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SupplySide West Expo 2011

By Mike Gottschalk

Laszlo Torma inside the Venetian Hotel & Casino

The Supplyside West Conference is a very important Herbal Supplement Industry event. It provides important educational and networking opportunities to this $29 billion market. Since the FDA set out required current good manufacturing practices (cGMP) in 2007, the Herbal Supplement producers are working to meet the new requirements before the FDA audits. These regulations are intended to insure the quality, purity and safety of the Herbal Supplement products available today.  


The show is held in Las Vegas, Nevada, October 19-23. Pickering Laboratories exhibited at the show. We introduced our instruments, and methods to the industry. Of primary concern are Mycotoxins and Amino Acids, but also pesticides. Our GPC Clean-up and post-column instruments are well-suited to these applications. 

In addition to the literature and instruments in the booth, we presented two posters:

“Immunoaffinity Clean-up and  Analysis of Aflatoxins and Ochratoxin A in Herbs & Spices using HPLC with Post-column Photochemical Derivatization”

The production of herbal supplements and spices is a fast growing industry. There are numerous reports on the presence of Mycotoxins in commercially available herbs and spices such as chamomile, black and white tea leaves, ginkgo leaves, paprika and cumin. We developed a simple, sensitive and robust HPLC-Post Column Derivatization method for analyzing Aflatoxins B1, B2, G1, G2 and Ochratoxin A in herbs and spices. AflaOTAClean Immunoaffinity columns contain antibodies specific for both classes of Mycotoxins and allow for fast and efficient sample clean-up. We used the AcceClean automated workstation, which processes three samples simultaneously.


“Accelerated Amino Acids using HPLC with Post-Column Derivatization”

We developed an accelerated amino acids analysis method for Physiological and Protein Hydrolysate samples that utilizes temperature and eluant gradients. Protein Hydrolysates can be analyzed in 48min (inject-to-inject). Amino Acid Analysis is an important step in the Quality Control and R&D of dietary supplements, sports drinks, pharmaceuticals and in any type of sample where the amino acid content is of importance. The objective of the study was to reduce the total run time of Amino Acid Analysis by implementing both a column temperature gradient and a linear buffer gradient using HPLC with Post-column derivatization.
If you would like a copy of either or both of these posters or any additional information  about our products, please feel free to send us an email or give us a call:

Phone: Toll-free: 800-654-3330 Direct: 650-694-6700

Dinner on the canal in “Venice”

AOAC International 2011

By Mike Gottschalk
Any trip to New Orleans requires a visit to
Cafe du Monde for coffee and beignets

The annual meeting of the AOAC International in New Orleans, Louisiana on September  18-21, had a strong emphasis on Herbal Supplements testing. The AOAC organization is central to FDA efforts to provide analytical structure to testing methods for this newly regulated industry. 

Pickering Laboratories participated in the AOAC sponsored Single Laboratory Validation of Multi-residue Mycotoxin Analysis in Feeds and Grains. For this work, Pickering Laboratories was awarded the “Single Lab Validation of the Year”. This pivotal work in the analysis of Mycotoxins continues in Herbal Supplements as well as agricultural products. 

We presented our new instrumentation and a poster titled “Analysis of Paralytic Shellfish Toxins in Bivalve Mollusks using HPLC with Post-column Derivatization and Fluorescence Detection”

In support of our new instrumentation, the incredibly versatile FREESTYLE series, we presented the highlights and capabilities in our Vendor session on Tuesday afternoon. You can find more details about Freestyle in a separate blog post and on the LCTech website: http://www.lctech.de/english/FREESTYLE-GPC.html

The post-column method for Paralytic Shellfish Toxins presented in our poster is now a official AOAC Method:  OMA 2011.02. Earlier in 2011, we attended the 2nd Joint Symposium & AOAC Task Force Meeting on Marine & Freshwater Toxins meeting in Spain in support of the work done by Mr. Jeffery van der Riet to complete method 2011.02.  You can read about the meeting and the method in an earlier blog post.
If you would like a copy of the poster or any additional information  about our products, please feel free to send us an email or give us a call:

Phone: Toll-free: 800-654-3330 Direct: 650-694-6700


Good Toys Stimulate Imagination

By Michael Pickering

A sandbox is a reasonably scaled and so infinitely variable a toy that it should be an important consideration for any family with children and the use of about 20 square feet of ground.  The basic design is simple: 1) Make a collar of the depth you want out of rot-resistant material (i.e. heart redwood, cedar, et. al.) and 2) fill to desired level with sand.

That is the most obvious design consideration but not the most important factor by far.  Sand management is the important issue.  Sand is predominantly silica (aka quartz) and as purchased is fine grained and fairly uniform in size.  Thus it packs densely.  The most critical property is the extremely hydrophilic nature of silica.  It can sustain a great deal of water just by surface tension.  So, if you put sand in a blind hole on dirt, once it gets wet it can readily puddle and take weeks or months to dry, depending on where you live.  It rains sometime where most people live.  And to maximize the “toy-ness,” the sandbox must quickly drain so the children can add a dribbling hose to the party.

