Strong Fluorescence Intensity Research Articles

Liposomes loaded with dual clinical photosensitizers for enhanced photodynamic therapy of cervical cancer.

Photodynamic therapy (PDT) has become a potential anti-cancer strategy owing to its negligible invasiveness, low toxicity, and high selectivity. The photosensitizer (PS) plays an indispensable role in PDT. Herein, a novel type of PS (Ce6-MB@Lips) which can be excited by a near-infrared (NIR) laser was designed and synthesized. Methylene blue (MB) and Chlorin e6 (Ce6), two organic dyes approved by the Food and Drug Administration (FDA), were used to prepare Ce6-MB@Lips by thin-film dispersion method, which improve the water solubility of Ce6 and reduce the cytotoxicity of MB. The Ce6-MB@Lips were shown to have a spherical nanostructure with an average particle size of 160.3 nm and excellent water solubility. Then the optical properties of Ce6-MB@Lips were further studied. Ce6-MB@Lips showed absorption peaks at 413 nm/670 nm and fluorescence peak at 697 nm. Compared with Ce6@Lips and MB@Lips, Ce6-MB@Lips showed better stability, stronger fluorescence intensity, and higher singlet oxygen (1O2) generation ability. Cell experimental analysis exhibited that the stable Ce6-MB@Lips showed low cytotoxicity, high phototoxicity and high reactive oxygen species (ROS) production capacity. After effective cell internalization, the prepared Ce6-MB@Lips showed excellent ability to promote tumor cell apoptosis in vitro. The Ce6-MB@Lips could be a promising candidate for PDT of cervical cancer.

A simple and fast strategy for rare earth doped phosphors prepared by 980 nm laser thermal effect

The phosphors synthesize by the sol-gel method show low cost and good homogeneity, but it also requires furnace annealing at high-temperatures. This report uses a 980 nm laser annealing strategy to replace the furnace annealing in the sol-gel combustion synthesis. The fast laser annealing can improve the preparation efficiency of rare earth doped phosphor. Er3+/Li+ co-doped Y2O3 nanocrystals are synthesized by laser annealing strategy. The structures and spectral properties of the phosphors prepared by laser annealing are studied. The phosphors prepared by laser annealing have the same crystal structure and spectral properties as those organized by furnace annealing. In addition, phosphors can be heated into crystals using a high-power 980 nm laser. Under 980 nm excitation, the crystal prepared by laser annealing shows a much stronger fluorescence intensity than phosphors.

Expeditious Synthesis of Fluorescent Bis(phenylfuryl)benzenes

AbstractVersatile fluorescent polyaromatic compounds of alternating benzene and furan rings, para- and meta-bis(5-phenylfur-3-yl)benzenes, were expeditiously synthesized by double Mn(OAc)3-catalyzed oxidative decarbonylation and Paal–Knorr reactions of β-ketoesters, prepared from the conjugate addition of ethyl acetoacetate to para- and meta-bis(chalcones). Stronger fluorescence intensity was observed for meta-bis(phenylfuryl)benzene with ortho-methoxy substitution, whereas longer fluorescence wavelength was observed for para-bis(phenylfuryl)benzene with para-methoxy substitution.

An exploratory human study of superstable homogeneous lipiodol-indocyanine green formulation for precise surgical navigation in liver cancer.

The clinical applications of transcatheter arterial embolization (TAE) conversion therapy combined with hepatectomy have been severely restricted by ill-defined tumoral boundaries and miniscule hidden lesions. Fluorescent surgical navigation is a promising method for overcoming these barriers. However, sufficient delivery of the fluorescent probe into the tumor region after long-term TAE is challenging due to blockade of the tumor-supplying artery. Here, a super-stable homogeneous intermix formulating technology (SHIFT) to physically mix lipiodol and indocyanine green (ICG) formulation (SHIFT and ICG) for fluorescent surgical navigation after long-term TAE conversion therapy is provided. Through the retrospective study of 45 clinical liver cancer patients, it is found that SHIFT and ICG formulation have excellent tumor deposition effect and safety. During surgical resection after long-term TAE conversion therapy, SHIFT and ICG could clearly identify in real time the full tumor regions and boundaries and had a high signal-to-normal tissues ratio-even the indistinguishable satellite lesions could be identified with a strong fluorescence intensity. Meanwhile, SHIFT and ICG could improve operative, anesthetic, and postoperative variables associated with postoperative complications. This simple and effective SHIFT could provide precise fluorescent navigation for surgical resection following long-term embolization therapy in clinical practice and has great potential for a translational pipeline.

