共查询到20条相似文献,搜索用时 15 毫秒
1.
Repizo LM Martinez LD Olsina RA Cerutti S Raba J 《Analytical and bioanalytical chemistry》2012,402(2):965-973
A novel, simple, and rapid reversed-phase liquid chromatography–tandem mass spectrometric methodology was developed for the
analysis of natamycin in wine samples. Natamycin was protonated to form singly charged ions in an electrospray positive ion
mode. Data acquisition under MS/MS was achieved by applying multiple reaction monitoring (MRM) of three fragment ion transitions
(666.3 → 648.2, 666.3 → 503.3, and 666.3 → 485.2) to provide a high degree of sensitivity and specificity. Chromatographic
separation was performed on a rapid resolution column using a mobile phase consisting of an acetonitrile/water mixture with
a total run time of 5.0 min. After only filtration as pretreatment, the sample was injected into the chromatographic system.
The proposed method was validated in terms of selectivity, trueness, precision, decision limit (CCα), and detection capability (CCβ) according to 2002/657/EC Commission decision. The values for trueness, reported as bias (%), agreed with those established
by the aforementioned document. Repeatability (intraday variability) values were 12.37% at a concentration of 1.0 μg L−1 and 8.99–4.19% at concentrations between 2.5 and 10 μg L−1. The overall within-laboratory (interday variability) reproducibility was 15.47% at a concentration of 1.0 μg L−1, which was significantly lower than the indicative value reported in the EU decision. The results indicated that the proposed
approach is a sensitive, fast, reproducible, and robust methodology suitable for the analysis of natamycin levels in wine
samples. 相似文献
2.
A rapid, sensitive and environmentally friendly method for the analysis of 14 anilines in water samples by dispersive liquid–liquid
microextraction based on solidification of floating organic drop (DLLME-SFO) prior to gas chromatography–mass spectrometry
(GC-MS) was developed and optimized. In the proposed method, cyclohexane was used as the extraction solvent as its toxicity
was much lower than that of the solvent usually used in dispersive liquid–liquid microextraction (DLLME). In the optimized
conditions, the method exhibited good analytical performance. Based on a signal-to-noise ratio of 3, limits of detection for
anilines were in the range of 0.07 to 0.29 μg L−1, and the linear range was 0.5–200 μg L−1 with regression coefficients (r
2) higher than 0.9977. It was efficient for qualitative and quantitative analysis of anilines in water samples. The relative
standard deviations varied from 2.9 to 8.6 % depending on different compounds indicating good precision. Tap water and river
water were selected for evaluating the application to real water samples. The relative recoveries of anilines for the two
real samples spiked with 10 μg L−1 anilines were in the scope of 78.2–114.6 % and 77.3–115.6 %, respectively. 相似文献
3.
Sangita Pal Suchismita Mishra S. K. Satpati G. G. Pandit P. K. Tewari V. D. Puranik 《Journal of Radioanalytical and Nuclear Chemistry》2011,289(1):67-73
A fast and simple multisyringe flow injection analysis (MSFIA) method for routine determination of thorium in water samples
was developed. The methodology was based on the complexation reaction of thorium with arsenazo (III) at pH 2.0. Thorium concentrations
were spectrophotometrically detected at 665 nm. Under optimal conditions, Beer’s law was obeyed over the range from 0.2 to
4.5 μg mL−1 thorium, a 3σ detection limit of 0.05 μg mL−1, and a 10σ quantification limit of 0.2 μg mL−1 were obtained. The relative standard deviations (RSD, %) at 0.5, 2.5 and 4.5 μg mL−1 was 2.8, 1.5 and 0.8%, respectively (n = 10). It was found that most of the common metal ions and anions did not interfere with the thorium determination. The proposed
method was successfully applied to its analysis in various water samples. 相似文献
4.
