High-sensitivity Mass Research Articles

A novel approach based on capillary liquid chromatography for the simultaneous determination of neonicotinoid residues in cereal samples

A simple and effective method using solid–liquid extraction followed by capillary liquid chromatography with diode array detection (CLC-DAD) has been established for the extraction and determination of seven neonicotinoid insecticides commercially available (imidacloprid, thiacloprid, clothianidin, thiamethoxam, acetamiprid, nitenpyram and dinotefuran) in cereal samples. The separation was achieved in less than 19 min using a Zorbax XDB-C18 column (150 mm × 0.5 mm i.d, 5 µm) at a 25 °C, with a mobile phase consisting of ultrapure water and acetonitrile at a flow rate of 10 µL/min. Detection wavelengths of 254 or 270 nm were used, depending on the analyte. Variables affecting the extraction efficiency were optimized, such as type and volume of extraction solvent, and extraction and centrifugation time. Under the optimal conditions, the proposed method was characterized according to SANTE/12682/2019 guideline, in terms of linearity (R2 ≥ 0.9901), repeatability (RSD ≤ 7.6%), reproducibility (RSD ≤ 10%) and trueness (recoveries ≥ 80%). The limits of detection and quantification were in the ranges of 3–5 and 9–18 µg/kg, respectively, being adequate for the determination of these compounds in cereal samples at levels below its maximum residue limits (MRLs) established by the European legislation. The advantages of a miniaturized technique such as CLC in terms of high mass sensitivity and reduced solvent consumption, combined with the simplicity of the solid–liquid extraction procedure, make this method a useful alternative for the monitoring of these residues at trace level in cereal samples.

JMorp updates in 2020: large enhancement of multi-omics data resources on the general Japanese population.

In the Tohoku Medical Megabank project, genome and omics analyses of participants in two cohort studies were performed. A part of the data is available at the Japanese Multi Omics Reference Panel (jMorp; https://jmorp.megabank.tohoku.ac.jp) as a web-based database, as reported in our previous manuscript published in Nucleic Acid Research in 2018. At that time, jMorp mainly consisted of metabolome data; however, now genome, methylome, and transcriptome data have been integrated in addition to the enhancement of the number of samples for the metabolome data. For genomic data, jMorp provides a Japanese reference sequence obtained using de novo assembly of sequences from three Japanese individuals and allele frequencies obtained using whole-genome sequencing of 8,380 Japanese individuals. In addition, the omics data include methylome and transcriptome data from ∼300 samples and distribution of concentrations of more than 755 metabolites obtained using high-throughput nuclear magnetic resonance and high-sensitivity mass spectrometry. In summary, jMorp now provides four different kinds of omics data (genome, methylome, transcriptome, and metabolome), with a user-friendly web interface. This will be a useful scientific data resource on the general population for the discovery of disease biomarkers and personalized disease prevention and early diagnosis.

Directed Self-Assembly of Block Copolymers for the Fabrication of Functional Devices.

Directed self-assembly of block copolymers is a bottom-up approach to nanofabrication that has attracted high interest in recent years due to its inherent simplicity, high throughput, low cost and potential for sub-10 nm resolution. In this paper, we review the main principles of directed self-assembly of block copolymers and give a brief overview of some of the most extended applications. We present a novel fabrication route based on the introduction of directed self-assembly of block copolymers as a patterning option for the fabrication of nanoelectromechanical systems. As a proof of concept, we demonstrate the fabrication of suspended silicon membranes clamped by dense arrays of single-crystal silicon nanowires of sub-10 nm diameter. Resulting devices can be further developed for building up high-sensitive mass sensors based on nanomechanical resonators.

