FIBRINOGEN QUANTIFICATION METHOD

To provide a fibrinogen quantification method capable of accurate fibrinogen quantification without requiring preparing reagents or dilute samples, applicable to perinatal and perioperative use.SOLUTION: The fibrinogen quantification method includes the steps of: after adding the sample to the fibri...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: OKA SHUICHI, TORAMI TAKAYOSHI, NAKAMOTO KAZUYA, KIKUCHI MASAYOSHI
Format: Patent
Sprache:eng ; jpn
Schlagworte:
Online-Zugang:Volltext bestellen
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue
container_start_page
container_title
container_volume
creator OKA SHUICHI
TORAMI TAKAYOSHI
NAKAMOTO KAZUYA
KIKUCHI MASAYOSHI
description To provide a fibrinogen quantification method capable of accurate fibrinogen quantification without requiring preparing reagents or dilute samples, applicable to perinatal and perioperative use.SOLUTION: The fibrinogen quantification method includes the steps of: after adding the sample to the fibrinogen quantitative drying reagent containing magnetic particles, moving magnetic particles in the reagent to monitor movement signals of the magnetic particles; and calculating multiple magnetic particle motion signal ratios at regular time intervals. Defining an arbitrary point in the section where the ratio is maintained within a certain range for a certain period as a starting point and a point that is 5-50% attenuated with respect to the peak value of the magnetic particle motion signal after the starting point as the endpoint, the solidification time is the time from the start point to the endpoint. With this, accurate fibrinogen quantification can be performed even when undiluted whole blood is used as the measurement sample.SELECTED DRAWING: Figure 4 【課題】周産期および周術期での使用に耐えうる、試薬の調製や検体の希釈操作を必要とせず、且つ、正確なフィブリノゲン定量が可能なフィブリノゲン定量方法の開発。【解決手段】磁性粒子を含有したフィブリノゲン定量乾燥試薬に検体を添加後、試薬中の磁性粒子を運動させ、磁性粒子運動シグナルをモニターするとともに、一定の時間間隔の磁性粒子運動シグナル比を複数算出し、その比が一定の範囲内で一定時間保たれた区間の任意の点を起点とし、起点以降の磁性粒子運動シグナルのピーク値に対して5〜50%減衰した点を終点とし、起点から終点までの時間を凝固時間とすることを特徴とするフィブリノゲン定量方法を適用することにより、測定試料を無希釈全血とした場合でも、正確なフィブリノゲン定量を可能とする。【選択図】図4
format Patent
fullrecord <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_JP2020173203A</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>JP2020173203A</sourcerecordid><originalsourceid>FETCH-epo_espacenet_JP2020173203A3</originalsourceid><addsrcrecordid>eNrjZFBw83QK8vTzd3f1UwgMdfQL8XTzdHYM8fT3U_B1DfHwd-FhYE1LzClO5YXS3AxKbq4hzh66qQX58anFBYnJqXmpJfFeAUYGRgaG5sZGBsaOxkQpAgBGXSJm</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>FIBRINOGEN QUANTIFICATION METHOD</title><source>esp@cenet</source><creator>OKA SHUICHI ; TORAMI TAKAYOSHI ; NAKAMOTO KAZUYA ; KIKUCHI MASAYOSHI</creator><creatorcontrib>OKA SHUICHI ; TORAMI TAKAYOSHI ; NAKAMOTO KAZUYA ; KIKUCHI MASAYOSHI</creatorcontrib><description>To provide a fibrinogen quantification method capable of accurate fibrinogen quantification without requiring preparing reagents or dilute samples, applicable to perinatal and perioperative use.SOLUTION: The fibrinogen quantification method includes the steps of: after adding the sample to the fibrinogen quantitative drying reagent containing magnetic particles, moving magnetic particles in the reagent to monitor movement signals of the magnetic particles; and calculating multiple magnetic particle motion signal ratios at regular time intervals. Defining