TW202118826A - Light curing retraction material - Google Patents
Light curing retraction material Download PDFInfo
- Publication number
- TW202118826A TW202118826A TW108140682A TW108140682A TW202118826A TW 202118826 A TW202118826 A TW 202118826A TW 108140682 A TW108140682 A TW 108140682A TW 108140682 A TW108140682 A TW 108140682A TW 202118826 A TW202118826 A TW 202118826A
- Authority
- TW
- Taiwan
- Prior art keywords
- light
- retraction material
- gingival retraction
- curing
- item
- Prior art date
Links
- 239000000463 material Substances 0.000 title claims abstract description 101
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 18
- 239000003999 initiator Substances 0.000 claims abstract description 17
- 239000003431 cross linking reagent Substances 0.000 claims abstract description 15
- 239000007787 solid Substances 0.000 claims abstract description 12
- 239000000203 mixture Substances 0.000 claims description 26
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 14
- PEDCQBHIVMGVHV-UHFFFAOYSA-N glycerol group Chemical group OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 14
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 claims description 12
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 claims description 12
- 239000002562 thickening agent Substances 0.000 claims description 11
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 10
- 229920002134 Carboxymethyl cellulose Polymers 0.000 claims description 8
- 239000001768 carboxy methyl cellulose Substances 0.000 claims description 8
- 235000010948 carboxy methyl cellulose Nutrition 0.000 claims description 8
- 239000008112 carboxymethyl-cellulose Substances 0.000 claims description 8
- OKKRPWIIYQTPQF-UHFFFAOYSA-N Trimethylolpropane trimethacrylate Chemical group CC(=C)C(=O)OCC(CC)(COC(=O)C(C)=C)COC(=O)C(C)=C OKKRPWIIYQTPQF-UHFFFAOYSA-N 0.000 claims description 7
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 7
- 239000000679 carrageenan Substances 0.000 claims description 7
- 235000010418 carrageenan Nutrition 0.000 claims description 7
- 229920001525 carrageenan Polymers 0.000 claims description 7
- 229940113118 carrageenan Drugs 0.000 claims description 7
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical group O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 7
- 239000000843 powder Substances 0.000 claims description 7
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 claims description 7
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 claims description 6
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical group CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 claims description 6
- GUCYFKSBFREPBC-UHFFFAOYSA-N [phenyl-(2,4,6-trimethylbenzoyl)phosphoryl]-(2,4,6-trimethylphenyl)methanone Chemical group CC1=CC(C)=CC(C)=C1C(=O)P(=O)(C=1C=CC=CC=1)C(=O)C1=C(C)C=C(C)C=C1C GUCYFKSBFREPBC-UHFFFAOYSA-N 0.000 claims description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 6
- 235000011187 glycerol Nutrition 0.000 claims description 6
- 239000000600 sorbitol Substances 0.000 claims description 6
- 239000005995 Aluminium silicate Substances 0.000 claims description 5
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 claims description 5
- 235000012211 aluminium silicate Nutrition 0.000 claims description 5
- 239000003906 humectant Substances 0.000 claims description 5
- 238000002347 injection Methods 0.000 claims description 5
- 239000007924 injection Substances 0.000 claims description 5
- 239000004909 Moisturizer Substances 0.000 claims description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N acetone Substances CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 4
- 230000001333 moisturizer Effects 0.000 claims description 4
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 claims description 3
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 claims 1
- QPMJENKZJUFOON-PLNGDYQASA-N ethyl (z)-3-chloro-2-cyano-4,4,4-trifluorobut-2-enoate Chemical compound CCOC(=O)C(\C#N)=C(/Cl)C(F)(F)F QPMJENKZJUFOON-PLNGDYQASA-N 0.000 claims 1
- 238000001723 curing Methods 0.000 description 32
- VNQXSTWCDUXYEZ-UHFFFAOYSA-N 1,7,7-trimethylbicyclo[2.2.1]heptane-2,3-dione Chemical compound C1CC2(C)C(=O)C(=O)C1C2(C)C VNQXSTWCDUXYEZ-UHFFFAOYSA-N 0.000 description 5
- 229930006711 bornane-2,3-dione Natural products 0.000 description 5
- 230000004048 modification Effects 0.000 description 5
- 238000012986 modification Methods 0.000 description 5
