Fluorescence Quantum Efficiency Research Articles

Near-infrared voltage-sensitive dyes based on chromene donor

Voltage-sensitive dyes (VSDs) are used to image electrical activity in cells and tissues with submillisecond time resolution. Most of these fast sensors are constructed from push-pull chromophores whose fluorescence spectra are modulated by the electric field across the cell membrane. It was found that the substitution of naphthalene with chromene produces a 60 to 80 nm red-shift in absorption and emission spectra while maintaining fluorescence quantum efficiency and voltage sensitivity. One dye was applied to ex vivo murine heart with excitation at 730 nm, by far the longest wavelength reported in voltage imaging. This VSD resolves cardiac action potentials in single trials with 12% ΔF/F per action potential. The well-separated excitation spectra between these long-wavelength VSDs and channelrhodopsin (ChR2) enabled monitoring of action potential propagation in ChR2 hearts without any perturbation of electrical dynamics. Importantly, by employing spatially localized optogenetic manipulation, action potential dynamics can be assessed in an all-optical fashion with no artifact related to optical cross-talk between the reporter and actuator. These new environmentally sensitive chromene-based chromophores are also likely to have applications outside voltage imaging.

Spectral properties and theoretical analysis of Dy3+:KGd(WO4)2 crystals in the visible wavelength band

Yellow laser has been widely applied in various fields such as biomedicine, optical communication technology and chip processing. This study focuses on the preparation and characterization of a 3 at.% Dy3+:KGd(WO4)2 crystal. The crystal was grown by the top-seeded solution growth method. The absorption spectrum, excitation spectrum, emission spectrum, and fluorescence decay curve were measured at room temperature, and the fluorescence properties of the crystal in the yellow region were explored. Analysis of the absorption spectrum revealed an absorption cross-section σabs of 4.81 × 10−21 cm2 at 453 nm (E//Y), corresponding to the 6H15/2 → 4I15/2 transition. Utilizing the Judd-Ofelt theory, the J-O intensity parameters Ωt, radiative transition probability, fluorescence branching ratio, and radiative lifetime were calculated. The F-L theory was used to calculate the emission cross-section σem at 575 nm (E//Y), which was found to be 2.43 × 10−20 cm2, along with a fluorescence lifetime τf of 148.5 μs and a fluorescence quantum efficiency of 80.35% for 4F9/2. These findings suggest that Dy3+:KGd(WO4)2 crystal shows significant promise as a yellow laser material, with the potential to contribute to both commercial and scientific fields.

Fluorescence Quantum Efficiency Enhancement in Size-Controlled 3.5 Monolayer Cadmium Telluride Nanoplatelets

Fluorescence Quantum Efficiency Enhancement in Size-Controlled 3.5 Monolayer Cadmium Telluride Nanoplatelets

Synthesis, Structure, and Properties of Monodispersed and Highly Luminescent Organoborane Oligomers.

Organoborane oligomers with well-defined molecular structures and high luminescence are scarce, among which those with boron not used as bridging atoms are even more so. Here, a series of well-defined ethynyl-linked or butadiynyl-linked conjugated organoborane oligomers with high fluorescence quantum yield and extinction coefficient (i.e., high brightness) were prepared by coupling different building blocks featuring dithienooxadiborepine moieties. Single crystal structures of hexyl modified dithienooxadiborepine (1a-hex) and hexyl-modified butadiynyl-linked conjugated dimer (D2-hex) not only verified the identity of the molecular structures but also revealed that the introduction of the hexyl chains distorted the molecular structures due to steric hindrance. Optical measurements showed that the absorption and emission maxima of the six oligomeric molecules bathochromic shifted with increasing numbers of repeating units. Molecules without hexyl chains emit efficient fluorescence upon photoexcitation, and the fluorescence quantum efficiency of the ethynyl-linked conjugated dimer (D1) is close to unity. Theoretical calculation results using density functional theory methods are consistent with the single crystal data, allowing a better understanding of the spectral properties. Such results indicate that the method is efficient for expanding small organoborane molecules into π-conjugated oligomers, which can be used to modulate to emit different colors with high efficiency.

