• 폴리머
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• 제28권6호
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• pp.538-544
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• 2004

Z-라이신 올리고머를 사슬연장제로 하고 D-다이페닐이소시아네이트와 폴리테트라메틸글리콜을 반응시켜 주사슬에 L-라이신 분절을 함유하는 폴리우레틴 (PULL)을 합성하였다. PULL 표면의 아민기와 인슐린의 공유 결합으로 인슐린 고정화 폴리우레탄 (PULL-In)을 제조하였다. Bradfold법으로 측정한 고정화 인슐린의 양은 약 0.30 nmol/$\textrm{cm}^2$이였다. $^3$H-thymidine 분석방법과 광학 현미경법으로 NIH/3T3 섬유아세포와 표면 개질된 PULL의 상호작용을 조사하였다. 그 결과 PULL-In 필름 표면에서의 세포 성장 속도는 다른 기질에서보다 높았다. 또한 고정화된 인슐린에서의 세포증식이 배양액에 용해된 인슐린에서와 거의 유사한 특성을 나타내었다.

• 공업화학
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• 제21권4호
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• pp.377-384
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• 2010

에너지 함유 쇄연장제인 3-azidopropane-1,2-diol (AzPD)로 쇄연장된 에너지 함유 폴리우레탄의 특성을 고찰하기 위하여 비교연구법을 수행하였다. 이를 위하여 AzPD, 1,4-BD, 또는 1,5-PD 쇄연장제를 갖는 poly(glycidyl azide)/poly(tetramethylene oxide)계 에너지 함유 세그멘티드 폴리우레탄(energetic segmented polyurethane, GAP/PTMG ESPU)을 dimethyl formamide (DMF) 용매에서 합성하여 상거동을 고찰하였다. 상거동은 fourier transform infrared.attenuated total reflection spectroscopy (ATR FT.IR), differential scanning calorimetry (DSC), 및 dynamic mechanical analysis (DMA)를 이용하여 분석하였다. ATR FT.IR spectrum 분석결과 7일 경과 시편의 GAP/PTMG AzESPU의 수소결합하지 않은 C=O 분율이 0.5로 각각 0.44 및 0.41인 GAP/PTMG BDESPU 및 GAP/PTMG PDESPU 보다 높았고, 제조 후 60일 경과 시편의 경우 0.26~0.29의 범위로 큰 차가 없었다. 제조 후 7일 경과 GAP/PTMG AzESPU 시편의 DMA curves는 무정형 고분자의 거동과 유사하였으며, GAP/PTMG BDESPU과 GAP/PTMG PDESPU는 고무평탄구간과 연성 흐름 구간을 갖는 점탄성 거동을 나타냈다. 그러나, 제조 후 60일 경과 GAP/PTMG AzESPU의 DMA curves는 GAP/PTMG PDESPU와 같이 고무평탄구간과 연성 흐름 구간을 갖는 점탄성 거동을 나타냈다. ATR FT-IR, DSC 및 DMA 분석을 이용한 상거동 고찰로부터 AzPD로 쇄연장된 GAP/PTMG ESPU는 1,4-BD 또는 1,5-PD로 쇄연장된 GAP/PTMG ESPU보다 구성성분간의 상혼합이 잘 이루어지나 적절한 조건에서 상형평에 도달되면 GAP/PTMG PDESPU와 유사한 TPE의 점탄성 거동을 나타냈다.

• Journal of Microbiology and Biotechnology
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• 제18권3호
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• pp.427-433
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• 2008

The cephabacins produced by Lysobacter lactamgenus are ${\beta}$-lactam antibiotics composed of a cephem nucleus, an acetate residue, and an oligopeptide side chain. In order to understand the precise implication of the polyketide synthase (PKS) module in the biosynthesis of cephabacin, the genes for its core domains, ${\beta}$-ketoacyl synthase (KS), acyltransferase (AT), and acyl carrier protein (ACP), were amplified and cloned into the pET-32b(+) expression vector. The sfp gene encoding a protein that can modify apo-ACP to its active holo-form was also amplified. The recombinant KS, AT, apo-ACP, and Sfp overproduced in the form of $His_6$-tagged fusion proteins in E. coli BL21(DE3) were purified by nickel-affinity chromatography. Formation of stable peptidyl-S-KS was observed by in vitro acylation of the KS domain with the substrate [L-Ala-L-Ala-L-Ala-L-$^3H$-Arg] tetrapeptide-S-N-acetylcysteamine, which is the evidence for the selective recognition of tetrapeptide produced by nonribosomal peptide synthetase (NRPS) in the NRPS/PKS hybrid. In order to confirm whether malonyl CoA is the extender unit for acetylation of the peptidyl moiety, the AT domain, ACP domain, and Sfp protein were treated with $^{14}C$-malonyl-CoA. The results clearly show that the AT domain is able to recognize the extender unit and decarboxylatively acetylated for the elongation of the tetrapeptide. However, the transfer of the activated acetyl group to the ACP domain was not observed, probably attributed to the improper capability of Sfp to activate apo-ACP to the holo-ACP form.

