2005
DOI: 10.1016/j.bios.2004.09.001
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Culture of neural cells on polymers coated surfaces for biosensor applications

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Cited by 51 publications
(21 citation statements)
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“…They assigned this limited cell growth to surface tension and irregular roughness in the oxidized films, with the possibility that tosylate diffusion into the culture media worsened the outcome on overoxidized films. Poor proliferation was also reported by Lakard et al (2004Lakard et al ( , 2005 for a rat neuronal cell line on PPy when compared to other substrates including those that were electrodeposited (figure 6). Furthermore, Castano et al (2004) showed a dependence on film thickness as controlled by monomer concentration during admicellar polymerization, where a surfactant, monomer and initiator are used to form the polymer, for the viability and differentiation of mesenchymal stem cells towards the osteoblastic phenotype.…”
Section: Mattioli-belmonte Et Al (2003) Studied the Tissuementioning
confidence: 94%
“…They assigned this limited cell growth to surface tension and irregular roughness in the oxidized films, with the possibility that tosylate diffusion into the culture media worsened the outcome on overoxidized films. Poor proliferation was also reported by Lakard et al (2004Lakard et al ( , 2005 for a rat neuronal cell line on PPy when compared to other substrates including those that were electrodeposited (figure 6). Furthermore, Castano et al (2004) showed a dependence on film thickness as controlled by monomer concentration during admicellar polymerization, where a surfactant, monomer and initiator are used to form the polymer, for the viability and differentiation of mesenchymal stem cells towards the osteoblastic phenotype.…”
Section: Mattioli-belmonte Et Al (2003) Studied the Tissuementioning
confidence: 94%
“…66 In addition, electrodeposited PEI films were superior in the growth of olfactory cells, as compared with other positively charged biopolymers. 60 As shown in Figures 5-7, an increase in the concentration of PEI from 210 to 300 lg/mL in the surface-modified scaffolds exhibited few improvements in the culture of BKCs. This indicated that the optimal upper limit of the concentration of PEI could be about 210 lg/mL in the case of surface modification.…”
Section: Culture Of Constructsmentioning
confidence: 95%
“…Briefly, one construct was digested by 95.24 lg of papain in 2 mL of Tris buffer, containing 55 mM trisodium citrate, 150 mM NaCl, 5 mM cysteine, and 5 mM EDTA at 60 C over 24 h. The amount of BKCs was determined by Hoechst No. 33258 with a fluorescence spectrophotometer (F-4500, Hitachi, Tokyo, Japan) at 365 nm excitation wavelength and 458 nm emission wavelength.…”
Section: Cultivation Of Constructs and Biochemical Analysismentioning
confidence: 99%
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“…4 Factors, such as the composition, hydrophobicity, and topography of the surface, electrical charges, materials viscosity, and protein interactions play an important role in the cell proliferation on alloplastic materials. [5][6][7] Ideally, directly influencing the biocompatibility via fabrication of an appropriate "design" of the surface should be possible. This might also have a beneficial effect on negative long-term side effects which may to a certain extent result from the mesh, such as pain syndromes.…”
Section: Introductionmentioning
confidence: 99%