Fluorescence Color Research Articles

Molecular and carbon isotopic geochemistry of oils with different fluorescence color from the Upper Jurassic Qigu formation and oil accumulation process in Yongjin area, Junggar Basin in China.

Molecular and carbon isotopic geochemistry of oils with different fluorescence color from the Upper Jurassic Qigu formation and oil accumulation process in Yongjin area, Junggar Basin in China.

Identification of conservation and restoration materials for iron relics through ultraviolet-induced visible luminescence imaging and pyrolysis-gas chromatography/mass spectrometry

Understanding the previous protection and restoration efforts and the current state of cultural relics is essential before compiling a conservation and restoration plan. The lack of detailed archival records for some early conservation operations, the identification of restoration materials necessitates the use of scientific analytical methods. In this study, the composition and spatial distribution of historical restoration materials on five iron relics were investigated through pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS) and ultraviolet-induced visible luminescence imaging (UVL). The relics studied were iron weight 20791, iron adze head 2335, and iron axe 2334 from the Gansu Provincial Museum, iron sword D0008 from the Zhaotong Municipal Museum, and iron sword 450 from the National Museum of China. All five relics had undergone restoration without accompanying archival records. UVL revealed the distribution of various conservation materials. Notably, two distinct layers of the conservation material were observed on iron axe 2334. Differences in the fluorescence color and intensity of iron sword 450 provided information regarding the sampling strategy. The samples were collected under ultraviolet light emitting diode illumination to ensure representativeness and minimize damage to the relics. Through Py-GC/MS, the coating materials for iron weight 20791 and iron adze head 2335 were identified as boiled tung oil mixed with rosin resin. Iron axis 2334 had a two-layer coating: a base layer of boiled tung oil and a top layer of shellac. The coating material for iron sword D0008 was determined to be paraffin wax. The protective layer of iron sword 450 included multiple materials, including shellac, polystyrene, and bisphenol-A-type epoxy resin. This study confirms that UVL combined with Py-GC/MS serves as an effective technique for analyzing historical restoration materials. UVL guided the selection of representative samples for Py-GC/MS, reducing the time and amount of sampling required and minimizing further damage to the relics. This research provides valuable data for the restoration archives of five iron artifacts, offering a scientific basis for conservators to evaluate conservation methods, devise future conservation strategies, and exclude ineffective conservation materials.

Synergistic effect induces self crystallization of CsPbBr3 quantum dots in Borosilicate glass matrix By LiF

Cesium lead halide perovskite (CsPbX3) quantum dots (QDs) are recognized as viable substitutes for conventional fluorescent powder color converters, which can improve the color gamut and reproducibility of liquid crystal displays (LCDs). Encapsulating QDs in glass can effectively solve the water oxygen stability of QDs, but the glass matrix impedes the nucleation of QDs and the precipitation of QDs requires secondary heating. In our research, we successfully accomplished the self-crystallization of CsPbBr3 QDs facilitated by LiF within a B2O3-SiO2-ZnO borosilicate glass matrix.The results indicate that the self crystallization of CsPbBr3 QDs induced by LiF in borosilicate glass matrix has a synergistic effect. The Li+ ions can break the glass network structure and facilitate ionic migration and transport, while F- ions have good electronegativity due to ion aggregation, and can strongly attract Cs+ and Pb2+ ions with larger atomic radii, thereby promoting the rapid nucleation and growth of CsPbBr3 QDs, ultimately synthesizing QDs with uniform particle size, narrow half peak width, good optical properties, and thermal stability.

