Selective colorimetric and fluorescent quenching determination of uranyl ion via its complexation with curcumin.

Under pH4.0 HAc-NaAc buffer medium, curcumin alone possesses extraordinary weak fluorescence emission. Nevertheless, the introduction of Triton X-100 micelles can largely enhance the fluorescence intensity of curcumin. Uranyl ions can complex with micelles-capped curcumin, along with the slight red shift of curcumin fluorescence (about 1-7 nm), a clear decrement of absorbance (424 nm) and fluorescence (507 nm) intensities, and a distinct color change from bright yellow to orange. The fluorescence decrements (ΔF, 507 nm) are positively correlated to the amount of uranyl ions in the concentration range of 3.7×10(-6)-1.4×10(-5) mol L(-1). The detection limit of this fluorescence quenching methods is 3.7×10(-6) mol L(-1), which is nearly 9000 times lower than the maximum allowable level in drinking water proposed by World Health Organization. Good selectivity is achieved because of a majority of co-existing substances (such as Ce(4+), La(3+), and Th(4+)) do not affect the detection. The content of uranyl ions in tap water samples was determined by the proposed method with satisfactory results.

Interaction of proteins with aluminum(III)-chlorophosphonazo III by resonance Rayleigh scattering method.

In weak acid medium, aluminum(III) can react with chlorophosphonazo III [CPA(III), H(8)L] to form a 1:1 coordination anion [Al(OH)(H(4)L)](2-). At the same time, proteins such as bovine serum albumin (BSA), lysozyme (Lyso) and human serum albumin (HSA) existed as large cations with positive charges, which further combined with [Al(OH)(H(4)L)](2-) to form a 1:4 chelate. This resulted in significant enhancement of resonance Rayleigh scattering (RRS), second-order scattering (SOS) and frequency doubling scattering (FDS). In this study, we investigated the interaction between [Al(OH)(H(4)L)](2-) and proteins, optimization of the reaction conditions and the spectral characteristics of RRS, SOS and FDS. The maximum RRS wavelengths of different protein systems were located at 357-370 nm. The maximum SOS and FDS wavelengths were located at 546 and 389 nm, respectively. The scattering intensities (ΔI) of the three methods were proportional to the concentration of the proteins, within certain ranges, and the detection limits of the most sensitive RRS method were 2.6-9.3 ng/mL. Moreover, the chelate reaction mechanism or the reasons for the enhancement of RRS were discussed through absorption spectra, fluorescence spectra and circular dichroism (CD) spectra.

Fluorescence quenching method for the determination of carbazochrome sodium sulfonate with aromatic amino acids.

In Britton-Robinson (BR) buffer medium (pH 3.3), carbazochrome sodium sulfonate (CSS) can react with some aromatic amino acids such as tryptophan (Trp), tyrosine (Tyr) and phenylalanine (Phe) to form a 1:1 complex by electrostatic attraction, aromatic stacking interaction and Van der Waals' force, resulting in fluorescence quenching of these amino acids. Maximum quenching wavelengths were located at 352 nm (CSS-Trp system), 303 nm (CSS-Tyr system) and 284 nm (CSS-Phe system), respectively. The fluorescence quenching value (ΔF) was proportional to the concentration of CSS in a certain range. The fluorescence quenching method for the determination of CSS showed high sensitivity, with detection limits of 31.3 ng/mL (CSS-Trp system), 44.6 ng/mL (CSS-Tyr system) and 315.0 ng/mL (CSS-Phe system), respectively. The optimum conditions of the reaction conditions and the effect of coexisting substances were investigated and results showed that the method had good selectivity. The method was successfully applied for the rapid determination of CSS in blood and urine samples. Based on the bimolecular quenching constant Kq , the effect of temperature and Stern-Volmer plots, this study showed that quenching of fluorescence of amino acids by CSS was a static quenching process.

Studying the interaction between CdTe quantum dots and Nile blue by absorption, fluorescence and resonance Rayleigh scattering spectra.

