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Direct microscopic monitoring of initial and dynamic clot lysis using plasmin or rt-PA in an in vitro flow system

Abstract Introduction Plasmin is a direct-acting thrombolytic agent with a favorable safety profile upon intra-arterial delivery in pre-clinical and phase I studies. However, the thrombolytic efficacy of plasmin, relative to that of rt-PA, remains to be established. We have compared the dynamics of...

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Published in:Thrombosis research 2014-05, Vol.133 (5), p.908-913
Main Authors: Bizjak, Nina, Bajd, Franci, Vidmar, Jernej, Blinc, Aleš, Perme, Maja Pohar, Marder, Victor J, Novokhatny, Valery, Serša, Igor
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container_end_page 913
container_issue 5
container_start_page 908
container_title Thrombosis research
container_volume 133
creator Bizjak, Nina
Bajd, Franci
Vidmar, Jernej
Blinc, Aleš
Perme, Maja Pohar
Marder, Victor J
Novokhatny, Valery
Serša, Igor
description Abstract Introduction Plasmin is a direct-acting thrombolytic agent with a favorable safety profile upon intra-arterial delivery in pre-clinical and phase I studies. However, the thrombolytic efficacy of plasmin, relative to that of rt-PA, remains to be established. We have compared the dynamics of clot lysis with plasmin or rt-PA in an in vitro perfusion system, in which thrombolytic agent is administered locally, allowed to induce lysis for short intervals, then washed with plasma in a re-circulation circuit. Materials and Methods Whole blood human clots were prepared in observation chambers, exposed to plasmin or rt-PA at equimolar concentrations (1.2/1.0, 1.8/1.5 and 2.4/2.0 mg/ml) for measured intervals of time, followed by perfusion with human plasma. Clot size was monitored by digital analysis of sequential photographs obtained through an optical microscope. Results Plasma perfusion after incubation with thrombolytic agent rapidly removed superficial clot fragments. This initial decrease in clot size was greater with plasmin than with rt-PA when tested at the highest concentrations of agent (0.63 ± 0.11 vs. 0.30 ± 0.11, p = 0.001 for clots with non-cross-linked fibrin and 0.53 ± 0.15 vs. 0.14 ± 0.15, p = 0.02, for clots with cross-linked-fibrin). Subsequent clot lysis during plasma flow was greater after prior incubation with rt-PA. Longer incubation times of plasmin resulted in larger portions of the clot being washed free. Repeated plasmin incubations and plasma perfusions of a clot successfully induced stepwise reductions in clot size. Conclusions Initial clot lysis is greater with direct exposure using plasmin than rt-PA. During washout and circulation with plasma, rt-PA induced continued clot lysis, while plasmin lysis was curtailed, presumably because of plasmin inhibition.
doi_str_mv 10.1016/j.thromres.2014.02.008
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However, the thrombolytic efficacy of plasmin, relative to that of rt-PA, remains to be established. We have compared the dynamics of clot lysis with plasmin or rt-PA in an in vitro perfusion system, in which thrombolytic agent is administered locally, allowed to induce lysis for short intervals, then washed with plasma in a re-circulation circuit. Materials and Methods Whole blood human clots were prepared in observation chambers, exposed to plasmin or rt-PA at equimolar concentrations (1.2/1.0, 1.8/1.5 and 2.4/2.0 mg/ml) for measured intervals of time, followed by perfusion with human plasma. Clot size was monitored by digital analysis of sequential photographs obtained through an optical microscope. Results Plasma perfusion after incubation with thrombolytic agent rapidly removed superficial clot fragments. This initial decrease in clot size was greater with plasmin than with rt-PA when tested at the highest concentrations of agent (0.63 ± 0.11 vs. 0.30 ± 0.11, p = 0.001 for clots with non-cross-linked fibrin and 0.53 ± 0.15 vs. 0.14 ± 0.15, p = 0.02, for clots with cross-linked-fibrin). Subsequent clot lysis during plasma flow was greater after prior incubation with rt-PA. Longer incubation times of plasmin resulted in larger portions of the clot being washed free. Repeated plasmin incubations and plasma perfusions of a clot successfully induced stepwise reductions in clot size. Conclusions Initial clot lysis is greater with direct exposure using plasmin than rt-PA. During washout and circulation with plasma, rt-PA induced continued clot lysis, while plasmin lysis was curtailed, presumably because of plasmin inhibition.