Highly bright stable organic radicals encapsulated by amphiphilic polypeptide for efficient near-infrared phototheranostics

Stable organic radical molecules have received extensive attention due to their unique electronic structure and photophysical properties, and the highly fluorescent quantum efficiency has great appeal to bioimaging. However, still scarce reports on the application of them on the therapy of tumors, especially theranostics. Here, 3,6-dibromocarbazole modified tris (2,4,6-trichlorophenyl) methane radical (TB) has been synthesized with high NIR fluorescence quantum efficiency, and free radical nanoparticles (NPs) have been prepared using the precursor of the radical doping strategy. The free radical molecule TB and its precursor molecule HTB were mixed in proportion and encapsulated with an amphiphilic polypeptide (PEG-PAsp) to obtain the NPs. The 4% NPs can achieve a high fluorescence quantum efficiency (18.68%) in the NIR region. In addition, the NPs also have a good ability to produce reactive oxygen species (ROS) under either normoxia or hypoxia conditions, which makes it possible for photodynamic therapy (PDT). Interestingly, the NPs also show preferable photothermal ability (PCE = 42.39%) for photothermal therapy (PTT). Both in vitro and in vivo studies reveal that the as-prepared radical NPS show a NIR fluorescence imaging-guided synergistic PTT and type I/II PDT to tumors. It provides new strategies and new clues for the application of free radical molecules in the theranostics of tumors.

Optical property and Judd-Ofelt analysis of Dy3+, Na+:PbGa2S4 crystal grown by Bridgman method

In this research, the high quality Dy3+, Na+:PbGa2S4 single crystal was grown by Bridgman method. The crystal devices with high transmittance were successfully processed. The crystal structure and crystallization property were characterized by the XRD and XRC patterns. The transmission spectrum, temperature-dependent emission spectrum from 77 K to 350 K and decay curves at room temperature of crystal were measured. The strong absorption at 1315 nm of 6H15/2 → 6F11/2+6H9/2 transition could match well with high power 1310 nm semiconductor laser. The spectroscopic parameters were calculated by Judd-Ofelt theory based on the absorption spectra. The fluorescence lifetime of 6H11/2 energy level was fitted to be 2.09 ms and the corresponding fluorescence quantum efficiency η was calculated to be 77%. The emission cross-section at 4325 nm of 6H11/2 → 6H13/2 transition was also calculated to be 0.9 × 10−20 cm2. The experiment results show the advantage of Dy3+, Na+:PbGa2S4 crystal in emitting mid-infrared lasers.

The Introduction of Different Types of OLEDs

As display technology advances, organic light emitting diodes (OLEDs) have attracted a lot of attention worldwide due to their light weight, flexibility, wide viewing angle, etc. This paper briefly introduces the history and the different historical OLEDs, including phosphorescence, thermally activated delayed fluorescence (TADF), and triplet-triplet annihilation (TTA). Then, this article mainly presents two kinds of OLEDs. The first is small-molecule OLED with typical three organic layers. The purity of the material is quite high, and it can produce high-quality films with high fluorescence quantum efficiency, which can produce a variety of colors of light. Its disadvantages are poor thermal stability and limited carrier transport capacity. The second is polymer based OLED. Compared with small molecule organic luminescence materials, polymer materials have higher physical strength, better processibility, mechanical properties, and thermal stability. In this regard, recent research progress and the comparison between these two types of OLEDs are proposed. They both are considered the most promising display technologies.

Side-chain engineering of highly efficient solid-state red fluorophore based on diaminoterephthalate with steric ortho-substituents

A series of 2,5-diaminoterephthalate-based fluorophores (Me, Et, iPr, and tBu) with steric ortho-substituents were designed and synthesized. There is an optical changing tendency of the four crystals with distinct red-shifted emissions. The crystal characteristics suggest that the enhanced anti-aromaticity of the central benzene rings of four compounds in the ground state might be an important reason for achieving long-wavelength fluorescence emission, which matches well with the changing tendency of C–N bond lengths. Moreover, all compounds exhibit highly efficient solid-state emission with fluorescence quantum efficiency reaching up to 69%.

