Abstract: Isolated antibodies that bind to human CD38 and cynomolgus CD38 are disclosed. Also disclosed are pharmaceutical compositions comprising the disclosed antibodies, and therapeutic and diagnostic methods for using the disclosed antibodies.

Abstract: A method for decreasing the immunogenicity of antibody variable domains is disclosed.

Abstract: The present invention is concerned with antigen binding polypeptides, and in particular conventional antibodies derived from camelid species, that specifically bind to target antigens that are either self-antigens or highly conserved antigens. The present invention also relates to anti-idiotype antigen binding peptides which bind to a target antigen comprising the variable region of an antibody obtained from a species within the family Camelidae.

Abstract: Disclosed are targeting constructs for targeting a target site, including a molecule or complex of interest. The targeting constructs comprise a polymer chain and a plurality of multi-specific molecules each of which includes an affinity moiety for binding with the polymer chain and a targeting ligand for binding with the target site. The polymer chain may be associated with a therapeutic or diagnostic agent and generally comprises a plurality of sites, wherein individual sites bind with a multi-specific molecule of the target construct. The present disclosure also relates to methods of preparing the targeting construct and to its use in therapeutic and diagnostic applications.

Abstract: Provided is a method for obtaining high-yield, stable expression cell clones from myeloma cell lines in a protein-free culture medium. The method is used for industrial production of a recombinant antibody, and includes three stage: (1) adapting to a protein-free culture medium, statically culturing cells at a low density, and gradually reducing a fat-rich supplement to a chemical culture medium; (2) adapting to a protein-free culture medium; culturing cells at a high density, and using a perfusion fermentation system in a laboratory scale; and (3) screening high-yield, stable expression cell clones from the cells after fermentation ends. The cell clone may be used to produce a humanized anti-NeuGcGM3 14F7 recombinant antibody.

Abstract: The invention provides for a domain-exchanged antibody comprising a light chain (LC) composed of VL-CH3, and a heavy chain (HC) comprising VH-CH3-CH2-CH3, wherein the VL-CH3 of the LC is dimerising with the VH-CH3 of the HC thereby forming a domain-exchanged LC/HC dimer comprising a CH3LC/CH3HC domain pair, and means and method for producing the same.

Abstract: The present invention provides a process for producing a nanocellulose material, comprising: fractionating a lignocellulosic biomass feedstock in the presence of a solvent for lignin and water, but no acid catalyst, to generate cellulose-rich solids; and then mechanically treating the cellulose-rich solids to form a nanocellulose material comprising cellulose nanofibrils and/or cellulose nanocrystals. Many organic or inorganic solvents are possible. In some embodiments, the solvent for lignin is an oxygenated organic compound, such as a C1-C18 alcohol, e.g. ethanol, ethylene glycol, propanol, propanediol, glycerol, butanol, or butanediol. The solvent for lignin may be an aromatic alcohol, such as phenol, cresol, or benzyl alcohol. The solvent for lignin may be a ketone, an aldehyde, or an ether, such as methyl ethyl ketone or diethyl ether. The solvent for lignin may be a non-oxygenated alkane, olefin, or aromatic hydrocarbon. In some embodiments, the solvent for lignin is an ionic liquid.

Abstract: A process for manufacturing a solid thermoset foam includes the following successive stages: (a) providing an expandable and thermosetting composition including a first reactant chosen from reducing sugars and a second reactant chosen from primary amines, primary amine acid addition salts, secondary amines, secondary amine acid addition salts, and ammonium salts of formula Rn?(NH4+)n where n is an integer at least equal to 1 and Rn? represents the residue of an organic or inorganic acid; (b) introducing the expandable and thermosetting composition into a mold or applying the expandable composition to a support so as to form a film having a thickness at least equal to 1 mm; and (c) heating the expandable and thermosetting composition to a temperature at least equal to 140° C. to react the first reactant with the second reactant and to form, by polymerization and chemical foaming, a block of solid thermoset foam.

Abstract: The invention relates to chitin, a hydrolysate and a method for the production of at least one desired product from insects. More specifically, the invention relates to a method for the production of at least one desired product from insects, comprising an insect cuticle pressing step, followed by the enzymatic hydrolysis of the insect cuticles using a proteolytic enzyme.

