Abstract:
PURPOSE: A method for preparing a delivery system for supporting physiologically active growth factors which are necessary for cell differentiation and proliferation is provided to maximize stem cell differentiation ability in vitro. CONSTITUTION: A growth factor delivery system comprises a core and shell structure containing two kinds of ingredients which are necessary for cell differentiation or proliferation. The delivery system is in the form of a microsphere of 100-400 um in dianeter. The delivery system is treated with a crosslinking agent of ethyl dimethyl amino propyl carbodiimide, genipin, or glutaraldehyde in the shell. A method for preparing the delivery system comprises: a step of preparing a polymeric microsphere containing a first ingredient needed for cell differentiation or proliferation; and a step of introducing the polymeric microsphere into other polymers containing a second ingredient needed for cell differentiation or proliferation.
Abstract:
본 발명은 생분해성 및 생체친화성이 우수한 조직재생용 주입형 온도감응성 생분해 플루로닉(pluronic) 유도체 하이드로겔 및 이의 제조방법에 관한 것으로, 구체적으로 플루로닉 고분자의 한쪽 또는 양쪽 말단에 생분해성 고분자가 도입되고, 상기 생분해성 고분자에 메타크릴옥시에틸 트라이멜리트산(methacryloxyethyl trimellitic acid) 무수물이 결합되고, 상기 메타크릴옥시에틸 트라이멜리트산 무수물의 카르복실기에 생리활성물질이 중합된 구조를 갖는, 조직재생용 주입형 온도감응성 생분해 플루로닉 유도체 하이드로겔 및 이의 제조방법에 관한 것이다. 본 발명에 따른 플루로닉 유도체 하이드로겔은 플루로닉 고분자의 온도감응성(thermosentitive)은 그대로 유지하면서 생분해성 고분자의 도입으로 인해 생체 내에서 일정 기간 후에 분해되어 배설될 수 있는 생분해성(biodegradability)이 탁월하고, 세포증식성 또는 세포분화성을 향상시킬 수 있는 생리활성물질이 결합되어 있어 생체친화성(biocompatibility)이 우수하기 때문에, 인공조직이나 장기를 조직공학적으로 재생하는데 유용하게 사용될 수 있다. 조직재생, 하이드로겔, 플루로닉 유도체, 생분해성, 생체친화성, 생리활성물질
Abstract:
PURPOSE: A method for preparing biodegradable covered porous polymer microspheres is provided to control a pore size of microspheres, and to prepare porous polymer microspheres capable of ensuring sustained release control and persistence of a sealed drug. CONSTITUTION: A method for preparing biodegradable covered porous polymer microspheres comprises the steps of: dissolving or suspending a bio-active material in a polymer solution that a biodegradable polymer is dissolved in an organic solvent to prepare a polymer solution containing a bio-active material; adding a hydrogen peroxide-containing compound to the polymer solution and mixing the mixture to prepare water-in-oil type emulsion; emulsifying the water-in-oil type emulsion in a emulsion stabilizer solution to prepare oil-in-water type emulsion; and adding a hydrogen peroxide decomposition catalyst to the oil-in-water type emulsion to degrade hydrogen peroxide and evaporate organic solvent.
Abstract:
A photopolymerizable composite material composition for dental service and orthopedics is provided to improve physical properties, mechanical properties and biocompatibility. A photopolymerizable composite material composition comprises 5-95 wt% of an organic matrix component; and 5-95 wt% of an inorganic filler. The organic matrix component comprises 15-80 wt% of a multifunctional methacrylate prepolymer selected from a bifunctional methacrylate prepolymer represented by the formula 2, a trifunctional methacrylate prepolymer represented by the formula 3, a tetrafunctional methacrylate prepolymer represented by the formula 4 and their mixture; 5-50 wt% of a diluent; 1-40 wt% of a polymerization monomer; 0.1-10 wt% of a photoinitiator; and 0.1-10 wt% of other additives, wherein n is a number of 0-2; and R is H, CH3, CH2CH3 or -C(CH3)3.
Abstract:
A method for preparing a biodegradable porous polymer scaffold is provided to produce a biodegradable porous polymer scaffold for tissue engineering, which has no phenomena for pore clogging and harmful substances excretion and remain, and has an open structure with higher surface area and porosity. A method for preparing a biodegradable porous polymer scaffold for tissue engineering comprises the steps of: (a) adding a hydrogen peroxide-containing compound to a polymer solution which is obtained by dissolving a biodegradable polymer into a solvent, and mixing the resulting solution homogeneously; (b) allowing the solution obtained in the step (a) to stand at a temperature of -196 deg.C to a normal temperature so as to evaporate the solvent; and (c) introducing the polymer specimen obtained in the step (b) into an aqueous solution containing a catalyst for decomposition of hydrogen peroxide and foaming the resultant, followed by drying.