• 한국응용약물학회:학술대회논문집
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• 한국응용약물학회 1994년도 춘계학술대회 and 제3회 신약개발 연구발표회
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• pp.196-196
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• 1994

DDS에 활용될 수 있는 고분자 소재를 개발할 목적으로 물성 및 응용성이 우수한 고분자 겔에 관한 연구를 수행하였다. Ethylene oxide,propylene oxide 각각의 copolymer인 poloxamer등의 prepolymer들을 triisocyanate로 가교시키고 diisocyanate 로 chain이 연장된 "soft hydrogel"을 제조하였다. 모델 약물을 선정하여 crosslinker와 extender의 조절에 따른 hydrogel의 약물 방출 조절능을 조사하였으며 그 기전을 규명하고자 하였다. 가교부위에 urethane bond를 함유한 soft hydtogel은 건조상태에서도 고무와 같은 전연성을 보여 일반적인 hydrogel과 대비되는 특성을 보였으며 이에 따른 다양한 활용성이 기대되었다. Extender및 crosslinker의 비율에 따라서 이 rubber elasticity가 조절되었다. 가교도가 감소할수록 팽윤도가 상승하였고 이에 따른 약물방출도 증가함을 확인하였다. 또한 Prepolymer의 분자량 및 친수/소수성등의 물성에 따라 약물방출을 조절할 수 있었다. 제조된 hydrogel에 조절방출시 필요한 기능을 부가시키고자 poly(carylic acid)류와 IPN 공중합체를 합성하여 물성을 조사하였고 비이온성/양이온성/음이온성 모델약물을 선정하여 pH에 따른 가변적 팽윤도와 이온성 상호작용등에 근거한 약물 조절방출기전을 조사하였다.기전을 조사하였다.

• Transactions on Electrical and Electronic Materials
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• 제14권4호
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• pp.199-202
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• 2013

In order to study the effect of reactive diluents on the electrical insulation breakdown strength and mechanical properties of, a polyglycol and an aliphatic epoxy were individually introduced to an epoxy system. Reactive diluents were used in order to decrease the viscosity of the epoxy system; polyglycol acted as a flexibilizer and 1,4-butanediol diglycidyl ether (BDGE) acted as an aliphatic epoxy, which then acted as a chain extender after curing reaction. The ac electrical breakdown strength was estimated in sphere-to-sphere electrodes and the electrical breakdown strength was estimated by Weibull statistical analysis. The scale parameters of the electrical breakdown strengths for the epoxy resin, epoxy-polyglycol, and epoxy-BDGE were 45.0, 46.2, and 45.1 kV/mm, respectively. The flexural and tensile strengths for epoxy-BDGE were lower than those of the epoxy resin and those for epoxy-polyglycol were lower than those of the epoxy resin.

• Transactions on Electrical and Electronic Materials
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• 제14권6호
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• pp.317-320
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• 2013

Partial discharge resistance for the epoxy systems with two diluents was investigated in the rod-plane electrodes arrangement, and the effect of electric frequency on the partial discharge resistance was also studied. Diglycidyl ether of bisphenol A (DGEBA) type epoxy was used as a base resin, and 1,4-butanediol diglycidyl ether (BDGE) or polyglycol (PG) as a reactive diluent was introduced to the DGEBA system, in order to decrease the viscosity of the DGEBA epoxy system. BDGE was acted as a chain extender, and PG acted as a flexibilizer, after the curing reaction. To measure the partial discharge resistance, 5 kV alternating current (ac) with three different frequencies (60, 500 and 1,000 Hz) was applied to the specimen in a rod-plane electrode arrangement, at $30^{\circ}C$. PG had a good effect, while BDGE had a bad effect on the partial discharge resistance of the DGEBA system, regardless of the electric frequency.

• 한국응용과학기술학회지
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• 제22권4호
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• pp.355-361
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• 2005

The physical characteristics of polyurethane were examined by SEM, FT-IR tensile strength and mole % [NCO/OH]. Growing concerns in the environment-friendly architecture and public works have led to the development of solvent-free formulations that can be cured and foamed in air. Compared with general packing materials, this resin is much stronger in intensity and much longer in durability. Polyurethane foam resins were mainly composed of polyol, MDI, silicone surfactant, fillers, catalyst and blowing agent. The rigid foam of polyurethane in mechanical characteristics were due to chain extender and the increase of mole % [NCO/OH]. The change in the microstructure of polyurethane should be taken into account when considering the process of construction and durability through the polyurethane polymer resin in lots of industries.

