• Bulletin of the Korean Chemical Society
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• 제8권2호
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• pp.102-105
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• 1987

2-Methoxy-6-methyl-3,4-dihydro-2H-pyran ($1_a$), 2-ethoxy-3,6-dimethyl-3,4-dihydro-2H-pyran ($1_b$), and 2-ethoxy-3-methyl-6-ethyl-3,4-dihydro-2H-pyran ($1_c$) were prepared by (4 + 2) cycloaddition reaction from the corresponding vinyl ketones and alkyl vinyl ethers. Compounds $1_{a-c}$ were ring-open polymerized by cationic catalyst to obtain alternating head-to-head (H-H) copolymers. For comparison, copolymer of head-to-tail (H-T) was also prepared by free radical copolymerization of the mixture of the corresponding monomers. The H-H copolymer exhibited some differences in its $^1H$ NMR and IR spectra. However, significant differences were showed between the H-H and H-T copolymers in the $^{13}C$ NMR spectra. Also noteworthy was that$T_g$ value of H-H copolymer was higher than that of the corresponding H-T structure. Decomposition temperature of the H-H copolymer was lower than that of the H-T copolymer. All the H-H and H-T copolymers were soluble in common solvents.

• Asian Pacific Journal of Cancer Prevention
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• 제15권5호
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• pp.2335-2340
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• 2014

Paclitaxel is hydrophobic in nature and is recognized as a highly toxic anticancer drug, showing adverse effects in normal body sites. In this study, we developed a polymeric nano drug carrier for safe delivery of the paclitaxel to the cancer that releases the drug in a sustained manner and reduces side effects. N-isopropylacrylamide/vinyl pyrrolidone (NIPAAm/VP) nanoparticles were synthesized by radical polymerization. Physicochemical characterization of the polymeric nanoparticles was conducted using dynamic light scattering, transmission electron microscopy, scanning electron microscopy and nuclear magnetic resonance, which confirmedpolymerization of formulated nanoparticles. Drug release was assessed using a spectrophotometer and cell viability assays were carried out on the MCF-7 breast cancer and B16F0 skin cancer cell lines. NIPAAm/VP nanoparticles demonstrated a size distribution in the 65-108 nm range and surface charge measured -15.4 mV. SEM showed the nanoparticles to be spherical in shape with a slow drug release of ~70% in PBS at $38^{\circ}C$ over 96 h. Drug loaded nanoparticles were associated with increased viability of MCF-7 and B16F0 cells in comparison to free paclitaxel. Nano loaded paclitaxel shows high therapeutic efficiency by sustained release action for the longer period of time, i increasing its efficacy and biocompatibility for human cancer therapy. Therefore, paclitaxel loaded (NIPAAm/VP) nanoparticles may provide opportunities to expand delivery of the drug for clinical selection.

• 공업화학
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• 제21권3호
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• pp.343-348
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• 2010

저밀도 폴리에틸렌(low density polyethylene, LDPE) 필름의 표면을 다양한 반응 조건하에서 함산소불소화하여 hydroperoxide 관능기를 도입시켜 표면특성을 변화시켰다. 또한 생성된 hydroperoxide 관능기를 반응 개시제로 친수성 그룹을 가지는 단량체인 acryl amide (AM)와 소수성 그룹을 가지는 단량체인 methyl methacrylate (MMA)를 그라프트 중합시켜 LDPE 필름의 표면을 2차 개질하였다. 또한 LDPE, 함산소불소화 된 LDPE (OFPE), AM 및 MMA 단량체가 그라프트 된 OFPE 필름의 표면특성은 1,1-diphenyl-2-picrylhydrazyl (DPPH), 감쇠전반사 분광법, 시차주사 열량분석기 및 접촉각 측정법 등으로 분석하였다. DPPH 라디칼 분석법의 결과로부터, OFPE의 hydroperoxide 관능기의 양은 함산소불소화 총압력과 F2 가스의 부분압이 증가함에 따라 증가함을 알 수 있었다. 접촉각 및 표면 자유에너지 분석결과로부터, 함산소불소화에 의해서 생성된 hydroperoxide 관능기와 AM과 같은 친수성 그룹을 가지는 단량체의 그라프트 중합은 LDPE 필름 표면에서 물과 같은 친수성 용매의 접촉각을 감소시키고, MMA와 같은 소수성 그룹을 가지는 단량체의 경우는 LDPE 필름 표면에서 methylene diiodide와 같은 비극성 용매의 표면 접촉각을 감소시켰다. 이는 AM 및 MMA 단량체의 그라프트 중합에 의한 것으로, LDPE 필름 표면은 친수성 및 소수성 용매에 대한 젖음성이 향상되었다.

