ELSD Research Articles

A wide range and high resolution one-filtration molecular weight cut-off method for aqueous based nanofiltration and ultrafiltration membranes

A new and superior one-filtration method for the determination of the molecular weight cut-off (MWCO) of aqueous based nanofiltration and ultrafiltration membranes has been developed using the widest range of polyethylene glycol oligomers as MWCO probes of any MWCO method so far. This method was enabled by a new, high resolution oligomer separation and detection using high performance liquid chromatography (HPLC) coupled with an evaporative light scattering detector (ELSD). The refined method can determine the MWCO of membranes over a MW range from 678 to 4594gmol−1 with a molecular weight difference of just 44gmol−1 and a bonus further one point extension to 6000gmol−1 – giving the widest range and most precise difference of MWs that can be resolved of any single filtration MWCO method that exists. MWCO determination of five commercial membranes from GE Osmonics™ and Millipore showed good agreement with manufacturer and literature values, confirming the accuracy of the method. As this new method has significant advantages over all other existing aqueous MWCO determinations (i.e. single filtration, higher resolution over a wider MW range, low cost MWCO molecular probes), it is suggested that it could be adopted as the new standard for determining aqueous MWCO over a MW range from 678 to 6000gmol−1.

Selection of crude Solidago virgaurea L. ssp. extracts based on two fast and efficient chromatographic methods (high-performance thin-layer chromatography or high-performance liquid chromatography) for the quantification of total saponins

A previous study on Solidago virgaurea extracts showed an inhibiting activity of Candida albicans yeast—hyphal transition due to a mixture of triterpene saponins, leading to applications in the field of oral care products. Such applications require the development of an efficient, fast, and simple quantification method of S. virgaurea total saponins. Two methods were developed: the first was based on high-performance liquid chromatography (HPLC) separation with gradient elution and evaporative light scattering detection (ELSD); the second was based on high-performance thin-layer chromatography (HPTLC) separation with in-situ hydrolysis followed by densitometric measurements at 366 nm. Both calibration curves showed good linear regressions (R2 > 0.99) within the range of the concentrations tested. The limit of detection (LOD) and the limit of quantitation (LOQ) were 2–4 μg and 10–16 μg, respectively. The intra- and inter-day variations were studied and found to remain below 5.6% in terms of relative standa...

Improvement in Thermal Stability of Sucralose by γ-Cyclodextrin Metal-Organic Frameworks.

To explain thermal stability enhancement of an organic compound, sucralose, with cyclodextrin based metal organic frameworks. Micron and nanometer sized basic CD-MOFs were successfully synthesized by a modified vapor diffusion method and further neutralized with glacial acetic acid. Sucralose was loaded into CD-MOFs by incubating CD-MOFs with sucralose ethanol solutions. Thermal stabilities of sucralose-loaded basic CD-MOFs and neutralized CD-MOFs were investigated using thermogravimetric analysis (TGA), differential scanning calorimetry (DSC) and high performance liquid chromatography with evaporative light-scattering detection (HPLC-ELSD). Scanning electron microscopy (SEM) and powder X-ray diffraction (PXRD) results showed that basic CD-MOFs were cubic crystals with smooth surface and uniform sizes. The basic CD-MOFs maintained their crystalline structure after neutralization. HPLC-ELSD analysis indicated that the CD-MOF crystal size had significant influence on sucralose loading (SL). The maximal SL of micron CD-MOFs (CD-MOF-Micro) was 17.5 ± 0.9% (w/w). In contrast, 27.9 ± 1.4% of sucralose could be loaded in nanometer-sized basic CD-MOFs (CD-MOF-Nano). Molecular docking modeling showed that sucralose molecules preferentially located inside the cavities of γ-CDs pairs in CD-MOFs. Raw sucralose decomposed fast at 90°C, with 86.2 ± 0.2% of the compound degraded within only 1h. Remarkably, sucralose stability was dramatically improved after loading in neutralized CD-MOFs, with only 13.7 ± 0.7% degradation at 90°C within 24h. CD-MOFs efficiently incorporated sucralose and maintained its integrity upon heating at elevated temperatures.

Temporal Changes of Human Breast Milk Lipids of Chinese Mothers.

