SE452106B - Sett och medel for att forbettra vidheftningen av kompositer vid dentin, emalj och andra substrat - Google Patents

Sett och medel for att forbettra vidheftningen av kompositer vid dentin, emalj och andra substrat

Info

Publication number: SE452106B
Authority: SE; Sweden
Prior art keywords: solution; article according; chamber; dentin; acetone
Prior art date: 1983-07-25

Application number

SE8501434A

Other languages

English (en)

Swedish (sv)

Other versions

SE8501434L (sv

SE8501434D0 (sv

Inventor

R L Bowen

Original Assignee

American Dental Ass

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1983-07-25

Filing date

1985-03-22

Publication date

1987-11-16

1985-03-22 Application filed by American Dental Ass filed Critical American Dental Ass

1985-03-22 Publication of SE8501434L publication Critical patent/SE8501434L/xx

1985-03-22 Publication of SE8501434D0 publication Critical patent/SE8501434D0/xx

1987-11-16 Publication of SE452106B publication Critical patent/SE452106B/sv

Links

210000003298 dental enamel Anatomy 0.000 title claims abstract description 45
239000000758 substrate Substances 0.000 title claims abstract description 40
239000002131 composite material Substances 0.000 title claims abstract description 24
239000000243 solution Substances 0.000 claims abstract description 102
210000004268 dentin Anatomy 0.000 claims abstract description 79
239000002904 solvent Substances 0.000 claims abstract description 65
238000000034 method Methods 0.000 claims abstract description 50
NPKSPKHJBVJUKB-UHFFFAOYSA-N N-phenylglycine Chemical compound OC(=O)CNC1=CC=CC=C1 NPKSPKHJBVJUKB-UHFFFAOYSA-N 0.000 claims abstract description 38
239000000203 mixture Substances 0.000 claims abstract description 30
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 27
150000001768 cations Chemical class 0.000 claims abstract description 27
150000001875 compounds Chemical class 0.000 claims abstract description 27
RMCCONIRBZIDTH-UHFFFAOYSA-N 2-(2-methylprop-2-enoyloxy)ethyl 1,3-dioxo-2-benzofuran-5-carboxylate Chemical compound CC(=C)C(=O)OCCOC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 RMCCONIRBZIDTH-UHFFFAOYSA-N 0.000 claims abstract description 24
229920005989 resin Polymers 0.000 claims abstract description 19
239000000805 composite resin Substances 0.000 claims abstract description 18
239000007795 chemical reaction product Substances 0.000 claims abstract description 17
150000001450 anions Chemical class 0.000 claims abstract description 16
239000002244 precipitate Substances 0.000 claims abstract description 16
239000007864 aqueous solution Substances 0.000 claims abstract description 15
WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 claims abstract description 13
238000007259 addition reaction Methods 0.000 claims abstract description 13
239000011575 calcium Substances 0.000 claims abstract description 11
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims abstract description 10
150000008043 acidic salts Chemical class 0.000 claims abstract description 10
229910052791 calcium Inorganic materials 0.000 claims abstract description 10
ANSXAPJVJOKRDJ-UHFFFAOYSA-N furo[3,4-f][2]benzofuran-1,3,5,7-tetrone Chemical compound C1=C2C(=O)OC(=O)C2=CC2=C1C(=O)OC2=O ANSXAPJVJOKRDJ-UHFFFAOYSA-N 0.000 claims abstract description 6
VQVIHDPBMFABCQ-UHFFFAOYSA-N 5-(1,3-dioxo-2-benzofuran-5-carbonyl)-2-benzofuran-1,3-dione Chemical compound C1=C2C(=O)OC(=O)C2=CC(C(C=2C=C3C(=O)OC(=O)C3=CC=2)=O)=C1 VQVIHDPBMFABCQ-UHFFFAOYSA-N 0.000 claims abstract description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 212
VEPSWGHMGZQCIN-UHFFFAOYSA-H ferric oxalate Chemical compound [Fe+3].[Fe+3].[O-]C(=O)C([O-])=O.[O-]C(=O)C([O-])=O.[O-]C(=O)C([O-])=O VEPSWGHMGZQCIN-UHFFFAOYSA-H 0.000 claims description 34
239000004094 surface-active agent Substances 0.000 claims description 33
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150000003839 salts Chemical class 0.000 claims description 16
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IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 10
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239000012047 saturated solution Substances 0.000 claims description 6
VLDPXPPHXDGHEW-UHFFFAOYSA-N 1-chloro-2-dichlorophosphoryloxybenzene Chemical compound ClC1=CC=CC=C1OP(Cl)(Cl)=O VLDPXPPHXDGHEW-UHFFFAOYSA-N 0.000 claims description 4
150000008064 anhydrides Chemical group 0.000 claims description 4
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NPFOYSMITVOQOS-UHFFFAOYSA-K iron(III) citrate Chemical compound [Fe+3].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NPFOYSMITVOQOS-UHFFFAOYSA-K 0.000 claims description 4
229910019142 PO4 Inorganic materials 0.000 claims description 3
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125000001931 aliphatic group Chemical group 0.000 claims description 2
150000004820 halides Chemical group 0.000 claims description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 2