an arbitrary point in the section where the ratio is maintained within a certain range for a certain period as a starting point and a point that is 5-50% attenuated with respect to the peak value of the magnetic particle motion signal after the starting point as the endpoint, the solidification time is the time from the start point to the endpoint. With this, accurate fibrinogen quantification can be performed even when undiluted whole blood is used as the measurement sample.SELECTED DRAWING: Figure 4 【課題】周産期および周術期での使用に耐えうる、試薬の調製や検体の希釈操作を必要とせず、且つ、正確なフィブリノゲン定量が可能なフィブリノゲン定量方法の開発。【解決手段】磁性粒子を含有したフィブリノゲン定量乾燥試薬に検体を添加後、試薬中の磁性粒子を運動させ、磁性粒子運動シグナルをモニターするとともに、一定の時間間隔の磁性粒子運動シグナル比を複数算出し、その比が一定の範囲内で一定時間保たれた区間の任意の点を起点とし、起点以降の磁性粒子運動シグナルのピーク値に対して5〜50%減衰した点を終点とし、起点から終点までの時間を凝固時間とすることを特徴とするフィブリノゲン定量方法を適用することにより、測定試料を無希釈全血とした場合でも、正確なフィブリノゲン定量を可能とする。【選択図】図4</description><language>eng ; jpn</language><subject>INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIRCHEMICAL OR PHYSICAL PROPERTIES ; MEASURING ; PHYSICS ; TESTING</subject><creationdate>2020</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=20201022&amp;DB=EPODOC&amp;CC=JP&amp;NR=2020173203A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25563,76318</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=20201022&amp;DB=EPODOC&amp;CC=JP&amp;NR=2020173203A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>OKA SHUICHI</creatorcontrib><creatorcontrib>TORAMI TAKAYOSHI</creatorcontrib><creatorcontrib>NAKAMOTO KAZUYA</creatorcontrib><creatorcontrib>KIKUCHI MASAYOSHI</creatorcontrib><title>FIBRINOGEN QUANTIFICATION METHOD</title><description>To provide a fibrinogen quantification method capable of accurate fibrinogen quantification without requiring preparing reagents or dilute samples, applicable to perinatal and perioperative use.SOLUTION: The fibrinogen quantification method includes the steps of: after adding the sample to the fibrinogen quantitative drying reagent containing magnetic particles, moving magnetic particles in the reagent to monitor movement signals of the magnetic particles; and calculating multiple magnetic particle motion signal ratios at regular time intervals. Defining an arbitrary point in the section where the ratio is maintained within a certain range for a certain period as a starting point and a point that is 5-50% attenuated with respect to the peak value of the magnetic particle motion signal after the starting point as the endpoint, the solidification time is the time from the start point to the endpoint. With this, accurate fibrinogen quantification can be performed even when undiluted whole blood is used as the measurement sample.SELECTED DRAWING: Figure 4 【課題】周産期および周術期での使用に耐えうる、試薬の調製や検体の希釈操作を必要とせず、且つ、正確なフィブリノゲン定量が可能なフィブリノゲン定量方法の開発。【解決手段】磁性粒子を含有したフィブリノゲン定量乾燥試薬に検体を添加後、試薬中の磁性粒子を運動させ、磁性粒子運動シグナルをモニターするとともに、一定の時間間隔の磁性粒子運動シグナル比を複数算出し、その比が一定の範囲内で一定時間保たれた区間の任意の点を起点とし、起点以降の磁性粒子運動シグナルのピーク値に対して5〜50%減衰した点を終点とし、起点から終点までの時間を凝固時間とすることを特徴とするフィブリノゲン定量方法を適用することにより、測定試料を無希釈全血とした場合でも、正確なフィブリノゲン定量を可能とする。