Fatty acids (FA), phospholipids (PL), and gangliosides (GD) play a central role in infant growth, immune and inflammatory responses. The aim of this study was to determine FA, PL, and GD compositional changes in human milk (HM) during lactation in a large group of Chinese lactating mothers (540 volunteers) residing in Beijing, Guangzhou, and Suzhou. HM samples were collected after full expression from one breast and while the baby was fed on the other breast. FA were assessed by direct methylation followed by gas chromatography (GC) analysis. PL and GD were extracted using chloroform and methanol. A methodology employing liquid chromatography coupled with an evaporative light scattering detector (ELSD) and with time of flight (TOF) mass spectrometry was used to quantify PL and GD classes in HM, respectively. Saturated FA (SFA), mono-unsaturated FA (MUFA), and PL content decreased during lactation, while polyunsaturated FA (PUFA) and GD content increased. Among different cities, over the lactation time, HM from Beijing showed the highest SFA content, HM from Guangzhou the highest MUFA content and HM from Suzhou the highest n-3PUFA content. The highest total PL and GD contents were observed in HM from Suzhou. In order to investigate the influence of the diet on maternal milk composition, a careful analyses of dietary habits of these population needs to be performed in the future.

Feasibility of Fraction Collection in HPLC Systems with Evaporative Light Scattering Detector: Analysis of Pectinatella magnifica.

The use of a liquid chromatography (LC) splitter inserted between an HPLC column and an evaporative light scattering detector (ELSD) is described. This paper aims to show the feasibility of using the splitter in an HPLC-ELSD system to fractionate a model mixture of analytes, namely salicin (2-(hydroxymethyl)-phenyl-β-d-glucopyranoside) and glucose. The retention factors and efficiency of the separation were studied under various temperatures and water contents in the mobile phase in order to clarify the mechanism of polyols separation on a diol column under the conditions of hydrophilic liquid chromatography (HILIC). Finally, the system was applied to a biological sample (a lyophilized colony gel of Pectinatella magnifica), where the presence of fructose and glucose was confirmed.

Statistical Optimization of Evaporative Light Scattering Detection for Molten Sucrose Octaacetate and Comparison With Ultraviolet Diode Array Detection Validation Parameters Using Tandem HPLC Ultraviolet Diode Array Detection/Evaporative Light Scattering Detection–Specific Stability-Indicating Method

A sucrose octaacetate (SOA) gradient HPLC evaporative light scattering detection (ELSD) and low-wavelength UV-diode array detection (UV-DAD)-specific stability-indicating method development and validation comparison is reported. A central composite response surface design and multicriteria optimization was used to maximize molten SOA area-under-the-curve response and signal-to-noise ratio. The ELSD data were also analyzed using multivariate principal component analysis, analysis of variance, and standard least squares effects modeling. The method suitability and validation parameters of both methods were compared. To the authors’ knowledge, this is the first report that validates an ELSD method using a molten analyte. SOA exhibited a low molar absorptivity of 439 absorption units/cm/M in water at 210 nm requiring low-wavelength UV-DAD detection. The low-wavelength UV-DAD method provided substantially better intraday and interday precision, intraday and interday goodness-of-fit, detection limit, and quantitation limit than ELSD. ELSD exhibited a 60-fold greater area-under-the-curve response, better resolution, and 58% more theoretical plates. On balance, the UV-DAD method was chosen for SOA chemical kinetic studies. This study illustrates that ELSD may not always be the best alternative to gradient HPLC low-wavelength UV detection.

Simultaneous Analysis of Free/Bound Phytosterols and Diosgenin in Taiwanese Yams

Gas chromatography (GC) and high performance liquid chromatography (HPLC) methods were developed for the simultaneous analysis of phytosterols and diosgenin in two representative Taiwanese yams, Dioscorea pseudojaponica Yamamoto and Dioscorea alata L. The major phytosterols found were β-sitosterol, stigmasterol, and campesterol. GC afforded good separation of phytosterols and diosgenin, with the diosgenin peak appearing between stigmasterol and β-sitosterol. For HPLC, UV detection had higher sensitivity (detection limits 0.03–0.09 μg); however, evaporative light scattering detection (ELSD) achieved higher noise tolerance and did not show baseline interference from solvent gradients. In addition, mixed solvents for extraction before acid hydrolysis, which is necessary to avoid fibers and acid hydrolysates binding to the target compounds, were evaluated. Phytosterol contents of 30.1 and 9.9 mg/100 g were found in D. pseudojaponica Yamamoto and D. alata L., respectively. Diosgenin was only found in D. pseudojaponica Yamamoto at a content of 15.2 mg/100 g.

