Aggregation behavior of fullerenes in aqueous solutions: a capillary electrophoresis and asymmetric flow field-flow fractionation study
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  • 作者:Alina Astefanei ; Oscar Nú?ez…
  • 关键词:Capillary zone electrophoresis ; Cosmetic products ; Micellar electrokinetic capillary chromatography ; Asymmetric flow field ; flow fractionation ; Fullerene aggregates
  • 刊名:Analytical and Bioanalytical Chemistry
  • 出版年:2015
  • 出版时间:October 2015
  • 年:2015
  • 卷:407
  • 期:26
  • 页码:8035-8045
  • 全文大小:1,796 KB
  • 参考文献:1.Kroto HW, Heath JR, O’Brien SC, Curl RF, Smalley RE (1985) C60: buckminsterfullerene. Nature 318:162-63CrossRef
    2.Tagmatarchis N, Shinohara H (2001) Fullerenes in medicinal chemistry and their biological applications. Mini-Rev Med Chem 1:339-48
    3.Xiao L, Takada H, Gana X, Miwa N (2006) The water-soluble fullerene derivative ‘radical sponge-exerts cytoprotective action against UVA irradiation but not visible-light-catalyzed cytotoxicity in human skin keratinocytes. Bioorg Med Chem Lett 16:1590-595CrossRef
    4.Kronholm D, Hummelen JC (2007) Fullerene-based n-type semiconductors in organic electronics. Mater Matters 2:16-9
    5.Meng H, Xing G, Sun B, Zhao F, Lei H, Li W, Song Y, Chen Z, Yuan H, Wang X, Long J, Chen C, Liang X, Zhang N, Chai Z, Zhao Y (2010) Potent angiogenesis inhibition by the particulate form of fullerene derivatives. ACS Nano 4:2773-783CrossRef
    6.Dugan LL, Lovett EG, Quick KL, Lotharious J, Lin TT, O’Malley KL (2001) Fullerene-based antioxidants and neurodegenerative disorders. Parkinson Relat Disord 7:243-46CrossRef
    7.Bosi S, Da Ros T, Spalluto G, Prato M (2003) Fullerene derivatives: an attractive tool for biological applications. Eur J Med Chem 38:913-23CrossRef
    8.Sitharaman B, Asokan S, Rusakova I, Wong MS, Wilson LJ (2004) Nanoscale aggregation properties of neuroprotective carboxyfullerene (C3) in aqueous solution. Nano Lett 4:1759-762CrossRef
    9.Friedman SH, DeCamp DL, Sijbesma RP, Srdanov G, Wudl F, Kenyon GL (1993) Inhibition of the HIV-1 protease by fullerene derivatives: model building studies and experimental verification. J Am Chem Soc 115:6506-509CrossRef
    10.Yamago S, Tokuyama H, Nakamura E, Kituchi K, Kananishi S, Sueki K, Nakahara H, Enmoto S, Ambe F (1995) In vivo biological behavior of a water-miscible fullerene: 14C labeling, absorption, distribution, excretion and acute toxicity. Chem Biol 2:385-89CrossRef
    11.Nel AE, Madler L, Velegol D, Xia T, Hoek EMV, Somasundaran P (2009) Understanding biophysicochemical interactions at the nano-bio interface. Nano Mater 8:543-47
    12.Vileno B, Marcoux PR, Lekka M, Sienkiewicz A, Feher T, Forro L (2006) Spectroscopic and photophysical properties of a highly derivatized C60 fullerol. Adv Funct Mater 16:120-28CrossRef
    13.Pickering KD, Wiesner MR (2005) Fullerol-sensitized production of reactive oxygen species in aqueous solution. Environ Sci Technol 39:1359-365CrossRef
    14.Sayes CM, Fortner JD, Guo W, Lyon D, Boyd AM, Ausman KD, Tao YJ, Sitharaman B, Wilson LJ, Hughes JB, West JL, Colvin VL (2004) The differential cytotoxicity of water-soluble fullerenes. Nano Lett 4:1881-887CrossRef
    15.Astefanei A, Nú?ez O, Galceran MT (2015) Characterisation and analysis of fullerenes: a critical review. Anal Chim Acta 882:1-1CrossRef
    16.Handy RD, Owen R, Valsami-Jones E (2008) The ecotoxicology of nanoparticles and nanomaterials: current status, knowledge gaps, challenges, and future needs. Ecotoxicology 17:315-25CrossRef
    17.Klaine SJ, Alvarez PJJ, Batley GE, Fernandes TF, Handy RD, Lyon DY, Mahendra S, McLaughlin MJ, Lead JR (2008) Nanomaterials in the environment: behavior, fate, bioavailability, and effects. Environ Toxicol Chem 27:1825-851CrossRef
    18.Astefanei A, Nú?ez O, Galceran MT (2014) Liquid chromatography in the analysis of fullerenes. In: Ellis SB (ed) Fullerenes, chemistry, natural sources and technological applications. Nova, New York, pp 35-3