Inkjet-printed CMUT humidity sensors with high sensitivity and low hysteresis

Capacitive micromachined ultrasonic transducer (CMUT) is a proven MEMS based gravimetric sensor featuring high mass sensitivity. It can be highly sensitive for relative humidity (RH) measurement when drop-casted with moisture-sensitive graphene oxide (GO) film. However, high hysteresis appears to be a critical problem for the sensor partially due to the non-uniformity of the sensing film. Here, we present miniaturized CMUTs that are functionalized by the inkjet-printed GO film and exhibit high sensitivity and meanwhile low hysteresis. Hexagon CMUTs with a side length of 500 μm were designed and fabricated by the nitride-to-oxide wafer bonding process. GO inks were prepared using a mixture of DI water and ethanol as the solvent. A square pattern formed by a 2D array of ink droplets was inkjet printed on the CMUT membranes. GO films with different thicknesses were deposited on three CMUTs. The humidity sensing performance of the sensors was evaluated by measuring the resonance frequency shifts induced by the added mass of adsorbed water molecules. The sensors delivered high RH sensitivity of up to 3.35 kHz/%RH, short response/recovery time down to 8 s/2 s, and hysteresis as low as 2.6 %RH. This work demonstrates that the inkjet printing technique is an excellent tool to functionalize CMUT with the advantages of minimized material consumption, batch-production capability, and exceptional control over the film thickness and quality. The CMUT printed with GO film has also shown to be a promising candidate as a miniaturized humidity sensing platform.

Emission drivers and variability of ambient isoprene, formaldehyde and acetaldehyde in north-west India during monsoon season

Isoprene, formaldehyde and acetaldehyde are important reactive organic compounds which strongly impact atmospheric oxidation processes and formation of tropospheric ozone. Monsoon meteorology and the topography of Himalayan foothills cause surface emissions to get rapidly transported both horizontally and vertically, thereby influencing atmospheric processes in distant regions. Further in monsoon, Indo-Gangetic Plain is a major rice growing region of the world and daytime hourly ozone can frequently exceed phytotoxic dose of 40 ppb O3. However, the sources and ambient variability of these compounds which are potent ozone precursors are unknown. Here, we investigate the sources and photochemical processes driving their emission/formation during monsoon season from a sub-urban site at the foothills of the Himalayas. The measurements were performed in July, August and September using a high sensitivity mass spectrometer. Average ambient mixing ratios (±1σ variability) of isoprene, formaldehyde, acetaldehyde, and the sum of methyl vinyl ketone and methacrolein (MVK+MACR), were 1.4 ± 0.3 ppb, 5.7 ± 0.9 ppb, 4.5 ± 2.0 ppb, 0.75 ± 0.3 ppb, respectively, and much higher than summertime values in May. For isoprene these values were comparable to mixing ratios observed over tropical forests. Surprisingly, despite occurrence of anthropogenic emissions, biogenic emissions were found to be the major source of isoprene with peak daytime isoprene driven by temperature (r ≥ 0.8) and solar radiation. Photo-oxidation of precursor hydrocarbons were the main sources of acetaldehyde, formaldehyde and MVK+MACR. Ambient mixing ratios of all the compounds correlated poorly with acetonitrile (r ≤ 0.2), a chemical tracer for biomass burning suggesting negligible influence of biomass burning during monsoon season. Our results suggest that during monsoon season when radiation and rain are no longer limiting factors and convective activity causes surface emissions to be transported to upper atmosphere, biogenic emissions can significantly impact the remote upper atmosphere, climate and ozone affecting rice yields.

Dual Functions of Ghz Frequency Acoustic Resonator System for Biosamples Capture and Sensing.

This work reports a novel acoustic resonator system integrated dual functions of biological samples capture and amount monitoring on a single chip. The system could capture samples from nano-sized proteins to micro-sized cells on micro-sized chip precisely with controllable concentration, meanwhile the high sensitivity mass sensing was achieved during the capture process. The devices were further applied to study the cell growth and cytotoxicity. Results indicated that it was possible to capture and monitor the physiological changes in a single cell level. This work explores a new opportunity on the development of miniaturized multiplex biosensing devices on a single chip.

Mass Spectrometry of Heavy Analytes and Large Biological Aggregates by Monitoring Changes in the Quality Factor of Nanomechanical Resonators in Air.

Nanomechanical resonators are routinely used for identification of various analytes such as biological and chemical molecules, viruses, or bacteria cells from the frequency response. This identification based on the multimode frequency shift measurement is limited to the analyte of mass that is much lighter than the resonator mass. Hence, the analyte can be modeled as a point particle and, as such, its stiffness and nontrivial binding effects such as surface stress can be neglected. For heavy analytes (>MDa), this identification, however, leads to incorrectly estimated masses. Using a well-known frequency response of the nanomechanical resonator in air, we show that the heavy analyte can be identified without a need for highly challenging analysis of the analyte position, stiffness, and/or binding effects just by monitoring changes in the quality factor (Q-factor) of a single harmonic frequency. A theory with a detailed procedure of mass extraction from the Q-factor is developed. In air, the Q-factor depends on the analyte mass and known air damping, while the impact of the intrinsic dissipation is negligibly small. We find that the highest mass sensitivity (for considered resonator dimensions ∼zg) can be achieved for the rarely measured lateral mode, whereas the commonly detected flexural mode yields the lowest sensitivity. Validity of the proposed procedure is confirmed by extracting the mass of heavy analytes (>GDa) made of protein and Escherichia coli bacteria cells, and the ragweed pollen nanoparticle adsorbed on the surface of the nanomechanical resonator(s) in air, of which the required changes in the Q-factor were previously experimentally measured. Our results open a doorway for rapid detection of viruses and bacteria cells using standard nanomechanical mass sensors.