【選択図】図4</description><subject>INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIRCHEMICAL OR PHYSICAL PROPERTIES</subject><subject>MEASURING</subject><subject>PHYSICS</subject><subject>TESTING</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2020</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZFBw83QK8vTzd3f1UwgMdfQL8XTzdHYM8fT3U_B1DfHwd-FhYE1LzClO5YXS3AxKbq4hzh66qQX58anFBYnJqXmpJfFeAUYGRgaG5sZGBsaOxkQpAgBGXSJm</recordid><startdate>20201022</startdate><enddate>20201022</enddate><creator>OKA SHUICHI</creator><creator>TORAMI TAKAYOSHI</creator><creator>NAKAMOTO KAZUYA</creator><creator>KIKUCHI MASAYOSHI</creator><scope>EVB</scope></search><sort><creationdate>20201022</creationdate><title>FIBRINOGEN QUANTIFICATION METHOD</title><author>OKA SHUICHI ; TORAMI TAKAYOSHI ; NAKAMOTO KAZUYA ; KIKUCHI MASAYOSHI</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_JP2020173203A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng ; jpn</language><creationdate>2020</creationdate><topic>INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIRCHEMICAL OR PHYSICAL PROPERTIES</topic><topic>MEASURING</topic><topic>PHYSICS</topic><topic>TESTING</topic><toplevel>online_resources</toplevel><creatorcontrib>OKA SHUICHI</creatorcontrib><creatorcontrib>TORAMI TAKAYOSHI</creatorcontrib><creatorcontrib>NAKAMOTO KAZUYA</creatorcontrib><creatorcontrib>KIKUCHI MASAYOSHI</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>OKA SHUICHI</au><au>TORAMI TAKAYOSHI</au><au>NAKAMOTO KAZUYA</au><au>KIKUCHI MASAYOSHI</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>FIBRINOGEN QUANTIFICATION METHOD</title><date>2020-10-22</date><risdate>2020</risdate><abstract>To provide a fibrinogen quantification method capable of accurate fibrinogen quantification without requiring preparing reagents or dilute samples, applicable to perinatal and perioperative use.SOLUTION: The fibrinogen quantification method includes the steps of: after adding the sample to the fibrinogen quantitative drying reagent containing magnetic particles, moving magnetic particles in the reagent to monitor movement signals of the magnetic particles; and calculating multiple magnetic particle motion signal ratios at regular time intervals. Defining an arbitrary point in the section where the ratio is maintained within a certain range for a certain period as a starting point and a point that is 5-50% attenuated with respect to the peak value of the magnetic particle motion signal after the starting point as the endpoint, the solidification time is the time from the start point to the endpoint. With this, accurate fibrinogen quantification can be performed even when undiluted whole blood is used as the measurement sample.SELECTED DRAWING: Figure 4 【課題】周産期および周術期での使用に耐えうる、試薬の調製や検体の希釈操作を必要とせず、且つ、正確なフィブリノゲン定量が可能なフィブリノゲン定量方法の開発。【解決手段】磁性粒子を含有したフィブリノゲン定量乾燥試薬に検体を添加後、試薬中の磁性粒子を運動させ、磁性粒子運動シグナルをモニターするとともに、一定の時間間隔の磁性粒子運動シグナル比を複数算出し、その比が一定の範囲内で一定時間保たれた区間の任意の点を起点とし、起点以降の磁性粒子運動シグナルのピーク値に対して5〜50%減衰した点を終点とし、起点から終点までの時間を凝固時間とすることを特徴とするフィブリノゲン定量方法を適用することにより、測定試料を無希釈全血とした場合でも、正確なフィブリノゲン定量を可能とする。【選択図】図4</abstract><oa>free_for_read</oa></addata></record>
fulltext fulltext_linktorsrc
identifier
ispartof
issn
language eng ; jpn
recordid cdi_epo_espacenet_JP2020173203A
source esp@cenet
subjects INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIRCHEMICAL OR PHYSICAL PROPERTIES
MEASURING
PHYSICS
TESTING
title FIBRINOGEN QUANTIFICATION METHOD
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-10T17%3A11%3A32IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-epo_EVB&rft_val_fmt=info:ofi/fmt:kev:mtx:patent&rft.genre=patent&rft.au=OKA%20SHUICHI&rft.date=2020-10-22&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3EJP2020173203A%3C/epo_EVB%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true