Thermochromic behavior of pigment red 254 in nylon 6 polymer for high-chromaticity engineering plastics

Advancement in Color-Material-Finishing (CMF) plays a crucial role in enhancing the visual appeal of plastic products, particularly for the high-chroma nylon plastics that are currently in vogue. However, it is inevitable to encounter pigment-dyeing issues in polar engineering plastics during the high-temperature extrusion process, which can lead to intense fluorescence and color fading. This phenomenon, characterized by the dissolution of pigments in a polar environment, can adversely affect the color saturation and weatherability of the pigment, which ultimately cause sharp reduction of aesthetic quality and durability of the plastic. Herein, we develop a modified strategy combined with thermal annealing to realize rapid color recovery in nylon 6, and further reveal the fluorescence and discoloration mechanism of pigment red 254 in nylon 6. Through improving the mobility of nylon chain segments, the rigid heterogeneous nucleation regions centered on the interfacial hydrogen bond between nylon 6 and the pigment molecules loosens with the help of heat treatment, and then the dissolved pigment molecules reaggregate to induce fluorescence quenching. Importantly, as a consequence of the increased lubricity segments, the required thermal annealing temperature and time for color recovery and fluorescence quenching could be significantly shortened from 180 °C for 5 h to 100 °C for 0.5 h. This work provides a feasible approach for the industrial production of high-chroma polar engineering plastics.

Polymer-stabilized cholesteric liquid crystals with multi-state reversibility for applications in advanced smart adjustable anti-counterfeiting and energy-saving displays

The creation of an anti-counterfeiting material with reflection color, fluorescence, infrared imaging, and electrical property information will increase the level of anti-counterfeiting. However, the creation of such a material has proved to be extremely challenging. In this study, twin anti-counterfeiting labels with intelligently tunable patterns were obtained through a strategy of PMMA loaded chiral molecules via diffusing on the micrometer scale. In order to enhance anti-counterfeiting ability, the multi-mode intelligently modulated advanced anti-counterfeiting material was obtained through the strategy of introducing photo-isomerizing dithienylethene and infrared-shielding Cs0.33WO3 nanoparticles. This material can be reversibly converted into fluorescent, reflected colors, infrared, and electrical characteristic signals. The encrypted information is displayed with red fluorescence under UV light irradiation. Furthermore, the encrypted information can be reversibly displayed and erased under repeated stimulation by voltage and pressure, heating and cooling, UV, visible and near infrared (NIR) light. The aim of our work is to create a simple method to prepare complex patterns of structural and fluorescent color anti-counterfeiting films with the improved anti-counterfeiting capability. Based on this, the strategy of co-doping fluorescent molecules and photochromic molecules in liquid crystals combined with etching technology has realized a multiple anti-counterfeiting mode with a higher level of security. The advanced multiple anti-counterfeiting mode can output encrypted information of multiple states which will greatly improve the level of anti-counterfeiting. In terms of display, we obtained billboards with complex patterns, price intelligently tunable and full-color display by diffusion S5011 in liquid crystals, thus extending their application in the field of electronic shelf labels.

A pH-responsive dual-emission composite for fast detection of BAs and visual monitoring seafood freshness with large luminescence color difference

Sensing biogenic amine (BAs) content is very important for assessing food freshness. To address the limitations such as small color difference values (ΔE) and complex preparation of probes for visualizing the freshness of seafood, a pH-responsive ratiometric fluorescent probe (EnEB) was prepared by Eu(NO3)3, trimeric acid (BTC), and hydrochloric acid norepinephrine (Enr). EnEB emitted blue (446 nm) and red fluorescence (616 nm) originating from Enr and Eu3+, respectively, and exhibiting a fluorescence wavelength difference up to 170 nm. The ratiometric fluorescent signals of EnEB showed a linear correlation with pH in the range of 5.5–8.0. Thus, EnEB can rapidly and precisely detect BAs, such as histamine, tyramine, and spermine, with detection limits and response times of 1.14 μmol/L (3 s), 1.04 μmol/L (8 s), and 0.41 μmol/L (2 s), respectively. Furthermore, an EnEB aerogel was prepared by loading EnEB in a matrix formed by polyvinyl alcohol (PVA) and agarose (AG). EnEB aerogel exhibited excellent acid-base gas-sensing properties. The fluorescence color of EnEB aerogel can change significantly with the deterioration of seafood. When seafood changed from fresh to decayed, the ΔE value of EnEB aerogel was as high as 80.9. Importantly, the results of seafood freshness by naked eye using EnEB aerogel was consistent well with the TVB-N content and the freshness standard stipulated by national food standard, indicating EnEB aerogel can accurately visually and real-time monitor seafood freshness. Furthermore, the strategy for sensing food freshness based on EnEB aerogel also offered multiple color variations to indicate fine freshness levels of seafood. This work provided a convenient, efficient, and accurate approach to assessing the freshness of seafood. Additionally, EnEB also has promising applications in security and anti-counterfeiting.