- 238000000016 photochemical curing Methods 0.000 description 5
- 238000002474 experimental method Methods 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000011010 flushing procedure Methods 0.000 description 3
- ICFXCSLDPCMWJI-UHFFFAOYSA-N 2,3-dimethylbut-2-enoic acid;2-ethyl-2-(hydroxymethyl)propane-1,3-diol Chemical compound CC(C)=C(C)C(O)=O.CCC(CO)(CO)CO ICFXCSLDPCMWJI-UHFFFAOYSA-N 0.000 description 2
- XMLYCEVDHLAQEL-UHFFFAOYSA-N 2-hydroxy-2-methyl-1-phenylpropan-1-one Chemical compound CC(C)(O)C(=O)C1=CC=CC=C1 XMLYCEVDHLAQEL-UHFFFAOYSA-N 0.000 description 2
- YDIYYWIAGKNHTK-UHFFFAOYSA-N [(2-phenylphenyl)-(2,4,6-trimethylbenzoyl)phosphoryl]-(2,4,6-trimethylphenyl)methanone Chemical compound C1(=CC=CC=C1)C1=C(C=CC=C1)P(C(C1=C(C=C(C=C1C)C)C)=O)(C(C1=C(C=C(C=C1C)C)C)=O)=O YDIYYWIAGKNHTK-UHFFFAOYSA-N 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229910052622 kaolinite Inorganic materials 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000005871 repellent Substances 0.000 description 2
- 230000002940 repellent Effects 0.000 description 2
- PDLCCNYKIIUWHA-UHFFFAOYSA-N 1-(4-propan-2-ylphenyl)ethanone Chemical compound CC(C)C1=CC=C(C(C)=O)C=C1 PDLCCNYKIIUWHA-UHFFFAOYSA-N 0.000 description 1
- ZEERWUUHFUFJJT-UHFFFAOYSA-N 2-hydroxy-2-methyl-1-phenylpropan-1-one Chemical compound CC(C)(O)C(=O)C1=CC=CC=C1.CC(C)(O)C(=O)C1=CC=CC=C1 ZEERWUUHFUFJJT-UHFFFAOYSA-N 0.000 description 1
- -1 IRGACURE 819) Chemical compound 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 201000005562 gingival recession Diseases 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 230000002439 hemostatic effect Effects 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 238000002690 local anesthesia Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000010297 mechanical methods and process Methods 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000010076 replication Effects 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
Landscapes
- Dental Preparations (AREA)
Abstract
Description
本發明係有關於一種排齦材料,特別是有關於可藉由光照射固化之排齦材料。 The present invention relates to a gingival retraction material, in particular to a gingival retraction material that can be cured by light irradiation.
排齦程序是一般在牙科臨床上,將病患牙齦溝暫時性地水平推開擴大後用以進行印模操作的先前程序。傳統中較常用排齦線(Gingival retraction cords)的方式,以機械力量擠壓排齦線入牙齦溝內,使牙齦溝水平擴大。然而,排齦線的操作需要相當高度的技巧才能將排齦線順利地填入牙齦溝中,且一般單顆牙齒操作約需要7-10分鐘。因此,排齦線在操作上難度高、費時,此外,也需先施行局部麻醉減輕排齦線操作時病患的不適感。再者,在使用排齦線排齦後,約會造成平均0.1mm牙齦退縮(Marginal recession)。 The gingival retraction procedure is generally used in dental clinics to temporarily push the patient's gingival sulcus horizontally and expand it to perform an impression operation. Gingival retraction cords are commonly used in the traditional way, which uses mechanical force to squeeze the retraction cord into the gingival sulcus to expand the gingival sulcus horizontally. However, the operation of the gingival cord requires a high degree of skill to smoothly fill the gingival cord into the gingival sulcus, and it usually takes about 7-10 minutes to operate a single tooth. Therefore, the operation of the retraction cord is difficult and time-consuming. In addition, local anesthesia must be applied first to reduce the patient's discomfort during the operation of the retraction cord. Furthermore, after using the retraction cord to retreat, dating causes an average of 0.1mm gingival recession (Marginal recession).
為了減少上述使用排齦線排齦的問題,也愈來愈多非排齦線(Cordless)的技術被提出來。例如,運用化學-機械的方式排齦,透過添加化學藥劑,例如三氯化鋁作為收斂劑的排齦材料,填入牙齦 溝排齦,操作上相對上更為便利,且也可解決排齦線的不適感。然而,此類型的排齦材料仍需花費一定時間擴大牙齦,且需利用沖水方式移除,無法保持乾燥,而導致後續印模操作上的困難。再者,現行的排齦材料若沒清除乾淨,也容易殘留、沾黏在牙齒、牙齦上。 In order to reduce the above-mentioned problem of using retraction cords to retreat, more and more cordless technologies have been proposed. For example, using a chemical-mechanical method to evacuate the gums, filling the gums by adding chemicals such as aluminum trichloride as an astringent evacuation material Groove retraction is relatively more convenient in operation, and can also solve the discomfort of the retraction line. However, this type of gingival retraction material still takes a certain amount of time to expand the gums, and needs to be removed by flushing, and cannot be kept dry, resulting in difficulties in subsequent impression operations. Furthermore, if the current gingival retraction material is not cleaned, it is easy to remain and stick to the teeth and gums.
因此,有需要提供一種新改良的排齦材料。 Therefore, there is a need to provide a new and improved gingival retraction material.
