Green nanotechnology incorporates the principles of green chemistry and green engineering to fabricate innocuous and eco-friendly nanoassemblies to combat the problems affecting the human health or environment. Subsequently, amalgamation of green nanotechnology with drug delivery area has actually commenced a new realm of “green nanomedicine”. The burgeoning demand for green nanotechnology-driven drug delivery systems has led to the development of different types of delivery devices, like inorganic (metallic) nanoparticles, quantum dots, organic polymeric nanoparticles, mesoporous silica nanoparticles, dendrimers, nanostructured lipid carriers, solid lipid nanoparticles, etc. The present article deals with a brief account of delivery devices produced from green methods and describes site-specific drug delivery systems (including their pros and cons) and their relevance in the field of green nanomedicine.

The objective of the present work was to develop solid lipid nanoparticles (SLNs) as drug-encapsulating structures by the solvent injection method. In this report, for the first time the inherent potential of lactonic sophorolipid (glycolipid) was exploited to formulate SLNs. A range of different Pluronic copolymers were screened by dynamic and static light scattering with the aim of obtaining most stable SLNs. To comprehend the structure of the SLNs, techniques such as transmission electron microscopy, differential scanning calorimetry, Fourier transform infrared spectroscopy, and X-ray diffraction were employed. A clear correlation between the type of Pluronic and size and stability of the SLNs could be drawn. The vector properties of the formed SLNs were assessed for both the encapsulated hydrophobic drugs-rifampicin and dapsone. To elucidate the transport mechanism of drug release, kinetic modeling was carried out on the drug release profiles. The promising results of sophorolipid-based SLNs have actually established a new arena beneath the significantly developed field of SLNs.

The template efficacy of solid lipid nanoparticles for generating porous silica materials with the amalgamation of Cu‐functionalized cetylpyridinium chloride (CPC; as a co‐emulsifier and as a metal source for generation of CuO oxide nanoparticles) has been explored. Impregnation of CuO nanoparticles (∼10–12 nm) onto the silica matrix proffers to be a propitious route for the fabrication of twin sized porous, highly active catalytic materials. The surface morphology and structural characterization of the synthesized CuO@meso‐macroporous silica framework was elucidated by TEM, field ‐emission (FE)‐SEM, energy‐dispersive X‐ray (EDX), wavelength dispersive (WD)‐XRF, X‐ray photoelectron spectroscopy (XPS), small‐angle X‐ray scattering (SAXS), XRD, and N2 adsorption/desorption studies. All the results have shown that there exists a structural network interconnecting the mesopores with macropores. The catalytic performance of the synthesized framework (ascribed catalyst) was checked for two model reactions. For the reduction of p‐nitrophenol to p‐aminophenol, only 0.25 % (w/v) catalyst was sufficient to accomplish the reaction in 6 min, giving 99.9 % yield. On the other hand, the redox reaction of potassium hexacyanoferrate(III) and sodium thiosulfate utilized 5 % (w/v) catalyst and completed the reaction in 40 min, yielding 98.43 %. Therefore, CuO@meso‐macroporous silica materials could hold great importance in the world of nanocatalysis owing to the present promising results.

No abstract

No abstract