Graphical Abstract Physicochemical characteristics of particle-based carriers influence their peritoneal residence time, biological fate and anticancer efficacy after intraperitoneal administration.Metal complexes were obtained by the reaction of zinc, cadmium and mercury(II) salts with Schiff base HL (N(salicylidene)benzylamine). HL was synthesized by the condensation reaction of benzylamine and 2-hydroxybenzaldehyde. The fluorescence properties of the Schiff base and its metal complexes were studied in ethanol-water solutions. HL was examined for its utility as a fuorescent chemosensor for the determination of Zn2+, Cd2+ and Hg2+ in aqueous samples. The HL chemosensor was found to be sensitive to Zn2+, Cd2+ and Hg2+ than some metal ions and its complexes emitted strong fluorescence at 452 nm for Zn2+ at 474 nm for Cd2+ and at 491 nm for Hg2+, respectively. It was determined that HL forms complexes with a ratio of 21 for Zn2+ and Hg2+ and with a ratio of 11 for Cd2+ by Job plots. For the detection of Zn2+, Cd2+ and Hg2+ in aqueous samples, pH, solvent type and ligand concentration were optimized for an analytical method based on HL chemosensor. HL gave a wide range of linearity with Zn2+, Hg2+ and Cd2+, the limit of detection was found to be 2.7 × 10-7 M, 7.5 × 10-7 M and 6.0 × 10-7 M, respectively.A significant challenge concerning the development of fluorescence lifetime (FL) based pH sensors is the paucity of fluorophores with sufficiently large FL variation with pH. Acridine is amongst the indicators with highest fluoresce lifetime responses to pH, with a change in lifetime of about 13 ns within a pH range of 5-8. Here we examine the two acridine derivatives, 9-acridinemethanamine (9-AMA) and acridine-9-carbaldehyde (9-ACA) in terms of their FL pH sensitivity and pH sensing range. Both indicators are characterized when dissolved in buffer solutions, as well as when immobilized in support materials. 9-AMA has a change in FL of 11 ns between pH 2-5, both when dissolved in solution and when immobilized in surfactant-filled mesoporous silica. The FL of 9-ACA is not sensitive to pH when dissolved in buffer solutions; however, when covalently bound to amine-modified silica, its FL changes 15 ns between pH 3-6. 9-AMA and 9-ACA represent promising FL in the pH range of pH 2-6, and could potentially form the basis of new FL pH sensors. Graphical Abstract.Dendrobium officinale is a rare and endangered perennial herb in China, which have been used in preparing Chinese tonic medicine for hundreds of years. The severe shortage of this herb and high price have caused that many similar plants were processed as an adulterant and it became difficult to distinguish genuine D. officinale by traditional authentication methods. A sensitive, convenient, and specific method for rapid identification of D. officinale is urgently needed. In the present study, 3D front-face fluorescence technique merged with Independent Component Analysis was used to get the "pure" independent fluorescence signals. The overall 3D-FFF spectra were decomposed into seven independent components (IC). https://www.selleckchem.com/products/sn-001.html To distinguish D. officinale from other species, IC1 and IC4 were chosen as fluorescence markers and the fluorescence intensity (FI) value at 340 nm/ 442 nm (excitation /emission wavelength) of IC1and 315 nm/ 468 nm of IC4 were used to build a linear model for identifying D. officinale successfully. Compared with other Dendrobium species, D. officinale showed much higher FI1 and FI4 value which is a direct criterion for identification. Meanwhile, even though the FI values of D. officinale may fluctuate due to the difference of growing conditions, the relation between FI1 and FI4 amazingly always fit the linear model constructed (FI4 = 9.9046 + 0.6119FI1, R2 = 0.9811). The linear model is an important finding and specific for D. officinale. Based on the FI value and the goodness of fit in the linear model, D. officinale can be identified quickly.Based on boron-dipyrromethene (BODIPY), taking 2-hydroxy-N-(2-hydroxyphenyl)benzamide as recognition site, a new fluorescent probe HHPBA-BODIPY aimed at sensitively detecting Cu ions was designed, synthesized and characterized.The emission spectra of HHPBA-BODIPY exhibited an intensive green fluorescence around 510 nm, with a maximum absorption near 500 nm. When Cu2+ ions are present, the fluorescence at 510 nm can be quenched with a good linearity between the copper ion concentrationand the fluorescence intensity and the detection limit is 0.35 μM. HHPBA-BODIPY is also selective toward Cu2+, while other metal ions show no interfere except Fe3+ and Cr3+ ions. In addition, HHPBA-BODIPY also proved efficient to detect Cu2+ in water samples which offers the possibility to detect trace amount of Cu2+ for environmental monitoring. Copper ions; BODIPY; fluorescent probe.The absorption and fluorescence spectra of synthesized 4-[5-(2,5-Dimethyl-pyrrol-1-yl)-[1, 3, 4] thiadiazol-2-ylsulfanylmethyl]-6-methoxy-chromen-2-one (DTYMC) compound were recorded in various solvents like acetone, acetonitrile, chloroform, dimethyl formamide (DMF),1,4-dioxane, ethanol, ethyl acetate, methanol, tetrahydrofuran (THF) and dimethylsulphoxide (DMSO) at room temperature in order to estimate the ground and excited state dipole moment. The ground state dipole moment (μg) and excited state dipole moment (μe) were calculated using solvatochromic shift method which involve equations proposed by Lippert, Bakshiev and Kawski-Chamma-Viallete. The results were signified that the excited state dipole moment is greater than the ground state dipole moment, which indicates the excited state is more polar than the ground state of the molecule. The bond angle between the ground state and excited state dipole moments were found to be 00, The change in dipole moment (∆μ) was calculated using microscopic solvent polarity parameter ([Formula see text]). Further multiple linear regression analysis of Kamlet-Taft parameter, HOMO-LUMO energy were determined by cyclic voltammetry using phosphate buffer solution.In this study, we developed two different very sensitive magnetite fluorescent Fe3O4@SiO2-TPED-BODIPY and Fe3O4@SiO2-TMPTA-BODIPY nano-sensors for the selective detection of Cr(VI) ions. The Cr(VI) metal ions sensing is based on the fluorescent quenching of BODIPY functionalized with Fe3O4@SiO2-TPED and Fe3O4@SiO2-TMPTA nanoparticles in the ethanol-water environment. Characterization of the newly synthesized fluorescent BODIPY compound was performed on a 1H and 13C-NMR spectrometer. The morphology, chemical and physical properties of the sensing nano-sensors were studied by transmission thermogravimetric analysis (TGA), X-ray diffraction (XRD), energy dispersive X-ray (EDX), scanning electron microscopy (SEM), FT-IR spectroscopy, and transmission electron microscopy (TEM). UV-visible and fluorescent spectroscopy were used to characterize BODIPY functionalized magnetite fluorescent nano-sensors. Characterization measurements revealed that the mean particle diameter of magnetite fluorescent Fe3O4@SiO2-TPED-BODIPY and Fe3O4@SiO2-TMPTA-BODIPY nano-sensors was 18.