Abstract: This invention relates to a new process for obtaining inulin from roots of cardoon plants, that is those belonging to the Cardueae tribe.

Abstract: The present invention provides a process for the preparation of (6-per-deoxy-6-per-(2-carboxyethyl)thio-?-cyclodextrin) sodium salt, comprising the steps of: reacting ?-cyclodextrin (SM1) with iodine in the presence of triphenylphosphine in an organic solvent to afford an intermediate, 6-per-deoxy-6-iodo-?-cyclodextrin (abbreviated as SGMD-1); adding methanol solution of sodium methoxide into the reaction system followed by the addition of acetone without removal of the solvent under reduced pressure to obtain the crude SGMD-1 as a solid after filtration; purifying the crude SGMD-1 by recrystallization; reacting a obtained recrystallized intermediate (SGMD-1) with 3-mercaptopropionic acid in basic medium e.g., sodium hydride, to obtain the crude 6-per-deoxy-6-per-(2-carboxyethyl)thio-?-cyclodextrin sodium salt (abbreviated as SGMD); purifying the crude SGMD by passing through adsorbents followed by recrystallization.

Abstract: Method of production of highly saturated nitrile rubber, including: polymerization step of polymerizing monomer mixture containing at least ?,?-ethylenically unsaturated nitrile monomer and diene monomer in medium to obtain dispersion or solution of nitrile rubber; coagulation step causing the nitrile rubber dispersion or solution to coagulate at 10-60° C.

Abstract: The present invention provides a modified conjugated diene polymer in which a phenoxy group of a polar group-containing phenoxy compound is bonded to at least one selected from the group consisting of the end, main chain, and side chain of a conjugated diene polymer, which can further improve a rubber composition in the low-heat-generation property and abrasion resistance, and a rubber composition using the same.

Abstract: A method of production of modified conjugated diene rubber includes causing an aromatic compound having three or more carbon atoms directly bonded to an aromatic ring in one molecule to react with an alkali metal atom so as to obtain an alkali metal-reacted aromatic compound; polymerizing a monomer at least containing a conjugated diene compound by using the alkali metal-reacted aromatic compound so as to obtain a conjugated diene rubber having an active end; causing the active end of the conjugated diene rubber having an active end to react with an activity control agent so as to obtain a conjugated diene rubber reacted with an activity control agent; and causing the active end of the conjugated diene rubber reacted with an activity control agent to react with a modifier having an alkoxy group and a halogen atom-containing group so as to obtain a modified conjugated diene rubber.

Abstract: Disclosed are photoinitiators that are ultra violet (UV) reactive. The photoinitiators can be polymerized into polymeric backbones for use in UV curable hot melt pressure sensitive adhesives. The preferred polymeric backbones are acrylic-based polymers. The photoinitiators are very UVC sensitive and have excellent hot melt viscosity stability that is many fold higher than existing photoinitiators. The subject photoinitiators feature aryl ketones linked through an ether linkage to a variety of connector sequences that allow for polymerization of the photoinitiators.

Abstract: A photoinitiator includes a benzophenone moiety, a nitrogen-containing moiety covalently bonded to the benzophenone moiety, and an unsaturated polymerizable moiety covalently bonded to the nitrogen-containing moiety. The unsaturated polymerizable moiety includes an acrylate group or a methacrylate group.

Abstract: The present disclosure relates to tertiary amine co-initiators that demonstrate reduced leaching and which may be utilized in dental restoration and other biomedical applications. Embodiments of the present disclosure provide compounds and compositions for use in preparing polymers and light curable dental resin composites, as well as methods for preparing photocurable polymer-based dental restorative materials. In one or more disclosed embodiments, a co-initiator for use in preparing a polymer comprises a tertiary amine core and two or more pendant, terminal methacrylate groups. In some embodiments, the co-initiator may also act as a co-monomer in a co-polymerization reaction.