</description><identifier>ISSN: 0049-3848</identifier><identifier>EISSN: 1879-2472</identifier><identifier>DOI: 10.1016/j.thromres.2014.02.008</identifier><identifier>PMID: 24613694</identifier><language>eng</language><publisher>United States: Elsevier Ltd</publisher><subject>Blood Coagulation - drug effects ; Fibrinolysin - pharmacology ; Fibrinolysis - drug effects ; Fibrinolytic Agents - pharmacology ; Hematology, Oncology and Palliative Medicine ; Hemodynamics ; Humans ; In Vitro Techniques ; Microscopy ; Plasmin ; Plasminogen - metabolism ; Plasminogen activator ; Recombinant Proteins - pharmacology ; Thrombolytic therapy ; Tissue Plasminogen Activator - pharmacology</subject><ispartof>Thrombosis research, 2014-05, Vol.133 (5), p.908-913</ispartof><rights>Elsevier Ltd</rights><rights>2014 Elsevier Ltd</rights><rights>Copyright © 2014 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c423t-bdb6967bae31383bebddaee5f2937b62a0c16e91a5206000307df1ec7b5106423</citedby><cites>FETCH-LOGICAL-c423t-bdb6967bae31383bebddaee5f2937b62a0c16e91a5206000307df1ec7b5106423</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24613694$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bizjak, Nina</creatorcontrib><creatorcontrib>Bajd, Franci</creatorcontrib><creatorcontrib>Vidmar, Jernej</creatorcontrib><creatorcontrib>Blinc, Aleš</creatorcontrib><creatorcontrib>Perme, Maja Pohar</creatorcontrib><creatorcontrib>Marder, Victor J</creatorcontrib><creatorcontrib>Novokhatny, Valery</creatorcontrib><creatorcontrib>Serša, Igor</creatorcontrib><title>Direct microscopic monitoring of initial and dynamic clot lysis using plasmin or rt-PA in an in vitro flow system</title><title>Thrombosis research</title><addtitle>Thromb Res</addtitle><description>Abstract Introduction Plasmin is a direct-acting thrombolytic agent with a favorable safety profile upon intra-arterial delivery in pre-clinical and phase I studies. However, the thrombolytic efficacy of plasmin, relative to that of rt-PA, remains to be established. We have compared the dynamics of clot lysis with plasmin or rt-PA in an in vitro perfusion system, in which thrombolytic agent is administered locally, allowed to induce lysis for short intervals, then washed with plasma in a re-circulation circuit. Materials and Methods Whole blood human clots were prepared in observation chambers, exposed to plasmin or rt-PA at equimolar concentrations (1.2/1.0, 1.8/1.5 and 2.4/2.0 mg/ml) for measured intervals of time, followed by perfusion with human plasma. Clot size was monitored by digital analysis of sequential photographs obtained through an optical microscope. Results Plasma perfusion after incubation with thrombolytic agent rapidly removed superficial clot fragments. This initial decrease in clot size was greater with plasmin than with rt-PA when tested at the highest concentrations of agent (0.63 ± 0.11 vs. 0.30 ± 0.11, p = 0.001 for clots with non-cross-linked fibrin and 0.53 ± 0.15 vs. 0.14 ± 0.15, p = 0.02, for clots with cross-linked-fibrin). Subsequent clot lysis during plasma flow was greater after prior incubation with rt-PA. Longer incubation times of plasmin resulted in larger portions of the clot being washed free. Repeated plasmin incubations and plasma perfusions of a clot successfully induced stepwise reductions in clot size. Conclusions Initial clot lysis is greater with direct exposure using plasmin than rt-PA. During washout and circulation with plasma, rt-PA induced continued clot lysis, while plasmin lysis was curtailed, presumably because of plasmin inhibition.</description><subject>Blood Coagulation - drug effects</subject><subject>Fibrinolysin - pharmacology</subject><subject>Fibrinolysis - drug effects</subject><subject>Fibrinolytic Agents - pharmacology</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>Hemodynamics</subject><subject>Humans</subject><subject>In Vitro Techniques</subject><subject>Microscopy</subject><subject>Plasmin</subject><subject>Plasminogen - metabolism</subject><subject>Plasminogen activator</subject><subject>Recombinant Proteins - pharmacology</subject><subject>Thrombolytic therapy</subject><subject>Tissue Plasminogen Activator - pharmacology</subject><issn>0049-3848</issn><issn>1879-2472</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqFkc1u1TAQRi1ERS-FV6i8ZJMwdhwn2SCqlj-pUisBa8uxJ-CLE9_aSVHevg63ZcGGjS1L55uRz0fIOYOSAZNv9-X8M4YxYio5MFECLwHaZ2TH2qYruGj4c7IDEF1RtaI9JS9T2gOwhnX1C3LKhWSV7MSO3F25iGamozMxJBMOztAxTG4O0U0_aBioyw-nPdWTpXaddCap8WGmfk0u0SVt3MHrNLqJhkjjXNxe5FQObOe9m2Oggw-_aVrTjOMrcjJon_D1431Gvn_88O3yc3F98-nL5cV1YQSv5qK3vexk02usWNVWPfbWasR64F3V9JJrMExix3TNQQJABY0dGJqmrxnIPOKMvDnOPcRwt2Ca1eiSQe_1hGFJitWs45I3UmRUHtHNQYo4qEN0o46rYqA23WqvnnSrTbcCrrLuHDx_3LH0I9q_sSe_GXh_BDD_9N5hVMk4nAzaP9qVDe7_O979M8L43InR_heumPZhiVP2qJhKOaC-bqVvnTORrbRNXT0AuGOq7g</recordid><startdate>20140501</startdate><enddate>20140501</enddate><creator>Bizjak, Nina</creator><creator>Bajd, Franci</creator><creator>Vidmar, Jernej</creator><creator>Blinc, Aleš</creator><creator>Perme, Maja Pohar</creator><creator>Marder, Victor