Chemistry: analytical and immunological testing – Involving an insoluble carrier for immobilizing immunochemicals
Reexamination Certificate
2006-10-17
2006-10-17
Mannifield, Nita (Department: 1645)
Chemistry: analytical and immunological testing
Involving an insoluble carrier for immobilizing immunochemicals
C435S004000, C435S006120, C435S007100, C435S174000, C435S180000, C435S181000, C436S525000, C436S527000, C436S529000, C436S530000, C436S531000
Reexamination Certificate
active
07122381
ABSTRACT:
A selective adsorption material made by the process comprising: a) non-cavalently or reversibly-covalently binding a print molecule to at least two styrene, acrylate or silica monomers, each of which monomers brinds to said print molecule by means of a different functional group; b) immobilizing said bound monomers by being polymerized to each other in the presence of an effective amount of cross-linker; and c) removing said print molecule from said polymer by extraction to leave a cavity in said polymer which is stereo-tailored to a biological molecule of interest; and wherein said print molecule is the biological molecule of interest.
REFERENCES:
patent: 4269605 (1981-05-01), Dean et al.
patent: 5110833 (1992-05-01), Mosbach
patent: 5310648 (1994-05-01), Arnold et al.
patent: 5372719 (1994-12-01), Afeyan et al.
patent: 5453199 (1995-09-01), Afeyan et al.
patent: 2 358 647 (1973-11-01), None
patent: 0 364 772 (1989-09-01), None
patent: 0 552 630 (1993-01-01), None
patent: 1133328 (1966-02-01), None
patent: 60 181155 (1985-09-01), None
patent: 6-323949 (1994-11-01), None
patent: 8404967 (1986-04-01), None
patent: WO 90/07527 (1990-07-01), None
patent: WO 02/19663 (1992-11-01), None
patent: WO 94/11403 (1994-05-01), None
patent: WO 94/14835 (1994-07-01), None
Ekberg et al. 1989. TIBTECH. vol. 7: 92-96.
Figueroa et al. 1986. J. of Chromatography. 371: 335-352.
Glad et al. 1985. J. of Chromatography. 347: 14-23.
O. Ramström et al., “Recognition Situ Incorporating Both Pyridinyl and Carboxy Functionalities Prepared by Molecules Inprinting,” J. Org. Chem. 1993, 58, 7562-7564.
“Molecular Imprinting: A Technique for Producing Specific Separation Materials”, TIBTECH, vol. 7, Apr. 1989, Björn Ekberg et al.
“Use of Silane Monomers for Molecular Imprinting and Enzyme Entrapment in Polysiloxane-Coated Porous Silica”, Journal of Chromatography, vol. 347, 1985, pp. 11-23, Magnus Glad, et al.
“Synthesis of Substrate-Selective Polymers by Host-Guest Polymerization”, Makromol. Chem. 182, 687-692, (1981), Reza Arshady et al.
“Imprinting Of Amino Acid Derivatives in Macroporous Polymers”, Lars Andersson et al., Tetrahedron Letters, vol. 25, No. 45, pp. 5211-5214, 1984.
“Polymeric Reagents and Catalyts”, ACS Symposium Series, Developed from a symposium sponsored by the Divisions of Organic and Polymer Chemistry at the American Chemical Society, Miami Beach, Florida, Apr. 28-May 3, 1985, pp. 186-230. Günter Wulff.
“Improved Chromatography: Prearranged Distances Between Boronate Groups by the Molecular Imprinting Approach”, Olof Norrlöw et al., Journal of Chromatography, 396 (1987) 374-377, Elsevier Science Publishers B.V. Amsterdam.
“Synthesis of Cellulosse Derivatives Containing the Dihydroxyboryl Group and a Study of Their Capacity to Form Specific Complexes with Sugars and Nucleic Acid Components”, H.L. Weith et al., Biochemistry, vol. 9, No. 22, 1970, pp. 4396-4401.
“The Interaction of Chain Molecules Carrying Reactive and Catalytic Chain Substituents”, H. Morawetz and W.R. Song, Journal of the American Chemical Society, 88:24, Dec. 20, 1966, pp. 5714-5718.
High-Performance Immobilized-Metal Affinity Chromatography of Proteins on Iminodiacetic Acid Silica-Based Bonded Phases, Alvaro Figueroa et al., Journal of Chromatography, 371, (1986) 335-377, Elsevier Science Publishers B.V. Amsterdam.
“The Synthesis of a D-Amino Acid Ester in an Organic Media With a α-Chymotryspin Modified by a Bio-Imprinting Procedure”, Marianne St{dot over (a)}hl et al., Biotechnology Letters, vol. 12, No. 3, pp. 161-166 (1990).
“Protein Separation and Purification in Neat Dimethyl Sulfoxide”, Nancy Chang et al., Biochemical and Biophysical Research Communications, vol. 176, No. 3, (1991) May 15, 1991, pp. 1462-1468.
