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221 results about "Lipid droplet" patented technology

Lipid droplets, also referred to as lipid bodies, oil bodies or adiposomes, are lipid-rich cellular organelles that regulate the storage and hydrolysis of neutral lipids and are found largely in the adipose tissue. They also serve as a reservoir for cholesterol and acyl-glycerols for membrane formation and maintenance. Lipid droplets are found in all eukaryotic organisms and store a large portion of lipids in mammalian adipocytes. Initially, these lipid droplets were considered to merely serve as fat depots, but since the discovery in the 1990s of proteins in the lipid droplet coat that regulate lipid droplet dynamics and lipid metabolism, lipid droplets are seen as highly dynamic organelles that play a very important role in the regulation of intracellular lipid storage and lipid metabolism. The role of lipid droplets outside of lipid and cholesterol storage has recently begun to be elucidated and includes a close association to inflammatory responses through the synthesis and metabolism of eicosanoids and to metabolic disorders such as obesity, cancer, and atherosclerosis. In non-adipocytes, lipid droplets are known to play a role in protection from lipotoxicity by storage of fatty acids in the form of neutral triacylglycerol, which consists of three fatty acids bound to glycerol. Alternatively, fatty acids can be converted to lipid intermediates like diacylglycerol (DAG), ceramides and fatty acyl-CoAs. These lipid intermediates can impair insulin signaling, which is referred to as lipid-induced insulin resistance and lipotoxicity. Lipid droplets also serve as platforms for protein binding and degradation. Finally, lipid droplets are known to be exploited by pathogens such as the hepatitis C virus, the dengue virus and chlamydia trachomatis among others.

Personal care formulations

Personal care and hygiene formulations for topical application to mucosal surfaces. These formulations include an amphiphilic lipid carrier in the form of a colloidal composition which can include a micellar aggregate or mixed micelles dispersed in a continuous aqueous phase, or an emulsion of lipid droplets suspended in a continuous aqueous phase, and an active agent which is an anti-microbial agent. The lipid carrier has high adhesiveness to mucous membranes such as the soft tissues of the oral cavity. The lipid carrier also has a high load capacity for the active agent to be carried to these tissues. These formulations have the desirable properties of carrying a large amount of active agent for controlled and prolonged release thereof at the desired site, such as mucous membrane surfaces and surrounding tissue. Accordingly, the present invention provides a formulation for oral or topical application including an anti-microbial agent and a lipid. The agent is held by the carrier through a hydrophobic interaction and is released from the carrier in a controlled manner over a prolonged period of time. The lipid is also characterized by having a high adhesive capability towards mucous membrane surfaces. The lipid and the agent are preferably present in a ratio in a range of from about 1:10 to 10:1, more preferably from about 1:5 to about 5:1, and most preferably from about 1:3 to about 3:1 in the formulation.
Owner:LURIYA ELENA +1

Compound with aggregation induced luminescence property and preparation method and application thereof

The invention discloses a compound with an aggregation induced luminescence property and a preparation method and application thereof in lipid droplet targeting light activating fluorescence imaging. The structure of the compound and the structure of an intermediate product of the compound are represented as the formula I and the formula II, and the formula I can be converted to generate the formula II under the light condition. The compound in the formula I is prepared through the following steps that a compound in the formula III and a compound in the formula IV are dissolved in acetonitrile under the protection of nitrogen, light avoiding reaction is conducted, and the 1,2-dihydro-2-diphenyleneimine ketone compound in the formula I is generated. The novel compound with the aggregation induced luminescence property has the aggregation induced luminescence advantage and can effectively overcome the aggregation induced quenching defect of traditional fluorescent dye, and thus lipid droplet targeting specificity light activating fluorescence imaging in a living cell can be achieved; in addition, the compound has the advantages that the light activating efficiency and the signal-to-noise ratio are high, the cytotoxicity is small, the Stokes shift is large, and the capability of the compound to enter cells is high; and cancer cells and normal cells can be effectively distinguished.
Owner:SOUTH CHINA UNIV OF TECH

Fluorescent probe based on fused ring oxidized thiophene and application of fluorescent probe in cell imaging