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-1 iron (III) oxalate Iron (III) oxalate Chemical compound 0.000 description 12
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230000015572 biosynthetic process Effects 0.000 description 9
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210000001519 tissue Anatomy 0.000 description 9
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RZXMPPFPUUCRFN-UHFFFAOYSA-N p-toluidine Chemical compound CC1=CC=C(N)C=C1 RZXMPPFPUUCRFN-UHFFFAOYSA-N 0.000 description 8
238000003786 synthesis reaction Methods 0.000 description 8
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239000003112 inhibitor Substances 0.000 description 7
238000002844 melting Methods 0.000 description 7
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VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 7
150000003254 radicals Chemical class 0.000 description 7
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 6
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 6
230000008901 benefit Effects 0.000 description 6
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OWZIYWAUNZMLRT-UHFFFAOYSA-L iron(2+);oxalate Chemical compound [Fe+2].[O-]C(=O)C([O-])=O OWZIYWAUNZMLRT-UHFFFAOYSA-L 0.000 description 6
239000010410 layer Substances 0.000 description 6
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238000002474 experimental method Methods 0.000 description 5
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229910052742 iron Inorganic materials 0.000 description 5
CERQOIWHTDAKMF-UHFFFAOYSA-M methacrylate group Chemical group C(C(=C)C)(=O)[O-] CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 5
239000000178 monomer Substances 0.000 description 5
238000010526 radical polymerization reaction Methods 0.000 description 5
238000003860 storage Methods 0.000 description 5
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AFBPFSWMIHJQDM-UHFFFAOYSA-N N-methyl-N-phenylamine Natural products CNC1=CC=CC=C1 AFBPFSWMIHJQDM-UHFFFAOYSA-N 0.000 description 4
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
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238000001878 scanning electron micrograph Methods 0.000 description 4
230000002269 spontaneous effect Effects 0.000 description 4
150000003512 tertiary amines Chemical class 0.000 description 4
JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 description 3
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239000004471 Glycine Substances 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
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125000003118 aryl group Chemical group 0.000 description 3
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FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 3
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125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 3
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CTFOHWIEFNJZHC-UHFFFAOYSA-N 2-(4-methylanilino)acetic acid Chemical compound CC1=CC=C(NCC(O)=O)C=C1 CTFOHWIEFNJZHC-UHFFFAOYSA-N 0.000 description 2
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DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
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229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
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239000012736 aqueous medium Substances 0.000 description 1
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230000009286 beneficial effect Effects 0.000 description 1
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239000012965 benzophenone Substances 0.000 description 1
235000019400 benzoyl peroxide Nutrition 0.000 description 1
230000005540 biological transmission Effects 0.000 description 1
WXNRYSGJLQFHBR-UHFFFAOYSA-N bis(2,4-dihydroxyphenyl)methanone Chemical compound OC1=CC(O)=CC=C1C(=O)C1=CC=C(O)C=C1O WXNRYSGJLQFHBR-UHFFFAOYSA-N 0.000 description 1
238000006664 bond formation reaction Methods 0.000 description 1
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244000309464 bull Species 0.000 description 1
235000010354 butylated hydroxytoluene Nutrition 0.000 description 1
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239000001110 calcium chloride Substances 0.000 description 1
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238000006555 catalytic reaction Methods 0.000 description 1
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150000002170 ethers Chemical class 0.000 description 1
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230000001747 exhibiting effect Effects 0.000 description 1
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229960002413 ferric citrate Drugs 0.000 description 1
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238000000338 in vitro Methods 0.000 description 1
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239000010985 leather Substances 0.000 description 1