Thioglycolic acid (TGA) capped CdTe quantum dots (QDs) with the diameter of 2-3nm were synthesized. The interaction between CdTe QDs and Nile blue (NB) was investigated by ultraviolet-visible (UV-vis) absorption, resonance Rayleigh scattering (RRS) and fluorescence spectroscopy. UV-vis absorption spectrum of CdTe QDs and NB obviously changed, showing that CdTe QDs could associate with NB to form a new complex. At pH 6.8, NB effectively quenched the fluorescence of CdTe QDs. It was proved that the fluorescence quenching of CdTe QDs by NB was mainly result of the formation of CdTe QDs-NB complex, electrostatic attraction and hydrophobic forces played a major role in stabilizing the complex. The binding molar ratio of CdTe QDs and NB was 5:1 by a mole-ratio method. The interaction between CdTe QDs and NB lead to the remarkable enhancement of RRS and the enchantments were in proportional to the concentration of NB in a certain range. The mechanism of the interaction between CdTe QDs and NB, reasons for the enhancement of RRS intensity were also discussed. The obtained results suggested the more satisfactory mechanism for the interaction between CdTe QDs and NB.

Study on the resonance Rayleigh scattering and resonance non-linear scattering spectra of ion-association complexes of [PdI4](2-)-protein systems and their analytical applications.

In an acid medium solution, proteins such as bovine serum albumin, human serum albumin, ovalbumin, hemoglobin, lysozyme, gamma-globulin, alpha-chymotrypsin and papain could react with [PdI(4)](2-) by virtue of electrostatic attraction and hydrophobic force to form ion-association complexes. As a result, the resonance Rayleigh scattering (RRS) and resonance nonlinear scattering such as second-order scattering (SOS) and frequency doubling scattering (FDS) intensities were enhanced greatly and new scattering spectra appeared. The maximum scattering peaks of RRS, SOS and FDS were at 367, 720 and 370 nm, respectively. The enhanced RRS, SOS and FDS intensities were directly proportional to the concentrations of proteins. The detection limits for the different proteins were 2.4-11.8 ng/mL for RRS method, 9.5-47.9 ng/mL for SOS method and 4.6-18.5 ng/mL for FDS method. In this work, the influences of the interaction of [PdI(4)](2-) with proteins on spectral characteristics of RRS, SOS and FDS were investigated and the optimum conditions were tested. Meanwhile, the effects of coexisting substances were tested and the results showed that the method exhibited a good selectivity. Based on the above research, a highly sensitive, simple and rapid method for the determination of trace amounts of proteins by resonance light scattering technique has been developed. It can be applied to the determination of proteins in tablet, human serum and urine samples.

[Fluorescence quenching reaction of tetracaine hydrochloride with erythrosine and their analytical applications].

In Britton-Robinson (BR) buffer solution at pH 4.0, erythrosine (ET) reacts with tetracaine hydrochloride (TA x HCl) to form an ion association complex that quenches the fluorescence of erythrosine and has a compound ratio of 1 : 1. The measurement wavelength of fluorescence quenching was located at lambda(ex)/lambda(em) = 525 nm/556 nm. The linear range for TA x HCl is from 0.28 microg x mL(-1) to 4.8 microg x mL(-1), and its detection limit is 0.083 microg x mL(-1). The influence of coexisting substance was also inspected, and the result shows that this method has a better selectivity. Therefore, a new fluorospectrophotometry, being high sensitive, sample and rapid, was developed to determinate TA x HCl at trace amounts. The method has been applied to the determination of TA x HCl in human serum and urine samples with satisfactory results. In this study, the spectral characteristics and the optimum reaction conditions were discussed with quantum chemistry AM1 method.

Fluorescence quenching of serum albumin by rifamycin antibiotics and their analytical application.

In neutral medium, rifamycin antibiotics such as rifapentin (RFPT), rifampicin (RFP), rifandin (RFD) and rifamycin SV (RFSV) can bind with human serum albumin (HSA) and bovine serum albumin (BSA) to form complexes, resulting in the quenching of the intrinsic fluorescence (lambda(ex)/lambda(em) = 285/355 nm) of the BSA and HSA. The quenching intensity (DeltaF) is directly proportional to the concentration of the rifamycin antibiotics. Therefore, a new analytical method was established to determine trace rifamycin antibiotics. The method had fairly high sensitivity and the detecting limits (3sigma) for RFPT, RFP, RFD and RFSV were 0.85, 0.98, 1.83, 1.89 ng/mL, respectively, for the HSA system and 0.76, 0.89, 1.55, 1.77 ng/mL, respectively, for the BSA system. All relative standard deviations (RSDs) were <3.8%. In this work, the characteristics of the fluorescence spectra were studied and the optimum reaction conditions and influencing factors were investigated. The influence of coexisting substances was tested and the results showed that the method had good selectivity and could be applied to determine trace rifamycin antibiotics in medicine capsules and urine samples. Taking the RFSV-serum albumin system as an example, the reaction mechanisms, such as binding constants, binding sites, binding distance and the type of fluorescence quenching, were investigated.

