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We always have a lot of new products and programs at Kirkman® so you may want to bookmark this page and check it frequently for updates.



October  2009 

IT'S HERE!

Kirkman® Introduces Biofilm DefenseTM

Several years ago, Dr. Anju Usman, a well-known physician from Illinois, introduced the revolutionary concept of a particular enzyme formulation to break down biofilm. She chose Kirkman® to help perfect that formulation. The result is a product being introduced this month called Biofilm Defense. Dr. Usman talked to Kirkman® about gut ecology, immunity, and biofilms, explaining the following issues.

The gut harbors the largest collection of microorganisms in the human body. Our gastrointestinal system is the first line of immunity against pathogens from the outside world. Healthy gut flora is imperative for a healthy immune system. Many patients with GI complaints have been found to have dysbiosis - a microbial imbalance. If dysbiosis persists after intervention with antibiotics, antifungals, therapeutic diet, digestive enzymes, and targeted nutrients, then we need to investigate further.   One possible explanation for persistent dysbiosis may be due to the production of pathogenic biofilm by bad "bugs" in the gut.

Pathogenic biofilm surrounds and protects the bad bugs like an impenetrable fortress, allowing them to thrive and reproduce. The microbes hiding under biofilm are highly resistant to both immunologic and non-specific defense mechanisms of the body. As the bad bugs reproduce, they continue to produce toxic byproducts that may be detrimental to the health of the host without the host even realizing the bad bugs are there. Some microbes even fail to express outer membrane proteins when iron is present. When outer membrane proteins are not expressed, the immune system is unable to recognize pathogens and, therefore, is not able to produce antibodies against the bugs.

The pathogens living in the biofilm are remarkably difficult to treat, often resistant to doses of antimicrobials, and 100- to 1000-fold over the minimum lethal dose for microbes outside of biofilm. Since the bacteria hiding under biofilm is difficult to see and culture since the immune system may not be producing antibodies against the pathogens, the bad bugs can be very difficult to diagnose.

Recently, scientists have been discovering ways to penetrate these pathogenic biofilms and expose the bad bugs beneath so that they can be addressed by the immune system. Probiotics, prebiotics, synbiotics, oral NaEDTA, iron chelating compounds (lactoferrin), chitosans as well as mucus and fibrin degrading enzymes all have the potential to help antimicrobials work with better efficiency to restore the balance of good bugs in the body.  Enzymes, in particular, have a long history of safety and efficacy in helping patients with a variety of issues.

Kirkman’s Biofilm Defense™ contains a combination of unique enzymes that have the ability to dissolve the polysaccharide and fibrin components of biofilm.  Because this enzyme lacks any significant amount of protease, which can irritate a sensitive GI tract, Biofilm Defense™ can be taken on an empty stomach. In fact, it may be recommended by clinicians to use this product on an empty stomach followed by appropriate natural or pharmaceutical antimicrobials that target a specific bug or bugs residing in biofilm. This enzyme should be used with other aforementioned strategies − in particular, high quality, high potency probiotics and prebiotics.  Prebiotics, which consist of fiber that is fermented in our gut, help fuel the cells that line the GI tract. Proper digestion of fats, carbohydrates and protein is essential to prevent putrefaction and further bacterial overgrowth in the bowel.  Digestive enzymes taken with food may also be needed to support this process.

Kirkman® will introduce Biofilm Defense at the DAN! Conference, which starts October 8. You may also order Biofilm Defense beginning October 8 on the Kirkman® website at www.kirkmangroup.com or by calling 1-800-245-8282.

 

 
September 2009

Kirkman® Introduces an Advanced Multi-Vitamin/Mineral for Adults
 
We had many requests for a multi-vitamin for adults that supported general goodAdvanced Adult Multi-Vitamin/Mineral health and was also suitable for the sensitive individual.  In response, Kirkman® recently released Advanced Adult Multi-Vitamin/Mineral hypoallergenic capsules, a formulation that contains twelve vitamins and eight minerals in forms and dosages that are supported by the latest scientific studies.
 
Most adult multiple vitamin formulations available commercially contain additives such as colors, flavors, gluten or other undesirable ingredients that may trigger reactions in sensitive individuals.  Furthermore, most of the commercially available products are tablets which can be hard to swallow for some people.  Kirkman’s new product is in capsule form and is free of common allergens and ingredients that cause these types of sensitivities.  
 
This new formulation also contains coenzyme Q10 and the Resvida™ brand of resveratrol.  These two antioxidants have shown dramatic health benefits in recent scientific evaluations.  
 

 
New and Improved Formulations
 
We've improved the formulas of the following products:

 
Folinic Acid Products Have Been Discontinued at Kirkman® - - Why?

 
 
By Larry Newman
Chief Operating Officer
Technical & Regulatory Affairs
Kirkman Group, Inc.
 
 
 
In an effort to provide our customers with the best products in the marketplace, Kirkman® does extensive and on-going testing of our products.  It has come to our attention that folinic acid has a tendency to decrease in potency over time in liquid products when in an acidic pH.  This degradation, over time, could affect the potency of folinic acid in such liquid products to the degree that they may not carry full potency through the “Best Used by” date that appears on the label.  This is not a satisfactory situation for Kirkman®, since we guarantee all our products to be full potency through the date on the label. 
 
