Electromagnetic radiation approximately equal to band-gap energy has been established as responsible for the dissociation of amorphous As2Se3 and As2S3. The dissociation is accompanied by an optical densification observable as a ``photographic'' effect in thin films of these materials. The dissociation can be expressed by the following equations: As2Se3→ lim hvxAs+As2−xSe3, 0<x<2 As2S3→ lim hv2As+3S.The densification is reversible by thermal cycling to higher temperatures. A detailed analysis of the experimental results is given and a mechanism is proposed which explains the photodecomposition reactions and the thermally induced reversibility in As2Se3. The photographic cycling characteristics of As2Se3 are discussed in the light of its potential device application.
Polystyrene culture dishes and polystyrene microcarriers were coated with Pronectin-F and poly-L-lysine (polylysine), either alone or in combination. Pronectin-F is a recombinant peptide containing repeats of the RGD cell-attachment sequence from fibronectin. Polylysine is a polymer of L-lysine. Pronectin-F supported attachment of Madin-Darby Canine Kidney (MDCK) cells at concentrations as low as 0.025 micrograms/cm2 of surface area. The cells rapidly spread after attachment. Polylysine at concentrations of 0.05-0.5 micrograms/cm2 also supported cell attachment but cells did not rapidly spread after attachment to this substrate. Higher concentrations of polylysine could not be used because of toxicity. When the two peptides were used in conjunction, MDCK cells attached and spread at lower peptide concentrations than they did when either substrate was used alone. These findings suggest that recombinant Pronectin-F alone or in conjunction with a cationic polymer could be a useful replacement for materials such as gelatin or collagen which are currently used as microcarrier surfaces.
The transport properties of vacuum evaporated films of “pure” selenium and selenium doped with small quantities of Cl (0–40 ppm) and As (∼12at.%) have been examined using a time-resolved drift technique. Addition of Cl alone acts as an electron trap, and addition of As alone acts as a hole trap while greatly increasing the electron free-carrier lifetime. When used in combination, controlled addition of these two impurities can be used to produce hole ranges greater than 7.5×10−6 cm2/V and electron ranges greater than 1.2×10−6 cm2/V in the same film. This hole range is approximately a factor of 3 greater and the electron range a factor of 5 greater than that observed in the best pure Se films.
Human squamous epithelial cells produce lower amounts of laminin and fibronectin when cultured on DEAE-dextran than when cultured on gelatin-coated polystyrene (Biotechnol. Bioeng., 33:1235). The epithelial cells also spread much more slowly on DEAE-dextran than they do on gelatin-coated polystyrene. To determine if the low level of matrix production by cells grown on DEAE-dextran contributed to the slowness of cell spreading on this substrate, microcarriers made from DEAE-dextran were treated with exogenous laminin (10 micrograms/cm2 of surface area) and then examined for ability to support cell adhesion. Squamous epithelial cells spread as rapidly on the laminin-treated DEAE-dextran as they did on gelatin-coated polystyrene (much more rapidly than on untreated DEAE-dextran). This indicates 1) that laminin can bind to DEAE-dextran in a fashion that is biologically usable by anchorage-dependent cells, and 2) that when laminin is bound to DEAE-dextran, the failure of squamous epithelial cells to rapidly spread is overcome. These data support the hypothesis that failure of the cells to synthesize an intact extracellular matrix on DEAE-dextran is responsible, at least in part, for the slowness with which cells spread on this substrate.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.