| Tech ID |
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| 23106 |
Inventory Control: Product Labeling to Indicate Authenticity
Available for licensing are patent rights in a method of marking products and goods with unique identifiers, using safe and consumable polymers. The system of marking can be applied as a coating or intrinsic to single or multiple ingredients that become a final product, allowing for authentication of a good, inventory control, and as a means to combat counterfeit goods.
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| 22966 |
An Aerosol Coating Process For Pharmaceutical Solids Based On Volatile, Non-Flammable Solvents
Hybrid polymer seed and tablet coating process
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| 21238 |
Energy Crops Engineered for Increased Sugar Extraction through Inhibition of snl6 Expression
Pamela Ronald and a team of researchers at the Joint BioEnergy Institute (JBEI) have engineered plants with inhibited expression of snl6, a cinnamoyl-CoA reductase-like (CCR-like) gene. As a result, the JBEI plants have reduced lignin or phenolic compounds compared to wild type plants and yield an increase of up to 10 percent of sugar extracted. The JBEI technology can be applied to a wide range of plants including rice, miscanthus, switchgrass, sugarcane, sugar beet, sorghum and corn, among others. In addition, the JBEI-engineered plants are developmentally normal. Until now, plants with decreased lignin content have exhibited defects such as reduced size or sturdiness that made them unsuitable biofuel feedstocks. Lignin significantly hinders the extraction of sugars from plant cells walls for saccharification, a key step in the production of biofuels from cellulosic biomass. The JBEI-engineered plants present less lignin or phenolics than control plants and lack the defects of other engineered species making them a superior biofuel feedstock. The Joint BioEnergy Institute (JBEI, www.jbei.org) is a scientific partnership led by the Lawrence Berkeley National Laboratory and including the Sandia National Laboratories, the University of California campuses of Berkeley and Davis, the Carnegie Institution for Science and the Lawrence Livermore National Laboratory. JBEI's primary scientific mission is to advance the development of the next generation of biofuels.
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| 20956 |
A Spray Dry Method to Encapsulate (Protect) Biological Moieties (e.g. Proteins, Cells, Probiotics, Nutraceuticals, etc.) in Crosslinked Alginate or Soy Protein Particles for Controlled Release Applications
Alginates have been used for decades for the encapsulation of biological molecules, cells and chemicals. The traditional encapsulation process involved dissolving or dispersing the active agent in a sodium alginate solution, forcing the solution through an orifice to form a droplet which was then cross-linked by contact with a calcium chloride solution. This process was not easily scaled-up and was limited to particles larger than 500 μm. Spray-drying would be a commercially viable process to form a calcium alginate matrix particle in the size range of 10 – 20 μm; however, one would have to find a way of cross-linking the sodium alginate solution during atomization. Researchers at the University of California Davis have developed a method that accomplishes this by spray-drying an aqueous formulation that contains sodium alginate, a calcium salt that is only soluble at reduced pH and an organic acid that has been neutralized to a pH just above the pKa with a volatile base. Under these conditions, the calcium salt is insoluble and calcium ions are not available for cross-linking. The solution in this fluid state is pumped through the nozzle of the spray dryer, where it is effectively atomized. Upon atomization, the volatile base is vaporized, which reduces the pH (hydrogen ions are released into solution) and in turn releases calcium ions from the calcium salt that cross-link the alginate. The incorporation of an additional polymer to the formulation allows for the control of hydration properties of the particles to control the release of the encapsulated compounds. This same process can be used for encapsulation using soy protein.
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| 19949 |
Nitrate-Responsive Synthetic Promoter Produces Nitrate-Regulated Gene Expression in Plants
Inorganic nitrogen is a vital nutrient for plants. Soil nitrate provides as much as 90 percent of the nitrogen taken up by most plants and leads to a dramatic change in gene expression, which is critical to direct the productivity and survival of the plant. Consequently, nitrate is commonly provided by way of fertilizer to improve crop yield. However, many crop plants are inefficient in their ability to utilize the nitrogen. For example, corn and wheat typically only utilize 50 percent of the nitrogen applied to the soil and paddy rice may recoup as little as 30 percent. Nitrogen not used by crops may contribute to severe environmental problems, including pollution of ground water, run-off into nearby bodies of water, and release of greenhouse gases into the atmosphere. Plants take up and assimilate nitrate in response to its availability in the soil and the demands of the plant, but with varying efficiency among species. Understanding and improving the ability of particular plant species to respond to and utilize nitrogen could therefore lead to increased crop productivity and decreased water and air pollution.
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| 19590 |
Monodisperse Silk Emulsions And Microspheres
Emulsions are commonly used in food products, cosmetics, paint, etc. Polymer microspheres have applications in, for example, drug delivery and tissue engineering. A challenge in creating polymer microspheres and emulsions is minimizing the polydispersity of the particles. The particles tend to have inconsistent size, shape and mass distribution. Silk is often used commercially as an emulsion, and has been demonstrated to be an extremely effective polymer for drug delivery. Microfluidic devices that produce microsphere have been demonstrated in the past. However, it has been difficult to produce particles with a consistent size and shape known as monodisperse particles. Researchers at UC Berkeley have developed a microfluidic methodology for producing monodisperse silk microspheres. The unique chemistry and method enables production of exact microsphere diameter and percent of crystallinity. Both the microsphere and crystallinity can be precisely adjusted which can be used in for a variety of applications. It is particularly useful to vary drug release characteristics in a drug delivery system.
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| 18101 |
Efficient Extraction of Hydrocarbons from Microalgae Colonies
Green microalgae of the genus Botryoccene synthesize long-chain terpenoid hydrocarbons that can amount to as much as 30-40% of the dry biomass weight. These hydrocarbons can serve as renewable biofuels, feedstock for synthetic chemicals, feedstock in drug manufacturing, and in cosmetics as an alternative to squalene. However, existing methods of extracting these hydrocarbons aren't economically viable. To address this opportunity, scientists at UC Berkeley have developed a more efficient method for extracting and quantifying extracellular terpenoid hydrocarbons from terprnoid-producing and secreting Botryoccene microalgae.
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| 17991 |
Determination of Bioproduct Content in Live Cell Cultures for Industrial Applications
There is great variability among different organisms in their ability to naturally or artificially synthesize and accumulate lipids, hydrocarbons, and polymers. Consequently, many organisms must be screened in order to achieve the desired maximal bio-product accumulation. After an ideal organism is selected, its product content can vary with lifecycle stage, cultivation conditions, cellular stress and/or time. This variability must be understood and controlled during R&D, process development and manufacturing scale-up in order to maximize product yields. The above process of screening and development can be time-consuming and consequently costly. To address this situation, scientists at UC Berkeley have developed a method for quick and precise estimation of lipid, hydrocarbon or biopolymer content in live cells -- whether grown as single cells or in colonies. This method can be used for screening a variety of microorganisms for product accumulation (microorganism prospecting), and to check yields throughout the production process -- allowing for more rapid improvement of production methods and shortened R&D timelines.
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