| Literature DB >> 30428975 |
Francesca Falcetta1, Lavinia Morosi1, Paolo Ubezio1, Silvia Giordano2, Alessandra Decio1, Raffaella Giavazzi1, Roberta Frapolli1, Mridula Prasad3, Pietro Franceschi4, Maurizio D'Incalci1, Enrico Davoli5.
Abstract
Mass spectrometry imaging is a valuable tool for visualizing the localization of drugs in tissues, a critical issue especially in cancer pharmacology where treatment failure may depend on poor drug distribution within the tumours. Proper preprocessing procedures are mandatory to obtain quantitative data of drug distribution in tumours, even at low intensity, through reliable ion peak identification and integration. We propose a simple preprocessing and quantification pipeline. This pipeline was designed starting from classical peak integration methods, developed when "microcomputers" became available for chromatography, now applied to MSI. This pre-processing approach is based on a novel method using the fixed mass difference between the analyte and its 5 d derivatives to set up a mass range gate. We demonstrate the use of this pipeline for the evaluating the distribution of the anticancer drug paclitaxel in tumour sections. The procedure takes advantage of a simple peak analysis and allows to quantify the drug concentration in each pixel with a limit of detection below 0.1 pmol mm-2 or 10 μg g-1. Quantitative images of paclitaxel distribution in different tumour models were obtained and average paclitaxel concentrations were compared with HPLC measures in the same specimens, showing <20% difference. The scripts are developed in Python and available through GitHub, at github.com/FrancescaFalcetta/Imaging_of_drugs_distribution_and_quantifications.git.Entities:
Keywords: Imaging data analysis; Mass spectrometry images; Preprocessing; Quantitative imaging; Tumour drug distribution
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Year: 2018 PMID: 30428975 DOI: 10.1016/j.aca.2018.06.067
Source DB: PubMed Journal: Anal Chim Acta ISSN: 0003-2670 Impact factor: 6.558