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1.
J Clin Monit Comput ; 32(3): 583-586, 2018 06.
Article in English | MEDLINE | ID: mdl-28593455

ABSTRACT

The purpose of this study was to characterize the heterogeneity of oxygen partial pressure in different adipose tissue zones and to assess the possibility of compensating these heterogeneities during optical glucose measurements. In this proof of concept study, the heterogeneity of oxygen partial pressure was determined in the adipose tissue of a pig by using 48 oxygen sensors in 3 zones of the abdominal region at two different blood oxygen levels. Sensor oxygen values correlated well with reference blood oxygen values and we identified heterogeneities in oxygen partial pressure among the defined zones of the abdominal region. Significant differences in the mean oxygen partial pressure were found when comparing the three abdominal zones but no significant differences were found when comparing two sensors located in close proximity (on one cannula). The low heterogeneity on one cannula allows the compensation of physiological oxygen variations for optical glucose measurements by using an additional oxygen sensor in close proximity to the glucose sensor. In addition, this setup can be used to continuously monitor tissue oxygenation e.g. in patients with adipose tissue dysfunction or serve limb ischemia.


Subject(s)
Adipose Tissue/diagnostic imaging , Monitoring, Physiologic/instrumentation , Oxygen/chemistry , Partial Pressure , Animals , Blood Glucose , Disease Models, Animal , Equipment Design , Glucose/analysis , Monitoring, Physiologic/methods , Optical Fibers , Swine
2.
Biosens Bioelectron ; 88: 240-248, 2017 Feb 15.
Article in English | MEDLINE | ID: mdl-27554063

ABSTRACT

The combination of continuous glucose monitoring (CGM) and continuous subcutaneous insulin infusion can be used to improve the treatment of patients with diabetes. The aim of this study was to advance an existing preclinical single-port system for clinical application by integrating the sensors of a phosphorescence based CGM system into a standard insulin infusion set. The extracorporeal optical phase fluorimeter was miniaturised and is now comparable with commercial CGM systems regarding size, weight and wear comfort. Sensor chemistry was adapted to improve the adhesion of the sensor elements on the insulin infusion set. In-vitro tests showed a linear correlation of R2=0.998 between sensor values and reference glucose values in the range of 0-300mg/dl. Electrical and cytotoxicity tests showed no negative impact on human health. Two single-port devices were tested in each of 12 patients with type 1 diabetes mellitus in a clinical set-up for 12h. Without additional data processing, the overall median absolute relative difference (median ARD) was 22.5%. For some of the used devices the median ARD was even well below 10%. The present results show that individual glucose sensors performance of the single-port system is comparable with commercial CGM systems but further improvements are needed. The new system offers a high extent of safety and usability by combining insulin infusion and continuous glucose measurement in a single-port system which could become a central element in an artificial pancreas for an improved treatment of patients with type 1 diabetes mellitus.


Subject(s)
Biosensing Techniques/instrumentation , Blood Glucose Self-Monitoring/instrumentation , Blood Glucose/analysis , Diabetes Mellitus, Type 1/blood , Insulin Infusion Systems , Adolescent , Aspergillus niger/enzymology , Equipment Design , Female , Fluorometry/instrumentation , Glucose Oxidase/chemistry , Humans , Male , Monitoring, Ambulatory/instrumentation
3.
Chem Commun (Camb) ; 51(20): 4172-5, 2015 Mar 11.
Article in English | MEDLINE | ID: mdl-25360563

ABSTRACT

We introduce here a dynamic optode for buffer capacity sensing based on photochromic spiropyran (Sp). It represents the first reversible optical sensor for buffer capacity. Sensing was possible using a non-equilibrium readout mode, a novelty for photoswitchable optical ion sensors. In addition to the buffer capacity, the final point of each measurement sequence provides the pH of the solution.

