANOSTRUCTURED MATERIALS; NANOTUBES; PROTEINS; PROTEOMICS; SINGLE-WALLED CARBON NANOTUBES (SWCN);

BIOLOGICAL CHARACTERIZATION; BRONCHOALVEOLAR LAVAGE FLUID; DOUBLE WALLED CARBON NANOTUBES; INFLAMMATION; NANOTOXICOLOGY; PHOSPHATE-BUFFERED SALINES; SINGLE WALLED NANOTUBE (SWNTS); TUMOR NECROSIS FACTOR ALPHA; BIOLOGICAL MEDIA; DOUBLE-WALLED CARBON NANOTUBES; PROTEOMICS; SINGLE-WALLED;

MULTIWALLED CARBON NANOTUBES (MWCN); CARBON NANOTUBES;

BOVINE SERUM ALBUMIN; DOUBLE WALLED NANOTUBE; INTERLEUKIN 6; PHOSPHATE BUFFERED SALINE; SINGLE WALLED NANOTUBE; TUMOR NECROSIS FACTOR ALPHA; CARBON NANOTUBE; GAMMA INTERFERON;

BIOLOGICAL METHOD; DISPERSION; PHOSPHATE; PHYSICOCHEMICAL PROPERTY; PROTEIN; TOXICITY; AGGREGATION; COAGULATION; FULLERENE; NANOTECHNOLOGY; PROTEOMICS; RODENT;

A549 CELL LINE; AMINO ACID SEQUENCE; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BALB/C NUDE MOUSE; BIOLOGICAL ACTIVITY; BLOOD CLOTTING; CONTROLLED STUDY; FEMALE; HUMAN; HUMAN CELL; LUNG LAVAGE; MEMBRANE STABILIZATION; MOUSE; NONHUMAN; PHYSICAL CHEMISTRY; PROTEIN AGGREGATION; PROTEIN BINDING; PROTEIN MODIFICATION; SAMPLING; BAGG ALBINO MOUSE; BIOLOGICAL PHENOMENA AND FUNCTIONS CONCERNING THE ENTIRE ORGANISM; IN VITRO STUDY; IN VIVO STUDY; SUSPENSION; ANIMAL; BOVINE; CHEMISTRY; TUMOR CELL LINE;

ANIMALS; BRONCHOALVEOLAR LAVAGE FLUID; CATTLE; CELL LINE, TUMOR; FEMALE; HUMANS; INTERFERON-GAMMA; INTERLEUKIN-6; MICE; MICE, INBRED BALB C; NANOTUBES, CARBON; SERUM ALBUMIN, BOVINE; TUMOR NECROSIS FACTOR-ALPHA;

EID: 84906489893     PISSN: 03043894     EISSN: 18733336     Source Type: Journal    
DOI: 10.1016/j.jhazmat.2014.07.069     Document Type: Article

References (43)