J</creator><creator>Novokhatny, Valery</creator><creator>Serša, Igor</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20140501</creationdate><title>Direct microscopic monitoring of initial and dynamic clot lysis using plasmin or rt-PA in an in vitro flow system</title><author>Bizjak, Nina ; Bajd, Franci ; Vidmar, Jernej ; Blinc, Aleš ; Perme, Maja Pohar ; Marder, Victor J ; Novokhatny, Valery ; Serša, Igor</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c423t-bdb6967bae31383bebddaee5f2937b62a0c16e91a5206000307df1ec7b5106423</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Blood Coagulation - drug effects</topic><topic>Fibrinolysin - pharmacology</topic><topic>Fibrinolysis - drug effects</topic><topic>Fibrinolytic Agents - pharmacology</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>Hemodynamics</topic><topic>Humans</topic><topic>In Vitro Techniques</topic><topic>Microscopy</topic><topic>Plasmin</topic><topic>Plasminogen - metabolism</topic><topic>Plasminogen activator</topic><topic>Recombinant Proteins - pharmacology</topic><topic>Thrombolytic therapy</topic><topic>Tissue Plasminogen Activator - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bizjak, Nina</creatorcontrib><creatorcontrib>Bajd, Franci</creatorcontrib><creatorcontrib>Vidmar, Jernej</creatorcontrib><creatorcontrib>Blinc, Aleš</creatorcontrib><creatorcontrib>Perme, Maja Pohar</creatorcontrib><creatorcontrib>Marder, Victor J</creatorcontrib><creatorcontrib>Novokhatny, Valery</creatorcontrib><creatorcontrib>Serša, Igor</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Thrombosis research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bizjak, Nina</au><au>Bajd, Franci</au><au>Vidmar, Jernej</au><au>Blinc, Aleš</au><au>Perme, Maja Pohar</au><au>Marder, Victor J</au><au>Novokhatny, Valery</au><au>Serša, Igor</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Direct microscopic monitoring of initial and dynamic clot lysis using plasmin or rt-PA in an in vitro flow system</atitle><jtitle>Thrombosis research</jtitle><addtitle>Thromb Res</addtitle><date>2014-05-01</date><risdate>2014</risdate><volume>133</volume><issue>5</issue><spage>908</spage><epage>913</epage><pages>908-913</pages><issn>0049-3848</issn><eissn>1879-2472</eissn><abstract>Abstract Introduction Plasmin is a direct-acting thrombolytic agent with a favorable safety profile upon intra-arterial delivery in pre-clinical and phase I studies. However, the thrombolytic efficacy of plasmin, relative to that of rt-PA, remains to be established. We have compared the dynamics of clot lysis with plasmin or rt-PA in an in vitro perfusion system, in which thrombolytic agent is administered locally, allowed to induce lysis for short intervals, then washed with plasma in a re-circulation circuit. Materials and Methods Whole blood human clots were prepared in observation chambers, exposed to plasmin or rt-PA at equimolar concentrations (1.2/1.0, 1.8/1.5 and 2.4/2.0 mg/ml) for measured intervals of time, followed by perfusion with human plasma. Clot size was monitored by digital analysis of sequential photographs obtained through an optical microscope. Results Plasma perfusion after incubation with thrombolytic agent rapidly removed superficial clot fragments. This initial decrease in clot size was greater with plasmin than with rt-PA when tested at the highest concentrations of agent (0.63 ± 0.11 vs. 0.30 ± 0.11, p = 0.001 for clots with non-cross-linked fibrin and 0.53 ± 0.15 vs. 0.14 ± 0.15, p = 0.02, for clots with cross-linked-fibrin). Subsequent clot lysis during plasma flow was greater after prior incubation with rt-PA. Longer incubation times of plasmin resulted in larger portions of the clot being washed free. Repeated plasmin incubations and plasma perfusions of a clot successfully induced stepwise reductions in clot size. Conclusions Initial clot lysis is greater with direct exposure using plasmin than rt-PA. During washout and circulation with plasma, rt-PA induced continued clot lysis, while plasmin lysis was curtailed, presumably because of plasmin inhibition.</abstract><cop>United States</cop><pub>Elsevier Ltd</pub><pmid>24613694</pmid><doi>10.1016/j.thromres.2014.02.008</doi><tpages>6</tpages></addata></record>
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subjects Blood Coagulation - drug effects
Fibrinolysin - pharmacology
Fibrinolysis - drug effects
Fibrinolytic Agents - pharmacology
Hematology, Oncology and Palliative Medicine
Hemodynamics
Humans
In Vitro Techniques
Microscopy
Plasmin
Plasminogen - metabolism
Plasminogen activator
Recombinant Proteins - pharmacology
Thrombolytic therapy
Tissue Plasminogen Activator - pharmacology
title Direct microscopic monitoring of initial and dynamic clot lysis using plasmin or rt-PA in an in vitro flow system
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