A design that worked for our four children:
Our sandbox is 6’ x 6’ x 1’ and is filled to 8” deep.  About 25 cubic feet of sand in all.  Although it is simple arithmetic, I’m going to give you the small numbers to inspire you.  Its position on the ground is controlled by gravity.  The mount is three layers:

  1. Gravel, also called drain rock, minimum one inch deep – 3 cubic feet
  2. Galvanized fencing, ¼ inch mesh, 36 square feet
  3. Aluminum screen, 36 square feet
  4. When not in use, protect your sandbox with a screen to keep the local cats out

Play Time:
You can also add a degree of nonsense.  I added marbles, surf tumbled beach glass and stainless flatware from the local Goodwill.  Our children would squirt water droplets into the air and the humming birds would come to collect them.  It was a four-act play that had a long run.

2nd Joint Symposium and AOAC Task Force Meeting on Marine and Freshwater Toxins Analysis

Held in Baiona, Spain, May 1-5, 2011
By David Mazawa

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Pickering Laboratories was proud to sponsor the Second Joint Symposium and AOAC Task Force Meeting of Marine and Freshwater Toxins Analysis. This growing symposium addressed new developments, method validation efforts, and method implementation in the analysis of marine and freshwater toxins. A variety of methods needs for detecting saxitoxins, domoic acids, okadaic acids, azaspiracids, other seafood toxins and the cyanobacterial toxins were addressed. Presentations and discussions addressed special needs of the community ranging from emerging toxins to the ongoing replacement of the mouse bioassay with modern and fully validated chemical methods. Principle sponsor of the symposium was the University of Vigo, Spain, Department of Analytical and Food Chemistry.

New methods have been recently validated in an effort to replace the Mouse Bioassay. Due to the hard work of Jeff van de Riet et al. in his single laboratory validated study, the HPLC post-column oxidation method for analysis of paralytic shellfish toxins (saxitoxins) in shellfish, is now an official AOAC method (AOAC OMA 2011.02). Pickering Laboratories was there to support this occasion and to show the symposium that we have instrumentation perfectly suited for this method. For details on the method, please visit our website or contact Pickering Laboratories Technical Support.  

To view the official method, members should log onto AOAC’s website: www.aoac.org

Secondary Metabolites


Secondary Metabolites
By Michael Pickering

Peyote Plants (1)

This name encompasses the category of chemicals that living organisms make which are not used in their normal growth, development, or reproduction.  They are a staggering array of chemical structures and properties.  Antibiotics are largely produced by bacteria, and a large variety of mammalian toxins are of fungal origin.  Pigments are produced by both botanicals and insects.  The peyote cactus, Lophophora williamsii, produces the hallucinogenic alkaloid mescaline.  Fugu, the Chinese puffer fish, harbor symbiotically produced tetrodotoxin.  

Puffer Fish at Japanese Market (2)

The producers of these exotic structures usually must isolate them to keep them out of the traffic of their living processes.  They can interfere with everyday life, or more often are toxic for the producer.  Dalea emoryi (aka dyebush) makes an intense red pigment that it stores in blister-like vesicles on its bark.  Coyotillo shrubs, Karwinskia humboldtiana, make deadly neurotoxins which they store in the seeds, discouraging browsing animals such as cattle, deer, and sheep from eating them. (You can read more about this plant in a previous newsletter:  Coyotillo in Del Rio, Texas

Lotus scoparius, or deer weed, makes a water-soluble flavinoid, which is a biodegradable germination inhibitor, and stores in its seeds.  Upon first rain, this compound sterilizes the surrounding ground so that no seeds can germinate.  The result is that competitive weed seeds rot.  When the second rain comes, the deer weed seeds germinate with nothing but clear sky surrounding them. 

Sometimes, we can see a competitive advantage of the presence of these chemicals: attracting pollinators, protective insects, or mates, or discouraging predators, competitors, or tramplers.  But often not.  Today’s musings are about two species (an insect and a botanical): Daclylopius coccus and Citrus sinensis

“Gusano Rojo”, Dactylopius coccus
Red dyes produced by insects have been and remain among the most important dyestuffs in human commerce.  Before the Americas were exploited, the most abundant source of red pigments was the Asian scale insects and their excretions.  This broad class of quinoid dyes bind permanently to proteinaceous substrates (in dye talk they are ‘fast’) such as wool and silk.  Historically, they have also been used as art pigments.

