The present disclosure relates to a method for preparing a colorant having a target color and the colorant. The method includes configuring submicron particles prepared from a predetermined material to have a predetermined size; adjusting a ratio of the submicron particles to cuttlefish juice submicron particles to a predetermined ratio; evaporating a predetermined solution mixed with the submicron particles and the cuttlefish juice submicron particles to obtain an amorphous photonic crystal structure; acquiring spectral data for reflected light generated by incident light irradiating the amorphous photonic crystal structure; determining whether the spectral data meets a predetermined condition, wherein the predetermined condition is associated with the target color; and responsive to determining that the spectral data does not meet the predetermined condition, adjusting at least one of the ratio or a size of each of the submicron particles until the spectral data meets the predetermined condition.

In various embodiments, the present invention is directed to a facile one-pot reverse emulsion process to assemble core-shell nanoparticles (CS-SMNPs) into bright and noniridescent photonic supraballs. In one or more embodiments, the present invention is directed to core-shell nanoparticles having an inner high refractive index (RI) core and an outer low RI shell. In one or more embodiment, the present invention includes core-shell nanoparticles using high RI (˜1.74) melanin cores and low-RI (˜1.45) silica shells. In various embodiments, these nanoparticles may be self-assembled into bright and noniridescent supraballs using a scalable one-pot reverse emulsion process. According to various embodiments of the present invention, it is possible to generate a full spectrum of structural colors with the combination of only two ingredients, synthetic melanin and silica.

A light-emitting colorant-containing particle contains an organic resin and a light-emitting colorant. A content of the light-emitting colorant is in a range of 10 to 80 mol % based on a total amount of a monomer forming the organic resin and the light-emitting colorant. The particle has an average particle diameter in a range of 1 to 100 nm.

The present disclosure provides a nano dye molecule, a color filter, and a display panel. The nano dye molecule comprises a gold nanocluster and a plurality of dye groups which are connected to the gold nanocluster by gold-sulfur bonds and cover an outer periphery of the gold nanocluster.

The present invention provides a method of producing dye-containing thermosetting resin particles, the method including: dispersing seed particles formed from a thermosetting resin in a dispersion medium; and polymerizing a monomer for thermosetting resin synthesis in the thus obtained dispersion in the presence of a dye and an acid catalyst. By the method of producing dye-containing thermosetting resin particles according to the present invention, dye-containing thermosetting resin particles whose particle size variation coefficient is small at, for example, 8% or less, can be produced without performing a post-treatment such as centrifugation. Therefore, when immunological observation is performed by a fluorescent labeling method using fluorescent dye-containing resin particles produced by the method of producing dye-containing thermosetting resin particles according to the present invention, a high bright spot detection accuracy can be attained.

Solid lipid nanoparticles (SLNs) and suspensions thereof in an aqueous phase are provided, in which the SLNs have high content of oil-soluble pigment and high stability. A food product, such as a beverage, comprising said SLNs is also provided.

The present disclosure provides a nano dye molecule, a color filter, and a display panel. The nano dye molecule comprises a gold nanocluster and a plurality of dye groups which are connected to the gold nanocluster by gold-sulfur bonds and cover an outer periphery of the gold nanocluster.

The present invention provides compositions relating to nanoparticles, such as nanocapsules, that selectively target cells associated with diseases or disorders (e.g., cancer cells). The present invention further relates to methods relating to the said nanoparticles for imaging, detection, and treatment of diseases or disorders in a subject. The present invention additionally provides kits that find use in the practice of the methods of the invention.

One embodiment of the present disclosure provides a method for producing an angle-independent colloidal particles-based structure, the method having: preparing two or more types of hollow colloidal particles, wherein the types are distinguished based on a size of the hollow colloidal particles thereof, wherein the types have different particle sizes; and dispersing the at least two types of hollow colloidal particles to produce an amorphous structure, wherein the amorphous structure realizes the same color independently of an angle of an incident light thereto.

The present invention provides compositions relating to nanoparticles, such as nanocapsules, that selectively target cells associated with diseases or disorders (e.g., cancer cells). The present invention further relates to methods relating to the said nanoparticles for imaging, detection, and treatment of diseases or disorders in a subject. The present invention additionally provides kits that find use in the practice of the methods of the invention.