Cell adhesion resisting surfaces

• US 20050153429A1
• Filed: 11/22/2004
• Published: 07/14/2005
• Est. Priority Date: 09/30/2002
• Status: Abandoned Application

• Current Assignee: Becton, Dickinson & Co
• Original Assignee: Becton, Dickinson & Co
• Inventors: Liebmann-Vinson, Andrea, Clarke, Richard P., Xu, Ruiling, Heidaran, Mohammad A.
• Application Number:
  US10/994,879
• Publication Number:
  US 20050153429A1
• Time in Patent Office: Days
• US Class Current: 435/287.200
• CPC Class Codes: C12N 2533/80 Hyaluronan
• CPC Class Codes: C12N 5/0068 General culture methods using substrates for specific animal cell type C12N5/06
• CPC Class Codes: Y10T 428/13 Hollow or container type article [e.g., tube, vase, etc.]
• CPC Class Codes: Y10T 428/1352 Polymer or resin containing [i.e., natural or synthetic]

Abstract

A coated surface that resists cell adhesion comprises hyaluronic acid directly bound to a plasma-treated polymer surface. A process for producing the coated surface is disclosed as are further modifications of the hyaluronic acid by attaching ligand-binding polypeptides (antibodies or antibody binding proteins).

Claims

1-58. -58. (canceled)

59. A process of coating a surface of an article with hyaluronic acid (HA) or alginic acid (AA) or a derivative of HA or AA, which consists essentially of the steps of

i) treating a surface of an article with a plasma that causes formation of nitrogen containing groups on said surface;

and

ii) exposing the treated surface of the article to a solution containing hyaluronic acid or alginic acid, or a derivative thereof, in the presence of a carbodiimide and a reactive intermediate ester stabilizing compound;

to obtain a coated surface.

60. The process of claim 59 wherein the reactive intermediate ester stabilizing compound is selected from the group consisting of N-hydroxysuccinimide, hydroxysulfosuccinimide and hydroxybenzotriazolohydrate.

61. The process of claim 59 comprising the further step of allowing the coated surface to dry.

62. The process of claim 59 wherein the surface is selected from the group consisting of polystyrene, polyethylene, polypropylene, polyethylene terephthalate, polytetrafluoroethylene, polylactide and cellulose.

63. The process of claim 62 wherein the surface is polystyrene.

64. The process of claim 59 wherein step (ii) is carried out within 60 minutes of step (i).

65. The process of claim 59 wherein the plasma treatment is an NH₃ plasma treatment.

66. The process of claim 65 wherein the plasma treatment is carried out by placing the polymer article into the plasma chamber, evacuating the chamber to a 20 mTorr base pressure, establishing a 375 mTorr NH₃ atmosphere, followed by a 25 sec plasma treatment.

67. The process of claim 59 wherein the concentration of HA is at least about 0.05% w/v.

68. The process of claim 67 wherein the concentration of HA is at least about 0.5% w/v.

69. The process of claim 59 wherein the ratio of carbodiimide and ester stabilizing compound-to-HA repeat unit is at least 1 and 0.5.

80. A method for producing a cell-adhesion resistive (CAR) solid phase surface to which is covalently bonded at least a first ligand binding polypeptide, comprising the steps of:

(a) coating a polymer surface with HA, AA, or derivative in accordance with claim 59;

(b) oxidizing said HA, AA or derivative to create an amine-reactive group; and

(c) exposing said oxidized HA, AA or derivative to a first ligand-binding polypeptide wherein covalent bonds are formed between amino groups of said polypeptide and said amine-reactive group, resulting in the covalent bonding of said polypeptide to the HA, AA or derivative,

thereby producing said CAR surface to which is covalently bonded first ligand-binding polypeptide.

81. The method of claim 80, wherein

(i) said oxidizing step (b) is performed by providing an oxidizing agent that generates reactive aldehyde groups on said HA, AA or derivative, and

(ii) step (c) additionally comprises providing a reducing agent to said polypeptide and said surface that effects reductive amination that results in said covalent bond formation between said amino groups of said polypeptide and said reactive aldehyde groups.

82. The method of claim 80, wherein, step (b) additionally comprises, either before step (c) or contemporaneously therewith, the step of converting carboxylate groups of said HA, AA or derivative to reactive esters by exposure to a carbodiimide and a reactive intermediate ester stabilizing compound

83. The method of claim 82 wherein the reactive intermediate ester stabilizing compound is selected from the group consisting of N-hydroxysuccinimide, hydroxysulfosuccinimide and hydroxybenzotriazolohydrate.

84. The method of claim 80, further comprising, after step (c),

(d) contacting said covalently bonded first ligand binding polypeptide with a second ligand binding polypeptide that is a ligand for said first ligand binding polypeptide under conditions that result in the noncovalent binding of said second polypeptide to said first polypeptide.