The invention belongs to the technical field of biochemistry, and discloses a fluorescent probe based on fused ring oxidized thiophene and application of the fluorescent probe in cell imaging. The fluorescent probe based on the fused ring oxidized thiophene is nano-particles coated with the fused ring oxidized thiophene. The fluorescent probe is applied to cell imaging, in particular to lipid droplet and lysosome imaging. The fluorescent probe can be used as a fluorescent imaging dye for lysosomes and lipid droplets, a tracer agent of mutual action between the lysosomes and the lipid droplets,and a tracer agent for lipid droplet formation and lipid droplet metabolism. The fluorescent probe shows blue-fluorescence in the lipid droplets, and shows red fluorescence in the lysosomes after entering cells, the fluorescent signal intensity and the color change are monitored, so that the high-sensitivity and high-resolution tracing of the movement of the droplets in a short time is realized;and the distribution and the metabolism conditions of the droplets are traced through long-time monitoring, and it is proved for the first time that the internal components of the droplets can be recovered by the lysosomes. The fluorescent probe is high in sensitivity and simple to operate.
Owner:SOUTH CHINA UNIV OF TECH

Enzymatically decomposed clam oligopeptide having recovery effect on non-alcoholic fatty liver disease cell model and preparation method of calm oligopeptide

The invention relates to an enzymatically decomposed clam oligopeptide having a recovery effect on a non-alcoholic fatty liver disease (NAFLD) cell model. The clam oligopeptide is characterized by comprising an amino acid sequence of Gln Leu Asn Trp Asp. The invention also relates to a preparation method of the enzymatically decomposed clam oligopeptide having the recovery effect on the NAFLD cell model. Compared with the prior art, the following advantages can be achieved: the NAFLD cell model is established by virtue of induction of palmitic acid and the damaged liver cells in a body are simulated sufficiently, and the result indicates that the TG content of the in-vitro NAFLD cell model established 48 hours after induction by 15 micrograms/milliliter palmitic acid increased remarkably in comparison with that of normal liver cells; oil red O staining shows that the number of intracellular lipid droplets of the model group is increased in contrast with that of the cells of a normal group, and the cell mortality rate is low and the repeatability is good, and therefore, the modeling method is simple, convenient and feasible; meanwhile, the enzymatically decomposed clam oligopeptide having the obvious recovery effect on the NAFLD cell model can be separated out from clams.
Owner:ZHEJIANG OCEAN UNIV

Carbon quantum dot fluorescent probe for lipid droplet specific labeling as well as preparation method and application thereof

ActiveCN112358873AStrong fluorescenceBright yellow fluorescentNanoopticsNano-carbonQuantum yieldThiourea
The invention discloses a carbon quantum dot fluorescent probe for lipid droplet specific labeling as well as a preparation method and application of the carbon quantum dot fluorescent probe, the carbon quantum dot fluorescent probe takes o-phenylenediamine and thiourea as raw materials, a product containing bright yellow orange fluorescent components is obtained through solvothermal reaction at 170-240 DEG C, and finally the carbon quantum dot fluorescent probe is obtained through filtration, separation and drying. The prepared carbon quantum fluorescent probe has good solubility and bright fluorescence performance in a non-polar hydrophobic oily medium, compared with weak fluorescence performance shown in an aqueous solution, the fluorescence intensity is improved by about 140 times, andthe carbon quantum fluorescent probe can be used for lipid droplet specific fluorescence imaging and has a high signal-to-noise ratio. The carbon quantum dot fluorescent probe provided by the invention can realize specific targeting of intracellular lipid droplets, is novel in performance, and has the characteristics of high fluorescent quantum yield, good light stability, low cytotoxicity, goodbiocompatibility and the like, so that the carbon quantum dot fluorescent probe has a wide application prospect in lipid droplet specific biological imaging.
Owner:SICHUAN UNIV

Establishment method for alcoholic fatty liver zebra fish model

The invention discloses an establishment method for an alcoholic fatty liver zebra fish model. The establishment method includes the following steps that AB-series wild zebra fishes are domesticated in a laboratory, and the healthy adult zebra fishes are picked out to be evenly divided into 16 groups at random; a central combinational design method is adopted, and the ethyl alcohol concentration, the exposure time and the test cycle are designed; after the adult zebra fishes in all the groups are fed according to design conditions, the survival rates and average lipid droplet areas of the adult zebra fishes in the groups are calculated; the obtained 16 groups of survival rates and average lipid droplet areas are subjected to standard deviation standardization, survival rate standardized values and average lipid droplet area standardized values of all the groups are added and then divided by 2 to obtain the comprehensive grades of the adult zebra fishes in the groups; the comprehensive grades of all the groups are subjected to multivariate regression analysis and binomial fitting to obtain a regression equation, and the optimal modeling condition of the alcoholic fatty liver zebra fish model is determined according to the regression equation. The establishment method is low in cost and short in cycle, the alcoholic fatty liver pathomechanism can be deeply researched, and a novel treatment means is found for the alcoholic fatty liver.
Owner:NANJING UNIV OF SCI & TECH
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