Static Adsorption of an Ethoxylated Nonionic Surfactant on Carbonate Minerals.

The static adsorption of C12-14E22, which is a highly ethoxylated nonionic surfactant, was studied on different minerals using high-performance liquid chromatography (HPLC) combined with an evaporative light scattering detector (ELSD). Of particular interest is the surfactant adsorption in the presence of CO2 because it can be used for foam flooding in enhanced oil recovery applications. The effects of the mineral type, impurities, salinity, and temperature were investigated. The adsorption of C12-14E22 on pure calcite was as low as 0.01 mg/m2 but higher on dolomite depending on the silica and clay content in the mineral. The adsorption remained unchanged when the experiments were performed using a brine solution or 0.101 MPa (1 atm) CO2, which indicates that electrostatic force is not the governing factor that drives the adsorption. The adsorption of C12-14E22 on silica may be due to hydrogen bonding between the oxygen in the ethoxy groups of the surfactant and the hydroxyl groups on the mineral surface. Additionally, thermal decomposition of the surfactant was severe at 80 °C but can be inhibited by operating in a reducing environment. Under reducing conditions, adsorption of C12-14E22 increased at higher temperatures.

Comprehensive Quantitative Analysis of SQ Injection Using Multiple Chromatographic Technologies.

Quality control of Chinese medicine injections remains a challenge due to our poor knowledge of their complex chemical profile. This study aims to investigate the chemical composition of one of the best-selling injections, Shenqi Fuzheng (SQ) injection (SQI), via a full component quantitative analysis. A total of 15 representative small molecular components of SQI were simultaneously determined using ultra-high performance liquid chromatography (UHPLC) coupled with quadrupole tandem time-of-flight mass spectrometry (Q-TOF-MS); saccharide composition of SQI was also quantitatively determined by high performance liquid chromatography (HPLC) with evaporative light scattering detector (ELSD) on an amino column before and after acid hydrolysis. The existence of polysaccharides was also examined on a gel permeation chromatography column. The method was well validated in terms of linearity, sensitivity, precision, accuracy and stability, and was successfully applied to analyze 13 SQI samples. The results demonstrate that up to 94.69% (w/w) of this injection product are quantitatively determined, in which small molecules and monosaccharide/sucrose account for 0.18%–0.21%, and 53.49%–58.2%, respectively. The quantitative information contributes to accumulating scientific evidence to better understand the therapy efficacy and safety of complex Chinese medicine injections.

LC with Evaporative Light-Scattering Detection for Quantitative Analysis of Organic Acids in Juices

In this work, a performing LC method with evaporative light-scattering detector was described for the analysis of tartaric, malic, ascorbic, citric and succinic acids in fruit juices. The method was optimized and validated in comparison with LC-UV, in terms of accuracy, LODs, LOQs and precision. The successive application to ACE, orange, pear, peach, mulberry and apple juices allowed separation and quantitative determination of organic acids in about 20 min just diluting and filtering the sample before LC determination. In the analysed juices, citric, malic and ascorbic acids were always present, and in all the samples, citric acid was the prevailing acid followed by malic acid except for peach and apple juices where an opposite trend was found. Tartaric and succinic acids were detected at lower concentrations and more rarely, except for peach juices, all containing tartaric acid, and ACE and orange juices, all containing succinic acid.

Chemical characterization of humic-like substances (HULIS) in PM2.5 in Lanzhou, China

Evaporative light scattering detection (ELSD) was applied to quantify HULIS (humic-like substances) for the first time in 2012 winter and 2013 summer at an urban site in Lanzhou. Water soluble organic carbon (WSOC), water soluble inorganic ions, and carbonaceous species (OC/EC) were also analyzed. The results show that OM (Organic Matter=OC×1.6, constituting 45.8% to PM2.5) was the most abundant species, followed by SNA (SO42−+NO3−+NH4+, constituting 23.4% to PM2.5). The chemical species were in the order of: OC>EC>SO42−>NO3−>NH4+>Cl−>Ca2+>K+. The annual average concentration of HULIS was 4.70μg/m−3 and HULISc (carbon content of HULIS) contributed 6.19% to PM2.5 and 45.6% to WSOC, indicating that HULIS was the most important components of WSOC. The concentration of HULIS was 2.14±0.80μg/m3 in summer and 7.24±2.77μg/m3 in winter, respectively. The concentrations of HULIS were relatively low and stable in summer, while high and varied dramatically in winter. The abundance of HULISc in WSOC shows a more concentrated distribution in Lanzhou, with a range between 0.28–0.57. The ratios of HULIS/K+ were 6.25±1.41 and 6.14±1.96 in summer and winter, respectively, suggesting there were other significant sources in addition to biomass burning emissions. HULIS and WSOC exhibited similar seasonal variation and had a strong positive correlation. In addition to the good relationship (0.89) between HULIS and Cl− in winter, the great enhancement of HULIS with significantly high Cl− and relatively low K+ in winter indicated that residential coal burning was probably an important HULIS source in winter. Correlation and back trajectory analysis suggested that biomass burning and secondary formation were also important HULIS sources and the contribution of HULIS from dust could be neglected. Adverse meteorological conditions were also important factors for the accumulation of HULIS in winter.