Abstract: A polymer compound has a group represented by Formula (1) or Formula (2) in a side chain. (In Formula (1), X1 represents a neutral amino acid residue or an ?-aminoalkanoic acid residue, X2 represents a membrane-permeable peptide residue, X3 represents a hydroxyl group, an amino group, an alkoxyl group having 1 to 4 carbon atoms, or a benzyloxy group, and a represents a number of from 1 to 50.) (In Formula (2), X4 represents a neutral amino acid residue or an ?-aminoalkanoic acid residue, X5 represents a membrane-permeable peptide residue, X6 represents a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, a benzyl group, an acyl group having 1 to 6 carbon atoms, an arylsulfonyl group, or a carboxyl group, and b represents a number of from 1 to 50.

Abstract: An olefin polymerization catalyst containing a complex of a ligand being a diimine compound represented by the formula (1) and at least one metal selected from the group consisting of Group 8 elements, Group 9 elements and Group 10 elements: wherein Ar1 and Ar2 are respectively a group represented by the formula (2): wherein R1 and R5 are respectively a hydrogen atom or a hydrocarbyl group having 1 to 5 carbon atoms, the total number of carbon atoms of R1 and R3 is 1 or more and 5 or less, and R2, R3 and R4 are respectively a hydrogen atom or an electron-donating group.

Abstract: A process for the continuous synthesis of diene elastomers with a high degree of conversion is provided. The process includes simultaneously: a) introducing continuously into a polymerisation reactor containing a gas phase and equipped with at least one stirring rotor and a discharge device, at least i. one or more monomers, including at least one conjugated diene monomer, and ii. from 0% to 70% by mass of an organic solvent, calculated relative to the total mass of monomers and of solvent, b) continuously polymerising the monomer(s), c) stirring the polymerisation medium via the continuous movement of at least one stirring rotor about a rotary axle, d) continuously discharging the elastomer paste, e) continuously conveying the discharged elastomer paste to a chopping device and chopping it into particles, f) removing solvent from the particles of the elastomer paste, and g) recovering diene elastomer.

Abstract: The present disclosure relates to a modified conjugated diene-based polymer having excellent affinity with a filler, a method for preparing the same, a rubber composition including the same and a tire manufactured using the rubber composition. The modified conjugated diene-based polymer according thereto has a tin-based compound-derived group bind on one end, and a silane-based compound-derived group bind on the other end, and therefore, may have excellent affinity with a carbon black-based filler as well as a silica-based filler. Accordingly, a rubber composition including the modified conjugated diene-based polymer may have excellent processability, and as a result, processed goods (for example, tires) manufactured using the rubber composition may have excellent tensile strength, wear resistance and viscoelastic property.

Abstract: The present invention relates to polyolefin powder for preparing fiber, and fiber comprising the same. According to the present invention, provided is polyolefin, which exhibits a high molecular weight range and narrow molecular weight distribution and in which the formation of a gel deteriorating the quality of fiber is reduced. Therefore, by using the polyolefin, the present invention exhibits molecular weight, density and narrow molecular weight distribution, which are equivalent to those of conventional polyolefin, but the number of gels having a large particle diameter is remarkably reduced, and therefore, the present invention can provide fiber having excellent tenacity and tensile strength half-life.

Abstract: The present invention relates to a vinyl chloride-based polymer which has improved thermal stability and a method for preparing the same. The vinyl chloride-based polymer includes silicate compound derived units, and a dehydrochloric acid (dehydrochlorination) reaction due to heat or ultraviolet rays may be suppressed, and thus, thermal stability may be improved, and discoloration and deformation of physical properties may be prevented. Accordingly, the vinyl chloride-based polymer and the method for preparing the same may be readily applied to industries requiring a vinyl chloride-based polymer, for example, industries related to a vinyl chloride-based resin and molded articles thereof.

Abstract: The low density polyethylene copolymer according to the present invention is characterized in that as LCB (Long Chain Branch) is introduced into LLDPE, the melt strength is remarkably high even without blending with LDPE, and thus it can be advantageously applied to blown film processing and the like.