Resonance Rayleigh scattering spectral method for the determination of raloxifene using gold nanoparticle as a probe.

When gold nanoparticles were being prepared by sodium citrate reduction method, citrate anions self-assembled on the surface of gold nanoparticles to form supermolecular complex anions with negative charges, and protonated raloxifene (Ralo) was positively charged and could bind with the complex anions to form larger aggregates through electrostatic force and hydrophobic effects, which could result in the remarkable enhancement of the resonance Rayleigh scattering intensity (RRS), and the appearance of new RRS spectra. At the same time, the second-order scattering (SOS) and frequency-doubling scattering (FDS) intensities were also enhanced. The maximum wavelengths were located near 370 nm for RRS, 520 nm for SOS, and 350 nm for FDS, respectively. Among them, the RRS method had the highest sensitivity and the detection limit was 5.60 ng mL(-1) for Ralo, and its linear range was 0.05-2.37 microg mL(-1). A new RRS method for the determination of trace Ralo using gold nanoparticles probe was developed. The optimum conditions of the reaction and influencing factors were investigated. In addition, the reaction mechanism and the reasons for the enhancement of RRS were discussed.

Resonance Rayleigh-scattering method for the determination of sildenafil citrate in a pharmaceutical formulation using Evans blue.

A highly sensitive resonance Rayleigh-scattering (RRS) method for the determination of sildenafil citrate has been developed, based on the fact that sildenafil (Sild) reacted with Evans Blue (EB) to form an ion-association complex in pH 1.1 - 4.6 aqueous solution. This resulted in a significant enhancement of the RRS intensity, and a new spectrum appeared. The wavelength of the maximum RRS was at 365 nm, and other scattering peaks were at 400, 442, 470 and 534 nm, respectively. The intensity of RRS was directly proportional to the concentration of Sild in the range 0 - 11.5 microg ml(-1), and the detection limit for Sild (3 sigma) was 30.3 ng ml(-1). The composition of the ion-association complex was Sild:EB = 1:1, as established by Job's method. The method had good selectivity and could be applied to the determination of Sild in the aqueous phase without using organic solvent extraction. The method was simple and rapid. In addition, the reaction mechanism and the reason for RRS enhancement were considered.

Fluorescence quenching method for the determination of sodium carboxymethyl cellulose with acridine yellow or acridine orange.

In near neutral to weak basic media, sodium carboxymethyl cellulose (NaCMC) will dissociate to become a macro polymeric anion, which can react with acridine yellow (AY) or acridine orange (AO) to form an ion-association complex resulting in fluorescence quenching of the acridine dyes. The maximum fluorescence quenching wavelength is 505 nm (lambda(ex)=440 nm) for AY system and 530 nm (lambda(ex)=493 nm) for AO system, respectively. The fluorescence quenching values (DeltaF) are directly proportional to the concentrations of NaCMC and the linear ranges are 20.0-4000 microg/L for AY system and 20.0-7000 microg/L for AO system, separately. This method has high sensitivity and the detection limits for NaCMC are 58.0 microg/L (AY system) and 157.2 microg/L (AO system). The effects of coexistent substance have been investigated, and the results show that this method has a relatively good selectivity. A fluorescence quenching method for the determination of NaCMC based on the ion-association reactions of CMC polymeric anion with a basic acridine dye was developed. The method is sensitive, simple and fast.

Resonance Rayleigh scattering study of interaction of hyaluronic acid with ethyl violet dye and its analytical application.

In near weak acid to neutral medium, ethyl violet (EV) can react rapidly with hyaluronic acid (HA) to form a complex, which results in a significant enhancement of resonance Rayleigh scattering (RRS) and an appearance of a new spectrum, and the scattering wavelengths appear at 231, 274, 326, 498 and 640 nm. The maximum scattering wavelength appears at 326 nm. The RRS intensity is directly proportional to the concentration of HA in the range of 0.4-48.0 microg mL(-1). A new method for the determination of trace amounts of HA based on the RRS method has been developed. The method exhibits high sensitivity, and the detection limit for HA is 9.6 x 10(-2) microg mL(-1). This method was applied for determining HA in eyedrops and in sodium hyaluronate injection samples with satisfactory results. Furthermore, the enhancement reasons of RRS and the relationship between RRS spectral characteristics of the HA-EV complex and its absorption spectrum have been discussed.

