<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11(4)</volume><submitter>Rajora MA</submitter><funding>Natural Sciences and Engineering Research Council of Canada</funding><funding>Princess Margaret Cancer Foundation</funding><funding>Terry Fox Research Institute</funding><funding>Peterborough K. M. Hunter Charitable Foundation</funding><funding>McLaughlin Centre, University of Toronto</funding><funding>Prostate Cancer Canada</funding><funding>Canada Foundation for Innovation</funding><funding>Canadian Institutes of Health Research</funding><funding>Institute of Cancer Research</funding><funding>Canada Research Chairs</funding><funding>CIHR</funding><pubmed_abstract>Microbubble-enabled focused ultrasound (MB-FUS) has revolutionized nano and molecular drug delivery capabilities. Yet, the absence of longitudinal, systematic, quantitative studies of microbubble shell pharmacokinetics hinders progress within the MB-FUS field. Microbubble radiolabeling challenges contribute to this void. This barrier is overcome by developing a one-pot, purification-free copper chelation protocol able to stably radiolabel diverse porphyrin-lipid-containing Definity® analogues (pDefs) with >95% efficiency while maintaining microbubble physicochemical properties. Five tri-modal (ultrasound-, positron emission tomography (PET)-, and fluorescent-active) [&lt;sup>64&lt;/sup> Cu]Cu-pDefs are created with varying lipid acyl chain length and charge, representing the most prevalently stu</pubmed_abstract><journal>Advanced science (Weinheim, Baden-Wurttemberg, Germany)</journal><pagination>e2304453</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10811482</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Quantitative Pharmacokinetics Reveal Impact of Lipid Composition on Microbubble and Nanoprogeny Shell Fate.</pubmed_title><pmcid>PMC10811482</pmcid><pubmed_authors>Dhaliwal A</pubmed_authors><pubmed_authors>Goertz D</pubmed_authors><pubmed_authors>Pellow C</pubmed_authors><pubmed_authors>Chen J</pubmed_authors><pubmed_authors>Zheng M</pubmed_authors><pubmed_authors>Choi V</pubmed_authors><pubmed_authors>Zheng G</pubmed_authors><pubmed_authors>Rajora MA</pubmed_authors><pubmed_authors>Overchuk M</pubmed_authors><pubmed_authors>Lou JWH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Quantitative Pharmacokinetics Reveal Impact of Lipid Composition on Microbubble and Nanoprogeny Shell Fate.</name><description>Microbubble-enabled focused ultrasound (MB-FUS) has revolutionized nano and molecular drug delivery capabilities. Yet, the absence of longitudinal, systematic, quantitative studies of microbubble shell pharmacokinetics hinders progress within the MB-FUS field. Microbubble radiolabeling challenges contribute to this void. This barrier is overcome by developing a one-pot, purification-free copper chelation protocol able to stably radiolabel diverse porphyrin-lipid-containing Definity® analogues (pDefs) with >95% efficiency while maintaining microbubble physicochemical properties. Five tri-modal (ultrasound-, positron emission tomography (PET)-, and fluorescent-active) [&lt;sup>64&lt;/sup> Cu]Cu-pDefs are created with varying lipid acyl chain length and charge, representing the most prevalently stu</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jan</publication><modification>2025-04-04T09:17:54.134Z</modification><creation>2025-04-04T09:17:54.134Z</creation></dates><accession>S-EPMC10811482</accession><cross_references><pubmed>38032129</pubmed><doi>10.1002/advs.202304453</doi></cross_references></HashMap>