{"id":{"repo_id":"chapman","oai_identifier":"oai:digitalcommons.chapman.edu:pharmaceutical_sciences_dissertations-1014"},"canonical_url":"https://search.dev.ndltd.org/etd/chapman/oai:digitalcommons.chapman.edu:pharmaceutical_sciences_dissertations-1014","repository":{"repo_id":"chapman","name":"Chapman University","base_url":"https://digitalcommons.chapman.edu/do/oai/"},"display":{"title":"The Use of Spectral Imaging to Reveal Inorganics and Organics Identity in The Biological Samples","abstract":"<p>The wavelength is used to identify the exact location and quantify the number of molecules in the spectral imaging system. It aids in identifying materials and studying their quantities by examining how they interact with light. A traditional spectrometer provides spectrum information of chemical compounds, while standard imaging provides the intensity at each pixel of the image. Spectral imaging (SI) combines these two aspects by equipping intensity and spectral data for each pixel. In biomedical research, it is important to assess the inorganics/organics molecules to understand drug activity, cellular toxicity, and distribution. Using the microscopy technique, we found for the first time that spectral imaging can provide a high temporal and spatial resolution of gold (Au) and silver (Ag) nanoparticles (NPs) in fixed, living cells and tissue samples. We discovered that SI has a tremendous potential to study NPs localization and identification in biological samples at a single living cell and tissue, based primarily on the spectra information. In addition, we revealed for the first time that without labeling the drug and destroying the samples, spectral imaging is a novel method that allows us to analyze the dynamics of drug distribution and metabolism in single living cells. The spectral microscopy provides a high image resolution to track and identifies doxorubicin (dox) metabolite, which is doxorubicinol (dox’ol). The microscopy approach confirms that both dox and dox’ol are translocated to the nucleus at different rates, while rhodamine remains in the cytoplasm.</p>","abstract_html":"&lt;p&gt;The wavelength is used to identify the exact location and quantify the number of molecules in the spectral imaging system. It aids in identifying materials and studying their quantities by examining how they interact with light. A traditional spectrometer provides spectrum information of chemical compounds, while standard imaging provides the intensity at each pixel of the image. Spectral imaging (SI) combines these two aspects by equipping intensity and spectral data for each pixel. In biomedical research, it is important to assess the inorganics/organics molecules to understand drug activity, cellular toxicity, and distribution. Using the microscopy technique, we found for the first time that spectral imaging can provide a high temporal and spatial resolution of gold (Au) and silver (Ag) nanoparticles (NPs) in fixed, living cells and tissue samples. We discovered that SI has a tremendous potential to study NPs localization and identification in biological samples at a single living cell and tissue, based primarily on the spectra information. In addition, we revealed for the first time that without labeling the drug and destroying the samples, spectral imaging is a novel method that allows us to analyze the dynamics of drug distribution and metabolism in single living cells. The spectral microscopy provides a high image resolution to track and identifies doxorubicin (dox) metabolite, which is doxorubicinol (dox’ol). The microscopy approach confirms that both dox and dox’ol are translocated to the nucleus at different rates, while rhodamine remains in the cytoplasm.&lt;/p&gt;","abstract_has_math":false,"creators":["Alshammari, Qamar"],"institution":null,"degree_name":"Doctor of Philosophy (PhD)","degree_level":"Dissertation","degree_discipline":"Pharmaceutical Sciences","degree_department":null,"school":null,"contributors":["Surya M. Nauli","Aftab Ahmed","Ajay Sharma","Amir Ahsan"],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2022,"date_issued":"2022-05-01T07:00:00Z","date_published":"2022-05-01T07:00:00Z","updated_at":"2026-07-24T01:38:24Z","subjects":["Investigative Techniques","Nanomedicine","Other Pharmacy and Pharmaceutical Sciences"],"languages":[],"rights":[],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"https://digitalcommons.chapman.edu/pharmaceutical_sciences_dissertations/14","outbound_label":"Repository record","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor","label":"Contributor","values":["Surya M. 