Jorge L. Guzmán Mar Leticia López Martínez Pedro L. López de Alba Nancy Ornelas Soto Víctor Cerdà Martín 《Journal of Radioanalytical and Nuclear Chemistry》2009,281(3):433-439
A multisyringe flow injection analysis method for the determination of uranium in water samples was developed. The methodology
was based on the complexation reaction of uranium with arsenazo (III) at pH 2.0. Uranium concentrations were spectrophotometrically
detected at 649 nm using a light emitting diode. Under the optimized conditions, a linear dynamic range from 0.1 to 4.0 μg mL−1, a 3σ detection limit of 0.04 μg mL−1, and a 10σ quantification limit of 0.10 μg mL−1 were obtained. The reproducibility (%) at 0.5, 2.5, and 4.0 μg mL−1 was 2.5, 0.9, and 0.6%, respectively (n = 10). The interference effect of some ions was tested. The proposed method was successfully applied to the determination
of uranium in water samples. 相似文献
5.
This work presents a comparison of convective interaction media (CIM) and controlled pore glass (CPG) as solid supports for
immunoglobulin antibodies used in bioanalytical detection of allergens in foodstuffs. A flow-injection manifold with highly
sensitive thermal lens spectrometric detection was used for this purpose. Using beta-lactoglobulin, a milk allergen, as a
model analyte, CIM disc supports had a higher linear range (0.2–3.5 μg L−1), better reproducibility (intra-day RSD = 1%, inter-day RSD = 10%), lower consumption of reagents, and better immunocolumn
stability (1 month, over 240 injections of substrate), while providing comparable LODs (0.1 μg L−1). Application of CIM discs as solid supports in immunocolumns for allergen detection enables fast and sensitive screening
of allergens in foodstuffs with sample throughput of up to eight samples per hour. 相似文献
6.
A simple and efficient method, based on ultrasound-enhanced surfactant-assisted dispersive liquid–liquid microextraction (UESA-DLLME)
followed by high-performance liquid chromatography (HPLC) has been developed for extraction and determination of ketoconazole
and econazole nitrate in human blood samples. In this method, a common cationic surfactant, cetyltrimethylammonium bromide
(CTAB), was used as dispersant. Chloroform (40 μL) as extraction solvent was added rapidly to 5 mL blood containing 0.068 mg mL−1 CTAB. The mixture was then sonicated for 2 min to disperse the organic chloroform phase. After the extraction procedure,
the mixture was centrifuged to sediment the organic chloroform phase, which was collected for HPLC analysis. Several conditions,
including type and volume of extraction solvent, type and concentration of the surfactant, ultrasound time, extraction temperature,
pH, and ionic strength were studied and optimized. Under the optimum conditions, linear calibration curves were obtained in
the ranges 4–5000 μg L−1 for ketoconazole and 8–5000 μg L−1 for econazole nitrate, with linear correlation coefficients for both >0.99. The limits of detection (LODs, S/N = 3) and enrichment factors (EFs) were 1.1 and 2.3 μg L−1, and 129 and 140 for ketoconazole and econazole nitrate, respectively. Reproducibility and recovery were good. The method
was successfully applied to the determination of ketoconazole and econazole nitrate in human blood samples. 相似文献
7.
A confirmatory and quantitative method based on liquid chromatography–electrospray ionization tandem mass spectrometry (LC-ESI/MS/MS)
has been developed for simultaneous determination of seven photoinitiator residues: benzophenone, (1-hydroxycyclohexyl)phenylketone
(Irgacure 184), isopropylthioxanthone (ITX), 2-ethylhexyl-(4-dimethylamino)benzoate (EHA or EHDAB), 2-methyl-1-[4-(methylthio)phenyl]-2-(4-morpholinyl)-1-propanone
(Irgacure 907), (2,4,6-trimethylbenzoyl)diphenylphosphine oxide (TPO) and 2-benzyl-2-(dimethylamino)-1-(4-morpholinophenyl)-1-butanone
(Irgacure 369) in packaged milk and related packaging materials. Residues of photoinitiators were extracted from milk using
acetonitrile, and further enriched and purified on HLB solid-phase extraction cartridges prior to being analyzed by LC-ESI/MS/MS
with selected reaction monitoring mode, while photoinitiators in packaging materials were extracted using the same solvent.
