• 제목/요약/키워드: poly(caprolactone)

검색결과 160건 처리시간 0.026초

Surfactant-free microspheres of poly($\alpha$-caprolactone)/poly(ethylene glycol)/poly($\varepsilon$-caprolactone) triblock copolymers as a novel protein carriers

  • Sun, Sang-Wook;Jeong, Young-Il;Jung, Sun-Woong;Kim, Sung-Ho
    • 대한약학회:학술대회논문집
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    • 대한약학회 2002년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2
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    • pp.408.2-409
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    • 2002
  • The aim of this study is to prepare biodegradable microspheres without use of any kind of surfactants or emulsifiers for a novel sustained delivery carriers of protein drugs. Poly(e-caprolactone)/poly(ethylene glycol)/poly(e-caprolactone) (CEC) triblock copolymer was synthesized by ring-opening of e-caprolactone with dihydroxy poly(ethylene glycol) and was used to make surfactant-free microspheres. (omitted)

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Synthesis and Microphase Separation of Biodegradable Poly($\varepsilon$-caprolactone)-Poly(ethylene glycol)-Poly($\varepsilon$-caprolactone) Multiblock Copolymer Films

  • You, Jae-Ho;Choi, Sung-Wook;Kim, Jung-Hyun;Kwak, Young-Tae
    • Macromolecular Research
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    • 제16권7호
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    • pp.609-613
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    • 2008
  • Poly($\varepsilon$-caprolactone)-poly(ethylene glycol)-poly($\varepsilon$-caprolactone) (PCL-PEG-PCL) multiblock copolymers at various hydrophobic-hydrophilic ratios were successfully synthesized by the chain extension of triblock copolymers through isocyanate (hexamethylene diisocyanate). Biodegradable films were prepared from the resulting multiblock copolymers using the casting method. The mechanical properties of the films were improved by chain extension of the triblock copolymers, whereas the films prepared by the triblock copolymers were weak and brittle. Atomic force microscopy (AFM) of the multiblock copolymer film showed that the hydrophilic PEG had segregated on the film surface. This is consistent with the observed contact angle of the films.

박리형 PCL/Clay 나노복합재료 제조와 특성 (Preparation of Exfoliated PCL/Clay Nanocomposite and Its Characterization)

  • 유성구;박대연;배광수;서길수
    • 폴리머
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    • 제25권3호
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    • pp.421-426
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    • 2001
  • Montmorillonite (MMT)의 층간에 poly(${varepsilon}-caprolactone$) diol과 반응할 수 있는 -COOH기를 삽입하기 위하여 11-aminododecanoic acid를, 그리고 MMT의 층간거리를 넓혀주기 위하여 세칠트리메칠암모늄 브로마이드(CTMA)를 각각 삽입시켰다. 이렇게 개질된 MMT를 THF 용액상태에서 poly(${varepsilon}-caprolactone$) diol ($M_n{=2000}$)와 $80^{\circ}C$에서 4시간 동안 반응하였다. 반응 후, poly(${varepsilon}-caprolactone$) ($A_n{=80000}$)을 이 용액에 삽입하여 같은 온도에서 12시간 동안 혼합하였다. 이 용액을 실리콘 몰드에 부어 6$0^{\circ}C$ 진공 오븐에서 6시간 동안 건조하여 poly(${varepsilon}-caprolactone$) (PCL)/clay 나노복합재료 필름을 제조하였다. XRD와 TEM으로 확인한 결과 실리케이트 층이 완전히 박리된 박리형 나노복합재료임을 확인하였다. 그리고 MMT의 양에 따른 PCL/clay 나노복합재료의 기계적 성질과 열적 성질을 tensile tester와 DSC로 확인하였다. MMT가 PCL 매트릭스에 균일하게 분산되어 있어 복합재료의 영율이 향상되었으나, 인장강도에는 영향이 거의 없었다. 그리고 MMT의 양이 PCL에 대하여 3wt%까지 증가함에 따라 PCL의 결정화 온도가 증가하였다.

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Preparation and Characterization of Nanoparticles Using Poly(N-isopropylacrylamide)-$Poly({\varepsilon}-caprolactone)$ and Poly(ethylene glycol)-$Poly({\varepsilon}-caprolactone)$ Block Copolymers with Thermosensitive Function