4.
J Mater Chem B ; 2(39): 6792-6801, 2014 Oct 21.
Article in English | MEDLINE | ID: mdl-32261875

ABSTRACT

Several new perylene bisimide (PBI) probes comprising oligo-guanidine conjugates and cationic hydrogel nanoparticle structures were designed for sensing intracellular pH in live cell fluorescence lifetime imaging microscopy (FLIM). Using adherent mammalian cells (2D) and neurosphere (3D) cell models, we evaluated their performance by confocal FLIM-TCSPC. The nanoparticle PBI probe showed stable pH calibration and lifetime changes from 4.7 to 3.7 ns between pH 4.4 and 8 attributed to photo-induced electron transfer (PET). The molecular oligo-guanidine probe showed fast cell penetration and bright staining, but its calibration is affected by the microenvironment being unreliable for quantitative FLIM. Thus, nanoparticle structures are preferred for the design of quantitative pH measurement by FLIM. High brightness and photostability, efficient staining of different cell types and positive optical response to acidification in fluorescence intensity and lifetime modalities are the advantages of the nanoparticle PBI probes compared to conventional pH probes such as BCECF (2',7'-bis-(2-carboxyethyl)-5,6-carboxyfluorescein). Other PBI derivatives with stronger PET can be developed for future high-resolution FLIM of intracellular pH.

7.
Anal Bioanal Chem ; 404(10): 2797-806, 2012 Dec.
Article in English | MEDLINE | ID: mdl-22811065

ABSTRACT

New sensing materials have been developed which rely on the use of luminescent europium(III) and gadolinium(III) complexes with thenoylacetylacetonate embedded in an acridone-polystyrene conjugate. Acridone acts as an antenna which efficiently absorbs violet light. Covalent coupling to the polystyrene backbone prevents aggregation and enables very high antenna loading (16% w/w). Energy transfer from the antenna to the lanthanide complexes results in efficient red luminescence from the Eu(III) complex or green phosphorescence originating from the Gd(III) chelate. The luminescence of the material based on the Eu(III) complex is only slightly affected by oxygen but is highly sensitive to temperature under physiological conditions (20-40 °C). The Gd(III) complex has long phosphorescence decay times of approximately 1 ms and high sensitivity to oxygen. Ultra-thin (250 nm) sensing layers with sufficient absorption at the excitation wavelength enable monitoring of rapid oxygen changes virtually in real time. Immobilization of both complexes in a single matrix results in a dual-luminescence material with emissions almost ideally matching the red and green channels of a digital camera. Thus, oxygen imaging using a very simple and inexpensive set-up can be realized. Additionally, the material can be used for simultaneous sensing of oxygen and temperature.

8.
J Microbiol Methods ; 85(1): 67-74, 2011 Apr.
Article in English | MEDLINE | ID: mdl-21277912

ABSTRACT

New transparent optodes for life-time based microscopic imaging of O2 were developed by spin-coating a µm-thin layer of a highly luminescent cyclometalated iridium(III) coumarin complex in polystyrene onto glass cover slips. Compared to similar thin-film O2 optodes based on a ruthenium(II) polypyridyl complex or a platinum(II) porphyrin, the new planar sensors have i) higher brightness allowing for much shorter exposure times and thus higher time resolution, ii) more homogeneous and smaller pixel to pixel variation over the sensor area resulting in less noisy O2 images, and iii) a lower temperature dependency simplifying calibration procedures. We used the new optodes for microscopic imaging of the spatio-temporal O2 dynamics at the base of heterotrophic biofilms in combination with confocal imaging of bacterial biomass and biofilm structure. This allowed us to directly link biomass distribution to O2 distribution under both steady state and non-steady state conditions. We demonstrate that the O2 dynamics in biofilms is governed by a complex interaction between biomass distribution, mass transfer and flow that cannot be directly inferred from structural information on biomass distribution alone.


Subject(s)
Bacteria/chemistry , Bacteria/growth & development , Biofilms/growth & development , Luminescent Measurements/methods , Microscopy/methods , Oxygen/analysis , Biomass
9.
Anal Chem ; 80(24): 9435-42, 2008 Dec 15.
Article in English | MEDLINE | ID: mdl-19006407

ABSTRACT

New optical oxygen-sensing materials make use of highly luminescent NIR platinum(II) and palladium(II) complexes with benzoporphyrins. Bulk optodes based on polystyrene and sensing nanobeads based on poly(styrene-block-vinylpyrrolidone) and polysulfone are prepared and characterized. The versatility of the new materials is demonstrated. The features include excellent compatibility with most common excitation sources, high brightness, and suitability for subcutaneous oxygen monitoring.

10.
J Microsc ; 222(Pt 2): 135-40, 2006 May.
Article in English | MEDLINE | ID: mdl-16774522

ABSTRACT

The use of ultrabright light-emitting diodes as a potential substitute for conventional excitation light sources in fluorescence microscopy is demonstrated. We integrated ultrabright light-emitting diodes in the filter block of a conventional fluorescence microscope together with a collimating Fresnel lens, a holographic diffuser and emission filters. This setup enabled convenient changes between different excitation light sources and resulted in high excitation efficiencies. Quantitative comparison of image intensities of test samples revealed that light-emitting diodes yielded intensities in the range of a mercury arc lamp depending on the wavelength. The use of ultrabright light-emitting diodes also enabled luminescence lifetime imaging without the need for image intensification.

