Multi-channel Small Animal Drug Metabolism Real-Time Monitoring Fluorescence System

Purpose The data acquisition of drug metabolism analysis requires a lot of time and animal resources. However, there are often many deviations in the results of pharmacokinetic analysis. Conventional methods cannot measure the blood drug concentration data in multiple tissues at the same time, and t...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Molecular imaging and biology 2024-02, Vol.26 (1), p.138-147
Hauptverfasser: Li, Yiran, Jin, Xiaofei, Wang, Feilong, Zhou, Huijing, Gu, Yueqing, Yang, Yamin, Qian, Zhiyu, Li, Weitao
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 147
container_issue 1
container_start_page 138
container_title Molecular imaging and biology
container_volume 26
creator Li, Yiran
Jin, Xiaofei
Wang, Feilong
Zhou, Huijing
Gu, Yueqing
Yang, Yamin
Qian, Zhiyu
Li, Weitao
description Purpose The data acquisition of drug metabolism analysis requires a lot of time and animal resources. However, there are often many deviations in the results of pharmacokinetic analysis. Conventional methods cannot measure the blood drug concentration data in multiple tissues at the same time, and the data is obtained by in vitro measurement, which produces time errors, in vitro data errors, and individual differences between animals. In the analysis of pharmacokinetic parameters, it will seriously affect the pass rate of clinical trials of R&D drugs and the accuracy of the dosing schedule. To the best of our knowledge, we have not found the study of in vivo blood drug concentration using multi-channel equipment. Therefore, the purpose of this paper is to build a set of multi-organ monitoring and analysis instruments for synchronously monitoring the metabolism of drugs in various tissues of small animals, so as to obtain real in vivo data of blood drug concentration in real time. Procedures Using the fluorescence properties and laser-induced fluorescence principle of drugs, we designed six channels to monitor the changes of fluorescence-labeled drugs in their main metabolic organs, a multi-channel calibration method was proposed to improve the accuracy of the time-division multiplexing, the real-time collection of drug concentration in vivo is realized, and the drug metabolism curve in vivo can be observed. Results The instrument satisfies the collection of small doses of drugs such as microgram; the detection sensitivity can reach 10 ng/ml, and can monitor and collect the drug metabolism of multiple small animal tissues at the same time, which greatly reduces the use of animals, reduces the differences between individuals, and reduces consumption cost and improve the detection efficiency of parameters, and obtain data information that is closer to the real biology. Conclusion The real-time continuous monitoring and data collection of the drug metabolism in the plasma of living small animals and the important organs such as kidney, liver, and spleen were realized. The research and development of new drugs and clinical research have higher practical value.
doi_str_mv 10.1007/s11307-023-01883-w
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2904156052</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2904156052</sourcerecordid><originalsourceid>FETCH-LOGICAL-c326t-3e67fc22d5a42233481577321bfb5001ae3e94f74c6e18551e42d9e09833f5d83</originalsourceid><addsrcrecordid>eNp9kMtO3EAQRVuIKDySH2CBLLHJppN6dPuxRCSESIyQGLJueTxlYtS2h25biL9PkwEisWBVtTh16-oodYTwFQGKbxGRodBArAHLkvXDjtrHMgdNALSbdsu5xpxpTx3EeAeABRJ_VHtcIpoCqn21XMx-6nTzpx4G8dmyr73PTocuzex7mG-zhUz1avRd7LNrqb2-6XrJFuPQTWPohtvs3M9jkNjI0Ei2fIyT9J_Uh7b2UT4_z0P1-_zHzdmFvrz6-evs9FI3TPmkWfKibYjWtjZEzKZEWxRMuGpXNnWthaUybWGaXLC0FsXQuhKoSubWrks-VF-2uZsw3s8SJ9d3qYj39SDjHB1VYNDmYCmhJ2_Qu3EOQ2qXKAIiw9YkirZUE8YYg7RuE5KJ8OgQ3JNyt1XuknL3T7l7SEfHz9Hzqpf168mL4wTwFoibJ2MS_v9-J_Yv0H6KnQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2920224354</pqid></control><display><type>article</type><title>Multi-channel Small Animal Drug Metabolism Real-Time Monitoring Fluorescence System</title><source>SpringerLink Journals - AutoHoldings</source><creator>Li, Yiran ; Jin, Xiaofei ; Wang, Feilong ; Zhou, Huijing ; Gu, Yueqing ; Yang, Yamin ; Qian, Zhiyu ; Li, Weitao</creator><creatorcontrib>Li, Yiran ; Jin, Xiaofei ; Wang, Feilong ; Zhou, Huijing ; Gu, Yueqing ; Yang, Yamin ; Qian, Zhiyu ; Li, Weitao</creatorcontrib><description>Purpose The data acquisition of drug metabolism analysis requires a lot of time and animal resources. However, there are often many deviations in the results of pharmacokinetic analysis. Conventional methods cannot measure the blood