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Case Study – Metabolites of Cyclosporin A Introduction:. Cyclosporin A (Csp A; Sandimmune®) is a natural product produced by the fermentation of the fungus Tolypocladium inflatum and is used extensively as an immunosuppressant. Its primary route of metabolism is via hepatic cytochrome P450s of the 3A family, the major human metabolites of cyclosporin being two different hydroxylated (AM9 & AM1) and an N-demethylated derivative (AM4N). Here we demonstrate that using microbial biotransformation, human and human-like metabolites of API’s can be produced efficiently and at a scale that facilitates not only bioanalytical applications, but toxicological, pharmacological, structure-activity relationship and other studies. Screening and confirmation: a panel of microbial species was screened for the potential to metabolise cyclosporin A by adding 100mg/L substrate to growing cultures. Several strains were seen to produce metabolites of interest, including mono- & di-hydroxylations, and N-demethylated derivatives, as well as combinations thereof. In all, nine putative metabolites were observed. Analysis of the products using HPLC-MS indicated the likely presence of AM9 and other hydroxylated metabolites among them. R = H Cyclosporine A Fig 1: Structure of Cys A indicating biotransformation to the AM9 metabolite, and chromatogram of some of the Scale up and purification: In order to produce quantities of metabolite sufficient for NMR analysis and for pharmacological/toxicological testing, the metabolite producing cultures were scaled up to a volume of 2.25L with an increased concentration of 200mg/L of substrate. Cultures were harvested at 24hrs and were sufficient for the isolation and purification of approx. 40mgs of the desired AM9 metabolite. Most of the other observed metabolites were of sufficient concentration in the culture medium to have been isolated in 2-30mg quantities if this had been required. Summary: Human and human-like metabolites of natural products can be efficiently produced using microbial biotransformation. Using this approach facilitates not only the production of metabolite reference standards, but allows for the production of other compound derivatives to determine structure activity relationships, discover new or improved activity and create intellectual property. Testimonial: “Hypha’s biotransformation service made available materials important to support our innovative drug delivery and development programs. Their expertise and professionalism made them easy to work with and we would gladly do so again if the occasion arises.” Dr Ivan Coulter, CEO Sigmoid Pharma
BOARD OF TRUSTEES Minutes of Regular Meeting September 13, 2005 PUBLIC SESSION: CALLED TO ORDER Board President Sue Roth called the Public Session to order at 5:08 p.m. in the Conference Room at the Scotts Valley Unified School District, 4444 Scotts Valley Drive, 5B, Scotts Valley. Board Members present: Sue Roth, Allison Niday, and Marshall Wolf with Joseph Espinola arriving at
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