有鑑於此,本發明之一目的在於提供一種光固化排齦材料,可利用UV光照射,將此排齦材料由膏狀形態轉變成固體形態,再將之移除。由於,本發明之排齦材料可利用UV光照射的方式,迅速固化,可節省排齦程序的時間,且固化後的排齦材料可直接利用夾取方式移除,而不會造成殘留,而不需如習知方式沖水的方式移除,故本發明之光固化排齦材料可保持例如牙齦溝的乾燥。本發明實施例之光固化排齦材料可保持乾燥,也有利於後續之印模操作時可得到完整的修磨邊緣複製模型,而可確保及提高假牙膺復物的製作精度。 In view of this, one object of the present invention is to provide a light-curable gingival retraction material, which can be irradiated with UV light to convert the gingival retraction material from a paste-like form to a solid form, and then remove it. Because the gingival retraction material of the present invention can be rapidly cured by UV light irradiation, it can save the time of the gingival retraction procedure, and the cured gingival retraction material can be directly removed by clamping without causing residue, and It does not need to be removed by flushing in a conventional manner, so the light-curable gingival retraction material of the present invention can keep, for example, the gingival sulcus dry. The light-curable gingival retraction material of the embodiment of the present invention can be kept dry, and is also conducive to obtaining a complete grinding edge replication model during the subsequent impression operation, and can ensure and improve the production accuracy of the artificial tooth complex.
為達到上述目的,本發明之一較佳實施例係提供一光固化排齦材料,其係以一膏狀形態存在,且該光固化排齦材料包含至少一光固化劑、一起始劑及一交聯劑,當曝露於一UV光底下時,該光固化排齦材料由膏狀形態轉變成固體形態。 To achieve the above objective, a preferred embodiment of the present invention provides a light-curable gingival retraction material, which exists in a paste form, and the light-curable gingival retraction material includes at least one light curing agent, an initiator, and one The cross-linking agent, when exposed to a UV light, the light-curable gingival repellent material changes from a paste-like form to a solid form.
較佳地,該光固化排齦材料以膏狀形態存在時,其具有一黏度範圍介於10x106~70x106cP之間。 Preferably, when the light-curable gingival retraction material exists in a paste form, it has a viscosity range between 10 ×10 6 and 70× 10 6 cP.
較佳地,該UV光包含一波長範圍介於400nm~500nm之間。 Preferably, the UV light includes a wavelength range between 400 nm and 500 nm.
較佳地,該UV光係由一能量範圍介於500~3000mW/cm2的光照機所發出。 Preferably, the UV light is emitted by an illuminator with an energy range of 500-3000 mW/cm 2 .
較佳地,該光固化排齦材料具有一由膏狀形態轉變為固體形態的固化時間,介於10~50秒之間。 Preferably, the light-curable gingival retraction material has a curing time from a paste form to a solid form, which is between 10 and 50 seconds.
較佳地,該光固化排齦材料在以該膏狀形態存在時,該光固化排齦材料係以一注射的方式注射至一目標物。 Preferably, when the light-curing gingival retraction material exists in the paste form, the light-curing gingival retraction material is injected into a target in an injection manner.
較佳地,該光固化排齦材料,包含該光固化劑、該起始劑、該交聯劑、一增稠劑、一保濕劑以及一賦形劑。 Preferably, the photocurable gingival retraction material includes the photocuring agent, the initiator, the crosslinking agent, a thickener, a humectant, and an excipient.
較佳地,光固化排齦材料的該光固化劑,係2-甲基丙烯酸(2-Hydroxyethyl methacrylate,HEMA)或甲基丙烯酸(Methacrylic acid,MMA),或者2-甲基丙烯酸及甲基丙烯酸的混合物。 Preferably, the light curing agent of the light curing gingival retraction material is 2-Hydroxyethyl methacrylate (HEMA) or Methacrylic acid (MMA), or 2-Hydroxyethyl methacrylate (HEMA) or Methacrylic acid (MMA), or 2-Methacrylic acid and methacrylic acid. mixture.
較佳地,光固化排齦材料的該起始劑,係苯基雙(2,4,6-三甲基苯甲酰基)氧化膦(Bis(2,4,6-trimethylbenzoyl)-phenylphosphineoxide)、2-羥基-2-甲基-1-苯基-1-丙酮(2-Hydroxy-2-methylpropiophenone)或苯酉昆崁酮 (Camphorquinone,CQ),或者其中二者或其三者的混合物。 Preferably, the initiator of the photocurable gingival retraction material is phenyl bis(2,4,6-trimethylbenzoyl)-phenylphosphineoxide (Bis(2,4,6-trimethylbenzoyl)-phenylphosphineoxide), 2-Hydroxy-2-methyl-1-phenyl-1-propanone (2-Hydroxy-2-methylpropiophenone) or benzoquinone (Camphorquinone, CQ), or a mixture of two or three of them.
