Substrate-Independently Surface-Coated Polymer By Aromatic-Amine Compound and Coating Method Thereof

Abstract

Disclosed herein is a substrate-independently surface-coated polymer by aromatic-amine compound and a coating method thereof, and in particular to a substrate-independently surface-coated polymer and a coating method thereof wherein an aromatic compound in which two or more amines are substituted on benzene, is substrate-independently surface-coated. The substrate-independently surface-coated polymer characterized in that the surface of a polymer substrate is coated in such a way to react, using a surface modifier, an aromatic compound of the following structural formula on at least one surface of the polymer substrate having a nucleophilic functional group or an electrophilic functional group.

Claims

1. A substrate-independently surface-coated polymer by an aromatic amine compound characterized in that the surface of a polymer substrate is modified in such a way to react, using a surface modifier, an aromatic amine compound of the following structural formula on at least one surface of the polymer substrate having a nucleophilic functional group or an electrophilic functional group, ##STR00005## wherein R.sub.1 is any of H, NH.sub.2 and NH-acyl.

2. The substrate of claim 1, wherein the surface modification is carried out in such a way that the aromatic compound is inputted in an aqueous solution and is oxidized, and is reacted with a nucleophilic functional group of the polymer substrate, thus modifying the substrate surface into the following structure. ##STR00006##

3. The substrate of claim 1, wherein the surface modification is carried out in such a way that the aromatic compound is inputted in an aqueous solution and is reduced into the structural formula, and is reacted with an electrophilic functional group of the polymer substrate, thus modifying the substrate surface into the following structure. ##STR00007##

4. The substrate of claim 2, wherein the aqueous solution is any of an acidic solution, a neutral solution and an alkaline solution.

5. The substrate of claim 3, wherein the aqueous solution is any of an acidic solution, a neutral solution and an alkaline solution.

6. The substrate of claim 2, wherein the aromatic amine compound of the modified substrate surface is polymerized into a polymer since it is polymerized with another aromatic amine compound.

7. The substrate of claim 3, wherein the aromatic amine compound of the modified substrate surface is polymerized into a polymer since it is polymerized with another aromatic amine compound.

8. The substrate of claim 1, wherein the polymer substrate is a solid mass formed in any of a bead shape, a plate shape, a tube shape and a spherical shape.

9. The substrate of claim 2, wherein a biochemical substance including a cell, a protein, a hexane or a synthesized polymer is fixed, using a linker molecule, on the modified substrate surface.

10. The substrate of claim 3, wherein a biochemical substance including a cell, a protein, a hexane or a synthesized polymer is fixed, using a linker molecule, on the modified substrate surface.

11. A method for preparing a surface-independently modified multifunctional polymer substrate, comprising: inputting an aromatic amine compound of the following structural formula in an aqueous solution in order to make an oxidation and reduction reaction; modifying at least one surface of a polymer substrate having a nucleophilic functional group or an electrophilic functional group in such a way to contact it with an aqueous solution wherein an aromatic compound of the following structural formula is oxidized; washing the surface-modified substrate; and drying the washed substrate, ##STR00008## wherein R.sub.1 is any of H, NH.sub.2 and NH-acyl.

12. The method of claim 11, wherein the aqueous solution is any of an acidic solution, a neutral solution and an alkaline solution.

13. The method of claim 11, wherein the polymer substrate is a solid mass formed in any of a bead shape, a plate shape, a tube shape and a spherical shape.

14. The method of claim 11, wherein in the step for modifying the surface, the aromatic amine compound of the modified substrate surface is polymerized into a polymer since it is polymerized with another aromatic amine compound.

15. The method of claim 11, wherein a biochemical substance including a cell, a protein, a hexane or a synthesized polymer is fixed, using a linker molecule, on the modified substrate surface.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0032] The above and other features of the present invention will now be described in detail with reference to certain exemplary embodiments thereof illustrated the accompanying drawings which are given hereinbelow by way of illustration only, and thus are not limitative of the present invention, and wherein:

[0033] FIG. 1 is a view illustrating an oxidation and reduction reaction of an aromatic amine compound according to the present invention;

[0034] FIG. 2 is a view for describing a reaction procedure between an aromatic amine compound and a nucleophilic substrate according to the present invention;

[0035] FIG. 3 is a view illustrating a polymerization reaction of an aromatic amine compound bond with a nucleophilic substrate according to the present invention;

[0036] FIG. 4 is a view for describing a state where an aromatic amine compound bond with a nucleophilic substrate has been polymerized according to the present invention;

[0037] FIG. 5 is a view for describing a reaction procedure between an aromatic amine compound and an electrophilic substrate according to the present invention;

[0038] FIG. 6 is a view for describing a polymerization reaction of an aromatic amine compound bound with an electrophilic substrate according to the present invention; and

[0039] FIG. 7 is a view for describing a state where an aromatic amine compound bond with an electrophilic substrate has been polymerized according to the present invention.

[0040] It should be understood that the appended drawings are not necessarily to scale, presenting a somewhat simplified representation of various preferred features illustrative of the basic principles of the invention. The specific design features of the present invention as disclosed herein, including, for example, specific dimensions, orientations, locations, and shapes will be determined in part by the particular intended application and use environment.

