Detection of Botanicals and Adulterants Using the Novel Dna-Based Technology 'SEQ
Award last edited on: 11/4/14

Sponsored Program
Awarding Agency
Total Award Amount
Award Phase
Solicitation Topic Code

Principal Investigator
Danica Taylor Harbaugh Reynaud

Company Information

AuthenTechnologies LLC (AKA: NSF AuthenTechnologies )

1341 Redwood Way
Petaluma, CA 94954
   (510) 914-3290
Location: Single
Congr. District: 05
County: Sonoma

Phase I

Contract Number: 1R43AT008292-01
Start Date: 7/1/14    Completed: 12/31/14
Phase I year
Phase I Amount
From cosmetics, to supplements and pharmaceuticals- natural products using a wide-array of botanicals play an important role in our health and wellbeing. However, deceitful adulteration poses a great risk to the natural products industry and the safety of its consumers; there are a number of well-known cases involving substitution by toxic species that have led to illness and even death. There are numerous methods commonly used for botanical authentication- from microscopy, to chemistry, and infrared radiation- that vary in their ability to detect and identify adulterants. Although DNA-based technologies have not yet been widely used in industry, there are a number of methods that offer great potential for solving our challenges with adulterant detection, especially of closely related species. In the proposed project, we will develop a new test, Detect IDNATM, specifically designed to affordably and reliably, detect and identify adulterants and contaminants, even in processed materials such as capsules and botanical extracts. Detect IDNA' is based on an innovative method that integrates and refines two well- established technologies: Site-Targeted PCR analysis and DNA sequencing, which we have named 'Sequenced Site-Targeted PCR' (SSTP). The objectives of this proposal are to prove the technology and demonstrate the commercial viability of our Detect IDNATM testing line. We will accomplish these objectives with the following Specific Aims: (1) Design and Optimize an Array of PCR Primers; (2) Validate the PCR Primer Sensitivity and Specificity; and (3) Test the Applicability on Commercial Materials. For Phase I, we will demonstrate the applicability and significance of our method by analyzing three species, which have significant issues with adulteration: black cohosh, skullcap, and American ginseng. While American ginseng is commonly substituted by inferior relatives, the others are prone to adulteration by toxic species leading to great safety concerns for consumers.

Thesaurus Terms:
American;Bacteria;Base;Biological Assay;Biological Factors;Botanicals;Capsule (Pharmacologic);Cessation Of Life;Chemistry;Cimicifuga Racemosa;Combat;Communities;Cosmetics;Design;Detection;Dna;Dna Sequence Analysis;Ensure;Environmental Pollution;Filler;Flour;Funding;Genomic Dna;Ginseng Preparation;Health;Industry;Inferior;Infrared Rays;Innovation;Manufacturer Name;Medicinal Herbs;Methods;Microscopy;Molds;Names;Novel;Pharmacologic Substance;Phase;Play;Probability;Process;Public Health Relevance;Regulation;Relative (Related Person);Research;Research Personnel;Risk;Role;Safety;Sampling;Sensitivity And Specificity;Services;Site;Soy;Technology;Testing;Tool;

Phase II

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Start Date: 00/00/00    Completed: 00/00/00
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