• 청정기술
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• 제11권2호
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• pp.69-74
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• 2005

본 연구에서는 AFM 양극산화법을 이용하여 서브마이크로 수준의 패턴을 구성하였다. 자기조립법으로 제조한 MPTMS/Si(100) 기질 위에 AFM 양극산화법으로 패턴을 형성하였고, 비에칭법을 이용하여 아민그룹을 지닌 기능기를 고정시켰다. 금속전극으로는 Frens 방법으로 제조한 금나노입자를 이용하였다. 금속이온의 흡착에 따른 전도도는 근거리의 경우 coherent tunneling에 의존하지만, 원거리 전극에서는 incoherent tunneling에 의존한다. 전극의 간격이 가까울수록 저항이 감소하여 센서의 감도와 최소검출능을 개선할 수 있었다. 또한 다중기능성을 부여하여 센서의 선택도를 부여하였으며, 패턴의 크기에 따른 최소검출농도를 낮출 수 있음을 확인하였다.

• Bulletin of the Korean Chemical Society
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• 제33권7호
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• pp.2359-2364
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• 2012

Two new chemosensors, rhodamine 6G derivative bearing hydroxyethyl group (1) and rhodamine base derivative bearing 15-crown-5 group (2) were synthesized and their sensing behaviors toward various metal ions were investigated by UV/Vis and fluorescence spectroscopies. Addition of $Hg^{2+}$ ion to a $CH_3CN$ solution of 1 and 2 gave visual color changes as well as fluorescent OFF-ON observations. Selectivity and sensitivity of 1 towards $Hg^{2+}$ are excellent enough to detect micromolar level of $Hg^{2+}$ ion, even in equeous media and biological sample (HeLa cell).

• 한국산학기술학회논문지
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• 제18권12호
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• pp.100-105
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• 2017

수질환경에서 구리이온을 검출하기 위하여 광섬유 센서의 구리 이온 감지 물질로 8-Hydroxyquinolin-2carboxaldehyde와 4-Aminoantipyrine으로 합성된 8-Hydroxyquinoline 합성유도체에 대해 광학적 반응 특성을 조사하였다. 실험은 광섬유를 이용한 측정시스템을 이용하여 수용액에 용해된 구리 이온의 농도에 대해 합성유도체에 의한 흡광도와 관계를 평가하기 위하여 수행되었다. 8-Hydroxyquinoline 합성유도체는 수질 환경에서 다양한 금속 이온들 중에서 구리 이온에 대해 노란색에서 붉은색으로 변화되는 높은 발색 현상을 나타냈으며 530 nm의 고유 흡광 파장을 보였다. 제작된 합성유도체의 Cu 이온에 대한 선택성을 평가하기 위하여 Hg 이온의 영향을 조사하였다. Cu와 Hg 이온의 다양한 농도 비 (Cu:Hg ratio 0.05부터 20까지)에서 흡광도를 측정한 결과, Cu 이온의 농도 증가에 따라 530nm에서 흡광도가 증가하는 경향을 보였다. 구리 이온의 고유 흡광 파장인 530 nm에서 합성 유도체에 의한 흡광도 세기는 구리 이온의 로그 농도에 선형으로 비례하였다. 따라서 8-Hydroxyquinoline합성유도체는 광섬유 센서의 구리 이온 감지 물질로 우수한 특성을 보임을 실험적으로 확인할 수 있었다.

• 한국염색가공학회지
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• 제24권3호
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• pp.158-164
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• 2012

Rhodamine dyes belong to xanthene family has excellent photostability and photophysical properties. In rhodamine dyes, Rhodamine 6G and its precursors also have xanthene chromophore and it shows high fluorescent quantum yield. Rhodamine 6G derivates are simple to synthesis and its high sensitivity and water solubility are suitable as good chemosensor. In this regard, Rhodamine 6G derivates which have selectivity to specific metal cation can used to detect various heavy metal ions. In this study, rhodamine 6G derivatives were synthesized by reaction of rhodamine 6G hydrazide and glyoxal and 4-phenyl thiosemicarbazide and it showed colorimetric and fluorescence sensing toward $Hg^{2+}$ ion. This novel chemosensor was analyzed and measured on UV-Vis and fluorescence spectrophotometer. HOMO/LUMO values were also calculated by computational calculation.

• 한국염색가공학회지
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• 제25권4호
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• pp.254-261
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• 2013

In this study, we synthesized a new fluorescent polypyridyl dye 2 containing a 2,2'-bipyridine in the center and two 2,2':6',2"-terpyridines at both ends. When exposed to various metal ions, the dye 2 showed selective fluorescence responses. In the presence of $Cu^{2+}$ and $Ni^{2+}$, it exhibited a highly effective fluorescence quenching, leading to large $K_{sv}$ values of up to $10^5$. In response to most other metal ions including $Al^{3+}$, in contrast, its fluorescence changes little, showing a small Ksv value at $10^2$. Meanwhile, the compound 2 revealed a differentiated fluorescence response to $Zn^{2+}$, which is evidenced by a large red shift of > 100 nm. Such a red shift from the ion binding is attributed to the planarization of the bipyridyl unit extending the effective conjugation length in conjunction. A polypyridyl compound will find important usefulness in chemosensor application due to its selective binding to metal ions. Subsequent research concerned with modified derivatives is currently going on, as a way to provide high solubility even after metal-complexing.