239000003446 ligand Substances 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
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150000002736 metal compounds Chemical class 0.000 description 1
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MQUIHBQDYYAEMH-UHFFFAOYSA-N methedrone Chemical compound CNC(C)C(=O)C1=CC=C(OC)C=C1 MQUIHBQDYYAEMH-UHFFFAOYSA-N 0.000 description 1
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230000000474 nursing effect Effects 0.000 description 1
238000005457 optimization Methods 0.000 description 1
229910052762 osmium Inorganic materials 0.000 description 1
230000003204 osmotic effect Effects 0.000 description 1
BBJSDUUHGVDNKL-UHFFFAOYSA-J oxalate;titanium(4+) Chemical compound [Ti+4].[O-]C(=O)C([O-])=O.[O-]C(=O)C([O-])=O BBJSDUUHGVDNKL-UHFFFAOYSA-J 0.000 description 1
239000007800 oxidant agent Substances 0.000 description 1
230000001590 oxidative effect Effects 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical compound COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 1
230000020477 pH reduction Effects 0.000 description 1
239000008188 pellet Substances 0.000 description 1
230000000737 periodic effect Effects 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
ZFACJPAPCXRZMQ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O.OC(=O)C1=CC=CC=C1C(O)=O ZFACJPAPCXRZMQ-UHFFFAOYSA-N 0.000 description 1
230000001766 physiological effect Effects 0.000 description 1
OXNIZHLAWKMVMX-UHFFFAOYSA-N picric acid Chemical compound OC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O OXNIZHLAWKMVMX-UHFFFAOYSA-N 0.000 description 1
239000004033 plastic Substances 0.000 description 1
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229920013657 polymer matrix composite Polymers 0.000 description 1
239000011160 polymer matrix composite Substances 0.000 description 1
239000002685 polymerization catalyst Substances 0.000 description 1
230000000379 polymerizing effect Effects 0.000 description 1
229920001343 polytetrafluoroethylene Polymers 0.000 description 1
229910052573 porcelain Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
HHDOORYZQSEMGM-UHFFFAOYSA-L potassium;oxalate;titanium(4+) Chemical compound [K+].[Ti+4].[O-]C(=O)C([O-])=O HHDOORYZQSEMGM-UHFFFAOYSA-L 0.000 description 1
238000002203 pretreatment Methods 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
239000003586 protic polar solvent Substances 0.000 description 1
230000005180 public health Effects 0.000 description 1
239000010453 quartz Substances 0.000 description 1
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230000004044 response Effects 0.000 description 1
230000000717 retained effect Effects 0.000 description 1
229910052702 rhenium Inorganic materials 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
229930195734 saturated hydrocarbon Natural products 0.000 description 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
238000002791 soaking Methods 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
239000011343 solid material Substances 0.000 description 1
230000007480 spreading Effects 0.000 description 1
238000003892 spreading Methods 0.000 description 1
238000010186 staining Methods 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
229910021653 sulphate ion Inorganic materials 0.000 description 1
239000006228 supernatant Substances 0.000 description 1
238000004381 surface treatment Methods 0.000 description 1
230000009044 synergistic interaction Effects 0.000 description 1
230000002194 synthesizing effect Effects 0.000 description 1
239000011975 tartaric acid Substances 0.000 description 1
235000002906 tartaric acid Nutrition 0.000 description 1
229910052713 technetium Inorganic materials 0.000 description 1
150000003510 tertiary aliphatic amines Chemical class 0.000 description 1
125000001302 tertiary amino group Chemical group 0.000 description 1
229930101283 tetracycline Natural products 0.000 description 1
XROWMBWRMNHXMF-UHFFFAOYSA-J titanium tetrafluoride Chemical compound [F-].[F-].[F-].[F-].[Ti+4] XROWMBWRMNHXMF-UHFFFAOYSA-J 0.000 description 1
150000004992 toluidines Chemical class 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
238000011269 treatment regimen Methods 0.000 description 1
YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
238000003828 vacuum filtration Methods 0.000 description 1
238000009423 ventilation Methods 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J4/00—Adhesives based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; adhesives, based on monomers of macromolecular compounds of groups C09J183/00 - C09J183/16
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J5/00—Adhesive processes in general; Adhesive processes not provided for elsewhere, e.g. relating to primers
- C09J5/02—Adhesive processes in general; Adhesive processes not provided for elsewhere, e.g. relating to primers involving pretreatment of the surfaces to be joined

