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Cheng Zhi Huang

Publications and source records attributed to Cheng Zhi Huang.

15 recordsLinked to original sources

Visual detection of Sudan dyes based on the plasmon resonance light scattering signals of silver nanoparticles.

A visual light scattering detection method of Sudan dyes is reported in food products based on the formation of silver nanoparticles (NPs) . Sudan dyes including I, II, III and IV have reducibility due to the nitrogen-nitrogen double bond and phenol group in their molecular structure, and a redox reaction could occur with AgNO3. Owing to the formation of silver NPs as a result of the redox reaction, color changes could be observed by eye from the red of Sudan to the brown of silver NPs, resulting in strong plasmon resonance light scattering (PRLS) signals characterized at 452 nm, which could be measured using a common spectrofluorometer. It was found that the PRLS intensities were proportional to the dye concentrations over the range of 0.2-2.4 microM Sudan I, 0.1-2.4 microM Sudan II, 0.1-2.4 microM Sudan III, and 0.2-3.0 microM Sudan IV, with the corresponding limits of determination (3 sigma) of 3.2, 3.0, 3.2, and 2.9 nM, respectively. Using hot chili as a model sample, detection could be made with the recovery of 90.8-103.3% and RSD of 4.0-4.9%, and the results are identical with that of a liquid chromatographic method approved by the European Commission. To make the PRLS method much more practical, we could visually detect the quantity of Sudan dyes based on the PRLS signals using simple devices such as a portable laser pointer (653 nm) and a light emitting diode (458 nm). Mechanism investigations show that the functional group of Sudan oxidized by AgNO3 is the phenol group, not the nitrogen-nitrogen double bond.

Azo Compounds↗

Pharmacokinetic detection of penicillin excreted in urine using a totally internally reflected resonance light scattering technique with cetyltrimethylammonium bromide.

A quantitative analysis method for penicillins including ampicillin (AmP), benzyl penicillin (BP), oxacillin (OA) and amoxycillin (AmO) is proposed that makes use of the totally internally reflected resonance light scattering (TIR-RLS) signal from the penicillin at the H2O/CCl4 interface in the presence of cetyltrimethylammonium bromide (CTMAB), and enables the pharmacokinetics of penicillin taken orally and excreted through urine to be monitored. Penicillin is coadsorbed with CTMAB at the H2O/CCl4 interface in neutral solution, resulting in the formation of ion associates that display greatly enhanced TIR-RLS signals (maximum at 368-372 nm). This enhanced TIR-RLS intensity was found to be proportional to the penicillin concentration over the range 0.2 x 10(-6) to 2.2 x 10(-6) mol L(-1), with limits of determination (3sigma) of 5.0 x 10(-8) to 7.0 x 10(-8) mol L(-1). Pharmacokinetics studies performed using the present method show that the excretion of orally-taken ampicillin through urine has a half-time of 1.05 h and an excremental quantum over 8 h of 49.3%, respectively.

Calibration↗

A backscattering light detection assembly for sensitive determination of analyte concentrated at the liquid/liquid interface using the interaction of quercetin with proteins as the model system.

We report on the construction of a backscattering light (BSL) detection assembly based on detecting angle-dependent light scattering signals, by changing the sample chamber of a common spectrofluorometer. The BSL detection assembly was used to detect, with high sensitivity, the analyte concentrated at the liquid/liquid interface. We applied this assembly to study the interaction of proteins with quercetin in the presence of cationic surfactant. The species resulting from the interaction of quercetin with proteins, when concentrated at the H2O/CCl4 interface, generate enhanced BSL signals characterized at 376.0 nm which were found to be proportional to human serum albumin (HSA) and bovine serum albumin (BSA) in the range of 1-1250 ng mL(-1) and 2-1250 ng mL(-1), respectively. Limits of determination (3sigma) of 75 and 180 pg mL(-1) are reported for the two proteins.

Animals↗

A selective and sensitive assay of berberine using total internal reflected resonance light scattering technique with fluorescein at the water/1,2-dichloroethane interface.

An assay of berberine (BE) was developed with good selectivity and sensitivity based on the total internal reflected resonance light scattering (TIR-RLS) signals from water/1,2-dichloroethane (H(2)O/DCE) interface. Under optimal conditions, amphiphilic complex formed by BE and fluorescein (Flu) was adsorbed to H(2)O/DCE interface, resulting in good separation of BE from the coexisting foreign substances in aqueous phase and significant enrichment of BE at the interface. This enriched species at the interface was found corresponding to enhanced TIR-RLS signals located at 370.0 nm. Proportional relationships were established between the enhanced TIR-RLS intensity and the BE in the range of 3.2 x 10(-9) to 3.2 x 10(-6) mol l(-1) with the limit of detections (3sigma) being 1.3 ng ml(-1). Favorable sensitivity of TIR-RLS technique was demonstrated superior to that of high-performance liquid-chromatography (HPLC) method. The feasibility of the proposed technique was validated by the satisfactory performance of intra-assay and inter-assay BE in tablets.