Controllable Preparation of a Cu NCs@Zn-MOF Hybrid with Dual Emission Induced by an Ion Exchange Strategy for the Detection of Explosives.

The precise synthesis of Cu NCs is a highly desirable and controllable route for the preparation of desired structures and properties, which facilitates the rational design of valuable probes for fluorescence sensing and the understanding of structure-property relationships. Herein, an ion-exchange strategy combined with a bottom-up synthetic approach was utilized in the synthesis process of Cu NCs for the first time, which achieved the controllable synthesis of Cu NCs and in situ anchoring of Cu NCs on the support material HPU-14. The as-prepared Cu NCs@HPU-14-4h not only had a good peroxidase-like property but also exhibited stable dual-emitting fluorescence at 470 and 620 nm. Notably, the peroxidase-like property endowed Cu NCs@HPU-14-4h with the capability of highly sensitive colorimetric detection of H2O2 in a linear concentration from 0.1 to 140 μM (detection limit of 86.7 nM), and a change in the fluorescent color from red to blue could be observed by the naked eye. Furthermore, due to the large overlap between the absorption of 2,4,6-trinitrophenol (TNP) and the excitation band of Cu NCs@HPU-14-4h, TNP could also be detected from 27 types of analogs and common ions with a limit of detection of 68 nM. Finally, a portable hydrogel probe with efficient wipe sampling was fabricated by polyvinyl alcohol (PVA) comprising Cu NCs@HPU-14-4h with the aim of on-site visualization of different explosives. Consequently, the current study not only provides a new idea for the precise synthesis of Cu NCs and their controllable anchoring on support materials but also offers an effective method for predicting H2O2 and TNP.

A dual-response fluorescent hemicyanine probe for the detection of mitochondrial hypochlorite and viscosity based on ESIPT/AIE and TICT

Viscosity and hypochlorite (ClO−) are two important factors affecting the physiological activity and function of mitochondria. Hypochlorite (ClO−) is a vital reactive oxygen species, and endogenous ClO− acts as an important germicidal oxidant in the immune system at low concentrations. While, fluctuations in viscosity can cause mitochondrial dysfunction that is linked to several diseases. We herein report on a hemicyanine-based probe (BDTB-PA) for the detection of hypochlorite (ClO−) and viscosity. The probe exhibits a very low fluorescence background in an aqueous solution due to twisted intramolecular charge transfer (TICT) and blocked excited-state intramolecular proton transfer (ESIPT). In a viscous solution, the TICT of the probe was inhibited, generating a strong emission at 580 nm. In contrast, upon treatment with ClO−, the phenylboronic acid pinacol ester group of probe BDTB-PA was removed, and the hydroxyl group was released, activating the ESIPT process. Coupled with its aggregation-induced emission (AIE) characteristics, the product of BDTB-PA with ClO− exhibited a distinct emission at 540 nm. As such a solution of the probe BDTB-PA exhibited a distinct fluorescent color change from colourless to green under UV light with the addition of ClO−. More importantly, probe BDTB-PA was used for monitoring ClO− and viscosity in the mitochondria of living cells, plants and zebrafish.