[0041] In the figures, reference numbers refer to the same or equivalent parts of the present invention throughout the several figures of the drawing.

DETAILED DESCRIPTION

[0042] The configuration and operation of an exemplary embodiment of the present invention will be described with reference to the accompanying drawings.

[0043] FIG. 1 is a view illustrating an oxidation and reduction reaction of an aromatic amine compound according to the present invention, FIG. 2 is a view for describing a reaction procedure between an aromatic amine compound and a nucleophilic substrate according to the present invention, FIG. 3 is a view illustrating a polymerization reaction of an aromatic amine compound bond with a nucleophilic substrate according to the present invention, FIG. 4 is a view for describing a state where an aromatic amine compound bond with a nucleophilic substrate has been polymerized according to the present invention, FIG. 5 is a view for describing a reaction procedure between an aromatic amine compound and an electrophilic substrate according to the present invention, FIG. 6 is a view for describing a polymerization reaction of an aromatic amine compound bound with an electrophilic substrate according to the present invention, and FIG. 7 is a view for describing a state where an aromatic amine compound bond with an electrophilic substrate has been polymerized according to the present invention.

[0044] As illustrated in FIG. 1, the surface modifier employed in the present invention is an aromatic amine compound. FIG. 1 is a view for describing an oxidation and reduction reactions of a benzene diamine 1 and a benzene diimine 2. As illustrated therein, during the aforementioned oxidation and reduction reactions, the benzene diamine 1 is oxidized into the benzene diimine 2, and the benzene diimine 2 is reduced into the benzene diamine 1. If the value of pKa is higher, the oxidation reaction of the benzene diamine may be carried out better. Thus, as the aqueous solution is gradually changed from the acidic state to the alkaline state, the oxidation reaction of the benzene diamine 1 may be carried out better by the chemical property of the amine. More specifically, since the amine is oxidized based on the degree of ionization, although the amine can be oxidized in the acidic state which the degree of ionization is low, the higher the degree of ionization is, the faster the oxidation of amine can be carried out. H, NH.sub.2 or NH-acyl may be substituted on an alkyl group (R.sub.1) of the benzene diamine 1 or the benzene diimine 2 which are the surface modifiers. The substrate employed in the present invention may be substrate-independent, but the aforementioned substrate should have a functional group which can be employed for the sake of a nucleophilic or electrophilic chemical bond. As the nucleophilic functional groups, there are —NH.sub.2, —SH, —OH etc. The benzene diamine 1 will be expressed as a surface modification monomer.

[0045] FIG. 2 is a view illustrating a procedure wherein in a state (2) where the amine, which is a surface modification monomer, has been oxidized into an imine, the nucleophilic functional group of the substrate 10 reacts with a carbon atom while sharing with a non-shared electron pair, and it is reduced into a surface modification monomer 1 and is bonded to a substrate. This procedure is referred to one surface modification monomer 1. If a plurality of surface modification monomers 1 react with a plurality of nucleophilic substrates and are bonded to the surface of polymer, the surface of the polymer may be modified into a substrate having an amine group, which is a reaction group, by a plurality of the surface modification monomers 1.

[0046] FIGS. 3 and 4 are views illustrating a procedure wherein the surface modification monomers 1 are polymerized through a polymerization reaction. As illustrated therein, the nitrogen atoms of the surface modification monomers 1 bonded to the substrate will nucleophilically react with the carbon atoms of other oxidized surface modification monomers 2 which are in free states, and the surface modification monomers 2 will be polymerized together into polymers as illustrated in FIG. 4. The amine group which is a functional group may be formed condensed in a highly polymerized compound 3 and may react with a biochemical substance, whereby the yield that the biochemical substances can be fixed or separated based on the number of amine groups can be greatly increased. A plurality of the surface modification monomers 1 or the surface modification polymers 3, therefore, may be formed on the surface of the polymer, whereupon the time that the biochemical substances are separated and extracted, can be greatly reduced. Moreover, if —NH.sub.2 or NH-acyl is substituted on the alkyl group (R1), more functional groups can be obtained, by means of which the separation and extraction functions of the biochemical substance can be more improved in terms of separation time and yield.