  • Choi, Chang-Yong;Jang, Mi-Kyeong;Nah, Jae-Woon
    • Macromolecular Research
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    • 제15권7호
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    • pp.623-632
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    • 2007
  • Thermosensitive nanoparticles were prepared via the self-assembly of two different $poly({\varepsilon}-caprolactone)$-based block copolymers of poly(N-isopropylacrylamide)-b-$poly({\varepsilon}-caprolactone)$ (PNPCL) and poly(ethylene glycol)-b-$poly({\varepsilon}-caprolactone)$ (PEGCL). The self-aggregation and thermosensitive behaviors of the mixed nanoparticles were investigated using $^1H-NMR$, turbidimetry, differential scanning microcalorimetry (micro-DSC), dynamic light scattering (DLS), and fluorescence spectroscopy. The copolymer mixtures (mixed nanoparticles, M1-M5, with different PNPCL content) formed nano-sized self-aggregates in an aqueous environment via the intra- and/or intermolecular association of hydrophobic PCL chains. The microscopic investigation of the mixed nanoparticles showed that the critical aggregation concentration (cac), the partition equilibrium constants $(K_v)$ of pyrene, and the aggregation number of PCL chains per one hydrophobic microdomain varied in accordance with the compositions of the mixed nanoparticles. Furthermore, the PNPCL harboring mixed nanoparticles evidenced phase transition behavior, originated by coil to the globule transition of PNiPAAm block upon heating, thereby resulting in the turbidity change, endothermic heat exchange, and particle size reduction upon heating. The drug release tests showed that the formation of the thermosensitive hydrogel layer enhanced the sustained drug release patterns by functioning as an additional diffusion barrier.

Surfactant-Free Microspheres of Poly(${\varepsilon}-caprolactone$)/Poly(ethylene glycol)/Poly(${\varepsilon}-caprolactone$) Triblock Copolymers as a Protein Carrier

  • Sun, Sang-Wook;Jeong, Young-Il;Kim, Sung-Ho
    • Archives of Pharmacal Research
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    • 제26권6호
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    • pp.504-510
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    • 2003
  • The aim of this study is to prepare biodegradable microspheres without the use of surfactants or emulsifiers for a novel sustained delivery carriers of protein drugs. A poly($\varepsilon$-caprolactone)/poly(ethylene glycol)/poly($\varepsilon$-caprolactone) (CEC) triblock copolymer was synthesized by the ring-opening of $\varepsilon$-caprolactone with dihydroxy poly (ethylene glycol) to prepare surfactant-free microspheres. When dichloromethane (DCM) or ethyl formate (EF) was used as a solvent, the formation of microspheres did not occur. Although the microspheres could be formed prior to lyophilization under certain conditions, the morphology of microspheres was not maintained during the filtration and lyophilization process. Surfactant-free microspheres were only formed when ethyl acetate (EA) was used as the organic solvent and showed good spherical micro-spheres although the surfaces appeared irregular. The content of the protein in the micro-sphere was lower than expected, probably because of the presence of water channels and pores. The protein release kinetics showed a burst release until 2 days and after that sustained release pattern was showed. Therefore, these observations indicated that the formation of microsphere without the use of surfactant is feasible, and, this the improved process, the protein is readily incorporated in the microsphere.

Poly(2, 6-dimethyl-1, 4-phenylene oxide)/Poly(styrene-co-acrylonitrile)블렌드에서 Macroinitiator로 합성한 Polystyrene-Poly(caprolactone) 블록공중합체의 상용제로서의 역할에 관한 연구 (Compatibilizing Effect of Polystyrene-Poly(caprolactone) Block Copolymer Synthesized from Macroinitiator in Poly(2, 6-dimethyl-1, 4-phenylene oxide)/Poly(styrene-co-acrylonitrile) Blend)

  • 정동권;정한모;양성봉;윤구식
    • 공업화학
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    • 제3권2호
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    • pp.247-255
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    • 1992
  • Macroazoinitiator를 이용하여 Polystyrene-poly(caprolactone) (PS-PCL) 블록공중합체를 합성하고, poly(2, 6-dimethyl-1, 4-phenylene oxide) (PPO)/poly(styrene-co-acrylonitrile) (SAN, acrylonitrile의 함량이 25wt%) 블렌드에서의 상용화 효과를 조사하였다. 공중합체 중 PS블록과 PCL블록은 각각 PPO, SAN과 상용성을 가졌으며, 블록공중합체는 SAN의 PPO 영역으로의 용해 정도를 증가시킴을 관찰할 수 있었다.

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Norfloxacin이 담지된 Poly(ε-caprolactone)/Poly(ethylene glycol) 이중블록공중합체 미셀의 제조 (Norfloxacin-Incorporated Polymeric Micelle Composed of Poly(ε-caprolactone)/Poly(ethylene glycol) Diblock Copolymer)

  • 정영일;장미경;나재운
    • 폴리머
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    • 제33권2호
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    • pp.137-143
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    • 2009
  • 이 연구에서 norfloxacin(NFX)이 담지된 poly($\varepsilon$-caprolactone)/poly(ethylene glycol)(PCL/PEG, abbreviated as CE) 이중블록공중합체로 구성된 고분자 미셀을 제조하였다. 입자크기는 PCL블록길이에 따라 60$\sim$200 nm사이였다. 임계회합농도는 소수성 PCL 블록길이가 증가함에 따라 감소하는 경향을 보였다. $^1H$-NMR 연구에서 PCL 블록은 내핵, PEG는 외피를 형성한 미셀구조로 형성되었음을 확인하였다. 약물의 방출은 약 2일간 지속되었으며 PCL블록길이와 약물함량이 증가함에 따라 감소하는 경향을 보였다. 항미생물 성능 실험에서 고분자 미셀은 기존의 NFX와 비슷한 독성을 보였다.

