• 보존과학회지
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• 제32권2호
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• pp.273-291
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• 2016

차령산맥 남북의 7개 유적에서 신석기시대 빗살무늬 토기부터 조선시대 백자까지 시대적으로 일부 시료를 선별하여 물리화학적 및 광물학적 정량분석을 통해 고대 세라믹의 제작기술과 특성을 해석하였다. 연구대상 선사시대 토기는 연질에 테쌓기한 흔적이 나타나며, 삼국시대 토기는 연질과 경질이 공존하나 자비와 저장용기는 모두 테쌓기한 반면 배식기는 물레성형하였다. 태토의 정선도가 높은 삼국시대 이후 토기와 달리 신석기 및 청동기시대 토기는 사질태토에 높은 광물 함량을 보이며, 태토보다 큰 비짐이 다량 확인된다. 청자와 백자 기질에서는 일차광물이 거의 나타나지 않으나 고온생성 광물의 함량이 높게 동정되었다. 분석시료들은 시기에 관계없이 유적에 따라 주성분 및 미량원소에 약간의 차이가 나타났다. 지구화학적 거동특성도 거의 동일하여 태토의 기본적 성질은 유사한 것을 지시한다. 작열감량은 0.01~12.59wt.% 범위를 보여 편차가 크나, 선사시대에서 삼국시대로 가며 급격히 감소한다. 이들은 소성에 따른 중량감소율과 관련이 있으며, 태토의 소성도와 고온생성 광물의 검출 함량에 따라 5그룹의 추정 소성온도로 분류된다. 신석기시대와 청동기시대 토기는 모두 $750{\sim}850^{\circ}C$ 그룹에 속하고, 삼국시대 토기는 $750{\sim}1,100^{\circ}C$의 소성온도 범위에서 다양하게 확인되며, 청자와 백자는 $1,150{\sim}1,250^{\circ}C$의 고온에서 소성된 것으로 나타났다. 제작시기에 따른 태토의 정선도와 소성온도 차이는 제작기술이 발전함에 따라 원료수급과 소성방식이 변화된 결과로 보인다. 그러나 같은 시기에도 제작방법에 차이를 보이기도 하여, 단순히 한 방향으로 진화된 발전보다는 사용 목적과 필요에 따라 활용한 것으로 해석된다.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2013년도 제45회 하계 정기학술대회 초록집
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• pp.88-89
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• 2013

A variety of influenza A viruses from animal hosts are continuously prevalent throughout the world which cause human epidemics resulting millions of human infections and enormous industrial and economic damages. Thus, early diagnosis of such pathogen is of paramount importance for biomedical examination and public healthcare screening. To approach this issue, here we propose a fully integrated Rotary genetic analysis system, called Rotary Genetic Analyzer, for on-site detection of influenza A viruses with high speed. The Rotary Genetic Analyzer is made up of four parts including a disposable microchip, a servo motor for precise and high rate spinning of the chip, thermal blocks for temperature control, and a miniaturized optical fluorescence detector as shown Fig. 1. A thermal block made from duralumin is integrated with a film heater at the bottom and a resistance temperature detector (RTD) in the middle. For the efficient performance of RT-PCR, three thermal blocks are placed on the Rotary stage and the temperature of each block is corresponded to the thermal cycling, namely $95^{\circ}C$ (denature), $58^{\circ}C$ (annealing), and $72^{\circ}C$ (extension). Rotary RT-PCR was performed to amplify the target gene which was monitored by an optical fluorescent detector above the extension block. A disposable microdevice (10 cm diameter) consists of a solid-phase extraction based sample pretreatment unit, bead chamber, and 4 ${\mu}L$ of the PCR chamber as shown Fig. 2. The microchip is fabricated using a patterned polycarbonate (PC) sheet with 1 mm thickness and a PC film with 130 ${\mu}m$ thickness, which layers are thermally bonded at $138^{\circ}C$ using acetone vapour. Silicatreated microglass beads with 150~212 ${\mu}L$ diameter are introduced into the sample pretreatment chambers and held in place by weir structure for construction of solid-phase extraction system. Fig. 3 shows strobed images of sequential loading of three samples. Three samples were loaded into the reservoir simultaneously (Fig. 3A), then the influenza A H3N2 viral RNA sample was loaded at 5000 RPM for 10 sec (Fig. 3B). Washing buffer was followed at 5000 RPM for 5 min (Fig. 3C), and angular frequency was decreased to 100 RPM for siphon priming of PCR cocktail to the channel as shown in Figure 3D. Finally the PCR cocktail was loaded to the bead chamber at 2000 RPM for 10 sec, and then RPM was increased up to 5000 RPM for 1 min to obtain the as much as PCR cocktail containing the RNA template (Fig. 3E). In this system, the wastes from RNA samples and washing buffer were transported to the waste chamber, which is fully filled to the chamber with precise optimization. Then, the PCR cocktail was able to transport to the PCR chamber. Fig. 3F shows the final image of the sample pretreatment. PCR cocktail containing RNA template is successfully isolated from waste. To detect the influenza A H3N2 virus, the purified RNA with PCR cocktail in the PCR chamber was amplified by using performed the RNA capture on the proposed microdevice. The fluorescence images were described in Figure 4A at the 0, 40 cycles. The fluorescence signal (40 cycle) was drastically increased confirming the influenza A H3N2 virus. The real-time profiles were successfully obtained using the optical fluorescence detector as shown in Figure 4B. The Rotary PCR and off-chip PCR were compared with same amount of influenza A H3N2 virus. The Ct value of Rotary PCR was smaller than the off-chip PCR without contamination. The whole process of the sample pretreatment and RT-PCR could be accomplished in 30 min on the fully integrated Rotary Genetic Analyzer system. We have demonstrated a fully integrated and portable Rotary Genetic Analyzer for detection of the gene expression of influenza A virus, which has 'Sample-in-answer-out' capability including sample pretreatment, rotary amplification, and optical detection. Target gene amplification was real-time monitored using the integrated Rotary Genetic Analyzer system.