11.
Bioconjug Chem ; 12(6): 883-9, 2001.
Article in English | MEDLINE | ID: mdl-11716677

ABSTRACT

A simple encapsulation technique is presented to produce highly phosphorescent, inert nanospheres that are suitable luminescent markers. It is based on the coprecipitation of phosphorescent ruthenium(II)-tris(polypyridyl) complexes and polyacrylonitrile (PAN) derivatives from a solution in N,N-dimethylformamide. The beads precipitate in the form of very small aggregates of spherical shape and a typical particle diameter of less than 50 nm. This process allows the encapsulation of phosphorescent and fluorescent dyes in an individual nanosphere provided that they are sufficiently lipophilic. Quenching by oxygen is negligible due to the use of PAN. The nanospheres were characterized with respect to their spectral properties (quantum yields of the luminophores, brightness, luminescence decay time), stability in aqueous buffered suspensions, and in terms of size, shape, and surface charge of the particles, as well as storage stability, quenching by oxygen, and dye leaching.


Subject(s)
Acrylic Resins/chemistry , Nanotechnology , Ruthenium/chemistry , Drug Compounding , Fluorescent Dyes , Luminescent Measurements , Microscopy, Electron , Microspheres , Organometallic Compounds , Particle Size , Scattering, Radiation , Spectrum Analysis
12.
Anal Chem ; 73(17): 4354-63, 2001 Sep 01.
Article in English | MEDLINE | ID: mdl-11569831

ABSTRACT

We present a referenced scheme for fluorescence intensity measurements that is useful for imaging applications. It is based on the conversion of the fluorescence intensity information into a time-dependent parameter. A phosphorescent dye is added in the form of approximately 10-microm particles to the sample containing the pH-sensitive fluorescent indicator. Both the reference dye and the pH probe are excited simultaneously by a blue LED, and an overall luminescence is measured. In the time-resolved imaging method presented here, two images taken at different time gates were recorded using a CCD camera. The first image is recorded during excitation and reflects the luminescence signal of both the fluorophore (pH) and the phosphor (reference). The second image, which is measured after a certain delay (after switching off the light source), is solely caused by the long-lived phosphorescent dye. Because the intensity of the fluorophore contains the information on pH, whereas phosphorescence is pH-independent, the ratio of the images displays a referenced intensity distribution that reflects the pH at each picture element (pixel). The scheme is useful for LED light sources and CCD cameras that can be gated with square pulses in the microsecond range. The fundamentals and potential of this new method, to which we refer as time domain dual lifetime referencing (t-DLR), are demonstrated.

13.
Anal Biochem ; 297(1): 32-41, 2001 Oct 01.
Article in English | MEDLINE | ID: mdl-11567525

ABSTRACT

A new concept to design phosphorescent nanospheres is presented. The spheres are distinguishable by their individual decay time and spectral distribution of their emission spectra. They are composed of a phosphorescent ruthenium metal-ligand complex (MLC) dissolved, along with certain strongly fluorescent cyanine dyes, in modified polyacrylonitrile-based nanospheres. Since the emission spectrum of the MLC overlaps the absorption spectrum of the cyanine and both the MLC (the donor) and the cyanine (the acceptor) are in close spatial proximity, efficient resonance energy transfer (RET) does occur. Thus, the nanospheres emit dual luminescence, one from the acceptor dye and the other from the donor MLC. Variation of the concentrations of the acceptor dye results in a varying efficiency of RET, thus making the spheres distinguishable. Hence, a set of multiplexable sphere labels is obtained by using one MLC (acting as the phosphorescent donor and present in constant concentration) and one acceptor dye (which varies in terms of both spectral properties and concentration). The nanospheres can be identified by the emission maximum (reflecting the kind of acceptor dye) and by decay time (reflecting its concentration). Since the same donor MLC is used throughout, all nanospheres can be excited with the same light source.


