KR20070116614A - 미생물 검출 기법 - Google Patents
미생물 검출 기법 Download PDFInfo
- Publication number
- KR20070116614A KR20070116614A KR1020077022159A KR20077022159A KR20070116614A KR 20070116614 A KR20070116614 A KR 20070116614A KR 1020077022159 A KR1020077022159 A KR 1020077022159A KR 20077022159 A KR20077022159 A KR 20077022159A KR 20070116614 A KR20070116614 A KR 20070116614A
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- KR
- South Korea
- Prior art keywords
- indicator
- volatile compounds
- microorganism
- identified
- substrate
- Prior art date
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Classifications
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/02—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving viable microorganisms
- C12Q1/04—Determining presence or kind of microorganism; Use of selective media for testing antibiotics or bacteriocides; Compositions containing a chemical indicator therefor
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/52—Use of compounds or compositions for colorimetric, spectrophotometric or fluorometric investigation, e.g. use of reagent paper and including single- and multilayer analytical elements
- G01N33/521—Single-layer analytical elements
- G01N33/523—Single-layer analytical elements the element being adapted for a specific analyte
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- General Physics & Mathematics (AREA)
- Pathology (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Investigating Or Analysing Materials By The Use Of Chemical Reactions (AREA)
- Other Investigation Or Analysis Of Materials By Electrical Means (AREA)
- Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)
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Families Citing this family (63)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7713266B2 (en) | 2005-05-20 | 2010-05-11 | Myoscience, Inc. | Subdermal cryogenic remodeling of muscles, nerves, connective tissue, and/or adipose tissue (fat) |
| US7850683B2 (en) | 2005-05-20 | 2010-12-14 | Myoscience, Inc. | Subdermal cryogenic remodeling of muscles, nerves, connective tissue, and/or adipose tissue (fat) |
| US20080057534A1 (en) * | 2006-08-31 | 2008-03-06 | Kimberly-Clark Worldwide, Inc. | Microbe-sensitive indicators and use of the same |
| US20080060550A1 (en) * | 2006-09-12 | 2008-03-13 | Macdonald Gavin | Color changing skin sealant with co-acid trigger |
| US20080063615A1 (en) * | 2006-09-12 | 2008-03-13 | Macdonald John Gavin | Color changing skin sealant |
| US20080145316A1 (en) * | 2006-12-14 | 2008-06-19 | Macdonald John Gavin | Skin coating with microbial indicator |
| US9254162B2 (en) | 2006-12-21 | 2016-02-09 | Myoscience, Inc. | Dermal and transdermal cryogenic microprobe systems |
| US8409185B2 (en) | 2007-02-16 | 2013-04-02 | Myoscience, Inc. | Replaceable and/or easily removable needle systems for dermal and transdermal cryogenic remodeling |
| US20090230300A1 (en) * | 2007-10-19 | 2009-09-17 | Jose Miguel Trevejo | Rapid detection of volatile organic compounds for identification of bacteria in a sample |
| US20090123569A1 (en) * | 2007-11-08 | 2009-05-14 | Macdonald John Gavin | Coverage indicating technology for skin sealants using tannates |
| WO2009065061A1 (en) | 2007-11-14 | 2009-05-22 | Myoscience, Inc. | Pain management using cryogenic remodeling |
| US8247220B2 (en) * | 2008-02-01 | 2012-08-21 | Kimberly-Clark Worldwide, Inc. | Optical indicator for detecting bacterial pathogens |