Satisfactory recovery (from 80 to 111%), intra- and inter-day precision (below 12%), and low limits of quantification (from
0.1 to 5.0 μg kg−1) were evaluated from spiked samples at three concentration levels (5.0, 10.0 and 25.0 μg kg−1 for Irgacure 184 and 2.5, 5.0 and 25.0 μg kg−1 for others). These excellent validation data suggested the possibility of using the LC-ESI/MS/MS method for simultaneous
determination of low-level photoinitiator residues migrating from printed food-packaging materials into milk. The method has
been successfully applied to the analysis of real samples of different fat contents ranging from 8 to 30 g L−1. The photoinitiator residues were revealed to be higher in milk with higher fat content and the most important contaminations
were benzophenone and ITX in concentration ranges of 2.84–18.35 and 0.83–8.87 μg kg−1, respectively. 相似文献
8.
Larivière D Tremblay M Durand-Jézéquel M Tolmachev S 《Analytical and bioanalytical chemistry》2012,403(2):409-418
This article describes a robust methodology using the combination of instrumental design (high matrix interface—HMI), sample
dilution and internal standardization for the quantification of beryllium (Be) in various digested autopsy tissues using inductively
coupled plasma mass spectrometry. The applicability of rhodium as a proper internal standard for Be was demonstrated in three
types of biological matrices (i.e., femur, hair, lung tissues). Using HMI, it was possible to achieve instrumental detection
limits and sensitivity of 0.6 ng L−1 and 157 cps L ng−1, respectively. Resilience to high salt matrices of the HMI setup was also highlighted using bone mimicking solution ([Ca2+] = 26 to 1,400 mg L−1), providing a 14-fold increase in tolerance and a 2.7-fold decrease in method detection limit compared to optimized experimental
conditions obtained without the HMI configuration. Precision of the methodology to detect low levels of Be in autopsy samples
was demonstrated using hair and blood certified reference materials. Be concentration ranging from 0.015 to 255 μg kg−1 in autopsy samples obtained from the U.S. Transuranium and Uranium Registries were measured using the methodology presented. 相似文献
9.
The worldwide contamination of winery by-products by mycotoxins may present a serious hazard to human and animal health. Mycotoxins
are secondary metabolites of fungi with possible adverse effects on humans, animals, and crops that result in illnesses and
economic losses. Mycotoxins are under continuous survey in Europe, but the regulatory aspects still need to be set up for
winery by-products, which may be used in animal feed. The aim of this study was to implement a simple but reliable analytical
methodology for ochratoxin A (OTA) quantification in grape pomaces in order to perform a survey of samples from the Douro
Demarcated Region, Portugal. The method involved a unique preparation step, solvent extraction, followed by high-performance
liquid chromatography (HPLC) with fluorescence (FL) detection. A comparative study was performed with two extraction solvents
(ethyl acetate and methanol) as well as using extraction on an immunoaffinity column. The linearity range for OTA analysis
was 0.05–23.5 μg L−1 with a detection limit of 0.05 μg L−1 and a precision (expressed by the coefficient of variation under repeatability conditions) of 0.4–14.7%. The percentage of
recovery was on average 23.5 ± 3.6% (extraction with ethyl acetate) or 70.1 ± 2.5% (extraction with 70% methanol). Accounting
for the recovery factor and the chromatographic detection limit, as well as the preconcentration factor, the limit of detection
in grape pomaces is 0.04 μg kg−1 (ethyl acetate extraction) and 0.33 μg kg−1 (methanol extraction). Samples from 12 out of 13 sites in the Douro Demarcated Region showed OTA presence with concentrations
not exceeding 0.4 μg kg−1. Both developed methods for evaluation of OTA in grape pomace are simple but efficient.