Berberine↗

Microscopic determination of tetracycline based on aluminum-sensitized fluorescence of a self-ordered ring formed by a sessile droplet on glass slide support.

A fluorescent microscopic determination of trace amount of tetracycline is reported based on the aluminum-sensitized fluorescence effect of a self-ordered ring formed by a sessile droplet on glass slide support. Since the evaporative loss of the solvent from the edge wedge of the droplet that is spotted on a hydrophobic-treated glass slide, an outward capillary flow of the interior solvent of the droplet occurs. The resulted outward capillary flow then carries the solute to the perimeter of the droplet spot where the solute accumulates to form a fluorescent self-ordered ring (SOR). Depending on the spotted volume of the aluminum-tetracycline chelate solution, different size of SOR with the outer diameter (o.d.) less than 1.1mm and the ring belt width less than 21.6 microm can be obtained. Data analysis for the imaged SOR by using a digitalized CCD camera showed that the chelate molecule across the fluorescent SOR belt section follows a Gaussian distribution, and the maximum fluorescent intensity (I(max)) was found to be proportional to tetracycline content. When a 0.1 microl droplet was spotted on the solid surface, tetracycline in the range of 7.5-800.0 fmol (or 7.9 x 10(-8) to 800.0 x 10(-8)moll (-1)) can be detected, and the limit of detection can reach 0.8 fmol (or 7.9 x 10(-9) moll (-1)). With present method, the contents of tetracycline in capsule, tablet, urine and fresh milk were satisfactorily detected with the recoveries of 97.0-106.5% and RSD of 1.2-4.2%, correspondingly.

Aluminum↗

Resonance light scattering imaging detection of proteins with alpha,beta,gamma,delta-tetrakis(p-sulfophenyl)porphyrin.

A resonance light scattering (RLS) imaging technique was introduced to measure the light scattering of aggregation species induced by proteins, and thus a method of detecting proteins in the range of picograms was proposed. In acidic medium, J-aggregation of alpha,beta,gamma,delta-tetrakis(p-sulfophenyl)porphyrin (TPPS(4)) in the presence of proteins occurs, resulting in strong RLS signals characterized at 490 nm. Under the excitation of a 488-nm light beam of argon ion laser source, the scattered light of single J-aggregation species could be observed with a common microscope, and the images could be captured with a cooled charge-coupled device camera. Data analysis for the digital images showed that the counts of aggregate species in the detection focus plane are proportional to the concentration of proteins in picograms. When 1.0 x 10(-7)M TPPS(4) was employed, 0.01-210 ng/ml bovine serum albumin and human serum albumin could be detected with limits of detection lower than 10 pg/ml (3 sigma). Three human blood serum samples were satisfactorily detected with relative standard deviations lower than 3.04%.

Animals↗

Capillary electrophoresis with laser induced-fluorescence detection of profens derivatized with the water-soluble fluorogenic reagent 4-N-(4-N'-aminoethyl)piperazino-7-nitro-2,1,3-benzoxadiazole.

Profens, including pranoprofen, fenoprofen, flurbiprofen, ketoprofen and ibuprofen (Ib), were derivatized by a water-soluble benzofurazan fluorescent reagent, 4-N-(4-N'-aminoethyl)piperazino-7-nitro-2,1,3-benzoxadiazole and then were run on capillary electrophoresis in a NH4Ac-HAc buffer of pH 3.1 containing 2.4 mM beta-cyclodextrin. At room temperature, the derivatization reaction was catalyzed by triphenyl phosphine and diphenyl disulfide in acetonitrile medium, and the derivatives fluoresce around 530 nm when excited at 488 nm. With the CE running on a 50 cm x 50 microm I.D. length fused-silica capillary of by using Ar+ laser induced-fluorescence detection, the detection limits attained were in the range of 0.16 to 0.3 fmol.

4-Chloro-7-nitrobenzofurazan↗

Determination of berberine by measuring the enhanced total internal reflected fluorescence at water/tetrachloromethane interface in the presence of sodium dodecyl benzene sulfonate.

