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Development of a simple indocyanine green measurement method using an automated biochemical analyser
Background The indocyanine green retention rate is important for assessing the severity of liver disorders. In the conventional method, blood needs to be collected twice. In the present study, we developed an automated indocyanine green method that does not require blood sampling before intravenous...
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Published in: | Annals of clinical biochemistry 2018-07, Vol.55 (4), p.491-495 |
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container_end_page | 495 |
container_issue | 4 |
container_start_page | 491 |
container_title | Annals of clinical biochemistry |
container_volume | 55 |
creator | Sato, Yuka Seimiya, Masanori Yoshida, Toshihiko Sawabe, Yuji Hokazono, Eisaku Osawa, Susumu Matsushita, Kazuyuki |
description | Background
The indocyanine green retention rate is important for assessing the severity of liver disorders. In the conventional method, blood needs to be collected twice. In the present study, we developed an automated indocyanine green method that does not require blood sampling before intravenous indocyanine green injections and is applicable to an automated biochemical analyser.
Methods
The serum samples of 471 patients collected before and after intravenous indocyanine green injections and submitted to the clinical laboratory of our hospital were used as samples. The standard procedure established by the Japan Society of Hepatology was used as the standard method. In the automated indocyanine green method, serum collected after an intravenous indocyanine green injection was mixed with the saline reagent containing a surfactant, and the indocyanine green concentration was measured at a dominant wavelength of 805 nm and a complementary wavelength of 884 nm.
Results
The coefficient of variations of the within- and between-run reproducibilities of this method were 2% or lower, and dilution linearity passing the origin was noted up to 10 mg/L indocyanine green. The reagent was stable for four weeks or longer. Haemoglobin, bilirubin and chyle had no impact on the results obtained. The correlation coefficient between the standard method (x) and this method (y) was r=0.995; however, slight divergence was noted in turbid samples.
Conclusion
Divergence in turbid samples may have corresponded to false negativity with the standard procedure. Our method may be highly practical because blood sampling before indocyanine green loading is unnecessary and measurements are simple. |
doi_str_mv | 10.1177/0004563217745895 |
format | article |
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The indocyanine green retention rate is important for assessing the severity of liver disorders. In the conventional method, blood needs to be collected twice. In the present study, we developed an automated indocyanine green method that does not require blood sampling before intravenous indocyanine green injections and is applicable to an automated biochemical analyser.
Methods
The serum samples of 471 patients collected before and after intravenous indocyanine green injections and submitted to the clinical laboratory of our hospital were used as samples. The standard procedure established by the Japan Society of Hepatology was used as the standard method. In the automated indocyanine green method, serum collected after an intravenous indocyanine green injection was mixed with the saline reagent containing a surfactant, and the indocyanine green concentration was measured at a dominant wavelength of 805 nm and a complementary wavelength of 884 nm.
Results
The coefficient of variations of the within- and between-run reproducibilities of this method were 2% or lower, and dilution linearity passing the origin was noted up to 10 mg/L indocyanine green. The reagent was stable for four weeks or longer. Haemoglobin, bilirubin and chyle had no impact on the results obtained. The correlation coefficient between the standard method (x) and this method (y) was r=0.995; however, slight divergence was noted in turbid samples.
Conclusion
Divergence in turbid samples may have corresponded to false negativity with the standard procedure. Our method may be highly practical because blood sampling before indocyanine green loading is unnecessary and measurements are simple.</description><identifier>ISSN: 0004-5632</identifier><identifier>EISSN: 1758-1001</identifier><identifier>DOI: 10.1177/0004563217745895</identifier><identifier>PMID: 29153028</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><ispartof>Annals of clinical biochemistry, 2018-07, Vol.55 (4), p.491-495</ispartof><rights>The Author(s) 2017</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c403t-9d1971a4c4143a1a4a06f9fab36e4fa49e0efee4e87ee29d158f48d8d8bab44d3</citedby><cites>FETCH-LOGICAL-c403t-9d1971a4c4143a1a4a06f9fab36e4fa49e0efee4e87ee29d158f48d8d8bab44d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925,79364</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29153028$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sato, Yuka</creatorcontrib><creatorcontrib>Seimiya, Masanori</creatorcontrib><creatorcontrib>Yoshida, Toshihiko</creatorcontrib><creatorcontrib>Sawabe, Yuji</creatorcontrib><creatorcontrib>Hokazono, Eisaku</creatorcontrib><creatorcontrib>Osawa, Susumu</creatorcontrib><creatorcontrib>Matsushita, Kazuyuki</creatorcontrib><title>Development of a simple indocyanine green measurement method using an automated biochemical analyser</title><title>Annals of clinical biochemistry</title><addtitle>Ann Clin Biochem</addtitle><description>Background
The indocyanine green retention rate is important for assessing the severity of liver disorders. In the conventional method, blood needs to be collected twice. In the present study, we developed an automated indocyanine green method that does not require blood sampling before intravenous indocyanine green injections and is applicable to an automated biochemical analyser.
Methods
The serum samples of 471 patients collected before and after intravenous indocyanine green injections and submitted to the clinical laboratory of our hospital were used as samples. The standard procedure established by the Japan Society of Hepatology was used as the standard method. In the automated indocyanine green method, serum collected after an intravenous indocyanine green injection was mixed with the saline reagent containing a surfactant, and the indocyanine green concentration was measured at a dominant wavelength of 805 nm and a complementary wavelength of 884 nm.