Figure Extraction of ochratoxin A (OTA) from grape pomaces allows simple but efficient quantification of OTA in winery by-products
by HPLC-FL 相似文献
10.
López-Darias J Pino V Ayala JH González V Afonso AM 《Analytical and bioanalytical chemistry》2008,391(3):735-744
An environmentally friendly method to extract endocrine-disrupting phenols (EDPs) from seawaters was realized using nonionic
surfactant mixtures and micelle-mediated extractions. The preconcentration step was achieved directly in the seawater matrix,
and was followed by high-performance liquid chromatography (HPLC) with ultraviolet (UV) detection without any clean-up steps
to remove the surfactant mixture prior to injection. Various nonionic surfactant mixtures were used, and polyoxyethylene-10-laurylether
(POLE) with polyoxyethylene-4-laurylether (Brij 30) was found to be the best to work with. Method optimization involved maximizing
the preconcentration factor using the studied mixtures. The proposed method gave extraction recoveries ranging from 83.3 to
114.4% for an EDP spiking level of 46.7 μg L−1, and from 63.4 to 112.4% for a spiking level of 4.7 μg L−1 for EDPs studied in real seawater matrices, with relative standard deviations of <12.1%. The detection limits of the method
varied from 0.18 μg L−1 for bisphenol A (BPA) to 1.17 μg L−1 for 4-cumylphenol (4-CP). The method was applied to seawaters from the Canary Islands with successful results.
Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users. 相似文献
11.
Tatyana S. Baptista Marcelo M. Redígolo Cibele B. Zamboni Ivone M. Sato Jose R. Marcelino 《Journal of Radioanalytical and Nuclear Chemistry》2012,291(2):399-403
The World Health Organization states that envenomation is responsible for a high number of deaths per year, especially in
equatorial areas. The only effective specific treatment is the use of hyperimmune serum (antivenom). In Brazil, Crioula breed
horses are used for antivenom production, with great importance in the maintenance of public health programs. A strict biochemical
and metabolic control is required to attain specificity in antiserum. Inorganic elements represent only a small fraction of
whole blood. Nonetheless, they play important roles in mammalian metabolism, being responsible for controlling enzymatic reactions,
respiratory and cardiac functions and ageing. In this work, whole blood samples from Crioula breed horses were analyzed by
EDXRF technique. The reference interval values were determined for the elements Na (1955–2013 μg g−1), Mg (51–75 μg g−1), P (523–555 μg g−1), S (1628–1730 μg g−1), Cl (2388–2574 μg g−1), K (1649–1852 μg g−1), Ca (202–213 μg g−1), Cu (4.1–4.5 μg g−1) and Zn (2.4–2.8 μg g−1) and a comparative study with NAA results was outlined. The samples were obtained from Instituto Butantan. Both techniques
showed to be appropriate for whole blood sample analyses and offer a new perspective in Veterinary Medicine. 相似文献
12.
Neopterin is a valuable biomarker of cellular immunity associated with various pathological situations such as viral and bacterial
infections, autoimmune, cardiovascular, neurodegenerative and malignant disorders. To produce specific antibodies against
neopterin for a rapid multi-biomarker-based diagnosis, a novel hapten derivative was synthesized and attached to carrier proteins.
