Functionalization of MgZnO nanorod films and characterization by FTIR microscopic imaging

2017 ◽  
Vol 409 (27) ◽  
pp. 6379-6386 ◽  
Author(s):  
Yuan Chen ◽  
Qihong Zhang ◽  
Carol Flach ◽  
Richard Mendelsohn ◽  
Elena Galoppini ◽  
...  
Biopolymers ◽  
2000 ◽  
Vol 62 (1) ◽  
pp. 1-8 ◽  
Author(s):  
Nancy P. Camacho ◽  
Paul West ◽  
Peter A. Torzilli ◽  
Richard Mendelsohn

Molecules ◽  
2021 ◽  
Vol 26 (20) ◽  
pp. 6318
Author(s):  
Jun-Li Xu ◽  
Ana Herrero-Langreo ◽  
Sakshi Lamba ◽  
Mariateresa Ferone ◽  
Amalia G. M. Scannell ◽  
...  

This work investigates the application of reflectance Fourier transform infrared (FTIR) microscopic imaging for rapid, and non-invasive detection and classification between Bacillus subtilis and Escherichia coli cell suspensions dried onto metallic substrates (stainless steel (STS) and aluminium (Al) slides) in the optical density (OD) concentration range of 0.001 to 10. Results showed that reflectance FTIR of samples with OD lower than 0.1 did not present an acceptable spectral signal to enable classification. Two modelling strategies were devised to evaluate model performance, transferability and consistency among concentration levels. Modelling strategy 1 involves training the model with half of the sample set, consisting of all concentrations, and applying it to the remaining half. Using this approach, for the STS substrate, the best model was achieved using support vector machine (SVM) classification, providing an accuracy of 96% and Matthews correlation coefficient (MCC) of 0.93 for the independent test set. For the Al substrate, the best SVM model produced an accuracy and MCC of 91% and 0.82, respectively. Furthermore, the aforementioned best model built from one substrate was transferred to predict the bacterial samples deposited on the other substrate. Results revealed an acceptable predictive ability when transferring the STS model to samples on Al (accuracy = 82%). However, the Al model could not be adapted to bacterial samples deposited on STS (accuracy = 57%). For modelling strategy 2, models were developed using one concentration level and tested on the other concentrations for each substrate. Results proved that models built from samples with moderate (1 OD) concentration can be adapted to other concentrations with good model generalization. Prediction maps revealed the heterogeneous distribution of biomolecules due to the coffee ring effect. This work demonstrated the feasibility of applying FTIR to characterise spectroscopic fingerprints of dry bacterial cells on substrates of relevance for food processing.


The Analyst ◽  
2007 ◽  
Vol 132 (7) ◽  
pp. 647 ◽  
Author(s):  
Christoph Krafft ◽  
Reiner Salzer ◽  
Sebastian Seitz ◽  
Christina Ern ◽  
Matthias Schieker

2015 ◽  
Vol 4 (1) ◽  
pp. 57-66 ◽  
Author(s):  
Claudia Beleites ◽  
O. Guntinas-Lichius ◽  
G. Ernst ◽  
Jürgen Popp ◽  
Christoph Krafft

2008 ◽  
Vol 1 (2) ◽  
pp. 154-169 ◽  
Author(s):  
Christoph Krafft ◽  
Daniela Codrich ◽  
Gloria Pelizzo ◽  
Valter Sergo

Cells ◽  
2021 ◽  
Vol 10 (3) ◽  
pp. 499
Author(s):  
Tracy W. Liu ◽  
Seth T. Gammon ◽  
David Piwnica-Worms

Intravital microscopic imaging (IVM) allows for the study of interactions between immune cells and tumor cells in a dynamic, physiologically relevant system in vivo. Current IVM strategies primarily use fluorescence imaging; however, with the advances in bioluminescence imaging and the development of new bioluminescent reporters with expanded emission spectra, the applications for bioluminescence are extending to single cell imaging. Herein, we describe a molecular imaging window chamber platform that uniquely combines both bioluminescent and fluorescent genetically encoded reporters, as well as exogenous reporters, providing a powerful multi-plex strategy to study molecular and cellular processes in real-time in intact living systems at single cell resolution all in one system. We demonstrate that our molecular imaging window chamber platform is capable of imaging signaling dynamics in real-time at cellular resolution during tumor progression. Importantly, we expand the utility of IVM by modifying an off-the-shelf commercial system with the addition of bioluminescence imaging achieved by the addition of a CCD camera and demonstrate high quality imaging within the reaches of any biology laboratory.


Sign in / Sign up

Export Citation Format

Share Document