- 标题
- 摘要
- 关键词
- 实验方案
- 产品
-
Determination of curcuminoid content in turmeric using fluorescence spectroscopy
摘要： The potential of fluorescence spectroscopy is exploited for the characterization and comparison of different turmeric varieties based on curcuminoids content in turmeric powders. Fluorescence spectra from turmeric powders has been acquired by using excitation wavelengths from 300 to 470 nm with step of 10 nm to investigate the effect of excitation wavelengths on the emission of valuable ingredients for their characterization. Emission spectra revealed that fresh wet turmeric rhizomes show emission bands at 571 nm which is due to curcumin. It is found that main ingredient of turmeric powder is curcumin and best excitation wavelength is 467 nm for its maximum emission intensity. High Pressure Liquid Chromatography (HPLC) was used as alternate standard technique for determination of curcuminoid content in the reference samples. The curcumin content in the commercially available local turmeric brands were also evaluated, one brand showed significant covariance from standard fluorescent spectra of turmeric meaning this particular brand contained minimum curcumin content or have been severely adultered. In the next step the powders were heated at different temperatures from 60 ℃ to 150 ℃ (Normal cooking & frying temperatures) to observe the difference in emission spectra particularly keeping in view the molecular composition and curcuminoid content in turmeric. The results indicate that curcumin content gradually decreases above 90 ℃. Principal component analysis (PCA) has been employed on all the data to statistically differentiate small molecular changes and adulteration by covariance calculations.
关键词： Anti-inflammatory.,Turmeric,Fluorescence emission spectroscopy,Anti-oxidant,Curcumin
更新于2025-09-23 15:22:29
-
New perspective on the fluorescence and sensing mechanism of TNP chemosensor 2-(4,5-bis(4-chlorophenyl)-1H-imidazol-2-yl)-4-chlorolphenol
摘要： For TNP chemosensor 2-(4,5-Bis(4-Chlorophenyl)-1H-Imidazol-2-yl)-4-Chlorolphenol (HPICI), previous thought with no theoretical basis was that excited-state intramolecular proton transfer (ESIPT) process and the ground-state HPICI-TNP complex are mainly responsible for its fluorescence emission and the detection of TNP. However, this interpretation has been proved to be wrong by the present theoretical DFT/TDDFT explorations. Actually, the strong fluorescence of HPICI is mainly induced by the local excitation of the enol form HPICI(E) without ESIPT, and the fluorescence quenching by TNP is due to the photo-induced electron transfer (PET) process together with the cooperative effect of hydrogen-bonding interaction and π-π stacking interaction coexisting in the HPICI-TNP complex. The strengthened excited-state hydrogen bond promotes the PET process, thus facilitates the fluorescence quenching. This mechanism is proposed on the basis of the theoretical analyses on molecule geometry, binding energy, Gibbs free energy, electronic transitions, and frontier molecular orbitals (FMOs).
关键词： Fluorescence emission,Fluorescence quenching,Photo-induced electron transfer,Hydrogen-bonding interaction,Dynamical sensing mechanism,π-π stacking interaction
更新于2025-09-19 17:15:36
-
Fluorescence coupled with electrochemical approach at the bulk and the interface region of hydrogen-bonding self assemblies of urea derivatives with DDP dye in aqueous solution
摘要： Photophysical and electrochemical techniques were employed to hydrogen-bonding self assemblies forming solutes (Urea, Dimethylurea and Tetramethylurea) in the presence of 4-dicyanomethylene 2, 6-dimethyl-4H-pyran (DDP) dye. Addition of urea derivatives to DDP dye (Intramolecular Charge Transfer (ICT)) results in a fluorescence enhancement accompanied with a significant shift. Fluorescence lifetime behavior exhibits a tri-exponential decay with a large variation in the fluorescence lifetime and relative amplitude distribution. The co-existence of three different fluorescence lifetime components of DDP with urea derivatives signifies the existence of heterogeneous micro environment. The dye is surrounded by varying proportion of solute and water molecules are established from fluorescence lifetime studies. Urea derivatives govern the excited state characteristics of DDP dye resulting in the formation and promotion of different microenvironment which are clearly distinguishable. The existence of multi environment attributed to urea-water structural behaviour is authenticated by electrochemical impedance spectral studies (EIS). A large variation in the contour pattern, shape and intensity in 3D fluorescence contour spectra of dye with urea validate the existence of dye in a heterogeneous micro environment. The hydrophobicity of urea derivatives along with the hydrogen-bonding properties of urea-water and urea-urea influence the photophysical and electrochemical nature of dye is emphasized.