Design and synthesis of dicyanoethylene derivatives functionalized with carbazole possessing the properties of obvious aggregation-induced emission and reversible high-contrast mechanofluorochromism

This study devotes to the design, preparation, and examination of two novel D-A structured molecules, designated as CCEDBF and BCCEDBF, which are derived from carbazole unit, dicyanoethylene segment, and dibenzofuran unit. The distinctive D-A molecular architectures and highly twisted spatial configurations of these compounds facilitate pronounced intramolecular charge transfer (ICT) while also imparting robust solid-state luminescence, exhibiting emission efficiencies of 0.518 and 0.739, respectively, and notable aggregation-induced emission (AIE) with AIE factors of 43 and 30. Significantly, both CCEDBF and BCCEDBF demonstrate reversible mechanofluorochromic (MFC) behavior characterized by high fluorescence contrast. Mechanical grinding of the initial powders results in a shift in their emission colors, transitioning from green and yellow-green to yellow and orange-red, respectively, alongside a corresponding shift in emission peaks from 525 nm to 536 nm–558 nm and 597 nm. Powder X-ray diffraction (PXRD) examination of the initially synthesized, mechanically processed, and vaporized samples reveals that the observed fluorescence color change is due to a structural transformation between ordered crystalline and disordered amorphous configurations induced by the application of the external force. The red shift in photoluminescence (PL) spectra post-grinding is attributed to a reduced band gap, driven by factors such as extended π-conjugation length, enhanced planar intramolecular charge transfer (PICT) effect, strengthened π-π interactions and exciton coupling, as well as the increase in the orbitals overlap between neighboring molecular. Moreover, the presence or absence of tert-butyl substituents attaching to the 3- and 6-positions of the carbazole units significantly impacts the photophysical properties of these materials.

Reversible Emission Color, Brightness, and Shape Changes of AIEgen‐containing Bulk Polymers

AbstractBulk polymers generally exhibit faster response, higher shape‐deformation speed, and stronger mechanical properties than the hydrogels. However, it still remains a formidable challenge to enable bulk polymers to exhibit reversible changes in shape and fluorescence simultaneously. Herein, for the first time, the temperature‐responsive reversible changes in fluorescence color, brightness, and shape of semi‐crystalline poly(ε‐caprolactone) (PCL) network doped with a D‐A based aggregation‐induced emission luminogen (AIEgen) is realized. The fabricated flower‐like and dragonfly‐shaped actuators show reversible blooming‐closing and wing fanning behaviors, respectively, as well as reversible fluorescence‐changing effects. Notably, the response and shape‐deformation speed as well as mechanical properties of the system is much better than the reported hydrogels. Moreover, a smart switch is developed to demonstrate the potential applications. The stick fabricated by the sample can lift and release an object 1000 times larger than its weight, serving as a color‐changing artificial muscle. This material design strategy may shine light on the design and preparation of other reversible shape‐deformation polymers in combination with stimuli‐responsive luminescence‐changing AIEgens, such as mechanochromic, thermochromic, and photochromic luminogens.

Fluorescent-based bile acid triazole-phenothiazine derivatives: Multiphase detection of biogenic amines and application in spoiled foods

Amines are ubiquitous in biological world, yet are toxic and harmful in nature. To preserve the quality and safety of these packaged meals, it’s critical to identify biogenic amines that are emitted from spoiled meat, fish, or dairy products. To this endeavour, herein we report bile acid based triazole derivative with phenothiazine that are capable of sensing various amines by rapid change of fluorescence colour or intensity. The triazole derivatives exhibit a multiphase sensing platform by effectively sensing amine vapours or solutions in both solid and solution phases. Probes in the vapour state exhibit very quick interaction to primary amines (26 s for CTPTZ) and strong sensitivity to putrescine, which is a common example of biogenic amines (BAs). We have employed our unique sensing triazole derivative as a spoilage indication for meat. It detects biogenic amines from spoiled food and produces an optical response. Significant changes in both visual and luminescent were noted within 4–18 h of packaging at room temperature (∼25 °C). The rapid response that biogenic amines provide to these molecular sensors makes them highly promising for applications in the food packaging industry, medical diagnostics, and other sensory devices.

