Marianneza Chatzipetrou

Superamphiphobic Polymeric Surfaces Sustaining Ultrahigh Impact Pressures of Aqueous High‐ and Low‐Surface‐Tension Mixtures, Tested with Laser‐Induced Forward Transfer of Drops

Superamphiphobic, (quasi-)ordered plasma-textured surfaces, coated with a perfluorinated monolayer, exhibit extreme resistance against drop-pinning for both water-like and low-surface-tension mixtures (36 mN m(-1)). The highest values reported here are 36 atm for a water-like mixture, 5 times higher than previously reported in the literature, and 7 atm for a low-surface-tension mixture, the highest ever reported value for lotus-leaf-inspired surfaces.

Label-free DNA biosensor based on resistance change of platinum nanoparticles assemblies

A novel nanoparticle based biosensor for the fast and simple detection of DNA hybridization events is presented. The sensor utilizes hybridized DNAs charge transport properties, combining them with metallic nanoparticle networks that act as nano-gapped electrodes. The DNA hybridization events can be detected by a significant reduction in the sensors resistance due to the conductive bridging offered by hybridized DNA. By modifying the nanoparticle surface coverage, which can be controlled experimentally being a function of deposition time, and the structural properties of the electrodes, an optimized biosensor for the in situ detection of DNA hybridization events is ultimately fabricated. The fabricated biosensor exhibits a wide response range, covering four orders of magnitude, a limit of detection of 1nM and can detect a single base pair mismatch between probe and complementary DNA.

Direct Creation of Biopatterns via a Combination of Laser-Based Techniques and Click Chemistry.

In this paper, we present the immobilization of thiol-modified aptamers on alkyne- or alkene-terminated silicon nitride surfaces by laser-induced click chemistry reactions. The aptamers are printed onto the surface by laser-induced forward transfer (LIFT), which also induces the covalent bonding of the aptamers by thiol-ene or thiol-yne reactions that occur upon UV irradiation of the thiol-modified aptamers with ns laser pulses. This combination of LIFT and laser-induced click chemistry allows the creation of high-resolution patterns without the need for masks. Whereas the click chemistry already takes place during the printing process (single-step process) by the laser pulse used for the printing process, further irradiation of the LIFT-printed aptamers by laser pulses (two-step process) leads to a further increase in the immobilization efficiency.

Time-resolved imaging and immobilization study of biomaterials on hydrophobic and superhydrophobic surfaces by means of laser-induced forward transfer

In this work, we present the generation of high velocity liquid jets of a photosynthetic biomaterial in buffer solution (i.e. thylakoid membranes) and a test solution, using the laser-induced forward transfer (LIFT) technique. The high impact pressure of the collision of the jets on solid substrates, ranging from 0.045 MPa–35 MPa, resulted in strong physical immobilization of the photosynthetic biomaterial on superhydrophobic (SH) poly(methyl methacrylate) (PMMA) surfaces and hydrophobic gold surfaces. The immobilization efficiency was evaluated by fluorescence microscopy, while time-resolved imaging of the LIFT process was carried out to study the corresponding LIFT dynamics. The results show that this simple, direct and chemical-linkers-free immobilization technique is valuable for several biosensors and microfluidic applications since it can be applied to a variety of hydrophobic and SH substrates, leading to the selective immobilization of the biomaterials, due to the high spatial printing resolution of the LIFT technique.