This disclosure relates to pectin-based polymer compositions and methods of use thereof to cover, protect, and seal injuries, e.g., surgical wounds, in a mesothelial tissue. The methods include obtaining a bioadhesive pectin-based polymer composition including a complex of high-methoxyl pectin (HMP) and carboxymethylcellulose (CMC) in a ratio from about 10 to 1 to 1 to 10 by weight; applying the composition to an injured mesothelial tissue; and applying pressure for at least one minute to enable the composition to bind to the mesothelial tissue.

Paste compositions for additive manufacturing and methods for the same are provided. The paste composition may include an organic vehicle, and one or more powders dispersed in the organic vehicle. The organic vehicle may include a solvent, a polymeric binder, a thixotropic additive, and a dispersant. The organic vehicle may be configured to provide the paste composition with a suitable viscosity. The organic vehicle may also be configured to provide a stable paste composition for a predetermined period of time.

The present solution can temporarily impart the handling characteristics of corneal stroma to the otherwise very thin, flimsy, coiling, and fragile Descemet membrane endothelial keratoplasty (DMEK) tissue during its insertion into the anterior chamber and positioning in apposition against the cornea of the recipient eye. The device of the present solution can be configured in a number of ways. In a first configuration, a scaffold can be coupled with the endothelial side of the DMEK graft. In a second configuration, the scaffold can be coupled with the stromal side of the DMEK graft. In a third configuration, one or more scaffolds can be coupled with both the endothelial and stromal side of the DMEK graft.

The present solution can temporarily impart the handling characteristics of corneal stroma to the otherwise very thin, flimsy, coiling, and fragile Descemet membrane endothelial keratoplasty (DMEK) tissue during its insertion into the anterior chamber and positioning in apposition against the cornea of the recipient eye. The device of the present solution can be configured in a number of ways. In a first configuration, a scaffold can be coupled with the endothelial side of the DMEK graft. In a second configuration, the scaffold can be coupled with the stromal side of the DMEK graft. In a third configuration, one or more scaffolds can be coupled with both the endothelial and stromal side of the DMEK graft.

Dry solids of anionically modified cellulose nanofibers with good redispersion are provided by incorporating 5 to 300% by mass of a water-soluble polymer relative to the anionically modified cellulose nanofibers during the preparation of the dry solids of anionically modified cellulose nanofibers.

Dry solids of anionically modified cellulose nanofibers with good redispersion are provided by incorporating 5 to 300% by mass of a water-soluble polymer relative to the anionically modified cellulose nanofibers during the preparation of the dry solids of anionically modified cellulose nanofibers.

A double-layered medical membrane and a method for manufacturing the same are provided. The double-layered medical membrane includes a hydrophilic material layer and a hydrophobic material layer disposed thereon. The hydrophilic material layer includes hydrophilic fibers, hydrophilic particles, or a combination thereof. The hydrophilic fibers and the hydrophilic particles include a hydrophilic polymer as a material. The method includes the following steps: using an electrospinning solution to form the hydrophilic material layer by electrospinning or using a hydrophilic solution to form the hydrophilic material layer; and producing the double-layered medical membrane that includes the hydrophilic material layer. The hydrophilic material layer includes the hydrophilic fibers, the hydrophilic particles, or the combination thereof. The hydrophilic fibers or the hydrophilic particles include the hydrophilic polymer as a material.

A double-layered medical membrane and a method for manufacturing the same are provided. The double-layered medical membrane includes a hydrophilic material layer and a hydrophobic material layer disposed thereon. The hydrophilic material layer includes hydrophilic fibers, hydrophilic particles, or a combination thereof. The hydrophilic fibers and the hydrophilic particles include a hydrophilic polymer as a material. The method includes the following steps: using an electrospinning solution to form the hydrophilic material layer by electrospinning or using a hydrophilic solution to form the hydrophilic material layer; and producing the double-layered medical membrane that includes the hydrophilic material layer. The hydrophilic material layer includes the hydrophilic fibers, the hydrophilic particles, or the combination thereof. The hydrophilic fibers or the hydrophilic particles include the hydrophilic polymer as a material.

The present invention relates to a method for preparing a superabsorbent polymer, and a superabsorbent polymer prepared thereby. A superabsorbent polymer prepared by the preparation method exhibits minimized deterioration of physical properties after being pulverized, and thus basic absorbance performance is excellent and an excellent liquid permeability and absorbance rate can be exhibited.

The present invention relates to a method for preparing a superabsorbent polymer, and a superabsorbent polymer prepared thereby. A superabsorbent polymer prepared by the preparation method exhibits minimized deterioration of physical properties after being pulverized, and thus basic absorbance performance is excellent and an excellent liquid permeability and absorbance rate can be exhibited.