Simultaneous enhancement of emission and thermal sensitivity via phase transition in Gd2(MoO4)3:Yb3+/Er3+ crystals

AbstractThe effects of site symmetric distortion induced by the phase transition on up‐conversion emission and thermal sensing performance of Gd2(MoO4)3:Yb3+/Er3+ (GMO) crystals were elaborately studied by minimizing interference from many factors. Monoclinic GMO showed a much stronger fluorescence intensity and larger fluorescence intensity ratio under the irradiation of 980 nm laser in comparison to the orthorhombic counterpart. These remarkable up‐conversion properties stemmed from the low site symmetry with large site symmetric distortion in monoclinic GMO. Moreover, the thermal sensing property of the samples was assessed based on the fluorescence intensity ratio technique, where monoclinic GMO exhibited much higher maximum absolute sensitivity (Sa = 0.0257 K−1 at 510 K) due to the site symmetric distortion, which was further explained by the Judd–Ofelt theory and polarizability of the chemical bond volume model. Results opened an efficient avenue for achieving highly sensitive thermometry in many daily scenarios via finely tailoring the local site symmetry.

Effect of rare earth ion on fluorescent properties of Eu(TTA)3phen/PMMA temperature sensitive paint

The temperature sensitive paint (TSP) technology is widely used in the temperature distribution measurement of large area solid field, especially for the in-depth research in the mechanical behavior of complex flow gas around the aircraft, because of its advantages of non-contact, full-field measurement, easy manufacture and use. In this work, we synthesized the rare earth ion(Y3+, Er3+) doped Eu(TTA)3phen/PMMA temperature sensitive paint respectively based on the probe molecules of the rare earth ion (Y3+, Er3+) doped Eu(TTA)3phen and polymethyl methacrylate(PMMA). The structure of probe molecules and the fluorescent properties of TSP were also studied. The result show that the optimal ratio of Eu3+:Y3+ (or Er3+) is 0.5:0.5, rare earth ions are coordinated with ligands and the doping of Y3+ and Er3+ do not affect the structure of Eu(TTA)3phen. Y3+ and Er3+ have gain effect on the fluorescent emission of Eu(TTA)3phen/PMMA and the strongest fluorescent intensity (616 nm) is decreased with the increasing of temperature, which show that the Y3+ and Er3+ doped Eu (TTA)3phen/PMMA have temperature quenching properties in the temperature range of 20–80 °C. What’s more, the doping of Y3+ and Er3+ can improve the change rate of the fluorescent intensity and the temperature measurement sensitivity.

Development of a novel highly specific fluorescent probe for detecting HOCl in living cells and zebrafish, as well as real water samples

Hypochlorous acid (HOCl), a member of reactive oxygen species (ROS), plays an important role in living systems. Highly sensitive probes for detection of hypochlorous acid are in great demand. A novel chromene derivative fluorescent probe was constructed for determining hypochlorous acid. When HOCl was absent, the probe itself exhibited strong fluorescence intensity, while the fluorescence was quenched with the presence of HOCl. The fluorescent probe exhibited high selectivity and sensitivity for HOCl in a linear response range of 0 -15 μM with a low detection limit of 0.12 μM. The probe has been successfully applied for the confocal imaging of HOCl in the RAW 264.7 cells and zebrafish with low cell toxicity. It also was used to detect HOCl in tap water and lake water.