Abstract: A polysulfide material having reactive vinyl end groups and a method of making a vinyl end-capped polysulfide material are described. The vinyl end-capped polysulfide material has potential applications as a sealant, an adhesive, a coating, a caulking, or the like. In a specific example, the polysulfide material may be used as a precursor material for a sealant resin in the manufacturing of an integral fuel tank of an aircraft. An example method for making polysulfide materials includes contacting a vinyl-functionalized aryl halide and/or a vinyl-functionalized heteroaryl halide with dithiols and/or trithiols in the presence of an organic solvent.

Abstract: An integrating sphere includes twelve pentagonal spherical shells and twenty hexagonal spherical shells. The hexagonal spherical shell includes a first circular spherical shell having a first diameter and six first auxiliary spherical shells formed by cutting the first circular spherical shell. The pentagonal spherical shell includes a first circular spherical shell having the first diameter and five second auxiliary spherical shell formed by cutting a second circular spherical shell having a second diameter.

Abstract: A copolymer having tetrafluoroethylene units, hexafluoropropylene units, and units independently represented by formula in a range from 0.001 to 2 mole percent, based on the total amount of the copolymer. In these units, a is 0 or 1, each b is independently from 1 to 4, c is 0 to 4, d is 0 or 1, and e is 1 to 6. In the —SO2X groups, X is independently —F, —NH2, —OH, or —OZ, wherein Z is independently a metallic cation or a quaternary ammonium cation. The copolymer has a melt flow index in a range from 20 grams per 10 minutes to 40 grams per 10 minutes. The copolymer can be extruded to make articles, such as insulated cables. A method of making the copolymer is also disclosed.

Abstract: The present invention is a composition comprising a stable aqueous dispersion of polymer particles comprising structural units of a phosphorus acid monomer or a salt thereof and structural units of a photoinitiator monomer. Gloss retention of paints containing the latex described herein is markedly improved over paints that do not have photoinitiator chemically bound to the latex particles.

Abstract: This disclosure provides a solvent-borne system for forming an n-acyl urea coating on a substrate. In one embodiment, the solvent-borne system comprises a polycarbodiimide-polyurethane hybrid. The solvent-borne system also comprises an acid functional polymer and an organic solvent, and comprises less than or equal to 10 weight percent of water based on a total weight of said solvent-borne system. The solvent-borne system also comprises less than about 100 parts by weight of toluene diisocyanate per one million parts by weight of the solvent-borne system.

Abstract: Co-distilling a mixture of para-phenylene diisocyanate (PPDI) and solvent, collecting the mixture of solvent and PPDI as a solution, reacting this solution with a polyol to form a prepolymer, and then removing unreacted PPDI by distillation in the presence of one or more solvents provides lower color prepolymer and higher quality polyurethane resin than a similar process that omits the co-distillation of PPDI and solvent prior to reaction with the polyol.

Abstract: The invention provides foam forming methods that comprise: (a) preparing a foamable system comprising at least one hydrohaloolefin; and (b) ensuring either (i) the substantial absence of long-term decomposition-inducing contact between said hydrofluoroolefin and an amine-containing catalyst; (ii) that an effective amount of surfactant is available in the system under conditions which prevent long term exposure of the surfactant to a long-term decomposition reaction environment; or (iii) a combination of (i) and (ii). Related methods, foamable systems and foams are also disclosed. Preferred embodiments provide polyurethane and polyisocyanurate foams and methods for the preparation thereof, including closed-celled, polyurethane and polyisocyanurate foams and methods for their preparation. The preferred foams are characterized by a fine uniform cell structure and little or no foam collapse.

Abstract: Partially crosslinked polyurethane polymers comprising diisocyanates and aliphatic hydrocarbon soft segments with a short-chain diol chain extender and a multifunctional amine and/or alcohol crosslinker to provide a polyurethane polymer with useful properties for the production of medical implant devices such as heart valves, are described. The polymers have an unexpected linear elastic region in a range from 5-100% and preferably between 10-35%. In some embodiments the polyurethanes are a thermally convertible gel formulation which may be converted to a liquid formulation by extended heating to render the polymer suitable for solvent processing techniques such as casting, spraying, spinning, etc. The invention also provides for living hinge polyurethane polymers which are thermally modifiable from a gel to a liquid and reaction injection moulded (RIM) polyurethanes with an enhanced flex life.

