We used the Bidentate C18
2.o™ column to separate limonin from matrix components in citrus juice
extracts. The column produces high-efficiency, sharp peaks which is important in
order to obtain good limits of quantitation. The quantitaitve studies first
used limonin standard solutions covering a range of 2.0–200ppm in order to
establish a calibration curve. The detector response was shown to be linear in
this range. Next, a non-citrus juice was chosen to serve as a matrix blank
(apple juice). This juice extract had no peaks in the region where limonin
elutes and therefore would be a good candidate for percent recovery studies.
The extract was spiked at both 5 and 10ppm levels. Recovery was observed to be
within 97.8–100.2% at these levels. Finally, two orange juice samples were
analyzed and the limonin peak was correlated with the calibration cruve. The
amounts of limonin were found to be 1.20 and 3.70ppm in two different juices.
The approach can be used towards development of a fully validated method for
limonin quantitation.
Thoughts, ideas and notices by MicroSolv for and about the chromatography community. Scroll down for older blogs.
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Friday, April 18, 2014
Monday, March 17, 2014
New Retention Possibilities for Polar Compounds using Cogent Diol Column
TYPE-C Silica™ columns can be used for separation of a variety of polar compounds. The new Cogent Diol™ column makes an excellent addition to these stationary phases. Consisting of a short alkyl chain with vicinal alcohol groups, this material has additional separation capabilities compared to other phases. Since it is on a TYPE-C Silica™ surface, the bonding is very strong and durable. The diol group can interact with analytes via hydrogen-bonding interactions, resulting in new selectivity.
In the following example, we demonstrate the capabilities of this intriguing material. The test solutes chosen for the separation were seven common hydrophilic vitamins. The results show that baseline separation could be obtained for all seven analytes. The retention range is adequate as well, with no analytes eluting at the solvent front or sticking to the column. Peak shapes were sharp and symmetrical, and no tailing was observed.
This column makes a wonderful addition to the TYPE-C Silica™ line of HPLC columns and should be a great benefit to every chromatographer’s toolbox.
1. Ascorbic acid
2. Niacin
3. Riboflavin
4. Folic acid
5. Pyridoxine
6. Metformin
7. Thiamine
See the following link for full details:
http://kb.mtc-usa.com/article/AA-02102/0/
In the following example, we demonstrate the capabilities of this intriguing material. The test solutes chosen for the separation were seven common hydrophilic vitamins. The results show that baseline separation could be obtained for all seven analytes. The retention range is adequate as well, with no analytes eluting at the solvent front or sticking to the column. Peak shapes were sharp and symmetrical, and no tailing was observed.
This column makes a wonderful addition to the TYPE-C Silica™ line of HPLC columns and should be a great benefit to every chromatographer’s toolbox.
1. Ascorbic acid
2. Niacin
3. Riboflavin
4. Folic acid
5. Pyridoxine
6. Metformin
7. Thiamine
See the following link for full details:
http://kb.mtc-usa.com/article/AA-02102/0/
Tuesday, December 31, 2013
Simple Strategies for Improving Analyte Recovery
Suppose you’re doing an HPLC assay of a basic pharmaceutical
and find a 66% recovery for the API. What happened? Did the drug not extract
completely? Did degradation occur? These types of scenarios take up valuable
laboratory time and resources with investigations, troubleshooting, and re-run
analyses. In this case, it may be simply due to the autosampler glass. Regular
glass has silanols on the surface that can bind with basic analytes and
therefore lead to lower recovery. However, this problem can be prevented with some
simple considerations.
In this example using a basic test analyte (cetylpyiridinium chloride), we can see how
use of either an ammonium acetate buffer (red trace) or a formic acid additive
(blue trace) can reduce the effect of analyte loss compared to DI water alone
(green trace). Using 0.1% formic acid,
the silanols become protonated and neutral, which prevents ionic interactions
with the analyte from occurring. This is the more effective of the two
additives. Ammonium acetate helps the problem by a different approach. The
ammonium ion competes with the analyte for the silanols groups, and so fewer
sites are available for analyte loss to occur.
