목적 : 천연 항균, 항산화 물질인 망고스틴의 크산톤 화합물로 코팅된 콘택트렌즈를 제조하여 안과적 질환 예 방을 위한 기능성 콘택트렌즈의 물리·화학적 특성을 연구하였다. 방법 : 콘택트렌즈를 제조하여 IPN기술을 통해 감마망고스틴을 코팅하였다. 제조된 렌즈를 ISO와 식약처기준 을 참고하여 광투과율, 함수율, 산소투과율(Dk/t), 항균, 항산화성 실험을 진행하였다. 결과 : 감마망고스틴 코팅 콘택트렌즈의 가시광선투과율은 93%이다. 자외선은 70% 이상 청광은 30% 이상 차 단한다. 항균 실험에서는 감마망고스틴 코팅 콘택트렌즈의 항균성이 일반렌즈에 비해 5배 이상 효과 있고, 항산화 는 시험별 17.49, 28.46, 36.99%의 항산화율을 보였다. 결론 : 감마망고스틴으로 코팅된 콘택트렌즈는 UV와 청광의 차단율이 일반렌즈에 비해 매우 뛰어나다. 또한, 일반렌즈에 없는 항균, 항산화 활성을 보여 안과적 질환을 예방할 수 있을 것으로 보인다.

Indoor air environments for people are recently being observed because the time we spend inside the house or a building throughout the day has been extended during the present circumstances. This is why formaldehyde and volatile organic compounds (VOCs) are regulated, which can cause Sick Building Syndrome (SBS). There might be other VOCs not regulated by law in newly built collective housing, however, in order to compensate for the reduced concentration of regulated VOCs such as benzene, toluene, ethylbenzene, xylene, and styrene. In this study, the concentration of unregulated VOCs in newly built collective housing structures located in the Seoul Special City was researched to find potential indoor hazards for citizens and to prepare basic data for further research.

최근에 상용화된 SWRO 막은 플럭스 감소만으로 파울링을 평가하기 어렵다. 따라서 본 실험에서는 열역학 모델식을 통해 유기막오염과 세정에 따른 투수계수(Lp)와 농도분극계수(fcp), 파울링에 의한 여과저항(Rf) 변화를 분석해보았다. 파울런트 미주입시, 원수 TDS농도별, 압력별로 Lp와 fcp를 분석하였고 그 후, 유기 파울런트를 주입하여 막오염 진행에 따른 Lp와 fcp 변화를 분석하였다. 실험 결과, 파울런트를 주입하지 않은 경우, Lp와 fcp는 동일한 원수의 TDS 농도에서 압력이 증가함에 따라 증가하고, 동일한 운전 압력에서 원수의 TDS 농도가 증가할수록 감소하였고, 막오염 진행에 따른 Lp와 fcp의 감소 경향은 플럭스 감소 경향과 일치하지 않으며 막오염 물질 별로 다른 양상을 보였다.

In the present study, the effect of cysteine and NT or bisphenol A (BP) on in vitro aturation (IVM) of porcine oocytes were examined. COCs was cultured in NCSU-23 medium supplement with 10% FCS which had previously been covered with mineral oil and equilibrated in a humidified atmosphere of 5% CO2 and 95% air at 38℃. The IVM rate of oocytes cultured for 48 hrs in NCSU-23 medium supplement with 0.5～10.0 mM cysteine were 34.0±3.2%, 36.0±3.5%, 48.0±3.8%, 22.0±3.2%, respectively. The IVM rate of oocytes cultured in NCSU-23 medium supplement with 0.5～5.0 mM NT for 48 hrs were 24.0±4.2%, 18.0±4.9%, 8.0±2.2%, respectively. NT affects oocyte in vitro maturation rate in a dose-dependent. This result were significantly lower than the control group. The IVM rate of oocytes cultured for 48 hrs in NCSU-23 medium supplement with 1.0 mM NT+5.0 mM cysteine (38.0±4.3%) were significantly higher than that of NT treatment. The IVM rate of oocytes cultured in NCSU-23 medium supplement with 0.05～5.0 mM BP for 48 hrs were 20.0±4.7%, 10.0±5.3%, 6.0±3.2%, respectively. The IVM rate of oocytes cultured in NCSU-23 medium supplement with BP was significantly lower cultured non supplement of BP (44.0±3.5%). BP affects porcine oocyte maturation rate in a dose-dependent manner. The IVM rate of oocytes cultured for 48 hrs in NCSU-23 medium supplement with 1.0 mM BP+5.0 mM cysteine (32.0±3.2%) were increased than that of BP treatment.