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Dental Preparations (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Adhesives Or Adhesive Processes (AREA)
Paints Or Removers (AREA)

SE8501434A 1983-07-25 1985-03-22 Sett och medel for att forbettra vidheftningen av kompositer vid dentin, emalj och andra substrat SE452106B (sv)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US06/516,956 US4521550A (en)	1983-01-10	1983-07-25	Method for obtaining strong adhesive bonding of composites to dentin, enamel and other substrates

Publications (3)

Publication Number	Publication Date
SE8501434L SE8501434L (sv)	1985-03-22
SE8501434D0 SE8501434D0 (sv)	1985-03-22
SE452106B true SE452106B (sv)	1987-11-16

Family

ID=24057769

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SE8501434A SE452106B (sv)	1983-07-25	1985-03-22	Sett och medel for att forbettra vidheftningen av kompositer vid dentin, emalj och andra substrat

Country Status (12)

Country	Link
US (1)	US4521550A (pt)
EP (1)	EP0151612B1 (pt)
JP (1)	JPS60502055A (pt)
AU (1)	AU558786B2 (pt)
BR (1)	BR8406987A (pt)
CA (1)	CA1227383A (pt)
CH (1)	CH669518A5 (pt)
DE (2)	DE3490336C2 (pt)
GB (1)	GB2159067B (pt)
IT (1)	IT1181806B (pt)
SE (1)	SE452106B (pt)
WO (1)	WO1985000514A1 (pt)