Manganese‐Induced Highly Fluorescent Oligodopamine for Sensitive Detection of Dopamine Neurotransmitter by Catalytic Action of H2O2/MnO2 Nanosheets

Dopamine (DA) is a catecholamine, which plays an important role as neurotransmitter in the central nervous system. Optical sensing technology is commonly used for the rapid detection of DA through the formation of fluorescent polydopamine (PDA). However, it is difficult to quantify low levels of DA (≤10−8 m) because the resulting PDA has a low fluorescence (FL) efficiency. In this study, DA analyte is polymerized into highly fluorescent oligodopamine (F‐ODA) by the catalytic action of H2O2/MnO2 nanosheets, so‐called Mn2+@F‐ODA (i.e., manganese (2+) coordinated oligodopamine derivatives). Compared to the F‐ODA prepared by NaOH oxidation, Mn2+@F‐ODA exhibits a stronger FL intensity with a maximal peak at 465 nm. Mn2+@F‐ODA produces a distinct FL emission that allows for the detection of trace DA (10−8–10−12 m) with a detection limit of 10−13 m. The FL intensity of Mn2+@F‐ODA shows a suitable logarithmic linearity over four orders of the magnitude from 10−8–10−11 m. The developed chemical strategy suggests potential applications of Mn2+@F‐ODA for the sensitive detection of DA neurotransmitters.

Magnetic capture of sulfur quantum dots encapsulated in MOF-5-NH2 via a target-driven self-cycling catalyzed hairpin assembly for the sensitive detection of patulin

Tools to detect low molecular weight mycotoxin patulin (PAT) are urgently needed because of its harm to human health. Here, we report a simple, effective, and sensitive fluorescent aptasensor based on sulfur quantum dots encapsulated in MOF-5-NH2 ([email protected]2) and self-cycling catalyzed hairpin assembly (scCHA) for the detection of PAT in apple juice. The [email protected]2 synthesized by a “bottle-around-ship” solvothermal method works as a fluorescent probe and offers enhanced fluorescence intensity and good water-solubility versus MOF-5-NH2 due to the encapsulation of water-soluble SQDs. Meanwhile, the scCHA designed by the two DNA hairpins is initiated after the formation of PAT/aptamer, which further recycles PAT to effectively capture multiple fluorescence probes ([email protected]2) and amplify the detection signal. Attributed to the synergistic effect between the strong fluorescence intensity of [email protected]2 and the efficient PAT utilization of scCHA, the fluorescent aptasensor exhibits high sensitivity with detection limits as low as 0.753 pg/mL. The system has satisfactory specificity, anti-interference, and reproducibility (RSDs of intra-assay and inter-assay were 3.24% and 8.60%, respectively). The recoveries in apple juice were between 89.03% and 107.67%, which were with good consistency versus high-performance liquid chromatography (HPLC). These data collectively show that the developed fluorescent aptasensor has a good practical application value.

Preparation of Cadmium Telluride Quantum Dots Modified by Thioglycolic Acid

A CdTe quantum dot modified with thioglycolic acid as stabilizer was prepared. The structure of CdTe quantum dots was characterized by IR, UV and fluorescence spectra, transmission electron microscopy (TEM) scanning and X-ray diffraction (XRD). The effects of reactants, temperature, time and PH on the luminescence properties of the quantum dots were investigated. It is found that the quantum dots have strong fluorescence intensity. The synthesized QDS have small and uniform particle size and high crystallinity. The optimum conditions were determined as follows: n (Cd2+): n (Te2-): n (TGA) = 2:1:4, heating temperature 140°C, reaction time 60min, pH 11.

Tumor-Selective Cascade-Amplified Dual-Prodrugs Activation for Synergistic Oxidation-Chemotherapy

Tumor-Selective Cascade-Amplified Dual-Prodrugs Activation for Synergistic Oxidation-Chemotherapy

Novel Cuboid-like Crystalline Complexes (CLCCs), Photon Emission, Fluorescent Fibers, and Bright Red Fabrics of Eu3+ Complexes Adjusted by Amphiphilic Molecules.

