• 대한전자공학회:학술대회논문집
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• 대한전자공학회 2006년도 하계종합학술대회
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• pp.877-878
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• 2006

In this paper, we propose a skin lesion detection to develop the system of fluorescence image analysis to identify the fluorescence of topical methyl aminolevulinate(MAL) idduced PpIX in patients with BCC accurately. By fluorescence image analysis we define the border between tumo and tumor-free areas on fluorescence image after topical application of MAL ointment. We excised both the tumor and peri-tumoral areas widely from the 10 patients with BCC, and divided tissue samples into 3 area, such as tumor area, suspected tumor area, tumor-free area, respectively. Our proposed method migt play a role as an adjunctive tool to define the border between tumor and tumor-free areas for Mohs' micrographic surgery.

• 한국콘텐츠학회논문지
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• 제7권1호
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• pp.40-47
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• 2007

단백질 매크로 어레이 영상에서 단백질 칩 각각의 특징을 규명하는 것은 중요한 것이다. 사람의 시각에 의한 판단은 많은 단백질 칩 영상을 실험할 경우, 장시간의 관찰과 그로 인한 오류가 발생할 수 있다. 따라서 시뮬레이터를 통한 특성 파악이 필요하게 되고, 매크로 어레이 스캔 영상에 대해 특성 분석을 할 경우 효율을 극대화할 수 있다. 형광 스캔 영상에 있어서, 각 셀의 반응도는 컬러 영상의 R, G, B 분포에 의존하여 왔다. 그러나 중첩되는 영상의 경우는 한쪽으로 구분하여 분류하기가 어렵다. 본 논문은 이러한 단점을 극복하기 위해 사용자가 원하는 색상에 대한 퍼지 측도 값을 적용한 퍼지 적분 값으로서 단백질 칩의 반응색상을 구분 지었다. Scan Array 5000에 의해 구성된 매크로 어레이 형광 영상들에 대해 실험한 결과, 퍼지 적분을 사용한 제안 방법이 모호한 색상에 대해 결정을 내릴 수 있는 요소가 됨을 보여 주었다.

• 멤브레인
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• 제21권2호
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• pp.171-176
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• 2011

분리막을 이용한 수처리 공정에서 유입 수에 함유된 부유물질이나 기타 오염물질이 막 표면 또는 내부에 축적 흡착 등의 막 오염현상으로 인해 막 성능 감소와 함께 막 분리 공정에 큰 영향을 미치게 된다. 본 연구에서는 막 표면에서의 막 오염현상을 실시간으로 모니터링 할 수 있는 기술을 연구하였다. 투명한 오염물질에 의한 분리막 표면 오염을 측정하기 위해 막 표면에 360 nm 파장의 가시광선을 조사하여 이미지를 R. G. B 값으로 추출하여 막의 오염현상을 실시간으로 모니터링 하였다. 추출된 이미지 중 400~499 nm 파장영역인 B 값이 가장 강도가 강하게 나타났다. 막 오염정도의 변화를 이미지의 강도 차이로 관찰함으로써 실시간 분석이 가능함을 확인하였다.

• 대한의용생체공학회:의공학회지
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• 제44권3호
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• pp.176-181
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• 2023

During cancer treatment, the patient's response to drugs appears differently at the cellular level. In this paper, an image-based cell phenotypic feature quantification and key feature selection method are presented to predict the response of patient-derived cancer cells to a specific drug. In order to analyze the viability characteristics of cancer cells, high-definition microscope images in which cell nuclei are fluorescently stained are used, and individual-level cell analysis is performed. To this end, first, image stitching is performed for analysis of the same environment in units of the well plates, and uneven brightness due to the effects of illumination is adjusted based on the histogram. In order to automatically segment only the cell nucleus region, which is the region of interest, from the improved image, a superpixel-based segmentation technique is applied using the fluorescence expression level and morphological information. After extracting 242 types of features from the image through the segmented cell region information, only the features related to cell viability are selected through the ReliefF algorithm. The proposed method can be applied to cell image-based phenotypic screening to determine a patient's response to a drug.

• 전자공학회논문지SC
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• 제43권4호
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• pp.11-20
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• 2006

본 논문에서는 초분광 형광영상과 반사영상 융합을 이용한 닭의 종양인식방법을 제안하였다. 형광영상에 밴드비율을 적용하여 피부의 정상과 종양부분을 구분한다. 이를 위해 각각 부분의 확률밀도함수의 중첩된 면적을 최소화하는 방법을 사용하였다. 이 방법으로 획득한 4개의 특정영상에 분할-합병법을 적용하여 형광영상 분류결과를 얻었다. 반사영상 분석에서는 단일 밴드가 정보량에 주는 영향에 근거하여 밴드 선택 방법을 제안하였다. 학습데이터에 의해 투영 축을 선택하는 선형변환을 정의함으로써 영상분류에 효과적인 많은 특징을 확보하였다. 이에 따라 반사영상에서도 세밀한 영상의 해석이 가능하였고 특징 선택의 자동화를 실현하였다. 반사영상에서 획득한 특정영상도 분할-합병법으로 분류하였으며 형광영상의 분류결과와 융합하여 종양을 인식하였다. 모의실험을 통해 제안한 방법은 기존의 방법에 비해 오인식이 낮음을 확인하였다.

• 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.

• Archives of Plastic Surgery
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• 제34권6호
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• pp.679-684
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• 2007

Purpose: DMH(1,2-dimethylhydrazine) has been known to induce vascular neoplasm such as malignant endothelioma in animal experiment, through induction of abnormal proliferation of HUVECs. In our previous studies, 11 types of PKC isoenzymes were determined by RT-PCR and the expression of $PKC{\alpha}$, and ${\mu}$ was more prominent than other PKC isoenzymes in the DMH-treated group. However, this result was not based on objective assessment. In this study, we further evaluated the role of $PKC{\alpha}$ on the DMH-induced abnormal proliferation of HUVECs by two different methods to identify its presence with high relevance in objective view. $PKC{\mu}$ will be investigated in further study. Methods: The study was conducted with the cultured HUVECs group(control) and the $0.75{\times}10^{-9}M$ DMH-treated group. After processing protein extraction in 0 and 24 hour, extracted protein was treated of quantitative test through BCA protein assay. In the western blot analysis, electrophoresis was performed in the order of gel preparation, sample preparation, and gel running. Electrotransfer to nitrocellulose membrane and reaction with antibody were done. Detection of $PKC{\alpha}$ was achieved through "Gel Image Analysis System". In the fluorescence immunocytochemical analysis, the grading of radiance of the intracellular $PKC{\alpha}$ particles was detected with confocal microscope after treating with primary and fluorescent secondary antibody in 0 and 24 hours. Results: The Western blot analysis showed increased $PKC{\alpha}$ expression from the specimen obtained in 24 hour of the DMH treatment group when compared to those in control group. Under confocal fluorescence microscope, the emitting radiance in the DMH treated group was brighter at 24 hours as well. Conclusion: We believe that $PKC{\alpha}$ plays a role in DMH-induced abnormal proliferation of the vascular endothelium, which may provide insights in understanding the vascular neoplasm.