Disclosed are a blood filter which exhibits excellent leukocyte elimination performance as well as significantly improved blood throughput per unit time and erythrocyte recovery rate and a method of manufacturing the same. The blood filter of the present invention includes a pre-treatment filter which is a laminate of first non-woven fabrics having a mean fiber diameter of 5 to 30 μm and a mean pore size of 10 to 30 μm, and a main filter which is a laminate of second non-woven fabrics having a mean fiber diameter of 1 to 5 μm, a mean pore size of 5 to 10 μm and a mean pore size distribution rate of 30% or more. A filling density of the pre-treatment filter and a filling density of the main filter, with respect to a target blood throughput of the blood filter, are 0.1 g/100 ml to 1 g/100 ml and 1 g/100 ml to 3 g/100 ml, respectively.

Disclosed are a blood filter which exhibits excellent leukocyte elimination performance as well as significantly improved blood throughput per unit time and erythrocyte recovery rate and a method of manufacturing the same. The blood filter of the present invention includes a pre-treatment filter which is a laminate of first non-woven fabrics having a mean fiber diameter of 5 to 30 μm and a mean pore size of 10 to 30 μm, and a main filter which is a laminate of second non-woven fabrics having a mean fiber diameter of 1 to 5 μm, a mean pore size of 5 to 10 μm and a mean pore size distribution rate of 30% or more. A filling density of the pre-treatment filter and a filling density of the main filter, with respect to a target blood throughput of the blood filter, are 0.1 g/100 ml to 1 g/100 ml and 1 g/100 ml to 3 g/100 ml, respectively.

A polyphenylene sulfide monofilament is characterized by having a continuous heat-shrinking stress variation of at most 5% and a size uniformity (U %, Normal value) of at most 1.2%; and a drum-shaped fiber package includes the wound polyphenylene sulfide monofilament described. The polyphenylene sulfide monofilament has a very small aperture variation rate and is optimal for high-precision filters.

Nonwoven fabrics having a plurality of fibers that are bonded to each other to form a coherent web, wherein the fibers comprise a blend of a polylactic acid (PLA) and at least one secondary alkane sulfonate are provided. The nonwoven fabrics exhibit increased tensile strengths, elongation and toughness.

Nonwoven fabrics having a plurality of fibers that are bonded to each other to form a coherent web, wherein the fibers comprise a blend of a polylactic acid (PLA) and at least one secondary alkane sulfonate are provided. The nonwoven fabrics exhibit increased tensile strengths, elongation and toughness.

Provided is a method of manufacturing fiber with aligned porous structure, an apparatus, and applications of the fiber. The apparatus comprises: a fiber extrusion unit, a freezing unit, and a collection unit for collecting the frozen fibers, wherein fibers extruded from the fiber extrusion unit pass through the freezing unit. Continuous and large scale preparation of such fiber with aligned porous structure is achieved by combining directional freezing and solution spinning.

The present disclosure relates to methods and systems for manufacturing rotational spun materials. The rotational spun materials are medical appliances or other prostheses made of, constructed from, covered or coated with rotational spun materials, such as polytetrafluoroethylene (PTFE).

The present disclosure relates to methods and systems for manufacturing rotational spun materials. The rotational spun materials are medical appliances or other prostheses made of, constructed from, covered or coated with rotational spun materials, such as polytetrafluoroethylene (PTFE).

Provided is a dental cord using a nanofiber multiple yarn having a large specific surface area and a large number of three-dimensional pores, thereby effectively impregnating a drug such as a hemostatic agent, and a method of manufacturing the dental cord. The dental cord includes: a nanofiber multiple yarn which is obtained by plying and twisting at least two nanofiber tape yarns and which is impregnated with a drug, wherein the at least two nanofiber tape yarns are integrated by nanofibers made of fiber moldability polymer materials and having an average diameter of less than 1 μm, to thus be formed of a nanofiber web having three-dimensional micropores.

Provided is a dental cord using a nanofiber multiple yarn having a large specific surface area and a large number of three-dimensional pores, thereby effectively impregnating a drug such as a hemostatic agent, and a method of manufacturing the dental cord. The dental cord includes: a nanofiber multiple yarn which is obtained by plying and twisting at least two nanofiber tape yarns and which is impregnated with a drug, wherein the at least two nanofiber tape yarns are integrated by nanofibers made of fiber moldability polymer materials and having an average diameter of less than 1 μm, to thus be formed of a nanofiber web having three-dimensional micropores.