較佳地,光固化排齦材料的該交聯劑,係三羥甲基丙烷三甲基丙烯酸酯(Trimethylolpropane trimethylacrylate,TMPTMA)或二甲基兩烯酸乙二醇酯(Ethylene glycol dimethacrylate,EGDMA),或者三羥甲基丙烷三甲基丙烯酸酯(TMPTMA)及二甲基兩烯酸乙二醇酯(EGDMA)的混合物。 Preferably, the crosslinking agent of the light-curable gingival retraction material is trimethylolpropane trimethylacrylate (TMPTMA) or ethylene glycol dimethacrylate (EGDMA) , Or a mixture of trimethylolpropane trimethacrylate (TMPTMA) and ethylene glycol dimethyl dienoate (EGDMA).
較佳地,光固化排齦材料的該增稠劑,係羧甲基纖維素(Carboxymethyl Cellulose)或卡拉膠(Carrageenan),或者羧甲基纖維素及卡拉膠的混合物。 Preferably, the thickener of the light-curable gingival retraction material is carboxymethyl cellulose (Carboxymethyl Cellulose) or carrageenan, or a mixture of carboxymethyl cellulose and carrageenan.
較佳地,光固化排齦材料的該保濕劑,係甘油(Glycerol)或山梨糖醇(Sorbitol),或者甘油及山梨糖醇的混合物。 Preferably, the moisturizer of the light-curable gingival retraction material is glycerol or sorbitol, or a mixture of glycerol and sorbitol.
較佳地,光固化排齦材料的該賦形劑,係高嶺土(Kaolinite)或氧化鋁粉(Alumina powder),或者高嶺土及氧化鋁粉的混合物。 Preferably, the excipient of the light-curable gingival retraction material is kaolinite or alumina powder, or a mixture of kaolinite and alumina powder.
較佳地,光固化排齦材料的該光固化劑之重量百分比約為20%。 Preferably, the weight percentage of the light curing agent of the light curing gingival retraction material is about 20%.
較佳地,光固化排齦材料的該起始劑整重量百分比約為4%。 Preferably, the total weight percentage of the initiator of the light-curable gingival retraction material is about 4%.
較佳地,光固化排齦材料的該交聯劑之重量百分比約 為3%。 Preferably, the weight percentage of the crosslinking agent of the light-curable gingival retraction material is about Is 3%.
較佳地,光固化排齦材料的該增稠劑之重量百分比範圍介於18~28%之間。 Preferably, the weight percentage of the thickener of the light-curable gingival retraction material is in the range of 18-28%.
較佳地,光固化排齦材料的該保濕劑之重量百分比範圍介於15~30%之間。 Preferably, the weight percentage of the moisturizer of the light-curable gingival retraction material is in the range of 15-30%.
較佳地,光固化排齦材料的該賦形劑之重量百分比範圍介於20~40%之間。 Preferably, the weight percentage of the excipient of the light-curable gingival retraction material is in the range of 20-40%.
較佳地,光固化排齦材料固化後,藉由一外物將該固化之排齦材料從該目標物處移除。 Preferably, after the light-curable gingival retraction material is cured, the cured gingival retraction material is removed from the target by an external object.
本發明之一較佳實施例的光固化排齦材料,可以膏狀形態存在,且可利用例如針筒注射的方式,將排齦材料精準地注射至目標物,例如牙齦溝,接著,再利用一UV光照機,照射光固化排齦材料,以將排齦材料由膏狀形態轉變至固體形態。利用注射方式,除可精準置放光固化排齦材料外,亦可節省其用量。在經由UV光照射後,本發明之排齦材料可迅速固化,固化後,排齦材料亦不會沾黏於例如牙齒及牙齦的目標物上,可直接利用如鑷子的外物直接將之夾取出,而不會殘留。再者,由於本發明之光固化排齦材料固化後,可輕易取出,而不需如習知的沖水方式排出,故可保持排齦溝的乾燥,以利於後續印模的操作,並可確保及提高假牙膺復物的製作精度。 The light-curable gingival retraction material of a preferred embodiment of the present invention can exist in a paste form, and can be injected into the target object, such as the gingival sulcus, by using, for example, a syringe injection method, and then reused A UV light machine irradiates light to cure the gingival retraction material to transform the gingival retraction material from a paste-like form to a solid form. The injection method can not only accurately place the light-curing gingival retraction material, but also save its consumption. After being irradiated by UV light, the gingival retraction material of the present invention can be cured quickly. After curing, the gingival retraction material will not stick to the target objects such as teeth and gums. It can be directly clamped by foreign objects such as tweezers. Take it out without leaving behind. Furthermore, since the light-curable gingival retraction material of the present invention can be easily taken out after being cured, and does not need to be discharged as in the conventional flushing method, the gingival sulcus can be kept dry to facilitate subsequent impression operations. To ensure and improve the accuracy of the production of artificial dentures.
為使本發明實施的目的、技術方案和優點更加清楚,下面將對本發明實施例進行溝楚、完整地描述及說明,顯然地,所描述之實施例僅是本發明可具以實施之一部份實施例,而不是全部的實施例。在不脫離本發明的精神內,對所揭露之實施例潤飾、修飾、修改或簡單的變更,皆仍屬於本發明的範籌。 In order to make the purpose, technical solutions and advantages of the implementation of the present invention clearer, the embodiments of the present invention will be discussed, fully described and illustrated below. Obviously, the described embodiments are only part of the implementation of the present invention. Partial examples, not all examples. Without departing from the spirit of the present invention, retouching, modification, modification or simple changes to the disclosed embodiments still belong to the scope of the present invention.
