Application Notes: General

Heparin is well-known as an anti-coagulant, antithrombotic drug. Chemically, it is a linear polysaccharide that is derived from animal tissues. For some time it has been known that heparin is not a homogeneous substance; rather, it is a heterogeneous mixture of molecules ranging in molar mass from less than 5,000 to more than 30,000 Daltons. Heparin can be chemically or enzymatically depolymerized to obtain low molecular weight (LMW) heparin products, which exhibit an improved pharmacological profile.

This application details a fast, reliable and highly selective trace-level screening method for the quantification of polychlorinated biphenyls (PCBs) in environmental, food and biological samples, using gas chromatography and a triple stage quadrupole mass spectrometer. The analytical strategy is analogous to the well-established US Environmental Protection Agency (USEPA) Method 1668A.

An ultrafast gradient LC separation method was developed to separate a 5-component drug mixture in 30 seconds, with peak widths of 1 second. maXis mass accuracy at sub-ppm levels and true isotopic pattern of the spectra from the peaks lead to a confident elemental formula assignment for each drug compound with the SmartFormula algorithm.

The success of evaporative light scattering detection relies on evaporating the eluent without destroying the analyte particle. Where the analyte is non-volatile, evaporator temperatures of 50-100 °C can be used without compound degradation, thus giving maximum sensitivity. However, when compounds have high vapor pressures and the eluent has a high boiling point (e.g. water), detection of semi-volatile compounds is problematic, because the evaporation temperature needs to be set at 30 °C or above in order to evaporate the solvent.

Improve the separation of 14 drugs of abuse in a complex mixture by employing a ternary solvent gradient.

Studies of odd-electron CID behaviors reveal that free radical fragmentation is structure-dependent and is directly correlated with the functional groups that stabilize the newly-formed free radicals.

QC test probes serve a vital function in ensuring the reproducibility of modern GC columns. These probes ensure that the columns have been properly deactivated, contain the correct amount of stationary phase, and have the same relative retention as the last column purchased. The choice of individual compounds in these test mixes varies widely and can have profound consequences on the performance of a column in the users' applications.

Synthetic fused silica capillary tubing is commonly used as the preferred substrate for chromatographic separation columns. In limited instances the absorption and diffusion of molecules into and through the fused silica deserves consideration.

Transforming "standard" gradient HPLC systems into extremely fast gradient systems is readily achievable with proper application of chromatographic principles, particularly temperature control, combined with utilization of advanced HPLC columns. Bottom line: You don't have to buy a new LC to achieve ultra high quality and speed!

A novel centrifugal fraction collector CFCâ„¢ enables SFC users to simultaneously collect and concentrate fractions. The technique is particularly useful for chiral separations where large volumes of enantiomers are being purified by stacked injection methods.

In size exclusion chromatography, obtaining calibration curves over a wide range of molecular weights is a difficulty investigators often encounter when analyzing polymers with a broad molar mass distribution. To overcome this problem two procedures are typically used. One option is to use multiple columns of different pore sizes linked together in series. A second is to use a column packed with a mixed bed resin of different pore sizes at an optimized mix ratio. However, problems can occur with both of these methods, which include distortion of the chromatogram or deviations between the actual calibration curve and the calibration curve approximated from data obtained from the molecular weight standards.

Our work focuses on the synthesis of branched (functionalized) polydienes via a facile two-step synthesis. Despite the numerous strategies developed for the preparation of branched polymers in recent years, there is still a limited number of simple synthetic strategies based on common vinyl monomers.

The SHISEIDO CAPCELL PAK C18 MGIII is an HPLC column packed with a silicone polymer-coated phase, providing excellent peak profiles for basic compounds under acidic conditions, and generating ultimately minimized column bleeding in LC–MS.

In general, polymer-based columns have a broad pH range (pH 2 to 13), and some have high temperature tolerance (up to 150°C or higher). Considerably large selectivity changes can be obtained by varying analysis temperature and mobile phase pH. Having control on these two parameters over wide ranges can be especially useful in method development.

Viscotek has been a strong advocate of good chromatography as a prerequisite for GPC (Gel Permeation Chromatography) data accuracy. Our recent work in application development has been driven by extremely difficult samples from industrial, biopharmaceutical, and academic sources. These samples present challenges ranging from sample solubility, column adsorption, as well as detection issues. This report will attempt to highlight a new approach that could be very helpful in certain advanced GPC applications.

