Industrial

This application note provides a method for comprehensive detection of pesticides in vegetable juice matrices using GC/MS and LC/MS methods. Methods have been developed on Agilent GC/MS and LC/MS instrument platforms that reliably detect and quantitate 39 pesticides in a vegetable juice matrix. Most of the limits of quantitation (LOQ) values for GC/MS SIM ranged from 5 to 50 ng/mL, compared with 0.25 ng/mL to 10 ng/mL for GC/MS/MS, and 0.1 ng/mL to 10 ng/mL for LC/MS/MS. Both sensitivity and selectivity are improved using MS/MS and recovery of most spiked pesticides ranged from 70 to 120%.

An analytical method for screening and confirming the presence of 84 pharmaceuti- cals and 23 labeled standards in water samples for a total of 107 components was developed using the Agilent 6460 Triple Quadrupole Mass Spectrometer (Triple Quad MS) with Jet Stream Technology.

This application note describes the implementation of US EPA 200.7 guidelines for the analysis of trace elements in water using the Agilent SVS 2, a new and innovative sample introduction system for the Agilent 720/730 Series ICP-OES.

This application note demonstrates sensitive and reproducible HPLC analysis of N-linked glycans of human immunoglobulin G using the Agilent 1260 Infinity Bio-inert Quaternary LC System with fluorescence detection. The precision of retention times and areas was determined for analysis of a N-linked human IgG glycan library. In addition, good linearity in a range from 0.008 to 1 pmol was determined for a mix of five glycan standards (Man5, G2, G2S1, G2FS1, and G2S2) with low limits of detection and quantification. The Agilent 1260 Infinity Bio-inert Quaternary LC System with fluorescence detection is an optimal system for sensitive and reproducible analysis of 2-AB derivatized N-glycans released from human immunoglobulin G.

This Application Note shows that unwanted retention and peak tailing of adenosine triphosphate can be completely prevented when using the Agilent 1260 Infi nity Bio-inert Quaternary LC System. Due to the iron and steel-free design of the Agilent 1260 Infi nity Bio-inert Quaternary LC System, phosphate compounds can be analyzed without any issues regarding the formation of phosphate-iron complexes found with stainless steel systems. Even in the presence of high organic mobile phases, good peak shapes were observed without peak tailing or area reduction.

The THS6042/3 is a high-performance, low-power ADSL CPE line driver from TI that offers 350 mA of output current and supports ±12 V operation. The device features low noise, wide output range, and high speed, making it ideal for ADSL and G.Lite applications.

This is a Toshiba CompactFlash™ card that is based on flash technology and uses an ATA interface flash memory card. It is constructed with a flash disk controller chip and a NAND-type （Toshiba） flash memory device. The card supports both 5-Volt and 3.3-Volt power supplies. It comes in capacity of 8, 16, 32, 48, 64, 96, 128, 160, 192, 256, 320, 384 and up to 512 MB unformatted for type-I card. It is a perfect choice of solid-state mass-storage cards for battery backup handheld devices such as Digital Camera, Audio Player, PDA, or the applications that require high environment tolerance with high performance sustained write speed.

This article describes an LC/MS/MS method for the determination of buprenorphine and norbuprenorphine in whole blood using an Agilent Bond Elut Plexa PCX and an Agilent Poroshell 120 column

This document introduces the method of optimizing the method parameters of detecting steroids in wastewater using Agilent 6490 Triple Quadrupole LC/MS System with iFunnel Technology, resulting in a sensitivity as low as sub-1 ng/L (1 part per trillion).

A method for simultaneous determination of malachite green and crystal violet, and their metabolites leuco-malachite green and leuco-crystal violet in fish, was developed and validated. The analytes were extracted by solid phase extraction and quantified by liquid chromatography coupled to electrospray ionization tandem mass spectrometry operating in positive ion multiple reaction monitoring mode. The method provided a 0.5 ng/g limit of quantification for all these compounds in fish. The dynamic calibration ranges for these compounds were obtained from 0.5 to 100 ng/g. The overall recoveries ranged from 96 to 109% with RSD values between 1.7 and 4.5%.

This series of 500 W Transient Voltage Suppressors (TVSs) provides the highest level of Peak Pulse Power (PPP) in the industry for the DO-213AB size MELF package.

This application note describes a rapid method for detecting benzoylecgonine (BZE), the major metabolite of cocaine, in urine using the Agilent RapidFire High-throughput Mass Spectrometry System. Results were achieved with much faster sample cycle times and similar analytical output compared to GC/MS or LC/MS assays.

TGA8349-SCC is a high-performance low-noise distributed amplifier with a frequency range of DC to 14GHz, an output power of 16dBm, and a noise figure of 3.1dB.

This application note describes a method using high resolution accurate mass (HRAM) LC/MS for the quantitation of cystine and related metabolites in white blood cells. Excellent assay performance was achieved for cystine quantitation in white blood cells (WBCs) using the ultra-high resolving power and mass accuracy of an Agilent 6530 Accurate-Mass Q-TOF LC/MS System. Further, related metabolites were successfully identified and quantitatively profiled. The HRAM LC/MS data acquired in this study can be retrospectively analyzed to search for more metabolites and biomarkers without sample re-injection.

Mercury is one of the more toxic elements to living organisms. It is encountered at relatively low concentrations in the environment but with its amplification through the food chain, the final concentration in some foods can be relatively high. In addition, its toxicity is not only linked to its total concentration but is also dependent on the species. Mercury speciation in food analysis is necessary to fully estimate the toxic potential of this element to humans. Due to the low detection limits required for the analysis of Hg species, GC-ICP-MS has been the preferred method. However, with the sensitivity improvements in modern ICP-MS systems, the use of HPLC has become practical for the separation. Coupling HPLC and ICP-MS is particularly attractive due to the simple and fast connection between the techniques. Furthermore, in contrast to a GC analysis, sample extracts are directly injected into the system and no species derivatization is required, greatly simplifying the sample preparation and reducing the cost of the total analytical procedure.