Proteomic Analysis of the Cerebrospinal Fluid in Patients With Essential Tremor Before and After Deep Brain Stimulation Surgery: A Pilot Study

Electrical neuromodulation by deep brain stimulation (DBS) is a well-established method for treatment of severe essential tremor (ET). The mechanism behind the tremor relieving effect remains largely unknown. Our aim of this study was to evaluate alterations in proteomics pre- and post-DBS in patients diagnosed with severe ET. Ten right-handed ET patients were included in this study. Cerebrospinal fluid (CSF) was obtained by lumbar puncture preoperatively (N = 10) and six months postoperatively (N = 7). The samples were analyzed by high sensitive liquid chromatography tandem mass spectrometry. Twenty-two proteins were statistically significantly altered in the CSF of ET patients before and after DBS treatment. Downregulated proteins were involved in regulatory processes of protein activation, complement activation, humoral immune response as well as acute inflammatory response. The upregulated proteins were involved in pathways for cell secretion, adhesion as well as response to axon injury. DBS in ET patients effects the neurochemical environment in the CSF. These findings further elucidate the mechanisms of DBS and may lead to new biomarkers for evaluating the effect of DBS treatment.

Measurement of the mass sensitivity of QCM with ring electrodes using electrodeposition

A practical method for calculating the mass sensitivity of quartz crystal microbalance (QCM) resonators with ring-shaped Au electrodes on one side based on electrodeposition is presented in this communication. While for standard QCMs, an average mass sensitivity can be calculated despite its approximately Gaussian distribution, the mass sensitivity of QCMs with an asymmetrical electrode structure is difficult to calculate. However, non-standard electrode geometries might be beneficial for sensor applications especially in the area of electrochemistry. By measuring the resonance frequency change of a quartz crystal during deposition and applying Faraday’s law, we determined the mass sensitivity of QCM resonators with a ring electrode. We also studied the influence of the gold electrode thicknesses on the mass sensitivity of the ring-shaped and disc shaped electrodes. The experimental results showed that the mass sensitivity of the ring-shaped electrodes was 5%∼20% higher than those of the disc shaped electrodes. This method is practical and convenient for determining the mass sensitivity of the QCM with ring electrode, and it can be extended to measure QCMs with symmetrical and asymmetrical electrode structures. Such resonators with modified electrode structures may be of interest for studying electrochemical processes where a higher mass sensitivity is desirable.

Optimization of Ultra-High-Performance Liquid Chromatography-Electrospray Ionization-Mass Spectrometry Detection of Glutamine-FMOC Ad-Hoc Derivative by Central Composite Design

Glutamine (Gln) is converted to excitatory (glutamate, aspartate) and inhibitory (γ-amino butyric acid) amino acid neurotransmitters in brain, and is a source of energy during glucose deprivation. Current research utilized an Analytical Quality by Design approach to optimize levels and combinations of critical gas pressure (sheath, auxiliary, sweep) and temperature (ion transfer tube, vaporizer) parameters for high-sensitivity mass spectrometric quantification of brain tissue glutamine. A Design of Experiments (DOE) matrix for evaluation of relationships between these multiple independent variables and a singular response variable, e.g. glutamine chromatogram area, was developed by statistical response surface methodology using central composite design. A second-order polynomial equation was generated to identify and predict singular versus combinatory effects of synergistic and antagonistic factors on chromatograph area. Predicted versus found outcomes overlapped, with enhanced area associated with the latter. DOE methodology was subsequently used to evaluate liquid chromatographic variable effects, e.g. flow rate, column temperature, and mobile phase composition on the response variable. Results demonstrate that combinatory AQbD-guided mass spectrometric/liquid chromatographic optimization significantly enhanced analytical sensitivity for Gln, thus enabling down-sized brain tissue sample volume procurement for quantification of this critical amino acid.

