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        <identifier>oai:figshare.com:article/33794058</identifier>
        <datestamp>2026-09-15T12:55:02Z</datestamp>
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          <dc:title>A dose-unit-aware predictive toxicology framework for literature-derived &lt;i&gt;in vitro&lt;/i&gt; carbon nanotube cytotoxicity</dc:title>
          <dc:creator>Deniz Özkan Vardar (24934119)</dc:creator>
          <dc:creator>Necati Vardar (24934122)</dc:creator>
          <dc:subject>Space Science</dc:subject>
          <dc:subject>Medicine</dc:subject>
          <dc:subject>Pharmacology</dc:subject>
          <dc:subject>Chemical Sciences not elsewhere classified</dc:subject>
          <dc:subject>Biological Sciences not elsewhere classified</dc:subject>
          <dc:subject>Cancer</dc:subject>
          <dc:subject>Carbon nanotubes</dc:subject>
          <dc:subject>predictive toxicology</dc:subject>
          <dc:subject>computational toxicology</dc:subject>
          <dc:subject>nanotoxicology</dc:subject>
          <dc:subject>in vitro cytotoxicity</dc:subject>
          <dc:description>&lt;p&gt;Carbon nanotubes (CNTs) are increasingly used as engineered nanomaterials, but their &lt;i&gt;in vitro&lt;/i&gt; cytotoxicity remains difficult to synthesize because reported viability outcomes vary across dose metrics, exposure durations, CNT types, functionalization states, cell models, and assay systems. This study developed an exploratory, literature-derived, dose-unit-aware predictive toxicology framework for binary classification of CNT-induced cytotoxicity using standardized cell viability data. Experimental-condition-level records were extracted from eligible &lt;i&gt;in vitro&lt;/i&gt; CNT studies and harmonized according to dose, dose unit, exposure duration, CNT type, functionalization, cell line, assay type, and viability outcome. Cytotoxicity was defined as cell viability below 70%. A primary-core dataset, including 146 µg/mL records from 11 articles, was used for nominal concentration-based modeling, whereas a secondary unit-aware dataset, including 212 records from 13 articles, incorporated both µg/mL and µg/cm&lt;sup&gt;2&lt;/sup&gt; observations while retaining dose-unit identity as an explicit predictor. Logistic Regression and Random Forest classifiers were trained using log-transformed dose-related variables and experimental-context predictors. Performance was assessed using stratified cross-validation, article-grouped cross-validation, leave-one-article-out validation, and leave-one-family-out validation with fold-level variability considered to reflect uncertainty and to mitigate overoptimistic estimates arising from within-study similarity. Random Forest showed higher point estimates under conventional stratified validation, whereas Logistic Regression provided comparatively stable discrimination under stricter grouped-validation settings. Ablation-based stress testing identified high-dose nontoxic A549/MTT observations as a major source of false-positive toxicity predictions, particularly for Random Forest. A dose × dose-unit interaction sensitivity analysis did not consistently improve grouped or leave-one-out validation; therefore, the additive unit-aware model was retained as the primary unit-aware analysis. The unit-aware analysis demonstrated that surface-dose records can be incorporated without assuming equivalence between nominal mass concentration and surface-area-normalized exposure. The framework provides a transparent strategy for curating, validating, stress-testing, and cautiously modeling heterogeneous literature-derived CNT viability data in nanosafety research.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-15T12:55:02Z</dc:date>
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          <dc:identifier>10.6084/m9.figshare.33794058.v1</dc:identifier>
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          <dc:rights>CC BY 4.0</dc:rights>
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