A highly sensitive method for determination of berberine is proposed based on the measurements of total internal reflected fluorescence (TIRF) at water/ tetrachloromethane (H(2)O/CCl(4)) interface. In the pH range of 2.6-5.7, the co-adsorption of the berberine with the anionic surfactants such as sodium dodecyl benzene sulfonate (SDBS), sodium dodecylsulfonate (SDS), and sodium lauryl sulfate (SLS) occurs at the H(2)O/CCl(4 )interface, resulting in greatly enhanced TIRF signal characterized by the emission at 526 nm when excited with a 351 nm light beam. The enhanced TIRF intensity is in proportion to the berberine concentration in the range 0.2-10.0x10(-7) mol L(-1). The limit of detection is 1.7x10(-9) mol L(-1) (3sigma). It was found that ions such as Ca(II), Cu(II), Fe(III), Cd(II), Mg(II), Zn(II), Pb(II), and Al(III) can be allowed larger than 1.0x10(-4) mol L(-1). Meanwhile, the organic compounds such as vitamin B, saccharine, and amino acid do not display any effect for the present TIRF method even if they are larger than 1.0x10(-2) mol L(-1)in high concentration levels (larger than 1.0x10(-5) mol L(-1)). The results of determination for synthetic samples were agreement with the desired values, and the ones for tablets were identical with those obtained according to the method of Chinese Pharmacopoeia.

Amino Acids↗

Determination of proteins with Fast Red VR by a corrected resonance light-scattering technique.

A simple corrected resonance light-scattering (CRLS) technique was established to correct for any distortion of the resonance light scattering (RLS) spectra resulting from molecular absorption. By using an absorption cell holder to change the propagation direction of the incident light beam of a common spectrofluorometer, the molecular absorption was directly measured through a spectrofluorometer. With measurements of the CRLS signals of the interaction of Fast Red VR (FRV) and proteins, we proved that the present correction for the RLS spectra in terms of the molecular absorption of excitation and scattering radiation can improve the detection sensitivity by about two fold.

Coloring Agents↗

Fluorescence assay based on preconcentration by a self-ordered ring using berberine as a model analyte.

A novel assay for trace amounts of fluorescent analytes is proposed based on the assembly of a self-ordered ring (SOR) through capillary flow in a sessile droplet on a glass slide support. After solvent evaporation of the sessile droplet containing a fluorescent analyte on a hydrophobic-treated glass slide, an outward capillary flow of the solvent from the interior of the droplet occurs. The resultant outward capillary flow then carries the analyte to the perimeter of the droplet spot where the analyte deposits and forms a fluorescent SOR. For the model analyte of berberine, SORs with outer diameter less than 1.2 mm and ring belt width less than 19 microm can be obtained depending on the droplet volume of the berberine solution. Data analysis for the digitally imaged SOR by using a CCD camera showed that the berberine molecules across the SOR belt section follow a Gaussian distribution, and the maximum fluorescent intensity (Imax) was found to be proportional to berberine content at the femtomole level. With the proposed technique, the content in tablets and the average excretion rates of berberine through human urine after oral administration could be satisfactorily monitored.

Berberine↗

Determination of cationic surfactants in water samples by their enhanced resonance light scattering with azoviolet.

A simple assay of cationic surfactants in water samples was developed based on the measurements of enhanced resonance light scattering (RLS). At pH 6.09 and ionic strength 0.03 M, the interactions of azoviolet (AV) with cationic surfactants, including zephiramine (Zeph) and cetyl trimethyl ammonium bromide (CTMAB), result in enhanced RLS signals characterized by the peaks of 470.0, 485.0 and 495.0 nm. The enhanced RLS intensity is proportional to the concentration of cationic surfactant of Zeph in the range of 0.2~6.0x10(-6) M, and to that of CTMAB in the range of 0.4~4.8x10(-6 )M. The limit of determination (3 sigma) is 2.1x10(-8) M and 3.8x10(-8) M for the two surfactants, respectively. Determinations of cationic surfactants in synthetic and tap water samples were successfully made with a recovery of 90.5~108.6%.

Azo Compounds↗

Direct quantification of human serum albumin in human blood serum without separation of gamma-globulin by the total internal reflected resonance light scattering of thorium-sodium dodecylbenzene sulfonate at water/tetrachloromethane interface.

A direct quantification of human serum albumin (HSA) in blood serum samples without separation is proposed based on the measurements of total internal reflected resonance light scattering (TIR-RLS) at water/tetrachloromethane (H(2)O/CCl(4)) interfaces. In the pH range of 6.37-6.59, the coadsorption of the binary complex of HSA-Th(IV) with sodium dodecylbenzene sulfonate occurs at the H(2)O/CCl(4) interface, forming an amphiphilic layer and displaying greatly enhanced TIR-RLS signals with the maximum peak located at 340-370 nm. The enhanced TIR-RLS intensity is in proportion to the HSA concentration in the range 0.15-1.0 micro gml(-1). The limit of detection is 14.4 ngml(-1). The contents of HSA in blood serum samples were determined with the recovery of 97.1-102.3% and RSD of 0.6-2.9%, which are identical to those obtained according to the spectrofluorimetric method using chrome azurol S.