The thoroughly characterized conjugates were used for immunization of BALB/c mice and rabbits. The produced monoclonal antibody
reached in both direct and indirect enzyme-linked immunosorbent assay (ELISA) format LoD of 0.18 and 0.45 μg L−1, respectively, and was a superior immunoreagent for further biosensor developments with regard to assay sensitivity and material
availability. The best polyclonal antibody was somewhat more sensitive in direct ELISA with LoD of 0.05 μg L−1. The optimized ELISA method was evaluated with blood samples collected from patients with renal insufficiency, patients with
sepsis, patients without confirmed clinical diagnosis, and healthy volunteers. In plasma samples, neopterin concentrations
ranging from 3.2 to 103 μg L−1 could be determined with the monoclonal ELISA whereas twofold lower results were obtained with the polyclonal ELISA. A satisfactory
correlation of results was found between the polyclonal ELISA and IBL Neopterin ELISA kit within the concentration range 0.5–16 μg L−1 (R = 0.874; n = 40), and slightly lower correlation was found for monoclonal-based ELISA (R = 0.819; n = 40). These data show that the generated antibodies may be used as functional analytical reagents for the integration into
multianalyte biochip detection systems. 相似文献
13.
L. Giannetti F. Longo F. Buiarelli M. V. Russo B. Neri 《Analytical and bioanalytical chemistry》2010,398(2):1017-1023
A specific, sensitive and robust liquid chromatography tandem mass spectrometry method for determining oxytetracycline, tetracycline,
chlortetracycline and doxycycline in royal jelly and honey samples is presented. Extraction of drug residues was performed
by ammonium acetate buffer as extractant followed by a clean-up with metal chelate affinity chromatography and solid-phase
extraction. Tetracycline analysis was performed using liquid chromatography–electrospray ionisation–tandem mass spectrometry.
The presented method is the first validated for royal jelly and in accordance with the requirements set by Commission Decision
2002/657/EC. Recoveries of the methods, calculated spiking the samples at 5.0, 10.0, 20.0 and 30.0 μg kg−1, were 79% to 90% for honey and 77% to 90% for royal jelly. The intra-day precision (RSD) ranged between 8.1% and 15.0% for
honey and from 9.1% to 16.3% for royal jelly, while inter-day precision values were from 10.2% to 17.6% and from 10.6% to
18.4% respectively for honey and royal jelly. Linearity for the four analytes was calculated from 5.0 to 50.0 μg kg−1. The decision limits (CCα) ranged from 6.2 to 6.4 μg kg−1 and from 6.1 to 6.5 μg kg−1 for honey and royal jelly, respectively. Detection capabilities values (CCβ) ranged between 7.2 and 7.7 μg kg−1 and from 7.3 to 7.9 μg kg−1 respectively for honey and royal jelly. The developed method is currently in use for confirmation of the official control
analysis of honey and royal jelly samples. 相似文献
14.
D. Leyva J. Estévez A. Montero I. Pupo 《Journal of Radioanalytical and Nuclear Chemistry》2012,291(3):699-705
A sensitive and non chromatographic analytical procedure for the separation of inorganic selenium species in natural water
has been performed. A combination of APDC coprecipitation and determination by an absolute thin layer Energy dispersive X-ray
fluorescence spectrometry method was used. The influence of various analytical parameters such as element concentration, oxidation
states and pH on the recoveries of Se (IV) was examined. The presence of organic matter and bicarbonate anions, typical components
in Cuban groundwater samples, was also tested. Negligible matrix effects were observed. At pH 4 a 100% recovery was found
for Se (IV). The coprecipitation recovery of the oxidized selenium species (Se (VI)) was null for the selected concentration
range (5–100 μg L−1). When the Se (VI) was reduced by heating the solution with 4 mol L−1 HCl, quantitative recovery was also obtained. The determination of total selenium was conducted by the application of the
oxidation–reduction process and the analytical procedure for Se (IV). Se (VI) content was calculated as the difference between
total selenium and Se (IV). The detection limit was 0.13 μg L−1. The relative standard deviation was lower than 3.5% for 5 μg L−1 of Se (IV). The trueness of the method was verified by using standardized hydride generation-atomic absorption spectrometry
technique. The results obtained using the EDXRF technique were in good agreement with the ones determined by HG-AAS. The proposed
method was applied to the determination of Se (IV) in surface water and groundwater samples. 相似文献
15.