Traditionally the analysis of water-soluble vitamins by reversed-phase HPLC has been complicated by the lack of retention for these compounds on conventional silica C18 columns. Here we demonstrate efficient, multi-mode, baseline resolution of six water-soluble vitamins in 6 min using a ZirChrom®-SAX column.

Amylose is an occasionally-branched biopolymer and, together with amylopectin, the hyper-branched component, a constituent of starch. Determination of branching in amylopectin on the basis of amyloses may be performed with the help of synthetic amyloses. Synthetic amyloses from enzymatic (phosphorolytic) reaction were checked for their linearity.

The analysis of polar compounds in support of clinical and preclinical pharmacokinetic studies requires an analytical methodology capable of achieving ultra-low detection and quantification limits. The high sensitivity afforded by coupling HPLC with tandem mass spectrometry (MS–MS) has made it the technique of choice in this environment, but it is subject to the following limitations when reversed-phase liquid chromatography (RPLC) is used

Capillary flow technology (CFT) devices are microfluidic components that extend capillary GC capabilities through simple and robust connections between pressure/flow modules and columns. One of the most powerful and simple is the CFT Tee. This is especially useful in GC–MS analysis providing (1) rapid column and inlet maintenance without MSD venting and (2) the capability of rapidly removing late eluting interferences from the column by forcing their retreat into the injection port through "backflushing". Removing these interferences improves column and detector longevity and analytical integrity. Backflushing is very valuable for trace GC–MS analysis in samples from complex matrices like soil, foods or tissues. The CFT Tee uses pressure-pulsed injections and constant flow mode with minimal loss in the MS signal. This approach will be useful to all GC–MS users who want to improve their instrument uptime.

An effective UHPLC–MS method for high throughput separation, identification and quantification of pseudoephedrine was developed on a Hypersil GOLD PFP 1.9 µm, 2.1 Ã- 100 mm column.

A new APCI/APLI source enables a high resolution TOF-MS to be coupled on LC and GC, thus increasing flexibility and performance of TOF-MS in combination with GC.

Under the registration, evaluation and authorization of chemicals (REACH) Regulations (EG) no. 1907/2006 the producer, manufacturer or importer of chemical substances/formulations have to register their products (more than 1 ton/year) at the chemical agency.

PEGylation, the process by which polyethylene glycol (PEG) chains are attached to protein and peptide drugs is a common practice in the development of biopharmaceuticals to prolong serum half-life and improve pharmacokinetics of a drug. There is increasing demand for chromatographic methods to separate the modified isoforms from the native protein. This application note describes the use of size exclusion and ion exchange chromatography for the characterization of PEGylated lysozyme.

Short analyses time and high resolution are in great demand from R&D and QC departments within the pharmaceutical industry. Sub-two micron ODS reversed phase columns have recently been introduced to meet these requirements, but these columns require an ultra-high pressure HPLC system to achieve optimum performance. TSK-GEL ODS-140HTP, 2.3mm columns from Tosoh Bioscience have been developed to offer a combination of short analyses time and high resolution separations that can be run at modest pressures, making these columns compatible with conventional HPLC instrumentation. The polylayer bonding chemistry of these columns results in highly efficient and physically stable columns when operated at high linear velocities. In addition, TSK-GEL ODS-140HTP, 2.3mm columns can be efficiently operated at pressures not exceeding 9000psi in UPLC® and other ultra-high pressure HPLC systems, as well as in traditional HPLC systems.

Synthetic fused silica capillary tubing has proven to be a vital component in many separation science techniques. Recently, it has expanded to serve an array of scientific markets. In most cases, an understanding of the internal surface chemistry is of fundamental importance.

There are many misconceptions about what it means to perform fast gas chromatography (GC) and what the term fast GC implies. Fast GC is often associated with the use of hydrogen as a carrier gas and, although this is certainly a good approach, it is not always necessary to shorten the analysis time. A second misconception is that changing column dimension results in time-consuming method development. Using high-efficiency GC columns can greatly reduce the analysis time and when coupled with the method translation software, the time spent on method development can be greatly minimized.

Viscotek has been a strong advocate of good chromatography as a prerequisite for GPC (Gel Permeation Chromatography) data accuracy. Our recent work in application development has been driven by extremely difficult samples from industrial, biopharmaceutical, and academic sources. These samples present challenges ranging from sample solubility, column adsorption as well as detection issues. This report will attempt to highlight a new approach that could be very helpful in certain advanced GPC applications.

An effective UHPLC-MS method for high throughput separation, identification and quantitation of pseudoephedrine was developed on a Hypersil GOLD™ PFP 1.9 µm, 2.1 x 100 mm column.