Mitigation of Salinity Stress on Soybean Seedlings Using Indole Acetic Acid-Producing Acinetobacter pittii YNA40

Soybean is an important oil crop with multiple uses. Soybeans can grow in various soil types and climates; however, salt stress reduces their yield. Plant growth-promoting microorganisms are an environmentally benign way to combat stress and boost plant tolerance. In the present study, we have identified plant growth-promoting bacteria that can produce indole acetic acid (IAA) and induce distinct growth characteristics in soybean plants under salt stress. The YNA40 isolate was identified as Acinetobacter pittii through 16S rRNA sequencing and phylogenetic analysis. A pure culture of Acinetobacter pittii YNA40 was subjected to chromatographic and mass spectrometry selected-ion monitoring (GC-MS/SIM) for IAA quantification. The results revealed that the YNA40 bacterial strain showed a significantly higher IAA concentration (473.88 ng/mL) at 4% sodium chloride (NaCl). Moreover, in a salt-stress condition, inoculation with Acinetobacter pittii YNA40 was able to induce increased shoot length (23.48%), shoot weight (24%), root length (2.47%), and root weight (44.82%) compared to the uninoculated control. Therefore, soybean seedlings were inoculated with YNA40 to examine their potential for promoting growth and reprogramming after salt stress. Inoculation with YNA40 isolates mitigated the salt stress and significantly improved the growth of the plant, enhanced the chlorophyll contents, and improved the quantum efficiency of chlorophyll fluorescence, total phenolic content, flavonoid content, the diphenyl-1-picrylhydrazyl (DPPH) activity, and antioxidant activities of soybean plants during and after salt stress. The present research demonstrated that the application of the YNA40 isolate is promising for reducing salt stress in soybean plants and helps plants grow better in a salt-stressed environment.

Effect of shortened alkyl chain on photothermal properties of D-A-D conjugated small molecules

Through the study of the molecular formula of p1-AQM2AF, it is found that 9-methylenedecane, as the electron donor system, has strong electron donor capacity, but due to its huge steric hindrance, the p1-AQM2AF molecule may be seriously distorted, resulting in the reduction of the fluorescence quantum efficiency of p1-AQM2AF due to the angular momentum energy loss during the electron transmission process. Therefore, we have made a bold guess, The length of alkyl chain may also be one of the factors affecting the fluorescence efficiency of D-A-D conjugated small molecules. We converted the 9-methylene-19decane originally attached to the molecule into 3-methylenenonane, and explored its influence on the fluorescence molecule by reducing the length of the donor alkyl chain.

Physiological and Biochemical Changes in Soybean Plants Caused by Iodine-Selenium Chelates and Phytopathogenic Bacteria

