Various formulations consisting of biomaterials zirconium imidazolate framework-8 (ZIF-8), choline acetate ([Ch][Ac]), and arginine hydrochloride (argHCl) are optimized to study the stability of antibody, Immunoglobulin G (IgG). We have performed several instrumentations including UV−visible spectroscopy, dynamic light scattering (DLS), circular dichroism (far UV CD), and atomic force microscopy (AFM) in the presence of all the formulations to investigate the conformational and colloidal stability of the antibodies. Alongside, the packing efficiency of all the formulations was also explored by storing IgG at 4 °C for 3 months. We have tried to investigate the interactions between biomaterials and antibodies with the motive of designing aggregation-resistant formulations. The overall stability of IgG was improved in the presence of [Ch][Ac]; however, ZIF-8 and argHCl cause relatively more aggregation, although the structure was retained in all the formulations. The key aspect of this study is that the presence of [Ch][Ac] increases ZIF-8@IgG's thermal stability and resistance to IgG-argHCl aggregation. All over, for the first time, with different experimental approaches, the impact of each biomaterial individually and in combination is explored to study their effect on the stability of antibodies. Thus, better efficient formulations can be designed for the storage/packaging of IgG-based drugs which ultimately will have more applicability in pharmaceuticals.
Surface modification of metallic nanoparticles (NPs) by stimuli-responsive polymers is a benign method to prepare smart colloidal composites which tune the characteristic properties of individual systems. The temperature-dependent transition of diblock copolymer poly(N-isopropylacrylamide)-block-poly(N-vinylcaprolactam) (PNIPMA-b-PVCL) synthesized using reversible addition–fragmentation chain transfer polymerization was studied by incorporating anisotropic gold NPs (AGPs) such as spheres (AuNSs), rods (AuNRs), cubes (AuNCs), and rhombic dodecahedrals (AuRDs). Shape-dependent physiochemical properties of nanostructures alter the lower critical solution temperature (LCST) of the chemical inhomogeneous diblock copolymer. Heterogeneous nucleation of AuNPs was facilitated by seed-mediated synthesis for incorporating uniformity. In the mixed system, the presence of PNIPAM-b-PVCL modifies the surface of AGPs through physisorption which is supported by transmission electron microscopy and field emission scanning electron microscopy showing the NPs embedding in the polymeric matrix. Furthermore, steady state fluorescence spectroscopy and Fourier transform infrared spectroscopy were performed to examine the phase transition behavior of PNIPAM-b-PVCL in AGPs. The formation of a smart polymer nanocomposite alters the physiochemical properties of the diblock copolymer as demonstrated from the variation of LCST in the dynamic light scattering measurement. Henceforth, functionalizing the surfaces of AGPs with a thermoresponsive diblock copolymer provides combinatorial benefits in the properties of smart polymeric colloidal systems with potential applications in bioimaging and drug delivery.
The proteins can easily lose their native conformation in presence of denaturants which unfolds protein structure. Since, the introduction of deep eutectic solvents (DESs), there are numerous studies in which...
Thermoresponsive polymers (TRPs) have attracted considerable interest in the scientific community because of their potential applications in sensors, gels, drug delivery devices, biotechnology, and pharmacology. Certain biomolecules alter the phase transition behavior of TRPs by acting as external biological stimuli. Herein, we describe recently reported results and trends for TRP/biomolecule mixed systems in which biological stimuli modulate temperature-dependent polymer transitions and reviewed studies related to protein–polymer assembly formation, interactions, and temperature-dependent protein adsorption. Modifying polymer properties in response to biomolecules, which are inherently present in the human body, designs polymeric biomaterials with envisaged applications. We hope this review sheds light on scientific problems concerning biomolecule–polymer mixed systems and helps in designing next-generation “smart” polymers.
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