• 한국해양환경ㆍ에너지학회지
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• 제8권4호
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• pp.179-185
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• 2005

다환방향족 탄화수소는 주요한 독성환경오염물질풍의 하나이며 해양퇴적물에 축적이 된다. 다환방향족 탄화수소가 가지고 있는 위해성으로 인해 해양퇴적물내의 다환방향족 탄화수소 제거는 많은 관심사가 되어오고 있다. 본 연구에서는 다환방향족 탄화수소로 오염된 해양퇴적물의 생물정화를 위해 bioslurry reactor를 사용하기 위한 전단계로 ex situ bioremediation을 위한 최적 조건을 찾기 위해 멸균 유무의 퇴적물에서 균주접종과 혼합 cyclodextrin (M-CD)공급의 효과를 알아보았다. 비멸균상태의 퇴적물에서 분해균주의 접종여부에 상관없이 M-CD가 첨가된 실험구의 전자전달계활성이 증가되었고 멸균상태의 퇴적물에서는 분해균주가 접종되고 M-CD가 첨가된 실험구의 전자전달계활성이 증가되었다. 멸균상태의 퇴적물에서 M-CD와 함께 단일 균주가 접종되었을 때 퇴적물내의 다환방향족 탄화수소의 분해율이 9-20%로 나타났으며 동일한 조건에서 혼합균주가 접종되었을 때는 24-37%로 나타났다. 비멸균상태의 퇴적물에서 동일한 조건으로 실험하였을 때는 유의한 분해가 일어나지 않았으며 군집분석 결과 접종 균주도 감소하였다. 또한 M-CD 첨가 없이는 2일후 접종균주를 찾아볼 수 없었다. 결론적으로 퇴적물내의 다환방향족 탄화수소 제거를 위해 퇴적물내의 토착미생물과 포식자가 제거된 상태에서 적절한 탄소원과 함께 균주를 접종하는 것이 효과적인 것으로 나타났다.

• Journal of Pharmaceutical Investigation
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• 제31권3호
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• pp.151-160
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• 2001

The purpose of this study is to investigate the interaction of progesterone with various cyclodextrins (CDs) in the aqueous solution and in solid state, and finally to formulate a parenteral aqueous formulation. CDs used were ${\alpha}-$, ${\beta}-$, and ${\gamma}-CD$, $2-hydroxypropyl-{\beta}-CD$ (HPCD), sulfobutyl $ether-{\beta}-CD$ (SBCD), $dimethyl-{\beta}-CD$ (DMCD) and $trimethyl-{\beta}-CD$ (TMCD). The solubility studies of progesterone were performed in the presence of various CDs as a function of concentration or temperature. The solubility of progesterone increased in the rank order of ${\alpha}-CD$ < ${\beta}-CD$ < ${\gamma}-CD$ < TMCD$ < HPCD < DMCD < SBCD. Addition of SBCD (200 mg/ml) in water increased the aqueous solubility $(9.36\;{\mu}g/ml)$ about 3,200 times, and lowering the temperature facilitated the solubilization of progesterone. However, the addition of HPCD and SBCD in 20:80 (v/v) polyethylene glycol 300-water and propylene glycol-water cosolvents markedly decreased the solubility of progesterone, compared with solubilizing effects in water. Physical mixtures and solid dispersions of progesterone with HPCD or SBCD were prepared, and evaluated by differential scanning calorimetry (DSC), Fourier-transform infrared spectroscopy (FT-IR), near IR spectroscopy and dissolution studies. By DSC and IR studies, it was found that progesterone was dispersed in HPCD in monotectic state and dissolved rapidly from both solid dispersions. Based on solubility studies, new aqueous progesterone fonnulations (5 mg/ml) containing SBCD (200 mg/ml) could be prepared and did not form precipitates even after 2 months at $4^{\circ}C$. The solution was transparent when mixed with normal saline and 5% dextrose injection at 1: 1, 1:10 and 1:20 (v/v) even after 7 days. Permeation rates of progesterone through a cellulose membrane from 20% PEG 300 solution $(50\;{\mu}g/ml)$ containing HPCD or SBCD were compared with oily formulation. Permeation of progesterone from oily formulation did not occur up to 8 hr, but aqueous formulations showed fast permeation rates from early stage of permeation study. The addition of HPCD or SBCD retarded the permeation rates of progesterone with the increase of CD concentrations, suggesting the possibility of a controlled absorption from the site administered intramuscularly. These results demonstrate that it is feasible to develop a new progesterone parenteral aqueous injection (5 mg/ml) using SBCD.