An Efficient Thermal Elimination Pathway toward Phosphodiester Hydrogels via a Precursor Approach

Phosphodiester hydrogels offer a wide range of fascinating properties. Not only do they exhibit excellent hemocompatibility and cellular compatibility, they also show a remarkable resistance to protein adsorption, thereby limiting the foreign body response. In this work, phosphodiester-crosslinked hydrogels are produced by a simple free-radical polymerization of a phosphotriester crosslinker. In a second step, this material is transformed to the phosphodiester, by heating it up to 60 degrees C in phosphate-buffered saline. Compared to earlier methods, there is no need for acids, bases, or oxidizing agents to achieve this final conversion to the phosphodiester. This method thus reduces the risk to damage or degrade any sensitive biomolecules that might be of interest to tissue engineers, such as various growth factors or other proteins. The phosphotriester crosslinker is readily synthesized out of common laboratory chemicals in multigram quantities with good yield and easy workup and purification

An Efficient Thermal Elimination Pathway toward Phosphodiester Hydrogels via a Precursor Approach

Phosphodiester hydrogels offer a wide range of fascinating properties. Not only do they exhibit excellent hemocompatibility and cellular compatibility, they also show a remarkable resistance to protein adsorption, thereby limiting the foreign body response. In this work, phosphodiester-crosslinked hydrogels are produced by a simple free-radical polymerization of a phosphotriester crosslinker. In a second step, this material is transformed to the phosphodiester, by heating it up to 60 degrees C in phosphate-buffered saline. Compared to earlier methods, there is no need for acids, bases, or oxidizing agents to achieve this final conversion to the phosphodiester. This method thus reduces the risk to damage or degrade any sensitive biomolecules that might be of interest to tissue engineers, such as various growth factors or other proteins. The phosphotriester crosslinker is readily synthesized out of common laboratory chemicals in multigram quantities with good yield and easy workup and purification

Monitoring the Chloride Concentration in International Scheldt River Basin District Water Using a Low-Cost Multifunction Data Acquisition Board

In analytical chemistry laboratories, to gather in the shortest time as many data as possible with the utmost accuracy and precision, high throughput automated setups are indispensable. In the present study, to determine the chloride concentration in the international Scheldt river basin district, experiments are carried out utilizing a thermostatically controlled semi-automated setup. A novel ICT-based method is developed using a low-cost multifunction Data Acquisition Board (DAQ) controlled by a homebuilt LabVIEW™ program. Specifically, this approach enables a correlation between different parameters i.e., droplet volume, temperature, A/D voltage conversions. Here, processing experimental data of a potentiometric precipitation titration utilizing a silver nitrate standard solution as titrant in a manual burette equipped with a controllable electronic valve allows for a preliminary indication of the titration end point via the Virtual Instrument (VI) numerical first derivative tool in the LabVIEW software. The LabVIEW tool is compared with the well-known Gran method implemented in the LabVIEW program, emphasizing an accurate performance of the setup to determine the chloride concentration in fresh river water. We are confident that our findings are evidence of the versatile and powerful features of the LabVIEW controlled DAQ in the analytical chemistry laboratory

High Electronic Conductance through Double-Helix DNA Molecules with Fullerene Anchoring Groups

Determining the mechanism of charge transport through native DNA remains a challenge as different factors such as measuring conditions, molecule conformations, and choice of technique can significantly affect the final results. In this contribution, we have used a new approach to measure current flowing through isolated double-stranded DNA molecules, using fullerene groups to anchor the DNA to a gold substrate. Measurements were performed at room temperature in an inert environment using a conductive AFM technique. It is shown that the π-stacked B-DNA structure is conserved on depositing the DNA. As a result, currents in the nanoampere range were obtained for voltages ranging between ±1 V. These experimental results are supported by a theoretical model that suggests that a multistep hopping mechanism between delocalized domains is responsible for the long-range current flow through this specific type of DNA.status: publishe

Direct immobilization of engineered nanobodies on gold sensors

Single-domain antibodies, known as nanobodies, have great potential as biorecognition elements for sensors because of their small size, affinity, specificity, and robustness. However, facile and efficient methods of nanobody immobilization are sought that retain their maximum functionality. Herein, we describe the direct immobilization of nanobodies on gold sensors by exploiting a modified cysteine strategically positioned at the C-terminal end of the nanobody. The experimental data based on secondary ion mass spectrometry, circular dichroism, and surface plasmon resonance, taken together with a detailed computational work (molecular dynamics simulations), support the formation of stable and well-oriented nanobody monolayers. Furthermore, the nanobody structure and activity is preserved, wherein the nanobody is immobilized at a high density (approximately 1 nanobody per 13 nm2). The strategy for the spontaneous nanobody self-assembly is simple and effective and possesses exceptional potential to be used in numerous sensing platforms, ranging from clinical diagnosis to environmental monitoring

High Electronic Conductance through Double-Helix DNA Molecules with Fullerene Anchoring Groups

Determining the mechanism of charge transport through native DNA remains a challenge as different factors such as measuring conditions, molecule conformations, and choice of technique can significantly affect the final results. In this contribution, we have used a new approach to measure current flowing through isolated double-stranded DNA molecules, using fullerene groups to anchor the DNA to a gold substrate. Measurements were performed at room temperature in an inert environment using a conductive AFM technique. It is shown that the π-stacked B-DNA structure is conserved on depositing the DNA. As a result, currents in the nanoampere range were obtained for voltages ranging between ±1 V. These experimental results are supported by a theoretical model that suggests that a multistep hopping mechanism between delocalized domains is responsible for the long-range current flow through this specific type of DNA.ChemE/Opto-electronic Material