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The LC-2010 is a completely integrated
chromatography system. It comprises a quaternary gradient low-pressure
mixing pump with integral degasser, autosampler, column oven, dual-wavelength
UV-Vis detector and system controller in one ultra-small footprint.
Available in both Peltier cooled and ambient autosampler versions,
the LC-2010 has set new standards in precision, throughput and
regulatory compliance.
LC-2010 is an integrated HPLC system full of the most advanced
technologies; provides you with high performance and useful functions
which help you do chromatography more productively.
Higher Speed. Higher capacity -- Never-ending desire for High
Throughput is addressed by the Autosampler. High speed of injection
(15 sec for 10 µL injection) for 4 MTP, standard or Deep-well
plate cooling capability in a compact footprint provides you with
up to 1536 unattended analyses ! In addition to rapid throughput,
the system provides more robust, durable and reproducible injection
capability.
Automation frees you from repetitious daily operations, such as
changing mobile phases, waiting for the baseline stability, and
rinsing the column after analyses by automated these functions.
Automated standalone system operation provides the estimated ending
time of the analyses, amount of remaining mobile phases.
A High level validation is mandated in order to comply with GLP/GMP
requirements. The time, effort and increased costs to meet these
requirements are now addressed by the automated validation and
verification of the operation of the overall system. Also CMD (Column
Management Device) enables users to manage the column history and
term of validity.
For most users, analytical equipment is just another tool. If
that tool is difficult to operate or requiring a steep learning
curve, no benefit can be gained no matter how numerous its capabilities.
Graphical operating screens and wizard functions make it simple
to use even for the first time user. Moreover, users can run gradient
analyses as well as isocratic analyses even more easily by using
Simple Mode of operation.
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The CoSense Series is an automated
sample pre-treatment system designed to facilitate the processing
of complex samples and augment the efficiency of NMR and MS measurements.
HPLC column switching is used to separate, purify and concentrate
target compounds as well as perform desalting and solvent replacement.
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The process of purifying target compounds
from the sample, including concentration, desalting and (most importantly)
deuterated solvent replacement is completely automated on CoSense
for NMR. Manual handling of large quantities of expensive deuterated
solvents is entirely eliminated, shortening analysis times and
reducing costs.
While LC-NMR and LC-MS are useful analytical methods, for the
structural analysis of compounds, the conditions most often used
for HPLC are not optimum for NMR or MS. For that reason, analysis
of samples in a complex matrix require cumbersome procedures involving
initial separation-purification using HPLC, followed by desalting
and other processes before NMR/MS analysis can be performed.
Co-Sense LC-NMR / LC-MS is an automated sample pretreatment system
designed to facilitate the processing of complex samples and augment
the efficiency of NMR and MS measurements. HPLC column-switching
technology is used to separate, purify and concentrate target compounds,
and perform desalting and solvent replacement. This eliminates
the bother and expense of performing such operations manually.
Further, the separation of target compounds using HPLC is not limited
by NMR and MS restrictions, allowing HPLC parameter selection as
desired.
System is designed for LC-NMR and LC-MS sample preparation. After
a semi-preparative or analytical separation the peaks can be collected
and pre-concentrated on a trap column to reach the necessary concentration
for an NMR analysis. The expansive D²-solvents will be used
only in the last step, when the samples are re-eluted after trapping.
Full automation allow online or offline measurements and can reduce
the time for manual preparation.
For LCMS use the separation can be done with typical high concentrated
buffers, the solvents will be exchanged direct before the LCMS
inlet. Especially if LCMS is not the standard method and is asked
to confirm the results of other techniques this could be an alternative,
because validated methods are not need to change.
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Problems associated with non-volatile
buffers or compromised LC separations arising from running solvents
best for MS analysis are prevented with the CoSense for MS. Optimum
separations can be run, with target compounds being purified, concentrated,
desalted and re-eluted into the MS in a suitable volatile solvent
system.
While LC-NMR and LC-MS are useful analytical methods, for the
structural analysis of compounds, the conditions most often used
for HPLC are not optimum for NMR or MS. For that reason, analysis
of samples in a complex matrix require cumbersome procedures involving
initial separation-purification using HPLC, followed by desalting
and other processes before NMR/MS analysis can be performed.
