CN1026005C - Antibacterial antiplaque oral composition contaning copolymer of styrene phosphonic acid - Google Patents

Abstract

An apparatus and a method for identifying handwritten characters is provided, each of the characters being a member of a set and being formed from a number of predetermined primitives. The apparatus includes an input device receiving successively each primitive forming a character. The input device generates input signals for each primitive forming the handwritten character. The input signals are conveyed to a processor. The processor examines the input signals and attempts to identify each of the primitives used to form the handwritten character. A primitive code is generated for each identified primitive and an unidentified primitive code is generated for each unidentified primitive. The primitive and unidentified primitive codes are combined to form an input character code. A memory is provided and stores a character code and an international output code for each of the characters in the set of characters. A comparator compares the input character code generated for the handwritten character with each of the character codes stored in the memory. When the input character code is equivalent to a character code associated with only one output code, the output code is conveyed to an output device such as a printer wherein a reproduction of the handwritten character is formed. When the character code is equivalent to a character code associated with more than one output code, a differentiator detects the correct output code associated with the input character code so that the handwritten character can be reproduced.

Description

Antibacterial antiplaque oral composition contaning copolymer of styrene phosphonic acid

The present invention relates to improve effectively the styryl phosphonic acid polymkeric substance of the anti-spot effect of antibacterial antiplaque oral composition.

Dental plaque is the soft settling that forms on tooth, and relative with it is the tooth dirt, and it is the hard calcified deposits thing that forms on tooth.Dental plaque is different with the tooth dirt, and it can form at any position of dental surface, especially also is included in the gingival edge place and generates.Therefore, dental plaque except that look indecency, also can cause gingivitis.

Therefore, wish very much the known antimicrobial drug that can reduce dental plaque is included in the composition for oral cavity.Through what use always is cationic antimicrobial drug.And, at United States Patent (USP) 4,022, Vinson etc. has announced that a compound that can provide zine ion as the agent of anti-tooth dirt, mixes mutually with a kind of antiseptic-germicide of dental plaque bacteria growing that can stop effectively, and narrated multiple antimicrobial drug and mixed with zn cpds in 880, these compounds include cationic material, for example guanidine compound and quaternary ammonium compound, and non-cationic type compound, for example halogenated Salicylanlide and halogenated dihydroxy diphenyl ether class.Saxton etc. discloses the halogenation dihydroxy diphenyl ether of the antibacterial antiplaque of non-cationic type in the Europe patent 0161,899, and triclosan share with three hydration zinc citrates.

Cationic antimicrobial substance is Tubulicid for example, and benzthonium Chloride, cetylpyridinium chloride are the key subjects of antibacterial antiplaque drug research.But these materials and anionic material are invalid usually when share.Yet, non-cationic type antimicrobial substance but can with anionic composition compatibility, make composition for oral cavity.

Yet composition for oral cavity generally is multiple mixture of ingredients, even typical neutral substance all can influence the performance of this composition as wetting agent.

An advantage of the invention is, the composition for oral cavity that is provided contains water-fast basically non-cationic type antiseptic-germicide, and include new β-styryl phosphonic acid homopolymer and with the antimicrobial enhancing agent of the multipolymer of vinyl phosphonate, this polymkeric substance can strengthen said antiseptic-germicide and transport to oral surfaces, and keeping thereon, thereby the formation of inhibition dental plaque.

An object of the present invention is to provide a kind of transhipment that can improve antiseptic-germicide, and make it remain on antimicrobial enhancing agent on tooth and the oral soft tissue.

An advantage of the invention is that this oral cavity is effective with the antiplaque composition to what reduce gingivitis.

Can be conspicuous in the examination of another advantage of the present invention detailed description below.

According to some content of the present invention, the present invention relates to a kind of polymkeric substance, it is by one group of β-styryl phosphonic acid polymkeric substance, α-styryl phosphonic acid polymkeric substance, and α-or β-styryl phosphonic acid multipolymer that other undersaturated polymerisable monomer that contains ethene forms with at least one in select.