Families Citing this family (48)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4659751A (en) *	1983-01-10	1987-04-21	American Dental Association Health Foundation	Simplified method for obtained strong adhesive bonding of composites to dentin, enamel and other substrates
US4719149A (en) *	1986-02-28	1988-01-12	Minnesota Mining And Manufacturing Company	Method for priming hard tissue
US4744759A (en) *	1986-05-13	1988-05-17	American Dental Association Health Foundation	Inserts for composite dental restorations
JPH06689B2 (ja) *	1986-09-05	1994-01-05	宇部興産株式会社	光重合性歯科材料
US4880660A (en) *	1987-08-28	1989-11-14	Minnesota Mining And Manufacturing Company	Method for priming hard tissue
US4964911A (en) *	1987-10-13	1990-10-23	Den-Mat Corporation	Adhesive bonding of acrylic resins, especially in dentistry
JP2756275B2 (ja) *	1987-10-13	1998-05-25	デン・マット・コーポレーション	基体表面を製造するための製品
USRE34937E (en) *	1987-10-13	1995-05-16	Den-Mat Corporation	Adhesive bonding of acrylic resins, especially in dentistry
US4863993A (en) *	1987-12-09	1989-09-05	Opi Products, Inc.	Surface priming composition for proteinaceous substrates; method of making and using same
US4913939A (en) *	1987-12-09	1990-04-03	Rem Systems, Inc.	Method of making and using surface priming composition for proteinaceous substrates
EP0423430B1 (de) *	1989-10-19	1993-04-21	Heraeus Kulzer GmbH	Dentales Haftmittel
JP2634276B2 (ja) *	1990-02-15	1997-07-23	株式会社松風	プライマー組成物
US5218070A (en) *	1991-02-11	1993-06-08	Dentsply G.M.B.H.	Dental/medical composition and use
US5133957A (en) *	1991-09-18	1992-07-28	Bisco, Inc.	Composition and method for desensitizing dentin
US5320886A (en) *	1991-11-14	1994-06-14	American Dental Association Health Foundation	Hydrophilic crosslinking monomers and polymers made therefrom
US5525648A (en)	1991-12-31	1996-06-11	Minnesota Mining And Manufacturing Company	Method for adhering to hard tissue
US5270351A (en) *	1992-06-15	1993-12-14	American Dental Association Health Foundation	Adhesion-promoting agents incorporating polyvalent cations
IL102274A (en) *	1992-06-21	1995-06-29	B J M Lab Ltd	Dental adhesives
JP3399573B2 (ja) *	1993-01-29	2003-04-21	株式会社ジーシー	歯面処理キット
US5710194A (en) *	1993-04-19	1998-01-20	Dentsply Research & Development Corp.	Dental compounds, compositions, products and methods
US6391940B1 (en)	1993-04-19	2002-05-21	Dentsply Research & Development Corp.	Method and composition for adhering to metal dental structure
US6500879B1 (en)	1993-04-19	2002-12-31	Dentsply Research & Development Corp.	Dental composition and method
US5338773A (en) *	1993-04-19	1994-08-16	Dentsply Research & Development Corp.	Dental composition and method
US5425641A (en) *	1993-07-27	1995-06-20	Ultradent Products, Inc.	Dental kit and process for sealing pits and fissures in enamel
US5498643A (en) *	1994-02-01	1996-03-12	The United States Of America As Represented By The Secretary Of Commerce	Method and composition for promoting improved adhesion to substrates
US5525647A (en) *	1994-08-01	1996-06-11	American Dental Association Health Foundation	Method and device for controllably affecting the reaction of dental adhesives
DE4433987A1 (de) *	1994-09-23	1996-03-28	Muehlbauer Ernst Kg	Polymerisierbare Oligo- und/oder Polyalkensäuren
DE19544670C2 (de) *	1995-11-30	2003-01-09	Heraeus Kulzer Gmbh & Co Kg	Verfahren zur Herstellung oligomerer Kondensationsprodukte aromatischer Tricarbonsäuren und Epoxy(meth)acrylaten
US5866629A (en) *	1995-12-05	1999-02-02	The University Of Toronto Innovations Foundation	Dental and medical primer formulations containing tissue infiltrating agents
US5859089A (en) *	1997-07-01	1999-01-12	The Kerr Corporation	Dental restorative compositions
DE19749349A1 (de) *	1997-11-07	1999-05-12	Espe Dental Ag	Polymerisierbare Zusammensetzung und ihre Verwendung als Haftvermittler
US6114408A (en)	1998-02-06	2000-09-05	American Dental Association Health Foundation	Single-solution adhesive resin formulations
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1983
- 1983-07-25 US US06/516,956 patent/US4521550A/en not_active Expired - Lifetime
1984
- 1984-07-16 JP JP59502975A patent/JPS60502055A/ja active Granted
- 1984-07-16 WO PCT/US1984/001109 patent/WO1985000514A1/en active IP Right Grant
- 1984-07-16 DE DE3490336A patent/DE3490336C2/de not_active Expired - Fee Related
- 1984-07-16 GB GB08506987A patent/GB2159067B/en not_active Expired
- 1984-07-16 EP EP84902974A patent/EP0151612B1/en not_active Expired
- 1984-07-16 BR BR8406987A patent/BR8406987A/pt not_active IP Right Cessation
- 1984-07-16 AU AU32118/84A patent/AU558786B2/en not_active Ceased
- 1984-07-16 DE DE19843490336 patent/DE3490336T1/de active Pending
- 1984-07-24 CA CA000459512A patent/CA1227383A/en not_active Expired
- 1984-07-24 IT IT48620/84A patent/IT1181806B/it active
1985
- 1985-03-22 SE SE8501434A patent/SE452106B/sv not_active IP Right Cessation
- 1985-07-16 CH CH1391/85A patent/CH669518A5/de not_active IP Right Cessation

