The invention discloses a method for improving triboelectric output performance of a protein film by changing a protein structure. Indissolvable protein powder and a trace amount of another protein powder are co-dissolved in a strong alkaline aqueous solution and maintained for a period of time, and then acidifying treatment is performed to achieve neutral condition to allow charge redistribution to induce refolding of the protein, which results in burying of hydrophobic groups of the protein and exposure of charged groups. Therefore, the solubility of the protein is remarkably improved, and a uniform protein solution is formed under a neutral condition. The plant protein structure is changed through a pH cycle process, a surface group exposure condition is adjusted, and the output performance of the plant protein film is greatly improved.

A method for making a silk protein film includes providing an aqueous solution of a silk protein, and annealing a mixture including the aqueous solution of the silk protein and a water-soluble polyhydroxy compound that is present in an amount ranging from 20 wt % to 60 wt % based on a total amount of the silk protein and the water-soluble polyhydroxy compound at an annealing temperature that is higher than 50° C. and lower than 180° C. and under a relative humidity of not higher than 30%, so as to form the silk protein film.

Embodiments of the present invention provide users with a system and method for manufacturing water-based hydrophobic aerogels and aerogel composites. The system and method can be carried out in a manner which is more rapid than typical ways and can be readily scalable. The method of manufacture is useful for producing water based hydrophobic aerogels and aerogel composites on a large scale with good homogeneity and consistency. Advantageously, the method of manufacture also has the benefit of a shorter processing time due to the vacuum homogenizing and mixing processes, the use of microwave assisted vacuum freeze drying for ease of synthesis of water-based hydrophobic aerogels.

We have developed novel shear-thinning biomaterials using silica nanoparticles, gelatin-based polymers and polypeptides such as anti-PD-1 antibodies. Shear-thinning biomaterial technology offers enables polymers and drugs loaded inside such polymers to be easily delivered directly through catheters into target area for use, for example, in cancer therapy and immunotherapy. When a force above a certain threshold is applied to inject such materials, they “thin” and behaves as a semi-solid, allowing the material to readily flow through a catheter. When the force is removed, the material instantly becomes a soft solid with significant cohesive properties that prevent it from dislodging or breaking up.

Disclosed a preparation method of a green, biodegradable, and multifunctional collagen-based nanocomposite film, and overcomes the problems of difficult biodegradation, poor barrier property, and single function of food packaging materials in the existing technologies. The present invention includes the following steps: adding silicate nanosheet into deionized water for ultrasonic dispersion; then adding polyphenolic acid into the mixture, wherein a mass ratio of the polyphenolic acid to the silicate nanosheet is 1:(0.2˜1); and adjusting the pH value to 3.0˜4.0 to obtain a solution A; adding collagen with a concentration of 5 g/L into an acetic acid solution, and fully dissolving the collagen to obtain a solution B; isovolumetrically mixing the solution A with the solution B, stirring at room temperature, and adjusting the pH value to 4.5˜5.5 to obtain a casting solution; and pouring the casting solution into a polytetrafluoroethylene mold, and naturally drying to obtain a nanocomposite film.

Biocompatible phase invertible proteinaceous compositions and methods for making and using the same are provided. The subject phase invertible compositions are prepared by combining a crosslinker and a proteinaceous substrate. The proteinaceous substrate includes one or more proteins and a polyamine, where the polyamine and a proteinaceous substrate are present in synergistic viscosity enhancing amounts, and may also include one or more of: a carbohydrate, a tackifying agent, a plasticizer, or other modification agent. In certain embodiments, the crosslinker is a heat-treated dialdehyde, e.g., heat-treated glutaraldehyde. Also provided are kits for use in preparing the subject compositions. The subject compositions, kits and systems find use in a variety of different applications.

Provided herein is a method for preparing microcarrier particles, comprising the steps of allowing the dispersed phase liquid flow through a multi-hole plate at a low temperature to form liquid microspheres in a continuous phase, and enabling a synthetic polymer and/or natural biological macromolecules within the liquid microspheres to be subject to a curing reaction at a low temperature to form particles. Further provided herein are the method for preparing an emulsion and an apparatus and process system for preparing microcarrier particles, which can be used for preparing emulsions and microcarrier particles on a large scale.

An aspect of the present disclosure provides a synthetic polymer containing a first segment containing a polypeptide skeleton and one or a plurality of second segments bonded directly to the first segment, in which the second segment contains a molecular group having a plasticizing function for the polypeptide skeleton.

The invention relates to a method for providing control data of a laser device (10) for the non-destructive laser-induced property change of a polymer structure (14). As steps, the method includes ascertaining (S10) a respective irradiation parameter range for preset irradiation parameters of the laser device (10) by means of an irradiation model, wherein a property change model is provided in the irradiation model, in which a caused property change of the polymer structure (14) is modelled depending on the irradiation parameters, wherein a destruction threshold value model is provided in the irradiation model, in which at least one threshold value for a laser-induced optical breakthrough of the polymer structure is modelled depending on the irradiation parameters, and wherein the caused property change from the property change model is optimized while limiting by the threshold value from the destruction threshold value model for ascertaining the irradiation parameter ranges.

A method is disclosed for controlling a laser device for a laser-induced refractive index change (URIC) of a polymer structure. The laser device is controlled by a control device such that it emits pulsed laser pulses in a shot sequence in a preset pattern into the polymer structure. The laser pulses are emitted with preset irradiation parameters for refractive index change of the polymer structure, wherein for adjusting an order of magnitude of the refractive index change, a spatial pulse distance of the laser pulses in the polymer structure is adapted and the further irradiation parameters are kept within respective preset irradiation parameter ranges.