• Journal of Microbiology and Biotechnology
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• 제21권1호
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• pp.28-36
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• 2011

Diblock copolymers composed of poly(${\varepsilon}$-caprolactone) (PCL) and poly(N,N-dimethylamino-2-ethyl methacrylate) (PDMAEMA), or methoxy polyethylene glycol(PEG), were synthesized via a combination of ring-opening polymerization and atom-transfer radical polymerization in order to prepare polymeric nanoparticles as an antifungal drug carrier. Amphotericin B (AmB), a natural antibiotic, was incorporated into the polymeric nanoparticles. The physical properties of AmB-incorporated polymeric nanoparticles with PCL-b-PDMAEMA and PCL-b-PEG were studied in relation to morphology and particle size. In the aggregation state study, AmB-incorporated PCL-b- PDMAEMA nanoparticles exhibited a monomeric state pattern of free AmB, whereas AmB-incorporated PCL-b- PEG nanoparticles displayed an aggregated pattern. In in vitro hemolysis tests with human red blood cells, AmBincorporated PCL-b-PDMAEMA nanoparticles were seen to be 10 times less cytotoxic than free AmB (5 ${\mu}g$/ml). In addition, an improved antifungal activity of AmBincorporated polymeric nanoparticles was observed through antifungal activity tests using Candida albicans, whereas polymeric nanoparticles themselves were seen not to affect activity. Finally, in vitro AmB release studies were conducted, proving the potential of AmB-incorporated PCL-b-PDMAEMA nanoparticles as a new formulation candidate for AmB.

• 멤브레인
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• 제23권4호
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• pp.290-296
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• 2013

촉매 1,8-diazabicyclo[5,4,0]undec-7-ene(DBU)를 이용하여, poly(vinylidenefluoride-co-chlorotrifluoroethylene) P(VDF-co-CTFE) 고분자와 methacrylic acid (MAA)를 반응시켜, P(VDF-co-CTFE)-MAA 공중합체를 제조하였다. 또한 P(VDF-co-CTFE)-MAA와 2-sulfoethyl methacrylate (SEMA) 단량체를 4',4'-azobis(4-cyanovaleric acid) (ACVA) 개시제 하에서 자유 라디칼 중합하여 수소 이온 전도성 막을 제조하였다. SEMA 함량이 많아짐에 따라 술폰산 그룹이 증가하였다. SEMA 함량이 50%일 때 최대 이온교환 용량값이 0.82 meq/g에 도달하였으며 이는 함수량 결과와 일치하였다. 또한, SEMA 함량이 50%일 때 수소이온 전도도가 0.041 S/cm까지 도달하였다. 이러한 결과는 분리막에서 SEMA 함량이 증가할수록 수소 이온을 전달시킬 수 있는 이온그룹이 증가하기 때문이다.

• Bulletin of the Korean Chemical Society
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• 제34권9호
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• pp.2616-2622
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• 2013

A novel zwitterionic monomer 3-[(2-acrylamido)dimethylammonio]propanesulfonate (DMADAS) was designed and synthesized in this study. Then it was polymerized with acrylamide (AM) by free radical polymerization in 0.5 mol/L NaCl solution with ammonium persulfate ($(NH_4)_2S_2O_8$) and sodium sulfate ($NaHSO_3$) as initiator. The structure and composition of DMADAS and acrylamide-3-[(2-acrylamido)-dimethylammonio]propanesulfonate copolymer (P-AM-DMADAS) were characterized by FT-IR spectroscopy, $^1H$ NMR and elemental analyses. Isoelectric point (IEP) of P-AM-DMADAS was tested by nanoparticle size and potential analyzer. Solution properties of copolymer were studied by reduced viscosity. Antipolyelectrolyte behavior was observed and was found to be enhanced with increasing DMADAS content in copolymer. The results showed that the viscosity of P-AM-DMADAS is 5.472 dl/g in pure water. Electrolyte was added, which weakened the mutual attraction between sulfonic acid group and quaternary ammonium group. The conformation became loose, which led to the increase of reduced viscosity. The ability of monovalent and divalent cation influencing the viscosity of zwitterionic copolymer obeyed the following sequence: $Li^+$ < $Na^+$ < $K^+$, $Mg^{2+}$ < $Ca^{2+}$ < $Ba^{2+}$, and that of anion is in the order: $Cl^-$ < $Br^-$ < $I^-$, $CO{_3}^{2-}$ > $SO{_3}^{2-}{\approx}SO{_4}^{2-}$.