Abstract: Disclosed herein is a coating material system containing (A) at least one polyhydroxy group-containing compound, (B) at least one polyisocyanate-containing compound, and (C) at least one catalyst comprising lithium (Li) and bismuth (Bi) as metal components and where the molar ratio of lithium to bismuth is at least 7:1 [mol/mol], in which i) components (A), (B), and (C) are present separately from one another, or ii) are mixed wholly or at least partly with one another. Methods for producing and using the coating material system are also disclosed herein.

Abstract: Polycarbonate based polyurethane prepolymers having a low amount of free isocyanate monomer with excellent handling and processing properties are prepared and used in the preparation of cast polyurethane polymers with excellent performance and handling properties.

Abstract: Transparent, impact-resistant, anti-icing coatings are disclosed. In some variations, a transparent anti-icing coating comprises: a continuous matrix of a hardened material; asymmetric templates that inhibit wetting of water, wherein the asymmetric templates have a length scale from about 10-300 nanometers; porous voids surrounding the asymmetric templates, wherein the porous voids have a length scale from about 15-500 nanometers; and nanoparticles that inhibit heterogeneous nucleation of water, wherein the nanoparticles have an average size from about 5-50 nanometers. Disclosed coatings have transparencies of 90% or higher light transmission. These coatings utilize lightweight and environmentally benign materials that can be rapidly formed into coatings. A uniform distribution of particles and asymmetric templates throughout the coating allows it to be abraded, yet retain its anti-icing function as well as transparency.

Abstract: A binder dispersion includes water and polyurethane. The polyurethane is formed from polyisocyanate; polyol having two hydroxyl (OH) groups at one chain end, no OH groups at an opposed chain end, and a number average molecular weight (Mn) ranging from ˜500-˜5,000; an alcohol, diol or amine having a Mn<500; and one of i) a carboxylic acid; ii) a sulfonate or sulfonic acid having one amino group; iii) i and ii; iv) i and a homopolymer or copolymer of poly(ethylene glycol) (PEG) having one or two OH or amino groups at one chain end; v) ii and a homopolymer or copolymer of PEG having one or two OH or amino groups at one chain end; or vi) i, ii, and a homopolymer or copolymer of PEG having one or two OH or amino groups at one chain end.

Abstract: The present invention relates to functional polyurethane which can be widely used in preparation of foams, elastomers, adhesives, coating materials, sealants, etc., and its preparation method and use.

Abstract: The present invention provides a polyisocyanate composition comprising a modified polyisocyanate obtained by a reaction between a polyisocyanate and a polyalkylene glycol alkyl ether having a specific structure. In the polyisocyanate composition, the average number of isocyanate functional groups is 1.8 or more and 4.0 or less, the moiety derived from the polyalkylene glycol alkyl ether in the modified polyisocyanate is contained in an amount of 10 mass % or more and 18 mass % or less based on the total amount of the polyisocyanate composition, and the polydispersity index of molecular weight distribution of the moiety derived from the polyalkylene glycol alkyl ether in the modified polyisocyanate is 1.05 or more and 2.00 or less.

Abstract: The present invention relates to an epoxy resin composition, comprising the following components: (A) an epoxy resin containing oxazolidinone structure having the structure of the formula (1), (B) an active ester curing agent, and (C) a curing accelerator. The epoxy composition, prepreg, laminate and printed circuit board prepared from such epoxy composition have the following features of low coefficient of thermal expansion, low dielectric loss factor Df less than or equal to 0.0084, low water absorption and excellent moisture and heat resistance.

Abstract: An adhesive material which comprises an epoxy component including a first flame retardant and a curing component which includes an adhesion promoter and a second flame retardant The epoxy component and curing component are present in a ratio of about 1:1 and the adhesive is formed when the epoxy component is combined with the curing component

Abstract: A water-based primer composition is particularly suitable for the pre-treatment of polycarbonate substrates, and has a component K1 having an aqueous epoxy resin dispersion, an aqueous polyester-polyurethane dispersion and an aqueous polyacrylate dispersion, and optionally a water-miscible organic solvent, and a second component K2 containing a water-dispersible curing agent based on isocyanate. The primers provide a strong bonding of subsequently applied adhesives to polycarbonate substrates, and permit a processing with a significant reduction in VOC emissions and the prevention of the occurrence of stress-cracks.