The search for effective and environmentally sound measures to fight against plant diseases caused by phytopathogenic microorganisms is of great importance. It is especially important to investigate alternative measures to protect cultivated plants that combine elements beneficial to human health such as iodine and selenium. Purpose. The study of physiological and biochemical changes in soybean leaves after artificial inoculation of plants with different strains of phytopathogenic bacteria on the background of pre-sowing treatment of seeds with a solution of iodine-selenium (I-Se) chelates. Methods. Soybean plants of the Artemis variety were grown in field conditions. Before sowing, the seeds were treated with a 1% I-Se chelated solution (I — 80 mg/L and Se citrate — 0.05 mg/L). The experimental plants were inoculated with phytopathogenic bacteria from the microbiological collection of the Zabolotny Institute of Microbiology and Virology of the National Academy of Sciences, namely Pseudomonas savastanoi pv. glycinea IMВ B-9190, P. agglomerans IMВ B-9185, and P. syringae pv. syringae IMВ B-8531. The contents of chlorophyll-a, b and carotenoids in the leaves were determined by extraction in DMSO followed by spectrophotometry. Catalase activity was determined by the method of titrimetric permanganatometry with a 0.01M solution of KMnO4, the activity to non-specific peroxidases — according to Boyarkin’s method. Evaluation of the photochemical activity of photosynthesis according to the parameters F0, Fv/Fm, and RFd was carried out by the method of induction of chlorophyll fluorescence using a portable device «Floratest». Statistical processing of experimental data was carried out using the built-in functions of the Microsoft Excel program. Results. The increase of peroxidase activity of leaves was revealed after both pre-sowing treatment with 1% I-Se solution of intact plants and inoculation of them with different strains of bacterial pathogens in the following order: I-Se > I-Se+P. syringae pv. syringae 8531 > I-Se+P. agglomerans 9185 > I-Se+P. savastanoi pv. glycinea 9190. The catalase activity of leaves tissues increased only when infected with a specific pathogen P. savastanoi pv. glycinea 9190 (by 20.6%). After artificial inoculation with strains of both specific and facultative bacterial pathogens and the pre-sowing treatment with I-Se, there was observed an increase in the quantum efficiency of PSII (Fv /Fm) and fluorescence in decline index (Rfd). An increase in the content of chlorophyll-a (by 18%), b and carotenoids (by 7%) in the leaves after the pre-sowing treatment with I-Se has been shown. The content of chlorophyll-a in soybean leaves due to pre-sowing treatment with I-Se had the most significant increase after inoculation of P. agglomerans 9185 (20%). Due to the inoculation with a specific pathogen P. savastanoi pv. glycinea 9190 (after the pre-sowing treatment with I-Se), the content of chlorophyll-a tended to decrease, and the content of chlorophyll-b decreased by 7%. The carotenoid content in leaves increased significantly at inoculation of plant with facultative pathogens: P. agglomerans 9185 (by 28.2%) and P. savastanoi pv. syringae 8531 (by 20.7%). The chlorophyll a/b ratio increased in all experimental variants. Conclusions. 1. It was found that pre-sowing seed treatment with 1% I-Se chelated solution results in increasing disease resistance in nonspecific adult soybean plants, including increasing their thermotolerance. This is evidenced by increasing the peroxidase activity of leaves and the content of photosynthetic pigments in natural conditions: chlorophyll-a and carotenoids. 2. Inoculation of soybean plants with a specific pathogen causes an increase in catalase and peroxidase activities in leaves. The significant increase in peroxidase activity after plant inoculation with facultative pathogens was shown. 3. A significant increase in the content of chlorophyll-a in soybean leaves after inoculation with P. agglomerans 9185 and pre-sowing treatment with I-Se was observed. The significant reduction of chlorophyll-b in leaves due to the inoculation of plants with P. savastanoi pv. glycinea 9190 and pre-sowing treatment of the seeds with I-Se was shown. The most significant increase in the content of carotenoids in leaves was detected after inoculation of plants with facultative pathogens — P. agglomerans 9185 and P. syringae pv. syringae 8531. 4. Significant stimulation of both maximum quantum yield of PSII photochemistry (Fv /Fm) and the rate of carbon assimilation (Rfd) due to the pre-sowing seed treatment with I-Se and inoculation of plants with different strains of phytopathogens was observed. It resulted from the activation of antioxidant systems and increased need for assimilates due to changes in plant metabolism.

Amplified Spontaneous Emission and Lasing from Zn-Processed AgIn5S8 Core/Shell Quantum Dots

I-III-VI ternary quantum dots (QDs) have emerged as favorable alternatives to the toxic II-VI QDs for optoelectronic and biological applications. However, their use as optical gain media for microlasers is still limited by a low fluorescence efficiency. Here, we demonstrate amplified spontaneous emission (ASE) and lasing from colloidal QDs of Zn-processed AgIn5S8 (AIS) for the first time. The passivation treatment on the AIS QDs yields a 3.4-fold enhancement of fluorescence quantum efficiency and a 30% increase in the two-photon absorption cross section. ASE is achieved from the AIS/ZnS core/shell QD films under both one- and two-photon pumping with a threshold fluence of ∼84.5 μJ/cm2 and 3.1 mJ/cm2, respectively. These thresholds are comparable to the best optical gain performance of Cd based-QDs reported in the literature. Moreover, we demonstrate a facile whispering-gallery-mode microlaser of the core/shell QDs with a lasing threshold of ∼233 μJ/cm2. The passivated AIS QDs can be promising optical gain media for photonic applications.

Self-Assembled BODIPY Nanoparticles for Near-Infrared Fluorescence Bioimaging

In vivo optical imaging is an important application value in disease diagnosis. However, near-infrared nanoprobes with excellent luminescent properties are still scarce. Herein, two boron-dipyrromethene (BODIPY) molecules (BDP-A and BDP-B) were designed and synthesized. The BODIPY emission was tuned to the near-infrared (NIR) region by regulating the electron-donating ability of the substituents on its core structure. In addition, the introduction of polyethylene glycol (PEG) chains on BODIPY enabled the formation of self-assembled nanoparticles (NPs) to form optical nanoprobes. The self-assembled BODIPY NPs present several advantages, including NIR emission, large Stokes shifts, and high fluorescence quantum efficiency, which can increase water dispersibility and signal-to-noise ratio to decrease the interference by the biological background fluorescence. The in vitro studies revealed that these NPs can enter tumor cells and illuminate the cytoplasm through fluorescence imaging. Then, BDP-B NPs were selected for use in vivo imaging due to their unique NIR emission. BDP-B was enriched in the tumor and effectively illuminated it via an enhanced penetrability and retention effect (EPR) after being injected into the tail vein of mice. The organic nanoparticles were metabolized through the liver and kidney. Thus, the BODIPY-based nanomicelles with NIR fluorescence emission provide an effective research basis for the development of optical nanoprobes in vivo.

