• Bulletin of the Korean Chemical Society
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• 제25권8호
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• pp.1238-1240
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• 2004

• Bulletin of the Korean Chemical Society
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• 제33권11호
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• pp.3535-3536
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• 2012

• Bulletin of the Korean Chemical Society
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• 제26권6호
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• pp.975-978
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• 2005

• Bulletin of the Korean Chemical Society
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• 제28권1호
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• pp.29-30
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• 2007

• 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.

• 대한화장품학회지
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• 제33권2호
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• pp.127-135
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• 2007

본 연구는 한방화장품의 원료로써 사용이 되는 약용식물들의 부위별 및 추출용매에 따른 추출물의 효능의 차이를 기술하였다. 기존의 단일성분 분석법보다 실제로 성분의 복합체인 추출물에 대하여 항산화와 UV흡수 관련 효능효과 시험법을 적용하였다. 약효를 가지는 약용식물들을 추출할 때 고려해야 할 조건이 있다. 같은 약용식물이라도 채취시기, 채취장소, 채취부위와 같은 채취조건들과 용매의 종류, 추출시간, 추출온도와 같은 추출조건들을 고려하여야 한다. 조건 중에서 추출용매와 채집부위는 효과에 있어서 매우 중요한 요인이다. 약용식물에 대한 관심이 증가하면서 여러 가지의 채취조건과 추출조건을 연구하여 한방원료의 개발에 있어 좀더 다양한 적용이 요청되고 있다. 본 연구에서는 약용과 식용으로 널리 사용되는 식물(Terminalia chebula, Syzygium aromaticum, Paeonia lactiflora, Morus alba, Scutellaria baicalensis)을 선정하여 추출용매와 채집부위를 변경시킴으로써 용매와 부위에 따른 효능의 차이를 확인하였다. 이 결과로 추출시 적당한 조건을 선택한다면 사용되는 약용식물의 양을 줄이거나 좀더 효과적인 결과를 얻을 수 있다.

• Bulletin of the Korean Chemical Society
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• 제31권8호
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• pp.2361-2367
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• 2010

$TiO_2-ZrO_2$ was prepared with surfactant through a sol-gel method. Catalysts containing 5 - 35% $H_3PO_4$ were prepared using these oxides. Subsequently the catalytic performance of prepared catalysts was determined for liquid phase esterification of aromatic acids. $H_3PO_4/TiO_2-ZrO_2$ has been used as catalyst to synthesize various novel esters by esterification of some aromatic acids with aliphatic alcohols (2-propanol, 1-butanol, iso butanol, 3-pentanol, 1-hexanol, heptanol, cyclo heptanol, octanol and decanol). Under optimized conditions, maximum yields and selectivity (100%) to the corresponding ester, was obtained by using 25 wt % $H_3PO_4/TiO_2-ZrO_2$ as catalyst. The Catalyst can be easily recycled after reaction and can be reused without any significant loss of activity/selectivity performance. No by-product formation, high yields, short reaction times, mild reaction conditions, operational simplicity with reusability of the catalyst are the salient features of the present synthetic protocol. The reaction was carried out under solvent-free condition.

• Bulletin of the Korean Chemical Society
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• 제32권7호
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• pp.2311-2315
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• 2011

Alumina supported polyphosphoric acid (PPA/$Al_2O_3$) was successfully prepared by impregnation of alumina support by polyphosphoric acid and characterized using FT-IR spectroscopy, the $N_2$ adsorption/desorption analysis (BET), thermal analysis (TG/DTG), and X-ray diffraction (XRD) techniques. The catalytic behavior of this new solid acid supported heterogeneous catalyst was checked in the synthesis of 14-aryl-14H-dibenzo[a, j]xanthenes by cyclocondensation reaction of ${\beta}$-naphthol and aryl aldehydes under solvent-free conditions. The results showed that the novel catalyst has high activity and the desired products were obtained in very short reaction times with high yields. Moreover, the catalyst can be easily recovered by filtration and reused at least three times with only slight reduction in its catalytic activity.

• Bulletin of the Korean Chemical Society
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• 제32권7호
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• pp.2385-2390
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• 2011

Preparation of ammonium dihydrogenphosphate supported on alumina ($NH_4H_2PO_4/Al_2O_3$) and its primary application as a solid acid supported heterogeneous catalyst to the synthesis of 1,2,4,5-tetrasubstituted imidazoles by a one-pot, four-component condensation of benzil, aromatic aldehydes, primary amines, and ammonium acetate under thermal solvent-free conditions were described. The results showed that the novel catalyst has high activity and the desired products were obtained in high yields. Furthermore, the products could be separated simply from the catalyst, and the catalyst could be recycled and reused with only slight reduction in its catalytic activity. Characterization of the catalyst was performed by FT-IR spectroscopy, the $N_2$ adsorption/desorption analysis (BET), thermal analysis (TG/DTG), and X-ray diffraction (XRD) techniques.

• Bulletin of the Korean Chemical Society
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• 제34권5호
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• pp.1521-1524
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• 2013

N-Propylsulfamic acid supported onto magnetic $Fe_3O_4$ nanoparticles (MNPs-PSA) was used as an efficient and magnetically recoverable catalyst for synthesis of 2H-Indazolo[2,1-b]phthalazine-1,6,11(13H)-trione derivatives from the three-component, one-pot condensation reaction of phthalhydrazide, aromatic aldehydes and cyclic 1,3-diones, in good to excellent yields at $100^{\circ}C$ under solvent-free conditions. The catalyst was easily separated with the assistance of an external magnetic field from the reaction mixture and reused for several consecutive runs without significant loss of its catalytic efficiency. In order to compare, the synthesis of 2H-Indazolo[ 2,1-b]phthalazine-1,6,11(13H)-trione derivatives in the presence of catalytic amount of sulfamic acid (SA) under same reaction condition was also reported.