CN101360515A - 荧光纳米微粒 - Google Patents
荧光纳米微粒 Download PDFInfo
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- CN101360515A CN101360515A CNA2006800491702A CN200680049170A CN101360515A CN 101360515 A CN101360515 A CN 101360515A CN A2006800491702 A CNA2006800491702 A CN A2006800491702A CN 200680049170 A CN200680049170 A CN 200680049170A CN 101360515 A CN101360515 A CN 101360515A
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
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- C09K11/56—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials containing sulfur
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- C09K11/74—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials containing arsenic, antimony or bismuth
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- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
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Abstract
Description
设置 | 值 |
白平衡(WB) | “日光直接照射”(固定的) |
曝光表 | “点测光” |
连续拍摄 | “单映像” |
最佳拍摄选择器 | “关” |
包围曝光(Bracketing) | “包围曝光” |
闪光补偿 | “0” |
反差 | “正常” |
锐化 | “关” |
色饱和度 | “+/-0” |
ISO灵敏度 | 64 |
图像质量 | “良好” |
图像尺寸 | “2592×1944” |
压缩 | “中等” |
自动聚焦 | “单次自动聚焦” |
固定光阑 | “开” |
噪声减低 | “关” |
曝光补偿 | 变量(std.-2) |
Claims (28)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP05025022.4A EP1787659B1 (de) | 2005-11-16 | 2005-11-16 | Fluoreszenz-Nanopartikel |
EP05025022.4 | 2005-11-16 | ||
PCT/EP2006/010996 WO2007057182A2 (de) | 2005-11-16 | 2006-11-16 | Fluoreszenz-nanopartikel |
Publications (2)
Publication Number | Publication Date |
---|---|
CN101360515A true CN101360515A (zh) | 2009-02-04 |
CN101360515B CN101360515B (zh) | 2014-03-19 |
Family
ID=37752631
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN200680049170.2A Expired - Fee Related CN101360515B (zh) | 2005-11-16 | 2006-11-16 | 荧光纳米微粒 |
Country Status (9)
Country | Link |
---|---|
US (1) | US8974767B2 (zh) |
JP (2) | JP5537808B2 (zh) |
KR (1) | KR20080070746A (zh) |
CN (1) | CN101360515B (zh) |
AU (1) | AU2006314773B2 (zh) |
CA (1) | CA2628678C (zh) |
ES (1) | ES2627998T3 (zh) |
HK (1) | HK1129567A1 (zh) |
WO (1) | WO2007057182A2 (zh) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102366632A (zh) * | 2011-08-22 | 2012-03-07 | 长春工业大学 | 顺磁性金属配合物功能化的荧光金纳米簇磁共振和荧光成像造影剂 |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
MX2010009526A (es) | 2008-02-29 | 2010-11-26 | Signalomics Gmbh | Fragmentos de adhesina optimizados y nanoparticulas correspondientes. |
WO2010016803A1 (en) * | 2008-08-05 | 2010-02-11 | Agency For Science, Technology And Research | Methods, compositions, and articles comprising stabilized gold nanoclusters |
KR101032307B1 (ko) * | 2008-10-02 | 2011-05-06 | 전북대학교병원 | 생체적합성 분자광학영상용 양자점 및 이의 제조방법 |
CA2764028A1 (en) * | 2009-06-05 | 2010-12-09 | Institut National D'optique | Hybrid-multimodal magneto-optical contrast marker |
US20130099162A1 (en) * | 2010-04-30 | 2013-04-25 | Ocean's King Lighting Science & Technology Co.,Ltd | Borate based red light emitting material and preparation method thereof |
WO2013123390A1 (en) * | 2012-02-16 | 2013-08-22 | Qd Vision, Inc. | Method for preparing semiconductor nanocrystals |
DE102013206077A1 (de) * | 2013-04-05 | 2014-10-09 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Blau-emittierende Leuchtdioden auf Basis von Zinkselenid-Quantenpunkten |
PT2886126T (pt) | 2013-12-23 | 2017-09-13 | Exchange Imaging Tech Gmbh | Nanopartícula conjugada a péptidos de ligação a cd44 |
EP3028721A1 (en) * | 2014-12-05 | 2016-06-08 | Exchange Imaging Technologies GmbH | Nanoparticle formulation having reverse-thermal gelation properties for injection |
JP6683571B2 (ja) * | 2016-08-10 | 2020-04-22 | トヨタ自動車株式会社 | 排ガス浄化触媒 |
JP2019535805A (ja) * | 2016-10-04 | 2019-12-12 | ナノコ テクノロジーズ リミテッド | 重合可能量子ドットナノ粒子、並びにそれを用いた治療薬、除去剤及び刺青剤 |
JP2018115315A (ja) * | 2017-01-18 | 2018-07-26 | 三菱マテリアル株式会社 | 可視蛍光を発するCdを含まないコロイダル量子ドット及びその製造方法 |
