Joseph Kimball

ORCID: 0000-0001-5869-4883
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About
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Research Areas
  • Luminescence and Fluorescent Materials
  • Advanced Fluorescence Microscopy Techniques
  • Analytical Chemistry and Sensors
  • Molecular Sensors and Ion Detection
  • Porphyrin and Phthalocyanine Chemistry
  • Photochemistry and Electron Transfer Studies
  • Protein Interaction Studies and Fluorescence Analysis
  • Nanoplatforms for cancer theranostics
  • Advanced biosensing and bioanalysis techniques
  • Advanced X-ray and CT Imaging
  • Diamond and Carbon-based Materials Research
  • Medical Imaging Techniques and Applications
  • Advanced Biosensing Techniques and Applications
  • Advanced Surface Polishing Techniques
  • Photodynamic Therapy Research Studies
  • Supramolecular Chemistry and Complexes
  • Biosensors and Analytical Detection
  • Electron Spin Resonance Studies
  • Advanced Optical Sensing Technologies
  • Ionic liquids properties and applications
  • Optical Imaging and Spectroscopy Techniques
  • Integrated Circuits and Semiconductor Failure Analysis
  • Organic Light-Emitting Diodes Research
  • Photoreceptor and optogenetics research
  • Spectroscopy Techniques in Biomedical and Chemical Research

Texas Christian University
2014-2024

Fort Worth Library
2014-2016

Fluorescence properties of a novel homodimeric BODIPY dye rotor for Lifetime Imaging Microscopy (FLIM) are reported.

10.1039/c4cp04260c article EN cc-by Physical Chemistry Chemical Physics 2014-01-01

Fluorescence technologies have been the preferred method for detection, analytical sensing, medical diagnostics, biotechnology, imaging, and gene expression many years. becomes essential studying molecular processes with high specificity sensitivity through a variety of biological processes. A significant problem practical fluorescence applications is apparent non-linearity intensity resulting from inner-filter effects, sample scattering, absorption intrinsic components samples. Sample can...

10.1088/2050-6120/ab947c article EN Methods and Applications in Fluorescence 2020-05-19

Abstract Fluorescence is an established technology for studying molecular processes and interactions. More recently fluorescence became a leading method detection, sensing, medical diagnostics, biotechnology, imaging, DNA analysis, gene expression. Consequently, precise accurate measurements in various conditions have become more critical proper result interpretations. Previously, Part 1, we discussed inner filter effect type I, which consequence of the instrumental geometrical sensitivity...

10.1088/2050-6120/ac0243 article EN Methods and Applications in Fluorescence 2021-05-17

Photophysical behaviour of a novel trimeric BODIPY rotor with high extinction coefficient is reported. Steady state and time resolved fluorescence measurements established that the trimer could be used as viscometer for molecular solvents, membrane-like environments several cancer cell lines.

10.1039/c5cp07214j article EN cc-by Physical Chemistry Chemical Physics 2016-01-01

The fluorescent lifetimes of the BODIPY–BODIPY dyad appear to correlate with viscosity media, thus making this rotor a suitable small molecule viscometer.

10.1039/c4ra09757b article EN cc-by RSC Advances 2015-01-01

Structure of the cationic and anionic counterparts ionic liquids has a significant impact on conformational bias porphyrin rotor; an apparent correlation between conformation viscosity was noted, albeit it found to be distinct more complex from that in molecular solvents.

10.1039/c3ra43001d article EN cc-by RSC Advances 2013-01-01

We studied room temperature phosphorescence of tryptophan (TRP) embedded in poly (vinyl alcohol) films. With UV (285 nm) excitation, the spectrum appears at about 460 nm. also observed TRP with blue light excitation 410 nm, well outside S0→S1absorption. This reaches triplet state directly without involvement singlet excited state. The lifetime is sub-millisecond range. long-wavelength direct to results high anisotropy which can be useful macromolecule dynamics study via time-resolved phosphorescence.

10.1088/2050-6120/ac4c9a article EN Methods and Applications in Fluorescence 2022-01-18

The signal-to-background ratio is the limiting factor for fluorescence based detection, sensing, and imaging. A typical background signal will include direct scattering of excitation Raman sample as well autofluorescence from additives. To improve ratio, fluorophores high brightness and/or concentration need to be used. Most instantaneous short-lived (picosecond nanosecond time scale), using long-lived probes combined with time-gated detection allows significant suppression unwanted...

10.1088/2050-6120/2/2/024009 article EN Methods and Applications in Fluorescence 2014-05-14

We report the spectral properties of 2-Phenylindole (2PI) embedded in rigid poly (vinyl alcohol) (PVA) film. The 2PI PVA film shows relatively strong and structured fluorescence with a maximum at 370 nm surprisingly room temperature phosphorescence an emission about 500 nm. dye is highly immobilized polymer matrix, thus presenting high anisotropy isotropic 0.3 temperature. excited usual way through electronic singlet state excitation (S0 → S1 absorption) results very low, near zero...

10.1088/2050-6120/ab6366 article EN Methods and Applications in Fluorescence 2019-12-18

Fluorescence signal enhancement induced by the binding of intercalators to DNA has been broadly utilized in various detection methods. In most instances increase fluorescence intensity is associated with a concomitant lifetime. This lifetime presents an additional opportunity sensitivity. this paper, we present new approach significantly enhance sensitivity detecting minute concentrations. The based on simultaneous use time-gated and multi-pulse pumping. By using calibrated burst short...

10.1039/c8an00136g article EN The Analyst 2018-01-01

This article presents a novel approach to increase the detection sensitivity of trace amounts DNA in sample by employing Förster resonance energy transfer (FRET) between intercalating dyes. Two intercalators that present efficient FRET were used enhance and improve specificity detecting minute DNA. Comparison steady-state acceptor emission spectra with without donor allows for simple specific (acceptor bound DNA) down 100 pg/μL. When utilizing as an dye significantly longer lifetime (e.g.,...

10.1021/acs.analchem.1c05275 article EN Analytical Chemistry 2022-03-14

We present a comprehensive spectroscopic study supported by theoretical quantum chemical calculations conducted on molecular system (4-(5-methyl-1,3,4-thiadiazol-2-yl)benzene-1,3-diol (C1) and the antibiotic Amphotericin B (AmB)) that exhibits highly synergistic properties. previously reported strong synergism of this now wish to related stationary measurements UV-Vis absorption, fluorescence, fluorescence anisotropy in polar, aprotic solvent (DMSO PBS buffer), followed time-resolved...

10.1038/s41598-024-83180-2 article EN cc-by-nc-nd Scientific Reports 2024-12-30

Although BSA Au clusters fluoresce in red region (λmax: 650nm), they are of limited use due to low fluorescence quantum yield (~6%). Here we report an enhanced imaging application fluorescent bio-nano probe using multipulse excitation scheme. Multipulse takes advantage long lifetime (> 1µs) and enhances its intensity 15 times over short lived cellular auto-fluorescence. Moreover have also shown that by time gated detection strategy signal (fluorescence clusters) noise (auto-fluorescence)...

10.2174/1389201015666140523161038 article EN Current Pharmaceutical Biotechnology 2014-06-01
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