Wavelength-Based luminescence sensing via Turn-On responses for acid detection in complex Environments

One possible way to address the shortcomings of current acid detection is to add fluorescence detection capabilities, however, there is little data regarding wavelength-based luminescence sensing, which makes possible for the naked eye to perceive various colors through wavelength variations. In this paper, we achieved turn-on response and wavelength-based luminescence sensing on acids detection by using donor-accepter complex Fe-L, which display significant fluorescence discoloration in the presence of a wide range of inorganic and organic acids, including benzoic acids, providing the fluorescence response for a more intuitive and convenient acid detection. The simultaneous achievement of fluorescence enhancement and color change as the acid concentration changes enables visual detection of the acid concentration, which provides a foundation for future research into convenient detection methods for various types of acids.

Effects of different beverages on the color stability and fluorescence of resin composites: in situ study.

To evaluate the color change (ΔE) and fluorescence (FL) of resin composites after the consumption of beverages. One hundred and sixty disc-shaped specimens (6 × 2mm) of Filtek Z350 XT (FZX) and Forma (FOR) resin composites were randomized for use in devices by five volunteers who ingested 100ml daily of red wine (RW), beer (BE), energy drink (ED) and water (WT) over 15 days. The data were collected from digital photographs and analyzed using the CIE-Lab and RGB scales to obtain ΔE and FL and statistics via two-way ANOVA (for ΔE) and ANOVA for repeated measures (for FL), α = 0.05. The highest ΔE values were obtained for FZX and FOR in the RW (ΔE = 10.5 for FZX and ΔE = 9.90 for FOR) and BE (ΔE = 6.3 for FZX and ΔE = 6.1 for FOR) drinks. For FL, there were different levels of change between the composites, with a much more significant reduction in FL intensity with RW. Beverages have the potential to stain the composites evaluated, especially alcoholic beverages. Before carrying out an esthetic treatment with resin composites, it is ideal to investigate the types of drinks consumed by patients, for greater predictability of treatment.

Fluorescent Microneedle‐Based Theranostic Patch for Naked‐Eye Monitoring and On‐Demand Photo‐Therapy of Bacterial Biofilm Infections

AbstractThe eradication of recalcitrant bacterial biofilm infections necessitates the development of speedy diagnostics and prompt therapeutics. However, constructing a portable versatile platform that enables in situ monitoring of biofilm infections accompanied by potent antibiofilm activity remains challenging. To address this conundrum, a microneedle theranostic patch (Mn: C/G@MN) is devised by incorporating an innovative biophotonic probe (manganese‐doped carbon dots, Mn: CDs) into methacrylated gelatin for visual monitoring of biofilm infection and on‐demand photo‐therapy. The Mn: C/G@MN patch penetrates the physical barrier of biofilms to track their acidic microenvironment, exhibiting a visualized fluorescence color change (from yellow to turquoise) to enable naked‐eye monitoring of biofilm infection. Furthermore, the Mn: C/G@MN patch can drastically eradicate biofilm on‐demand through the synergy of local hyperthermia and hydroxyl radical (•OH) storm under 808 nm near‐infrared light illumination, enabling the damaging of extracellular polymeric substances (EPS) matrix to disperse biofilms and subsequently kill detached bacteria. Both in vitro and in vivo findings authenticate that biofilm infection monitoring‐and‐treating can be achieved. Moreover, the versatile Mn: C/G@MN patch is conducive to suppressing inflammatory responses, expediting collagen deposition, stimulating angiogenesis, and accelerating biofilm‐infected wound healing. As envisaged, this work highlights the potential of such a versatile platform for application in integrated theranostics for biofilm infection.

Photoluminescent Multicolor Carbon Dots for UV Detection and Dynamic Anticounterfeiting.

