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1.
Front Chem ; 5: 62, 2017.
Article in English | MEDLINE | ID: mdl-28894734

ABSTRACT

A rugged and high throughput capillary column (cLC) LC-MS switching platform using large volume injection and on-line automatic filtration and filter back-flush (AFFL) solid phase extraction (SPE) for analysis of environmental water samples with minimal sample preparation is presented. Although narrow columns and on-line sample preparation are used in the platform, high ruggedness is achieved e.g., injection of 100 non-filtrated water samples did not result in a pressure rise/clogging of the SPE/capillary columns (inner diameter 300 µm). In addition, satisfactory retention time stability and chromatographic resolution were also features of the system. The potential of the platform for environmental water samples was demonstrated with various pharmaceutical products, which had detection limits (LOD) in the 0.05-12.5 ng/L range. Between-day and within-day repeatability of selected analytes were <20% RSD.

2.
J Chromatogr A ; 1218(20): 2954-62, 2011 May 20.
Article in English | MEDLINE | ID: mdl-21477803

ABSTRACT

An investigation into the preparation of monolithic separation media utilising a cyanine dye sensitiser/triphenylbutylborate/N-methoxy-4-phenylpyridinium tetrafluoroborate initiating system activated by 660 nm light emitting diodes is reported. The work demonstrates multiple uses of red-light initiated polymerisation in the preparation of monolithic stationary phases within polyimide and polyimide coated channels and the modification of monolithic materials with molecules which absorb strongly in the UV region. This initiator complex was used to synthesise poly(butyl methacrylate-co-ethylene dimethacrylate) and poly(methyl methacrylate-co-ethylene dimethacrylate) monolithic stationary phases in polyimide coated fused silica capillaries of varying internal diameters, as well as within polyimide micro-fluidic chips. The repeatability of the preparation procedure and resultant monolithic structure was demonstrated with a batch of poly(butyl methacrylate-co-ethylene dimethacrylate) monoliths in 100 µm i.d. polyimide coated fused silica capillary, which were applied to the separation of a model protein mixture (ribonuclease A, cytochrome C, myoglobin and ovalbumin). Taking an average from 12 chromatograms originating from each batch, the maximum relative standard deviation of the retention factor (k) for the protein separations was recorded as 0.53%, the maximum variance for the selectivity factor (α) was 0.40% while the maximum relative standard deviation in peak resolution was 8.72%. All maxima were recorded for the Ribonuclease A/Cytochrome C peaks. Scanning electron microscopy confirmed the success of experiments in which poly(butyl methacrylate-co-ethylene dimethacrylate) monoliths were prepared using the same initiation approach in capillary and micro-fluidic chips, respectively. The initiating system was also applied to the photo-initiated grafting of a chromophoric monomer onto poly(butyl methacrylate-co-ethylene dimethacrylate) monoliths within poly(tetrafluoroethylene) coated fused silica capillaries.


Subject(s)
Imides/chemistry , Light , Methacrylates/chemistry , Microfluidic Analytical Techniques/instrumentation , Benzopyrans/chemistry , Indoles/chemistry , Microfluidic Analytical Techniques/methods , Microscopy, Electron, Scanning , Nitro Compounds/chemistry , Particle Size , Photochemical Processes , Polymerization , Proteins/chemistry , Proteins/isolation & purification , Reproducibility of Results , Spectrophotometry/methods , Surface Properties
3.
Analyst ; 135(3): 477-81, 2010 Mar.
Article in English | MEDLINE | ID: mdl-20174698

ABSTRACT

Evanescent wave-initiated photopolymerisation in an optically wave guiding PTFE-coated fused silica capillary using light-emitting diode as a light source, is established here as a way to fabricate monolithic porous layer open-tubular capillary columns with a potential in capillary separation methods; application of the obtained open-tubular columns as enzymatic microreactors for on-line protein digestion is demonstrated.


Subject(s)
Enzymes/metabolism , Mass Spectrometry/methods , Polytetrafluoroethylene/chemistry , Proteins/metabolism , Animals , Bioreactors , Capillary Electrochromatography , Horses , Myoglobin/chemistry , Myoglobin/metabolism , Pepsin A/metabolism , Porosity , Proteins/chemistry , Silicon Dioxide/chemistry , Ultraviolet Rays
4.
Analyst ; 134(12): 2394-6, 2009 Dec.
Article in English | MEDLINE | ID: mdl-19918606

ABSTRACT

A 255 nm deep-UV-light-emitting diode (deep-UV-LED) is investigated as a novel light source for photometric detection in view of fundamental properties of UV-LEDs, in particular emission spectra and energy conversion. Its performance in on-capillary photometric detection in capillary electrophoresis (CE) is determined and the potential of deep-UV-LEDs in optical detection is discussed.

5.
Anal Chem ; 81(12): 5095-8, 2009 Jun 15.
Article in English | MEDLINE | ID: mdl-19441833

ABSTRACT

A simple microfluidic-based technique to quantitate the binding affinity between the glycopeptide antibiotics teicoplanin from Actinoplanes teicomyceticus and vancomycin from Streptomyces orientalis and 5-carboxyfluorescein-D-Ala-D-Ala-D-Ala (5-FAM-(DA)(3)) is described. In this work, (3-aminopropyl)triethoxysilane is used to modify the surfaces of a series of microchannels, and each channel is subsequently exposed to a solution of antibiotic for a few minutes. The antibiotic is retained after washing through electrostatic interactions, and the series of channels are subsequently exposed to an increasing concentration of 5-FAM-(DA)(3) followed by washing to exclude any nonspecific binding. The extent of fluorescence is quantified using a microscope fitted with a CCD camera. The binding constants for the interaction of teicoplanin and vancomycin with the fluorescent peptide were determined to be 6.03 +/- 0.97 x 10(4) and 4.93 +/- 1.13 x 10(4) M(-1), respectively, in good agreement with previous data. The ease of quantifying the extent of interaction in this microchip technique may prove powerful for exploration of a myriad of receptor-ligand pairs.


Subject(s)
Microfluidic Analytical Techniques/methods , Microfluidics/methods , Oligopeptides/chemistry , Silanes/chemistry , Anti-Bacterial Agents/chemistry , Ligands , Microfluidic Analytical Techniques/instrumentation , Microfluidics/instrumentation , Microscopy, Fluorescence , Propylamines , Teicoplanin/chemistry , Vancomycin/chemistry
6.
Chem Commun (Camb) ; (48): 6504-6, 2008 Dec 28.
Article in English | MEDLINE | ID: mdl-19057760

ABSTRACT

The spatially controlled synthesis of poly(glycidyl methacrylate-co-ethylene dimethacrylate) monolithic stationary phases in polyimide coated fused silica capillaries by visible light induced radical polymerisation using a three-component initiator and a 660 nm light emitting diode (LED) as a light source is presented here.

7.
Analyst ; 133(7): 864-6, 2008 Jul.
Article in English | MEDLINE | ID: mdl-18575635

ABSTRACT

For the first time photopolymerisation of polymer monoliths has been realised with UV-light emitting diodes (LEDs) as light source and demonstrated with polymethacrylate monoliths created in fused silica capillaries and plastic chips.

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