30 GHz surface acoustic wave transducers with extremely high mass sensitivity

A nano-patterning process is reported in this work, which can achieve surface acoustic wave (SAW) devices with an extremely high frequency and a super-high mass sensitivity. An integrated lift-off process with ion beam milling is used to minimize the short-circuiting problem and improve the quality of nanoscale interdigital transducers (IDTs). A specifically designed proximity-effect-correction algorithm is applied to mitigate the proximity effect occurring in the electron-beam lithography process. The IDTs with a period of 160 nm and a finger width of 35 nm are achieved, enabling a frequency of ∼30 GHz on lithium niobate based SAW devices. Both centrosymmetric type and axisymmetric type IDT structures are fabricated, and the results show that the centrosymmetric type tends to excite lower-order Rayleigh waves and the axisymmetric type tends to excite higher-order wave modes. A mass sensitivity of ∼388.2 MHz × mm2/μg is demonstrated, which is ∼109 times larger than that of a conventional quartz crystal balance and ∼50 times higher than a conventional SAW device with a wavelength of 4 μm.

Metabolic reprogramming of fibro/adipogenic progenitors facilitates muscle regeneration.

In Duchenne muscular dystrophy (DMD), the absence of the dystrophin protein causes a variety of poorly understood secondary effects. Notably, muscle fibers of dystrophic individuals are characterized by mitochondrial dysfunctions, as revealed by a reduced ATP production rate and by defective oxidative phosphorylation. Here, we show that in a mouse model of DMD (mdx), fibro/adipogenic progenitors (FAPs) are characterized by a dysfunctional mitochondrial metabolism which correlates with increased adipogenic potential. Using high-sensitivity mass spectrometry-based proteomics, we report that a short-term high-fat diet (HFD) reprograms dystrophic FAP metabolism in vivo. By combining our proteomic dataset with a literature-derived signaling network, we revealed that HFD modulates the β-catenin-follistatin axis. These changes are accompanied by significant amelioration of the histological phenotype in dystrophic mice. Transplantation of purified FAPs from HFD-fed mice into the muscles of dystrophic recipients demonstrates that modulation of FAP metabolism can be functional to ameliorate the dystrophic phenotype. Our study supports metabolic reprogramming of muscle interstitial progenitor cells as a novel approach to alleviate some of the adverse outcomes of DMD.

A new method for measurement of lithium isotopes with nuclear applications

Extreme isotope abundance ratios occur naturally, but also result from enrichment processes required for various industrial applications. The range of elements used for these industrial applications spans essentially the entire periodic table; thus, the need for a low cost (both in labor and finance) analytical technique to measure isotopic enrichments that create extreme isotope abundance ratios has never been greater. Molten salt reactors are one such application, where high purity 7Li is required for cooling processes due to its low neutron cross-section compared to 6Li. Several new technologies are required for these reactors to be viable, both technically and financially, including an efficient method for enrichment of 7Li. Many methods are being tested, but there is a need for a high-performance, high-throughput method for determination of extreme lithium isotope abundance ratios. High abundance sensitivity mass spectrometry provides a path forward for measurement of lithium isotopes. Here, we present a new method for measuring enriched lithium isotope ratios by using multi-collector inductively coupled plasma mass spectrometry and combined faraday-ion counting detectors. We carefully characterize the abundance sensitivity and background signals associated with combined Faraday-ion counting techniques. To test the accuracy of the method, we measured lithium isotopic compositions of a suite of pure lithium salts using the standard static faraday measurement and compare those results to isotope ratios measured using the new method. Isotope ratios of the two techniques agree to within 1.5‰. We also achieved 7Li isotope abundance for a previously characterized enriched lithium salts within 0.0035%, indicating that the technique will provide a way forward for measuring enriched lithium isotope ratios in nuclear materials. The technique can be applied to any element with unnatural isotopic compositions and/or extreme abundance ratios.

