Topics (20) View all

Skills (14)

Research experience

  • Jan 2010
    Research: Universidad de Zaragoza
    Universidad de Zaragoza
    Spain · Zaragoza
  • Jan 2009–
    Dec 2011
    Research: NanoTrap (MAT2008-01319/NAN)
    Centros de Investigacion Biomédica en Red de Bioingeniería, Biomateriales y Nanomedicina (CIBER-BBN) · Centros de Investigacion Biomédica en Red de Bioingeniería, Biomateriales y Nanomedicina (CIBER-BBN)
    Zaragoza
    Nanotechnology; Risk Analsys
  • Jun 2008–
    May 2010
    Research: NanoSost
    Universidad de Zaragoza · IUI en Nanociencia de Aragón - INA · Universidad de Zaragoza
    Nanostructured Films and Particles · Zaragoza
    Nanotechnology; Risk Analysis; Nanoparticle Aerosol
  • Jan 2006–
    Dec 2007
    Research: Chubu University
    Chubu University
    Japan · Kasugai
  • Dec 2003–
    Mar 2005
    Research: Development of Bone-Bonding Materials
    Japan Science and Technology Agency
    Biomaterials
  • Jan 1999–
    Dec 2010
    Research: Universidad Complutense de Madrid
    Universidad Complutense de Madrid · Facultad de Farmacia
    Spain · Madrid

Education

  • May 2003–
    Dec 2003
    Nara Institute of Science and Technology
    Graduate School of Materials Science · Post-Doctoral
    Japan · Nara
  • Oct 2001–
    Mar 2003
    Kyoto University
    Graduate School of Engineering · Post-Doctoral
    Japan · Kyoto
  • Dec 1996–
    Oct 2001
    Universidad Complutense de Madrid
    Faculty of Pharmacy · PhD
    Spain · Madrid
  • Sep 1991–
    Jun 1996
    Universidad Complutense de Madrid
    BSc (Chemistry)
    Spain · Madrid

Awards & achievements

  • Oct 2001
    Scholarship: Scholarship of the Japanese Ministry of Education (Monbukagaku-sho)
  • Jan 1997
    Scholarship: FPI Scholarship

Other

  • Languages
    Spanish; English; Japanese
  • Other Interests
    Reading, running and enjoying time together with my wife and daughter, Nat. Nanotech.; Nano Lett.; J. Am. Chem. Soc.; Angew. Chem.; Chem. Commun.

Questions and Answers (8) View all

  • Answer added in Nanotechnology
    177 Does anyone know of a physical method to obtain nanoparticles?
    By V. M. Lenart · State University of Ponta Grossa
    Francisco Balas · University of Zaragoza
    Any aerosol pyrolysis procedure allows the synthesis of nanoparticles. Of course, you will need to prepare an aerosol of small drops of a precursor in... [more]
  • Answer added in Controlled Drug Delivery
    26 In case of drug delivery study using porous material, how to differentiate the drug delivery is from the surface or from the pores?
    By Sanjay Thorat · Italian Institute of Technology (IIT)
    Francisco Balas · University of Zaragoza
    It will depend on the pore size and pore volume of the material. If drug molecules are small enough to be retained in the pores and these pores accoun... [more]
  • Answer added in Nanotechnology
    10 Is there any procedure for functionalizing SiO2 nanoparticles with rhodamine isothiocyanate with sizes under 100 nm?
    By Francisco Balas · University of Zaragoza
    Francisco Balas · University of Zaragoza
    Thank you al for your answers. We did try using PEG as coating to prevent agglomeration during the synthesis but it seems that rhodamine might react w... [more]
  • Question asked in Nanotechnology
    10 Is there any procedure for functionalizing SiO2 nanoparticles with rhodamine isothiocyanate with sizes under 100 nm?
    We have had good results with FITC-functionalized SiO2 NPs using micro-emulsions, but rhodamine derivatives give large sizes (about 200 nm) and usuall... [more]
    By Francisco Balas · University of Zaragoza
  • 7 Why does Krypton work better than N2 or Ar for BET surface area measurement of porous thin films?
    By Michael Riley · Rensselaer Polytechnic Institute
    Francisco Balas · University of Zaragoza
    In fact the low sublimation level of Kr at 77K is the reason why it is mainly used for low-k materials and thin films. Gas adsorption is based in the ... [more]