Subject(s)
Biological Assay/instrumentation , Biological Assay/methods , Coloring Agents/metabolism , Luminescent Measurements , Carbocyanines/chemistry , Carbocyanines/metabolism , Coloring Agents/chemistry , Energy Transfer , Ligands , Microspheres , Ruthenium/chemistry , Ruthenium/metabolism , Spectrum Analysis/instrumentation , Spectrum Analysis/methods , Time Factors
14.
Anal Chem ; 73(9): 2097-103, 2001 May 01.
Article in English | MEDLINE | ID: mdl-11354496

ABSTRACT

A membrane with an optical response to chloride has been developed that contains two luminophores that display two largely different decay times. The first luminophore (the "reference") is a chloride-insensitive ruthenium metal-ligand complex possessing a decay time in the microsecond range. The second luminophore is the short-lived chloride-quenchable fluorescent probe lucigenin. Both are contained in a hydrogel matrix and are excited by a blue LED emitting sinusoidally modulated light. Under these conditions, the chloride-dependent fluorescence intensity of lucigenin can be converted in an analyte-dependent fluorescence phase shift that depends on the ratio of the two luminescence intensities and can be measured at modulation frequencies of typically 45 kHz. The dynamic range of this sensor can be adjusted by either varying the ratio of the two luminophores or selecting a particular optical filter combination.


Subject(s)
Chlorides , Fluorescent Dyes , Organometallic Compounds , Ruthenium , Acridines , Algorithms , Chlorides/analysis , Chlorides/chemistry , Luminescent Measurements , Membranes, Artificial , Reference Standards , Spectrometry, Fluorescence/instrumentation
15.
Anal Chem ; 73(5): 1053-6, 2001 Mar 01.
Article in English | MEDLINE | ID: mdl-11289417

ABSTRACT

An optical sensor for aqueous 1-butylamine is presented which combines two novel techniques: A fluorescent indicator dye (fluoro reactand) embedded in a thin polymer layer performs a reversible chemical reaction with the analyte, causing changes in luminescence intensity. At the same time, inert phosphorescent beads dispersed within the polymer layer provide luminescence signals that act as an internal reference for the indicator dye. As a consequence, the optical sensor is independent of light source fluctuations, ambient light, drifts in optoelectronic setup, or optical fiber bending.

16.
Biosens Bioelectron ; 15(1-2): 69-76, 2000 Mar.
Article in English | MEDLINE | ID: mdl-10826645

ABSTRACT

Various types of thin-film glucose biosensors based on the use of the enzyme glucose oxidase (GOx) have been developed. The luminescent oxygen probe Ru(dpp)--whose emission is quenched by oxygen--is used to measure the consumption of oxygen. Three different combinations of oxygen transducer and sol-gel immobilized GOx were tested. In the first, GOx was sandwiched between a sol-gel layer doped with Ru(dpp) and a second sol-gel layer composed of pure sol-gel (the 'sandwich' configuration). In the second, a sol-gel layer doped with Ru(dpp) was covered with sol-gel entrapped GOx (the 'two-layer configuration'). In the third, both GOx and a sol-gel powder containing GOx were incorporated into a single sol-gel phase (the 'powder configuration'). In all cases, it was found to be essential to add sorbitol which results in a more porous sol-gel in which diffusion is not impaired. The sandwich configuration provides the highest enzyme activity and the largest dynamic range (0.1-15 mM), but suffers from a distinct decrease in sensitivity upon prolonged use. The two-layer configuration has the fastest response time (t90 = 50 s), while the 'powder configuration' provides the best operational lifetime. The storage stability of all configurations exceeds 4 months if stored at 4 degrees C. In an Appendix, equations are derived which describe the response of such sensors, how the effect of varying oxygen supply can be compensated for by making use of two sensors, one sensitive to oxygen only, the other to both oxygen and glucose, and how such sensors can be calibrated using two calibrators only.


Subject(s)
Biosensing Techniques , Glucose/analysis , Oxygen/analysis , Calibration , Glucose Oxidase/metabolism , Hydrogen-Ion Concentration
17.
Fresenius J Anal Chem ; 366(5): 481-7, 2000 Mar.
Article in English | MEDLINE | ID: mdl-11220343

ABSTRACT

A fast responding fiber-optic microsensor for sensing pCO2 in marine sediments with high spatial resolution is presented. The tip diameter varies typically between 20 and 50 microm. In order to make the pH-indicator 8-hydroxypyrene-1,3,6-trisulfonate soluble in the ethyl cellulose matrix, it was lipophilized with tetraoctylammonium as the counterion [HPTS-(TOA)4]. The microsensor was tuned to sense very low levels of dissolved carbon dioxide which are typically present in marine systems. The detection limit is 0.04 hPa pCO2 which corresponds to 60 ppb CO2 of dissolved carbon dioxide. A soluble Teflon derivative with an extraordinarily high gas permeability was chosen as a protective coating to eliminate interferences by ionic species like chloride or pH. Response times of less than 1 min were observed. The performance of the new microsensor is described with respect to reproducibility of the calibration curves, dynamic range, temperature behavior, long term stability and storage stability. The effect of hydrogen sulfide as an interferent, which is frequently present in anaerobic sediment layers, was studied in detail.