These polymkeric substance can improve the antiplaque effect of composition for oral cavity effectively, contain water-fast substantially antibiotic antiplaque medicine in the said composition, for example content is 0.01～5%(weight) the halogenated diphenyl ethers class, 2 ', 4,4 '-three chloro-2-hydroxyl-phenyl ether (triclosan), or 2,2 '-dihydroxyl-5,5 '-two bromo-phenyl ether, and halogenated Salicylanilide, benzoates, halogenated diphenylurea and phenol compound.

Antimicrobial enhancing agent (AEA) can improve the transhipment of this antiseptic-germicide to oral surfaces, and And keeps thereon.For realizing that this strengthens purpose, used significant quantity scope is the about 0.05% to 4% of composition for oral cavity, and scope is 0.1%～3% preferably, is more preferably in about 0.5%～2.5%(weight).

AEA can be simple compound, is preferably polymerisable monomer, preferably a polymkeric substance.This polymkeric substance one language is a general name, for example comprises oligopolymer, homopolymer, and the multipolymer that two or more monomers forms, ionomer, segmented copolymer, graft copolymer, cross-linked polymer and multipolymer, or the like.AEA can be natural or the synthetic product, is insoluble in water, or is more preferably water (saliva) dissolving or expand (but hydration, form hydrogel).Its molecular-weight average is approximately 100～4, and 000,000, be preferably 1,000～1,000,000, preferably about 2,000 or 2,5000 to 250,000 or 500,000.

AEA generally contains at least a transhipment and strengthens group, and this group is tart preferably, sulfonic group for example, phosphonate group, more preferably phosphonate group or carboxylic acid group, or their salt, for example alkali metal salts or ammonium salt.AEA contains a kind of organic group that strengthens retention time at least, preferably has the group that strengthens transhipment and strengthen two kinds of functions of retention time concurrently, and this group preferably has the n-R of general formula-(X), and X is O in the formula, N, S, SO, SO ₂, p, pO, Si or the like.R is hydrophobic alkyl, and thiazolinyl, acyl group, aryl, alkaryl, aralkyl, the derivative that heterocycle or their inertia group replace, n are 0,1 or greater than 1.Above-mentioned " derivative that inertia group replaces ", be meant the substituting group that is included among the R, be generally non-hydrophilic; And and to AEA as improving antiseptic-germicide to the oral surfaces transhipment or keep the group that thereon desirable function does not have significant interference effect, halogen for example, as Cl, Br, I, and carbonyl or the like.During the group of this kind enhancing retention time is listed in the table below

n X -（X）nR

0-methyl, ethyl, propyl group, butyl, isobutyl-, the tertiary butyl, cyclohexyl, alkene

Propyl group, benzyl, phenyl, chloro-phenyl-, xylyl, pyridyl, furans

Base, ethanoyl, benzoyl, butyryl radicals, terephthaloyl etc.,

1 O oxyethyl group, benzyloxy, thioacetyl oxygen base, phenoxy group, ethoxycarbonyl, benzyl

Oxygen carbonyl etc.,

The N ethylamino, diethylin, third amino, benzyl amino, benzamido, benzene second

Amido etc.,

The S butylthio, isobutyl sulfenyl, allyl sulfenyl, benzylthio-, thiophenyl, sulfo-third

Acyl group, the phenyl ethanethioyl, thiobenzoyl etc.,

SO butyl sulfoxide group, the allyl sulfoxide group, the benzyl sulfoxide group, phenyl sulfoxide group etc.,

SO ₂The butyl sulfuryl, the allyl sulfuryl, the benzyl sulfuryl, phenyl sulfuryl etc.,

P diethyl phosphino-, the ethyl vinyl phosphino-, the allyl ethyl phosphino-, the Ethylbenzyl phosphino-, ethylphenyl phosphino-etc.,

PO diethyl phosphine oxygen base, ethyl vinyl phosphine oxygen base, methacrylic phosphine oxygen base,

Methyl-benzyl phosphine oxygen base, aminomethyl phenyl phosphine oxygen base etc.,

The Si TMS, the dimethylbutyl silylation, the dimethyl benzyl silylation,

Dimethyl vinyl silanes base, dimethyl-allyl silylation etc.

