子分类：
| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 121 | Test system | JP2010537916 | 2008-05-29 | JP5329562B2 | 2013-10-30 | バウアー，ジェイコブ・エス; ブラウン，ダーレン; チェン，ジュン; ケイツ，リチャード; レビン，ジェニファー・エム; リーバー，ハリス; シュワルツ，エミー・エル; ヤオ，レイモンド |
| A portable data-management system may be easily employed with multiple processing devices by eliminating the need to pre-install additional programs, agents, device drivers, or other software components on the hosts. A portable storage device contains software for a data-management application, which receives and processes test data from a meter that measures an analyte. The portable device may employ an interface protocol that makes the portable device immediately compatible with different operating systems and hardware configurations. Once the portable device is connected to the host, the data-management application can be automatically launched. The convenience and portability of a data-management system may be enhanced by integrating advanced data processing and display features with the portable device. The users may access some advanced presentations of health data without having to launch the data-management application on a separate host. | ||||||
| 122 | Seal of the reaction cuvette for bio affinity assay | JP2013511714 | 2011-05-24 | JP2013526721A | 2013-06-24 | コスキネン、ジャンヌ; ルオナモ、リスト−マッチ; ソイニ、アレクシ |
| 本発明は、少なくとも１つの反応チャンバ（６）を備えたバイオアッセイカートリッジ（４）用の穿孔可能な密封カバー（２）に関する。 本発明の特徴は、カバー（２）が少なくとも最上層（８）と、中間層（１０）と、最下層（１２）と、穿孔用の箇所（１４）とを備え、穿孔用の箇所（１６）において、カバー（２）が最上層（１４）と最下層（１２）との間に空洞スペース（１８）を有することである。 本発明はまた、バイオアッセイカートリッジ（４）と、カートリッジ（４）用のカバー（２）とを備えたシステム（２０）に関する。 本発明はさらに、カートリッジ（４）を覆うためのカバー（２）の使用に関する。 | ||||||
| 123 | Novel products | JP2012287581 | 2012-12-28 | JP2013099745A | 2013-05-23 | COULSON STEPHEN |
| PROBLEM TO BE SOLVED: To provide a laboratory consumable having a nano coating of super non-adhesiveness.SOLUTION: A laboratory consumable having a polymeric coating, formed by exposing the consumable to pulsed plasma comprising a compound of formula (I) where R, Rand Rare independently selected from hydrogen, alkyl, haloalkyl or aryl optionally substituted by halo; and Ris a group X-Rwhere Ris an alkyl or haloalkyl group and X is a bond; a group of formula -C(O)O(CH)Y- where n is an integer of from 1 to 10 and Y is a bond or a sulphonamide group; or a group -(O)R(O)(CH)- where Ris aryl optionally substituted by halo, p is 0 or 1, q is 0 or 1 and t is 0 or an integer of from 1 to 10, provided that where q is 1, t is other than 0, for a sufficient period of time to allow a polymeric layer to form on the surface of the laboratory consumable. | ||||||
| 124 | Pressure type apparatus for producing vesicle having uniform diameter | JP2009249506 | 2009-10-29 | JP2011092860A | 2011-05-12 | TAKEUCHI SHOJI; KURAKAZU TOMOAKI |
| <P>PROBLEM TO BE SOLVED: To develop a technique for producing a bilayer membrane vesicle having almost the same size as that of a bio-cell more easily by using a pressure generator inexpensive than that of the conventional technique-based apparatus for producing the vesicle. <P>SOLUTION: An apparatus for producing the bilayer membrane vesicle includes a plurality of structures each of which includes a main flow path, a plurality of micro-diverticula opened to the main flow path, and a loculus adjacent to each of the plurality of micro-diverticula while interposing a deformable partition wall between them. A method for producing the bilayer membrane vesicle comprises a step of exerting pressure on the loculus, in such a state that a phase-separating fluid layer is suspended from the side wall surface of the micro-diverticulum, to deform and project the deformable partition wall into the micro-diverticulum and wash away a first aqueous solution and expanding the phase-separating fluid layer so that the tip of the phase-separating fluid layer enters the main flow path from an opening of the micro-diverticulum. <P>COPYRIGHT: (C)2011,JPO&INPIT | ||||||