• 폴리머
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• 제25권5호
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• pp.736-743
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• 2001

N,N-Methylenebisacrylamide (MBAA)로 가교 결합된 electro-active 고분자(EAP) (poly(2-acrylamido-2-methylpropane sulfonic acid), PAMPS) 겔을 수용액 상에서 potassium persulfate를 개시제로 하여 라디칼 중합시켜 제조하였다. PAMPS 겔의 구동성을 부여하기 위하여 계면활성제로 팽윤하며 치환하였다. 계면활성제가 치환된 PAMPS 겔은 용액내의 인가된 전압하에서, 그 전기장 변화에 의해 큰 변위를 나타내는 구동특성을 보였다. PAMPS 겔은 빠른 응답속도와 가역적인 bending을 나타내었다. 겔의 구동원리는 양극과 PAMPS 겔 음이온간의 정전기 인력, 겔의 swelling-deswelling 효과 그리고 계면활성제의 소수성 반응의 협동적 과정으로 나타난다. PAMPS 겔의 응답속도는 인가된 전압 및 가교도가 증가할수록 증가하였으며, 구동이 반복적으로 진행됨에 따라 응답속도는 증가하였다. 겔의 두께가 증가하면 응답속도는 감소하였다.

• 폴리머
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• 제34권1호
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• pp.79-83
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• 2010

Poly(N-isopropylacrylamide-co-dimethylamino ethyl methacrylate)(P(NIPAM-co-DMAEMA))가 고정화된 알지네이트 비드를 제조하였다. 알지네이트와 P(NIPAM-co-DMAEMA)의 정전기적 인력을 이용하여 P(NIPAM-co-DMAEMA)로 코팅된 알지네이트 비드와 P(NIPAM-co-DMAEMA)을 함유한 알지네이트 비드를 제조하였다. P(NIPAM-co-DMAEMA)은 자유 라디칼 반응으로 제조하였고 핵자기 공명분광기를 통해 확인하였다. 비드의 온도 민감성 방출 거동을 관찰하였으며, 모델시약으로 blue dextran과 fluorescein isothiocyanate-dextran을 사용하였다. P(NIPAM-co-DMAEMA)가 고정화된 알지네이트 비드로부터의 방출 정도는 온도 의존성이 낮았고, 방출모델시약의 분자량이 작을수록 더 높았다.

• Biotechnology and Bioprocess Engineering:BBE
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• 제6권5호
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• pp.326-331
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• 2001

With the aim of developing of pH-sensitive controlled drug release system, a poly(Llysine) (PLL) based cationic semi-interpenetrating polymer network (semi-IPN) has been synthesized. This cationic hydrogel was designed to swell at lower pH and de-swell at higher pH and therefore be applicable for achieving regulated drug release at a specific pH range. In addition to the pH sensitivity, this hydrogel was anticipated to interact with an ionic drug, providing another means to regulate the release rate of ionic drugs. This semi-IPN hydrogel was prepared using a free-radical polymerization method and by crosslinking of the polyethylene glycol (PEG)-methacrylate polymer through the PLL network. The two polymers were penetrated with each other via interpolymer complexation to yield the semi-IPN structures. The PLL hydrogel thus prepared showed dynamic swelling/de-swelling behavior in response to pH change, and such a behavior was influenced by both the concentrations of PLL and PEG-methacrylate. Drug release from this semi-IPN hydrogel was also investigated using a model protein drug, streptokinase. Streptokinase release was found to be dependent on its ionic interaction with the PLL backbones as well as on the swelling of the semi-IPN hydrogel. These results suggest that a PLL semi-IPN hydrogel could potentially be used as a drug delivery platform to modulate drug release by pH-sensitivity and ionic interaction.

• 멤브레인
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• 제29권6호
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• pp.323-328
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• 2019

인류의 에너지 수급은 항상 인간의 삶에 중요한 문제이며, 최근에는 전기 생산 및 공급 문제로 이어지고 있다. 이에 관련하여 본 연구에서는 에너지 저장장치의 일환으로 슈퍼커패시터 용도의 고체 전해질막을 제조하였다. 제조한 전해질막은 poly(vinyl alcohol) (PVA) 주사슬에 poly(oxyethylene methacrylate) (POEM) 곁사슬을 그래프팅하여 사용하였으며, 그래프팅은 자유 라디칼 중합법을 통해 합성하였다. 본 연구에서 사용한 PVA-g-POEM 가지형 공중합체를 슈퍼커패시터 전해질에 적용한 사례는 처음이다. POEM 그래프팅을 통해 PVA가 고유하게 가지고 있던 구조가 변화하였으며, 이를 FT-IR을 통해 분석하였다. 또한, 합성한 공중합체를 이용한 슈퍼커패시터 성능은 cyclic voltammetry (CV), galvanostatic charge/discharge(GCD), ragone plot 등을 통해 분석하였다. 이를 통해 기존에 수계 전해질로 PVA 단일 고분자만 사용하던 분야에 그래프팅 방법이라는 새로운 접근법을 제시하였다.