Enhancing used herein transhipment group is meant and is connected in, or is bonded in or is bonded in the group on the AEA securely, or is bonded on the AEA, and the latter carries antiseptic-germicide to oral surfaces (for example tooth and gums), thereby antiseptic-germicide is transported on these surfaces.The organic group that strengthens retention time is normally hydrophobic, antiseptic-germicide is linked to or is bonded on the AEA, thereby impel antiseptic-germicide to remain on the AEA, remains on the oral surfaces indirectly.In some cases, the binding of antiseptic-germicide is because they are held back by AEA physics, when especially AEA is cross-linked polymer.The structure of cross-linked polymer provides this required position of increasing of holding back congenitally.When molecular weight is higher, can hold back to (or quilt) crosslinked AEA polymer physics by further promotion antiseptic-germicide in the more hydrophobic part of cross-linked polymer.

Select preferably to be, AEA is an anionic polymer, it is to be made of a chain or a skeleton that contains repeating unit, each repeating unit preferably contain at least a carbon atom And and preferably univalent of side joint transhipment at least directly or indirectly strengthen group, also univalent of side joint strengthens the group of retention time at least directly or indirectly, and the latter strengthens group with transhipment and preferably is connected on the same carbon atom or adjacent carbons of carbochain, is connected on other atom relatively poor.Relatively poor selection is, polymkeric substance can contain transhipment and strengthen group, and/or keeps and strengthen group, and/or other bivalent atom or group be as the chain link of polymer chain, replacing the atom beyond carbon atom or the carbon, or as crosslinked segment.

The transhipment that do not contain described here strengthens group and all examples and the explanation that keep the AEA that strengthens group, can and preferably carry out in a known manner chemical modification with the AEA ， And that preferably contained these two kinds of groups and preferably each such group have two kinds of character concurrently.Preferred AEA polymkeric substance, in order to be directly transferred into oral surfaces to antiseptic-germicide to greatest extent, wish to contain 10% of polymer weight at least at the polymer chain or the repeating unit on the skeleton that contain acid transhipment enhancing group, be preferably 50%, preferably at least 80%～95%, or 100%.

According to an embodiment preferred of the present invention, AEA is a kind of polymkeric substance of being made up of repeating unit, and one or more phosphonic acids transhipments strengthen group bonding on one or more carbon atoms of polymer chain in the repeating unit.The example of this AEA is poly-(vinylphosphonic acid), contains the unit of formula I:

But it does not contain the enhancing group of withing a hook at the end.Yet, poly-(1-phosphono propylene) enhancing group of can withing a hook at the end, it has formula II unit

Here the used phosphonic AEA that preferably contains is poly-(β-styryl phosphonic acid), contains formula III unit:

Ph is a phenyl in the formula, chain closes the phosphonate group of the enhancing transhipment on the carbon atom of the ortho position of polymeric chain and strengthens the phenyl that keeps, or the multipolymer of β-styryl phosphonic acid and vinyl phosphonic acyl chlorides, it has formula III unit and is connected with formula I units alternately, or link at random, or poly-(α-styryl phosphonic acid), contain formula IV unit:

The transhipment of this polymer unit-and keep the enhancing group bonding on the same carbon of main chain.

These styryl phosphonic acid polymkeric substance and they and other inert contain the multipolymer of the unsaturated monomer formation of ethene, and molecular weight ranges generally about 2,000～30,000, is preferably 2,500～10 000.This 'inertia' monomer is to herein as AEA and the function of the multipolymer of usefulness does not have significant interference effect.