As a result, Kirkman® has had to discontinue several liquids containing folinic acid or folic acid from a folinic acid source.  An attempt was made to lower the acidity of these products to a stable pH; however, at the pH required for the stability of the folinic acid, the vitamin B-12, also contained in some of the products, then became unstable.  To correct this situation, Kirkman® has discontinued the following liquid products:
  • Folinic Acid w/ B-12 Liquid
    • Product # 274/8
  • Folic  Acid w/B-12 Liquid
    • Product # 012/8
  • DMG Liquid w/Folinic Acid and B-12
    • Product # 272/16
  • TMG Liquid w/Folinic Acid and B-12
    • Product  # 273/16 and 273/32
For those customers who use the discontinued items that are listed above, a slight variation in protocol will be necessary to result in the same potencies and supplementation as were obtained when using the discontinued items.  These variations in administration are outlined below:
  • Customers using Folinic Acid w/B-12 Liquid should switch to the capsule form (275/200).
  • Customers using Folic Acid w/B-12 Liquid should switch to the capsule form (040/200).
  • Customers using DMG Liquid w/Folinic Acid and B-12 Liquid should switch to DMG Liquid plain and then supplement with the capsule form (275/200) for the Folinic Acid and B-12.  
  • Customers using TMG Liquid w/Folinic Acid and B-12 Liquid should switch to a new product, TMG Liquid plain (available in September 2009) and then supplement with the capsule form (275/200) for the Folinic Acid and B-12.
Kirkman is adding a TMG liquid (plain ) in September 2009, and with that addition an alternative is provided for all discontinued products. 

Kirkman® regrets any inconveniences these changes may cause, but Kirkman’s number one priority is that we provide the best quality products to our customers.   Our quality assurance to you is what makes these changes necessary.
 


 
Kirkman Group Purchases New Laboratory
 
The Kirkman Group has acquired Food Quality Labs, Inc. (FQL), of Portland, OR.  The purchase was completed in June.
 
The laboratory has been in operation since 1969.  It performs a wide range of analyses and tests including:
 
"We are very pleased to add FQL to the Kirkman Group," said David Humphrey, CEO and president of Kirkman Group, Inc. 
 
"New FDA regulations which were effective on June 25, 2009, require additional testing of both our raw materials and finished products.  Food Quality Labs will help us expedite testing procedures so that we can continue to provide fast delivery of our products to our customers. 
 
"With more than 40 years experience in high-quality laboratory testing, we found Food Quality Labs to be an ideal fit for Kirkman®," Humphrey said.


 
Kirkman® Discontinues Selected Products
 
Last month we featured all the new products that Kirkman® has added to our product offerings in our Kirkman Family Newsletter.  At the same time that our "new" product list is growing, Kirkman® will be discontinuing some of our products. In some cases, we will be only discontinuing a particular size/s of the product but more popular sizes will still be offered.
 
The list that follows will show you which products have been discontinued and which products will be discontinued in the near future.
 
If you currently use items on our "To Be Discontinued List," you may want to order these while our supplies last.
 
Discontinued
053/180
DMSA (Di-Sulfhydryl) 25 mg
057/90
DMSA w/12.5 Alpha Lipoic Acid (Di-Sulfhydryl) Capsules
061/90
DMSA (Di-Sulfhydryl) 50 mg Capsules
122/1134 & 122/454
Pancake/Waffle Mix
123/434
Doughnut Mix
To Be Discontinued
006/8 & 006/Trial
MSM (Methylsulfonylmethane) Powder – Flavored
013/4
(013/8 and 013/Trial are still available).
TMG (Trimethylglycine) with Folic Acid & B-12 Powder
090/90
Detoxification Aid Pro-Support II - Hypoallergenic 
121/594
Five Recipe Cookie Base 
124/7
Tropical Punch Drink Mix
809/8 & 809/Trial
MSM (Methylsulfonylmethane) Powder - Unflavored - Hypoallergenic 
868/3
Toothpaste Gel
 


New FDA Testing Requirements Causes Delays

On June 25th, new regulations were enacted by the FDA that requires more extensive testing of raw materials that go into nutritional supplements and complete testing of nutritional supplements before their release to be sold.  This is a positive step by the FDA to ensure the overall quality of nutritional products in the marketplace and Kirkman® supports their effort.

What has occurred as a result of the increased testing requirements is that testing laboratories are experiencing considerable increases in their work loads which has in turn lengthened testing lead times for Kirkman® and other companies.  This has caused a few shipping delays on select Kirkman® products. 

Kirkman® is working diligently to improve scheduling and eliminate these temporary out of stocks.    Customer service and quality have always been priorities at Kirkman® and will continue to be our main focus.  Thank you for your understanding in this matter. 

These statements have not been evaluated by the Food and Drug Administration.  Products mentioned are anot intended to diagnose, treat, cure or prevent any disease.
   
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