Resonance Rayleigh scattering study on the interaction of gold nanoparticles with berberine hydrochloride and its analytical application.

The interaction of gold nanoparticles with berberine hydrochloride has been studied by using resonance Rayleigh scattering (RRS) spectra. In pH 3.8-5.5 aqueous solution, citrate acid ([H2L2-]) self-assembled on the surface of positively charged gold nanoparticles (average diameter is about 12.0 nm) to form a supermolecular complex with negative charges. By virtue of electrostatic attraction, hydrophobic force and charge transfer, the complex bound with berberine to form complex, which had bigger diameter (35 nm) than gold nanoparticles. The formation of the binding production not only resulted in the red shift of absorption of gold nanoparticles from 518 to 672 nm, but also led to the greatly enhancement of RRS intensity. At the same time, the intensities of second-order scattering (SOS) and frequency-doubling scattering (FDS) were also increased. Under definite condition, the increment of the RRS (DeltaI) were proportional to the concentration of berberine. A sensitive and simple method for the determination of berberine based on the RRS technique has been developed. The detection limit (3sigma) for berberine was 0.40 ng mL(-1) and the quantitative determination range was 1.33-240 ng mL(-1). In this work, the optimum conditions of reaction, the effect of foreign substances and the analytical application had been investigated.

[Resonance-scattering spectral determination of H2O2 using rhodamine 6G association particles].

Under the conditions of 0.02 mol x L(-1) HCl-4.0 x 10(-4) mol x L(-1) KI-1.6 x 10(-5) mol x L(-1) Mo(VI), there is a fluorescence peak at 540 nm and a synchronous fluorescence peak at 540 nm for Rhodamine 6G (RhG). When there exists H2O2, it reacts with I- to form I3-. RhG and I3- combine to form an ion association particle. The particles exhibit three resonance scattering peaks at 320 nm, 400 and 595 nm respectively. And there is fluorescence quenching at 540 nm. H2O2 concentration in the range of 0.068-34 microg x mL(-1) is proportional to the resonance scattering peak at 400 nm. And a new resonance scattering spectral method has been described for the determination of H2O2 in water samples. The spectral results have verified that the formation of (RhG-I3)n association particles and the interface are the main factor that causes the fluorescence quenching and resonance scattering effects.

[The interface fluorescence and resonance scattering spectral properties of Ag2S nanoparticles in liquid phase].

S2- and Ag+ form stable Ag2S nanoparticles in the presence of sodium dodecyl sulphate (SDS). It exhibits a strong resonance scattering peak at 470 nm and a strong fluorescence peak at 470 nm when excitation wavelength is at 200 nm. The effects of TAA and Ag+ concentration on the fluorescence intensities are consistent with those on the resonance scattering signals. The resonance scattering and fluorescence intensities all increase with Ag+ concentration in the range of 0-8.0 x 10(-5) mol x L(-1). The results verified that there is a correlation between the fluorescence and resonance scattering. The fluorescence is the interface fluorescence of Ag2S nanoparticles in liquid phase.

A study on the sizes and concentrations of gold nanoparticles by spectra of absorption, resonance Rayleigh scattering and resonance non-linear scattering.

Liquid phase gold nanoparticles with different diameters and colors can be prepared using sodium citrate reduction method by controlling the amounts of sodium citrate. The mean diameters of gold nanoparticles are measured by transmission electron microscope (TEM). Gold nanoparticles with different sizes have specific absorption spectra. When the diameters of nanoparticles is between 12 and 41 nm, the maximum absorption peaks locate at 520-530 nm and there are red shifts gradually with the increase of diameters of gold nanoparticles. And when the size of gold nanoparticle is constant, the absorbance is proportional to the concentration of gold. Obvious resonance Rayleigh scattering (RRS) and the resonance non-linear scattering such as second-order scattering (SOS) and frequency-doubling scattering (FDS) appear at the same time as well, and the maximum scattering peaks are located at 286 nm (RRS), 480 nm (SOS) and 310 nm (FDS), respectively. When the concentration of gold is constant, absorbance and the intensities of RRS, SOS and FDS (I(RRS), I(SOS) and I(FDS)) have linear relationships with the diameters of gold nanoparticles. When the diameter of gold nanoparticle is constant, the absorbance and I(RRS), I(SOS), I(FDS) are directly proportional to the concentrations of gold nanoparticles. Therefore, it is very useful for studying the liquid phase gold nanoparticles by investigating the absorption, RRS, SOS and FDS spectra.