    19.Chao TC, Song G, Hansmeier N, Westerhoff P, Herckes P, Halden RU (2011) Characterization and liquid chromatography-MS/MS based quantification of hydroxylated fullerenes. Anal Chem 83:1777-783CrossRef
    20.Silion M, Dascalu A, Pinteala M, Simionescu BC, Ungurenasu C (2013) A study on electrospray mass spectrometry of fullerenol C60(OH)24. Beilstein J Org Chem 9:1285-295CrossRef
    21.Astefanei A, Nú?ez O, Galceran MT (2012) Non-aqueous capillary electrophoresis separation of fullerenes and C60 fullerene derivatives. Anal Bioanal Chem 404:307-13CrossRef
    22.Wan TSM, Leung GNW, Tso TSC, Komatsu K, Murata Y (1995) Non-aqueous capillary electrophoresis as a new method for the separation of fullerenes. Proc - Electrochem Soc 95:1474-487
    23.Su HL, Kao WC, Lee C, Chuang SC, Hsieh YZ (2010) Separation of open-cage fullerenes using nonaqueous capillary electrophoresis. J Chromatogr A 1217:4471-475CrossRef
    24.Treubig JM, Brown PR (2000) Novel approach to the analysis and use of fullerenes in capillary electrophoresis. J Chromatogr A 873:257-67CrossRef
    25.Cerar J, Pompe M, Gucek M, Cerkovnik J, Skerjanc J (2007) Analysis of sample of highly water-soluble Th-symmetric fullerenehexamalonic acid C66(COOH)12 by ion-chromatography and capillary electrophoresis. J Chromatogr A 1169:86-4CrossRef
    26.Tamisier-Karolak SL, Pagliarusco S, Herrenknecht C, Brettreich M, Hirsch A, Ceolin R, Bensasson RV, Szwarc H, Moussa F (2001) Electrophoretic behavior of a highly water-soluble dendro[60]fullerene. Electropho
  • 作者单位:Alina Astefanei (1)
    Oscar Nú?ez (1) (2)
    Maria Teresa Galceran (1)
    Wim Th. Kok (3)
    Peter J. Schoenmakers (3)

    1. Department of Analytical Chemistry, University of Barcelona, Martí i Franquès 1-11, 08028, Barcelona, Spain
    2. Serra Húnter Fellow, Generalitat de Catalunya, Barcelona, Spain
    3. Analytical Chemistry Group, HIMS, University of Amsterdam, PO Box 94157, 1090 GD, Amsterdam, The Netherlands
  • 刊物类别:Chemistry and Materials Science
  • 刊物主题:Chemistry
    Analytical Chemistry
    Food Science
    Inorganic Chemistry
    Physical Chemistry
    Monitoring, Environmental Analysis and Environmental Ecotoxicology
  • 出版者:Springer Berlin / Heidelberg
  • ISSN:1618-2650
文摘
In this work, the electrophoretic behavior of hydrophobic fullerenes [buckminsterfullerene (C60), C70, and N-methyl-fulleropyrrolidine (C60-pyrr)] and water-soluble fullerenes [fullerol (C60(OH)24); polyhydroxy small gap fullerene, hydrated (C120(OH)30); C60 pyrrolidine tris acid (C60-pyrr tris acid); and (1,2-methanofullerene C60)-61-carboxylic acid (C60CHCOOH)] in micellar electrokinetic capillary chromatography (MECC) was evaluated. The aggregation behavior of the water-soluble compounds in MECC at different buffer and sodium dodecyl sulfate (SDS) concentrations and pH values of the background electrolyte (BGE) was studied by monitoring the changes observed in the electrophoretic pattern of the peaks. Broad and distorted peaks that can be attributed to fullerene aggregation were obtained in MECC which became narrower and more symmetric by working at low buffer and SDS concentrations (below the critical micelle concentration, capillary zone electrophoresis (CZE) conditions). For the characterization of the suspected aggregates formed (size and shape), asymmetrical flow field-flow fractionation (AF4) and transmission electron microscopy (TEM) were used. The results showed that the increase in the buffer concentration promoted the aggregation of the particles, while the presence of SDS micelles revealed multiple peaks corresponding to particles of different aggregation degrees. Furthermore, MECC has been applied for the first time for the analysis of C60 in two different cosmetic products (i.e., anti-aging serum and facial mask). Keywords Capillary zone electrophoresis Cosmetic products Micellar electrokinetic capillary chromatography Asymmetric flow field-flow fractionation Fullerene aggregates

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