With the growing needs for flexible fluorescence emission materials, emission fibers and related wearable fabrics with bright emission properties have become key factors for wearable applications. In this article, novel cuboid-like crystals of Eu3+ complexes were generated. Except for light-energy-harvesting ligands of thenoyltrifluoroacetone (TTA) and 1,10-phenanthroline hydrate (Phen), the crystal structures were adjusted by other functional amphiphilic molecules. Not only does ETPC-SA, adjusted by stearic acid, have a regular cuboid-like crystal with a size of about 2 μm size, but it also generates the best photon emission property, with a fluorescence quantum yield of 98.4% fluorescence quantum yield in this report. Furthermore, we succeeded in producing novel fluorescent fibers by mini-twin-screw extrusion, and it was easy to form bright red fabrics, which are equipped with strong fluorescence intensity, flexibility, and a smooth hand feeling, with the normal fabricating method in our work. It is worth noting that ETPC-HQ fibers, which carry a crystal complex adjusted by hydroquinone, possess the lowest quantum yield but have the longest average fluorescence lifetime of 1259 µs. This result means that a low-density polyethylene (LDPE) matrix could make excited electrons stand in the excited state for a relatively long time when adjusted by hydroquinone, so as to increase the afterglow property of fluorescent fibers.

Facile strategy for preparing rhodamine B/ZrO2 composite fluorescent film with combined advantages of high emission intensity and outstanding water-resistance

The RB/ZF composite film prepared by immobilizing rhodamine B (RB) on ZrO2 film (ZF) exhibits strong fluorescence intensity but poor water-resistance. In this paper, rosin, octadecane-1, 18-dicarboxylic acid (OA) and silane coupling agent were used as hydrophobic modifiers to investigate the method to improve water-resistance of RB/ZF and maintain its strong fluorescence intensity as well. The influencing factors including modifier dosage, molecular structure, RB concentration and alkyl chain length of coupling agent on fluorescence performance and water-resistance of composite film were studied in detail and the related reasons were discussed. Results demonstrate that the film modified by the combination of rosin, OA and coupling agent has both favorable fluorescence performance and excellent water-resistance. The emission intensity of the optimized film is 94.5% of that of RB/ZF. Meanwhile, after immersion in various aqueous environments, there is no obvious difference in emission spectrum or intensity.

Preparation of 2D Periodic Nanopatterned Arrays through Vertical Vibration-Assisted Convective Deposition for Application in Metal-Enhanced Fluorescence

The performance of a metal-enhanced fluorescence (MEF) substrate is fundamentally based on the orientation of the metal nanostructures on a solid substrate. In particular, two-dimensional (2D) periodic metallic nanostructures exhibit a strong confinement of the electric field between adjacent nanopatterns due to localized surface plasmon resonance (LSPR), leading to stronger fluorescence intensity enhancement. The use of vertical vibration-assisted convective deposition, a novel, simple, and highly cost-effective technique for preparing the 2D periodic nanostructure of colloidal particles with high uniformity, was therefore proposed in this work. The influences of vertical vibration amplitude and frequency on the structure of thin colloidal film, especially its uniformity, monolayer, and hexagonal close-packed (HCP) arrangement, were also investigated. It was found that the vibration amplitude affected film uniformity, whereas the vibration frequency promoted the colloidal particles to align themselves into defect-free HCP nanostructures. Furthermore, the results showed that the self-assembled 2D periodic arrays of monodisperse colloidal particles were employed as an excellent template for a Au thin-film coating in order to fabricate an efficient MEF substrate. The developed MEF substrate provided a strong plasmonic fluorescence enhancement, with a detection limit for rhodamine 6G as low as 10−9 M. This novel approach could be advantageous in further applications in the area of plasmonic sensing platforms.

