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        <datestamp>2026-09-14T05:32:06Z</datestamp>
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          <dc:title>Supplementary file 1_Hollow-degree-tuned Prussian blue–mesoporous silica nanoplatforms for chemo-photothermal cancer therapy with preliminary microfluidic perfusion evaluation.docx</dc:title>
          <dc:creator>Jingjing Xi (8936492)</dc:creator>
          <dc:creator>Jingjing Liu (305549)</dc:creator>
          <dc:creator>Heyao Zhang (12321162)</dc:creator>
          <dc:creator>Mengxi Wang (231051)</dc:creator>
          <dc:creator>Chenyi Lu (17037744)</dc:creator>
          <dc:creator>Tinghan Wang (24868132)</dc:creator>
          <dc:creator>Xijun Piao (1630693)</dc:creator>
          <dc:creator>Ri Huang (17271975)</dc:creator>
          <dc:creator>Keyun Ren (24868135)</dc:creator>
          <dc:creator>Xiao Mei (12884465)</dc:creator>
          <dc:subject>Biotechnology</dc:subject>
          <dc:subject>chemo-photothermal therapy</dc:subject>
          <dc:subject>drug delivery</dc:subject>
          <dc:subject>hollow-degree engineering</dc:subject>
          <dc:subject>mesoporous silica</dc:subject>
          <dc:subject>microfluidic evaluation</dc:subject>
          <dc:subject>prussian blue</dc:subject>
          <dc:description>Background&lt;p&gt;Balancing photothermal performance and drug-delivery capacity remains a key challenge in the structural design of multifunctional nanomedicines. Hollowing can increase internal space for drug accommodation but may simultaneously reduce the amount of NIR-absorbing Prussian blue (PB), creating an inherent trade-off between drug-delivery capacity and photothermal performance.&lt;/p&gt;Methods&lt;p&gt;The hollow state of hollow mesoporous Prussian blue (HMPB) nanocubes was regulated by controlled HCl etching, followed by a common mesoporous silica (mSiO&lt;sub&gt;2&lt;/sub&gt;) coating, to generate low-, intermediate-, and high-hollow formulations. The resulting formulations were evaluated for physicochemical properties, photothermal performance, doxorubicin (DOX) loading and release, cellular response, intracellular fluorescence, chemo-photothermal interaction, and preliminary microfluidic perfusion performance.&lt;/p&gt;Results&lt;p&gt;Increasing hollowing enhanced DOX loading from 525 to 867 μg⋅mg&lt;sup&gt;−1&lt;/sup&gt; and promoted drug release, but progressively reduced photothermal performance. The measured photothermal conversion efficiencies of 1-, 2-, and 3-HMPB@mSiO&lt;sub&gt;2&lt;/sub&gt; were 23.37%, 18.62%, and 14.41%, respectively. ICP-MS showed decreasing Fe contents with increasing hollowing, while PB-equivalent-mass-matched measurements yielded similar photothermal conversion efficiencies (16.80%, 15.80%, and 14.41%), indicating that PB abundance is a major contributor to the observed photothermal differences. DOX release was enhanced by both mild acidity and mild hyperthermia relative to pH 7.4/37 °C. After treatment-matched correction for nanoparticle-related optical interference, the blank carriers showed limited acute carrier-associated cytotoxicity in HeLa cells over 24 h, and quantitative fluorescence imaging confirmed effective intracellular DOX delivery. At an equal total formulation concentration, the intermediate-hollow 2-HMPB@mSiO&lt;sub&gt;2&lt;/sub&gt;-DOX formulation produced the strongest combined therapeutic response. Multi-dose combination-index, Bliss-independence, and Loewe-additivity analyses further supported increasingly synergistic chemo-photothermal interactions with increasing treatment effect. Preliminary syringe-pump-driven microfluidic perfusion in physiological medium preserved the principal structure-dependent trends in particle dispersion, drug leakage, and NIR heating.&lt;/p&gt;Conclusion&lt;p&gt;These results demonstrate that hollow-state engineering provides a practical strategy for balancing competing photothermal and drug-delivery functions in PB-based nanoplatforms.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-14T05:32:06Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.3389/fbioe.2026.1932857.s001</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Supplementary_file_1_Hollow-degree-tuned_Prussian_blue_mesoporous_silica_nanoplatforms_for_chemo-photothermal_cancer_therapy_with_preliminary_microfluidic_perfusion_evaluation_docx/33718774</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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