Abstract Hepatitis associated antigen is removed from plasma and plasma fractions by admixing the plasma with ethylene oxide-propylene glycol condensation product at a temperature of from about 0° to 39° centigrade. Under these conditions a precipitate is formed. The concentration of condensation product is adjusted so that all of the hepatitis associated antigen remains either in the precipitate or the liquid phase. Separation of the resultant liquid and solid phases produces a liquid phase which is entirely free of the undesired antigen. The concentration of condensation product which is required to cause complete precipitation of hepatitis associated antigen increases with increasing temperature from a value of about 9 percent, on a weight per volume basis, at about 0° centigrades to a value of about 28 percent at about 39° centigrade. All of the hepatitis associated antigen remains in the liquid phase at condensation product concentrations of less than about 7 percent at about 9° centigrade and about 15 percent at about 39° centigrade. At intermediate concentrations hepatitis associated antigen appears in both phases.
Process for separating hepatitis associated antigen from certain desired blood plasma fractions comprising: preparing an aqueous admixture including the desired blood plasma fraction and from about 2 to 7 weight per volume percent of a block copolymer of ethylene oxide and polyoxypropylene polymer at a temperature of approximately 22 degrees centigrade and a pH of from about 6.5 to 7.5 to form a precipitate in said admixture; separating said precipitate from said admixture; and retaining said precipitate for beneficial use.
Claim 2
Dependent Claim
80 words
Process for separating hepatitis associated antigen from certain desired blood plasma fractions comprising: preparing an aqueous admixture including the desired blood plasma fraction and from about 2 to 7 weight per volume percent of a block copolymer of ethylene oxide and polyoxypropylene polymer at a temperature of approximately 22 degrees centigrade and a pH of from about 6.5 to 7.5 to form a precipitate in said admixture; separating said precipitate from said admixture; and retaining said precipitate for beneficial use.
Claim 3
Dependent Claim
36 words
Process of claim 1 wherein said temperature is adjusted to a value of about 20 degrees centigrade and the concentration of said block copolymer is adjusted to a value of about 2 weight per volume percent.
Claim 4
Dependent Claim
12 words
Process of claim 1 including selecting a concentrated aqueous blood plasma composition.
Claim 5
Dependent Claim
94 words
Process for removing hepatitis associated antigen from blood plasma comprising: selecting a quantity of said blood plasma; adjusting the pH of said quantity of blood plasma to a value of from about 6.5 to 7.5; adjusting the temperature of said quantity of blood plasma to a value of approximately 22° centigrade; admixing said quantity of blood plasma with from about 2 to 7 weight per volume percent of a block copolymer of ethylene oxide and polyoxypropylene polymer; separating the resultant liquid and solid phases; and recovering the resultant hepatitis associated antigen free solid phase.
Claim 6
Dependent Claim
94 words
Process for removing hepatitis associated antigen from blood plasma comprising: selecting a quantity of said blood plasma; adjusting the pH of said quantity of blood plasma to a value of from about 6.5 to 7.5; adjusting the temperature of said quantity of blood plasma to a value of approximately 22° centigrade; admixing said quantity of blood plasma with from about 2 to 7 weight per volume percent of a block copolymer of ethylene oxide and polyoxypropylene polymer; separating the resultant liquid and solid phases; and recovering the resultant hepatitis associated antigen free solid phase.