Preparation of new MOF-808/chitosan composite for Cr(VI) adsorption from aqueous solution: Experimental and DFT study.

In this study, a series of Zirconium-based MOF and chitosan composites (MOF-808/chitosan) were synthesized as efficient adsorbent for Cr(VI) ions elimination from aqueous solution. MOF-808/chitosan structure and morphology was characterized by FE-SEM, EDX, XRD, BET, zeta potential analysis, FT-IR, XPS techniques. The kinetic studies ascertained that Cr(VI) adsorption over MOF-808/chitosan followed pseudo-second-order kinetic model. The adsorption isotherms fitted the Langmuir isotherm model, implying on homogeneously adsorption of Cr(VI) on the surface of MOF-808/chitosan. According to the Langmuir model, the maximum capacity was obtained to be 320.0 mg/g at pH 5. Thermodynamic investigation proposed spontaneous (ΔG° < 0), disordered (ΔS° > 0) and endothermic (ΔH° > 0) for adsorption process. Besides, MOF-808/chitosan displayed an appropriate reusability for the elimination of Cr(VI) ions from their aqueous solutions for six successive cycles. DFT study of the adsorption process displayed and confirmed the role of hydrogen bonding and electrostatic attraction simultaneously.

Stimulus-responsive liposomes as smart nanoplatforms for drug delivery applications.

Liposomes are known to be promising nanoparticles (NPs) for drug delivery applications. Among different types of self-assembled NPs, liposomes stand out for their non-toxic nature, and their possession of dual hydrophilic-hydrophobic domains. Advantages of liposomes include the ability to solubilize hydrophobic drugs, the ability to incorporate different hydrophilic and lipophilic drugs at the same time, lessening the exposure of host organs to potentially toxic drugs and allowing modification of the surface by a variety of different chemical groups. This modification of the surface, or of the individual constituents, may be used to achieve two important goals. Firstly, ligands for active targeting can be attached that are recognized by cognate receptors over-expressed on the target cells of tissues. Secondly, modification can be used to impart a stimulus-responsive or "smart" character to the liposomes, whereby the cargo is released on demand only when certain internal stimuli (pH, reducing agents, specific enzymes) or external stimuli (light, magnetic field or ultrasound) are present. Here, we review the field of smart liposomes for drug delivery applications.