<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Cheah HY</submitter><funding>Malaysian Ministry of Higher Education’s HIR-MoHE grants</funding><funding>PPP grant, University of Malaya, Malaysia</funding><funding>Ministry of Education, Science and Technological Development, Republic of Serbia</funding><funding>Malaysian Ministry of Higher Education’s HIR-MoHE</funding><funding>University of Malaya</funding><funding>Ministry of Education, Science and Technological Development of the Republic of Serbia</funding><pagination>210-222</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5964453</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(2)</volume><pubmed_abstract>Conjugation of Doxorubicin (DOX) to N-(2-hydroxypropyl) methylacrylamide copolymer (HPMA) has significantly reduced the DOX-associated cardiotoxicity. However, the reports on the impact of HPMA-DOX conjugates on the cardiovascular system such as blood pressure (BP) and heart rate (HR) were in restrained animals using tail cuff and/or other methods that lacked the resolution and sensitivity. Herein, we employed radiotelemetric-spectral-echocardiography approach to further understand the in vivo cardiovascular hemodynamics and variability post administration of free DOX and HPMA-DOX. Rats implanted with radio-telemetry device were administered intravenously with DOX (5 mg/kg), HPMA-DOX (5 mg DOX equivalent/kg) and HPMA copolymer and subjected to continuous cardiovascular monitoring and echoc</pubmed_abstract><journal>Nanotoxicology</journal><pubmed_title>Hemodynamic effects of HPMA copolymer based doxorubicin conjugate: A randomized controlled and comparative spectral study in conscious rats.</pubmed_title><pmcid>PMC5964453</pmcid><funding_grant_id>III 41013</funding_grant_id><funding_grant_id>UM.C/625/1/HIR/MOHE/MED/33</funding_grant_id><funding_grant_id>PG024-2015A</funding_grant_id><funding_grant_id>UM.C/625/1/HIR/MOHE/MED/17,UM.C/625/1/HIR/MOHE/MED/33</funding_grant_id><funding_grant_id>UM.C/625/1/HIR/MOHE/MED/17</funding_grant_id><funding_grant_id>III41013</funding_grant_id><pubmed_authors>Hindmarch CC</pubmed_authors><pubmed_authors>Sarenac O</pubmed_authors><pubmed_authors>Lee HB</pubmed_authors><pubmed_authors>Japundzic-Zigon N</pubmed_authors><pubmed_authors>Vasic M</pubmed_authors><pubmed_authors>Murphy D</pubmed_authors><pubmed_authors>Arroyo JJ</pubmed_authors><pubmed_authors>Hoe SZ</pubmed_authors><pubmed_authors>Lozic M</pubmed_authors><pubmed_authors>Glumac S</pubmed_authors><pubmed_authors>Cheah HY</pubmed_authors><pubmed_authors>Kiew LV</pubmed_authors><pubmed_authors>Vicent MJ</pubmed_authors><pubmed_authors>Chung LY</pubmed_authors></additional><is_claimable>false</is_claimable><name>Hemodynamic effects of HPMA copolymer based doxorubicin conjugate: A randomized controlled and comparative spectral study in conscious rats.</name><description>Conjugation of Doxorubicin (DOX) to N-(2-hydroxypropyl) methylacrylamide copolymer (HPMA) has significantly reduced the DOX-associated cardiotoxicity. However, the reports on the impact of HPMA-DOX conjugates on the cardiovascular system such as blood pressure (BP) and heart rate (HR) were in restrained animals using tail cuff and/or other methods that lacked the resolution and sensitivity. Herein, we employed radiotelemetric-spectral-echocardiography approach to further understand the in vivo cardiovascular hemodynamics and variability post administration of free DOX and HPMA-DOX. Rats implanted with radio-telemetry device were administered intravenously with DOX (5 mg/kg), HPMA-DOX (5 mg DOX equivalent/kg) and HPMA copolymer and subjected to continuous cardiovascular monitoring and echoc</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Mar</publication><modification>2025-04-05T10:58:37.593Z</modification><creation>2019-03-26T23:39:51Z</creation></dates><accession>S-EPMC5964453</accession><cross_references><pubmed>28098511</pubmed><doi>10.1080/17435390.2017.1285071</doi></cross_references></HashMap>