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        <identifier>oai:figshare.com:article/33770917</identifier>
        <datestamp>2026-09-15T04:28:05Z</datestamp>
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          <dc:title>Supplementary file 1_A multifunctional Fe3O4@Au-HPG-Glc theranostic platform for MRI/fluorescence-guided photothermal ablation of osteosarcoma.docx</dc:title>
          <dc:creator>Shengren Xiong (22633154)</dc:creator>
          <dc:creator>Xiaomei Zheng (2531440)</dc:creator>
          <dc:creator>Zhe Wu (582498)</dc:creator>
          <dc:creator>Shenghui Wu (2602330)</dc:creator>
          <dc:creator>Zhongliang Yao (24912061)</dc:creator>
          <dc:creator>Weilin Zheng (7513565)</dc:creator>
          <dc:subject>Biotechnology</dc:subject>
          <dc:subject>Fe3O4@Au-HPG-Glc</dc:subject>
          <dc:subject>in vivo</dc:subject>
          <dc:subject>Nanotecehnology</dc:subject>
          <dc:subject>osteosarcoma</dc:subject>
          <dc:subject>photothermal therapy</dc:subject>
          <dc:description>Background&lt;p&gt;The clinical management of osteosarcoma is challenged by its aggressive growth and deep anatomical location. Photothermal therapy offers a minimally invasive approach through localized thermal ablation, but its effectiveness is constrained by poor tissue penetration and inaccurate targeting of deep tumors without real-time guidance.&lt;/p&gt;Methods&lt;p&gt;We synthesized flower-like Fe&lt;sub&gt;3&lt;/sub&gt;O&lt;sub&gt;4&lt;/sub&gt;@Au nanoparticles coated with hyperbranched polyglycerol (HPG) and conjugated with glucose (Glc) (Fe&lt;sub&gt;3&lt;/sub&gt;O&lt;sub&gt;4&lt;/sub&gt;@Au-HPG-Glc). In an osteosarcoma mouse model, the photothermal efficacy of the nanoprobes was evaluated by comparing two groups: the control group receiving phosphate-buffered saline plus laser irradiation (phosphate-buffered saline (PBS) + Laser) and the treatment group receiving Fe&lt;sub&gt;3&lt;/sub&gt;O&lt;sub&gt;4&lt;/sub&gt;@Au-HPG-Glc nanoprobes plus laser irradiation (NPs + Laser). Intratumoral temperature was monitored by infrared thermography, with longitudinal tracking of tumor volume and body weight. Major organs were examined by H&amp;E staining. Tumor accumulation was assessed via whole-body fluorescence and T&lt;sub&gt;2&lt;/sub&gt;-weighted magnetic resonance imaging (MRI); pharmacokinetics and biodistribution were quantified by inductively coupled plasma mass spectrometry (ICP-MS).&lt;/p&gt;Results&lt;p&gt;The NPs + Laser regimen produced rapid intratumoral heating during the 0–4 min irradiation window and significantly delayed tumor growth compared with the PBS + Laser control group, with stable body weight and no overt organ lesions on H&amp;E staining. Whole-body fluorescence and T&lt;sub&gt;2&lt;/sub&gt;-weighted MRI confirmed tumor-site accumulation of the nanoprobes. ICP-MS-based pharmacokinetic and biodistribution analyses provided quantitative exposure context, including systemic clearance, reticuloendothelial system capture, and measurable tumor uptake. Together, these data facilitated interpretation of the subsequent photothermal response.&lt;/p&gt;Discussion&lt;p&gt;Flower-like Fe&lt;sub&gt;3&lt;/sub&gt;O&lt;sub&gt;4&lt;/sub&gt;@Au-HPG-Glc enables image-guided photothermal treatment in an osteosarcoma model, supported by quantitative pharmacokinetic and biodistribution measurements and an acceptable short-course safety profile. This work establishes a clear imaging-exposure-response relationship and provides a strong foundation for further optimization of magnetic-optical combination strategies in precision cancer therapy.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-15T04:28:05Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.3389/fbioe.2026.1868939.s001</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Supplementary_file_1_A_multifunctional_Fe3O4_Au-HPG-Glc_theranostic_platform_for_MRI_fluorescence-guided_photothermal_ablation_of_osteosarcoma_docx/33770917</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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