| ES2538497T3 (es) * | 2008-10-31 | 2015-06-22 | Biomerieux, Inc | Métodos para la identificación de microorganismos usando espectrometría de masas |
| AU2009330012A1 (en) | 2008-12-22 | 2011-07-21 | Myoscience, Inc. | Integrated cryosurgical system with refrigerant and electrical power source |
| WO2010126856A1 (en) * | 2009-04-27 | 2010-11-04 | The Charles Stark Draper Laboratory, Inc. | Rapid detection of volatile organic compounds for identification of mycobacterium tuberculosis in a sample |
| FR2952436B1 (fr) | 2009-11-10 | 2014-10-31 | Commissariat Energie Atomique | Materiau et procede pour pieger, detecter et quantifier des composes aromatiques heterocycliques et autres. |
| USD656852S1 (en) | 2010-08-06 | 2012-04-03 | Kimberly-Clark Worldwide, Inc. | Wetness indicator |
| US9018434B2 (en) | 2010-08-06 | 2015-04-28 | Kimberly-Clark Worldwide, Inc. | Absorbent articles with intricate graphics |
| US9522396B2 (en) | 2010-12-29 | 2016-12-20 | S.D. Sight Diagnostics Ltd. | Apparatus and method for automatic detection of pathogens |
| FR2976952A1 (fr) * | 2011-06-27 | 2012-12-28 | Commissariat Energie Atomique | Procede pour caracteriser la presence ou l'absence d'un microorganisme dans un milieu biologique |
| US8933292B2 (en) | 2011-10-28 | 2015-01-13 | Kimberly-Clark Worldwide, Inc. | Absorbent article with sensor array for body exudate detection |
| US8816149B2 (en) | 2011-10-28 | 2014-08-26 | Kimberly-Clark Worldwide, Inc. | System for detection and monitoring of body exudates using a gas emitting substance for use in interactive toilet training |
| US9119748B2 (en) | 2011-10-28 | 2015-09-01 | Kimberly-Clark Worldwide, Inc. | Electronic discriminating device for body exudate detection |
| CA2866148C (en) * | 2011-11-14 | 2021-05-18 | Smiths Detection Inc. | Solid phase micro-extraction (spme) devices |
| EP2798350B1 (en) | 2011-12-29 | 2021-07-28 | Sight Diagnostics Ltd. | Methods and systems for detecting a pathogen in a biological sample |
| WO2013106859A1 (en) | 2012-01-13 | 2013-07-18 | Myoscience, Inc. | Cryogenic needle with freeze zone regulation |
| CA2860893A1 (en) | 2012-01-13 | 2013-07-18 | Myoscience, Inc. | Skin protection for subdermal cryogenic remodeling for cosmetic and other treatments |
| CA2861116A1 (en) | 2012-01-13 | 2013-07-18 | Myoscience, Inc. | Cryogenic probe filtration system |
| US9017318B2 (en) | 2012-01-20 | 2015-04-28 | Myoscience, Inc. | Cryogenic probe system and method |
| CN102911997B (zh) * | 2012-11-06 | 2015-08-12 | 沈阳建筑大学 | 生物除磷微生物检测用培养基及检测生物除磷微生物除磷能力的方法 |
| US9610112B2 (en) | 2013-03-15 | 2017-04-04 | Myoscience, Inc. | Cryogenic enhancement of joint function, alleviation of joint stiffness and/or alleviation of pain associated with osteoarthritis |
| US9295512B2 (en) | 2013-03-15 | 2016-03-29 | Myoscience, Inc. | Methods and devices for pain management |
| WO2014146126A1 (en) | 2013-03-15 | 2014-09-18 | Myoscience, Inc. | Cryogenic blunt dissection methods and devices |
| WO2014146122A1 (en) | 2013-03-15 | 2014-09-18 | Myoscience, Inc. | Methods and systems for treatment of occipital neuralgia |
| EP2999988A4 (en) | 2013-05-23 | 2017-01-11 | S.D. Sight Diagnostics Ltd. | Method and system for imaging a cell sample |
| IL227276A0 (en) * | 2013-07-01 | 2014-03-06 | Parasight Ltd | A method and system for preparing a monolayer of cells, particularly suitable for diagnosis |