在本發明實施例中使用的技術用語僅僅是出於描述特定實施例的目的,而非旨在限制本發明。在本發明實施例和所附申請專利範圍中所使用的單數形式,並不侷限於單數,除非上述文明確表示其它含義。 The technical terms used in the embodiments of the present invention are only for the purpose of describing specific embodiments, and are not intended to limit the present invention. The singular form used in the embodiments of the present invention and the scope of the attached patent application is not limited to the singular, unless the above text clearly indicates other meanings.
本發明實施例揭露一種光固化排齦材料,平常可以是以膏狀形態存在,並可利用例如是針筒等設備將膏狀之光固化排齦材料注射至需治療病患的牙齦溝,藉由排齦材料的黏度所提供之降伏強度(Yield Strength)可將牙齦溝適度的擴大,接著使用一UV光光照機,照射本發明之光固化排齦材料,使之固化,以利後續印模的操作。最 後,可利用例如是鑷子的外物將固化之排齦材料直接取出。在本發明一較佳實施例中,固化後的光固化排齦材料的體積也可以是大於膏狀形態排齦材料的體積,藉此,在固化後,也可增加排齦的效果。 The embodiment of the present invention discloses a light-curable gingival retraction material, which can usually exist in a paste form, and can use equipment such as a syringe to inject the paste-like light-curing gingival retraction material into the gingival sulcus of a patient to be treated. The Yield Strength provided by the viscosity of the gingival retraction material can appropriately expand the gingival sulcus, and then use a UV light illuminator to irradiate the light-curable gingival retraction material of the present invention to cure it to facilitate subsequent impressions Operation. most Later, the solidified gingival retraction material can be directly taken out by using foreign objects such as tweezers. In a preferred embodiment of the present invention, the volume of the cured light-curable gingival retraction material can also be greater than the volume of the paste-like gingival retraction material, so that the effect of gingival retraction can also be increased after curing.
本發明之一較佳實施例中,光固化排齦材料,在以膏狀形態存在時,具有黏度範圍介10x106~70x106cP之間,使得可使用注射的方式膏狀形態的光固化排齦材料,注射至牙齦溝。另外,在一較佳實施例中,上述UV光照機可以是具有能量範圍介於500~3000mW/cm2之間,且可發出波長範圍介於400nm~500nm之間的光線。在又一較佳實施例中,光固化排齦材料可以是在UV光底下曝露、曝射約10~50秒之間,使得本發明之排齦材料可由膏狀形態轉變成為固體形態。上述數值僅是用來說明本發明實施例可具體實施的方式,並不用來限定本發明。 In a preferred embodiment of the present invention, the light-curable gingival retraction material has a viscosity range of 10x10 6 ~70x10 6 cP when it exists in the form of paste, so that the light-curing paste can be used in the form of injection. Gum material, injected into the gingival sulcus. In addition, in a preferred embodiment, the above-mentioned UV illuminator may have an energy range between 500-3000 mW/cm 2 and can emit light with a wavelength range between 400 nm and 500 nm. In another preferred embodiment, the photocurable gingival retraction material may be exposed under UV light for about 10-50 seconds, so that the gingival retraction material of the present invention can be transformed from a paste form to a solid form. The above-mentioned numerical values are only used to illustrate the specific implementation modes of the embodiments of the present invention, and are not used to limit the present invention.
如上所述之實施例,光固化排齦材料包含至少光固化劑、起始劑及交聯劑,其曝露在UV光波長範圍的光線下時,可產生活性反應而由液態或膏狀形態轉變成固態。在本發明之一較佳實施例中,光固化排齦材料可以是由上述光固化劑、上述起始劑、上述交聯劑、增稠劑、保濕劑以及賦形劑等成份組成。本發明的排齦材料並不限定於上述組成,可視消費者需求,額外增加其它成份,以增加光固化排齦材料的特性,例如硬度、外觀等。在一實施例中,可添加食用 藍色一號增加外觀上顏色差異,以利識別。或者,在另一實施例中,也可以添加些許三氯化鋁(Aluminium(III)chloride)增加在排齦時的止血效果等。 In the above-mentioned embodiment, the light-curable gingival retraction material includes at least a light-curing agent, an initiator, and a cross-linking agent. When exposed to light in the wavelength range of UV light, it can generate an active reaction and transform from a liquid or paste form. Into a solid state. In a preferred embodiment of the present invention, the light-curable gingival retraction material may be composed of the above-mentioned light-curing agent, the above-mentioned initiator, the above-mentioned crosslinking agent, thickener, moisturizer, excipients and other ingredients. The gingival retraction material of the present invention is not limited to the above composition, and other components can be added according to the needs of consumers to increase the characteristics of the light-curing gingival retraction material, such as hardness and appearance. In one embodiment, you can add food The blue number one increases the color difference in appearance to facilitate identification. Alternatively, in another embodiment, a small amount of aluminum trichloride (Aluminium(III) chloride) can also be added to increase the hemostatic effect during gingival evacuation.