drug concentration data in multiple tissues at the same time, and the data is obtained by in vitro measurement, which produces time errors, in vitro data errors, and individual differences between animals. In the analysis of pharmacokinetic parameters, it will seriously affect the pass rate of clinical trials of R&amp;D drugs and the accuracy of the dosing schedule. To the best of our knowledge, we have not found the study of in vivo blood drug concentration using multi-channel equipment. Therefore, the purpose of this paper is to build a set of multi-organ monitoring and analysis instruments for synchronously monitoring the metabolism of drugs in various tissues of small animals, so as to obtain real in vivo data of blood drug concentration in real time. Procedures Using the fluorescence properties and laser-induced fluorescence principle of drugs, we designed six channels to monitor the changes of fluorescence-labeled drugs in their main metabolic organs, a multi-channel calibration method was proposed to improve the accuracy of the time-division multiplexing, the real-time collection of drug concentration in vivo is realized, and the drug metabolism curve in vivo can be observed. Results The instrument satisfies the collection of small doses of drugs such as microgram; the detection sensitivity can reach 10 ng/ml, and can monitor and collect the drug metabolism of multiple small animal tissues at the same time, which greatly reduces the use of animals, reduces the differences between individuals, and reduces consumption cost and improve the detection efficiency of parameters, and obtain data information that is closer to the real biology. Conclusion The real-time continuous monitoring and data collection of the drug metabolism in the plasma of living small animals and the important organs such as kidney, liver, and spleen were realized. The research and development of new drugs and clinical research have higher practical value.</description><identifier>ISSN: 1536-1632</identifier><identifier>EISSN: 1860-2002</identifier><identifier>DOI: 10.1007/s11307-023-01883-w</identifier><identifier>PMID: 38114709</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Animal tissues ; Animals ; Blood ; Blood levels ; Clinical trials ; Data acquisition ; Data collection ; Drug development ; Drug metabolism ; Drugs ; Errors ; Fluorescence ; Imaging ; In vivo methods and tests ; Laser induced fluorescence ; Medicine ; Medicine &amp; Public Health ; Metabolism ; Monitoring ; Organs ; Parameters ; Pharmacokinetics ; R&amp;D ; Radiology ; Real time ; Research &amp; development ; Research Article ; Time division multiplexing</subject><ispartof>Molecular imaging and biology, 2024-02, Vol.26 (1), p.138-147</ispartof><rights>The Author(s), under exclusive licence to World Molecular Imaging Society 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2023. The Author(s), under exclusive licence to World Molecular Imaging Society.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c326t-3e67fc22d5a42233481577321bfb5001ae3e94f74c6e18551e42d9e09833f5d83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11307-023-01883-w$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11307-023-01883-w$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27903,27904,41467,42536,51297</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38114709$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Yiran</creatorcontrib><creatorcontrib>Jin, Xiaofei</creatorcontrib><creatorcontrib>Wang, Feilong</creatorcontrib><creatorcontrib>Zhou, Huijing</creatorcontrib><creatorcontrib>Gu, Yueqing</creatorcontrib><creatorcontrib>Yang, Yamin</creatorcontrib><creatorcontrib>Qian, Zhiyu</creatorcontrib><creatorcontrib>Li, Weitao</creatorcontrib><title>Multi-channel Small Animal Drug Metabolism Real-Time Monitoring Fluorescence System</title><title>Molecular imaging and biology</title><addtitle>Mol Imaging Biol</addtitle><addtitle>Mol Imaging Biol</addtitle><description>Purpose The data acquisition of drug metabolism analysis requires a lot of time and animal resources. However, there are often many deviations in the results of pharmacokinetic analysis. Conventional methods cannot measure the blood drug concentration data in multiple tissues at the same time, and the data is obtained by in vitro measurement, which produces time errors, in vitro data errors, and individual differences between animals. In the analysis of pharmacokinetic parameters, it will seriously affect the pass rate of clinical trials of R&amp;D drugs and the accuracy of the dosing schedule. To the best of our knowledge, we have not found the study of in vivo