| EP3039477B1 (en) | 2013-08-26 | 2021-10-20 | S.D. Sight Diagnostics Ltd. | Digital microscopy systems, methods and computer program products |
| EP3065658B1 (en) | 2013-11-05 | 2021-03-31 | Pacira CryoTech, Inc. | Secure cryosurgical treatment system |
| CN103823063B (zh) * | 2014-02-25 | 2015-09-30 | 上海理工大学 | 检测猪霍乱沙门氏菌的方法及其单抗 |
| KR101692969B1 (ko) * | 2014-07-15 | 2017-01-16 | 을지생명과학 주식회사 | 활성산소 진단용 조성물 및 그 분석 방법 |
| CN107077732B (zh) | 2014-08-27 | 2020-11-24 | 思迪赛特诊断有限公司 | 用于对数字显微镜计算聚焦变化的系统及方法 |
| EP3859425B1 (en) | 2015-09-17 | 2024-04-17 | S.D. Sight Diagnostics Ltd. | Methods and apparatus for detecting an entity in a bodily sample |
| TWI621744B (zh) * | 2015-10-20 | 2018-04-21 | 聚泰環保材料科技股份有限公司 | 製備石墨烯摻混天然纖維素紡黏不織布的方法 |
| TWI588089B (zh) * | 2015-10-20 | 2017-06-21 | Acelon Chem & Fiber Corp | 製備石墨烯摻混天然纖維素熔噴不織布的方法 |
| ITUB20155975A1 (it) * | 2015-11-27 | 2017-05-27 | Alifax Srl | Procedimento per la rilevazione di attivita' batterica in un campione biologico e relativa unita' di rilevazione |
| WO2017168411A1 (en) | 2016-03-30 | 2017-10-05 | S.D. Sight Diagnostics Ltd | Image processing device for identifying blood parasites |
| EP4177593A1 (en) | 2016-05-11 | 2023-05-10 | S.D. Sight Diagnostics Ltd. | Sample carrier for optical measurements |
| CN115266540B (zh) | 2016-05-11 | 2025-11-28 | 思迪赛特诊断有限公司 | 对样品实施的光学测量 |
| EP4349396A3 (en) | 2016-05-13 | 2024-05-01 | Pacira CryoTech, Inc. | Systems for locating and treating with cold therapy |
| CA3033762A1 (en) * | 2016-08-19 | 2018-02-22 | Becton, Dickinson And Company | Adapter assembly for attachment to a bottle |
| CN106381461B (zh) * | 2016-09-12 | 2018-11-02 | 西北师范大学 | 花瓣褶皱状纳米氧化铁涂层的制备方法 |
| CN106282903B (zh) * | 2016-09-12 | 2018-11-30 | 西北师范大学 | 火焰法制备块状纳米氧化铁涂层的工艺 |
| JP7214729B2 (ja) | 2017-11-14 | 2023-01-30 | エス．ディー．サイト ダイアグノスティクス リミテッド | 光学測定用試料収容器 |
| EP4541302A3 (en) | 2017-11-15 | 2025-07-16 | Pacira CryoTech, Inc. | Integrated cold therapy and electrical stimulation systems for locating and treating nerves |
| US20210130764A1 (en) * | 2018-06-12 | 2021-05-06 | The Trustees Of Dartmouth College | Method and apparatus of qr-coded, paper-based, colorimetric detection of volatile byproduct for rapid bacteria identification |
| WO2020097043A1 (en) * | 2018-11-08 | 2020-05-14 | The University Of Massachusetts | Method and system for chromogenic array-based food testing |
| US11460410B2 (en) * | 2019-04-08 | 2022-10-04 | Puma SE | Bioindicator component applied to an article |
| CN110412168A (zh) * | 2019-08-12 | 2019-11-05 | 西南民族大学 | 基于代谢标记物检测食品中金黄色葡萄球菌活菌的方法 |
| CN110331184B (zh) * | 2019-08-12 | 2023-10-24 | 西南民族大学 | 3-甲基-丁酸作为葡萄球菌的代谢标记物在非疾病诊断和治疗中的应用 |
| US12498325B2 (en) | 2019-10-22 | 2025-12-16 | S.D. Sight Diagnostics Ltd. | Accounting for errors in optical measurements |
| JP7677972B2 (ja) | 2019-12-12 | 2025-05-15 | エス．ディー．サイト ダイアグノスティックス リミテッド | カラー血液スミア画像の人工的な生成 |
| WO2021116959A1 (en) | 2019-12-12 | 2021-06-17 | S.D. Sight Diagnostics Ltd | Analyzing an analyte disposed within a medium |
| CN116536223B (zh) * | 2023-07-03 | 2023-10-03 | 中国食品发酵工业研究院有限公司 | 一种梭菌菌种及其应用 |
Family Cites Families (52)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4100324A (en) * | 1974-03-26 | 1978-07-11 | Kimberly-Clark Corporation | Nonwoven fabric and method of producing same |
| US4073691A (en) * | 1976-08-24 | 1978-02-14 | Johnston Laboratories, Inc. | Method for detecting the presence of biologically active agents |