Other contains the phosphonic polymkeric substance has, and for example, monomer is the phosphine acidifying ethene of formula V:

Ⅴ -〔CH ₂） ₁₄CHpO ₃H ₂〕n-

N for example can be an integer in the formula, or can draw the numerical value that molecular weight is approximately 3000 polymkeric substance; Have unitary poly-(butylene-4, the 4-di 2 ethylhexyl phosphonic acid) sodium of formula VI:

Unitary poly-(allyl group two (phosphono ethamine)) with formula VII:

The polymkeric substance of other phosphonoization; for example poly-(allyl group phosphinylidyne acetic acid ester); the polymethacrylate of phosphonoization etc.; and in European patent 0321233, announce and the gem-diphosphonate polymkeric substance here used as AEA, certainly they contain or modification after contain the organic group that above-mentioned enhancing keeps.

New α-and β-styryl phosphonic acid polymkeric substance and to contain the general preparation method of the multipolymer of unsaturated monomer of ethene with other be with monomer or monomeric mixture heating up, be preferably under the nitrogen, under the existence of the radical initiator of significant quantity, as 2.5～5%AIBN Benzoyl Peroxide, peroxy tert-butyl alcohol, persulphate (ester) or the like, the solution such as the acetonitrile that need not solvent or form in inert solvent, methylene dichloride or 1, the 2-ethylene dichloride; At high temperature, for example reach as high as the reflux temperature of about 125 ℃ or solvent, reacted 8～200 hours.

After removing inert solvent, the crude product of polymerisate mixes with water, for example with aqueous sodium hydroxide solution mixing solutions is transferred to pH8～11.Solid impurity is after filtering, and filtrate is isolated the polymkeric substance of purifying certainly to water saturating (for example by the end of 3500 dalton) through lyophilize in the solution of Bao Liuing.

According to another kind of embodiment preferred, AEA can comprise the polycarboxylate of synthetic anionic.Though the anti-tooth dirt of it and polyphosphonate of no use in the present invention agent synergy, but molecular weight is 1,000～1,000,000(preferably about 30, the polycarboxylate (ester) of synthetic anionic 000～500,000), at the anti-tooth dirt of the dehydration polyphosphonate of optimizing linear molecule on, the inhibitor that is used as alkaline phosphatase, as United States Patent (USP) 4,627,977Gaffer etc. are disclosed.In fact, English Patent 2200551 discloses the composition of polycarboxylate (ester) as alternative composition for oral cavity, contains the dehydrated polyphosphate and the non-cationic type antiseptic-germicide of linear molecule in this composition.Be also noted that, in text of the present invention, this polycarboxylate strengthens when keeping group if contain (or containing) after modification, during even without other composition of can act synergistically with polycarboxylate (be molecule dehydration poly-phosphate), the antibacterial antiplaque agent that also can strengthen the non-cationic type widely is to dental surface transhipment and the effectiveness that keeps; For example, when especially being non-cationic type antiseptic-germicide with the synergistic composition of polycarboxylate, its effect can be stronger.

The mixture that synthetic anionic polycarboxylate and they and various cationic sterilant, zinc and magnesium form, before dirty agent came forth as anti-tooth, and for example Shedlovsky is at United States Patent (USP) № .3,429,963, Gaffer is at United States Patent (USP) 4,152,420, Dichter equals United States Patent (USP) 3,956,480, Gaffer is at United States Patent (USP) 4,138,477 and Gaffer etc. at United States Patent (USP) 4,183, announced on 914.Recognize the synthetic anionic polycarboxylate of in this several patents, being announced, when containing (or after modification, containing) above-mentioned enhancing and keep group, it plays the sample as AEA in composition, the method for its invention and open combined with the reference form in this sense.

These synthetic anionic polycarboxylates usually use with the form of its free acid, perhaps even more preferably with the part neutralization, perhaps preferably basic metal of (but hydration, form gel) of the water miscible or water-swelling after the neutralization (as potassium sodium preferably) or ammonium salts are used fully.Maleic anhydride or toxilic acid and another polymerisable unsaturated monomer that contains ethene, methylvinylether/maleic anhydride preferably, ratio preferably 1: 4～4: 1, the preferred molecular weight of its multipolymer is approximately 30,000～1,000,000, preferably about 30,000～500,000.These multipolymers can have been bought, and for example commodity are called Gantrez, AN139(molecular weight 500,000), AN119(molecular weight 250,000); Be preferably other product of S97 pharmaceutical grade that GAF company produces, molecular weight 70,000.