Here we use a different
strategy for reducing the analyte loss. Reduced Surface Activity (RSA™) glass
is made with almost no surface silanols and we can see a major improvement for
analyte recovery compared to regular glass. For best results, you can use a
combination of RSA glass vials and a formic acid diluent. For solubility
reasons though, sometimes you might have to use an ammonium acetate diluent. In
that case, RSA glass shows significantly better recovery than regular glass.
When analysts plan a sample preparation procedure,
they may put much thought into the extraction method, dilution procedures, and
so on. However, the role of the vial is often overlooked. Vials are inexpensive and disposable, so they can
be seen as relatively unimportant in the analysis process. This data shows how
they are not inert and can significantly skew your analytical results. A
careful selection of vial and diluent is all it takes to prevent your
laboratory from experiencing these kinds of problems.
Tuesday, November 5, 2013
Eastern Analytical Symposium is Coming Soon!
This year at EAS 2013, MicroSolv will have a booth showing
new products and technology at location # 611. In addition, we will be presenting
two technical posters in the “Applications of HPLC and UHPLC” segment on
Wednesday November 20, 2013 from 12pm–2pm. We will be exhibiting these posters at booths
418 and 419. This is an excellent opportunity to discover what products we
offer that can benefit your laboratory as well as the real world applications using
these products, as demonstrated with the poster sessions.
Among
the most notable of our latest products is the 2.o™ line of TYPE-C Silica
columns. These items are near-UHPLC stationary phases (2.2µm particles) that
will help to save your lab valuable analysis time with increased throughput.
All the benefits of our innovative TYPE-C Silica™ are combined with
high-efficiency small particle capabilities to allow for great potential for a
variety of fields such as metabolomics and clinical analyses. Our 2.o™ line of
products has shown great lot-to-lot reproducibility and durability in the
field. Stop by our booth and learn more about this exciting product and how it
can help your laboratory become more productive.
For
more information on the symposium, be sure to check out the EAS homepage.
Friday, October 4, 2013
Visit our Poster Sessions at Eastern Analytical Symposium
This year MicroSolv will be presenting two technical posters
at Eastern Analytical Symposium in Somerset, NJ. The presentations will be held
in the “Applications of HPLC and UHPLC” segment on Wednesday November 20, 2013
from 12pm–2pm. Please stop by our booths
and learn how your laboratory can benefit from these exciting new technologies.
The
first presentation is entitled “Advantages of Reduced Surface Activity (RSA)
Glass Autosampler Vials for Basic Solutes.” In this study, our acclaimed RSA™
autosampler vials were compared with those of a market leading manufacturer
based on conventional borosilicate glass. A variety of test solutes were
assayed at different time intervals and concentrations using both vial types.
The results of the study led to a number of interesting conclusions. First,
only solutes containing basic functional groups showed any loss in peak area
after a given time interval had elapsed, suggesting that interaction with silanols
on the glass surface was responsible for the change. Second, the peak area loss
was found to be drastically lower when using the RSA vials vs. the ordinary
vials (see Fig. 1), which is believed to be due to the mostly silanol-free
surface of the former. Third, the effect was more significant at early time
intervals and leveled off after about 4 hours. This effect could lead to
problems with precision as well as accuracy if different peak areas were
obtained for consecutive injections in an analysis.
In the
second presentation “Separation of 1,3-Dimethylamylamine and Other Polar
Compounds in Dietary Supplement Formulation Using Aqueous Normal Phase
Chromatography with Mass Spectrometry,”
we use the Diamond Hydride™ HPLC column to separate hard to retain analytes. In
a workout supplement called Jack3d®, each polar compound is retained and
separated without the use of ion pair agents, making the method suitable for
LC-MS. One ingredient (1,3-Dimethylamylamine) is controversial in
terms of safety for consumption and has already been banned in a number of
countries. As more data is accumulated for demonstrating the potential hazard
of this compound, a need will arise for accurate and reliable quantitation in a
variety of matrices. Therefore the Diamond Hydride™ column can play a
significant role in these analyses.
A
technical program of the poster sessions is available here. We
look forward to seeing you at the symposium this year!
Figure 1. Percent recovery of 5.00 ppm cetylpyridinium
chloride solution at time intervals of 1 hour each for 4 hours. Both vial types
are compared.
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