• Archives of Pharmacal Research
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• 제18권1호
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• pp.18-21
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• 1995

Poly(ethylene glycol)(PEG) macrocers teminated with acrylate groups and semi-interpenetrating polymer networks (IPNs) composed of poly-.epsilon.-capolactone(PCL) and PEG macromer were syntheswized with the aim of obtaining a bioerodible hydrogel that could be used to release drugs for implantable delivery system. Polymerization of PEG macromer resulted in the formation of cross-linked gels due to the multifunctionality of macromer. Non-crosslinked PCL chains were interpenetrated into the cross-linked three-dimensions networks of PEG. The IPNs, largw drug loading lower concentration of PEG macromer in the IPNs concentration and the higher molecular weight of PEG macromer. Also, 5-FU was more fast released than hydrocortisone to the increased water solubility.

• 대한의용생체공학회:의공학회지
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• 제17권3호
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• pp.291-296
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• 1996

Poly(ethylene glycol)(PEG) macromers terminated with diacrylate Iyoups and interpenetrating poly- mer networks(IPN) composed of poly(hydroxyethyl methacrylate)(PHEMA) or poly(hydroxyethyl methacrylate-co-hydronypropyl methacrylate-co- N-vinyl pyrrolidone ) [ P( HEM A-co- HPM A-co- NVP) ] and PEG macromer were synthesized with the aim of obtaining protein adsorption resistant soft contact lens. Polymerization of PEC macromer resulted in the formation of cross-linked gels due to the multifunctionality of macromer. Crosslinked P(HEMA) or P(HEMA-co-HPMA-co-WVP) chains were interpenetrated into the cross-linked three-dimensional networks of PEG. It was found that albumin adsorption onto the contact lens prepared by P(HEMA-co-HPMA-co-NVP) /PEG IPW decreases with an increase of molecular weight of PEG. Also, it was found that albumin adsorption onto the both contact lens decreases with an increase of concentration of PEC macromer in the IPN preparation. There are also more adequate in the bioinertnen for the contact lens by P(HEMA)/PEG IPN or P (HEMA-co-HPMA-co-NVP)/PEG IPN than that by P(HEMA) or P(HEMA-co-HPMA-co-NVP)

• 공업화학
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• 제4권3호
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• pp.627-636
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• 1993

마크로머를 이용한 음이온성 아크릴 수지를 제조하기 위하여 음이온 리빙 중합법으로 TBMA를 합성하였고 이들을 다시 MMA와 공중합 시켜 아크릴계 그라프트 공중합체를 제조하였다. 그라프트 공중합체의 음이온 site 함량을 제어하기 위하여 (TBMA)마크로머의 MMA의 weight 비율을 7/93, 10/90, 15/85, 20/80, 30/70, 40/60, 50/50가지 변화시켜 합성하였다. (TBMA)마크로머의 음이온 리빙 중합과정에서는 반응온도를 $-78^{\circ}C$로 유지하면서 n-butyllithium-diphenylethylene계 개시제 시스템을 사용하였으며 정지반응 단계에서는 말단에 이중결합을 도입하기 위하여 capping material로 benzaldehyde를 사용한 후, methacryloyl chloride와 반응시켰으나, 넓은 분자량 분포(1.4~1.5)가 나타났다. 또한 그라프트 공중합체 내의 TBMA는 p-toluenesufonic acid인 촉매로 가수분해하였고 중화제로 triethylamine을 사용한 중화 반응은 아크릴 수지의 음이온성을 부여하였다. (TBMA)마크로머의 분자량과 분자량 분포에 대한 측정은 GPC를 이용하였으며 TBMA의 가수분해 반응과 더불어 아크릴 수지의 이온화 반응을 IR과 NMR을 이용하여 분석하였다. (TBMA)수분산성 및 분산 안정성의 관점에서 그라프트 공중합체내의 (TBMA)마크로머 분자량에 대한 가지(branch)의 길이와 TBMA함량을 관련지어 검토한 결과 분자량이 작은(TBMA) 마크로머에서는 적은 TBMA 함량으로도 안정된 수분산화 현상이 일어남을 알았다.

• Advances in materials Research
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• 제2권1호
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• pp.51-64
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• 2013

Enantioselective macromer of trimesic acid was prepared using S(-) menthol with trimesoyl chloride on polyimide (PI) ultrafiltration membrane. The chemical composition of macromer as well as polyimide ultrafiltration membrane was determined by ATR-FTIR Spectroscopy. The optical resolution of chiral alcohols was performed in pressure driven process. The effect of monomer solutions concentration, effect of air-drying time of S(-) menthol solution, effect of reaction time, effect of operating pressure, effect of feed concentration of racemate on the performance of macromer was studied. The synthesised material exhibits separation of chiral alcohols (menthol ~23% and sobrelol ~21%).

• Archives of Pharmacal Research
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• 제19권1호
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• pp.18-22
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• 1996

Acrylate-terminated poly (ethylene glycol) (PEG) macromer was prepared by the reaction of PEG with acryloyl chloride. Photopolymerization of PEG macromer resulted in the formation of cross-linked PEG network. Interpenetrating polymer networks (IPNs) based on PEG and poly(acrylic acid) (PAA) was obtained via template polymerization of AA to the PEG network by UV curing. The swelling degree of the IPNs hydrogel increased with an increase of pH value due to the association-dissociation between carboxylic acid of PAA and either of PEG through hydrogen bounding. The swelling-deswelling behavior proceeded reversibly for the IPNs upon changing pH. Release of indomethacin from the IPNs demonstrated "on-off" regulation with pH fluctuation.

