The invention relates to a method for predicting or diagnosing a risk of bioprosthetic valve degeneration. Further, the invention relates to a medical device, in particular a bioprosthetic valve coated with EPCR less prone to degeneration and/or calcification once implanted.

Particulate binder compositions and methods for making and using same are provided. The binder composition for producing composite lignocellulose products can include an aldehyde based resin and a filler, an extender, or a combination thereof. The binder composition can be in the form of particulates. The particulates can each comprises the filler, the extender, or the combination thereof and the aldehyde based resin.

Particulate binder compositions and methods for making and using same are provided. The binder composition for producing composite lignocellulose products can include an aldehyde based resin and a filler, an extender, or a combination thereof. The binder composition can be in the form of particulates. The particulates can each comprises the filler, the extender, or the combination thereof and the aldehyde based resin.

A method for producing a biodegradable floral arrangement media that includes obtaining a pre-formed mixture by mixing together: (a) a matrix of natural or inert inorganic fibers and/or powders; (b) a water insoluble, meltable compostable binder; and (c) optionally, additives; and heating the pre-formed mixture to fuse the binder with the matrix. Also, a biodegradable floral arrangement media made by the process, which is preferably compostable.

A method for producing a biodegradable floral arrangement media that includes obtaining a pre-formed mixture by mixing together: (a) a matrix of natural or inert inorganic fibers and/or powders; (b) a water insoluble, meltable compostable binder; and (c) optionally, additives; and heating the pre-formed mixture to fuse the binder with the matrix. Also, a biodegradable floral arrangement media made by the process, which is preferably compostable.

The present disclosure provides methods of preparing heteroaryl-containing compounds, wherein an azide-alkyne cycloaddition is accelerated in the presence of lauryldimethylamine oxide (LDAO). The present disclosure further provides conjugates of polypeptides and antigens prepared using such methods.

A process for producing a thermoplastic material for use as powder or slurry for further processing such as injection molding or coating, comprising the steps of mixing a biomass containing prolamins, such as a grain source or a water insoluble fraction of a grain, having prolamins and lipids, and an organic solvent to obtain undissolved components and dissolved components comprising dissolved prolamin, lipids and other dissolved components, extracting the dissolved components into a first liquid and extracting undissolved components in a first solid under the specific conditions. separating the first solid from the first liquid, recovering the thermoplastic material from the first liquid as powder by removing organic solvent under the conditions of maintaining temperature of the prolamins below 80° C., preferably below 75° C., maintaining a dielectric constant εr between 30 and 42 at 25° C., and maintaining a pressure level at below 2 bar.

A process for producing a thermoplastic material for use as powder or slurry for further processing such as injection molding or coating, comprising the steps of mixing a biomass containing prolamins, such as a grain source or a water insoluble fraction of a grain, having prolamins and lipids, and an organic solvent to obtain undissolved components and dissolved components comprising dissolved prolamin, lipids and other dissolved components, extracting the dissolved components into a first liquid and extracting undissolved components in a first solid under the specific conditions. separating the first solid from the first liquid, recovering the thermoplastic material from the first liquid as powder by removing organic solvent under the conditions of maintaining temperature of the prolamins below 80° C., preferably below 75° C., maintaining a dielectric constant εr between 30 and 42 at 25° C., and maintaining a pressure level at below 2 bar.

The present invention refers to a process for preparing a biomaterial scaffold said method comprising, (a) providing a hydrogel comprising a fibrin network and a polysaccharide network; (b) subjecting the hydrogel of step a) to a freeze-thawing process to physically crosslink the hydrogel; and (c) subjecting the physically cross-linked hydrogel obtained after conducting the step b), to a lyophilization. The invention also relates to the biomaterial scaffold obtainable by the process as defined above, as well said biomaterial scaffold for its use to partially or completely increase, restore or replace the functional activity of a diseased or damaged oral mucosa.

The present invention refers to a process for preparing a biomaterial scaffold said method comprising, (a) providing a hydrogel comprising a fibrin network and a polysaccharide network; (b) subjecting the hydrogel of step a) to a freeze-thawing process to physically crosslink the hydrogel; and (c) subjecting the physically cross-linked hydrogel obtained after conducting the step b), to a lyophilization. The invention also relates to the biomaterial scaffold obtainable by the process as defined above, as well said biomaterial scaffold for its use to partially or completely increase, restore or replace the functional activity of a diseased or damaged oral mucosa.