A novel H129-based anterograde monosynaptic tracer exhibits features of strong labeling intensity, high tracing efficiency, and reduced retrograde labeling

BackgroundViral tracers are important tools for mapping brain connectomes. The feature of predominant anterograde transneuronal transmission offers herpes simplex virus-1 (HSV-1) strain H129 (HSV1-H129) as a promising candidate to be developed as anterograde viral tracers. In our earlier studies, we developed H129-derived anterograde polysynaptic tracers and TK deficient (H129-dTK) monosynaptic tracers. However, their broad application is limited by some intrinsic drawbacks of the H129-dTK tracers, such as low labeling intensity due to TK deficiency and potential retrograde labeling caused by axon terminal invasion. The glycoprotein K (gK) of HSV-1 plays important roles in virus entry, egress, and virus-induced cell fusion. Its deficiency severely disables virus egress and spread, while only slightly limits viral genome replication and expression of viral proteins. Therefore, we created a novel H129-derived anterograde monosynaptic tracer (H129-dgK) by targeting gK, which overcomes the limitations of H129-dTK.MethodsUsing our established platform and pipeline for developing viral tracers, we generated a novel tracer by deleting the gK gene from the H129-G4. The gK-deleted virus (H129-dgK-G4) was reconstituted and propagated in the Vero cell expressing wildtype H129 gK (gKwt) or the mutant gK (gKmut, A40V, C82S, M223I, L224V, V309M), respectively. Then the obtained viral tracers of gKmut pseudotyped and gKwt coated H129-dgK-G4 were tested in vitro and in vivo to characterize their tracing properties.ResultsH129-dgK-G4 expresses high levels of fluorescent proteins, eliminating the requirement of immunostaining for imaging detection. Compared to the TK deficient monosynaptic tracer H129-dTK-G4, H129-dgK-G4 labeled neurons with 1.76-fold stronger fluorescence intensity, and visualized 2.00-fold more postsynaptic neurons in the downstream brain regions. gKmut pseudotyping leads to a 77% decrease in retrograde labeling by reducing axon terminal invasion, and thus dramatically improves the anterograde-specific tracing of H129-dgK-G4. In addition, assisted by the AAV helper trans-complementarily expressing gKwt, H129-dgK-G4 allows for mapping monosynaptic connections and quantifying the circuit connectivity difference in the Alzheimer’s disease and control mouse brains.ConclusionsgKmut pseudotyped H129-dgK-G4, a novel anterograde monosynaptic tracer, overcomes the limitations of H129-dTK tracers, and demonstrates desirable features of strong labeling intensity, high tracing efficiency, and improved anterograde specificity.

High-quantum yield alloy-typed core/shell CdSeZnS/ZnS quantum dots for bio-applications

BackgroundQuantum dots (QDs) have been used as fluorophores in various imaging fields owing to their strong fluorescent intensity, high quantum yield (QY), and narrow emission bandwidth. However, the application of QDs to bio-imaging is limited because the QY of QDs decreases substantially during the surface modification step for bio-application.ResultsIn this study, we fabricated alloy-typed core/shell CdSeZnS/ZnS quantum dots (alloy QDs) that showed higher quantum yield and stability during the surface modification for hydrophilization compared with conventional CdSe/CdS/ZnS multilayer quantum dots (MQDs). The structure of the alloy QDs was confirmed using time-of-flight medium-energy ion scattering spectroscopy. The alloy QDs exhibited strong fluorescence and a high QY of 98.0%. After hydrophilic surface modification, the alloy QDs exhibited a QY of 84.7%, which is 1.5 times higher than that of MQDs. The QY was 77.8% after the alloy QDs were conjugated with folic acid (FA). Alloy QDs and MQDs, after conjugation with FA, were successfully used for targeting human KB cells. The alloy QDs exhibited a stronger fluorescence signal than MQD; these signals were retained in the popliteal lymph node area for 24 h.ConclusionThe alloy QDs maintained a higher QY in hydrophilization for biological applications than MQDs. And also, alloy QDs showed the potential as nanoprobes for highly sensitive bioimaging analysis.Graphical

Development of a powerful synthetic hybrid promoter to improve the cellulase system of Trichoderma reesei for efficient saccharification of corncob residues

