Azlactone-derivatized polyamides

Details Azlactone-derivatized polyamides Azlactone-derivatized polyamides

1999-01-06

2002-05-07

Woodward, Ana (Department: 1711)

Stock material or miscellaneous articles

Hollow or container type article

Polymer or resin containing

C428S036800, C428S036900, C428S304400, C428S395000, C428S036500, C428S308400, C428S311510, C428S313500, C428S361000, C428S376000, C427S212000, C525S426000

Reexamination Certificate

active

06383584

ABSTRACT:

The invention relates to azlactone-derivatized polyamides, to shaped articles comprising azlactone-derivatized polyamides, and to processes for their preparation.
Azlactone-derivatized carrier materials are known from the literature; for example, U.S. Pat. No. 4,737,560 discloses crosslinked carrier materials which comprise azlactone groups. EP 0 392 783 discloses processes for the graft polymerization of substrate polymers, where the grafted-on side chains comprise aclactone [sic] groups. These carrier materials are suitable for binding proteins insofar as the azlactone groups are sufficiently accessible to compounds of high molecular mass. Porous membranes of polyamides exhibit outstanding flow properties; membranes of polyamides can also be produced with pores whose internal surfaces are readily accessible to compounds of high molecular mass. Polyamides, moreover, exhibit low levels of nonspecific binding with respect to proteins.
The patent application DE 195 01 726.9 (WO 96/22 316) discloses derivatized polyamide membranes which are in the form of block polymers. The monomers polymerized on can also be reacted to form azlactone groups. The preparation of these azlactone-containing polyamide membranes is relatively complex, since first of all it is necessary to prepare a polymerizable derivative of the polyamide and then the block polymer has to be prepared, with the monomers used in its preparation including precursor compounds for the azlactone group. Finally, the precursor compounds must be converted into the azlactone group. The object is therefore to provide a simplified process for preparing azlactone-derivatized polyamides.
It has been found that amino groups, which are usually present terminally in polyamides, can be reacted with vinylazlactone derivatives, the vinyl group reacting with the amino group to produce, in a simple manner, an azlactone-derivatized polyamide. Since the azlactone group is known to react with amino groups, this reaction possibility is unexpected. Where the polyamides used as the substrate polymer contain carboxyl groups, these carboxyl groups can first of all be reacted with diamino compounds by the process disclosed in DE 196 24 813.2 (PCT/EP97/02 768) to provide additional amino groups.
The invention provides azlactone-derivatized polyamides obtainable by reacting polyamides with a solution comprising an azabicyclo compound and a vinylazlactone derivative of the formula I
in which
R
1
, R
2
and R
3
independently of one another denote H or CH
3
;
R
4
and R
5
independently of one another denote H or C
1
- to C
5
-alkyl.
Preferably, R
1
, R
2
and R
3
are H and R
4
and R
5
are methyl.
The invention provides for the use of the azlactone-derivatized polyamides for the binding of amino-containing compounds. Examples of suitable amino-containing compounds are proteins, including enzymes and antibodies.
The invention provides separation materials obtained by reacting an azlactone-derivatized polyamide of the invention with an amino-containing separation effector. Examples of suitable amino-containing separation effectors are antibodies and other affinity ligands for affinity chromatography. Other separation effectors are known to the person skilled in the art.
The invention provides immobilized enzymes obtainable by reacting an azlactone-derivatized polyamide of the invention with an enzyme.
Polyamides suitable as the base polymer are known to the person skilled in the art and are also obtainable commercially. They include, for example, the polymers known under the trade name NYLON®, e.g. NYLON® 66 and NYLON® 6. Porous or nonporous shaped articles consisting of such polyamides are likewise known and are also obtainable commercially; they include, for example, bead-shaped articles, membranes, hoses, hollow fiber membranes, and sponges. The reaction of such shaped articles is preferred, since under the reaction conditions as used in DE 195 01 726.9 and DE 196 24 813.2 (reaction temperature below 80° C.) their shape is retained whereas other processes for derivatizing polyamide are performed in the melt or in solution.
The reaction sequence of the invention is preferably performed at between 0 and 70° C., in particular at between 10 and 60° C.; that is, at temperatures below the melting point of the starting polyamide. Since the starting polyamide need not be dissolved, the reaction sequence of the invention can preferentially also be applied to polyamide mouldings without any notable change in their form. The reaction is catalyzed by azabicyclo compounds, examples being 1,8-diazabicyclo-[5.4.0]undec-7-ene (DBU), 1,5-diazabicyclo[4.3.0]non-5-ene (DBN) and 1,5,7-triazabicyclo[4.4.0]dec-5-ene (TBD). The vinylazlactone derivative is dissolved together with the catalyst in a solvent which is inert to the azlactone derivative. Preferred solvents are those which do not attack the polyamide; examples are dimethylformamide (DMF) and dimethyl sulfoxide (DMSO).
Even without further statements it is assumed that a person skilled in the art will be able to utilize the above description in the widest scope. The preferred embodiments are therefore to be interpreted merely as a descriptive disclosure which in no way has any limiting nature whatsoever.
The complete disclosure content of all above- and belowmentioned applications, patents and publications, and of the corresponding application(s) DE 196 27 302.1, filed on Jun. 7, 1996, are hereby incorporated by reference into this application.


REFERENCES:
patent: 4737560 (1988-04-01), Heilmann et al.
patent: 5408002 (1995-04-01), Coleman et al.
patent: 5451453 (1995-09-01), Gagnon et al.
patent: 5866673 (1999-02-01), Müller et al.
patent: 5993935 (1999-11-01), Rasmussen et al.
patent: 0 392 783 (1990-10-01), None

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