| JPS5392195A (en) * | 1977-01-25 | 1978-08-12 | Dojindo Lab | Simple rapid determination method and apparatus for volatile matter in aqueous solution |
| CH648052A5 (de) * | 1980-02-14 | 1985-02-28 | Ciba Geigy Ag | Verfahren zur herstellung von triarylmethanverbindungen. |
| US4477635A (en) * | 1982-01-04 | 1984-10-16 | Minnesota Mining And Manufacturing Company | Polymeric triarylmethane dyes |
| US4703017C1 (en) * | 1984-02-14 | 2001-12-04 | Becton Dickinson Co | Solid phase assay with visual readout |
| JPH0611870B2 (ja) * | 1986-06-27 | 1994-02-16 | 徳山曹達株式会社 | 無機化合物／染料複合体粒子 |
| US5036000A (en) * | 1986-12-16 | 1991-07-30 | Enzymatics, Inc. | Threshold color control system |
| US4816414A (en) * | 1987-10-02 | 1989-03-28 | Crystal Diagnostics, Inc. | Methods and apparatus for detecting an analyte of interest capable of being converted into a carbonyl-containing composition |
| US4839331A (en) * | 1988-01-29 | 1989-06-13 | Rohm And Haas Company | Carbonaceous adsorbents from pyrolyzed polysulfonated polymers |
| JP2763635B2 (ja) * | 1988-02-08 | 1998-06-11 | ユニバーシティ カレッジ カーディフ コンサルタンツ リミティド | 生体液中のジアミンの検出 |
| US5094955A (en) * | 1988-03-15 | 1992-03-10 | Akzo N.V. | Device and method for detecting microorganisms |
| TW225511B (enExample) * | 1989-12-14 | 1994-06-21 | Nissan Chemical Ind Ltd | |
| US5196177A (en) * | 1990-01-17 | 1993-03-23 | Nissan Chemical Industries, Ltd. | Production of stable aqueous silica sol |
| US5691206A (en) * | 1990-04-02 | 1997-11-25 | Pawliszyn; Janusz B. | Method and device for solid phase microextraction and desorption |
| US5100581A (en) * | 1990-02-22 | 1992-03-31 | Nissan Chemical Industries Ltd. | Method of preparing high-purity aqueous silica sol |
| US6537827B1 (en) * | 1990-04-02 | 2003-03-25 | Janusz B. Pawliszyn | Method and device for solid phase microextraction and desorption |
| CA2027536C (en) * | 1990-05-14 | 1993-02-16 | George Chang | Method for determination of e.coli in water |
| CA2048905C (en) * | 1990-12-21 | 1998-08-11 | Cherie H. Everhart | High pulp content nonwoven composite fabric |
| IL97318A0 (en) * | 1991-02-20 | 1992-05-25 | Diagnostic Markers Inc | Method for the very rapid detection of polyamines |
| US5407600A (en) * | 1991-07-23 | 1995-04-18 | Nissan Chemical Industries, Ltd. | Stable aqueous alumina sol and method for preparing the same |
| US5332548A (en) * | 1991-12-30 | 1994-07-26 | Moore Robert E | Analytical device and method of using same |
| TW284848B (enExample) * | 1992-06-05 | 1996-09-01 | Supelco Inc | |
| US5468469A (en) * | 1992-08-11 | 1995-11-21 | The United States Of America As Represented By The Department Of Health And Human Services | Methods of using azo dyes and their derivatives |
| US5350624A (en) * | 1992-10-05 | 1994-09-27 | Kimberly-Clark Corporation | Abrasion resistant fibrous nonwoven composite structure |
| JPH07155792A (ja) * | 1993-12-06 | 1995-06-20 | Canon Inc | 誘導物質を用いた微生物による有機塩素化合物の分解方法、及び係る方法に用いる装置 |
| US5464739A (en) * | 1994-08-22 | 1995-11-07 | Bayer Corporation | Composition method for determining the presence of leukocyte cells, esterase or protease in a test sample |
| US6117090A (en) * | 1994-08-25 | 2000-09-12 | Caillouette; James C. | Method and apparatus for detecting amine producing organisms in the vagina |
| US5753285A (en) * | 1995-02-16 | 1998-05-19 | Horan; Thomas J. | Method for determining bacteria contamination in food package |