Carbon dots (CDs) are an emerging type of fluorescent carbon nanomaterial with broad application prospects. Among them, photochromic CDs have been widely used in the field of optoelectronic devices but rarely in ultraviolet (UV) detection. In this work, we successfully developed photochromic CDs that exhibit reversible emission under light stimulation in an amine solvent system. Notably, the CDs showed ultrafast photochromic behavior in diethylamine solvent, shifting the fluorescence color from cyan-green to orange-red after 2 s of irradiation, with the solution color changing from pale yellow to pale purple. Furthermore, this performance could recover without additional stimuli, simply by standing for several tens of seconds. Structural analysis indicated that rapid photochromism arises from changes in the surface functional group radicals of the CDs, with the reversibility attributed to fluctuation in these radicals. Leveraging the excellent photochromic properties of CDs, we further developed a device for detecting UV indices in sunlight. This opens up broad prospects for developing high-performance UV detection devices based on CDs.

Sustainable engineering polymer composites fabricated using delignified bamboo fiber as reinforcement and walnut shell powder as filler

Developing sustainable engineering materials using renewable resources and agro-wastes represents an effective method for reducing carbon emissions and environmental pollution. In this study, a novel approach to fabricating high-performance biomass-based polymer composites was presented. Specifically, partially delignified bamboo fiber (DBF) and walnut shell powder (WSP) were incorporated into the matrix, namely melamine-hexamethylenediamine-urea (MHU) resin which was previously known for its excellent interfacial compatibility. Mechanical property investigations show that the DBF, acting as the reinforcement, provided the hybrid composites with high flexural and tensile strength up to 220 and 120 MPa, respectively, greatly surpassing those of commercial wood-plastic composites, wood-based composites, and natural wood, making them promising structural materials. As the filler, walnut shell powder endowed the composites with high hardness (Shore D > 90) and an appealing mirror-like surface gloss. Owing to the protection provided by the MHU matrix, the composite containing 38 % MHU exhibited outstanding flame retardancy (UL 94-V0 grade), which was further supported by cone calorimeter test (CCT) results. An unexpected and intriguing finding is that the composites exhibited fluorescence under UV irradiation. The rare silvery-grey fluorescence color imparted self-anticounterfeiting property to the composites. This study demonstrated the significant potential of bamboo fiber and walnut shell in the development of sustainable engineering materials.

Multi-Objective Design of DNA-Stabilized Nanoclusters Using Variational Autoencoders With Automatic Feature Extraction.

DNA-stabilized silver nanoclusters (AgN-DNAs) have sequence-tuned compositions and fluorescence colors. High-throughput experiments together with supervised machine learning models have recently enabled design of DNA templates that select for AgN-DNA properties, including near-infrared (NIR) emission that holds promise for deep tissue bioimaging. However, these existing models do not enable simultaneous selection of multiple AgN-DNA properties, and require significant expert input for feature engineering and class definitions. This work presents a model for multiobjective, continuous-property design of AgN-DNAs with automatic feature extraction, based on variational autoencoders (VAEs). This model is generative, i.e., it learns both the forward mapping from DNA sequence to AgN-DNA properties and the inverse mapping from properties to sequence, and is trained on an experimental data set of DNA sequences paired with AgN-DNA fluorescence properties. Experimental testing shows that the model enables effective design of AgN-DNA emission, including bright NIR AgN-DNAs with 4-fold greater abundance compared to training data. In addition, Shapley analysis is employed to discern learned nucleobase patterns that correspond to fluorescence color and brightness. This generative model can be adapted for a range of biomolecular systems with sequence-dependent properties, enabling precise design of emerging biomolecular nanomaterials.

Multi-color emission composites of white carbon dots and dyes through inner filter effect

A series of multi-color carbon dot composites were obtained by transforming white carbon dots (WCDs) into three primary colors using the dyes' inner filter effect (IFE). WCDs were combined with three distinct dyes (methyl red, bromocresol green, and methylene blue), and three fluorescence colors (red, yellow, and blue) were obtained. The colors of the emitting light excited by the same UV light were similar to the colors of the respective dyes, and have a large Stokes shift. The presence of the IFE between WCDs and dyes was proved through a variety of methods, the analysis of the relationship between the UV of dyes and fluorescence spectra of WCDs, the excitation-emission matrix, as well as the comparison PL decay profiles of WCDs before and after dye addition. The Stern-Volmer quenching constant KSV exhibited no temperature dependence during the IFE process with increasing concentrations of dyes. The UV spectra of the mixture of WCDs and dyes were simply the sum of two individual components, which implies that there is no chemical interaction between WCDs and dyes. Since methyl red and bromocresol green are acid-base indicators, the fluorescence color of the carbon dot composite also changed continuously during the dilute NaOH solution titration process. In furtherment, distributing the binary system of “WCDs + dye” within poly (vinyl alcohol) (PVA), three colors fluorescent composite films of “WCDs / Dye / PVA” were produced successfully.

