Towards Sustainable Diagnostics: Replacing Unstable H2O2 By Photoactive Tio2 In Testing Systems For Visible And Tangible Diagnostics For Use By Blind People

Blind and color blind people cannot use colorimetric diagnostics; the problem is especially severe in rural areas where high temperatures and the absence of electricity challenge modern diagnostics. Here we propose to replace the unstable component of a diagnostic test, H2O2, with stable TiO2. Under UV irradiation, TiO2 forms reactive oxygen species that initiate polymerization of acrylamide causing liquid-to-gel transition in an analyte-dependent manner. We demonstrate that specific DNA sequences can be detected using this approach. This development may enable the detection of biological molecules by users with limited resources, for example in developing countries or for travelers in remote areas

Photodeposition of Hydroxyapatite into a Titanium Dioxide Nanotubular Layer Using Ca(EDTA) Complex Decomposition

A new photocatalytic hydroxyapatite (HA) synthesis method has been developed. This method is based on the unique ability of the TiO2 photocatalyst to decompose the Ca(EDTA) complex under UV illumination. As a result, released Ca2+ ions react with PO43− ions forming the HA particles. The photocatalytic formation of hydroxyapatite is found to have a fractional order, which may indicate the complex reaction mechanism and the presence of several limiting stages. The TNT-HA samples were studied by XRD, FTIR, SEM, GDOES, and biocompatibility study. High biocompatibility of the surfaces is proven by pre-osteoblast cell growth

Photocatalytic Deposition of Hydroxyapatite onto a Titanium Dioxide Nanotubular Layer with Fine Tuning of Layer Nanoarchitecture

A new effective method of photocatalytic deposition of hydroxyapatite (HA) onto semiconductor substrates is proposed. A highly ordered nanotubular TiO2 (TNT) layer formed on titanium via its anodization is chosen as the photoactive substrate. The method is based on photodecomposition of the phosphate anion precursor, triethylphosphate (TEP), on the semiconductor surface with the following reaction of formed phosphate anions with calcium cations presented in the solution. HA can be deposited only on irradiated areas, providing the possibility of photoresistfree HA patterning. It is shown that HA deposition can be controlled via pH, light intensity, and duration of the process. Energy-dispersive X-ray spectroscopy profile analysis and glow discharge optical emission spectroscopy of HA-modified TNT prove that HA deposits over the entire TNT depth. High is proven by protein adsorption and pre-osteoblast cell growth

Biomimetic materials based on hydroxyapatite patterns for studying extracellular cell communication

The study of cellular ion channels forms a basic understanding of healthy organ functioning and the body as a whole; however, the native role of signal transmission through ion channels between cells remains unclear. The success of the signal transmission investigation depends on the methods and materials used. Therefore, it is necessary to develop a new approach and system for studying detecting cell–cell communication. In this work, we suggest the system of hydroxyapatite patterns demonstrating piezoresponse in conjunction with fiber-based biosensors for detection of electrical signaling in cellular communities. Our system does not disrupt the integrity of cell membrane. The cells are located on self-assembled hydroxyapatite patterns forming the tissue patterns and communicating via spatially propagating waves of calcium, sodium, and potassium ions. These waves result from positive feedback caused by the activation of Ca2+ channels. The fiber-based ion-selective microelectrodes fixed above the patterns are used to detect the sodium, potassium, calcium ion currents in the extracellular space. We use norepinephrine to activate the Ca2+ channels result in intracellular Ca2+ release between the cell communities on different patterns. This system could be perspective as an efficient platform to lab-on-a-chip study as well as fundamental understanding of cellular communication during regeneration

Humidity-driven transparent holographic free-standing polyelectrolyte films

In the present work, transparent holographic poly(diallyldimethylammonium chloride) (PDADMAC)/heparin and PDADMAC/poly(styrenesulfonate) (PSS) films were synthesized via polyelectrolyte coacervates. PDADMAC/heparin films were obtained without temperature treatment. Thin holographic free-standing films with a 1 μm grating period and uniform surface of a polyelectrolyte complex were readily and quickly made by pressing polyelectrolyte coacervate, the hydrated viscoelastic fluid-like form of polyelectrolyte complex precursor, between a flat surface and holographic mask. Heparin replaces PSS in film composition to prepare the sheer film. Thus, the PDADMAC/heparin holographic film demonstrates transparency and reversible response for humidity under diffraction detection. In addition to diffraction humidity signal measurements, the cobalt(II) chloride was impregnated in polyelectrolyte coacervate to make an additional colorimetric signal response. In this case, the free-standing film serves both as the substrate for the hygroscopic salt and as a diffraction humidity sensor. The PDADMAC/heparin/Co(II) chloride film demonstrates a linear humidity range from 50 to 90%. Additionally, due to hydrated inorganic salt ion size, cobalt chloride prevents film porosity, which initiates under film swelling. Based on the results and calculations obtained, the study proposes the mechanism of water incorporation, including the reptation model and polyelectrolyte complex behavior. Results of density functional theory calculations prove that binding of cobalt aqua complexes [Co(H2O)6]2+ with the dimeric associates heparin/PDADMAC via noncovalent interactions (hydrogen bonds) additionally is much more energetically favorable compared with the alternative association of heparin/PDADMAC with water molecules