Other the AEA effect arranged, contain the polycarboxylate that (or containing) strengthens the reservation group after modification, comprise that those are at above-mentioned United States Patent (USP) № .3,956,480 disclosed polymkeric substance, for example maleic anhydride and ethyl propenoate, hydroxyethyl methylacrylate, 1: 1 the multipolymer that N-vinyl-2-Pyrrolidone or ethene form, the multipolymer of maleic anhydride and ethene can have been bought, for example Meng Shan has more the EMA № .1103 of product, molecular weight 10,000 and the EMA61 level, and vinylformic acid and hydroxyethyl methylacrylate or methyl esters, methyl acrylate or ethyl ester, 1: 1 multipolymer of IVE or N-vinyl-2-Pyrrolidone.

The United States Patent (USP) № .4 that mentions in the above, 138,477 and 4,183,914 disclosed containing (or containing after modification) strengthen the other effective polycarboxylate of reservation group, comprise maleic anhydride and vinylbenzene, the multipolymer that iso-butylene or ethyl vinyl ether form, polyacrylic acid, poly-methylene-succinic acid, polymaleic acid, the sulphonyl acrylic acid oligomer, molecular weight is low to 1,000, and commodity are called Uniroyal ND-2.

The enhancing that contains polymeric thiazolinyl or vinyl unsaturated carboxylic acid (this carboxylic acid contains an activatory carbon-to-carbon double bond and at least one carboxyl) keeps group and generally suits, promptly this carboxylic acid contains the two keys of alkene, because of this pair key in monomer molecule in the alpha-beta position of carboxyl or be terminal methylene group, be easy in polymerization, work.The example of this class acid has, vinylformic acid, methacrylic acid, ethylacrylic acid, α-Lv Daibingxisuan, Ba Dousuan, β-acryloxy propionic, 2, the 4-Sorbic Acid, alpha-chloro Sorbic Acid, styracin, β-styrene acrylic, muconic acid, methylene-succinic acid, citraconic acid, methylfumaric acid, propene dicarboxylic acid, equisetic acid, α-Ben Jibingxisuan, 2 benzyl acrylic acid, 2-cyclohexyl vinylformic acid, angelicic acid, umbellic acid, fumaric acid and toxilic acid and their acid anhydrides.The various of other can comprise with the vinyl monomer of these carboxylic acid monomer's copolymerization: vinyl-acetic ester, vinylchlorid, dimethyl maleate or the like.Multipolymer contains enough carboxylate groups usually and is beneficial to water-soluble.

So-called carboxy vinyl polymer also is useful at this, and these polymkeric substance equal United States Patent (USP) 3 as the composition of toothpaste by Chown, 980,767, Roberts equals United States Patent (USP) 3,935,306, Perla equals United States Patent (USP) 3,919,409, Harrison is in United States Patent (USP) 3,911,904, Colodney equals United States Patent (USP) 3, disclosed in 711,604.They can have been bought, and for example the trade mark of producing for B.F.Goodrich company is CarboPol934, and 940 and 941.

These products mainly are the water miscible polymkeric substance of colloidal that polyacrylic acid and about 0.75%～2.0% is cross-linked to form as the polyene propyl group sucrose or polyene propyl group five tetrahydroxybutanes of linking agent.The hydrophobicity of this crosslinking structure and cross-link bond and/or the physics of antiseptic-germicide and other or the like held back provide desirable reservation enhanced propertied.PolycarboPhil is substantially also similar, is polyacrylic acid and be lower than 0.2% crosslinked the forming of divinyl oxalic acid.The content of this linking agent, molecular weight and/or hydrophobicity are lower, and the enhancing stick effect is just healed little or do not had the enhancing stick effect.2,5-dimethyl-1,5-hexadiene are the examples of the linking agent of more effective enhancing stick effect.

The composition of synthetic anionic polycarboxylate usually is kind of a hydrocarbon, and optional on it have halogen and oxygen containing substituting group, is connected with for example existing way of ester, ether and hydroxyl.

