Raman micro spectroscopy for in vitro drug screening: subcellular localisation and interactions of doxorubicin
Literature Information
Z. Farhane, F. Bonnier, A. Casey, H. J. Byrne
Vibrational spectroscopy, including Raman micro spectroscopy, has been widely used over the last few years to explore potential biomedical applications. Indeed, Raman micro spectroscopy has been demonstrated to be a powerful non-invasive tool in cancer diagnosis and monitoring. In confocal microscopic mode, the technique is also a molecularly specific analytical tool with optical resolution which has potential applications in subcellular analysis of biochemical processes, and therefore as an in vitro screening tool of the efficacy and mode of action of, for example, chemotherapeutic agents. In order to demonstrate and explore the potential in this field, established, model chemotherapeutic agents can be valuable. In this study paper, Raman micro spectroscopy coupled with confocal microscopy were used for the localization and tracking of the commercially available drug, doxorubicin (DOX), in the intracellular environment of the lung cancer cell line, A549. Cytotoxicity assays were employed to establish clinically relevant drug doses for 24 h exposure, and Confocal Laser Scanning Fluorescence Microscopy was conducted in parallel with Raman micro spectroscopy profiling to confirm the drug internalisation and localisation. Multivariate statistical analysis, consisting of PCA (principal components analysis) was used to highlight doxorubicin interaction with cancer cells and spectral variations due to its effects before and after DOX spectral features subtraction from nuclear and nucleolar spectra, were compared to non-exposed control spectra. Results show that Raman micro spectroscopy is not only able to detect doxorubicin inside cells and profile its specific subcellular localisation, but, it is also capable of elucidating the local biomolecular changes elicited by the drug, differentiating the responses in different sub cellular regions. Further analysis clearly demonstrates the early apoptotic effect in the nuclear regions and the initial responses of cells to this death process, demonstrating the potential of the technique to monitor the mechanisms of action and response on a molecular level, with subcellular resolution.
Related Literature
Nucleic acid biosensors for environmental pollution monitoring
Ilaria Palchetti, Marco Mascini
DOI: 10.1039/B802920M
Describing chemical transformations in multiple spiking isotope dilution: fundamental aspects and definitions
Juris Meija, Laurent Ouerdane, Zoltán Mester
DOI: 10.1039/B814388A
Spatial metabolic fingerprinting using FT-IR spectroscopy: investigating abiotic stresses on Micrasterias hardyi
Soyab A. Patel, Felicity Currie, Nalin Thakker, Royston Goodacre
DOI: 10.1039/B809441A
Preparation and characterization of silica confined ionic liquids as chromatographic stationary phases through surface radical chain-transfer reaction
Hongdeng Qiu, Licheng Wang, Xia Liu, Shengxiang Jiang
DOI: 10.1039/B809125K
Facile analysis of metabolites by capillary electrophoresis coupled to matrix-assisted laser desorption/ionization mass spectrometry using target plates with polysilazane nanocoating and grooves
Andrea Amantonico, Pawel L. Urban, Renato Zenobi
DOI: 10.1039/B907039G
Electrochemical sensor highly selective for estradiol valerate determination based on a modified carbon paste with iron tetrapyridinoporphyrazine
Isabelle V. Batista, Marcos R. V. Lanza, Iara L. T. Dias, Sônia M. C. N. Tanaka, Auro A. Tanaka, Maria D. P. T. Sotomayor
DOI: 10.1039/B804462G
Recognition of single-base mismatch DNA by Au nanoparticle-assisted electroelution
Qing Wang, Xiaohai Yang, Kemin Wang, Weihong Tan, Jun Gou
DOI: 10.1039/B803239D
Gold nanoparticle-based immunoassay by using non-stripping chemiluminescence detection
Chun-Feng Duan, Yu-Qi Yu, Hua Cui
DOI: 10.1039/B807163B
An electrochemiluminescent biosensor for uric acid based on the electrochemiluminescence of bis-[3,4,6-trichloro-2-(pentyloxycarbonyl)-phenyl] oxalate on an ITO electrode modified by an electropolymerized nickel phthalocyanine film
Zhenyu Lin, Zhihuang Chen, Yan Liu, Jian Wang, Guonan Chen
DOI: 10.1039/B716281B
Differentiation of liquid analytes in gel films by permeability-modulated double-layer chemo-chips
Aniket R. Thete, G. Alexander Gross, J. Michael Koehler
DOI: 10.1039/B808257J
You might also like
What industries use 4-(4-tert-Butylphenyl)-1H-pyrazol-3-amine (CAS: 1015845-73-4)?
4-(4-tert-Butylphenyl)-1H-pyrazol-3-amine finds applications in various industri...
What industries use H3TATAB (CAS: 63557-10-8)?
H3TATAB is used in the pharmaceutical industry for the synthesis of certain orga...
What are the main uses of 1-Ethyl-3-fluorobenzene (CAS: 696-39-9)?
1-Ethyl-3-fluorobenzene (CAS: 696-39-9) is primarily used as a precursor in the ...
What are the main uses of 1-(tert-Butoxycarbonyl)-4-(4-methoxyphenyl)pyrrolidine-3-carboxylic acid (CAS: 851484-94-1)?
1-(tert-Butoxycarbonyl)-4-(4-methoxyphenyl)pyrrolidine-3-carboxylic acid is prim...
What are the physical and chemical properties of 1-Cyclobutyl-4-piperidinone (CAS: 359880-05-0)?
1-Cyclobutyl-4-piperidinone (CAS: 359880-05-0) is a colorless or white crystalli...
What is Pyridine-2,6-dicarboxylic acid mono-tert-butyl ester (CAS: 575433-76-0)?
Pyridine-2,6-dicarboxylic acid mono-tert-butyl ester (CAS: 575433-76-0) is a che...
What is the market or research trend for 2,3-Difluorophenylalanine (CAS: 236754-62-4)?
The market for 2,3-Difluorophenylalanine (CAS: 236754-62-4) is growing with incr...
How is (2-Hydroxy-1-naphthyl)boronic acid (CAS: 898257-48-2) typically synthesized?
(2-Hydroxy-1-naphthyl)boronic acid can be synthesized through the reduction of 2...
What are the physical and chemical properties of tert-Butyl (5-bromo-6-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)carbamate (CAS: 1315351-28-0)?
This compound is a crystalline solid with a molecular weight of approximately 52...
Are there alternatives to 5,7-Dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)-4H-chromen-3-yl beta-D-glucopyranoside (CAS: 19833-12-6) in synthesis?
While 5,7-Dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)-4H-chromen-3-yl beta-D-gluc...
Source Journal
Analyst

Analyst publishes analytical and bioanalytical research that reports premier fundamental discoveries and inventions, and the applications of those discoveries, unconfined by traditional discipline barriers.










![6-Nitro-2-(4-nitrophenyl)imidazo[1,2-a]pyridine structure 6-Nitro-2-(4-nitrophenyl)imidazo[1,2-a]pyridine structure](https://static.chemtradehub.com/structs/118/118000-57-0-cb82.webp)