| 125 | Self-contained device for the detection of biological contaminants | JP2001587908 | 2001-06-04 | JP4477809B2 | 2010-06-09 | ティム エイ． ケリー，; ジョージ エム． ハス，; フィリップ ティー． フェルドサイン， |
| 126 | Automatic analysis dexterity reaction vessel | JP2009545978 | 2008-01-23 | JP2010517005A | 2010-05-20 | ジャン−フランソワ・ジェラン |
| 反応容器は、自動分析器での使用を意図しており、その頂部における開口部（１４）と、上記開口部を部分的に閉塞する１つまたは２つのフラップ（１８）と、を有し、フラップは、液体注入またはサンプル抽出の針を通過可能としかつ容器内に収容されている攪拌手段が脱出することを防止するスロット（２２）によって離間している。 | ||||||
| 127 | Biochip substratum and method for production thereof | JP2008171322 | 2008-06-30 | JP2010008378A | 2010-01-14 | NOKIHARA SEISHI; HIRATA AKIYOSHI; OKA YASUO; TAKEBAYASHI YASUSHI |
| <P>PROBLEM TO BE SOLVED: To provide a substrate for biochips having a high probe immobilization ratio, a uniform immobilization density, high detection sensitivity by preventing the nonspecific adsorption of proteins, and high reproducibility, when used as a substrate for biochips for immobilizing a probe comprising bio-related substances, such as, proteins and nucleic acids. <P>SOLUTION: The substrate for biochips can uniformly, at a high density, and stably bond an amino group onto a substrate surface, by immobilizing an amino-group-containing polymer to the surface of the substrate through a covalent bond; have high probe immobilization ratio and a uniform immobilization density by immobilizing the probe comprising bio-related substances; such as, proteins and nucleic acids though the use of the amino group, and have high detection sensitivity and high reproducibility by preventing nonspecific adsorption of proteins. <P>COPYRIGHT: (C)2010,JPO&INPIT | ||||||
| 128 | Tapered cuvette and method for collecting magnetic particles | JP2007527655 | 2005-06-07 | JP2008501980A | 2008-01-24 | ゲイリー シュレーダー，; マーク タルマー，; キャスリン リマリック， |
| A vessel for use in clinical analysis including an open top, a closed bottom, and at least four tapered sides. A vessel cartridge for loading vessels in an automated clinical diagnostic device, comprising:a plurality of vessels for optical analysis, each vessel comprising, a) a vertical axis, b) an open top substantially perpendicular to said vertical axis, c) a closed bottom, and d) four sides comprising a pair of opposite sides for the optical analysis and another pair of opposite sides for magnetic particle engagement, each of the four sides extending from the vessel open top to the vessel closed bottom, and each side of the pair of opposite sides for the optical analysis or each side of the pair of opposite sides for the magnetic particle engagement comprise a projection comprising a planar surface substantially parallel to the vertical axis of the vessel positioned on the exterior surface of the vessel adjacent said vessel open top and extending toward said vessel closed bottom, each said projection comprising a length such that when the vessel is stacked with a like vessel to from said vessel cartridge, the exterior surface of a first vessel of the plurality of vessels and the interior surface of a second vessel of the plurality of vessels define a gap. | ||||||
| 129 | Container for immunological analysis | JP2000591430 | 1999-10-28 | JP3681983B2 | 2005-08-10 | 速雄 田中 |
| 130 | Disposable apparatus for performing the blood cell count | JP2000534334 | 1999-03-02 | JP3593315B2 | 2004-11-24 | ウォードロウ、スチーブン、シー |