85. The method of claim 81, further comprising, after step (c),

(d) contacting said covalently bonded first ligand binding polypeptide with a second ligand binding polypeptide that is a ligand for said first ligand binding polypeptide under conditions that result in the noncovalent binding of said second polypeptide to said first polypeptide.

86. The method of claim 82, further comprising, after step (c),

(d) contacting said covalently bonded first ligand binding polypeptide with a second ligand binding polypeptide that is a ligand for said first ligand binding polypeptide under conditions that result in the noncovalent binding of said second polypeptide to said first polypeptide.

87. The method of claim 80, wherein said surface is selected from the group consisting of polystyrene, polyethylene, polypropylene, polyethylene terephthalate, polytetrafluoroethylene, polylactide and cellulose.

88. The method of claim 81, wherein said oxidizing agent of step (b) is periodate.

89. The method of claim 80, wherein said first ligand-binding polypeptide is (a) an antibody, (b) a receptor, (c) an immunoglobulin binding protein, (d) avidin or streptavidin, (e) a lectin, (f) a cell adhesion molecule or (f) an extracellular matrix protein or (g) a synthetic peptide.

90. The method of claim 89 wherein said first ligand-binding polypeptide is an immunoglobulin-binding protein selected from the group consisting of a native or recombinant staphylococcal protein A, a native or recombinant staphylococcal protein G, and recombinant protein A/G.

91. The method of claim 89 wherein said first ligand-binding polypeptide is (a) an antibody or antigen-binding fragment thereof, (b) an immunoglobulin binding protein, or (c) avidin or streptavidin.

92. The method of claim 84 wherein said second ligand-binding polypeptide is (a) an antibody or antigen-binding fragment thereof, (b) a receptor, (c) a lectin, (d) a cell adhesion molecule or (e) an extracellular matrix protein or (f) a synthetic peptide.

93. The method of claim 84 wherein

(a) said first ligand-binding polypeptide is protein A, protein G, or recombinant protein A/G;

and

(b) said second ligand binding polypeptide is an antibody or antigen-binding fragment thereof.

94. The method of claim 84 wherein

(a) said first ligand-binding polypeptide is avidin or streptavidin;

and

(b) said second ligand binding polypeptide is a biotinylated antibody.

95. The method of any of claim 80 wherein said first ligand-binding polypeptide is a anti-CD34 monoclonal antibody.

96. The method of claim 91 wherein said first ligand-binding polypeptide is a anti-CD34 monoclonal antibody.

97. The method of claim 89, wherein said extracellular matrix polypeptide is selected from the group consisting of collagen, laminin, fibronectin and thrombospondin 1, vitronectin, elastin, tenascin, aggrecan, agrin, bone sialoprotein, cartilage matrix protein, fibrinogen, fibrin, fibulin, a mucin, entactin, osteopontin, plasminogen, restrictin, serglycin, SPARC/osteonectin, versican, von Willebrand Factor, a cadherin, a connexin, and a selectin.

98. The method of claim 92, wherein said extracellular matrix polypeptide is selected from the group consisting of a collagen, laminin, fibronectin and thrombospondin 1, vitronectin, elastin, tenascin, aggrecan, agrin, bone sialoprotein, cartilage matrix protein, fibrinogen, fibrin, fibulin, a mucin, entactin, osteopontin, plasminogen, restrictin, serglycin, SPARC/osteonectin, versican, von Willebrand Factor, a cadherin, a connexin, and a selectin.

70. A process of coating a plasma-treated surface of an article, which surface comprises nitrogen-containing groups, with HA or AA or a derivative of HA or AA, said process comprising:

exposing the plasma-treated surface to a solution of HA, AA or said derivative in the presence of a carbodiimide and a reactive intermediate stabilizing compound, to obtain a coated surface.

71. The process of claim 70 wherein the reactive intermediate ester stabilizing compound is selected from the group consisting of N-hydroxysuccinimide, hydroxysulfosuccinimide and hydroxybenzotriazolohydrate.

72. The process of claim 70 comprising the further step of allowing the coated surface to dry.

73. The process of claim 70 wherein the surface is selected from the group consisting of polystyrene, polyethylene, polypropylene, polyethylene terephthalate, polytetrafluoroethylene, polylactide and cellulose.

74. The process of claim 73 wherein the surface is polystyrene.

75. The process of claim 70 wherein the plasma treated surface is an NH₃ plasma treated surface.

76. The process of claim 70 wherein the article is Primaria™

treated.

77. The process of claim 70 wherein the plasma treatment is carried out by placing the polymer article into the plasma chamber, evacuating the chamber to a 20 mTorr base pressure, establishing a 375 mTorr NH₃ atmosphere, followed by a 25 sec plasma treatment.

78. The process of claim 70 wherein the concentration of HA is at least about 0.05% w/v.

79. The process of claim 78 wherein the concentration of HA is at least about 0.5% w/v.