Abstract: Degradable polycarbonates network based bulk materials are provided. The bulk materials of the present disclosure may be produced having a wide range of tunable mechanical, physical, and thermal properties and are hydrolytically degradable. The bulk materials of the present disclosure may be suitable for the manufacture of a variety of sport fishing equipment or other equipment for water use or that may benefit from hydrolytic degradation in the environment.

Abstract: The present invention is a polyether-based polymer composition includes: a polyether-based polymer including an oxirane monomer unit and having one cationic group substantially only at one terminal of a polymer chain, and a nanocarbon material. The polyether-based polymer composition of the present invention can be suitably used, for example, as a bucky gel or as a master batch for preparing a nanocarbon material aqueous dispersion in which a nanocarbon material is favorably dispersed.

Abstract: The present invention provides specific alkoxylation products, a process for preparing them, compositions comprising these alkoxylation products, and their use. In particular the present invention provides an alkoxylation product comprising at least one non-terminal alkoxysilyl group, formed from monomers of at least one alkylene oxide and at least one epoxide bearing alkoxysilyl groups, wherein at least 30% of all the free OH groups on the chain end of the alkoxylation product have been converted to acetoacetate groups.

Abstract: The present disclosure is drawn to polymeric amine synergists, photo curable inks containing the polymeric amine synergists, and methods of making the photo curable inks. A polymeric amine synergist can include an aminobenzene modified with a polyether chain connecting to the aminobenzene through an amide linkage.

Abstract: The polyamide resin of the present invention is a polymer of a monomer mixture including a dicarboxylic acid and an amine-based compound, wherein the amine-based compound comprises diamine and triamine and a branching rate measured using 1H—NMR is approximately 1% to approximately 8%.

Abstract: Disclosed herein is a friable polyimide powder having a weight average molecular weight, as determined by gel permeation chromatography (GPC) using polystyrene standards, of less than or equal to 24,500 Daltons and a reactive aromatic amine end group concentration greater than or equal to 3 mole percent, wherein 90 weight percent of the powder particles are reducible to less than or equal to 75 micrometers by mechanical grinding. Also disclosed is a method of making the friable polyimide powder, a processed polyimide resulting from the friable polyimide powder and compositions comprising the processed polyimide.

Abstract: The present invention relates to the field of perfumery. More particularly, it concerns co-polymers, derived from aspartic acid and comprising at least one ?- or ?-aspartic acid derivative capable of liberating an active molecule such as, for example, an ?,?-unsaturated ketone or aldehyde. The present invention concerns also the use of polymers or co-polymers in perfumery as part of a perfuming or malodor counteracting composition, as well as the perfuming compositions or perfumed articles comprising the invention's compounds.

Abstract: The present invention provides a polyorganosiloxane compound having a low viscosity, a process for the manufacture of such polyorganosiloxane compounds, polyorganosiloxane compositions comprising said polyorganosiloxane compound and another polyorganosiloxane compound which is different from the polyorganosiloxane compound, aqueous emulsions comprising the polyorganosiloxane compound, and a method of surface treatment using the polyorganosiloxane compound.

Abstract: The invention relates to a crosslinkable composition X, comprising: at least one organopolysiloxane compound A comprising, per molecule, at least two C2-C6 alkenyl radicals bonded to silicon atoms; at least one organohydrogenopolysiloxane compound B comprising, per molecule, at least two hydrogen atoms bonded to an identical or different silicon atom; at least one catalyst C which is a complex corresponding to the following formula: [Co(L1)2] in which: the symbol Co represents cobalt at degree of oxidation II; the symbols L1, which may be identical or different, represent a ligand which is a ?-dicarbonylato anion or the enolate anion of a ?-dicarbonylated compound; optionally at least one adhesion promoter D; and optionally at least one charge E.