Co-Sense LC-NMR / LC-MS is an automated sample pretreatment system
designed to facilitate the processing of complex samples and augment
the efficiency of NMR and MS measurements. HPLC column-switching
technology is used to separate, purify and concentrate target compounds,
and perform desalting and solvent replacement. This eliminates
the bother and expense of performing such operations manually.
Further, the separation of target compounds using HPLC is not limited
by NMR and MS restrictions, allowing HPLC parameter selection as
desired.
System is designed for LC-NMR and LC-MS sample preparation. After
a semi-preparative or analytical separation the peaks can be collected
and pre-concentrated on a trap column to reach the necessary concentration
for an NMR analysis. The expansive D²-solvents will be used
only in the last step, when the samples are re-eluted after trapping.
Full automation allow online or offline measurements and can reduce
the time for manual preparation.
For LCMS use the separation can be done with typical high concentrated
buffers, the solvents will be exchanged direct before the LCMS
inlet. Especially if LCMS is not the standard method and is asked
to confirm the results of other techniques this could be an alternative,
because validated methods are not need to change.
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Utilising the unique and newly developed
MAYI-ODS on-line SPE column and dilution flow channel, the Bioanalysis
CoSense seamlessly conducts all processes from sample pre-treatment
to analysis. Automatic, On-line pre-treatment of biological samples
such as serum or plasma minimises handling and enhances application
efficiency.
Co-Sense for BA features the dilution bypass added in the sample
introduction flow channel leading to the MAYI pretreatment columns.
Different type of MAYI columns enable to use this approach for
various type of components. This dilution bypass eliminates the
need for preliminary dilution of the sample by automatically diluting
it on-line. Use of a buffer solution as the sample introduction
mobile phase or adding a small amount of organic solvent to it
ensures effective trapping and concentration of even drugs with
a high rate of protein binding, leading to highly efficient deproteinisation
and a high recovery rate. Thus, direct injection of unprocessed
blood plasma or blood serum has become possible.
HPLC is widely employed in the analysis of drugs within bio-samples.
Conditions of the sample pretreatment, as well as chromatographic
conditions, are important factors that significantly affect the
accuracy and sensitivity of the analysis. Co-Sense for BA, with
its unique configuration comprised of the newly developed MAYI-ODS
on-line SPE column and the on-line dilution flow channel, automatically
and seamlessly conducts all processes from sample pretreatment
to analysis. On-line pretreatment of bio-samples such as blood
serum or plasma will remarkably enhance the efficiency, as well
as reduce the labor, of the analysis.
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Cleaning validation of manufacturing
equipment involved in pharmaceutical production is an essential
factor in GMP. CoSense for CV addresses the needs for a highly
sensitive yet simple method for sample pre-treatment, analysis
and residue evaluation. Wizard navigation with authorisation levels
allow intuitive, secure operation.
Cleaning validation of manufacturing equipment involved in pharmaceutical
production is an essential factor in GMP. However, it requires
complicated and laborious processes such as sampling from the equipment,
sample pretreatment, analysis of the compound concerned, and evaluation
of the residue amount. Setting the threshold values, which have
to be determined taking into consideration various factors such
as the effective amount and dosage of the medicine, the size of
the production batch, and the size of the equipment, is also a
difficult procedure. The Co-Sense CV is an HPLC application system
addressing this demand. The unique system configuration and special
software dramatically enhance the efficiency of cleaning validation
by automatically conducting all processes from sample concentration
to analysis and data processing.
A column-switching technique is used to concentrate the target
component within the sample onto the concentration column, then
send it to the analysis column for separation and detection. Complex
sample pretreatment is therefore unnecessary, as the target component
is concentrated from a large amount of sample, even a trace amount
of component can be detected with high sensitivity.
The target component is concentrated while diluting the sample
by any desired rate, assuring creation of a clear peak, as well
as a high recovery rate regardless of the type of the sample solvent
used for extraction (patent pending).
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