Abstract:
본 발명은 치과용 접착제 조성물에 관한 것으로, 생체와 조성물의 내수성, 강도, 접착, 색조 및 저장 안정성에 영향을 미치는 일정 온도 범위 및 습윤 범위 내에서 경화성이 우수한 치과용 접착성 조성물에 관한 것이다. 구체적으로 복합레진과 치아와의 접착성을 향상시키는 기존의 제품인 2,2-비스(4-(2-히드록시-3-메타크릴로일옥시프로폭시)페닐)프로판(Bis-GMA)에, 이 Bis-GMA 분자 중의 히드록시기 (-OH)의 수소원자를 메타크릴레이트기로 치환한 멀티메타크릴레이트기 함유 다관능성 프리폴리머를 혼합한 프리폴리머 혼합물을 기재로 하고, 접착 단량체, 친수성 단량체, 광개시제 및 환원제, 희석용매를 함유하는 것을 특징으로 하며, 본 발명의 조성물은 Bis-GMA를 포함하는 종래의 것보다 법랑질 및 상아질에 접착효과가 좋을 뿐만 아니라 우수한 물리적 특성을 보이고 시술을 간편하게 하는 효과를 나타낸다. 치과용 접착제, 다관능성 프리폴리머 혼합물, 접착 단량체, 친수성 단량체, 광경화성, 법랑질 접착, 상아질 접착
Abstract:
본 발명은 1단계 시술을 위한 치과용 고기능성 접착제 조성물에 관한 것으로, 본 발명에 따른 조성물은 2,2-비스[4-(2-히드록시-3-메타크릴로일옥시프로폭시)페닐]프로판 (이하, "Bis-GMA"라 칭함)에, 이 Bis-GMA 분자 중의 히드록시기의 수소 원자를 메타크릴레이트기로 치환한 멀티메타크릴레이트기 함유 다관능성 프리폴리머를 혼합한 프리폴리머 혼합물을 기재로 하고, 산성 단량체, 접착 단량체, 친수성 단량체, 희석 용매, 물, 무기 충전재, 광개시제 시스템을 포함하는 1단계 광중합형 치과용 고기능성 접착제 조성물에 관한 것이다. 본 발명의 조성물은 산부식제 처리 없이도 접착효과가 좋을 뿐만 아니라 치아와의 접착성이 뛰어나고 지각과민 현상 억제와 항우식성 등의 뛰어난 물성을 나타내고 생체 친화성도 우수한 효과를 나타낸다.
Abstract:
PURPOSE: A photopolymerizable composite resin composition for dental restoration using a multifunctional prepolymer mixture as a base material is provided, which has increased biocompatibility as well as exhibiting better physical and mechanical properties as compared to conventional compositions based on only Bis-GMA itself. CONSTITUTION: This composite resin composition comprises 2 to 40% by weight of multifunctional prepolymer mixture of 2,2-bis-(4-(2-hydroxy-3-methacryloyloxypropoxy)phenyl)propane ("Bis-GMA") of formula 1 and tri-GMA of formula 2 in a ratio of 95:5 to 5:95, 1 to 20% by weight of a diluent, 40 to 95% by weight of an inorganic filler, a photoinitiation system, and other additives. The composition has almost no cytotoxicity and high strength and hardness.
Abstract:
PURPOSE: The pyridyl benzoxazole derivatives, their copolymers, and a fluorescence image making method are provided, thereby the pyridyl benzoxazole copolymers have good sensor properties in solution, film and particle status, so that they can be used as recording materials or sensor materials. CONSTITUTION: The pyridyl benzoxazole derivative is represented by formula (1), in which A and B are independently CH and N; R1 is alkyl or phenyl; R2 is O or NH, R3 is vinyl, acryl, allyl, alpha-methylvinyl or 4-vinylphenyl; m is an integer from 0 to 20. The pyridyl benzoxazole copolymer represented by formula (2) is produced by radical polymerization of comonomer selected from the group consisting of pyridyl benzoxazole derivatives, styrene, maleimide and methacrylate, in which A and B are independently CH and N; R1 is alkyl or phenyl; R2 is O or NH, m is an integer from 0 to 20; R4 is hydrogen or methyl; R5 is methyloxycarbonyl or phenyl; and x and y are integer from 10 to 5000. The fluorescence image making method comprises the steps of: dissolving pyridyl benzoxazole copolymer of formula (2) wherein A is CH and B is N, AIBN, organic acid or inorganic acid in an organic solvent; coating the solution on board and drying to form a thin layer; prebaking the thin layer; and exposing the thin layer to light using photomask and post-exposure baking it.
Abstract:
PURPOSE: Provided are hydroxy protected 1,4-dihydroxyanthraquinone derivatives used as a precursor of material for forming fine fluorescent image, copolymers thereof applied to material for recording and a sensor, and a process for forming the fine fluorescent image by using the copolymers. CONSTITUTION: The hydroxy protected 1,4-dihydroxyanthraquinone derivatives are represented by the formula (1), and the copolymers thereof represented by the formula (2) are produced by radical polymerizing the hydroxy protected 1,4-dihydroxyanthraquinone derivatives and comonomers selected from the group consisting of styrene, maleimide, and methacrylate in the presence of a polymerization initiator. And the process for forming the fine fluorescent image comprises the steps of: dissolving the copolymers containing the hydroxy protected 1,4-dihydroxyanthraquinone and a photoacid generator in an organic solvent; spreading the solution on a substrate and drying to from a thin film; prebaking the thin film coated substrate; treating under the condition of chemical amplification to remove the hydroxy protecting group from the copolymers. In the formula, R1 is hydroxy protecting group, one of A and B is H, R2 is O or NH, R3 is vinyl, alpha-methyl vinyl, or 4-biphenyl, one of C and D is H and the other is represented by the formula (c) or (d), R4 is hydrogen or methyl, R5 is methyloxycarbonyl or phenyl, m is an integer of 0-20, x and y are independently an integer of 10-5000.