Alternative solvents for improving the greenness of normal phase liquid chromatography of lipid classes

An evaluation of solvents alternative to n-heptane (d-limonene and hexamethyldisiloxane) and chloroform (cyclopentyl methyl ether, 2-methyltetrahydrofuran and isopentyl acetate) was developed for lipid classes separation of non-polar cholesteryl ester to highly polar phospholipids by high-performance liquid chromatography on bare silica stationary phase and evaporative light-scattering detection. Screening of alternative solvents was used to estimate their compatibility with liquid chromatography and evaporative light-scattering detection and to evaluate their chromatographic selectivity. This work shows that n-heptane can be advantageously replaced by hexamethyldisiloxane. An increase of non-polar lipids retention is observed with hexamethyldisiloxane as weak solvent. Chloroform, which is largely used for lipid analysis, might be replaced efficaciously by cyclopentyl methyl ether, 2-methyltetrahydrofuran or isopentyl acetate. Aside from offering a different selectivity, the gradients composed by one or both alternative solvents gave efficient and comparable or even better separations than those obtained with conventional solvents.

Interspecies and Intraspecies Analysis of Trehalose Contents and the Biosynthesis Pathway Gene Family Reveals Crucial Roles of Trehalose in Osmotic-Stress Tolerance in Cassava.

Trehalose is a nonreducing α,α-1,1-disaccharide in a wide range of organisms, and has diverse biological functions that range from serving as an energy source to acting as a protective/signal sugar. However, significant amounts of trehalose have rarely been detected in higher plants, and the function of trehalose in the drought-tolerant crop cassava (Manihot esculenta Crantz) is unclear. We measured soluble sugar concentrations of nine plant species with differing levels of drought tolerance and 41 cassava varieties using high-performance liquid chromatography with evaporative light-scattering detector (HPLC-ELSD). Significantly high amounts of trehalose were identified in drought-tolerant crops cassava, Jatropha curcas, and castor bean (Ricinus communis). All cassava varieties tested contained high amounts of trehalose, although their concentrations varied from 0.23 to 1.29 mg·g−1 fresh weight (FW), and the trehalose level was highly correlated with dehydration stress tolerance of detached leaves of the varieties. Moreover, the trehalose concentrations in cassava leaves increased 2.3–5.5 folds in response to osmotic stress simulated by 20% PEG 6000. Through database mining, 24 trehalose pathway genes, including 12 trehalose-6-phosphate synthases (TPS), 10 trehalose-6-phosphate phosphatases (TPP), and two trehalases were identified in cassava. Phylogenetic analysis indicated that there were four cassava TPS genes (MeTPS1–4) that were orthologous to the solely active TPS gene (AtTPS1 and OsTPS1) in Arabidopsis and rice, and a new TPP subfamily was identified in cassava, suggesting that the trehalose biosynthesis activities in cassava had potentially been enhanced in evolutionary history. RNA-seq analysis indicated that MeTPS1 was expressed at constitutionally high level before and after osmotic stress, while other trehalose pathway genes were either up-regulated or down-regulated, which may explain why cassava accumulated high level of trehalose under normal conditions. MeTPS1 was then transformed into tobacco (Nicotiana benthamiana). Results indicated that transgenic tobacco lines accumulated significant level of trehalose and possessed improved drought stress tolerance. In conclusion, cassava accumulated significantly high amount of trehalose under normal conditions due to multiplied trehalose biosynthesis gene families and constant expression of the active MeTPS1 gene. High levels of trehalose subsequently contributed to high drought stress tolerance.

