The hydrogel consisting of an oligomeric electrolyte, poly[pyridinium-1,4-diyl-iminocarbonyl-1,4-phenylenemethylene chloride] (1-Cl) underwent self-healing at temperatures lower than its gelation temperature after destruction of the gel network in a shear flow. The self-healing mechanism was investigated by rheological measurements on three different kinds of gels including a low-molecular weight organogelator and a polymeric hydrogelator. Although all of the three gels exhibited thermo-reversible hysteresis loops in the shear moduli, only 1-Cl hydrogel recovered its mechanical properties after vigorous agitation. It is conjectured that the self-healing is due to formation of network structure via a chlorine ion mediated hydrogen bond for which the activation energy is on the order of 10 kJ/mol.

Dynamic light scattering and oscillatory rheology experiments were performed to study the effects of various salts on the hydrogel consisting of an oligomeric electrolyte gelator, poly(pyridinium-1,4-diyliminocarbonyl-1,4-phenylenemethylene chloride) (1-Cl). Sol-gel transition temperature increased with increasing salt concentration that suggested the salt-in behavior. The concentration dependence of the dynamic shear moduli showed power-law scaling behavior and was compared with the predictions made by the fractal gel model. The brittleness was increased by increasing salt concentration, indicating that 1-Cl hydrogel became better packed into stronger networks in ionic solutions. After certain salt concentrations, 1-Cl hydrogel started precipitation that might be due to the excessive network formation resulting in collapse of the network structure. The recovery of the mechanical properties of 1-Cl hydrogel was completely reduced in the presence of salts.

Proteins and genes of therapeutic interests in conjunction with different delivery systems are growing towards new heights. “Next generation delivery systems” may provide more efficient platform for delivery of proteins and genes. In the present review, snapshots about the benefits of proteins or gene therapy, general procedures for therapeutic protein or gene delivery system, and different next generation delivery system such as liposome, PEGylation, HESylation, and nanoparticle based delivery have been depicted with their detailed explanation.

Broadband dielectric spectroscopy has been used to analyze the temperature, frequency, and concentration dependences of the molecular dynamics of a nematic liquid crystal (5CB) mixed with the nonpolar solvent benzene. Differential scanning calorimetry measurement has been also performed to confirm the phase transitions of 5CB/benzene mixtures. The phase transition temperatures (crystalline to isotropic phases) thus obtained have been described very accurately from the temperature-dependent relaxation strength, the relaxation time, and the symmetric shape parameter of the relaxation function obtained from the fitting procedure. Two relaxation processes reflecting overall rotations around the short and long molecular axes are observed in both the nematic and isotropic phases. In the crystalline phase, the former process with the longer relaxation time disappeared, and latter process with shorter relaxation time shows a discontinuity at the freezing temperature. The relaxation process with shorter relaxation time obtained in the crystalline phase is larger than that obtained in the nematic phase because of the large restrictions in the crystalline phase. For the first time, we have precisely explained the molecular mechanism and structure of liquid crystalline materials as a function of concentration, temperature, and frequency.