在本發明一較佳實施例中,上述光固化劑可以是2-甲基丙烯酸羥乙酯(2-Hydroxyethyl methacrylate,HEMA)或甲基丙烯酸(Methacrylic acid,MAA)。光固化劑也可以是2-甲基丙烯酸羥乙酯(HEMA)及甲基丙烯酸(MAA)的混合物。在本發明實施例中,光固化劑的重量百分比可以是約為20wt%。在本發明一較佳實施例中,上述起始劑可以是苯基雙(2,4,6-三甲基苯甲酰基)氧化膦(Bis(2,4,6-trimethylbenzoyl)-phenylphosphineoxide,IRGACURE 819)、2-羥基-2-甲基-1-苯基-1-丙酮(2-Hydroxy-2-methylpropiophenone,IRGACURE 1173)或苯酉昆崁酮(Camphorquinone,CQ)。在另一實施例中,起始劑也可是由苯基雙(2,4,6-三甲基苯甲酰基)氧化膦、2-羥基-2-甲基-1-苯基-1-丙酮及苯酉昆崁酮其中兩者或三者的混合物。而,在一較佳實施例中,起始劑的重量百分比可以是約為4wt%。在本發明一實施例,光固化排齦材料的交聯劑可以是三羥甲基丙烷三甲基丙烯酸酯(Trimethylolpropane trimethylacrylate,TMPTMA)或二甲基兩烯酸乙二醇酯(Ethylene glycol dimethacrylate,EGDMA),或者三羥甲基丙烷三甲基丙烯酸酯(TMPTMA)及二甲基丙烯酸乙二醇酯(EGDMA) 的混合物。在一較佳實施例中,交聯劑的重量百分比可以是約為3wt%。在本發明實施例中,上述起始劑在UV光的照射底下,產生自由基而可作為誘發或引發光固化劑產生聚合、交聯等活性反應,並使排齦材料由膏狀形態轉變成固態。也就是說,在本發明實施例的光固化排齦材料,主要是可藉由上述光固化劑、起始劑或稱光引發劑以及交聯劑,在適當UV光波長下,而產生的活性反應,而將可膏狀形態的排齦材料轉變成固體形態。 In a preferred embodiment of the present invention, the photocuring agent may be 2-Hydroxyethyl methacrylate (HEMA) or Methacrylic acid (MAA). The light curing agent may also be a mixture of 2-hydroxyethyl methacrylate (HEMA) and methacrylic acid (MAA). In the embodiment of the present invention, the weight percentage of the photocuring agent may be about 20 wt%. In a preferred embodiment of the present invention, the above-mentioned initiator may be phenyl bis(2,4,6-trimethylbenzoyl)-phenylphosphineoxide (Bis(2,4,6-trimethylbenzoyl)-phenylphosphineoxide, IRGACURE 819), 2-Hydroxy-2-methylpropiophenone (2-Hydroxy-2-methylpropiophenone, IRGACURE 1173) or Camphorquinone (CQ). In another embodiment, the initiator can also be phenylbis(2,4,6-trimethylbenzoyl) phosphine oxide, 2-hydroxy-2-methyl-1-phenyl-1-acetone And a mixture of two or three of them. However, in a preferred embodiment, the weight percentage of the initiator may be about 4 wt%. In an embodiment of the present invention, the cross-linking agent of the light-curable gingival retraction material may be Trimethylolpropane trimethylacrylate (TMPTMA) or Ethylene glycol dimethacrylate (Ethylene glycol dimethacrylate, EGDMA), or trimethylolpropane trimethacrylate (TMPTMA) and ethylene glycol dimethacrylate (EGDMA) mixture. In a preferred embodiment, the weight percentage of the cross-linking agent may be about 3 wt%. In the embodiment of the present invention, the above-mentioned initiator generates free radicals under the irradiation of UV light, which can be used as inducing or initiating the photocuring agent to produce polymerization, cross-linking and other active reactions, and transform the gingival repellent material from a paste form to Solid state. That is to say, the photo-curable gingival retraction material in the embodiments of the present invention is mainly activated by the above-mentioned photo-curing agent, initiator or photoinitiator and cross-linking agent under the appropriate UV light wavelength. Reaction, and transform the gingival retraction material in a paste-like form into a solid form.