| DE69609967T2 (de) * | 1995-06-05 | 2001-04-12 | Kimberly-Clark Worldwide, Inc. | Farbstoffvorläufer und diese enthaltende zusammensetzungen |
| US5853859A (en) * | 1995-07-07 | 1998-12-29 | Kimberly-Clark Worldwide, Inc. | Room temperature latex printing |
| WO1997008337A1 (en) * | 1995-08-25 | 1997-03-06 | Unipath Limited | Methods and apparatus for detecting microorganisms |
| US5985229A (en) * | 1995-09-21 | 1999-11-16 | Toagosei Co., Ltd. | Solid silica derivative and process for producing the same |
| US6787366B1 (en) * | 1996-12-11 | 2004-09-07 | The United States Of America As Represented By The Secretary Of The Army | Microspot test kit and method for chemical testing |
| US5846292A (en) * | 1997-05-06 | 1998-12-08 | Board Of Supervisors At Louisiana State University & Agricultural & Mechanical College | Chromatograph with column extraction |
| US6849847B1 (en) * | 1998-06-12 | 2005-02-01 | Agilent Technologies, Inc. | Ambient pressure matrix-assisted laser desorption ionization (MALDI) apparatus and method of analysis |
| US6759126B1 (en) * | 1998-09-21 | 2004-07-06 | University Of South Florida | Solid phase microextraction fiber structure and method of making |
| US6589761B1 (en) * | 1999-06-19 | 2003-07-08 | Marv Freadman | Method and apparatus for detecting bacteria |
| EP1274983B1 (en) * | 2000-03-21 | 2012-02-01 | The Board Of Trustees Of The University Of Illinois | Colorimetric artificial nose having an array of dyes and method for artificial olfaction |
| EP1332357B1 (en) * | 2000-10-14 | 2006-05-24 | Alex M. Saunders | Ligand based solution assay for low concentration analytes |
| JP4520621B2 (ja) * | 2000-11-01 | 2010-08-11 | 信和化工株式会社 | クロマトグラフィー用分離カラム、固相抽出用媒体、及びクロマトグラフィーの試料注入システム |
| US6428748B1 (en) * | 2001-01-31 | 2002-08-06 | Grouptek, Inc. | Apparatus and method of monitoring an analyte |
| JP2002236124A (ja) * | 2001-02-07 | 2002-08-23 | Takasago Internatl Corp | 口臭の判定方法 |
| US6691053B2 (en) * | 2001-11-30 | 2004-02-10 | Agilent Technologies, Inc. | Method of matching retention times among multiple chromatographic system |
| US6646256B2 (en) * | 2001-12-18 | 2003-11-11 | Agilent Technologies, Inc. | Atmospheric pressure photoionization source in mass spectrometry |
| US6989246B2 (en) * | 2002-01-10 | 2006-01-24 | Becton, Dickinson And Company | Sensor formulation for simultaneously monitoring at least two components of a gas composition |
| US6607580B1 (en) * | 2002-03-04 | 2003-08-19 | Agilent Technologies, Inc. | Separation column for a gas chromatograph |
| US20040265440A1 (en) * | 2002-09-16 | 2004-12-30 | Agcert International, Llc | Food borne pathogen sensor and method |
| JP4402597B2 (ja) * | 2002-12-19 | 2010-01-20 | スリーエム イノベイティブ プロパティズ カンパニー | ジアセチレン物質から構築される比色分析センサー |
| US7666410B2 (en) * | 2002-12-20 | 2010-02-23 | Kimberly-Clark Worldwide, Inc. | Delivery system for functional compounds |
| US7282349B2 (en) * | 2003-12-16 | 2007-10-16 | Kimberly-Clark Worldwide, Inc. | Solvatochromatic bacterial detection |
| US20050191704A1 (en) * | 2004-03-01 | 2005-09-01 | Kimberly-Clark Worldwide, Inc. | Assay devices utilizing chemichromic dyes |
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| WO2006107370A1 (en) | 2006-10-12 |
| DE602006010835D1 (enExample) | 2010-01-14 |
| EP1864128B1 (en) | 2009-12-02 |
| EP1864128A1 (en) | 2007-12-12 |
| JP2008538179A (ja) | 2008-10-16 |
| US20060223052A1 (en) | 2006-10-05 |
| MX2007011964A (es) | 2007-12-07 |
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