Mohana Krishna Reddy Mudiam Rajeev Jain Virendra K. Dua Amit Kumar Singh V. P. Sharma R. C. Murthy 《Analytical and bioanalytical chemistry》2011,401(5):1699-1705
A simple and rapid analytical method based on in-matrix ethyl chloroformate (ECF) derivatization has been developed for the
quantitative determination of bisphenol-A (BPA) in milk and water samples. The samples containing BPA were derivatised with
ECF in the presence of pyridine for 20 s at room temperature, and the non-polar derivative thus formed was extracted using
polydimethylsiloxane solid-phase microextraction (SPME) fibres with thicknesses of 100 μm followed by analysis using gas chromatography–mass
spectrometry. Three alkyl chloroformates (methyl, ethyl and isobutyl chloroformate) were tested for optimum derivatisation
yields, and ECF has been found to be optimum for the derivatisation of BPA. Several parameters such as amount of ECF, pyridine
and reaction time as well as SPME parameters were studied and optimised in the present work. The limit of detection for BPA
in milk and water samples was found to be 0.1 and 0.01 μg L−1, respectively, with a signal-to-noise ratio of 3:1. The limit of quantitation for BPA in milk and water was found to be 0.38
and 0.052 μg L−1, respectively, with a signal-to-noise ratio of 10:1. In conclusion, the method developed was found to be rapid, reliable
and cost-effective in comparison to silylation and highly suitable for the routine analysis of BPA by various food and environmental
laboratories. 相似文献
16.
Ru-Song Zhao Xia Wang Jing Sun Shan-Shan Wang Jin-Peng Yuan Xi-Kui Wang 《Analytical and bioanalytical chemistry》2010,397(4):1627-1633
A novel and environmentally friendly microextraction method, termed ionic liquid dispersive liquid-phase microextraction (IL-DLPME),
has been developed for rapid enrichment of triclosan and triclocarban before analysis by high-performance liquid phase chromatography–electrospray
tandem mass spectrometry (HPLC–ESI-MS–MS). Instead of using toxic organic solvents, an ionic liquid was used as a green extraction
solvent. This also avoided the instability of the suspending drop in single-drop liquid-phase microextraction, and the heating
and cooling step in temperature-controlled ionic liquid dispersive liquid phase microextraction. Factors that may affect the
enrichment efficiency, for example volume of ionic liquid, type and volume of dispersive solvent, pH, extraction time, and
NaCl content were investigated in detail and optimized. Under optimum conditions, linearity of the method was observed over
the range 0.2–12 μg L−1 for triclocarban and 1–60 μg L−1 for triclosan with correlation coefficients ranging from 0.9980 to 0.9990, respectively. The sensitivity of the proposed
method was found to be excellent, with limits of detection in the range 0.040–0.58 μg L−1 and precision in the range 7.0–8.8% (RSD, n = 5). This method has been successfully used to analyze real environmental water samples and satisfactory results were achieved.
Average recoveries of spiked compounds were in the range 70.0–103.5%. All these results indicated that the developed method
would be a green method for rapid determination of triclosan and triclocarban at trace levels in environmental water samples. 相似文献
17.