• 대한전기학회:학술대회논문집
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• 대한전기학회 2009년도 제40회 하계학술대회
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• pp.1551_1552
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• 2009

In this paper, we presented the packaging technologies of CMOS ISFET(Ion Sensitive Field Effect Transistor) pH sensor using post-CMOS process and MCP(Multi Chip Packaging). We have proposed and developed two types of packaging technology. one is one chip, which sensing layer is deposited on the gate metal of standard CMOS ISFET, the other is two chip type, which sensing layer is separated from CMOS ISFET and connected by bonding wire. These proposed packaging technologies would make it easy to fabricate CMOS ISFET pH sensor and to make variety types of pH sensor.

• Korean Chemical Engineering Research
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• 제49권4호
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• pp.393-399
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• 2011

지난 수십년 동안, 환경오염물질에 대한 광학적 전기화학적 검출 방법에 관한 다양한 연구가 진행되었다. 최근에는 저렴하고, 장치가 불필요한 육안 식별 가능한 환경색센서가 개발되고 있다. 시각적 정성분석은 대상물질에 대한 즉각적인 정보를 제공하여, 실시간 현장 분석이 가능하게 해준다. 또한 정량분석이 가능한 색센서에 대한 관심도 높아지고 있다. 환경색센서는 기상의 VOC, 액상의 중금속 분석용으로 주로 개발되고 있다. 이에 본 총설에서는 다양한 환경색센서의 활용분야를 살펴보고, 기존 색센서의 문제점을 파악한 다음 환경색센서 기술의 발전방향에 관하여 전망하였다.

• 한국소성가공학회:학술대회논문집
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• 한국소성가공학회 2005년도 춘계학술대회 논문집
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• pp.237-240
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• 2005

The demand of micro electrical mechanical system (MEMS) bio/chemical sensor is rapidly increasing. To prevent the contamination of sensing area, a filtration system is required in on-chip total analyzing MEMS bio/chemical sensor. A nano-filter was mainly applied in some application detecting submicron feature size bio/chemical products such as bacteria, fungi and so on. We suggested a simple nano-filter fabrication process based on replication process. The mother pattern was fabricated by holographic lithography and reactive ion etching process, and the replication process was carried out using polymer mold and UV-imprinting process. Finally the nano-filter is obtained after removing the replicated part of metal deposited replica. In this study, as a practical example of the suggested process, a nano-dot array was replicated to fabricate nano-filter fur bacteria sensor application.

• Journal of Microbiology and Biotechnology
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• 제29권10호
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• pp.1522-1542
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• 2019

To adapt to environmental changes and to maintain cellular homeostasis, microorganisms adjust the intracellular concentrations of biochemical compounds, including metal ions; these are essential for the catalytic function of many enzymes in cells, but excessive amounts of essential metals and heavy metals cause cellular damage. Metal-responsive transcriptional regulators play pivotal roles in metal uptake, pumping out, sequestration, and oxidation or reduction to a less toxic status via regulating the expression of the detoxification-related genes. The sensory and regulatory functions of the metalloregulators have made them as attractive biological parts for synthetic biology, and the exceptional sensitivity and selectivity of metalloregulators toward metal ions have been used in heavy metal biosensors to cope with prevalent heavy metal contamination. Due to their importance, substantial efforts have been made to characterize heavy metal-responsive transcriptional regulators and to develop heavy metal-sensing biosensors. In this review, we summarize the biochemical data for the two major metalloregulator families, SmtB/ArsR and MerR, to describe their metal-binding sites, specific chelating chemistry, and conformational changes. Based on our understanding of the regulatory mechanisms, previously developed metal biosensors are examined to point out their limitations, such as high background noise and a lack of well-characterized biological parts. We discuss several strategies to improve the functionality of the metal biosensors, such as reducing the background noise and amplifying the output signal. From the perspective of making heavy metal biosensors, we suggest that the characterization of novel metalloregulators and the fabrication of exquisitely designed genetic circuits will be required.

• 약학회지
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• 제47권6호
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• pp.356-360
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• 2003

Nitroso-2-naphthol-3,6-disulfonic acid, disodium salt (NRS) was used as an organic ligand to prepare basic drug-selective polymeric membrane electrode. The sensing membrane of the electrode consited of basic drug-meta1(II)-NRS as an ion-exchanger site in a poly(vinyl chloride) matrix plasticized with 2-nitrophenyl octyl ether (NPOE). The metal ions used were Fe$^{2+}$, Co$^{2+}$, Ni$^{2+}$ and Cu$^{2+}$. The electrodes exhibited fast and wide linear response in the basic drug concentration of 10$^{-5}$ ∼10$^{-3}$ mol/l with a response slope of 50∼60 mV/decade in a buffer solution of pH 4∼8. The electrodes exhibited good selectivity for many basic compounds.mpounds.