1. Wu W., Jiang X. A practical strategy for constructing nanodrugs using carbon nanotubes as carriers. Methods Mol. Biol. 2011, 751:565-582.
2. Kam N.W., Liu Z., Dai H. Functionalization of carbon nanotubes via cleavable disulfide bonds for efficient intracellular delivery of siRNA and potent gene silencing. J. Am. Chem. Soc. 2005, 127:12492-12493.
3. Kolhe S., Parikh K. Application of nanotechnology in cancer: a review. Int. J. Bioinform. Res. Appl. 2012, 8:112-125.
4. Shvedova A.A., Pietroiusti A., Fadeel B., Kagan V.E. Mechanisms of carbon nanotube-induced toxicity: focus on oxidative stress. Toxicol. Appl. Pharmacol. 2012, 261:121-133.
5. Tian L., Lin Z.Q., Lin B.C., Liu H.L., Yan J., et al. Single wall carbon nanotube induced inflammation in cruor-fibrinolysis system. Biomed. Environ. Sci. 2013, 26:338-345.
6. Laverny G., Casset A., Purohit A., Schaeffer E., Spiegelhalter C., et al. Immunomodulatory properties of multi-walled carbon nanotubes in peripheral blood mononuclear cells from healthy subjects and allergic patients. Toxicol. Lett. 2013, 217:91-101.
7. Xu J., Futakuchi M., Shimizu H., Alexander D.B., Yanagihara K., et al. Multi-walled carbon nanotubes translocate into the pleural cavity and induce visceral mesothelial proliferation in rats. Cancer Sci. 2012, 103:2045-2050.
8. Zook J.M., Maccuspie R.I., Locascio L.E., Halter M.D., Elliott J.T. Stable nanoparticle aggregates/agglomerates of different sizes and the effect of their size on hemolytic cytotoxicity. Nanotoxicology 2011, 5:517-530.
9. Baier G., Costa C., Zeller A., Baumann D., Sayer C., et al. BSA adsorption on differently charged polystyrene nanoparticles using isothermal titration calorimetry and the influence on cellular uptake. Macromol. Biosci. 2011, 11:628-638.
10. Oberdörster G., Maynard A., Donaldson K., Castranova V., Fitzpatrick J., et al. Principles for characterizing the potential human health effects from exposure to nanomaterials: elements of a screening strategy. Part Fibre Toxicol. 2005, 2:8.
11. 2 nanoparticles dispersion for biological study. J. Nanosci. Nanotechnol. 2010, 10:5213-5219.
12. Vippola M., Falck G.C., Lindberg H.K., Suhonen S., Vanhala E., et al. Preparation of nanoparticle dispersions for in vitro toxicity testing. Hum. Exp. Toxicol. 2009, 28:377-385.
13. Bihari P., Vippola M., Schultes S., Praetner M., Khandoga A.G., et al. Optimized dispersion of nanoparticles for biological in vitro and in vivo studies. Part Fibre Toxicol. 2008, 5:14.
14. Carter D.C., Ho J.X. Structure of serum albumin. Adv. Protein Chem. 1994, 45:153-203.
15. Gasser M., Wick P., Clift M.J., Blank F., Diener L., et al. Pulmonary surfactant coating of multi-walled carbon nanotubes (MWCNTs) influences their oxidative and pro-inflammatory potential in vitro. Part Fibre Toxicol. 2012, 9:17.
16. Ehrenberg M.S., Friedman A.E., Finkelstein J.N., Oberdörster G., McGrath J.L. The influence of protein adsorption on nanoparticle association with cultured endothelial cells. Biomaterials 2009, 30:603-610.
17. Ruh H., Kuhl B., Brenner-Weiss G., Hopf C., Diabate S., et al. Identification of serum proteins bound to industrial nanomaterials. Toxicol. Lett. 2012, 208:41-50.
18. Jones T., Berube K. The bioreactivity of the sub-10 mum component of volcanic ash: Soufriere Hills volcano, Montserrat. J. Hazard. Mater. 2011, 194:128-134.
19. Moreno T., Gibbons W., Jones T., Richards R. The geology of ambient aerosols: characterising urban and rural/coastal silicate PM10-2.5 and PM2.5 using high-volume cascade collection and scanning electron microscopy. Atmos. Environ. 2003, 37:4265-4276.
20. Chiang L.L., Chen H.C., Lee C.N., Chuang K.J., Chen T.T., et al. Serum protein oxidation by diesel exhaust particles: effects on oxidative stress and inflammatory response in vitro. Chem. Biol. Interact. 2013, 206:385-393.
21. Wilson M.R., Lightbody J.H., Donaldson K., Sales J., Stone V. Interactions between ultrafine particles and transition metals in vivo and in vitro. Toxicol. Appl. Pharmacol. 2002, 184:172-179.
22. Chuang H.C., Fan C.W., Chen K.Y., Chang-Chien G.P., Chan C.C. Vasoactive alteration and inflammation induced by polycyclic aromatic hydrocarbons and trace metals of vehicle exhaust particles. Toxicol. Lett. 2012, 214:131-136.