| 131 | Self-contained device for the detection of biological contaminants | JP2001587908 | 2001-06-04 | JP2003535318A | 2003-11-25 | ティム エイ． ケリー，; ジョージ エム． ハス，; フィリップ ティー． フェルドサイン， |
| (57)【要約】 本発明は、種々の設備において生物学的汚染を検出するための新規な方法および独立式デバイスを提供する。 １つの局面において、標的物質を収集するためのサンプラーおよびこの標的物質の存在を伝達するためにこの標的物質に結合し、この標的物質の存在を合図する色素を含むシグナル発生器を有する独立式サンプリング／試験デバイスが提供される。 このデバイスはまた、洗浄溶液を有するサンプラー洗浄器を含む。 他の実施形態において、このデバイスは吸収体材料を有し、ここで、このサンプラーは、多孔性サンプル収集パッドを有し、そして吸収体材料、サンプラーおよびサンプラー洗浄器は、このサンプル収集パッドが吸収体材料とサンプラー洗浄器との間に配置されるように構成および配置され、その結果、この洗浄溶液が、このサンプル収集パッド上に固定された標的物質の結合した色素と未結合の色素とを分離する。 | ||||||
| 132 | Processing method and apparatus of the substance in a single container | JP2001568587 | 2001-03-21 | JP2003527953A | 2003-09-24 | デワルチ、ビンツ |
| In one example embodiment of the present invention, a vessel having an open end and a closed end is provided. The vessel further comprises a filtering means. The filtering means is disposed generally toward the closed end of the vessel. Subsequently the closed end of the tube or vessel can be pierced so that the liquid and waste products can be removed from the vessel through the pierced aperture. In another example embodiment, a method for processing at least one substance in a vessel capable of retaining at least one substance is provided. The method comprises introducing the at least one substance into the vessel. The method further comprises processing the at least one substance. The method further comprises creating an aperture in the vessel; and removing at least one substance through the aperture. | ||||||
| 133 | Disposable apparatus for performing the blood cell count | JP2000534334 | 1999-03-02 | JP2003526081A | 2003-09-02 | ウォードロウ、スチーブン、シー |
| (57)【要約】 チャンバー（１２）とラベル（１４）とを含む、分析のために生体液体試料を保持する容器を提供する。 チャンバーには、第一の壁（２６）、透明な第二の壁（２８）、およびチャンバー内に空間的に位置する特徴を含む複数の特徴が含まれる。 透明な第二の壁によって、チャンバー内に静かに存在する液体試料を第二の壁を通じて造影することができる。 チャンバー内に空間的に存在する特徴を含む複数の特徴は、生体液体の分析を可能にするために操作可能である。 ラベルは特徴に関する情報、およびチャンバー内の特徴の空間的位置を直接または間接的に含む。 試料はラベルによって伝達される情報を利用する分析装置によって分析される。 | ||||||
| 134 | Liquid sample test system | JP2000556252 | 1999-06-23 | JP2002519642A | 2002-07-02 | チェン，シューキ |
| (57)【要約】 試料試験システムは、液体試料材料を含むチャンバーを支持し、チャンバーの複数部分を複数の区画にシールするチャンバー・シール装置を有する。 試薬注入カートリッジ・アクチュエータは、試薬タンクに液体を連絡する少なくとも一つのニードルを有する試薬注入カートリッジを支持し、試薬注入カートリッジを動かし、ある量の試薬をチャンバーの区画の一つに注入する。 より好ましくは、流量制御装置で、区画内に試料の流れを生じさせる。 センサーは、混合状態に応じた信号を生成する。 | ||||||
| 135 | Incubation station for test sample card | JP19721298 | 1998-07-13 | JPH1189560A | 1999-04-06 | GUREGORII AARU MEEZU; DENISU EMU KONAA; BURENTO DEII FURAINAA; KURIFUOODO DABURIYUU KAARU; RON ROBINSUN; REIMONDO EMU SHIERUTON; GEIRII AARU TEGURAA; MAIKURU JIEIMUZU JIYASUTEIN |
| PROBLEM TO BE SOLVED: To provide an incubation station completely automatized for an analytical instrument of test sample cards and not requiring the hand mount of the cards. SOLUTION: This incubation station 600 for plural test sample cards 28 is provided by being equipped with a ring state carrousel 604 having plural slots, an enclosure having an opening of the carrousel and an air distributing plate, having a substantially uniform and constant temperature in the carrousel and opening up the rear part of the carrousel adjacent to the air distributing plate so as not to interrupt an air flow from the air distributing plate over the whole test sample cards. | ||||||
| 136 | JPH0588424B2 - | JP5171784 | 1984-03-16 | JPH0588424B2 | 1993-12-22 | MASUDA YOSHIJI; YASUDA YUKIO |
| 137 | JPH0365498B2 - | JP4933083 | 1983-03-24 | JPH0365498B2 | 1991-10-14 | |
| 138 | JPS6329225B2 - | JP199680 | 1980-01-11 | JPS6329225B2 | 1988-06-13 | KEUIN JEI SARIUAN |
