The present invention relates to a process for the preparation of a composition comprising a gold (111) chlorite-cyanide coordination compound, a composition comprising the gold (111) compound obtainable by this process, as well as the afore-mentioned composition for use in therapy, more particularly for use in the treatment of cancer.

A nanosample capable of near-infrared light-triggered release of therapeutic molecules. The nanosample includes a plurality of nanocomplexes. Each of the nanocomplexes includes a nanoshell; a host molecule linked to the nanoshell; and a guest molecule linked to the host molecule. The nanoshell includes a shell. The nanocomplex has a plasmon resonance wavelength. When irradiated with electromagnetic radiation of the plasmon resonance wavelength, plasmon resonance of the nanocomplex releases the guest molecule. The nanoshell may also include a core, where the shell surrounds the core. The nanoshell may be a nanomatryoshka. A link between the nanoshell and the host molecule may be a gold-thiol interaction. The shell may include at least one metal, such as gold or silver. The core may be a liposome and/or silica. The host molecule may be: synthetic polymers, biopolymers, polynucleotides, nucleic acids, polypeptides, polysaccharides, polyterpenes, lipids, aptamers, and/or proteins. The guest molecule may be: pharmaceutical molecules, biopharmaceutical molecules, oligonucleotides, nucleic acids, dye molecules, and/or imaging contrast agents. The host molecule may be: aptamer, single-stranded DNA, double-stranded DNA, and/or human serum albumin. The guest molecule may be: docetaxel, lapatinib, and/or tumor necrosis factor alpha. The plasmon resonance wavelength may be in a near-infrared (NIR) water window.

The present invention relates to a superparamagnetic gold nanoparticle cluster-protein nanoparticle fusion body for magnetic resonance imaging and magnetic thermotherapy. According to the present invention, a superparamagnetic gold nanoparticle cluster-protein nanoparticle fusion body which has target directionality and a high density of ultrafine gold nanoparticles uniformly coupled to the surface of protein nanoparticles can be fabricated with neither a separate surface stabilization process nor a separate target directionality conferring process. Hence, the superparamagnetic gold nanoparticle cluster-protein nanoparticle fusion body according to the present invention is superior to conventional gold nanoparticles in terms of biocompatibility and has excellent target directionality as well as being identified to have a temperature elevation potential in an alternating magnetic field and a functionality as a T2-MRI contrast medium thanks to the superparamagnetism property of the ultrafine gold nanoparticles. Therefore, the superparamagnetic gold nanoparticle cluster-protein nanoparticle fusion body according to the present invention can be utilized as a core technology in the fields of magnetic thermotherapy and magnetic resonance imaging contrast media.

A method and plant for gold recovery from any gold-bearing ore by low-temperature chlorination, wherein the finely-divided gold-bearing feedstock is chlorinated gaseous chlorine at a temperature of about 245 C. to form a highly volatile chloride compound, which after leaving a reactor is directed to a low-temperature nitrogen plasma unit having a temperature of 900-1100 C., wherein the said compound decomposes and turns into high-purity gold powder, which is cooled with gaseous nitrogen at a cooling reactor's inlet, which is equipped with a water chamber, and collected in a dumping hopper. Some embodiments allow recovery of high-purity 999.9 fine gold using an environmentally friendly, cost effective and inexpensive method implemented on an industrial scale.

A method and plant for gold recovery from any gold-bearing ore by low-temperature chlorination, wherein the finely-divided gold-bearing feedstock is chlorinated gaseous chlorine at a temperature of about 245 C. to form a highly volatile chloride compound, which after leaving a reactor is directed to a low-temperature nitrogen plasma unit having a temperature of 900-1100 C., wherein the said compound decomposes and turns into high-purity gold powder, which is cooled with gaseous nitrogen at a cooling reactor's inlet, which is equipped with a water chamber, and collected in a dumping hopper. Some embodiments allow recovery of high-purity 999.9 fine gold using an environmentally friendly, cost effective and inexpensive method implemented on an industrial scale.

A method and plant for gold recovery from any gold-bearing ore by low-temperature chlorination, wherein the finely-divided gold-bearing feedstock is chlorinated gaseous chlorine at a temperature of about 245 C. to form a highly volatile chloride compound, which after leaving a reactor is directed to a low-temperature nitrogen plasma unit having a temperature of 900-1100 C., wherein the said compound decomposes and turns into high-purity gold powder, which is cooled with gaseous nitrogen at a cooling reactor's inlet, which is equipped with a water chamber, and collected in a dumping hopper. Some embodiments allow recovery of high-purity 999.9 fine gold using an environmentally friendly, cost effective and inexpensive method implemented on an industrial scale.

The recovery of gold and/or silver from gold and/or silver containing material is generally described. The gold and/or silver can be recovered selectively, in some cases, such that gold and/or silver are at least partially separated from non-silver and/or non-gold material. Gold and/or silver may be recovered from material using mixtures of acids, in some instances. In some cases, the mixture can comprise nitric acid and at least one supplemental acid, such as sulfuric acid or phosphoric acid. The amount of nitric acid within the mixture can be, in some instances, relatively small compared to the amount of sulfuric acid or phosphoric acid within the mixture. In some cases, the recovery of gold and/or silver using the acid mixtures can be enhanced by transporting an electric current between an electrode and the gold and/or silver of the material. In some cases, acid mixtures can be used to recover silver from particular types of materials, such as material comprising silver metal and cadmium oxide and/or material comprising silver metal and tungsten metal.

The recovery of gold and/or silver from gold and/or silver containing material is generally described. The gold and/or silver can be recovered selectively, in some cases, such that gold and/or silver are at least partially separated from non-silver and/or non-gold material. Gold and/or silver may be recovered from material using mixtures of acids, in some instances. In some cases, the mixture can comprise nitric acid and at least one supplemental acid, such as sulfuric acid or phosphoric acid. The amount of nitric acid within the mixture can be, in some instances, relatively small compared to the amount of sulfuric acid or phosphoric acid within the mixture. In some cases, the recovery of gold and/or silver using the acid mixtures can be enhanced by transporting an electric current between an electrode and the gold and/or silver of the material. In some cases, acid mixtures can be used to recover silver from particular types of materials, such as material comprising silver metal and cadmium oxide and/or material comprising silver metal and tungsten metal.

Disclosed are a pharmaceutical use of a gold cluster and a substance containing the gold cluster and the preparation method and use thereof. The gold cluster and substance containing the gold cluster can inhibit the aggregation of A and -syn, has excellent effects on the levels of cell models and animal models, and can be used to prepare drugs for preventing and treating Alzheimer's disease and/or Parkinson's disease.

The present invention provides a composition for antifreezing including a gold (Au) nanostructure in which at least a portion thereof is concave, thereby it is possible to increase a survival rate of cells due to having excellent effect of inhibiting ice recrystallization when cryopreservation of the cells, and maintain a texture of food even when using in the freezing of food.