23. Fertsch-Gapp S., Semmler-Behnke M., Wenk A., Kreyling W.G. Binding of polystyrene and carbon black nanoparticles to blood serum proteins. Inhal. Toxicol. 2011, 23:468-475.
24. Wen C.L., Chen K.Y., Chen C.T., Chuang J.G., Yang P.C., et al. Development of an AlphaLISA assay to quantify serum core-fucosylated E-cadherin as a metastatic lung adenocarcinoma biomarker. J. Proteomics 2012, 75:3963-3976.
25. Chen T.-T., Chuang K.-J., Chiang L.-L., Chen C.-C., Yeh C.-T., et al. Characterization of the interactions between protein and carbon black. J. Hazard. Mater. 2014, 264:127-135.
26. Huang D.W., Sherman B.T., Tan Q., Kir J., Liu D., et al. DAVID Bioinformatics Resources: expanded annotation database and novel algorithms to better extract biology from large gene lists. Nucleic Acids Res. 2007, 35:W169-W175.
27. Su C.L., Chen T.T., Chang C.C., Chuang K.J., Wu C.K., et al. Comparative proteomics of inhaled silver nanoparticles in healthy and allergen provoked mice. Int. J. Nanomed. 2013, 8:2783-2799.
28. Sitkauskiene B., Radinger M., Bossios A., Johansson A.K., Sakalauskas R., et al. Airway allergen exposure stimulates bone marrow eosinophilia partly via IL-9. Respir. Res. 2005, 6:33.
29. Schulze C., Schaefer U.F., Ruge C.A., Wohlleben W., Lehr C.M. Interaction of metal oxide nanoparticles with lung surfactant protein A. Eur. J. Pharm. Biopharm. 2011, 77:376-383.
30. Aggarwal P., Hall J.B., McLeland C.B., Dobrovolskaia M.A., McNeil S.E. Nanoparticle interaction with plasma proteins as it relates to particle biodistribution, biocompatibility and therapeutic efficacy. Adv Drug Deliv. Rev. 2009, 61:428-437.
31. Kocbach A., Totlandsdal A.I., Lag M., Refsnes M., Schwarze P.E. Differential binding of cytokines to environmentally relevant particles: a possible source for misinterpretation of in vitro results?. Toxicol. Lett. 2008, 176:131-137.
32. Donaldson K., Tran L., Jimenez L.A., Duffin R., Newby D.E., et al. Combustion-derived nanoparticles: a review of their toxicology following inhalation exposure. Part Fibre Toxicol. 2005, 2:10.
33. Shemetov A.A., Nabiev I., Sukhanova A. Molecular interaction of proteins and peptides with nanoparticles. ACS Nano 2012, 6:4585-4602.
34. Nithiyasri P., Balaji K., Brindha P., Parthasarathy M. Programmable self-assembly of carbon nanotubes assisted by reversible denaturation of a protein. Nanotechnology 2012, 23:465603.
35. Lin L.-Y., Liu I.J., Chuang H.-C., Lin H.-Y., Chuang K.-J. Size and composition effects of household particles on inflammation and endothelial dysfunction of human coronary artery endothelial cells. Atmos. Environ. 2013, 77:490-495.
36. Chuang H.C., Jones T., Chen T.T., Berube K. Cytotoxic effects of incense particles in relation to oxidative stress, the cell cycle and F-actin assembly. Toxicol. Lett. 2013, 220:229-237.
37. Cho W.S., Duffin R., Poland C.A., Duschl A., Oostingh G.J., et al. Differential pro-inflammatory effects of metal oxide nanoparticles and their soluble ions in vitro and in vivo; zinc and copper nanoparticles, but not their ions, recruit eosinophils to the lungs. Nanotoxicology 2012, 6:22-35.
38. Herzog E., Byrne H.J., Davoren M., Casey A., Duschl A., et al. Dispersion medium modulates oxidative stress response of human lung epithelial cells upon exposure to carbon nanomaterial samples. Toxicol. Appl. Pharmacol. 2009, 236:276-281.
39. Zhang W.J., Frei B. Albumin selectively inhibits TNF alpha-induced expression of vascular cell adhesion molecule-1 in human aortic endothelial cells. Cardiovasc. Res. 2002, 55:820-829.
40. Salvador-Morales C., Flahaut E., Sim E., Sloan J., Green M.L., et al. Complement activation and protein adsorption by carbon nanotubes. Mol. Immunol. 2006, 43:193-201.
41. Meng J., Cheng X., Liu J., Zhang W., Li X., et al. Effects of long and short carboxylated or aminated multiwalled carbon nanotubes on blood coagulation. PLoS ONE 2012, 7:e38995.
42. Inoue K., Takano H., Koike E., Yanagisawa R., Sakurai M., et al. Effects of pulmonary exposure to carbon nanotubes on lung and systemic inflammation with coagulatory disturbance induced by lipopolysaccharide in mice. Exp. Biol. Med. (Maywood) 2008, 233:1583-1590.
43. Mandal S., Hossain M., Devi P.S., Kumar G.S., Chaudhuri K. Interaction of carbon nanoparticles to serum albumin: elucidation of the extent of perturbation of serum albumin conformations and thermodynamical parameters. J. Hazard. Mater. 2013, 248/249:238-245.