전기방사로 제조된 Poly($\varepsilon$-caprolactone) 필라멘트를 이용한 직물의 제조 (Preparation of Woven Fabric Via Electrospun Poly($\varepsilon$-caprolactone) Filament)

  • 박희천;길명섭;김형준;김학용;이덕래
    • 한국섬유공학회:학술대회논문집
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    • 한국섬유공학회 2003년도 봄 학술발표회 논문집
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    • pp.374-375
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    • 2003
  • 최근 나노섬유기술의 중요성이 증가함에 따라 나노섬유를 제조할 수 있는 여러 방법들 중에 상용화의 가능성, 적용 고분자의 다양성, 제조 공정의 단순성, 다양한 제품기술 응용성을 고려할 때 전기방사는 가장 기대되는 방법으로 현재, 다양한 분야의 연구들이 활발히 진행되고 있다[1,3]. 본 연구는 전기 방사 방법을 이용하여 다공성의 Poly($\varepsilon$-caprolactone) 필라멘트를 제조하고, 제조한 필라멘트를 수직기를 이용하여 평직 직물을 제조하여 그 응용 가능성을 확인하는 것이다[2]. (중략)

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Synthesis of Polyethylene-block-Poly(${\varepsilon}-caprolactone$) and Polyethylene-block-Poly(methyl methacrylate) from Hydroxy-terminated Polyethylenes

  • Jeon, Man-Seong;Kim, Sang-Youl
    • 한국고분자학회:학술대회논문집
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    • 한국고분자학회 2006년도 IUPAC International Symposium on Advanced Polymers for Emerging Technologies
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    • pp.226-226
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    • 2006
  • Ethylene was polymerized with a catalyst having sterically hindered pentamethylcyclopentadienyl ligand, $Cp^{\ast}_{2}ZrCl_{2}/MAO$, and the polymerization mixture were treated with dry oxygen (oxidative workup) to produce hydroxyl-terminated polyethylenes (PE-OH). Polyethylene-block-Poly (${\Box}-caprolactone$) was synthesized from PE-OH and ${\cdot}\^{A}-caprolactone$A by using stannous octoate as a catalyst for ring opening polymerization of ${\cdot}\^{A}-caprolactone$. Polyethylene-block-Poly(methyl methacrylate) was obtained by transforming the hydroxyl-terminated polyethylenes to macroinitiators for atom transfer radical polymerization (ATRP) and by reacting them with MMA.

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향오일을 함유한 Poly(ε-caprolactone)/Poly(ethyleneimine) 마이크로캡슐의 방출거동 (Release Behaviors of Poly(ε-caprolactone)/Poly(ethyleneimine) Microcapsules Containing Fragrant Oil)

  • 박수진;석수자
    • Korean Chemical Engineering Research
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    • 제43권4호
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    • pp.482-486
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    • 2005
  • 향오일이 흡착된 $Al_2O_3$를 심물질로 함유한 생분해성 poly(${\varepsilon}$-caprolactone) (PCL)/poly(ethylene imine) (PEI) 마이크로캡슐을 PEI의 함량에 따라 제조하였다. 교반속도 그리고 유화제의 농도에 따른 마이크로캡슐의 직경과 모폴로지는 주사전자현미경을 이용하여 관찰하였고, 열적 거동은 DSC를 통해 알아보았다. 또한, 향오일 방출거동을 알아보기 위해 UV.vis. 흡광광도법으로 흡광도를 측정하여 방출된 향오일의 양을 측정하였다. 실험 결과, PCL/PEI 마이크로캡슐의 입자크기는 교반속도와 유화제의 농도가 증가할수록 감소하였다. 그리고 표면 모폴로지는 PEI의 함량이 증가함에 따라 표면은 변했고, 마이크로캡슐의 용융 엔탈피(${\Delta}H_m$)은 증가하는 것을 확인할 수 있었다. 향오일의 방출속도는 PEI의 함량이 증가함에 따라 증가하는 경향을 나타냈다. 또한, 이는 친수성인 PEI의 함량비가 증가함에 따라 캡슐표면의 친수성 그룹이 증가하였기 때문에 향오일의 확산이 용이하게 되었기 때문인 것으로 판단된다.