Purification of monoclonal antibodies

Claim 1

A method of obtaining essentially homongeneous monoclonal antibody type IgG from a sample of mouse ascites fluid containing said monoclonal antibody which comprises separating and recovering said monoclonal antibody from said sample by employing liquid chromatographic means wherein the chromatographic packing consists essentially of particulate silica gel having an average particle diameter of from about 3 to about 40 microns and an average pore size of from about 50 to about 1000 Angstrom units to which polyethylenimine functions are bound in covalently bound non-crosslinked form or in adsorbed crosslinked form.

Claim 2

A method of obtaining essentially homongeneous monoclonal antibody type IgG from a sample of mouse ascites fluid containing said monoclonal antibody which comprises separating and recovering said monoclonal antibody from said sample by employing liquid chromatographic means wherein the chromatographic packing consists essentially of particulate silica gel having an average particle diameter of from about 3 to about 40 microns and an average pore size of from about 50 to about 1000 Angstrom units to which polyethylenimine functions are bound in covalently bound non-crosslinked form or in adsorbed crosslinked form.

Claim 3

A method of obtaining essentially homongeneous monoclonal antibody type IgG from a sample of mouse ascites fluid containing said monoclonal antibody which comprises separating and recovering said monoclonal antibody from said sample by employing liquid chromatographic means wherein the chromatographic packing consists essentially of the reaction product of particulate silica gel having an average particle diameter of from about 3 to about 40 microns and an average pore size of from about 50 to about 1000 Angstrom units with polyethyleniminopropyl trimethoxy silane having an average molecular weight of from about 400 to about 1800.

Claim 4

A method of obtaining essentially homongeneous monoclonal antibody type IgG from a sample of mouse ascites fluid containing said monoclonal antibody which comprises separating and recovering said monoclonal antibody from said sample by employing liquid chromatographic means wherein the chromatographic packing consists essentially of the reaction product of particulate silica gel having an average particle diameter of from about 3 to about 40 microns and an average pore size of from about 50 to about 1000 Angstrom units with polyethyleniminopropyl trimethoxy silane having an average molecular weight of from about 400 to about 1800.

Claim 5

A method of obtaining essentially purified monoclonal antibody type IgG from a sample of particulate-free mouse ascites fluid containing said monoclonal antibody which comprises: a. equilibrating said sample of particulate-free mouse ascites fluid to an ionic strength equal to or less than the ionic strength of the lower ionic strength buffer used for gradient elution in the subsequent chromatographic separation and recovery step and to a pH greater than the pI of the particular monoclonal antibody; and b. separating and recovering said monoclonal antibody type IgG from said sample by employing liquid chromatographic means wherein the chromatographic packing consists essentially of the reaction product of particulate silica gel having an average particle diameter of from about 3 to about 40 microns and an average pore size of from about 50 to about 1000 Angstrom units with polyethyleniminopropyl trimethoxy silane having an average molecular weight of from about 400 to about 1800.

Claim 6

A method of obtaining essentially purified monoclonal antibody type IgG from a sample of particulate-free mouse ascites fluid containing said monoclonal antibody which comprises: a. equilibrating said sample of particulate-free mouse ascites fluid to an ionic strength equal to or less than the ionic strength of the lower ionic strength buffer used for gradient elution in the subsequent chromatographic separation and recovery step and to a pH greater than the pI of the particular monoclonal antibody; and b. separating and recovering said monoclonal antibody type IgG from said sample by employing liquid chromatographic means wherein the chromatographic packing consists essentially of the reaction product of particulate silica gel having an average particle diameter of from about 3 to about 40 microns and an average pore size of from about 50 to about 1000 Angstrom units with polyethyleniminopropyl trimethoxy silane having an average molecular weight of from about 400 to about 1800.

Claim 7

A method of obtaining essentially homongeneous monoclonal antibody type IgG from a sample of mouse ascites fluid containing said monoclonal antibody which comprises separating and recovering said monoclonal antibody from said sample by employing liquid chromatographic means wherein the chromatographic packing consists essentially of particulate silica gel having an average particle diameter of from about 3 to about 40 microns and an average pore size of from about 50 to about 1000 Angstrom units to which polyethylenimine functions are bound in adsorbed crosslinked form.

Claim 8

A method of obtaining essentially homongeneous monoclonal antibody type IgG from a sample of mouse ascites fluid containing said monoclonal antibody which comprises separating and recovering said monoclonal antibody from said sample by employing liquid chromatographic means wherein the chromatographic packing consists essentially of particulate silica gel having an average particle diameter of from about 3 to about 40 microns and an average pore size of from about 50 to about 1000 Angstrom units to which polyethylenimine functions are bound in adsorbed crosslinked form.

Claim 9

A method of obtaining essentially purified monoclonal antibody type IgG from a sample of particulate-free mouse ascites fluid containing said monoclonal antibody which comprises: a. equilibrating said sample of particulate-free mouse ascites fluid to an ionic strength equal to or less than the ionic strength of the lower ionic strength buffer used for gradient elution in the subsequent chromatographic separation and recovery step and to a pH greater than the pI of the particular monoclonal antibody; and b. separating and recovering said monoclonal antibody type IgG from said sample by employing liquid chromatographic means wherein the chromatographic packing consists essentially of particulate silica gel having an average particle diameter of from about 3 to about 40 microns and an average pore size of from about 50 to about 1000 Angstrom units to which polyethylenimine functions are bound in adsorbed crosslinked form.

Claim 10

A method of obtaining essentially purified monoclonal antibody type IgG from a sample of particulate-free mouse ascites fluid containing said monoclonal antibody which comprises: a. equilibrating said sample of particulate-free mouse ascites fluid to an ionic strength equal to or less than the ionic strength of the lower ionic strength buffer used for gradient elution in the subsequent chromatographic separation and recovery step and to a pH greater than the pI of the particular monoclonal antibody; and b. separating and recovering said monoclonal antibody type IgG from said sample by employing liquid chromatographic means wherein the chromatographic packing consists essentially of particulate silica gel having an average particle diameter of from about 3 to about 40 microns and an average pore size of from about 50 to about 1000 Angstrom units to which polyethylenimine functions are bound in adsorbed crosslinked form.