Nuevo-Ordóñez Y Montes-Bayón M Blanco-González E Paz-Aparicio J Raimundez JD Tejerina JM Peña MA Sanz-Medel A 《Analytical and bioanalytical chemistry》2011,401(9):2747-2754
Increased concentrations of circulating metal-degradation products derived from the use of Ti orthopaedic implants may have
deleterious biological effects over the long term. Therefore, there is an increasing need to establish the basal level of
Ti in the serum of the population (exposed and non-exposed) with appropriate highly sensitive techniques and strategies. With
this aim, we have developed a quantitative strategy for the determination of total Ti concentration in human serum samples
by isotope dilution analysis using a double-focussing inductively coupled plasma mass spectrometer. Minimizing sample handling
and therefore contamination issues, we obtained detection limits of about 0.05 μg L−1 Ti working at medium resolution (m/Δm 4000). Such extremely good sensitivity permitted us to establish the range of Ti concentration
in serum of 40 control individuals (mean 0.26 μg L−1) and also to compare it with the level in exposed patients with different Ti metal implants. On the other hand, Ti transport
“in vivo” studies have been enabled by online coupling of liquid chromatography (anion-exchange) separation and double-focussing
inductively coupled plasma mass spectrometry for sensitive detection of Ti. The development of a postcolumn isotope dilution
strategy permitted quantitative characterization of the Ti-transporting biomolecules in human serum. The results for unspiked
serum revealed that 99.8% of the Ti present in this fluid is bound to the protein transferrin, with column recoveries greater
than 95%. 相似文献
18.
An anodic stripping voltammetric procedure for the determination of Cu(II) at an in situ-plated stannum film electrode (SnFE)
was described. The results indicated that the SnFE had an attractive electroanalytical performance, with two distinct voltammetric
stripping signals for copper and stannum, and showed the superior advantage for the determination of copper compared with
the bismuth film electrode. Several experimental parameters were optimized. The SnFE exhibited highly linear behavior in the
concentration range from 1.0 to 100.0 μg L−1 of Cu(II) (r = 0.994) with the detection limit of 0.61 μg L−1 (S/N = 3), and the relative standard deviation for a solution containing 40.0 μg L−1 Cu(II) was 2.2% (n = 8). The procedure has been successfully applied for the determination of Cu(II) in lake water sample. 相似文献
19.
Summary A simple and sensitive method for the determination of trace amounts of bisphenol-A (BPA), bisphenol-A diglycidyl dimethacrylate
(bis-GMA), bisphenol-A dimethacrylate (bis-DMA) and triethyleneglycol dimethacrylate (TEGDMA) in human saliva is proposed.
These materials are used in dental restorations, as composites and sealants, and are sometimes detected in human saliva after
dental treatment. The proposed method involves protein precipitation using acetonitrile followed by acidification, evaporation
of the solvent and dissolution with dichloromethane prior to injection into a GC-MS.
Thermal derivatization in the injection system was used for the identification and quantification of bis-GMA. Clean-up is
not necessary using SIM mode. Bisphenol-F (BPF) was used as internal standard. The linear range was 15 to 1000 μg·L−1 for BPA, 50 to 10 000 μg·L−1 for bis-GMA, 50 to 1000 μg·L−1 for bis-DMA and 1 to 100 μg·L−1 for TEGDMA.
The detection limits were 3,15,10 and 0.3 μg·L−1 for BPA, bis-GMA, bis-DMA and TEGD-MA, respectively. Validation of the proposed method was carried out by using the standard
addition methodology.
Samples of 10 mL of human saliva collected 1 h after dental treatment were analysed in order to assess the applicability of
the method to detect and quantify such compounds originated from methacrylic resins used in odontological treatment. 相似文献
20.
The possibilities of different media formed by lecithin/n-butanol (n-BuOH)/water ternary mixtures for the analysis of all-trans-retinol by fluorescence have been studied. Fluorescence intensity of retinol increases in the presence of different types
of aggregates formed in these media. Analytical features are good, the detection limit and quantification limit have micrograms
per liter levels, and the linear range and sensitivity are appropriate to determine retinol in cosmetic samples. The analysis
of retinol in anti-wrinkle creams can be achieved directly without any pretreatment of the sample. The vesicles built up from
a biocompatible surfactant (lecithin) in aqueous solution with a low amount of n-BuOH permit an appropriated media for a simple, rapid, and sensitive analytical method. This method has a linear range between
64.1 and 800 μg L−1, a sensitivity of 202.3 L mg−1, and a low detection and quantification limit at 19.2 and 64.1 μg L−1, respectively. 相似文献