在本發明之實施例光固化排齦材料中,增稠劑可以是羧甲基纖維素(Carboxymethyl Cellulose)或卡拉膠(Carrageenan),或者羧甲基纖維素及卡拉膠的混合物。增稠劑可用來調整排齦材料在以膏狀形態存在時的稠度,在一較佳實施例中,增稠劑的重量百分比範圍可以是介18~28wt%之間。在本發明實施例中,保濕劑可以是甘油或山梨糖醇,或者其兩者的混合物,且較佳可以是具有一重量百分比範圍介於15~30%之間。在本發明實施例之光固化排齦材料,賦形劑可以是高嶺土或氧化鋁粉,或者高嶺土及氧化鋁粉的混合物,且較佳地,賦形劑的重量百分比範圍可以是介於20~40wt%。 In the light-curing gingival retraction material of the embodiment of the present invention, the thickening agent may be Carboxymethyl Cellulose or Carrageenan, or a mixture of Carboxymethyl Cellulose and Carrageenan. The thickener can be used to adjust the consistency of the gingival retraction material when it is in the form of a paste. In a preferred embodiment, the weight percentage of the thickener can range from 18 to 28 wt%. In the embodiment of the present invention, the humectant may be glycerin or sorbitol, or a mixture of the two, and preferably may have a weight percentage in the range of 15-30%. In the light-curing gingival retraction material of the embodiment of the present invention, the excipient may be kaolin or alumina powder, or a mixture of kaolin and alumina powder, and preferably, the weight percentage range of the excipient may be between 20~ 40wt%.
請參照表一所示,接下來將利用7個實驗例說明、展示本發明實施例之光固化排齦材料的組成、特性,以及在曝露在UV光底下的固化時間。 Please refer to Table 1. Next, 7 experimental examples will be used to illustrate and show the composition, characteristics, and curing time of the light-curable gingival retraction material of the embodiment of the present invention, as well as the curing time when exposed to UV light.
表一、各實驗例之光固化排齦材料成份組成及特性
表一續、各實驗例之光固化排齦材料成份組成及特性
實驗例一 Experimental example one
在製備此實驗例一的樣品時,可分別秤取15克之2-甲基丙烯酸羥乙酯(HEMA)及5克之甲基丙烯酸(MAA)、2克之IRGACURE 819、1克之IRGACURE 1173及1克之苯酉昆崁酮(CQ),以及2克之三羥甲基丙烷三甲基丙烯酸酯(TMPTMA)和1克之二甲基兩烯酸乙二醇酯(EGDMA),混合作為本實驗例一的光固化配方。接著,分別秤取18克之羧甲基纖維素和10克之卡拉膠、10克之甘油和5克之山梨糖醇,以及10克之高嶺土和20克之氧化鋁粉,並將其和上述光固化配方攪拌均勻混合,以製備本實驗例一的光固化排齦材料的樣品。 When preparing the sample of this experimental example 1, 15 g of 2-hydroxyethyl methacrylate (HEMA) and 5 g of methacrylic acid (MAA), 2 g of IRGACURE 819, 1 g of IRGACURE 1173, and 1 g of benzene can be weighed respectively. Unitary cuminone (CQ), 2 grams of trimethylolpropane trimethacrylate (TMPTMA) and 1 grams of ethylene glycol dimethyl dienoate (EGDMA), mixed as the light curing of the first example of this experiment formula. Then, weigh 18 grams of carboxymethyl cellulose, 10 grams of carrageenan, 10 grams of glycerin, 5 grams of sorbitol, 10 grams of kaolin and 20 grams of alumina powder, and mix them with the above light-curing formula. , In order to prepare a sample of the light-curing gingival retraction material in Example 1.
在製備完成樣品後,接著,取用些許樣品進行測量黏度及光固化時間。在本實驗例一,是在攝氏溫度25下,使用廠牌為BROOKFIELD,且型號為RVDV-E的黏度計測量樣品的黏度。此黏度計可藉由一轉子在樣品中旋轉時,液體樣品在轉子上所產生的黏度力矩,經由感測器檢測此黏度力矩並經由微電腦運算處理,即可得到實驗例一樣品的黏度為50 x106cp。接著,進行光固化時間的測試,本實驗例一採用廠牌Rainbow的LED紫外光光照機照射樣品,觀察樣品固化所需的時間。在此實驗例一的樣品,從膏狀形態轉變成固化約需10秒(sec)。 After preparing the samples, then take a few samples to measure the viscosity and light curing time. In the first example of this experiment, the viscosity of the sample was measured with a viscometer made of BROOKFIELD and model RVDV-E at a temperature of 25 degrees Celsius. This viscometer can use the viscosity torque generated by the liquid sample on the rotor when a rotor rotates in the sample. The viscosity torque is detected by the sensor and processed by a microcomputer. The viscosity of the sample in the first experiment can be obtained as 50 x10 6 cp. Then, the light curing time test was performed. In the first example of this experiment, a Rainbow LED ultraviolet light illuminator was used to irradiate the sample to observe the time required for the sample to cure. In the sample of Experimental Example 1, it takes about 10 seconds (sec) to change from the paste form to solidification.