WO2018135434A1 (ja) * | 2017-01-18 | 2018-07-26 | 三菱マテリアル株式会社 | 可視蛍光を発するCdを含まないコロイダル量子ドット及びその製造方法 |
Family Cites Families (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0979107A1 (en) * | 1997-04-29 | 2000-02-16 | Nycomed Imaging As | Light imaging contrast agents |
US6207392B1 (en) * | 1997-11-25 | 2001-03-27 | The Regents Of The University Of California | Semiconductor nanocrystal probes for biological applications and process for making and using such probes |
US6306610B1 (en) * | 1998-09-18 | 2001-10-23 | Massachusetts Institute Of Technology | Biological applications of quantum dots |
US6179912B1 (en) * | 1999-12-20 | 2001-01-30 | Biocrystal Ltd. | Continuous flow process for production of semiconductor nanocrystals |
US6748259B1 (en) * | 2000-06-15 | 2004-06-08 | Spectros Corporation | Optical imaging of induced signals in vivo under ambient light conditions |
US20050059031A1 (en) | 2000-10-06 | 2005-03-17 | Quantum Dot Corporation | Method for enhancing transport of semiconductor nanocrystals across biological membranes |
US20020127224A1 (en) * | 2001-03-02 | 2002-09-12 | James Chen | Use of photoluminescent nanoparticles for photodynamic therapy |
IL157576A0 (en) * | 2001-03-08 | 2004-03-28 | Nanosolutions Gmbh | Paramagnetic nanoparticle |
WO2003054507A2 (en) | 2001-09-17 | 2003-07-03 | Biocrystal, Ltd. | Nanocrystals |
US7205048B2 (en) * | 2001-09-17 | 2007-04-17 | Invitrogen Corporation | Functionalized fluorescent nanocrystal compositions and methods of making |
CN100356984C (zh) | 2002-01-24 | 2007-12-26 | 巴内斯-朱威胥医院 | 整联蛋白靶向的影像剂 |
CN1672052A (zh) | 2002-06-27 | 2005-09-21 | 佐治亚技术研究公司 | 纳米级光学荧光标记及其用途 |
US7939170B2 (en) * | 2002-08-15 | 2011-05-10 | The Rockefeller University | Water soluble metal and semiconductor nanoparticle complexes |
US20040101822A1 (en) * | 2002-11-26 | 2004-05-27 | Ulrich Wiesner | Fluorescent silica-based nanoparticles |
EP2530719B1 (en) * | 2003-05-07 | 2020-08-05 | Indiana University Research and Technology Corporation | Alloyed semiconductor concentration-gradient quantum dots, use and method of fabricating thereof |
US7790473B2 (en) | 2003-11-05 | 2010-09-07 | The United States Of America As Represented By The Department Of Health And Human Services | Biofunctionalized quantum dots for biological imaging |
JP2005226021A (ja) * | 2004-02-16 | 2005-08-25 | Nihon Medi Physics Co Ltd | マンノース受容体親和性化合物 |
-
2005
- 2005-11-16 ES ES05025022.4T patent/ES2627998T3/es active Active
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2006
- 2006-11-16 CN CN200680049170.2A patent/CN101360515B/zh not_active Expired - Fee Related
- 2006-11-16 AU AU2006314773A patent/AU2006314773B2/en not_active Ceased
- 2006-11-16 WO PCT/EP2006/010996 patent/WO2007057182A2/de active Application Filing
- 2006-11-16 US US12/093,977 patent/US8974767B2/en not_active Expired - Fee Related
- 2006-11-16 CA CA2628678A patent/CA2628678C/en not_active Expired - Fee Related
- 2006-11-16 JP JP2008540516A patent/JP5537808B2/ja not_active Expired - Fee Related
- 2006-11-16 KR KR1020087014538A patent/KR20080070746A/ko active Search and Examination
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102366632A (zh) * | 2011-08-22 | 2012-03-07 | 长春工业大学 | 顺磁性金属配合物功能化的荧光金纳米簇磁共振和荧光成像造影剂 |
Also Published As
Publication number | Publication date |
---|---|
US20090226371A1 (en) | 2009-09-10 |
CA2628678C (en) | 2016-01-05 |
JP2013079962A (ja) | 2013-05-02 |
WO2007057182A3 (de) | 2008-02-28 |
JP5537808B2 (ja) | 2014-07-02 |
JP2009516182A (ja) | 2009-04-16 |
WO2007057182B1 (de) | 2008-04-17 |
CA2628678A1 (en) | 2007-05-24 |
ES2627998T3 (es) | 2017-08-01 |
US8974767B2 (en) | 2015-03-10 |
CN101360515B (zh) | 2014-03-19 |
HK1129567A1 (zh) | 2009-12-04 |
WO2007057182A2 (de) | 2007-05-24 |
AU2006314773A1 (en) | 2007-05-24 |
KR20080070746A (ko) | 2008-07-30 |
AU2006314773B2 (en) | 2013-04-11 |
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