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      Determination of Paclitaxel Distribution in Solid Tumors by Nano-Particle Assisted Laser Desorption Ionization Mass Spectrometry Imaging

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          Abstract

          A sensitive, simple and reproducible protocol for nanoparticle-assisted laser desorption/ionization mass spectrometry imaging technique is described. The use of commercially available TiO 2 nanoparticles abolishes heterogeneous crystallization, matrix background interferences and enhances signal detection, especially in the low mass range. Molecular image normalization was based on internal standard deposition on tissues, allowing direct comparison of drug penetration and distribution between different organs and tissues. The method was applied to analyze the distribution of the anticancer drug paclitaxel, inside normal and neoplastic mouse tissue sections. Spatial resolution was good, with a linear response between different in vivo treatments and molecular imaging intensity using therapeutic drug doses. This technique distinguishes the different intensity of paclitaxel distribution in control organs of mice, such as liver and kidney, in relation to the dose. Animals treated with 30 mg/kg of paclitaxel had half of the concentration of those treated with 60 mg/kg. We investigated the spatial distribution of paclitaxel in human melanoma mouse xenografts, following different dosage schedules and found a more homogeneous drug distribution in tumors of mice given repeated doses (5×8 mg/kg) plus a 60 mg/kg dose than in those assigned only a single 60 mg/kg dose. The protocol can be readily applied to investigate anticancer drug distribution in neoplastic lesions and to develop strategies to optimize and enhance drug penetration through different tumor tissues.

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          Most cited references35

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          Paclitaxel (taxol)

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            Use of mass spectrometry for imaging metabolites in plants.

            We discuss and illustrate recent advances that have been made to image the distribution of metabolites among cells and tissues of plants using different mass spectrometry technologies. These technologies include matrix-assisted laser desorption ionization, desorption electrospray ionization, and secondary ion mass spectrometry. These are relatively new technological applications of mass spectrometry and they are providing highly spatially resolved data concerning the cellular distribution of metabolites. We discuss the advantages and limitations of each of these mass spectrometric methods, and provide a description of the technical barriers that are currently limiting the technology to the level of single-cell resolution. However, we anticipate that advances in the next few years will increase the resolving power of the technology to provide unprecedented data on the distribution of metabolites at the subcellular level, which will increase our ability to decipher new knowledge concerning the spatial organization of metabolic processes in plants. Published 2012. This article is a US Government work and is in the public domain in the USA.
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              MALDI-FTICR imaging mass spectrometry of drugs and metabolites in tissue.

              A new approach is described for imaging mass spectrometry analysis of drugs and metabolites in tissue using matrix-assisted laser desorption ionization-Fourier transform ion cyclotron resonance (MALDI-FTICR). The technique utilizes the high resolving power to produce images from thousands of ions measured during a single mass spectrometry (MS)-mode experiment. Accurate mass measurement provides molecular specificity for the ion images on the basis of elemental composition. Final structural confirmation of the targeted compound is made from accurate mass fragment ions generated in an external quadrupole-collision cell. The ability to image many small molecules in a single measurement with high specificity is a significant improvement over existing MS/MS based technologies. Example images are shown for olanzapine in kidney and liver and imatinib in glioma.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2013
                26 August 2013
                : 8
                : 8
                : e72532
                Affiliations
                [1 ]IRCCS Istituto di Ricerche Farmacologiche “Mario Negri”, Department of Oncology, Milano, Italy
                [2 ]IRCCS Istituto di Ricerche Farmacologiche “Mario Negri”, Department of Environmental Health Sciences, Mass Spectrometry Laboratory, Milano, Italy
                Virginia Commonwealth University, United States of America
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                Conceived and designed the experiments: LM PS MZ AC MDI RG ED. Performed the experiments: LM PS FP AC. Analyzed the data: LM PS MZ FP AC MDI RG ED. Contributed reagents/materials/analysis tools: LM PS FP AC. Wrote the paper: LM PS MZ MDI ED.

                Article
                PONE-D-13-17266
                10.1371/journal.pone.0072532
                3753243
                23991120
                442814d5-c68c-4340-ae3b-e8befcc28a69
                Copyright @ 2013

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 29 April 2013
                : 10 July 2013
                Page count
                Pages: 9
                Funding
                This work has been funded by Regione Lombardia under Institutional Agreement n. 14501A. The authors acknowledge support from AIRC Special Program Molecular Clinical Oncology “5 per mille” to LM and MDI. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Biology
                Biochemistry
                Metabolism
                Biological Transport
                Model Organisms
                Animal Models
                Mouse
                Chemistry
                Analytical Chemistry
                Chemical Analysis
                Engineering
                Signal Processing
                Image Processing
                Medicine
                Drugs and Devices
                Pharmacokinetics
                Drug Distribution
                Oncology
                Basic Cancer Research
                Tumor Physiology
                Cancer Treatment
                Chemotherapy and Drug Treatment
                Cancers and Neoplasms
                Skin Tumors
                Malignant Melanoma

                Uncategorized
                Uncategorized

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