A High Frequency Dual Inverted Mesa QCM Sensor Array with Concentric Electrodes

Quartz Crystal Microbalance (QCM) is a candidate technology for high sensitivity application. This mass sensor's property depends on the piezoelectric property of the AT-cut quartz crystal. QCM has been widely employed for gas detection due to its comparative advantages including high mass sensitivity, potential for array configuration, low cost, ease of fabrication as well as wide range of available sensitive material compatibility. However, its application has been limited due to two main disadvantages of the non-uniform mass sensitivity across the electrodes and lower frequency of operation. In this work, in order to overcome these disadvantages, a novel concentric electrode structure combined with the dual inverted mesa structure has been proposed and implemented. It is demonstrated that the developed and optimized concentric electrode has provided a uniform displacement across the QCM's sensing electrode. In addition, the dual inverted mesa design has been implemented in the QCM array in which a high fundamental resonant frequency of 33 MHz has been achieved without interference between the adjacent channels in the sensor array. The interference between the adjacent high frequency QCM channels has been eliminated and therefore, each QCM can function as an individual gas sensor when coated with the designed sensing layers. For 33 MHz, the interference has been eliminated at the optimal center to center between electrode distance (c2c). In the case of 10 MHz array, c2c value of 6 mm is achieved which is lower than the value of c2c achieved on a traditionally un-etched QCM array which was found equal to 6.5 mm. Therefore, the proposed QCM array design is shown to reduce the overall size while enhancing the device sensitivity, uniformity and performance.

Detection and prevalence of monoclonal gammopathy of undetermined significance: a study utilizing mass spectrometry-based monoclonal immunoglobulin rapid accurate mass measurement

High-sensitivity mass spectrometry assays are available to detect monoclonal immunoglobulins. To better assess the prevalence of monoclonal gammopathy of undetermined significance (MGUS), we identified 300 patients diagnosed with MGUS or related gammopathy who had a prior negative work-up for monoclonal proteins as part of the Olmsted County MGUS screening study. Two mass spectrometry-based detection methods (matrix-assisted laser desorption/ionization-time of flight (MALDI-TOF) and monoclonal immunoglobulin rapid accurate mass measurements (miRAMM) along with traditional immunofixation were performed on the Olmsted baseline and MGUS diagnostics serum samples. Among the 226 patients considered negative for MGUS based on protein electrophoresis and serum-free light-chain assay, a monoclonal protein could be detected at baseline in 24 patients (10.6%) by immunofixation, 113 patients (50%) by MADLI-TOF mass spectrometry, and 149 patients (65.9%) by miRAMM mass spectrometry. In addition, using miRAMM, some patients demonstrated an oligoclonal to monoclonal transition giving insight into the origin of MGUS. Using the sensitive miRAMM, MGUS is present in 887 of 17,367 persons from the Olmsted County cohort, translating into a prevalence of 5.1% among persons 50 years of age and older. This represents the most accurate prevalence estimate of MGUS thus far.

Coherent Optical Transduction of Suspended Microcapillary Resonators for Multi-Parameter Sensing Applications.

Characterization of micro and nanoparticle mass has become increasingly relevant in a wide range of fields, from materials science to drug development. The real-time analysis of complex mixtures in liquids demands very high mass sensitivity and high throughput. One of the most promising approaches for real-time measurements in liquid, with an excellent mass sensitivity, is the use of suspended microchannel resonators, where a carrier liquid containing the analytes flows through a nanomechanical resonator while tracking its resonance frequency shift. To this end, an extremely sensitive mechanical displacement technique is necessary. Here, we have developed an optomechanical transduction technique to enhance the mechanical displacement sensitivity of optically transparent hollow nanomechanical resonators. The capillaries have been fabricated by using a thermal stretching technique, which allows to accurately control the final dimensions of the device. We have experimentally demonstrated the light coupling into the fused silica capillary walls and how the evanescent light coming out from the silica interferes with the surrounding electromagnetic field distribution, a standing wave sustained by the incident laser and the reflected power from the substrate, modulating the reflectivity. The enhancement of the displacement sensitivity due to this interferometric modulation (two orders of magnitude better than compared with previous accomplishments) has been theoretically predicted and experimentally demonstrated.