Determination of the four major surfactant classes in cleaning products by reversed-phase liquid chromatography using serially connected UV and evaporative light-scattering detection

A method for the simultaneous determination of the most frequently used surfactant families –linear alkyl benzenesulphonates (LAS), alkyl ether sulphates (AES), fatty alcohol ethoxylates (FAE) and oleins (soaps, fatty acid salts) – in cleaning products, has been developed. The common reversed phase octyl (C8), pentafluorophenyl and biphenyl columns were not capable of separating the anionic LAS and AES classes; however, since only LAS absorbs in the UV, these two classes were independently quantified using a C8 column and serially connected UV and ELSD detection. The best compromise to resolve the four surfactant classes and the oligomers within the classes was achieved with a C8 column and an ACN/water gradient. To enhance retention of the anionic surfactants, ammonium acetate, as an ion-pairing agent compatible with ELSD detection, was used. Also, to shift the olein peaks with respect to that of the FAE oligomers, acetic acid was used. In the optimized method, modulation of the mobile phase, using ammonium acetate during elution of LAS and AES, and acetic acid after elution of LAS and AES, was provided. Quantitation of the overlapped LAS and AES classes was achieved by using the UV detector to quantitate LAS and the ELSD to determine AES by difference. Accuracy in the determination of AES was achieved by using a quadratic model, and by correcting the predicted AES concentration according to the LAS concentration previously established using the UV chromatogram. Another approach also leading to accurate predictions of the AES concentration was to increase the AES concentrations in the samples by adding a standard solution. In the samples reinforced with AES, correction of the predicted AES concentration was not required. FAE and olein were quantified using also quadratic calibration.

Supercritical Fluid Chromatography with Evaporative Light Scattering Detection (SFC-ELSD) for Determination of Oligomer Molecular Weight Distributions

Ultraviolet curable polyureas and polyurethanes enjoy a wide range of applications in the coatings industry. They demand less energy for curing compared to thermal processes that offer relatively low viscosities before photocuring, and provide mechanical property improvements due to hydrogen bonding physical crosslinks. Mechanical properties of the coatings are dependent on a variety of factors, including chemical composition, molecular weight, and molecular weight distribution. Formulations are designed for a wide variety of end use applications, ranging from soft, elastomeric coatings to harder, nonflexible sealants. This report demonstrates that the thermomechanical behavior of photocured coatings is a function of molecular weight distribution. Step-growth polymerization and endcapping afforded a variety of acrylate-terminated, urea-/urethane-containing photocurable oligomers from amine-terminated poly(propylene glycol), dicyclohexylmethane-4,4′-diisocyanate (HMDI), and 2-hydroxyethyl acrylate (HEA) at various stoichiometric ratios. The state-of-the-art supercritical fluid chromatography coupled with evaporative light-scattering detection (SFC-ELSD) enabled the elucidation of oligomeric molecular weight distributions as a function of reaction stoichiometry. SFC-ELSD demonstrated the efficient separation of oligomeric species with single repeat unit resolution (i.e., n = 2 vs. n = 3). Dynamic mechanical analysis probed thermomechanical response of photocured films as a function of molecular weight distribution and demonstrated that the presence of a hydrogen-bonding, small molecule photoactive reaction byproduct, i.e., HEA doubly-endcapped HMDI, had a much more profound effect on thermomechanical response as compared to changes in oligomer molecular weight in the molecular weight range investigated. This combination of chromatographic technique and thermomechanical analysis afforded an in-depth investigation of the structure–property relationships of urea-/urethane-containing photocurable oligomers.

Comparison of Stability-Indicating LC Methods Using Light Scattering and Photodiode Array Detection with Monolithic Column for Determination of Quinapril and Hydrochlorothiazide.

Rapid stability-indicating LC methods for simultaneous analysis of quinapril and hydrochlorothiazide were developed, validated and compared using evaporative light scattering detection (ELSD) and diode array detection (DAD). For the separation of quinapril, hydrochlorothiazide and its major degradation products, a monolithic column was used and the analytes were eluted within 7 min, applying gradient mobile phase in both methods. Quinapril was subjected to hydrolytic, oxidative, thermal, humidity and photolytic stress conditions. Degradation products were well resolved from main peaks and from each other, proving the stability-indicating power of the methods. The response with DAD was linear and the response with ELSD was fitted to a power function, for quinapril and hydrochlorothiazide concentrations of 20-160 and 12.5-100 µg mL(-1), respectively. DAD method achieved better precision than ELSD method, the LOQ of DAD was lower and the accuracy of the methods was similar. Quinapril degrade by hydrolysis and thermal stress, showing the formation of quinaprilat and quinapril diketopiperazine as degradants, which were identified by MS-MS. The methods were successfully applied to quantify quinapril and hydrochlorothiazide in commercial tablets. LC-DAD and LC-ELSD methods are suitable to assess the stability and routine analysis of quinapril and hydrochlorothiazide in pharmaceutical industry.