Publications (44) View all

  • Source
    Article: Surface functionalization for tailoring the aggregation and magnetic behaviour of silica-coated iron oxide nanostructures.
    [show abstract] [hide abstract]
    ABSTRACT: We report here a detailed structural and magnetic study of different silica nanocapsules containing uniform and highly crystalline maghemite nanoparticles. The magnetic phase consists of 5 nm triethylene glycol (TREG)- or dimercaptosuccinic acid (DMSA)-coated maghemite particles. TREG-coated nanoparticles were synthesized by thermal decomposition. In a second step, TREG ligands were exchanged by DMSA. After the ligand exchange, the ζ potential of the particles changed from -10 to -40 mV, whereas the hydrodynamic size remained constant at around 15 nm. Particles coated by TREG and DMSA were encapsulated in silica following a sol-gel procedure. The encapsulation of TREG-coated nanoparticles led to large magnetic aggregates, which were embedded in coalesced silica structures. However, DMSA-coated nanoparticles led to small magnetic clusters inserted in silica spheres of around 100 nm. The final nanostructures can be described as the result of several competing factors at play. Magnetic measurements indicate that in the TREG-coated nanoparticles the interparticle magnetic interaction scenario has not dramatically changed after the silica encapsulation, whereas in the DMSA-coated nanoparticles, the magnetic interactions were screened due to the function of the silica template. Moreover, the analysis of the AC susceptibility suggests that our systems essentially behave as cluster spin glass systems.
    Nanotechnology 03/2012; 23(15):155603. · 3.98 Impact Factor
  • Article: In vitro structural changes in porous HA/beta-TCP scaffolds in simulated body fluid.
    [show abstract] [hide abstract]
    ABSTRACT: Porous scaffolds of biphasic calcium phosphate (hydroxyapatite/beta-tricalcium phosphate (beta-TCP)) have been fabricated and changes induced both in phase composition and porous architecture by immersion in simulated body fluid (SBF) under static and orbital stirring conditions have been studied. The starting porous scaffolds exhibit a low and randomized micro- and mesoporosity, an interconnected macroporosity centered at 100 and 0.6microm, a fractal connectivity of D=2.981 and total percent porosity of ca. 80%. After immersion for up to 60days the micro- and mesoporosity increase slightly, which could be attributed to dissolution of the beta-TCP phase confirmed by transmission electron microscopy. The effects of the change in the porous framework with SBF immersion time favor the bioactive behavior of the tested materials, inducing a nucleation and growth of a nanocrystalline apatite phase as the interconnected macroporosity centered at 0.6microm is reduced. The macroporosity centered at 100microm is still stable after 60days in SBF. Therefore, these biphasic calcium phosphate porous scaffolds combine bioactive behavior with the stability of interconnected macroporosity over large periods of soaking time in SBF under static and orbital stirring conditions.
    Acta biomaterialia 04/2009; 5(7):2738-51. · 3.98 Impact Factor
  • Article: Functionalization of different polymers with sulfonic groups as a way to coat them with a biomimetic apatite layer.
    [show abstract] [hide abstract]
    ABSTRACT: Covalent coupling of sulfonic group (-SO 3H) was attempted on different polymers to evaluate efficacy of this functional group in inducing nucleation of apatite in body environment, and thereupon to design a simple biomimetic process for preparing bonelike apatite-polymer composites. Substrates of polyethylene terephthalate (PET), polycaprolactam (Nylon 6), high molecular weight polyethylene (HMWPE) and ethylene-vinyl alcohol co-polymer (EVOH) were subjected to sulfonation by being soaked in sulfuric acid (H2SO4) or chlorosulfonic acid (ClSO 3H) with different concentrations. In order to incorporate calcium ions, the sulfonated substrates were soaked in saturated solution of calcium hydroxide (Ca(OH)2). The treated substrates were soaked in a simulated body fluid (SBF). Fourier transformed infrared spectroscopy, thin-film X-ray diffraction, and scanning electron microscopy showed that the sulfonation and subsequent Ca(OH)2 treatments allowed formation of -SO3H groups binding Ca2+ ions on the surface of HMWPE and EVOH, but not on PET and Nylon 6. The HMWPE and EVOH could thus form bonelike apatite layer on their surfaces in SBF within 7 d. These results indicate that the -SO3H groups are effective for inducing apatite nucleation, and thereby that surface sulfonation of polymers are effective pre-treatment method for preparing biomimetic apatite on their surfaces.
    Journal of Materials Science Materials in Medicine 11/2007; 18(10):1923-30. · 2.32 Impact Factor
  • Article: Surface modification of organic polymers with bioactive titanium oxide without the aid of a silane-coupling agent.
    [show abstract] [hide abstract]
    ABSTRACT: Polyethylene (PE), polyethylene terephthalate (PET), ethylene-vinyl alcohol copolymer (EVOH), and poly(epsilon-caprolactam) (Nylon 6) were successfully modified with a thin crystalline titanium oxide layer on their surfaces by a simple dipping into a titanium alkoxide solution and a subsequent soak in hot HCl solution, without the aid of a silane-coupling agent. The surface modified polymers formed a bone-like apatite layer in a simulated body fluid (SBF) within a period of 2 days. PE, PET, and Nylon 6 formed an apatite layer faster and had a higher adhesive strength to the apatite. Three-dimensional fabrics with open spaces in various sizes containing such surface modified polymer fibers are expected to be useful as bone substitutes, since they may be able to form apatite on their constituent fibers in the living body, and thus, integrate with living bone.
    Journal of Materials Science Materials in Medicine 07/2007; 18(6):1167-74. · 2.32 Impact Factor
  • Source
    Article: Structural characterization of nanosized silica spheres
    Solid State Sciences. 01/2007; 9(5):351-356.

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