关键词： Hydrogen-bonding,Urea derivatives,Fluorescence lifetime,Electrochemical impedance spectra,Fluorescence emission,DDP dye
更新于2025-09-12 10:27:22
-
[IEEE 2019 Conference on Lasers and Electro-Optics Europe & European Quantum Electronics Conference (CLEO/Europe-EQEC) - Munich, Germany (2019.6.23-2019.6.27)] 2019 Conference on Lasers and Electro-Optics Europe & European Quantum Electronics Conference (CLEO/Europe-EQEC) - Anisotropic Fluorescence Emission at the Surface of 1D-Photonic Crystal Biochips
摘要： Novel disposable optical biochips based on one-dimensional photonic crystals (1DPC) sustaining Bloch surface waves (BSW) are a desirable tool for the detection of several disease-related biomarkers. In particular, cancer biomarkers have gained considerable attention, due to the increasing demand for cancer treatment. Within this framework, the herein proposed optical biochips can quantify low concentration (sub ng/mL) of the ERBB2 breast cancer biomarker in biological complex matrices. To discriminate ERBB2 levels in several different cell lysate samples, we made use of a biosensing platform based on 1DPC biochips and on a reading instrument that can work in both a label-free and a fluorescence detection mode. Such combined configuration provides the advantage of complementary information and lower limit of detection (LoD) in the fluorescence mode [1]. In the label-free configuration the BSW excitation is achieved by a prism coupling system (Kretschmann-Raether configuration), like in the surface plasmon resonance (SPR) technique, resulting in a dip in the angular reflectance spectrum, shifting its position due to the refractive index changes [2]. The fluorescence mode is carried out by making use of dye labeled antibodies bound at the 1DPC surface. Coupling between the dye labels and a BSW results in strongly directional fluorescence emission. The advantages brought by the 1DPC, when compared to metal structures, are smaller energy dissipation and narrower resonances [3]. Presently, there is no study about photobleaching in experiments with BSW sustained by 1DPC, while it is evident that such phenomenon cannot be neglected in biosensing assays carried out close to the LoD, where quantitative and accurate information is needed. Here we report for the first time on cancer detection assays carried out with our platform, in which the trustworthiness of the output is put in doubt by photobleaching, which not only affects the overall emission intensity but also its polarization distribution via the TE and TM BSW modes provided by the 1DPC. The experimental data is interpreted by means of a theoretical model for the orientational distribution of dye labels over time, taking into account the density of the optical states of the 1DPC, photobleaching and rotational diffusion of surface bound emitters. The approach permits to model anisotropic fluorescence emission and to manage photobleaching effects in biosensing assays, leading to their correct interpretation.
关键词： one-dimensional photonic crystals,optical biochips,Bloch surface waves,cancer biomarkers,fluorescence emission,photobleaching
更新于2025-09-12 10:27:22
-
Spectral Reshaping of Single Dye Molecules Coupled to Single Plasmonic Nanoparticles
摘要： Fluorescent molecules are highly susceptible to their local environment. Thus, a fluorescent molecule near a plasmonic nanoparticle can experience changes in local electric field and local density of states that reshape its intrinsic emission spectrum. By avoiding ensemble averaging while simultaneously measuring the super-resolved position of the fluorophore and its emission spectrum, single-molecule hyperspectral imaging is uniquely suited to differentiate changes in spectrum from heterogeneous ensemble effects. Thus, we uncover for the first time single-molecule fluorescence emission spectrum reshaping upon near-field coupling to individual gold nanoparticles using hyperspectral super-resolution fluorescence imaging, and we resolve this spectral reshaping as a function of the nanoparticle/dye spectral overlap and separation distance. We find dyes bluer than the plasmon resonance maximum are red-shifted and redder dyes are blue-shifted. The primary vibronic peak transition probabilities shift to favor secondary vibronic peaks, leading to effective emission maxima shifts in excess of 50 nm, and we understand these light-matter interactions by combining super-resolution hyperspectral imaging and full-field electromagnetic simulations.