實驗例二~七 Experimental example 2~7
實驗例二~七係依據實驗例一的步驟及方法,差別僅在各成份配方上的調整、改變,如上述表一所列。同樣地,黏度測量和固化時間也和實驗例一相同,藉此觀察不同成份配方組成的差異對黏度和固化時間的變化,如上述表一所示。值得一提的是,在表一中的實驗例五~七,主要是針對光固化劑、起始劑、交聯劑、增稠劑、保濕劑及賦形劑僅使用單一種成份,觀察此改變對黏度及光固化時間的影響。 Experimental examples 2 to 7 are based on the steps and methods of experimental example 1, and the difference is only in the adjustments and changes in the formulation of each ingredient, as listed in Table 1 above. Similarly, the viscosity measurement and curing time are the same as in Experimental Example 1, to observe the difference in the composition of different ingredients and the changes in viscosity and curing time, as shown in Table 1 above. It is worth mentioning that the experimental examples 5~7 in Table 1 mainly use a single ingredient for light curing agent, initiator, crosslinking agent, thickener, humectant and excipient. Observe this Change the effect on viscosity and light curing time.
應當說明的是,上述實施例及實驗例均可依據需要自由組合。上述說明及圖式僅是本發明的較佳實施方式,應當指出,對於本發明所屬領域中具有通常知識的技術人員來說,在不脫離本發明原理、精神的前提下,還可以做出各種改進和潤飾,此些改進和潤飾也應視為本發明的保護範圍。因此,本發明保護範圍應當以後續之申請專利範圍為準。 It should be noted that the above-mentioned embodiments and experimental examples can be freely combined according to needs. The above description and drawings are only the preferred embodiments of the present invention. It should be pointed out that for those skilled in the art to which the present invention belongs, those skilled in the art can also make various modifications without departing from the principle and spirit of the present invention. Improvements and modifications, these improvements and modifications should also be regarded as the protection scope of the present invention. Therefore, the scope of protection of the present invention should be subject to the scope of subsequent patent applications.
Claims (20)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| TW108140682A TW202118826A (en) | 2019-11-08 | 2019-11-08 | Light curing retraction material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| TW108140682A TW202118826A (en) | 2019-11-08 | 2019-11-08 | Light curing retraction material |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TW202118826A true TW202118826A (en) | 2021-05-16 |
Family
ID=77020706
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW108140682A TW202118826A (en) | 2019-11-08 | 2019-11-08 | Light curing retraction material |
Country Status (1)
| Country | Link |
|---|---|
| TW (1) | TW202118826A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN116392397A (en) * | 2023-04-13 | 2023-07-07 | 四川大学 | A light-responsive gingival retraction material, its preparation method and application |
-
2019
- 2019-11-08 TW TW108140682A patent/TW202118826A/en unknown
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN116392397A (en) * | 2023-04-13 | 2023-07-07 | 四川大学 | A light-responsive gingival retraction material, its preparation method and application |
| CN116392397B (en) * | 2023-04-13 | 2024-05-31 | 四川大学 | Photoresponse gingival retraction material and preparation method and application thereof |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN101909579B (en) | Cement for dental applications | |
| JP4093974B2 (en) | Photopolymerization initiator and dental composite resin containing the photopolymerization initiator | |
| JP7099721B2 (en) | Photocurable compositions and dental restoration filling materials | |
| JP2019505482A (en) | Two-component self-adhesive dental compositions, storage-stable initiator systems, and their use | |
| JP2014088439A (en) | Methods for making dental restorations using two-phase light-curing materials | |
| Dietschi et al. | Comparative efficiency of plasma and halogen light sources on composite micro-hardness in different curing conditions | |
| CN105456039A (en) | Visible light cured dental restorative composition and preparation method thereof | |
| WO2017154983A1 (en) | Photopolymerization initiator and photocurable composition | |
| JP4162738B2 (en) | Photopolymerization type orthodontic resin composition | |
| KR20220044261A (en) | Paste-phased composite material with lowered thermal degradation | |
| JP6016656B2 (en) | Dental curable composition | |
| JP2016169180A (en) | Dental photopolymerizable composition | |
| JP2005213231A (en) | Photo-curable dental composite restorative material | |
| TW202118826A (en) | Light curing retraction material | |
| Oook et al. | Influence of polymerization mode of dual-polymerized resin direct core foundation systems on bond strengths to bovine dentin | |
| JP5478860B2 (en) | Photopolymerization initiator and dental composite resin containing the photopolymerization initiator | |
| JP2000254152A (en) | Resin material for dental plate | |
| JP2002255722A (en) | Dental curable composition | |
| JP4148332B2 (en) | Light-curing dental restoration material | |
| JP2000175941A (en) | Repair material composition for denture base | |
| US10299897B2 (en) | Dental plate liner | |
| JP4698806B2 (en) | Denture base resin composition | |
| Damade et al. | Comparative Evaluation of Shear and Tensile Bond Strength of Cross Linked Acrylic Denture Teeth to Denture Base Resins Cured by Heat and Microwave Polymerisation Techniques-An in Vitro Study | |
| Calomeni | A wash technique using rubber-base impression material | |
| Lloret et al. | Flexural properties, microleakage, and degree of conversion of a resin polymerized with conventional light and argon laser. |