AEA contains the natural anionic polycarboxylate that strengthens the stick effect group.Carboxymethyl cellulose and other wedding agent natural gum and film forming agent owing to lack above-mentioned enhancing transhipment and/or strengthen the group that keeps, are not effective AEA.

Contain AEA representational that phosphonic acids and/or sulfonic acid strengthen the transhipment group, can mention the unit or pulsating polymkeric substance or the multipolymer that obtain by ethene or allyl group phosphonic acids and/or sulfonic acid polymerization, at C ₁Or C ₂(or C ₃) on be substituted with the organic group that can strengthen stick effect as required, for example just like the n-R of general formula defined above-(X).About the polycarboxylate of effective synthetic anionic, can be with these monomeric mixtures, and monomer and the polymerisable unsaturated monomer that contains ethylenic linkage of one or more inert, the multipolymer that generates of the monomer of ubi supra for example.As what it will be appreciated that, at these or other effective AEA polymkeric substance, have only a tart can strengthen the group of transhipment usually, be bonded to the skeleton of polymkeric substance or certain carbon atom on the side chain or other atom.The side group that contains (or containing) after modification strengthens group that shifts and the polysiloxane that strengthens the group of stick effect, also can be used as AEA here.Contain the ionomer that (or containing after modification) can strengthen transhipment and stick effect group, also be effective as AEA herein.Ionomer is described in " chemical encyclopedia of Kirk Othmer ", the third edition, and the 546th～573 page of ancillary volume, John Willie father and son company, copyright 1984, the content of being narrated is at this as a reference.If AEA contains (or containing) and strengthen to keep group after modification, they are polyester, polyureas alkane and include protein and protein-like substance such as collagen, and synthetic or natural polymeric amide such as poly arginine and other polyamino acid also are effective as AEA.

Needn't binding isotherm, will be convincing, AEA, especially polymeric AEA generally are that the material ， And that makes us desirably forming anionic membrane thinks and is incorporated on the dental surface, form continuous thin film on the flank of tooth, thereby have stoped the contact of bacterium to the flank of tooth.Antiseptic-germicide that possible right and wrong are cationic and AEA form mixture or other combining form, thereby have formed the film of mixture or the film of these two kinds of materials on tooth surface.Film forming character of AEA and enhancing antiseptic-germicide it seems it is to be unfavorable for the gathering of bacterium at dental surface to the character of dental surface transhipment and reservation, especially because antiseptic-germicide to the direct repression of bacterium, is being controlled the growth of bacterium.Therefore, three kinds of modes of action after merging: 1) strengthen transhipment; 2) keep for a long time at dental surface; 3) avoid contacting of bacterium and dental surface, thereby this composition for oral cavity is effective to reducing dental plaque.The soft tissue in oral cavity or can reach similar anti-spot effect near the gums place.

In oral preparations, can there be the acceptable vehicle in the oral cavity that comprises the wetting agent water.Wetting agent is glycerine and/or Sorbitol Powder preferably.Should avoid the polyoxyethylene glycol with suitable volume, especially molecular weight is 600 or bigger polyoxyethylene glycol, because polyoxyethylene glycol can suppress the anti-microbial activity of the antiseptic-germicide of non-cationic type effectively.For example, the weight ratio when polyoxyethylene glycol (pEG) 600 and triclosan is 25 triclosans: during 1pEG600, can reduce the anti-microbial activity of triclosan, the factor of reduction approximately is not have 16% under the polyoxyethylene glycol situation.

Basically dissolve the material that antiseptic-germicide makes antiseptic-germicide be transported to oral soft tissue place or nearly gums place and can be used in saliva, dissolve antiseptic-germicide.The representational dissolubility material that adds includes the moistening for example propylene glycol of poly-hydroxy alcohols that arrives, two propyleneglycoles and hexene ethylene glycol, cellosolve is methylcyclohexane for example, and ethyl cellosolve for example contains the vegetables oil of about at least 12 carbon atoms and wax on straight chain, sweet oil, Viscotrol C, vaseline ester such as pentyl acetate, ethyl acetate, Tristearoylglycerol, peruscabin.Propylene glycol preferably.Here " propylene glycol " comprises 1,2-propylene glycol and 1, ammediol.