• Macromolecular Research
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• 제9권6호
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• pp.332-338
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• 2001

Waterborne polyurethane as a new polymer electrolyte was synthesized by using relatively hydrophilic polyols. The morphology of polyurethane was changed as it was dispersed in water. In contrast to polyurethane ionomer, waterborne polyurethane did not form an ionic cluster but produced a binary system composed of hydrophilic and hydrophobic groups. In the colloidal system, the former and the latter existed at outward and inward, respectively. Waterborne polyurethane was prepared from poly(ethylene glycol) (PEG) /poly(propylene glycol) (PPG) copolymer, 4,4'-diphenylmethane diisocyanate(MDI), ethylene diamine as a chain extender, and three ionization agents, 1,3-propane sultone, sodium hydride and lithium hydroxide. PEG/PPG copolymer was used for suppressing the crystallinity of PEG and N-H bond was ionized for increasing the electrochemical stability of polyurethane. Low molecular weight poly(ethylene glycol) and poly(ethylene glycol dimethyl ether) (PEGDME) were used as plasticizers. DSC, FT-IR and $^1$H-NMR of the waterborne polyurethane were measured. Also, the ionic conductivity of solid polymer electrolytes based on waterborne polyurethane and various concentrations of low molecular weight poly(ethylene glycol) or PEGDME were measured by AC impedance.

• Bulletin of the Korean Chemical Society
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• 제20권6호
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• pp.672-676
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• 1999

Gas-Permeable polymeric membranes containing carboxyl groups which are suitable for enzyme immobilization were investigated in order to use them as gas electrode membranes in biosensors. Carboxylated polyurethane (CPU) was synthesized via a reaciton between 2,2-bis(hydroxymethyl)propionic acid as a chain extender and prepolymers prepared from polycarprolactone(Mn=2,000) and 4,4'-diphenylmethane diisocynate. It was difficult to prepared membranes from the pure CPU because of its high elasticity and cohesion. However, transparent free-standing membranes were easily prepared from the blend solution of CPU and carboxylated poly(vinyl chloride)(CPVC) in tetrahydrofuran. Both elasticity and cohesion of the CPU/CPVC membranes were decreased with increasing the content of CPVC. DSC experiment suggests that CPU and CPVC may be well mixed. Permeability coefficients for O₂and CO₂(Po₂and Pco₂)in the membranes increased as the proportion of CPU increased. The addition of dioxtyl phthalate(DOP), a plasticizer, significantly enhanced the Po₂and Pco₂which were 4,4 and 30 barrer, respectively, in the CPU/CPVC(80/20 wt/wt) membranes containing 20% of DOP at 25℃ and 100psi. Thus this type of membranes may have a potential for the use as gas electrode membranes in biosensors.

• 공업화학
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• 제3권4호
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• pp.595-604
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• 1992

음이온기를 갖는 카보네이트형 폴리우레탄을 NCO-말단 프레폴리머법으로 제조하여 이를 제막하고 에탄올수용액분리 성능을 검토하였다. 우레탄수지의 물성을 향상시키기 위해 카보네이트형 폴리올(PTMCG)을 사용하였고, 친수성 향상에는 사슬연장제로 ${\alpha}^{\prime},{\alpha}^{{\prime}{\prime}}$-dimethylpropionic acid를 이용하였으며, trimethylamine으로 우레탄 사슬내의 카르복실기를 이온화시켰다. 우레탄 사슬내의 음이온기 형성을 확인하기 위해 모델반응을 실시하여 IR 분광분석을 행하였으며, 합성한 우레탄수지의 IR 스펙트럼과 비교하였다. 사슬연장제와 폴리올의 반응몰비율이 3:1에서 5:1인 범위에서는 hard segment의 농도, 수소결합 등이 우레탄수지의 물성을 기여하고 있음을 알 수 있었다. DSC에 의한 열분석결과 카르복실기를 함유한 카보네이트형 폴리우레탄수지(PU)는 $Tg-25^{\circ}C$ 및 Tm $45^{\circ}C$의 값을 갖는 것으로 나타났으며, 이를 이온화하여 사슬내에 음이온성기를 갖게한 카보네이트형 폴리우레탄수지(APU)의 경우 PU 수지보다 $8{\sim}10^{\circ}C$ 정도씩 낮은 온도 영역으로 전이되는 경향을 나타내었다. PU 및 APU 수지를 용매로 N, N-dimethylformamide(DMF), 가교제로 hexamethylene diisocyanate(HMDI)를 사용하여 캐스팅법으로 투과증발막을 제조하였다. 팽윤도 측정결과 혼합물중 에탄올농도에 따라 증가하는 경향을 나타내었고, 가교를 통하여 막의 팽윤도를 조절하였으며, 이를 투과증발에 응용한 결과 선택도 2.3~9.8, 투과유량 $27{\sim}79.5g/m^2hr$를 갖는 것으로 나타났다. 또한 폴리올의 분자량을 2,000에서 1,000으로 줄임으로 분리성능을 향상시킬 수 있었다.