blood drug concentration using multi-channel equipment. Therefore, the purpose of this paper is to build a set of multi-organ monitoring and analysis instruments for synchronously monitoring the metabolism of drugs in various tissues of small animals, so as to obtain real in vivo data of blood drug concentration in real time. Procedures Using the fluorescence properties and laser-induced fluorescence principle of drugs, we designed six channels to monitor the changes of fluorescence-labeled drugs in their main metabolic organs, a multi-channel calibration method was proposed to improve the accuracy of the time-division multiplexing, the real-time collection of drug concentration in vivo is realized, and the drug metabolism curve in vivo can be observed. Results The instrument satisfies the collection of small doses of drugs such as microgram; the detection sensitivity can reach 10 ng/ml, and can monitor and collect the drug metabolism of multiple small animal tissues at the same time, which greatly reduces the use of animals, reduces the differences between individuals, and reduces consumption cost and improve the detection efficiency of parameters, and obtain data information that is closer to the real biology. Conclusion The real-time continuous monitoring and data collection of the drug metabolism in the plasma of living small animals and the important organs such as kidney, liver, and spleen were realized. The research and development of new drugs and clinical research have higher practical value.</description><subject>Animal tissues</subject><subject>Animals</subject><subject>Blood</subject><subject>Blood levels</subject><subject>Clinical trials</subject><subject>Data acquisition</subject><subject>Data collection</subject><subject>Drug development</subject><subject>Drug metabolism</subject><subject>Drugs</subject><subject>Errors</subject><subject>Fluorescence</subject><subject>Imaging</subject><subject>In vivo methods and tests</subject><subject>Laser induced fluorescence</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Metabolism</subject><subject>Monitoring</subject><subject>Organs</subject><subject>Parameters</subject><subject>Pharmacokinetics</subject><subject>R&amp;D</subject><subject>Radiology</subject><subject>Real time</subject><subject>Research &amp; development</subject><subject>Research Article</subject><subject>Time division multiplexing</subject><issn>1536-1632</issn><issn>1860-2002</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kMtO3EAQRVuIKDySH2CBLLHJppN6dPuxRCSESIyQGLJueTxlYtS2h25biL9PkwEisWBVtTh16-oodYTwFQGKbxGRodBArAHLkvXDjtrHMgdNALSbdsu5xpxpTx3EeAeABRJ_VHtcIpoCqn21XMx-6nTzpx4G8dmyr73PTocuzex7mG-zhUz1avRd7LNrqb2-6XrJFuPQTWPohtvs3M9jkNjI0Ei2fIyT9J_Uh7b2UT4_z0P1-_zHzdmFvrz6-evs9FI3TPmkWfKibYjWtjZEzKZEWxRMuGpXNnWthaUybWGaXLC0FsXQuhKoSubWrks-VF-2uZsw3s8SJ9d3qYj39SDjHB1VYNDmYCmhJ2_Qu3EOQ2qXKAIiw9YkirZUE8YYg7RuE5KJ8OgQ3JNyt1XuknL3T7l7SEfHz9Hzqpf168mL4wTwFoibJ2MS_v9-J_Yv0H6KnQ</recordid><startdate>20240201</startdate><enddate>20240201</enddate><creator>Li, Yiran</creator><creator>Jin, Xiaofei</creator><creator>Wang, Feilong</creator><creator>Zhou, Huijing</creator><creator>Gu, Yueqing</creator><creator>Yang, Yamin</creator><creator>Qian, Zhiyu</creator><creator>Li, Weitao</creator><general>Springer International Publishing</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20240201</creationdate><title>Multi-channel Small Animal Drug Metabolism Real-Time Monitoring Fluorescence System</title><author>Li, Yiran ; Jin, Xiaofei ; Wang, Feilong ; Zhou, Huijing ; Gu, Yueqing ; Yang, Yamin ; Qian, Zhiyu ; Li, Weitao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c326t-3e67fc22d5a42233481577321bfb5001ae3e94f74c6e18551e42d9e09833f5d83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Animal tissues</topic><topic>Animals</topic><topic>Blood</topic><topic>Blood levels</topic><topic>Clinical trials</topic><topic>Data acquisition</topic><topic>Data collection</topic><topic>Drug development</topic><topic>Drug metabolism</topic><topic>Drugs</topic><topic>Errors</topic><topic>Fluorescence</topic><topic>Imaging</topic><topic>In vivo methods and tests</topic><topic>Laser induced fluorescence</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Metabolism</topic><topic>Monitoring</topic><topic>Organs</topic><topic>Parameters</topic><topic>Pharmacokinetics</topic><topic>R&amp;D</topic><topic>Radiology</topic><topic>Real time</topic><topic>Research &amp; development</topic><topic>Research Article</topic><topic>Time division