The pH of oral preparations generally is in about 4.5～9 or 10 scope, preferably about 6.5～7.5.PH that it should be noted that composition is lower than at 5 o'clock and also can be used for the oral cavity, does not cause decalcification or damage tooth glaze basically.PH usable acid (as citric acid or phenylformic acid) or regulate with alkali (as sodium hydroxide) or damping fluid (as Trisodium Citrate, Sodium Benzoate, yellow soda ash, sodium bicarbonate, Sodium phosphate dibasic, SODIUM PHOSPHATE, MONOBASIC or the like).

Oral preparations can mainly be a liquid, for example mouth wash shua, or a kind of tooth powder that contains tooth with polishing agent.The oral cavity is mainly contained natural or synthetic thickening material or gelifying agent with dentifrice composition.

It is former that composition for oral cavity also can contain fluorion, or supply the fluorine composition as anti-caries agent.

Should understand that routinely, oral preparation will be sold or distribute with the packing of appropriate mark.Thereby toothpaste is placed in the compressible pipe usually, mainly contains aluminum pipe, with lead or plastic lining, or with other extruding type, the divider of pump pressure type to be to measure content, its material of containing of label explanation is arranged, as toothpaste or other analogous products are indicated.

Use organic surface active agent in the composition for oral cavity, so that improve prophylactic effect, promoting anti-spot antiseptic-germicide to disperse ， And to make this based composition in whole oral cavity for a full due is that the user accepts easily with makeup.Organic surface active agent is preferably anionic, non-ionic type or amphoteric in nature, and the preferred substance that uses as tensio-active agent is a washing composition, and it gives composition with the washing and the character of foaming.

Oral preparations can add other various materials, whitening agent for example, sanitas, silicone, chlorophyll compound and/or contain for example urea of ammoniacal substance, the mixture of diammonium phosphate and these compounds.

If during with these auxiliarys, the consumption that joins in the preparation does not have tangible detrimentally affect to desired character that has and characteristic.Should avoid using significant quantity zinc, magnesium and other metal salt and general solubility and can form the material of mixture with effective ingredient of the present invention,

Also available various suitable seasonings and increase sweet substance.

Composition for oral cavity preferably is used for tooth enamel and soft tissue regularly, particularly at the gums place or nearly gums place.For example once a day or per two days or per three days once, or preferably one day 1～3 time, pH is approximately 4.5～9, generally is 5.5～8, and is preferably about 6.5～7.5, at least 2 weeks of time of use preferably use to 8 weeks lifetime.

AEA and antiseptic-germicide can be mixed and made into lozenge, chewy gum or other products, and for example stirring is added in the warm glue nurse matrix, or wraps on the outside surface of glue nurse matrix, and the example of glue nurse matrix can be mentioned joint road flexible glue, latex, Vinylite or the like.Best with conventional softening agent or tenderizer, sugar or other sweetener or carbohydrate such as glucose, Sorbitol Powder or the like share.

Following example further is illustrated feature of the present invention, but should know that this Fa Ming And is not limited to these examples, and except that refering in particular to, all consumptions and ratio all are to represent with weight.

Example A

Poly-(β-styryl phosphonic acid)

18.1g(0.1M) β-styryl phosphonic acid and 0.82g(0.005M) Diisopropyl azodicarboxylate (AIBN) is in the mixture of 300ml anhydrous acetonitrile stirring and refluxing 96 hours under drying nitrogen.After the mixture cooling, crude product settles out, and filters and collects, and with the acetonitrile washing, air dries.Dissolving crude product is (pH11) in aqueous sodium hydroxide solution, and the water dialysis is held back in 3000 dalton.The solution that keeps drops to 100ml, and vacuum lyophilization obtains the white powder solid, is the purified polymer product, and output is 0.91g.Infrared spectra: 1610,1550,745Cm ^-1(5 adjacent H of aromatic ring); 1240,1020,950Cm ^-1(phosphonate radical).Proton NMR spectrum (D ₂O) three peaks, 6.4ppm(links the H on the phosphonate radical carbon); Multiplet, the hydrogen on 7.3ppm(aromatic ring and the benzyl); Area was than 1: 6.Nuclear magnetic resonance spectrum (the D of phosphorus ₂O): multiplet, 6.2ppm.(alkylphosphines acid group).