“Preparation and Properties of Porous Particles from Trimethylolpropane Trimethacrylate”, Per Reinholdsson et al., Die Angewandte Makromolekulare Chemie 192, (1991), pp. 113-132.
“Synthesis of Some and Amino Acid Derivatives of Styrene”, L.R. Morris et al., JACS, 81, (1959), pp. 377-382.
“Metal Chelate Affinity Chromatography, A New Approach to Protein Fractionation”, Jerker Porath et al., Nature, vol. 258, Dec. 18, 1975, pp. 598-599.
Lars Andersson, et al.; “Enantiomeric Resolution On Molecularly Imprinted Polymers Prepared With Only Non Covalent And Non-Ionic Interactions”; Journal of Chromatography: 516 (1990); pp. 313-322.
Andersson Li et al, Dialog Information Services, File 154, Medline, Dialog accession No. 07658968, Medline accession No. 91177968, J. Chromatogr. Sep. 21, 1990, 516(2): p. 323-331 (Abstract).
Andersson et al, Plennum Press, “Bioseparation and Catalysis in Molecularly Imprinted Polymers”; “Molecular Interactions in Bioseparations” (Ngo. T.T. ed.), 383-394.
Lars Andersson, et al; “Molecular Recognition In Synthetic Polymers: Preparation Of Chiral Stationary Phases By Molecular Imprinting Of Amino Acid Amides”; J. Chromatography; 513 (1990); pp. 167-179.
Braun et al, 108 Chemiker-Zeitung, 255-257 “Ionenselektive Austauscherharze durch vernetzende Copolymerisation vinylsubtituierter Metallkomplexe” (1984).
Styrbjörn Byström, et al.; “Selective Reduction Of Steroid 3- And 17-Ketones Using LiAlH4Activated Template Polymers”; J. Am. Chem. Soc.; Mar. 10, 1993; 115; pp. 2081-2083.
Wayne Danen, et al.; “Stereoselective Synthesis Via A Photochemical Template Effect”; J. American Chemical Society; Apr. 23, 1980; 102:9; pp. 3265-3267.
Julien Damen et al., “Stereoselective Syntheses . Via a Photochemical Template Effect”, Journal of the American Chemical Society, vol. 102, No. 9, Apr. 1980, pp. 3265-3267.
Bjorn Ekberg and Klaus Mosbach: “Molecular imprinting: a technique for producing specific separation materials”, TIBTECH, vol. 7, 1989, pp. 92-96.
Lutz Fischer, et al.; “Direct Enantioseparation of β-Adrenergic Blockers Using A Chiral Stationary Phase Prepared By Molecular Imprinting”; J. Am. Chem. Soc., 1991, 113, 9358-9360.
Magnus Glad et al: “Use of silane monomers for molecular imprinting and enzyme entrapment in polysiloxane-coated porous silica”, Journal of Chromatography, vol. 347, 1985, pp. 11-23, see especially pp. 20-21.
Hedborg E. et al., “Some studies of molecularly-imprinted polymer membranes in combination with field-effect devices” Dialog Information Services, File 34, Scisearch, Dialog accession No. 12613654, Sensors and Actuators A-physical, 1993, V37-8,jun-(Jun.-Aug.), p. 796-799 (Abstract).
Kempe, et al, “Chiral recognition of N. alpha protected amino acids and derivatives in non-covalently molecularly imprinted polymers”, Int. J. Pept. Protein Res. (1994), 44(6), 603-6, pp. 4-6.
Kempe et al, “Direct resolution of naproxen on a non-covalently molecularly imprinted chiral stationary phase” 664 J. Chromatogr., 276-279 (1994).
Kempe M et al, “Binding Studies on Substrate- And Enantio-Selective Molecularly Imprinted Polymers” Dialog Information Services, File 34, Scisearch, Dialog accession No. 10998079; Analytical Letters, 1991, V24, N7, P1137-1145 (abstract).
Mayes, et al; “Sugar Binding Polymers Showing High Anomeric And Epimeric Discrimination Obtained By Noncovalent Molecular Imprinting”; Analytical Biochemistry; vol. 222, No. 2, Nov. 1, 1994; pp. 483-488.
Klaus Mosbach, “Enzymes Bound to Artificial Matrixes”, Scientific America, Mar. 1971, pp. 26-33.
Ann-Christin Johansson and Klaus Mosbach, “Acrylic Copolymers As Matrices for the Immobilization of Enzymes” Biochimica et Diophysica Acta, Jun. 10, 1974, pp. 339-347.
H. Nilsson, R. Mosbach, and K. Mosbach, “The Use of Bead Polymerization of Acrylin Monomers for Immobilization of Enzymes”, Biochimica et Biophysica Acta, Feb. 18. 1972,
Glad Magnus
Kempe Maria
Mosbach Klaus
Hines J.
Mannifield Nita
Morgan & Finnegan L.L.P.
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