Pyrene carbaldehyde derived carbon dots for detecting water in alcohol and security printing

This study focuses on preparing Carbon dots (CDs) from Pyrene-1-carbaldehyde (PCA) using a solvothermal method and further purification using column chromatography. The aggregation-induced emission (AIE) of CDs was systematically investigated in a THF/water medium. The CDs showed red shifts in their photoluminescence (PL) spectra upon increase in water content. Scanning electron microscopic (SEM) images revealed the formation of aggregates, while X-ray diffraction (XRD) confirmed that the d-spacing values remains unchanged. The NMR spectrum of the CDs displayed peaks corresponding to aromatic carbon, which disappeared upon addition of water due to π-π stacking, indicating aggregate formation. Based on the aggregation-induced fluorescence emission mechanism, detection of water content in alcohol is demonstrated. Moreover, the synthesized CDs were used as fluorescent colorant in screen inks along with polyvinyl alcohol (PVA) and hydroxyethyl cellulose (HEC) as binders. The print proofs obtained on UV-dull paper using PVA-based screen ink exhibited fluorescence emission at longer wavelengths and showcased desirable photostability under prolonged UV exposure compared to the prints obtained using HEC-based ink. Moreover, though the PVA based print appeared blue or cyan fluorescent, the actual yellow emissions from the CDs can be visualised using UV block filter. Such features, masked to the forger, but known to the user can be utilised in checking the authenticity of the print.

Pharmacognostical evaluation and description of the leaf and root bark of Citropsis articulata Swingle & Kellerman

BackgroundCitropsis articulata Swingle & Kellerman (Family Rutaceae) is a renowned African traditional medicinal plant for the management of erectile dysfunction. The root bark is more commonly used than the leaves. Little has been done to evaluate the pharmacognostical parameters of both parts. PurposeThe aim of this study was to determine the pharmacognostical parameters of C. articulata leaves and root bark. MethodsThe plant parts were collected, washed, dried, and extracted by decoction and soxhlation. The World Health Organisation quality control methods for herbal materials were generally followed for the pharmacognostical evaluation of the root bark and leaf. This involved macroscopic and microscopic analysis, physicochemical analysis, hemolytic activity, and phytochemical analysis. ResultsMacroscopically, the distillate of the root bark showed a fluorescent blue colour under ultra violet light of wavelength 254 nm. Microscopic examination revealed the presence of cellulose, lignified, suberized and cuticular cell walls. Numerous aleurone grains were noted in the root bark. Phytochemical analysis showed the presence of reducing sugars, free amino acids, L-arginine, coumarin, glycosides, phenols, phytosterols, saponins, steroids, tannins, terpenoids, alkaloids and flavonoids. Thin layer and high performance liquid fingerprints were also developed. The C. articulata root bark decoction and Soxhlet extracts contained 12.35 ± 0.05, and 110.00 ± 0.03 while the leaf decoction and Soxhlet extracts contained 4.97 ± 0.03 and 39.65 ± 0.00 mg/g diosgenin equivalent saponins respectively. The L-arginine content for the dried root bark decoction and Soxhlet was 2681 ± 7.29, 1660 ± 2.99 µg/g, while that for the leaf decoction and Soxhlet extracts was 135.60 ± 8.28, and 130.20 ± 2.83 µg/g respectively. ConclusionThis study distinguished the root bark and leaf of Citropsis articulata and offered vital information for the quality control and standardization of the plant materials.