Example B

(β-styryl phosphonic acid/vinyl phosphonate) multipolymer

10.68g(0.058M) β-styryl phosphonic acid, 6.0ml(8.4g, the mixture of ethene phosphonyl dichloride 0.058M) and 0.5g Diisopropyl azodicarboxylate (AIBN) stirs down and heats in drying nitrogen a few hours, spends the night in 80～90 ℃ then.With reactant transfer in the beaker that fills 60～70ml water.

After the hot solution cooling, separate out the crystallinity precipitation.Mixture is filtered.Thin up is to 125ml again for aqueous filtrate, and the solution that the obtains water of dialysing is held back 3500 daltonian molecules.Evaporate in the left solution for vacuum, obtain 0.600g, be the acid of purified multipolymer.Proton NMR spectrum (D ₂O) show alkyl, 11H), 5H) be broad peak with 6.9～7.5ppm(aryl at 1.0～2.8ppm(.These data show that the ratio of β-styryl phosphonic acid and vinylphosphonic acid is 1: 3 in this multipolymer.Nuclear magnetic resonance spectrum (the D of phosphorus ₂O) show that the signal of two main phosphorus concentrates on about 23.4 and the 29.2ppm place respectively.

Example C

Poly-(α-styryl phosphonic acid)

2.21g(0.01M) α-vinylbenzene phosphonyl dichloride and mixture 115 ℃ of stirrings in nitrogen of the Diisopropyl azodicarboxylate of 0.01g.Every 12 hours, add the 0.01g Diisopropyl azodicarboxylate successively in reaction mixture.After 96 hours, mixture is put cold and soluble in water.Regulate pH to 8～10 with aqueous sodium hydroxide solution, cumulative volume is 125ml.After solution filtered, filtrate was dialysed water in the Mierocrystalline cellulose bag that 3500 dalton hold back.In a vacuum left liquid is approximately dropped to 50ml, lyophilize, the polymkeric substance that obtains is pale brown toner powder solid, output 0.08g, proton NMR spectrum (D ₂O): 23～25ppm(multiplet).

The present invention is made description by some preferred examples, should be known in tangible improvement of those skilled in the art or conversion all are included within the present invention and the appended claim scope.

Claims (7)

1, a kind of preparation method of novel styryl phosphonic acid polymkeric substance, this styryl phosphonic acid polymkeric substance is selected from β-styryl phosphonic acid homopolymer and β-styryl phosphonic acid and the monomeric multipolymer of vinyl phosphonate, this method comprises: in the presence of radical initiator, reaching as high as under 125 ℃ the temperature of rising, make monomer or monomer mixture generation polymerization with any mode commonly used, the polymer product crude product is mixed with water, regulate resulting solution to PH8-11, the saturating folding of water is fallen, and isolate purified polymer.

2, according to the process of claim 1 wherein that described monomer is β-styryl phosphonic acid monomer.

3, according to the process of claim 1 wherein that described monomer is β-styryl phosphonic acid monomer and the monomeric mixture of vinyl phosphonic acyl chlorides.

4, according to each method in the claim 1 to 3, the consumption of wherein said radical initiator is 2.5% to 5% of described monomer or a monomer mixture weight.

5, according to the method for claim 4, wherein said radical initiator is a Diisopropyl azodicarboxylate.

6, according to each method of claim 1 to 3, wherein said polymerization was carried out 8 to 200 hours.

7,, carry out under the wherein said existence that is aggregated in inert organic solvents according to each method of claim 1 to 3.