BackgroundThe filamentous fungus Trichoderma reesei is a widely used workhorse for cellulase production in industry due to its prominent secretion capacity of extracellular cellulolytic enzymes. However, some key components are not always sufficient in this cellulase cocktail, making the conversion of cellulose-based biomass costly on the industrial scale. Development of strong and efficient promoters would enable cellulase cocktail to be optimized for bioconversion of biomass.ResultsIn this study, a synthetic hybrid promoter was constructed and applied to optimize the cellulolytic system of T. reesei for efficient saccharification towards corncob residues. Firstly, a series of 5’ truncated promoters in different lengths were established based on the strong constitutive promoter Pcdna1. The strongest promoter amongst them was Pcdna1-3 (− 640 to − 1 bp upstream of the translation initiation codon ATG), exhibiting a 1.4-fold higher activity than that of the native cdna1 promoter. Meanwhile, the activation region (− 821 to − 622 bp upstream of the translation initiation codon ATG and devoid of the Cre1-binding sites) of the strong inducible promoter Pcbh1 was cloned and identified to be an amplifier in initiating gene expression. Finally, this activation region was fused to the strongest promoter Pcdna1-3, generating the novel synthetic hybrid promoter Pcc. This engineered promoter Pcc drove strong gene expression by displaying 1.6- and 1.8-fold stronger fluorescence intensity than Pcbh1 and Pcdna1 under the inducible condition using egfp as the reporter gene, respectively. Furthermore, Pcc was applied to overexpress the Aspergillus niger β-glucosidase BGLA coding gene bglA and the native endoglucanase EG2 coding gene eg2, achieving 43.5-fold BGL activity and 1.2-fold EG activity increase, respectively. Ultimately, to overcome the defects of the native cellulase system in T. reesei, the bglA and eg2 were co-overexpressed under the control of Pcc promoter. The bglA-eg2 double expression strain QPEB70 exhibited a 178% increase in total cellulase activity, whose cellulase system displayed 2.3- and 2.4-fold higher saccharification efficiency towards acid-pretreated and delignified corncob residues than the parental strain, respectively.ConclusionsThe synthetic hybrid promoter Pcc was generated and employed to improve the cellulase system of T. reesei by expressing specific components. Therefore, construction of synthetic hybrid promoters would allow particular cellulase genes to be expressed at desired levels, which is a viable strategy to optimize the cellulolytic enzyme system for efficient biomass bioconversion.

Ultrasensitive lateral flow immunoassay for staphylococcal enterotoxin B using nanosized fluorescent metal-organic frameworks.

Owing to their outstanding optical properties and superior physical/chemical stability, dye-doped fluorescent nanoparticles (NPs) are growing exponentially as signal labels of immunochromatographic lateral flow immunoassay (LFA) for the detection of various analytes. However, the key challenge in the design of these fluorescent NPs is to confine the fluorophores inside NPs at extreme concentrations, at which dyes tend to self-quench resulting from the formation of non-fluorescent aggregates. Looking for other advantageous nanomaterials, we propose for the first time the use of a nanosized fluorescent metal-organic framework (nanoMOF) in LFA for the detection of staphylococcal enterotoxin B (SEB) as a model analyte. Featured by the chromophore assembly, the nanoMOF exhibited a high dye loading (∼60%) and strong fluorescence intensity, which was due to the reduced self-quenching of dyes in a variety of MOF matrices. The strong green fluorescence intensity of the nanoMOF gives a high contrast against the background of the strips and the sensitivity reflected by photoluminescence was improved by the enhanced antenna effect. Furthermore, due to the high surface area for antibody stemming, the limit of detection (LOD) of the MOF based LFA for SEB detection was as low as 0.025 ng mL-1. The compatibility of the MOF based LFA with dairy samples and its stability under long-term storage conditions were also demonstrated. The integration of a nanoMOF into LFA to detect toxins could inspire the utilization of such nanomaterial-based labels in similar immunochromatographic testing methods to improve their performance.

Mesoporous Silica Nanoparticles Carrying MicroRNA-124 to Target P2Y12 Facilitates Cerebral Angiogenesis in Lacunar Cerebral Infarction Through Stem Cell Factor/c-Kit Signaling Pathway.

