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The insulin-protamine interaction is at the core of the mode of action in many insulin formulations (Zn + insulin + protamine) and to treat diabetes, in which protamine is added to the stable form of hexameric insulin (Zn-insulin). However, due to the unavailability of quantitative data and a high-resolution structure, the binding mechanism of the insulin-protamine complex remains unknown. In this study, it was observed that Zn-insulin experiences destabilization as observed by the loss of secondary structure in circular dichroism (CD), and reduction in thermal stability in melting study, upon protamine binding. In isothermal titration calorimetry (ITC), it was found that the interactions were mostly enthalpically driven. This is in line with the positive Δ

We have synthesized a series of poly(N-isopropylacrylamide/ionic liquid) with deposited Au nanoparticles. The size of the nanoparticle range was varied from 10 to 35 nm, and these were characterized by transmission electron microscopy analysis. Ionic liquids (IL) were chosen by varying the polymerizable unit to be both in cationic (allyl) and anionic (acrylate) moiety. One-pot polymerization was done with N-isopropylacrylamide and IL using ammonium persulphate as the initiator, to which were added already prepared Au NPs. These thermally sensitive composites formed, possessed reversible swelling/deswelling abilities in water, and demonstrated a reversible visible phase transition, which was detected by differential scanning calorimetric measurements. The lower critical solution temperature (LCST) showed dependency on the size of nanoparticles and the IL independently. It was seen that the LCST of PNIPAM-based composite films can be tuned from 32 °C to a range of 23-67 °C by choosing the desired Au NP size, its concentration and kind of IL.

This paper highlights the relation between the shape of iron oxide (Fe3O4) particles and their magnetic sensing ability. We synthesized Fe3O4 nanocubes and nanospheres having tunable sizes via solvothermal and thermal decomposition synthesis reactions, respectively, to obtain samples in which the volumes and body diagonals/diameters were equivalent. Vibrating sample magnetometry (VSM) data showed that the saturation magnetization (Ms) and coercivity of 100–225 nm cubic magnetic nanoparticles (MNPs) were, respectively, 1.4–3.0 and 1.1–8.4 times those of spherical MNPs on a same-volume and same-body diagonal/diameter basis. The Curie temperature for the cubic Fe3O4 MNPs for each size was also higher than that of the corresponding spherical MNPs; furthermore, the cubic Fe3O4 MNPs were more crystalline than the corresponding spherical MNPs. For applications relying on both higher contact area and enhanced magnetic properties, higher-Ms Fe3O4 nanocubes offer distinct advantages over Fe3O4 nanospheres of the same-volume or same-body diagonal/diameter. We evaluated the sensing potential of our synthesized MNPs using giant magnetoresistive (GMR) sensing and force-induced remnant magnetization spectroscopy (FIRMS). Preliminary data obtained by GMR sensing confirmed that the nanocubes exhibited a distinct sensitivity advantage over the nanospheres. Similarly, FIRMS data showed that when subjected to the same force at the same initial concentration, a greater number of nanocubes remained bound to the sensor surface because of higher surface contact area. Because greater binding and higher Ms translate to stronger signal and better analytical sensitivity, nanocubes are an attractive alternative to nanospheres in sensing applications.