Also Published As

Publication number	Publication date
US4521550A (en)	1985-06-04
AU558786B2 (en)	1987-02-05
SE8501434L (sv)	1985-03-22
EP0151612B1 (en)	1989-01-25
JPH0258244B2 (pt)	1990-12-07
CH669518A5 (pt)	1989-03-31
DE3490336C2 (de)	1994-12-01
GB2159067B (en)	1987-03-04
BR8406987A (pt)	1985-07-02
CA1227383A (en)	1987-09-29
GB8506987D0 (en)	1985-04-24
DE3490336T1 (de)	1985-09-19
GB2159067A (en)	1985-11-27
SE8501434D0 (sv)	1985-03-22
IT1181806B (it)	1987-09-30
WO1985000514A1 (en)	1985-02-14
EP0151612A1 (en)	1985-08-21
JPS60502055A (ja)	1985-11-28
AU3211884A (en)	1985-03-04
IT8448620A0 (it)	1984-07-24

Publication	Publication Date	Title
SE452106B (sv)	1987-11-16	Sett och medel for att forbettra vidheftningen av kompositer vid dentin, emalj och andra substrat
US4514527A (en)	1985-04-30	Method for obtaining strong adhesive bonding of composites to dentin enamel and other substrates
US4588756A (en)	1986-05-13	Multi-step method for obtaining strong adhesive bonding of composites to dentin, enamel and other substrates
Bowen et al.	1982	Adhesive bonding of various materials to hard tooth tissues: improvement in bond strength to dentin
US5789610A (en)	1998-08-04	Adhesion-promoting agents incorporating polyvalent cations
EP0266220B1 (en)	1993-01-07	Curable composition
EP1721949B1 (de)	2010-06-16	Haftverbessernde Additive für polymerisierbare Zusammensetzungen
JPS6340406B2 (pt)	1988-08-11
JPS5930877A (ja)	1984-02-18	歯科用接着性組成物
JPH0277478A (ja)	1990-03-16	含イオウ接着剤
TW200843797A (en)	2008-11-16	Polymerizable monomer, polymerizable composition and dental material
CA1276648C (en)	1990-11-20	Method for obtaining strong adhesive bonding of composites to dentin, enamel and other substrates
JPS5821687A (ja)	1983-02-08	（メタ）アクリロイルオキシアルキルジハイドロジエンホスフエ−ト
JP2004203773A (ja)	2004-07-22	硬化性組成物
US5294646A (en)	1994-03-15	N-alkyl-n-(meth)acryloyloxyalkylcarboxamides of aromatic carboxylic acids and aromatic carboxylic acid anhydrides, and adhesives containing these compounds
JPH10505868A (ja)	1998-06-09	環状カーボネート基を有する重合性芳香族カルボン酸及び芳香族カルボン酸無水物、並びにこれらの化合物を含有する配合物
EP0718386B1 (en)	1998-02-18	Air-activatable polymerizable compositions containing tetrazoles
CA2199623A1 (en)	1997-01-30	Derivatives of aromatic carboxylic acids from aromatic carboxyanhydridesand hydroxyalkyl (meth) acrylates, as well as preparations containing these compounds
JPH0567146B2 (pt)	1993-09-24
JP3465748B2 (ja)	2003-11-10	歯科用接着セット
JPS6013866A (ja)	1985-01-24	接着性被膜形成材
RU2729619C1 (ru)	2020-08-11	Способ получения стоматологической адгезивной компоненты
JPH04327513A (ja)	1992-11-17	歯質接着性促進化合物およびそれを含む前処理剤および接着性組成物
Van Hees	2019	Temperature responsive polyelectrolyte complexes: Bio-inspired wet-adhesives
Ikemura et al.	2011	Synthesis of novel acryloyloxyalkyl and methacryloyloxyalkyl 6, 8-dithiooctanoates and evaluation of their bonding performances to precious metals and alloys

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