Process for the selective extracorporeal separation of blood constituents

Claim 2

A process for the selective exteracorporeal separation of precipitates of macromolecular pathologic or toxic species from blood having serum and plasma constituents, which comprises passing the serum or plasma through a housing comprising a filter candle defining a filter body and further defining a filtering means having an inner core, said filtration means longitudinally disposed therein and providing for the collection of filtrate and the exclusion of precipitate, said housing further having an inlet and outlet in communication with said filter body and said filtering means having an effective filter surface in the range of from about 0.2 to about 2 square meters, a length in the range of from about 10 to about 60 cm, and a means pore diameter in the range of from about 0.2 to about 2 micron.

Claim 3

The process of claim 1, wherein said filter candle has an effective filter surface in the range of from about 0.8 to about 1.7 square meters, a length in the range of from about 10 to about 50 cm, and a mean pore diameter in the range of from about 0.4 to about 1 micron.

Claim 4

The process of claim 1, wherein said housing is made of plastic or glass.

Claim 5

A process for the selective extracorporeal separation of precipitates of macromolecular pathologic or toxic species from a plasma fraction which has been produced by a filter or the last filter of a cascade of several filters with molecular exclusion limits of 50,000 to 3,000,000 Dalton continuously from patient blood or fractions thereof, and which plasma fraction contains precipitates of macromolecular pathologic or toxic species, which process comprises introducing said plasma fraction at atmospheric pressure through a housing comprising a filter candle, said filter candle comprising a permeable filtration means having an inner core, said filtration means longitudinally disposed within a filter body defined by said filter candle, and is installed in a closed extracorporeal circulation system, whereby said plasma fraction sweeps said filtration means externally and plasma purified by filtering passes into said core, said precipitates being prevented from entering into said core and said purified plasma from said core is returned to a patient.

Claim 6

A process for the selective extracorporeal separation of precipitates of macromolecular pathologic or toxic species from a plasma fraction which has been produced by a filter or the last filter of a cascade of several filters with molecular exclusion limits of 50,000 to 3,000,000 Dalton continuously from patient blood or fractions thereof, and which plasma fraction contains precipitates of macromolecular pathologic or toxic species, which process comprises introducing said plasma fraction at atmospheric pressure through a housing comprising a filter candle, said filter candle comprising a permeable filtration means having an inner core, said filtration means longitudinally disposed within a filter body defined by said filter candle, and is installed in a closed extracorporeal circulation system, whereby said plasma fraction sweeps said filtration means externally and plasma purified by filtering passes into said core, said precipitates being prevented from entering into said core and said purified plasma from said core is returned to a patient.

Claim 7

The process of claim 4, which also comprises removing excess reagents from said purified plasma or adjusting the temperature thereof prior to returning said purified plasma to said patient.

Claim 8

The process of claim 4, which also comprises maintaining said plasma at body temperature in a cylindrical housing fabricated from plastic or glass.

Claim 9

The process of claim 4, which also comprises maintaining said plasma during filtration at temperatures in the range of from below body temperature to about 4° C.

Claim 10

The process of claim 4, which also comprises maintaining said plasma during filtration at temperatures from above body temperature to about 60° C.

Claim 11

The process of claim 4, wherein said filtering means has an effective filtering surface in the range of from about 0.2 to about 2 square meters, a length in the range of from about 10 to about 60 cm, and a mean pore diameter in the range of about 0.2 to about 2 micron.

Claim 12

The process of claim 4, wherein any portion of the plasma which is not filtered off by gravity is conducted out of said housing and is recirculated to the stream of fresh plasma being introduced into said housing.

Claim 13

A process for the selective exteracorporeal separation of precipitates of macromolecular pathological and toxic species from blood having serum and plasma constituents which comprises passing the serum or plasma through a housing having an inlet and outlet comprising a filter candle defining a filter body in communication with said inlet and further defining a permeable filtering means having an inner core in communication with the outlet longitudinally disposed within said filter body and having pores which exclude the precipitates from entering the inner core, and through which filter body the serum or plasma is passed such that the serum or plasma enters one end of the filter body through the inlet and contacts the filtering means through which is passed filtrate from the plasma or serum, excluding the precipitate.

Claim 14

A process for the selective exteracorporeal separation of precipitates of macromolecular pathological and toxic species from blood having serum and plasma constituents which comprises passing the serum or plasma through a housing having an inlet and outlet comprising a filter candle defining a filter body in communication with said inlet and further defining a permeable filtering means having an inner core in communication with the outlet longitudinally disposed within said filter body and having pores which exclude the precipitates from entering the inner core, and through which filter body the serum or plasma is passed such that the serum or plasma enters one end of the filter body through the inlet and contacts the filtering means through which is passed filtrate from the plasma or serum, excluding the precipitate.

Claim 15

The process according to claim 11, wherein the filtering means has an effective filter surface in the range of from about 0.2 to about 2 square meters, a length in the range of from about 10 to about 60 cm, a mean pore diameter in the range of from about 0.2 to about 2 microns.

Claim 16

The process according to claim 11, wherein the filtering means has an effective filter surface in the range of from about 0.8 to about 1.7 square meters, a length in the range of from about 10 to about 50 cm, and a mean pore diameter in the range of from about 0.4 to about 1 micron.

Claim 17

The process according to claim 11, wherein the volumes of the filtering means with its inner core and the filter body approximately equal the volume of the cylindrical housing in which they are disposed, and the filtering means is centrally disposed within the filter body.

Claim 18

The process according to claim 11, wherein the housing defines an additional outlet in communication with the filter body for the passage of precipitate and a portion of the serum or plasma not passed not passed through the filtering means

Claim 19

The process according to claim 11, wherein the filter body and filtering means are the same length as each other and the cylindrical housing.

Claim 20

The process according to claim 11, wherein the process is conducted at the ambient atmospheric pressure, without the need for applying a pressure differential across the permeable filtering means.

Claim 21

The process according to claim 11, wherein the macromolecular pathological and toxic species is beta-lipoprotein.

Claim 22

A process for the selective exteracorporeal separation of precipitates of beta-lipoprotein from blood having serum and plasma constituents which comprises passing the serum or plasma through a filter candle disposed in a substantially cylindrical housing, said filter candle comprising a selectively permeable filtering means having an inner core in communication with a filtrate outlet and having a mean pore diameter in the range of about 0.2 to about 2 microns and an effective filtering surface in the range of about 0.2 to 2 square meters and which is longitudinally disposed within a filter body having an inlet and an outlet, through which filter body the serum or plasma is passed such that the serum or plasma enters one end of the filter body through the inlet and contacts the filtering means through which is passed filtrate excluding the precipitate, and the remainder of the plasma or serum, including the precipitate, is permitted to exit the filter body at the outlet thereof.

Claim 23

A process for the selective exteracorporeal separation of precipitates of beta-lipoprotein from blood having serum and plasma constituents which comprises passing the serum or plasma through a filter candle disposed in a substantially cylindrical housing, said filter candle comprising a selectively permeable filtering means having an inner core in communication with a filtrate outlet and having a mean pore diameter in the range of about 0.2 to about 2 microns and an effective filtering surface in the range of about 0.2 to 2 square meters and which is longitudinally disposed within a filter body having an inlet and an outlet, through which filter body the serum or plasma is passed such that the serum or plasma enters one end of the filter body through the inlet and contacts the filtering means through which is passed filtrate excluding the precipitate, and the remainder of the plasma or serum, including the precipitate, is permitted to exit the filter body at the outlet thereof.