Pharmacokinetic Comparisons of Mangiferin and Mangiferin Monosodium Salt in Rat Plasma by UPLC-MS/MS

Mangiferin (MG) is an active component in natural medicines, and various studies have been reported on pharmacological effects, but the low solubility and bioavailability of MG limit its wide application. The aim of the present study was to investigate the pharmacokinetic profiles of mangiferin (MG) and mangiferin monosodium salt (MG-Na) in rat plasma by UPLC-MS/MS, which were then compared between the two groups. An appropriate high sensitivity and selectivity ultraperformance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method was applied to the comparison of plasma pharmacokinetics in MG and MG-Na using carbamazepine as internal standard (IS). These results showed that there were statistically significant differences in the pharmacokinetic parameters between MG and MG-Na after a single oral administration at 100 mg/kg. When compared with pharmacokinetic parameters of MG, the AUC(0-t), AUC(0–∞), Cmax,K10, and Ka of MG-Na were increased by 5.6-, 5.7-, 20.8-, 8-, and 83.6-fold, while the Tmax and CL/F were decreased by 4- and 5.7-fold (P<0.001), respectively. t1/2 value showed an increasing trend, but was statistically significant between the two groups. Moreover, the AUC value in the MG-Na group was significantly increased and the relative bioavailability was calculated to be 570% when compared with that of the MG group. These results suggested that the salification reaction of MG can effectively enhance gastrointestinal absorption and relative bioavailability by improving solubility and membrane permeability.

ZnO nanorod‐based Love wave delay line for high mass sensitivity: a finite element analysis

This study presents finite element time-domain simulation of a SiO 2 /36°-YX LiTaO 3 Love wave (LW) delay line to explore coupled resonance phenomenon with ZnO nanorods designed on the top surface of the device. The effect of variation in ZnO nanorods height on the propagation of LW, mode-transitions, area-averaged stress, insertion loss, and mass sensitivity of the device is studied. Simulation results show that at the critical height of ZnO nanorods, coupled resonance occurs that causes a sharp swing in the phase shift indicating a transition from inertial to elastic loading. Coupled resonance increases the acoustic impedance of the device and also the average stress between nanorod and substrate interface. Simulation of mass loading is performed by applying an incremental surface mass density on the active area of the device. A nanorod packing density of 1 μm -2 gives a high mass sensitivity of 728 m 2 kg -1 which is more than ten times the sensitivity of a plain LW device. At the coupled resonant height, the insertion loss of the sensor increases, and a swing of about 1 dB is observed with variation in the nanorod height.

Detection and Prevalence of Monoclonal Gammopathy of Undetermined Significance: A study utilizing mass spectrometry-based monoclonal immunoglobulin rapid accurate mass measurement

High-sensitivity mass spectrometry assays are available to detect monoclonal immunoglobulins. To better assess the prevalence of monoclonal gammopathy of undetermined significance (MGUS), we identified 300 patients diagnosed with MGUS or related gammopathy who had a prior negative work-up for monoclonal proteins as part of the Olmsted County MGUS screening study. Two mass spectrometry-based detection methods (matrix-assisted laser desorption/ionization-time of flight (MALDI-TOF) and monoclonal immunoglobulin rapid accurate mass measurements (miRAMM) along with traditional immunofixation were performed on the Olmsted baseline and MGUS diagnostics serum samples. Among the 226 patients considered negative for MGUS based on protein electrophoresis and serum-free light-chain assay, a monoclonal protein could be detected at baseline in 24 patients (10.6%) by immunofixation, 113 patients (50%) by MADLI-TOF mass spectrometry, and 149 patients (65.9%) by miRAMM mass spectrometry. In addition, using miRAMM, some patients demonstrated an oligoclonal to monoclonal transition giving insight into the origin of MGUS. Using the sensitive miRAMM, MGUS is present in 887 of 17,367 persons from the Olmsted County cohort, translating into a prevalence of 5.1% among persons 50 years of age and older. This represents the most accurate prevalence estimate of MGUS thus far.

SIFT-ing archaeological artifacts: Selected ion flow tube-mass spectrometry as a new tool in archaeometry

A fast non‐destructive approach based on the use of portable selected ion flow tube-mass spectrometry (SIFT-MS) was used for the first time to characterize organic materials in archaeological artifacts. The high sensitivity, specificity and selectivity SIFT soft chemical ionization mass spectrometry enabled us to investigate the composition of organic residues collected from ancient Egyptian findings in order to demonstrate the robustness of the techniques with different matrices. In addition, we tested SIFT-MS directly on an archaeological Egyptian amphora to prove its suitability as a completely non-invasive technique.Parallel investigations on all the samples were performed by GC/MS analysis to correlate and confirm the data obtained by SIFT-MS.The possibility of using a portable mass spectrometer on an excavation site or in a museum would be a significant step forward in the non-invasive analysis of organic archaeological materials, enabling archeologists and conservators to obtain real-time information on the molecular composition of organic residues.