[0047] FIG. 5 is a view illustrating a state where the electrophilic substrate 10′ is reacting with the surface modification monomer 1. As illustrated therein, the non-shared electron pair of nitrogen which form an amine group is involved in the reaction group (R.sub.3) of the electrophilic substrate 10′. The non-shaped electron pair of the nitrogen of a first amine group will react with the reaction group (R.sub.3) of the electrophilic substrate and will lose electrons and will be bonded to the electrophilic substrate 10′. Moreover, the non-shared electron pair of nitrogen of a second amine group will react with the reaction group (R.sub.3) of the electrophilic substrate 10′ and will lose electrons and will be bonded to the electrophilic substrate 10′. Two amine groups, therefore, will be bonded to the electrophilic substrate 10′, and the amine groups will be substituted on the remaining alkyl groups (R.sub.1) and will react with the biochemical substance, whereupon the separation and extraction can be carried out. For this reason, at least three amine groups should be substituted on the surface modification monomer 1 which may operate on the electrophilic substrate 10′. Any of the alkyl groups (R.sub.1), therefore, should be substituted into an amine group (NH.sub.2), and the rest thereof may be any of hydrogen, amine and acylimine. FIG. 6 is a view illustrating a polymerization reaction with other free surface modification monomers 2 which have been oxidized after the surface modification monomers 1 are bonded to the electrophilic substrate. As illustrated therein, the amine group of the surface modification monomer 1 will nucleophilically react with the carbon of other oxidized free surface modification monomers 2, whereupon a polymer 3′ as in FIG. 7 can be obtained. Since the amine group which is a functional group is condensed, the fixing and extraction of the biochemical substance can be quickly processed. Moreover, the yield that the biochemical substance, for example, DNA, etc. is extracted can be greatly increased due to the condensed amine group.

[0048] The aromatic amine compound employed in the present invention may be 1,2,4-benzene-triamine or 1,2,4,5-benzene-tetraamine (BTA). The 1,2,4,5-benzene-tetraamine can be called 1,2,4,5-tetraaminebenzene. In case of the aforementioned benzene-triamine, since it has three amine groups, one among the alkyl groups (R.sub.1) may be substituted into an amine group, and the other one may be in a hydrogen state. Moreover, the benzene-tetraamine is that the alkyl groups (R.sub.1) all are substituted into amine groups.

[0049] The method for coating the surface modification monomer on the polymer substrate according to the present invention will be described. The polymer substrate is formed of an organic polymer compound and should be a solid polymer substrate which may have a nucleophilic functional group (R.sub.2) or an electrophilic functional group (R.sub.3). First of all, a surface modification monomer 1 with a predetermined concentration is inputted in an aqueous solution and is mixed well. The polymer substrate to have nucleophilic functional group react with the surface modification monomer 1 that imine is oxidized from the amine, and the substrate to have electrophilic functional group react with the surface modification monomer 1 that amine is reduced from the imine. The aforementioned aqueous solution may be any of acidic, neutral and alkaline solutions, provided that if it is a alkaline solution, the reaction may be carried out faster since the degree of ionization is high, which, however, is not limited thereto. The solid substrate may be dipped in the aqueous solution that the surface modification monomer 1 makes an oxidation and reduction reaction or the aqueous solution inputted with the surface modification monomer 1 may be filled in the solid substrate. The aforementioned mixture is placed in this state for a predetermined time long enough to react with the solid substrate. The mixture may be heated or stirred to activate the bonding. Moreover, if it is available to use catalyst, a predetermined catalyst may be inputted so as to accelerate reaction. The solid substrate is washed after a predetermined time has passed, and the surface modification monomers 1 or any impurities which are not bonded or polymerized are removed. In case of the coating of polymer, any substances which are not bonded to the substrate having hydrophilic or hydrophobic property, are removed through multiple washing steps. When the monomers 1 or any impurities which are not bonded or polymerized to the substrate are removed, it is dried and packed in a vacuum state, thus finishing the preparation of a product. The solid polymer substrate may be formed in any of various shapes, for example, a bead shape, a plate shape, a tube shape or a spherical shape, which, however, is not limited thereto.

[0050] The fixing and separation of a biochemical substance, for example, DNA, etc. which is carried out using a surface-modified polymer substrate according to the present invention will be described. An acidic solution is inputted in the solid polymer substrate to which a plurality of the surface modification monomers 1 have been bonded or which has been coated with a polymerized highly polymerized compound. The amine group of the substrate surface may have proton in the acidic solution and may be electrified into positive electric charges. In a state where the acidic solution is inputted, a sample having a biochemical substance, for example, DNA, etc. is inputted. The solid substrate surface electrified into the positive electric charges is bonded with the DNA which has been electrified with the electrons from the given sample mixture, whereby it is possible to selectively capture the biochemical substances, for example, DNA, etc. The rest of the samples is removed in a state where the DNA is captured. An alkaline solution is inputted in the solid substrate. Since the amine of the polymer substrate surface loses protons in the alkaline state, the captured DNA molecules will release from the surface where the DNA molecules are coated. Likewise, a selective purification of DNA, etc. is available from the sample mixture.

[0051] Furthermore, since the amine can be modified through a standard linker reaction using a linker molecule, it is possible to fix various biological/chemical substances, for example, cells, proteins, hexanes, synthesized molecules. As a result, the present invention may be adapted to the purification, separation or detection of a predetermined target analysis substance.

[0052] The invention has been described in detail with reference to preferred embodiments thereof. However, it will be appreciated by those skilled in the art that changes may be made in these embodiments without departing from the principles and spirit of the invention, the scope of which is defined in the appended claims and their equivalents.

LEGENDS OF REFERENCE NUMBERS

[0053] 1: Aromatic amine [0054] 2: Aromatic imine [0055] 3, 3′: Highly polymerized compound of aromatic amine [0056] 10: Nucleophilic substrate [0057] 10′: Electrophilic substrate