<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Sebek J</submitter><funding>NIBIB NIH HHS</funding><pagination>584-594</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9717487</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>39(1)</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>Bio-effects following thermal treatments are a function of the achieved temperature profile in tissue, which can be estimated across tumor volumes with real-time MRI thermometry (MRIT). Here, we report on expansion of a previously developed small-animal microwave hyperthermia system integrated with MRIT for delivering thermal ablation to subcutaneously implanted tumors in mice.&lt;h4>Methods&lt;/h4>Computational models were employed to assess suitability of the 2.45 GHz microwave applicators for delivering ablation to subcutaneous tumor targets in mice. Phantoms and &lt;i>ex-vivo&lt;/i> tissues were heated to temperatures in the range 47-67 °C with custom-made microwave applicators for validating MRIT with the proton resonance frequency shift method against fiberoptic thermometry. HAC15 tumors implanted in nude mice (&lt;i>n&lt;/i> = 6) were ablated &lt;i>in vivo&lt;/i> and monitored with MRIT in multiple planes. One day post ablation, animals were euthanized, and excised tumors were processed for viability assessment.&lt;h4>Results&lt;/h4>Average absolute error between temperatures from fiberoptic sensors and MRIT was 0.6 °C across all &lt;i>ex-vivo&lt;/i> ablations. During &lt;i>in-vivo&lt;/i> experiments, tumors with volumes ranging between 5.4-35.9 mm&lt;sup>3&lt;/sup> (mean 14.2 mm&lt;sup>3&lt;/sup>) were ablated (duration: 103-150 s) to achieve 55 °C at the tumor boundary. Thermal doses ≥240 CEM43 were achieved across 90.7-98.0% of tumor volumes for four cases. Ablations were incomplete for remaining cases, attributed to motion-affected thermometry. Thermal dose-based ablative tumor coverage agreed with viability assessment of excised tumors.&lt;h4>Conclusions&lt;/h4>We have developed a system for delivering microwave ablation to subcutaneous tumors in small animals under MRIT guidance and demonstrated its performance &lt;i>in&lt;/i>-&lt;i>vivo&lt;/i>.</pubmed_abstract><journal>International journal of hyperthermia : the official journal of European Society for Hyperthermic Oncology, North American Hyperthermia Group</journal><pubmed_title>System for delivering microwave ablation to subcutaneous tumors in small-animals under high-field MRI thermometry guidance.</pubmed_title><pmcid>PMC9717487</pmcid><funding_grant_id>R01 EB028848</funding_grant_id><pubmed_authors>Basel MT</pubmed_authors><pubmed_authors>Faridi P</pubmed_authors><pubmed_authors>Zeinali N</pubmed_authors><pubmed_authors>Timmerman SA</pubmed_authors><pubmed_authors>Pyle M</pubmed_authors><pubmed_authors>Prakash P</pubmed_authors><pubmed_authors>Sebek J</pubmed_authors><pubmed_authors>O'Halloran M</pubmed_authors><pubmed_authors>Mali I</pubmed_authors><pubmed_authors>Bossmann SH</pubmed_authors><pubmed_authors>Payne M</pubmed_authors><pubmed_authors>Chamani F</pubmed_authors><pubmed_authors>Shrestha TB</pubmed_authors><pubmed_authors>Dennedy MC</pubmed_authors></additional><is_claimable>false</is_claimable><name>System for delivering microwave ablation to subcutaneous tumors in small-animals under high-field MRI thermometry guidance.</name><description>&lt;h4>Purpose&lt;/h4>Bio-effects following thermal treatments are a function of the achieved temperature profile in tissue, which can be estimated across tumor volumes with real-time MRI thermometry (MRIT). Here, we report on expansion of a previously developed small-animal microwave hyperthermia system integrated with MRIT for delivering thermal ablation to subcutaneously implanted tumors in mice.&lt;h4>Methods&lt;/h4>Computational models were employed to assess suitability of the 2.45 GHz microwave applicators for delivering ablation to subcutaneous tumor targets in mice. Phantoms and &lt;i>ex-vivo&lt;/i> tissues were heated to temperatures in the range 47-67 °C with custom-made microwave applicators for validating MRIT with the proton resonance frequency shift method against fiberoptic thermometry. HAC15 tumors implanted in nude mice (&lt;i>n&lt;/i> = 6) were ablated &lt;i>in vivo&lt;/i> and monitored with MRIT in multiple planes. One day post ablation, animals were euthanized, and excised tumors were processed for viability assessment.&lt;h4>Results&lt;/h4>Average absolute error between temperatures from fiberoptic sensors and MRIT was 0.6 °C across all &lt;i>ex-vivo&lt;/i> ablations. During &lt;i>in-vivo&lt;/i> experiments, tumors with volumes ranging between 5.4-35.9 mm&lt;sup>3&lt;/sup> (mean 14.2 mm&lt;sup>3&lt;/sup>) were ablated (duration: 103-150 s) to achieve 55 °C at the tumor boundary. Thermal doses ≥240 CEM43 were achieved across 90.7-98.0% of tumor volumes for four cases. Ablations were incomplete for remaining cases, attributed to motion-affected thermometry. Thermal dose-based ablative tumor coverage agreed with viability assessment of excised tumors.&lt;h4>Conclusions&lt;/h4>We have developed a system for delivering microwave ablation to subcutaneous tumors in small animals under MRIT guidance and demonstrated its performance &lt;i>in&lt;/i>-&lt;i>vivo&lt;/i>.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-19T04:42:44.675Z</modification><creation>2025-04-19T04:42:44.675Z</creation></dates><accession>S-EPMC9717487</accession><cross_references><pubmed>35435078</pubmed><doi>10.1080/02656736.2022.2061727</doi></cross_references></HashMap>