关键词： Plasmonic nanoparticles,Single-molecule hyperspectral imaging,Optoelectronics,Energy Conversion and Storage,Fluorescence emission spectrum reshaping,Plasmonics
更新于2025-09-11 14:15:04
-
Laser-Induced Fluorescence Emission (L.I.F.E.) as Novel Non-Invasive Tool for In-Situ Measurements of Biomarkers in Cryospheric Habitats
摘要： Global warming affects microbial communities in a variety of ecosystems, especially cryospheric habitats. However, little is known about microbial-mediated carbon fluxes in extreme environments. Hence, the methodology of sample acquisition described in the very few studies available implies two major problems: A) high resolution data require a large number of samples, which is difficult to obtain in remote areas; B) unavoidable sample manipulation such as cutting, sawing, and melting of ice cores that leads to a misunderstanding of in situ conditions. In this study, a prototype device that requires neither sample preparation nor sample destruction is presented. The device can be used for in situ measurements with a high spectral and spatial resolution in terrestrial and ice ecosystems and is based on the Laser-Induced Fluorescence Emission (L.I.F.E.) technique. Photoautotrophic supraglacial communities can be identified by the detection of L.I.F.E. signatures in photopigments. The L.I.F.E. instrument calibration for the porphyrin derivates chlorophylla (chla) (405 nm laser excitation) and B-phycoerythrin (B-PE) (532 nm laser excitation) is demonstrated. For the validation of this methodology, L.I.F.E. data were ratified by a conventional method for chla quantification that involved pigment extraction and subsequent absorption spectroscopy. The prototype applicability in the field was proven in extreme polar environments. Further testing on terrestrial habitats took place during Mars analog simulations in the Moroccan dessert and on an Austrian rock glacier. The L.I.F.E. instrument enables high resolution scans of large areas with acceptable operation logistics and contributes to a better understanding of the ecological potential of supraglacial communities in the context of global change.
关键词： chlorophyll,glacial melt,laser-induced fluorescence emission (L.I.F.E.),ice,cryospheric habitats,phycoerythrin,non-invasive
更新于2025-09-11 14:15:04
-
Computational Investigations about the Ground and Excited States?￠????Properties of Trans-4-N,N-Dimethylamino-4?￠????-Nitro-Stilbene (DNS) and Trans-4-N,N-Dimethyl-Amino-4?￠????-Cyanostilbene (DCS) Derivatives
摘要： The ground and lowest-lying singlet excited state geometries and dipole moments of trans-4-N,N-dimethylamino-4’-nitro-stilbene (DNS) derivative and the trans-4-N,N-dimethyl-amino-4’-cyanostilbene (DCS) derivative are calculated at the B3LYP level of theory for the first time in this work. The vertical excitation energies and the fluorescence emission energies are obtained for the two species. The calculated results are compared with available experimental results and show good consistency. The molecular orbital analyses in these molecules have been performed. The comparison of the atomic charge distributions in the ground and excited states of both the DNS derivative and DCS derivative implies the intra molecular charge transfer (ICT) process during the excitation period.
关键词： Ground state,Excitation energy,Fluorescence emission,Molecular orbital,Charge transfer
更新于2025-09-10 09:29:36
-
Regioisomeric synthesis of chlorin-e6 dimethyl esters and their optical properties
摘要： Chlorin-e6 dimethyl esters possessing a single carboxy group at the 13-, 151-, or 172-position were prepared by chemically modifying chlorophyll-a. These three synthetic regioisomers were fully characterized by their mass, NMR, and visible absorption spectra. Their molecular structures were unambiguously identified by the specific 1H–13C correlation at the 13-, 15-, and/or 17-substituents in their respective HMBC spectra. Methyl esterification of 13/151-COOH and hydrolysis of 13/151-COOMe affected small shifts of the Qy absorption and fluorescence emission maxima in a diluted CH2Cl2 solution, while no substitution effect of 172-COOH/Me was observed.
关键词： fluorescence emission,ester protection,Qy absorption,retro-Dieckmann condensation,chlorophyll-a derivative
更新于2025-09-09 09:28:46