Early in the 16th century, the Spanish introduced the world to the American cochineal, and the Asian scale insects were doomed to a mere historical reference. 
Cacti with Cochineal (3)
Cochineal Cluster (3)

The females of this American species that feeds on cactus provide the popular Latino name “red worm.”  Interestingly, Dactylopius coccus is not actually a worm, but is part of the cochineal family. By dry weight, the females can produce an astounding double digit percentage of pigment.  The pigments have great variation of color and intensity (Carminic Acid extinction coefficient 6800, Laccaic Acid A extinction coefficient 43700).  The commercial growers of the pigment use the cactus Indian Fig Opuntia (Opuntia ficus-indica) to feed the caterpillars, whose fruit and tender young shoots are also popular in Latino diets.  The same insects in a blue agave farm are considered a pest.               


Because of the significance of these insect-derived pigments in human history, they are the subject of anthropological study in ancient art.  In 2004, we were invited into the study by the Department of Conservation and Scientific Research of the Smithsonian Institute.  Although the pigments have long wavelength chromophores (little or no interference) and large extinction coefficients, the sample size is only 2-5 ng to minimize damage.  As the pigments are only a small component of the sample, adequate detection requires a post-column reaction to make the pigments fluorescent.  We made them an inert system as the reagent AlCl3 is a powerful reducing agent, which translates as very corrosive to hardware.  During the reaction, the Al3+ reduces the quinone to a hydroquinone, which chelates the spent Al3+ and makes the entire complex fluorescent.  

Oranges, Citrus sinensis
Valencia oranges produces two main bitter principles, Limonin, a terpenoid, and Naringin, a flavenoid, which it mainly stores in its seeds.  The seeds are easily removed when the fruit is harvested for juice.  Lacking seeds, the navel orange must develop a different storage strategy. 

The navel orange stores the Limonin and Naringin as tasteless precursors (at neutral pH) in the peel, concentrated in the vestigial seed, the navel end.  When the orange is juiced, the membranes are torn and spill their contents into the acidic juice.  The acidity catalyzes the hydrolytic elimination of a sugar from a tertiary alcohol and facilitates a ring-closure to form a lactone, the bitter Limonin.  
The tasteless Naringin precursor reacts similarly.

California, and I am sure other commercial orange-producing areas, has strict standards for exportability of the whole fruit, size being paramount.  Thus, the most important commercial value in un-exportable fruit is the juice.  One hundred percent navel orange juice is unpalatably bitter. 

It is my opinion, and I encourage you to compare, that non-specific blended frozen orange juice concentrates contain a noticeable amount of navel orange juice.  Pure Valencia concentrate is available, so do the experiment and voice your opinion.  We will post opinions (with your bylines, or make up a cool avatar name) in the next newsletter.   

Further Reading and Photo Credits:

http://www.teotitlan.com/naturaldyes.htm
http://en.wikipedia.org/wiki/Natural_dye

1) Peyote photo from Wikipedia:
http://en.wikipedia.org/wiki/File:Peyote_Cactus.jpg#file

2) Puffer fish Photo by Mikael:
http://www.gastroville.com/2009/12/06/tidbits-from-japan/
3) Cochineal Photos from Wikipedia:
http://en.wikipedia.org/wiki/Cochineal


Pickering Laboratories’ Mycotoxin Workshop held at MidWest AOAC in Lincoln, NE

Sculpture on U of NE-Lincoln campus
By Maria Ofitserova, PhD
At the Midwest AOAC meeting (Held from June 6-9, 2011 in Lincoln, Nebraska) Pickering Laboratories presented a workshop on analysis of Aflatoxins in different matrices such as animal feeds, corn and peanut butter. The workshop generated a lot of interest with representatives from several State Departments of Agriculture, State Universities, as well as companies like Silliker and General Mills attending the two sessions of the workshop. The participants were able to learn about new analytical equipment and have a discussion about different aspects of Mycotoxins analysis.

During the workshop the samples extracts were cleaned with AflaClean™ Immunoaffinity columns and analyzed using an HPLC method with post-column photochemical derivatization by UVE™ and fluorescence detection. We also demonstrated how AcceClean™ workstation automates the labor-intensive column clean up step. The participants were impressed with versatility of the AcceClean workstation capable of handling multi-step procedures with both Immunoaffinity and SPE columns.
To learn more about Pickering products for Mycotoxins Analysis please visit our website http://www.pickeringlabs.com/catalog/Mycotoxin_Analysis.asp or call (800)-654-3330

Third Latin American Pesticide Residue Workshop

Held in Montevideo, Uruguay, May 8-11, 2011
By David Mazawa

Laszlo Torma at LAPRW

The Latin American Pesticide Residue Workshop (LAPRW) is a biannual open forum for discussion on current concepts and future developments in the field of pesticide residues in food and the environment. Pickering Laboratories was proud to support this workshop by sponsoring and also presenting a poster titled “Glyphosate in soy beans, corn and sunflower seeds by HPLC with post-column Derivatization and fluorescence detection”

Downtown Montevideo

 If you would like a copy of the poster, please email support@pickeringlabs.com 

Famous sculpture on the beach at Punta del Este, Uruguay

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