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PhytoCeutica, Inc.

5 Science Park, Suite 13

New Haven, CT  06511

 

Phone: 203-777-3462

Fax: 203-777-3538

E-mail: info@phytoceutica.com

Figure 1: LC/MS characterization of PHY906. Utilizing high resolution MS (green), a far more detailed spectrum can be obtained of the phytochemicals present in PHY906 than with conventional UV/VIS detection (red).  This information rich methodology allows the identification of more than 90 of the observed 125 phytochemical peaks. Note how single peaks in the UV/VIS trace (red) can be resolved into multiple phytochemical peaks in the high-resolution mass dimension

>  PhytomicsQC™

>  Chemical Fingerprinting

>  Genomic Bioreponse Profiling

>  Phytomics Similarity Index™

>  PhytoViewer™/

     PhytoInformatics™

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Chemical Fingerprinting

 

 

In addition to the standard liquid chromatography with UV-VIS or MS detection for quantitative detection of single marker standards, PhytoCeutica has developed a rapid method to identify and characterize a broad range of low molecular weight phytochemicals in the range of 100-1000 amu. This method combines high sensitivity capillary (LC) coupled with high resolution mass spectrometry to provide a high resolution molecular fingerprint that, when coupled to a comprehensive database of phytochemicals, can be used both for accurate phytochemical identification and for the creation of detailed phytochemical fingerprints for QC comparisons.  These fingerprints can form the foundation as a signature profile for standardizing the botanical extract that defines the clinical batch for later batch-to-batch comparisons, as a reference to study stability, and as a comprehensive dataset to identify potential adulterated drugs or chemical contaminants.  An illustration of the approach is described in Figure 1, using our drug candidate PHY906.

 

PhytoCeutica’s software package, PhytoViewerCA™, has been written to analyze chemical fingerprint patterns, identify the compounds, define the signature pattern, calculate similarity coefficients, and assign quantitative pattern cut-offs acceptance or rejection of manufactured batches.