18.
Fresenius J Anal Chem ; 368(2-3): 196-202, 2000.
Article in English | MEDLINE | ID: mdl-11220579

ABSTRACT

An optical sensor for the measurement of salinity in seawater has been developed. It is based on a chloride-quenchable fluorescent probe (lucigenin) immobilized on a Nafion film. Two approaches for measuring salinity via chloride concentration are presented. In the first, a change in salinity corresponds to a change in the fluorescence intensity of lucigenin. In the second, the fluorescence intensity information is converted into a phase angle information by adding an inert phosphorescent reference luminophore (a ruthenium complex entrapped in poly(acrylonitrile) beads). Under these conditions, the chloride-dependent fluorescence intensity of lucigenin can be converted into a chloride-dependent fluorescence phase shift which serves as the analytical information. This scheme is referred to as dual lifetime referencing (DLR). The sensor was used to determine the salinity in seawater and brackish water of the North Sea.

19.
Appl Environ Microbiol ; 62(1): 237-43, 1996 Jan.
Article in English | MEDLINE | ID: mdl-16535211

ABSTRACT

We developed a noninvasive rapid fluorimetric method for the investigation of growth of adhering (benthic) phototrophic microorganisms. The technique is based on the sensitive detection of the in vivo fluorescence of chlorophylls chlorophyll a and bacteriochlorophyll a and monitors increases in signal over time as an indicator for growth. The growth fluorimeter uses modulated excitation light of blue-light-emitting diodes and a photodiode as the detector. The light-emitting diodes are mounted geometrically in an aluminum housing for efficient and uniform illumination of the bottoms of the growth containers. The fluorimeter was characterized with respect to detection limit and dynamic range. This system is capable of resolving in vivo chlorophyll a concentrations of 0.5 (mu)g liter(sup-1) in cyanobacteria and 0.03 (mu)g liter(sup-1) in diatoms as well as in vivo bacteriochlorophyll a concentrations in phototrophic bacteria of 0.3 (mu)g liter(sup-1), which points to an extremely high sensitivity compared with that of similar available techniques. Thus, the new fluorimeter allows the determination of growth at extremely low cell densities. The instrument was used successfully to measure the growth of several adhering isolates of the filamentous cyanobacterium Microcoleus chthonoplastes from benthic microbial mats in seawater of different salinities. The data obtained demonstrate broad growth responses for all strains, which thus can be characterized as euryhaline organisms.

20.
Adv Space Res ; 18(4-5): 139-48, 1996.
Article in English | MEDLINE | ID: mdl-11538790

ABSTRACT

The optical oxygen sensor is a novel device for the determination of oxygen in gases or dissolved in liquids. It is based on the measurement principle of fluorescence quenching, which is completely different from that of polarographic oxygen sensors (today the most widespread devices of oxygen detection). The new instrument offers features and advantages, which render it not only a realistic alternative, but, for specific applications, make it superior to existing electrochemical methods. The system is based on low-cost semiconductor devices (light-emitting diodes, photodiodes, low-cost analogue and digital components) and new LED-compatible oxygen-sensitive membranes. The flow cell of the instrument may be thermostatted and the sensor can be calibrated by a simple two-point calibration procedure. The optical oxygen sensor is particularly suitable for measuring dissolved oxygen in respirometry, since no oxygen is consumed by the device and the signal is independent of sample flowrate or stirring speed. Typical fields of application are monitoring of oxygen in ground and drinking water, in process control in bioreactors and in breath gas and blood gas analysis.


Subject(s)
Biosensing Techniques , Fiber Optic Technology/instrumentation , Membranes, Artificial , Oxygen/analysis , Signal Processing, Computer-Assisted/instrumentation , Environmental Monitoring/instrumentation , Equipment Design , Fluorescence , Gases , Polystyrenes/chemistry , Semiconductors , Silicones/chemistry , Technology Transfer , Water
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