Finite element analysis on the near field properties of metallic cavities with atomic sharpness

Using finite element calculations, we investigated the near field properties of two types of commonly used metal nanostructures (a tip-substrate model representing a scanning tunneling microscope type setup (TS) and a nanoparticle-on-mirror (NPoM) configuration) with atomic sharpness and extreme focusing capabilities. The spatial confinement and electric field enhancement of the local field as well as the fluorescence quantum efficiency of a model molecule (as represented by an oscillating dipole) in the cavity region of the two models were systematically studied. It was found that the TS model tends to support higher local electric field enhancement while the NPoM model can provide a more localized plasmon electric field near the nanoparticle. Calculations with the radiating model molecule indicate that both TS and NPoM can cause significant enhancements to the non-radiative decay rates at the order of 106 in the wavelength range of 500–1000 nm. The TS model shows better performance for the radiative enhancements and the resulting emission quantum yield. These results are not only helpful to improve the understanding of such important nanocavities but also supply a reference for their further applications in different areas.

Highly Efficient Blue Electro‐Fluorescence and Hybrid White Electroluminescence Basing on a Novel Hybrid Local and Charge‐Transfer (HLCT) Material with Weak Donor–Acceptor Structure and High Carrier Mobilities

AbstractHigh efficiency and luminance are critical for commercialized blue organic light‐emitting diodes (OLEDs). Herein, a novel donor–acceptor (D–A) blue‐emissive molecule with a weak donor and acceptor is synthesized. The moderate hybrid local and charge transfer (HLCT) state character endows PPIBPO with blue fluorescence and high quantum efficiency. More importantly, the rigid, rod‐like molecular structure gives rise to the regularity of the stacking pattern of PPIBPO, which enables its extraordinary carrier mobilities in non‐doped OLED, the hole mobility and electron mobility are as high as 5.09 × 10−5 cm2 V−1 s−1 and 3.22 × 10−4 cm2 V−1 s−1, respectively. The non‐doped blue OLED of PPIBPO achieves a maximum external quantum efficiency (EQE) of 12.0% and a maximum luminance of 55023 cd m−2, which is one of the best values among the non‐doped blue OLEDs based on HLCT molecules. Furthermore, high‐efficiency two‐color hybrid warm white OLED with a maximum EQE up to 22.5% and maximum power efficiency of 87.0 lm W−1 is also achieved using PPIBPO as blue‐fluorophor.

Near infrared voltage sensitive dyes based on chromene electron donors.

Excellent hemicyanine voltage sensitive dyes (VSDs) are available for optical electrophysiology over a wide spectral range out to the far red. Near infrared fluorescent VSDs would be advantageous because they allow deeper light penetration into tissue because of decreased light scattering and also because they can be used in combination with other fluorescent indicators or optogenetic actuators. The usual approach to constructing long wavelength chromophores is to lengthen the π-system; however, this is generally accompanied by a significant decrease in fluorescence quantum efficiency and can also decrease aqueous solubility, making it difficult to deliver the probes to the target tissue. The VSDs developed in our lab are generally composed of an amino-naphthyl electron donor moiety linked to a pyridinium acceptor. Here we show that replacing the naphthalene with chromene induces a 60-80 nm red-shift in the absorption and emission spectra while maintaining the structure at the same size and fluorescence quantum yield at the same level. The voltage sensitivity of these chromene-based VSDs is also comparable to our older VSDs and they display opposite polarity sensitivity when excited at the short and long wavelength edges of the absorbance spectra; thus they can be used in dual wavelength ratio measurements to eliminate artifacts from motion and bleaching. We have tested one of these VSDs in voltage imaging of a whole murine heart at 730 nm, by far the longest wavelength reported in voltage imaging. It resolves action potentials in single sweep scans with 10.1% ΔF/F per action potential. Chromene-based electron donors are likely to find wide applications in generating long wavelength hemicyanines or cyanines. (Supported by NIH grant MH116830. Conflict of Interest statement: LML, CDA, and PY are founders and owners of Potentiometric Probes LLC.)