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It aids in identifying materials and studying their quantities by examining how they interact with light. A traditional spectrometer provides spectrum information of chemical compounds, while standard imaging provides the intensity at each pixel of the image. Spectral imaging (SI) combines these two aspects by equipping intensity and spectral data for each pixel. In biomedical research, it is important to assess the inorganics/organics molecules to understand drug activity, cellular toxicity, and distribution. Using the microscopy technique, we found for the first time that spectral imaging can provide a high temporal and spatial resolution of gold (Au) and silver (Ag) nanoparticles (NPs) in fixed, living cells and tissue samples. We discovered that SI has a tremendous potential to study NPs localization and identification in biological samples at a single living cell and tissue, based primarily on the spectra information. In addition, we revealed for the first time that without labeling the drug and destroying the samples, spectral imaging is a novel method that allows us to analyze the dynamics of drug distribution and metabolism in single living cells. The spectral microscopy provides a high image resolution to track and identifies doxorubicin (dox) metabolite, which is doxorubicinol (dox’ol). The microscopy approach confirms that both dox and dox’ol are translocated to the nucleus at different rates, while rhodamine remains in the cytoplasm.</p>"]},{"key":"dc:source","label":"Dc Source","values":["Alshammari, QA. <em>The Use of Spectral Imaging to Reveal Inorganics and Organics Identity in The Biological Samples</em>. [dissertation]. Irvine, CA: Chapman University; 2022. <a href=\"https://doi.org/10.36837/chapman.000341\">https://doi.org/10.36837/chapman.000341</a>"]},{"key":"dc:title","label":"Title","values":["The Use of Spectral Imaging to Reveal Inorganics and Organics Identity in The Biological Samples"]}]}],"canonical_facts":{"dc:contributor":["Surya M. Nauli","Aftab Ahmed","Ajay Sharma","Amir Ahsan"],"dc:creator":["Alshammari, Qamar"],"dc:description.abstract":["<p>The wavelength is used to identify the exact location and quantify the number of molecules in the spectral imaging system. It aids in identifying materials and studying their quantities by examining how they interact with light. A traditional spectrometer provides spectrum information of chemical compounds, while standard imaging provides the intensity at each pixel of the image. Spectral imaging (SI) combines these two aspects by equipping intensity and spectral data for each pixel. In biomedical research, it is important to assess the inorganics/organics molecules to understand drug activity, cellular toxicity, and distribution. Using the microscopy technique, we found for the first time that spectral imaging can provide a high temporal and spatial resolution of gold (Au) and silver (Ag) nanoparticles (NPs) in fixed, living cells and tissue samples. We discovered that SI has a tremendous potential to study NPs localization and identification in biological samples at a single living cell and tissue, based primarily on the spectra information. In addition, we revealed for the first time that without labeling the drug and destroying the samples, spectral imaging is a novel method that allows us to analyze the dynamics of drug distribution and metabolism in single living cells. The spectral microscopy provides a high image resolution to track and identifies doxorubicin (dox) metabolite, which is doxorubicinol (dox’ol). The microscopy approach confirms that both dox and dox’ol are translocated to the nucleus at different rates, while rhodamine remains in the cytoplasm.</p>"],"dc:identifier":["https://digitalcommons.chapman.edu/pharmaceutical_sciences_dissertations/14"],"dc:source":["Alshammari, QA. <em>The Use of Spectral Imaging to Reveal Inorganics and Organics Identity in The Biological Samples</em>. [dissertation]. Irvine, CA: Chapman University; 2022. <a href=\"https://doi.org/10.36837/chapman.000341\">https://doi.org/10.36837/chapman.000341</a>"],"dc:subject":["Investigative Techniques","Nanomedicine","Other Pharmacy and Pharmaceutical Sciences"],"dc:title":["The Use of Spectral Imaging to Reveal Inorganics and Organics Identity in The Biological Samples"],"thesis:degree_discipline":["Pharmaceutical Sciences"],"thesis:degree_level":["Dissertation"],"thesis:degree_name":["Doctor of Philosophy (PhD)"]},"updated_at":"2026-07-24T01:38:24Z"}