Agilent Manuals

This application note describes an ultrafast SPE/MS/MS method, using the Agilent RapidFire High-Throughput Mass Spectrometry System, with a sample analysis time of <10 seconds per sample, for the analysis of levetiracetam in human serum. The Agilent RapidFire/MS System exhibited comparable accuracy, precision, linearity, and sensitivity to LC/MS/MS, but with a sample analysis cycle time 10-fold faster than LC/MS/MS.

This document mainly introduces Agilent 8800 triple quadrupole ICP-MS innovative reaction cell technology, which can effectively eliminate oxide polyatomic ion interference

This study focuses on the rapid screening of an entire hippocampus section of mouse brain for the study of Alzheimer’s disease. The aim was to investigate whether there was a correlation between the tissue’s chemical composition and protein secondary structure with tissue morphology, in order to provide insight into the disease process. Agilent’s 670 and 620 FTIR imaging analysis, combined with a chemical imaging microscope and FTIR spectrometer, were used for this research.

This application note introduces the Chinese Pharmacopoeia 2010 edition limit requirements for heavy metals and describes the application of Agilent Technologies 's microwave plasma atomic emission spectrometry (MP-AES) in the determination of heavy metal content in Chinese herbal medicines.

This Application Note describes the performance comparison and benchmark of the Agilent 2200 TapeStation system with the Agilent 2100 Bioanalyzer system, the industry standard for RNA quality control. The 2200 TapeStation system performs automated analysis of up to 96 samples with approximate analysis time of 1 minute per sample. This Application Note demonstrates the high correlation between RINe generated by the 2200 TapeStation system with the RIN quality assessment of the 2100 Bioanalyzer system. The high reproducibility of RINe achieved with the 2200 TapeStation system in RNA quality assessment is also shown. The 2200 TapeStation system is, therefore, a reliable system for RNA quality control.

Gene expression analysis is currently carried out using three methods that provide complementary data: microarrays, RNA-Seq, and RT-qPCR. Microarrays provide comprehensive whole-genome coverage in single experiments, with rapid data acquisition and results at a low price per sample.

This application note demonstrates the concordance in the results achieved with identical oligonucleotide probes on two versions of Agilent miRNA microarrays [(AMADID 021827, release 12.0) and (AMADID 031181, release 16.0)], based on different revisions of the miRBase database and provided on different microarray formats. Since probes for a given microarray will remain constant for subsequent versions of Agilent SurePrint G3 Human miRNA microarrays, barring any miRBase sequence changes, it is necessary to confirm that the TotalGeneSignal achieved is consistent. The data show Agilent’s strength in probe reproducibility, a crucial factor for identifying miRNA of differential expression.

This applications note describes using VnmrJ 3 Software to set up advanced experiments to resolve overlapping homonuclear resonances. These tools allow even novice users to gain critical information about their research samples, using the most advanced NMR experiments available.

This application note describes a method for characterizing olive oil using Agilent GC/Q-TOF MS and Mass Profiler Professional software. The method can detect a large number of compounds in olive oil and perform quantitative analysis.

Solid-phase extraction (SPE) coupled with high-performance liquid chromatography (HPLC) was optimized for extraction and quantification of two fungicides (carbendazim and thiabendazole) in apple juice. Results indicate that SPE using Agilent Bond Elut SCX (60 mg, 3 mL) and HPLC using an Agilent ZORBAX Eclipse Plus C18 column (4.6 mm × 100 mm, 3.5 µm) is an excellent combination for extraction and analysis of these compounds. Recoveries ranged from 92.1 to 99.4 percent with RSDs below 5 percent and limits of detection of 4 µg/kg.

This application note describes the optimization of a rapid LC/MS/MS method for vitamin B related compounds (4-aminobenzoic acid, nicotinamide, riboflavin, and nicotinic acid) on an Agilent ZORBAX Rapid Resolution High Definition HILIC Plus column using an Agilent 1290 Infinity LC System with an Agilent 6410A Triple Quadrupole Mass Spectrometer. The method uses isocratic elution with an acetonitrile rich mobile phase and an ammonium acetate buffer. All analytes have good peak shape with this hydrophilic interaction chromatography (HILIC) application. The method is then used to demonstrate the importance of choosing an appropriate injection solvent when performing LC analyses in HILIC mode. Various injection solvents are investigated, including water, acetonitrile, methanol, and combinations. Of the solvents explored, it was determined that pure acetonitrile yields the best retention and peak shape for all compounds, with water being the worst solvent for analytical performance and peak shape.

This application note uses Agilent ZORBAX RRHD columns with UHPLC/MS to compare Morphine’s HILIC and RPLC. Both methods use acetonitrile/ammonium acetate buffer mobile phase for isocratic elution. The results show that HILIC mode allows for more sensitive MS detection due to more efficient spraying and desolvation in the ESI-MS source, as a result of the volatile acetonitrile rich mobile phase used.

This document describes the advantages and disadvantages of copper and molybdenum sources on a dual source SuperNova diffractometer, and compares the two sources in terms of data collection and data processing.

This application note describes an analytical method for determination of carbendazim and 3 other fungicide residues in orange juice with easy sample preparation and LC/MS/MS detection. Developed for the 3 most important systemic fungicides, carbendazim, thiabendazole, and imazalil with its metabolite, this method can be easily expanded to include a broader range of pesticides. A simple and rapid extraction procedure provides clean extracts that without any preconcentration allow for detection of analytes at concentrations below 2 ppb. Quantification was performed using triphenyl phosphate as an internal standard. Excellent accuracy (% recovery) and precision (% CV) data were obtained for three concentration levels: 10, 50, and 250 ppb of each analyte.

This application note describes a rigorous QC column testing approach that employs active tests probes to verify the inertness performance of modern GC capillary columns.