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An effective and rapid bacterial killing nanotechnology strategy based on lysozyme-modified fuel-free nanomotors is demonstrated. The efficient antibacterial property of lysozyme, associated with the cleavage of glycosidic bonds of peptidoglycans present in the bacteria cell wall, has been combined with ultrasound (US)-propelled porous gold nanowire (p-AuNW) motors as biocompatible dynamic bacteria nanofighters. Coupling the antibacterial activity of the enzyme with the rapid movement of these p-AuNWs, along with the corresponding fluid dynamics, promotes enzyme-bacteria interactions and prevents surface aggregation of dead bacteria, resulting in a greatly enhanced bacteria-killing capability. The large active surface area of these nanoporous motors offers a significantly higher enzyme loading capacity compared to nonporous AuNWs, which results in a higher antimicrobial activity against Gram-positive and Gram-negative bacteria. Detailed characterization studies and control experiments provide useful insights into the underlying factors controlling the antibacterial performance of the new dynamic bacteria nanofighters. Rapid and effective killing of the Gram-positive Micrococcus lysodeikticus bacteria (69-84% within 1-5 min) is demonstrated.

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Efficient and controlled nanoscale propulsion in harsh environments requires careful design and manufacturing of nanomachines, which can harvest and translate the propelling forces with high spatial and time resolution. Here we report a new class of artificial nanomachine, named magneto-acoustic hybrid nanomotor, which displays efficient propulsion in the presence of either magnetic or acoustic fields without adding any chemical fuel. These fuel-free hybrid nanomotors, which comprise a magnetic helical structure and a concave nanorod end, are synthesized using a template-assisted electrochemical deposition process followed by segment-selective chemical etching. Dynamic switching of the propulsion mode with reversal of the movement direction and digital speed regulation are demonstrated on a single nanovehicle. These hybrid nanomotors exhibit a diverse biomimetic collective behavior, including stable aggregation, swarm motion, and swarm vortex, triggered in response to different field inputs. Such adaptive hybrid operation and controlled collective behavior hold considerable promise for designing smart nanovehicles that autonomously reconfigure their operation mode according to their mission or in response to changes in their surrounding environment or in their own performance, thus holding considerable promise for diverse practical biomedical applications of fuel-free nanomachines.

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The need for sensitive, selective, rapid and low-cost detection systems for DNA and DNA-drug interactions are in crucial demand for diagnostics and real-world applications. This work details the preparation of poly(3,4-ethylenedioxythiophene) (PEDOT) coated chitosan (CHIT) and the use of PEDOT coated CHIT modified disposable pencil graphite electrodes (PGEs) for DNA and DNA-anticancer drug interaction sensing. PEDOT coated CHIT (PEDOT/CHIT) was prepared with rotating plasma polymerization using radio frequency (RF: 13.56 MHz) power generator. Then, modification of PEDOT/CHIT onto PGE was performed. The use of the prepared electrode was carried out using differential pulse voltammetry (DPV). Cyclic voltammetry (CV) and scanning electron microscopy (SEM) were used to characterize the PEDOT/CHIT/PGE. The performance of the electrode was compared with CHIT/PGE and unmodified PGE. The electrode exhibited high sensitivity for the investigation of DNA sensing and DNA-anticancer drug interaction. Such disposable sensing platform hold considerable promise for diverse bioapplications.

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Plasma-modified chitosan and poly(3,4-ethylenedioxythiophene) were blended to obtain conducting nanofibers with polyvinyl alcohol as a supporting polymer at various volumetric ratios by electrospinning method. Chemical compositions and molecular interactions among nanofiber blend components were determined using Fourier transform infrared spectroscopy (FTIR). The conducting blends containing plasma-modified chitosan resulted in a superior antibacterial activity and thinner fiber formation than those containing chitosan without plasma-modification. The obtained nanofiber diameters of plasma-modified chitosan were in the range of 170 to 200 nm and those obtained from unmodified chitosan were in the range of 190 to 246 nm. The electrical and electrochemical properties of nanofibers were also investigated by four-point probe conductivity and cyclic voltammetry measurements.

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Chitosan nano powders were modified using RF hydrazine plasma produced at low pressure (26.66Pa) with 13.56MHz frequency at a power of 100W for 30min. Characterization and investigation of the properties of plasma-modified chitosan (PMCh) and non-modified chitosan (Ch) were carried out using an optical monochromator, FTIR, florescence analysis, TGA, SEM, and X-ray techniques. FTIR spectra of PMCh indicated a band broadening at 3436cm(-1) that confirmed increasing functional groups based on H-bonding. The number of NH(2) groups was determined from fluorescence analysis. TGA analysis shows that the moisture absorption is three times higher in the PMCh structure. Ch and PMCh in PVA solutions were used to produce nanofibers by the electrospinning method; average fiber diameters were 480 and 280nm for Ch and PMCh, respectively. It was found that the antibacterial effect of PMCh is better than the Ch for Gram-positive strains.

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