Resonance Rayleigh scattering study of interaction of heparin with some cationic surfactants and their analytical application.

Binding of heparin with a cationic surfactant such as cetyldimethyl benzylammonium chloride (CDBAC), tetradecyldimethyl benzylammonium chloride (Zeph), cetylpyridinium bromide (CPB), tetradecane pyridinium bromide (TPB) and cetyltrimethylammonium bromide (CTAB) in a near-neutral medium can result in a significant enhancement of resonance Rayleigh scattering (RRS) intensities. The results showed that the reaction conditions and RRS spectral characteristics of these reactions are similar, but their sensitivities are obviously different. Among them, the sensitivity of CDBAC with an aryl and large molecular weight is the highest, while that of CTAB without aryl and with small molecular weight is the lowest. The detection limit for heparin of the former is 11 ng ml(-1) while that of the latter is 33 ng ml(-1). The method has better selectivity and was applied to the determination of trace amounts of heparin in sodium heparin injection samples with satisfactory results. Furthermore, it is discovered that the RRS intensity is related to the structure and molecular weight of the cationic surfactant.

Resonance Rayleigh scattering study of the inclusion complexation of chloramphenicol with beta-cyclodextrin.

The interaction of chloramphenicol and beta-cyclodextrin (beta-CD) in aqueous solution was studied using resonance Rayleigh scattering (RRS) technology. The molar ratio of the inclusion complex was 1:1 established by spectrophotometry. The RRS technology was first applied to the determination of the inclusion constant of chloramphenicol to beta-CD. The RRS peak of chloramphenicol was at 331 nm. When beta-CD interacted with chloramphenicol to form an inclusion complex, the RRS intensity was enhanced and increased with an increase in beta-CD concentration. The inclusion constants at different temperatures were measured by the RRS technology. The determination results using the RRS technology corresponded with those of the UV-spectrophotometric method. Therefore, the RRS method can be used as a new technology for the determination of the inclusion constant. The thermodynamic parameters (DeltaH, DeltaS and DeltaG) associated with the inclusion process were also determined. These values indicated that van der waals forces and hydrogen bonding could be considered as a main driving force for the encapsulation of chloramphenicol by beta-CD.

[Photochemical preparation of Au nanoparticles with polyethyelene glycol and its resonance scattering spectral study].

The nano-photochemical reaction of polyethyelene glycol (PEG)-Au3+ was studied by resonance scattering and absorption spectrophotometry, and transmission electron microscopy. Influence of various factors on the preparation of gold nanoparticles was considered. There is a correlation between the molecular mass of PEG and the size of gold nanoparticles. A new photochemical method was proposed for the preparation of gold nanoparticles in size of 6-60 nm, using different molecular mass of PEG. The cause of obtaining gold nanoparticle with different size is the different space effect and hydrophobic property of PEG. A reasonable nano-reaction mechanism was developed.

Resonance Rayleigh scattering measurement of aminoglycoside antibiotics with Evans Blue.

In a weak acid medium, some aminoglycoside antibiotics, such as kanamycin (KANA), gentamicin (GEN), tobramycin (TOB) and neomycin (NEO), or acid bisazo dye Evans Blue (EB) can only produce very weak resonance Rayleigh scattering (RRS) signals. However, when two agents react with each other to form ion-association complexes, the RRS intensity can be greatly enhanced and a new RRS spectrum with a significant enhancement of the RRS intensity in the wavelength range from 350 nm to 600 nm can be observed. The maximum scattering peak is at 570 nm. There is a linear relationship between the RRS intensity and the antibiotic concentration in the range of 0.01-6.0 microg mL(-1) at 570 nm. This RRS method for the determination of aminoglycoside antibiotics at trace-amount levels has been developed. The detection limits (3sigma) of the four antibiotics, whose order of sensitivity from high to low ranks as KANA > NEO > TOB > GEN, are 5.2-6.9 ng mL(-1). This method has good selectivity and has been successfully applied to the quick determination of antibiotics not only for injections and ear drops, but for clinic serum samples as well. In addition, the reaction mechanism by using a quantum chemistry method and the influencing factors of the RRS spectra and the enhancement reasons of RRS have been discussed.