Highly Efficient and Stable Blue OLEDs Based on B—N Bonds Embedded 6,12‐Diphenyl‐5,11‐dihydroindolo[3,2‐b]carbazole with Narrowband Emission and Extended Lifetime†

Comprehensive SummaryEmitters with narrowband spectra are of great importance nowadays because of the growing demand for ultra‐high‐definition displays in the fields of panel displays and solid‐state lighting. Though the reported multiple resonance (MR) emitters have been widely studied with extremely sharp spectra and color‐tunable emissions, the electrophilic borylation synthetic strategies and stable narrowband blue devices still face great challenges. Herein, by virtue of the advantages of both the MR effect of conventional indolocarbazole skeleton and the easy‐to‐access of B—N covalent bonds, the linear tert‐butyl benzene and carbazole groups modified 6,12‐diphenyl‐5,11‐dihydroindolo[3,2‐b]carbazole derivatives (tPh[BN] and Cz[BN]) containing two B—N covalent bonds are easily constructed through amine‐directed double borylation strategy. Both emitters behaved bright blue emission with full‐width‐at‐half‐maximum (FWHM) of 20—27 nm in solution, high fluorescence quantum efficiency over 90%, and excellent stability toward moisture. By employing triplet‐triplet annihilation electroluminescent mechanism, blue OLED devices based on them showed a small FWHM of 48 nm and maximum external quantum efficiency of ~7.1% with negligible efficiency roll‐off, and long operational lifetime (LT80) of 87 h at an initial brightness of 1000 cd·m−2, demonstrating the enormous application potential of B—N bonds embedded emitters in achieving ideal narrowband blue emitters.

FD-1050@NPs-cRGD: A novel NIR-II fluorophore for triple-negative breast cancer imaging

Triple-negative breast cancer (TNBC) is a highly heterogeneous and aggressive disease that is prone to metastasis and recurrence. It accounts for 15–20% of all breast cancer cases. Surgical resection is effective in removing most of the malignant tissues for non-metastasized tumors; however, some residual tumor tissues would be left, leading to a poor prognosis. Thus, real-time monitoring of surgical resection would be beneficial for the surgical resection of tumors. Although NIR-II fluorescent probe-guided surgical resection has been widely used for other types of diseases, it is not currently used for TNBC in clinical practice. Here, we describe the design and synthesis of a novel NIR-II fluorescent probe, FD-1050@NPs-cRGD, that targets TNBC. We found that it has a high fluorescence quantum efficiency, good stability, and low cytotoxicity. In vivo imaging in mice demonstrated a high tumor signal/normal tissue signal ratio, indicating that FD-1050@NPs-cRGD has great potential to be applied in tumor imaging of TNBC.

Carbene-Catalyzed Activation of 2-Aminobenzaldehyde for Access to Chiral Fluorescent Quinazolinone.

A carbene-catalyzed reaction to synthesize a chiral quinazolinone with a new activation mode of an "aniline-like" N-H moiety is disclosed. Addition of the nitrogen atom of diphenyl o-aminobenzaldehydes via NHC activation to imines leads to chiral quinazolinones with high yields and optical purities. The acidity of the N-H moiety was extremely increased through the formation of an acyl azolium intermediate, which was investigated by DFT calculations. Moreover, the chiral quinazolinones were found to have high fluorescence quantum efficiency.

Fluorescence Quantum Yields and Lifetimes of Aqueous Natural Dye Extracted from Tradescantia pallida purpurea at Different Hydrogen Potentials

In this work, we monitored the fluorescence quantum efficiency (η) and the fluorescence lifetime (τ) of natural dye extracts from the leaves of Tradescantia pallida purpurea. The natural dye was extracted from leaves in aqueous solutions as a function of the potential of hydrogen (pH). The η was determined from conical diffraction (CD) pattern measurements due to thermally-driven self-phase modulation. The fluorescence spectra and time-resolved fluorescence measurements corroborate the CD results, and the average η ≈ 0.28 and τ ≈ 3.1 ns values were obtained in the pH range 3.96–8.02. In addition, the extracted natural dye was tested as a possible colorimetric and/or fluorometric pH indicator in milk.