<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhang DY</submitter><funding>NCATS NIH HHS</funding><funding>NINDS NIH HHS</funding><funding>NCI NIH HHS</funding><funding>NIH HHS</funding><pagination>477-486</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7050644</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>26(2)</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>Paclitaxel shows little benefit in the treatment of glioma due to poor penetration across the blood-brain barrier (BBB). Low-intensity pulsed ultrasound (LIPU) with microbubble injection transiently disrupts the BBB allowing for improved drug delivery to the brain. We investigated the distribution, toxicity, and efficacy of LIPU delivery of two different formulations of paclitaxel, albumin-bound paclitaxel (ABX) and paclitaxel dissolved in cremophor (CrEL-PTX), in preclinical glioma models.&lt;h4>Experimental design&lt;/h4>The efficacy and biodistribution of ABX and CrEL-PTX were compared with and without LIPU delivery. Antiglioma activity was evaluated in nude mice bearing intracranial patient-derived glioma xenografts (PDX). Paclitaxel biodistribution was determined in sonicate</pubmed_abstract><journal>Clinical cancer research : an official journal of the American Association for Cancer Research</journal><pubmed_title>Ultrasound-mediated Delivery of Paclitaxel for Glioma: A Comparative Study of Distribution, Toxicity, and Efficacy of Albumin-bound Versus Cremophor Formulations.</pubmed_title><pmcid>PMC7050644</pmcid><funding_grant_id>P50 CA221747</funding_grant_id><funding_grant_id>UL1 TR001422</funding_grant_id><funding_grant_id>R01 NS102669</funding_grant_id><funding_grant_id>P30 CA060553</funding_grant_id><funding_grant_id>DP5 OD021356</funding_grant_id><pubmed_authors>Canney M</pubmed_authors><pubmed_authors>Dmello C</pubmed_authors><pubmed_authors>Chen L</pubmed_authors><pubmed_authors>Magnusson LP</pubmed_authors><pubmed_authors>James CD</pubmed_authors><pubmed_authors>Sonabend AM</pubmed_authors><pubmed_authors>Kane JR</pubmed_authors><pubmed_authors>Carpentier A</pubmed_authors><pubmed_authors>Muzzio M</pubmed_authors><pubmed_authors>Baran A</pubmed_authors><pubmed_authors>Horbinski C</pubmed_authors><pubmed_authors>Stupp R</pubmed_authors><pubmed_authors>Zhang DY</pubmed_authors><pubmed_authors>Arrieta VA</pubmed_authors><pubmed_authors>Gonzalez-Buendia E</pubmed_authors><pubmed_authors>Desseaux C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Ultrasound-mediated Delivery of Paclitaxel for Glioma: A Comparative Study of Distribution, Toxicity, and Efficacy of Albumin-bound Versus Cremophor Formulations.</name><description>&lt;h4>Purpose&lt;/h4>Paclitaxel shows little benefit in the treatment of glioma due to poor penetration across the blood-brain barrier (BBB). Low-intensity pulsed ultrasound (LIPU) with microbubble injection transiently disrupts the BBB allowing for improved drug delivery to the brain. We investigated the distribution, toxicity, and efficacy of LIPU delivery of two different formulations of paclitaxel, albumin-bound paclitaxel (ABX) and paclitaxel dissolved in cremophor (CrEL-PTX), in preclinical glioma models.&lt;h4>Experimental design&lt;/h4>The efficacy and biodistribution of ABX and CrEL-PTX were compared with and without LIPU delivery. Antiglioma activity was evaluated in nude mice bearing intracranial patient-derived glioma xenografts (PDX). Paclitaxel biodistribution was determined in sonicate</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jan</publication><modification>2025-04-06T15:17:15.294Z</modification><creation>2020-10-29T12:31:30Z</creation></dates><accession>S-EPMC7050644</accession><cross_references><pubmed>31831565</pubmed><doi>10.1158/1078-0432.ccr-19-2182</doi><doi>10.1158/1078-0432.CCR-19-2182</doi></cross_references></HashMap>