Results
The coefficient of variations of the within- and between-run reproducibilities of this method were 2% or lower, and dilution linearity passing the origin was noted up to 10 mg/L indocyanine green. The reagent was stable for four weeks or longer. Haemoglobin, bilirubin and chyle had no impact on the results obtained. The correlation coefficient between the standard method (x) and this method (y) was r=0.995; however, slight divergence was noted in turbid samples.
Conclusion
Divergence in turbid samples may have corresponded to false negativity with the standard procedure. Our method may be highly practical because blood sampling before indocyanine green loading is unnecessary and measurements are simple.</description><issn>0004-5632</issn><issn>1758-1001</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kL1PwzAQxS0EoqWwMyGPLAE7cb5GVD6lSiwwR5f43LqK7WInSP3vcWlhQEI33J3e7550j5BLzm44L8tbxpjIiyyNs8irOj8iU17mVcIZ48dkupOTnT4hZyGs45qWjJ2SSVrzPGNpNSXyHj-xdxuDdqBOUaBBm02PVFvpui1YbZEuPaKlBiGMHr9Jg8PKSToGbZcULIVxcAYGlLTVrluh0R30UYB-G9CfkxMFfcCLQ5-R98eHt_lzsnh9epnfLZJOsGxIasnrkoPoBBcZxAFYoWoFbVagUCBqZKgQBVYlYhrpvFKikrFaaIWQ2Yxc73033n2MGIbG6NBh34NFN4aG10UhRMViJDPC9mjnXQgeVbPx2oDfNpw1u2ybv9nGk6uD-9galL8HP2FGINkDAZbYrN3o4__hf8MvN_uDCQ</recordid><startdate>20180701</startdate><enddate>20180701</enddate><creator>Sato, Yuka</creator><creator>Seimiya, Masanori</creator><creator>Yoshida, Toshihiko</creator><creator>Sawabe, Yuji</creator><creator>Hokazono, Eisaku</creator><creator>Osawa, Susumu</creator><creator>Matsushita, Kazuyuki</creator><general>SAGE Publications</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20180701</creationdate><title>Development of a simple indocyanine green measurement method using an automated biochemical analyser</title><author>Sato, Yuka ; Seimiya, Masanori ; Yoshida, Toshihiko ; Sawabe, Yuji ; Hokazono, Eisaku ; Osawa, Susumu ; Matsushita, Kazuyuki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c403t-9d1971a4c4143a1a4a06f9fab36e4fa49e0efee4e87ee29d158f48d8d8bab44d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sato, Yuka</creatorcontrib><creatorcontrib>Seimiya, Masanori</creatorcontrib><creatorcontrib>Yoshida, Toshihiko</creatorcontrib><creatorcontrib>Sawabe, Yuji</creatorcontrib><creatorcontrib>Hokazono, Eisaku</creatorcontrib><creatorcontrib>Osawa, Susumu</creatorcontrib><creatorcontrib>Matsushita, Kazuyuki</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Annals of clinical biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sato, Yuka</au><au>Seimiya, Masanori</au><au>Yoshida, Toshihiko</au><au>Sawabe, Yuji</au><au>Hokazono, Eisaku</au><au>Osawa, Susumu</au><au>Matsushita, Kazuyuki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of a simple indocyanine green measurement method using an automated biochemical analyser</atitle><jtitle>Annals of clinical biochemistry</jtitle><addtitle>Ann Clin Biochem</addtitle><date>2018-07-01</date><risdate>2018</risdate><volume>55</volume><issue>4</issue><spage>491</spage><epage>495</epage><pages>491-495</pages><issn>0004-5632</issn><eissn>1758-1001</eissn><abstract>Background
The indocyanine green retention rate is important for assessing the severity of liver disorders. In the conventional method, blood needs to be collected twice. In the present study, we developed an automated indocyanine green method that does not require blood sampling before intravenous indocyanine green injections and is applicable to an automated biochemical analyser.
Methods
The serum samples of 471 patients collected before and after intravenous indocyanine green injections and submitted to the clinical laboratory of our hospital were used as samples. The standard procedure established by the Japan Society of Hepatology was used as the standard method. In the automated indocyanine green method, serum collected after an intravenous indocyanine green injection was mixed with the saline reagent containing a surfactant, and the indocyanine green concentration was measured at a dominant wavelength of 805 nm and a complementary wavelength of 884 nm.
Results
The coefficient of variations of the within- and between-run reproducibilities of this method were 2% or lower, and dilution linearity passing the origin was noted up to 10 mg/L indocyanine green. The reagent was stable for four weeks or longer. Haemoglobin, bilirubin and chyle had no impact on the results obtained. The correlation coefficient between the standard method (x) and this method (y) was r=0.995; however, slight divergence was noted in turbid samples.
Conclusion
Divergence in turbid samples may have corresponded to false negativity with the standard procedure. Our method may be highly practical because blood sampling before indocyanine green loading is unnecessary and measurements are simple.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>29153028</pmid><doi>10.1177/0004563217745895</doi><tpages>5</tpages></addata></record> |
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title | Development of a simple indocyanine green measurement method using an automated biochemical analyser |
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