• 대한의용생체공학회:학술대회논문집
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• 대한의용생체공학회 1996년도 춘계학술대회
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• pp.223-225
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• 1996

Poly (ethylene glycol) (PEG)macromers terminated with acrylate groups and interpenetrating polymer networks(IPN) composed of poly(hydroxyethyl methacrylate)(PHEMA) or poly(hydroxyethyl methacrylate-co-hydropropyl methacrylate-co-N-vinyl pyrrolidone) [P(HEMA-co-HPMA-co-NVP)] and PEG macromer were synthesized with the aim of obtaining protein adsorption resisatnt soft contact lens. Polymerization of PEG macromer resulted in the formation of cross-linked gels due to the multifunctionality of macromer. Crosslinked P(HEMA) or P(HEMA-co-HPMA-co-NVP) chains were interpenetrated into the cross-linked three-dimensional networks of PEG. It was found that albumin adsorption onto the contact lens prepared by P(HWMA)/PEG IPN decreases with a decrease of molecular weight of PEG whereas its adsorption onto the contact lens prepared by P(HEMA-co-HPMA-co-NVP)/PEG IPN decreases with an increase of molecular weight of PEG. Also, it was found that albumin adsorption onto the both contact lens decreases with an increase of concentration of PEG macromer in the IPN preparation. There are also more adequate in the bioinertness and bioadhesion for the contact lens by P(HEMA)/PEG IPN or P(HEMA-co-HPMA-co-NVP)/PEG IPN than that by P(HEMA) or P(HEMA-co-HPMA-co-NVP).

• 폴리머
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• 제24권2호
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• pp.141-148
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• 2000

Polycaprolactone (PCL)을 base로 하는 효과적인 compost 필름을 만들기 위하여 옥수수전분을 블렌딩한 뒤 기계적 특성과 미생물에 의한 생분해도를 조사하였다. 비상용성을 보이는 옥수수전분/PCL 블렌드에 대한 상용화제로는 2-hydroxyethylmethacrylate (HEMA)-PCL macromer를 옥수수전분에 그래프팅시킨 공중합체를 사용하였는데 옥수수전분에 대한 HEMA의 그래프팅율이 가장 높은 것과 가장 낮은 것을 선택하여 일정한 조성의 $\varepsilon$-caprolactone에 그래프팅시킨 상용화제들의 상용화 효과를 비교하였다. 상용화제를 함유한 옥수수전분/PCL (50/50) 블렌드의 신장율이 상당히 증가하였으며 SEM 관찰 결과 이는 상용화제로 인해 옥수수전분 알갱이와 PCL 기질간의 계면 접착력이 증가하였기 때문으로 판단된다. 그러나 모듈러스와 인장강도는 상용화치 사용에도 불구하고 별다른 변화가 없었다.

• 접착 및 계면
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• 제11권3호
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• pp.106-111
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• 2010

PEGMA macromer를 Na-MMT에 삽입한 후 MMA 및 MA 단량체와의 공중합을 행하여 PEGMA/(Na-MMT)-co-MMA/MA 나노복합재료를 합성하고 이의 특성결정을 행하였다. 제조된 나노복합재료를 XRD로 관찰한 결과, Na-MMT에 PEGMA를 삽입하였을 경우 Na-MMT 양이 증가함에 따라 Na-MMT의 실리케이트 층간거리는 증가하였다. DSC 측정으로부터 Na-MMT 첨가량이 늘어날수록 Tg는 높아지는 경향을 보였다. TGA 측정을 통하여 PEGMA/(Na-MMT)-co-MMA/MA 나노복합재료는 순수한 PEGMA-co-MMA/MA보다 열안정성이 다소 향상됨을 확인하였다.

• Journal of the Korean Wood Science and Technology
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• 제23권4호
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• pp.1-9
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• 1995

This study was carried out to experiment the dimensional stabilization of woods of red pine (Pinus densiflora S. et Z.) and sugi(Cryptomeria japonica D. Don) by vacuum impregnation of polyehtylene glycols(PEG) with mo. wt. 200, 400, 600, 1000; polypropylene glycols (PPG) with mo. wt. 425,725 ; PEG-acryloylates, and PPG-acryloylates synthesized, and then by water soaking. The results obtained are as follows: 1. The density of sapwood and heartwood was different from each other in both species. 2. The PEG and PEG-macromers with lower molecular weight by impregnation has increased the density of wood specimens more higher, thereby caused their higher volume expansion, and those with higher molecular weight than 600 has tended to down their density increment. 3. Before and after water soaking, the density decrease of specimen impregnated was high in woods impregnated with simple PEG and PPG, while lower in specimens impregnated with PEG-macromers and PPG-macromers. 4. So PEG-macromer was expected to hold the original dimension of decayed wood for antiques, but it was necessary to develop another penetration method as well as aqueous solvent.

• Macromolecular Research
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• 제12권4호
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• pp.379-383
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• 2004

Poly(ethylene glycol)s (PEGs) are unique in their material properties, such as biocompatibility, non-toxicity, and water-solublizing ability, which are extremely useful for a variety of biomedical applications. In addition, a variety of functional PEGs with specific functionality at one or both chain ends have been synthesized for many specialized applications. Surface modifications using PEG have been demonstrated to decrease protein adsorption and platelet or cell adhesion on biomaterials. Furthermore, PEGs having anionic sulfonate terminal units have been proven to enhance the blood compatibility of materials, which has been demonstrated by the negative cilia concept. The preparation of telechelic PEGs having a sulfonic acid group at one end and a polymerizable methacryloyl group at the other is an interesting undertaking for providing macromers that can be used in various vinyl copolymerization and gel systems. In this paper, preliminary results on the synthesis and polymerization behavior of a novel PEG macromer is described with the aim of identifying a biocompatible material for applications in various blood-contacting devices.