multiplexing</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Yiran</creatorcontrib><creatorcontrib>Jin, Xiaofei</creatorcontrib><creatorcontrib>Wang, Feilong</creatorcontrib><creatorcontrib>Zhou, Huijing</creatorcontrib><creatorcontrib>Gu, Yueqing</creatorcontrib><creatorcontrib>Yang, Yamin</creatorcontrib><creatorcontrib>Qian, Zhiyu</creatorcontrib><creatorcontrib>Li, Weitao</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular imaging and biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Yiran</au><au>Jin, Xiaofei</au><au>Wang, Feilong</au><au>Zhou, Huijing</au><au>Gu, Yueqing</au><au>Yang, Yamin</au><au>Qian, Zhiyu</au><au>Li, Weitao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Multi-channel Small Animal Drug Metabolism Real-Time Monitoring Fluorescence System</atitle><jtitle>Molecular imaging and biology</jtitle><stitle>Mol Imaging Biol</stitle><addtitle>Mol Imaging Biol</addtitle><date>2024-02-01</date><risdate>2024</risdate><volume>26</volume><issue>1</issue><spage>138</spage><epage>147</epage><pages>138-147</pages><issn>1536-1632</issn><eissn>1860-2002</eissn><abstract>Purpose The data acquisition of drug metabolism analysis requires a lot of time and animal resources. However, there are often many deviations in the results of pharmacokinetic analysis. Conventional methods cannot measure the blood drug concentration data in multiple tissues at the same time, and the data is obtained by in vitro measurement, which produces time errors, in vitro data errors, and individual differences between animals. In the analysis of pharmacokinetic parameters, it will seriously affect the pass rate of clinical trials of R&amp;D drugs and the accuracy of the dosing schedule. To the best of our knowledge, we have not found the study of in vivo blood drug concentration using multi-channel equipment. Therefore, the purpose of this paper is to build a set of multi-organ monitoring and analysis instruments for synchronously monitoring the metabolism of drugs in various tissues of small animals, so as to obtain real in vivo data of blood drug concentration in real time. Procedures Using the fluorescence properties and laser-induced fluorescence principle of drugs, we designed six channels to monitor the changes of fluorescence-labeled drugs in their main metabolic organs, a multi-channel calibration method was proposed to improve the accuracy of the time-division multiplexing, the real-time collection of drug concentration in vivo is realized, and the drug metabolism curve in vivo can be observed. Results The instrument satisfies the collection of small doses of drugs such as microgram; the detection sensitivity can reach 10 ng/ml, and can monitor and collect the drug metabolism of multiple small animal tissues at the same time, which greatly reduces the use of animals, reduces the differences between individuals, and reduces consumption cost and improve the detection efficiency of parameters, and obtain data information that is closer to the real biology. Conclusion The real-time continuous monitoring and data collection of the drug metabolism in the plasma of living small animals and the important organs such as kidney, liver, and spleen were realized. The research and development of new drugs and clinical research have higher practical value.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>38114709</pmid><doi>10.1007/s11307-023-01883-w</doi><tpages>10</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1536-1632
ispartof Molecular imaging and biology, 2024-02, Vol.26 (1), p.138-147
issn 1536-1632
1860-2002
language eng
recordid cdi_proquest_miscellaneous_2904156052
source SpringerLink Journals - AutoHoldings
subjects Animal tissues
Animals
Blood
Blood levels
Clinical trials
Data acquisition
Data collection
Drug development
Drug metabolism
Drugs
Errors
Fluorescence
Imaging
In vivo methods and tests
Laser induced fluorescence
Medicine
Medicine & Public Health
Metabolism
Monitoring
Organs
Parameters
Pharmacokinetics
R&D
Radiology
Real time
Research & development
Research Article
Time division multiplexing
title Multi-channel Small Animal Drug Metabolism Real-Time Monitoring Fluorescence System
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-25T16%3A48%3A03IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Multi-channel%20Small%20Animal%20Drug%20Metabolism%20Real-Time%20Monitoring%20Fluorescence%20System&rft.jtitle=Molecular%20imaging%20and%20biology&rft.au=Li,%20Yiran&rft.date=2024-02-01&rft.volume=26&rft.issue=1&rft.spage=138&rft.epage=147&rft.pages=138-147&rft.issn=1536-1632&rft.eissn=1860-2002&rft_id=info:doi/10.1007/s11307-023-01883-w&rft_dat=%3Cproquest_cross%3E2904156052%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2920224354&rft_id=info:pmid/38114709&rfr_iscdi=true