MicroRNA (miRNA)-124 inhibitor may enhance cerebral blood vessel formation in lacunar cerebral infarction (LCI) and mesoporous silica nanoparticles are highlighted as a drug carrier which improves patients' outcome. This study explored the impact of miR-124 and its promising targeted gene P2Y12 encapsulated by mesoporous silica nanoparticles (MSNs) on progression of LCI, and its interaction between SCF/c-kit signaling pathway. After establishment of animal models, the animals were divided into 6 groups, namely: model group, blank group, empty carrier group, carrier + miR-124 inhibitor group, SCF/c-kit inhibitor group, and P2Y12 agonist group. Western blot analysis and microscope determined the expression level of miR-124 in the rat brain tissue slices. MVD, SCF and c-kit P2Y12 protein expression levels were detected and their targeting relationship was verified. miR-124 was poorly expressed in the cells of rats with LCI upon injection of MSNs carrying miR-124-inhibitor. The LCI model group had the highest number of VEGF-positive. Compared with the model group, the number in the carrier + miR-124 inhibitor group was lowest. Moreover, treatment with SCF/c-kit inhibitor and P2Y12 agonist also obtained reduction in the number of VEGF-positive cells with less prominent effect (P < 0.05). With elevation of MVD in the LCI rats, injection of P2Y12 agonist or SCF/c-kit inhibitor significantly decreased the amount of MVD, while miR-124 inhibitor-loaded MSNs better reduced the MVD level. Besides, the LCI rats exhibited up-regulated level of P2Y12 protein. Injection of P2Y12 agonist or SCF/c-kit inhibitor dramatically decreased the level of P2Y12, where the level was still higher than that of carrier + miR-124 inhibitor group. Moreover, administration of miR-124 inhibitor-loaded MSNs resulted in increased SCF and c-kit protein level, and SCF/c-kit inhibitor group and P2Y12 agonist group also had increased SCF and c-kit protein level, compared to the model group. Mechanistically, the miR-124 was indicated to target P2Y12 with stronger fluorescence intensity in mutant plasmid (P < 0.05). MSN-encapsulated miR-124 inhibitor increased the expression of SCF/c-kit protein by targeting P2Y12, thereby enhancing regeneration of cerebral blood vessels in LCI.

Selective Fe(ii)-fluorescence sensor with validated two-consecutive working range using N,S,I-GQDs associated with garlic extract as an auxiliary green chelating agent.

The goal of this work was to use the pyrolysis process to synthesize graphene quantum dots doped with garlic extract (as N,S-GQDs) and simultaneously co-doped with iodine (as I-GQDs). XPS, HR-TEM, FE-SEM/EDX, FT-IR, fluorescence, and UV-visible absorption spectroscopy were used to characterize the N,S,I-GQDs and analyze their morphological images. The quantum yield of N,S,I-GQDs was found to be 45%, greater than that of undoped GQDs (31%). When stimulated at 363 nm, the N,S,I-GQDs display a strong fluorescence intensity at a maximum wavelength of 454 nm. Using N,S,I-GQDs as a fluorescence quenching sensor for screening tests with various metal ions, it was discovered that they are extremely selective towards Fe2+ over Fe3+ and other ions. Thus, solution pH, concentration of N,S,I-GQDs, quantity of garlic extract, EDTA and AgNO3 concentration as masking agents, reaction duration under ultrasonic aid, and tolerable limit of Fe3+ presence in the target analyte were all optimized for Fe2+ detection. A highly sensitive detection of Fe2+ was obtained using a linear curve with y = 141.34x + 5.5855, R2 = 0.9961, LOD = 0.11 mg L−1, and LOQ = 0.35 mg L−1. The method precision, given as RSDs, was determined to be satisfactory at 1.04% for intra-day analysis and 3.22% for inter-day analysis, respectively. As a result, the selective determination of trace amounts of Fe2+ in real water samples using such labile multi-element doped GQDs in conjunction with garlic extract as a green chelating agent to maintain its enhanced sensitivity was successfully applied with good recoveries ranging from 89.16 to 121.45%.