Benzenesulfonates↗

Development of 7-(N,N-dimethylaminosulfonyl)-5-N-(4-N-aminoethyl)piperazino-2,1,3-benzoxadiazole as a water-soluble fluorogenic reagent for the sensitive liquid chromatographic determination of saturated carboxylic acids.

A reversed-phase high-performance liquid chromatographic (HPLC) method for the femtomole determination of nine saturated carboxylic acids, n-butyric (C4), n-hexanoic (C6), n-caprylic (C8), n-decanoic (C10), lauric (C12), n-tetradecanoic (C14), palmitic (C16), stearic (C18) and arachidic (C20), based on the condensation reaction of these acids with a newly synthesized water-soluble benzofurazan fluorescent reagent, 7-(N,N-dimethylaminosulfonyl)-4-N-(4-N-aminoethyl)piperazino-2,1,3-benzoxadiazole (DBD-PZ-NH2), was developed. The derivatization reaction proceeds with 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide (EDC) in the presence of the catalyst 4-(dimethylamino)pyridine (DMAP). A model derivative of the reagent with n-caprylic acid (C8) was synthesized for fluorescence excitation/emission characterization. Depending on the solvents, including water, methanol, acetonitrile, 1,4-dioxane or N.N-dimethyformamide (DMF), the C8 derivative has a fluorescence emission with a fluorescence quantum yield (phi) ranging from 0.01 to 0.20 in the region from 545 to 580 nm. An exponential increase in phi was observed with increasing acetonitrile content. The calculated detection limits (signal-to-noise ratio = 3:1) of the proposed method for the above nine carboxylic acids were 9.1, 4.0, 2.5, 2.2, 2.0, 1.8, 1.2, 1.0 and 1.3 fmol, respectively. Biological samples including Intralipos 20% and rat plasma were analysed satisfactorily.

Carboxylic Acids↗

A sensitive and selective assay of nucleic acids by measuring enhanced total internal reflected resonance light scattering signals deriving from the evanescent field at the water/tetrachloromethane interfacet.

A total internal reflected resonance light scattering (TIR-RLS) technique, the coupling of resonance light scattering (RLS) technique with total internal reflected light at the interface of two immiscible liquids, where the steep change of the refractive indexes occurs to result in an evanescent field, is proposed with the characteristics of separation and enrichment properties of analytes and direct use of oil-soluble reagents free from surfactants. At pH 8.69 and ion strength 0.008, ternary amphiphilic species formed by the interaction of nucleic acids, including calf thymus DNA (ctDNA), fish sperm DNA (fsDNA), and yeast RNA (yRNA), with Eu(III) in the presence of oil-soluble trioctylphosphine oxide (TOPO), are adsorbed to the water/tetrachloromethane (H20/CCl4) interface, giving rise to significantly enhanced TIR-RLS signals. It has been found that the enhanced TIR-RLS intensity at 348.0 nm is proportional to the concentration of thermally denatured ctDNA, fsDNA and yRNA in the range 0.002-2.5 microg ml(-1), 0.002-2.5 microg ml(-1) and 0.003-2.0 microg ml(-1), respectively and their limits of determination (3sigma) are 0.16 ng ml(-1), 0.19 ng ml(-1) and 0.28 ng ml(-1), correspondingly. Complicated artificial samples with highly interfering backgrounds were determined satisfactorily.

Nucleic Acids↗

A resonance light-scattering determination of proteins with fast green FCF.

The interaction of Fast Green FCF (FCF) with proteins (including bovine serum albumin (BSA), human serum albumin (HSA), pepsin (Pep) and alpha-chymotrypsin (Chy), and lysozyme (Lys)) was characterized by enhanced resonance light-scattering (RLS) measurements using a common spectrofluorometer. The enhanced RLS signals of FCF by proteins at 279.0 nm were obtained, and the mechanism of the RLS enhancement was considered in terms of the effects of the pH and ionic strength on the interaction. It was found that the enhanced RLS intensities were in proportion to the concentrations of proteins in the range of nanogram levels, displaying that the present assay is much more sensitive than the reported RLS methods, with the limits of determination being 4.54, 0.6, 22.8, 4.32 and 1.75 ng/ml for BSA, HSA, Pep, Chy, and Lys. respectively.

Animals↗