| Apparatus and method for assuring the quality of the results obtained from a blood gas analyzer. The apparatus comprises a device for storing blood gas quality control reagent comprising a first variable volume, gas impermeable container for receiving the reagent. The reagent is stored exclusively in the liquid phase therein. A valved exit passageway emanates from the container which container is situated in a second container surrounding the first, a space being present therebetween and a compressed gas situated in the space. Upon opening the valve, the compressed gas decreases the volume of the first container and reagent is expelled through the exit passageway. The present device is uneffected by changes in ambient temperature since the reagent is stored exclusively in the liquid phase. The device is reusable since a portion of the reagent may be expelled without contamination of the remaining contents. Further, a method is disclosed for storing blood gas quality control reagent such that it is stored exclusively in a liquid phase. | ||||||
| 139 | Sample vessel for analysis | JP25778384 | 1984-12-05 | JPS61134665A | 1986-06-21 | INAISHI TETSUO |
| PURPOSE:To improve analytical accuracy by using a heat resistant and solvent resistant material to form a net-like vessel part for holding a sample, a frame member which forms a sample charge port by being bound to the aperture of the net-like vessel and a cap fitted to the frame member. CONSTITUTION:The sample vessel for analysis has the net-like vessel part 1 for holding the sample, the sample feed port 2b, the frame member 2 and the cap 3. The vessel 1 is formed of a 200-mesh net and has the circular aperture 1a' at the bottom end. The vessel is formed to an inverted triangular shape having the diameter decreasing gradually toward the upper part and the top end thereof is formed to a spherical face projecting upward. The cap 3 is made into a shallow tray shape and is so designed that the peripheral face 3a thereof can be fitted and coupled to and removed from the tapered peripheral surface 2a. The operator charges the sample into the vessel after removing the cap 3. The sample is then subjected to solvent extraction, distillation and ashing. The labor for replacing the sample in the mid-way is thus eliminated and the loss of the weight of the sample as a result of the replacement is obviated. The improved accuracy of analysis is thus attained. | ||||||
| 140 | Container | JP4933083 | 1983-03-24 | JPS59174758A | 1984-10-03 | MURAMATSU KOUZOU |
| PURPOSE:To reduce significantly contact area of dosed-supply member material, such as pipet, etc. with liquid, by forming 2 chambers with intervention of a partition provided with a communicating passage at the bottom, forming a pipet inserting hole on one of said 2 chambers and constructing the other chamber available for hermetical sealing. CONSTITUTION:After pouring a reagent S into a larger chamber 4 through a pouring orifice 6 of reagent container B, the whole set is hermetically sealed with a cover 7 attached to the orifice 6. The reagent S is introduced into the smaller chamber 3 through a communicating passage 5 located at the bottom of a partition 2. The smaller chamber 3 is open to atmosphere through an insertion hole 8 of pipet P, however, as the chamber 4 is sealed, a level of the reagent S admitted in the chamber 3 rises only to that lower than that of the larger chamber 4. By immersion of an end of pipet P in the reaqent S, the specified quantity of reagent can be absorbed assuredly and the contact area of the reagent S and the pipet P can be reduced to a minimum. | ||||||
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