Büchi acquires Grace chromatography line

Büchi Labortechnik has acquired W.R. Grace’s portfolio of flash chromatography and evaporative light-scattering detector instruments. Grace built the business under Gregory E. Poling, who recently left to head GCP Applied Technologies, the construction and packaging business spun off of Grace. Büchi says it will integrate the Grace instruments into its chromatography portfolio. Grace will continue to provide silica-based purification media to Büchi and other customers.

Purification Of Natural Product Extracts Using Integrated Flash And Preparative Chromatography

Isolation and purification of active components from natural origins is a challenging process requiring multiple steps and often large amounts of organic solvent. The diversity of compounds present in an extract is large and adequate purification can require different chromatographic techniques for effective isolation. A further complication is that natural product extracts may contain critical components that are both chromophoric and non-chromophoric. Identifying non-chromophoric compounds in complex mixtures can be difficult. Traditional ultraviolet (UV) detection fails to detect targets and impurities that are present at low levels or lack chromophores. Evaporative light scattering detection (ELSD) provides advantages over spectroscopic detectors for detecting compounds that are deficient in a UV-absorbing chromophore or fluorophore.

Rapid analysis and quantification of major neutral lipid species and free fatty acids by HPLC‐ELSD from microalgae

A method based on normal‐phase high performance liquid chromatography combined with evaporative light‐scattering detector was developed to quantify major neutral lipids from microalgae. A binary gradient enabled a good resolution of hydrocarbons and major neutral lipids by classes in less than 13 min. A good linearity was observed from 0.9 to 30 μg. Limits of detection (LOD) and quantification (LOQ) was from 3 to 64 ng depending on the analyte. The intra‐ and inter‐run precision (% RSD) of analysis was found less than 10%. The method was successfully applied to microalgae lipid extracts from Botryococcus braunii, Chlorella vulgaris, Spirulina platensis, and Porphyridium cruentum. B. braunii was distinguished by the highest levels of lipids, triacylglycerol (TAGs), and diacylglycerol (DAGs) being the major compounds.Practical applications: Neutral lipids produced by the microalgae are an interesting way for the development of biofuel from renewable carbon. A simple quantification of these lipids is important in the implementation of oleaginous microalgae screening as well as in the bioprocess optimization of algal lipid production. Besides, determining quantitatively the major lipid classes provides information in the understanding of the biosynthetic pathways and the accumulation of these lipids in relation with algal culture conditions.Normal‐phase HPLC conditions were studied to establish a method allowing a rapid separation of TAGs, DAGs, MAGs, and FFA but also HC by classes in a single run. Their quantification through evaporative light‐scattering detector (ELSD) was performed. The developed method was applied on lipid extracts from the different algal cultures.

Simultaneous determination of sucralose and related compounds by high-performance liquid chromatography with evaporative light scattering detection

Sucralose is widely used in food and beverages as sweetener. Current synthesis approaches typically provide sucralose products with varying levels of related chlorinated carbohydrates which can affect the taste and flavor-modifying properties of sucralose. Quantification of related compounds in sucralose is often hampered by the lack of commercially available standards. In this work, nine related compounds were purified (purity>97%) and identified by liquid chromatography–mass spectrometry (LC–MS) and nuclear magnetic resonance (NMR), then a rapid and simple HPLC coupled with evaporative light scattering detection (ELSD) method has been developed for the simultaneous determination of sucralose and related compounds. Under optimized conditions, the method showed good linearity in the range of 2–600μgmL−1 with determination coefficients R2⩾0.9990. Moreover, low limits of detection in the range of 0.5–2.0μgmL−1 and good repeatability (RSD<3%, n=6) were obtained. Recoveries were from 96.8% to 101.2%. Finally, the method has been successfully applied to sucralose quality control and purification process monitoring.