CypExpress 2C9 Catalyzed Conversion of Diclofenac (DN) to to 4- Hydroxydiclofenac (HDN)

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TM CASE STUDY CypExpress 2C9 Catalyzed Conversion of Diclofenac (DN) to to 4- Hydroxydiclofenac (HDN) Shuvendu Das, 1 Enrique Martinez, 2 and Mani Subramanian 1 1 Center for Biocatalysis and Bioprocessing, University of Iowa 2 Oxford Biomedical Research, Inc. 2014 Oxford Biomedical Research, Inc.

CypExpress 2C9 Conversion of Diclofenac to 4- Hydroxydiclofenac Introduction: Reaction Conditions: Metabolite Identification in 24- well microplates: 250-1000 μm diclofenac, 20-100 mg/ml CypExpress2C9, 50 mm KPi buffer ph 7.5, 30 C, 600 rpm in microplate shaker, Reaction volume 200 μl, Reaction time 2 to 4 h Pilot- scale s were performed in a total volume of 1.0 ml in a 20x150 mm glass tube using the following final concentrations: Substrate = 20 to 500 μm MP (500 µm for scale- up) CypExpress 2C19 = 100 mg/ml Buffer = 50 100 mm KPi, or Tris- HCl (as specified in tables), ph 7.5 NADP+, G6P = NONE ADDED for 1 st cycle; see details for additional cycles G6PDH and Mg++ = NONE ADDED. Contained in CypExpress system. The 20 x 150 mm tube was placed in a tilted position on a shaker platform at 30 C, and agitated by rotation at 225 rpm for 3.0 h. At the end of the period, either A. The entire suspension was extracted and subjected to HPLC (figure 1). Or B. CypExpress2C19 was pelleted by centrifugation at 6,000 x g. a. The supernatant from cycle was analyzed by HPLC. b. The pellet was resuspended in fresh buffer containing G6P, but no additional substrate, and incubated for a second cycle. After which the entire suspension was extracted and subjected to HPLC. B. CypExpress2C19 was pelleted by centrifugation at 6,000 x g. a. The supernatant from cycle was analyzed by HPLC. b. The pellet was resuspended in fresh buffer containing G6P, but no additional substrate, and incubated for a second cycle. After which the entire suspension was extracted and subjected to HPLC. Large Scale (200 ml) Reaction Conditions for Product Isolations: 250-500 μm Diclofenac, 20 g washed CypExpress2C9, 50 mm KPi buffer ph 7.5, final concentration of NaG6P 12 mm, 30 C, 225 rpm in rotary orbital shaker, Reaction volume 200 ml, Reaction time 2 to 4 h Large Scale (200 ml) Reaction Conditions for Product Isolations: 250-500 μm Diclofenac, 20 g washed CypExpress2C9, 50 mm KPi buffer ph 7.5, final concentration of NaG6P 12 mm, 30 C, 225 rpm in rotary orbital shaker, Reaction volume 200 ml, Reaction time 2 to 4 h 2015 Oxford Biomedical Research, Inc. All Rights Reserved. Page 2 Page 2

CypExpress 2C9 2C9 Conversion of of Diclofenac to to 4- Hydroxydiclofenac Conversion of DN to HDC in 24- well microplates: CypExpress 2C9 (100 mg/ml) rapidly These catalyzed studies conversion were performed of Diclofenac using (DN) the FDA- recommended to 4- Hydroxydiclofenac substrate (HDN) in a Diclofenac single 2 hr. to evaluate cycle. the utility The conversion of CypExpress2C9 of 500 μm for DN drug to metabolism HDN in 50 and mm disposition KPi of ph 7.5 studies. at 30 C was investigated by RP- HPLC after extraction of the entire mixture with HPLC Mobile Phase containing 15% (v/v) Methanol, 84.5% (v/v) Water, and 0.5% (v/v) Acetic acid. Typical results are shown in Table 1. The HPLC profile of the sample taken after 2 hr incubation with CypExpress2C9 (blue curve) is shown in Figure 1 along with results obtained for a vector control (devoid of recombinant human CYP2C9) shown in black. Flow thru HDN DN The results clearly show the very specific formation of HDN from DN catalyzed by CypExpress2C9 The results clearly show the very specific formation of HDN from DN catalyzed by CypExpress2C9 2015 Oxford Biomedical Research, Inc. All Rights Reserved. Page 3 Page 3

CypExpress 2C9 Conversion of Diclofenac to 4- Hydroxydiclofenac Conversion of DN to HDN in a single cycle: Large scale (80 ml) CypExpress 2C9 (100 mg/ml) catalyzed conversion of 500 μm Diclofnac (DN) to 4- Hydroxydiclofenac (HDN) was performed in 500 μm MP, in 100 mm KPi of ph 7.5 at 30 C. Results obtained for aliquots that were extracted and subjected to HPLC after a single cycle are presented in Table 2: No. Sample μm of DN Reaction hrs μm of HDN 1 Supernatant 500 3 67.91 2 Cell Suspension 500 4 187.91 Discussion: Under these conditions, 37.6% of the DN was converted to HDN. Most of the HDN was retained in the CypExpress pellet after the 3 hr. incubation period, with about 1/3 of the total HDN found in the supernatant. HPLC Analysis of the product: Results obtained for RP- HPLC after extraction with HPLC Mobile Phase containing 15% (v/v) Methanol, 84.5% (v/v) Water, and 0.5% (v/v) Acetic acid of an aliquot of the suspension after cycle are shown in figure 2. Second cycle production of HDN: The ability of CypExpress2C9 to catalyze further generation of HDN from DN that was absorbed during cycle was investigated. Second cycle To production distinguish of HDN: catalysis The from ability release of CypExpress2C9 of product formed to catalyze during further generation cycle, of HDN the CypExpress from DN that pellet was from absorbed during cycle was resuspended cycle was in investigated. buffer + G6P. To An distinguish aliquot was catalysis removed from (T=0) release extracted of product and subjected formed during to HPLC. The remainder cycle, of the the suspension CypExpress was pellet incubated, from the without first adding cycle additional was resuspended DN, for an additional in buffer + (2 G6P. nd ) 3 An hr. aliquot was cycle. removed Results (T=0) are extracted shown in Table and subjected 3: to HPLC. The remainder of the suspension was incubated, without adding additional DN, for an additional (2 nd ) 3 hr. cycle. Results are shown in Table 3: 2015 Oxford Biomedical Research, Inc. All Rights Reserved. Page 4 Page 4

CypExpress 2C9 Conversion of Diclofenac to 4- Hydroxydiclofenac 2 nd Cycle Sample Reaction Sample μm of HDN 0 hr Resuspended CypExpress (after cycle 1) 160.98 3 hr Extracted CypExpress suspension 308.74 3 hr CypExpress supernatant 113.83 Discussion: In addition to the large quantity of HDN that is retained by CypExpress2C9 after one cycle, a even larger quantity of the DN substrate is also retained. Incubation of this CypExpress suspension for an additional 3 hr. yields significant amounts of additional HND product. The total yield for 2 cycles of this large scale CypExpress catalyzed = 68 µm (Cycle 1 supernate) + 309 µm (extracted Cycle 2 suspension) = 376 µm DNH, which is a yield of 75% from the initial 500 µm DN. HPLC analysis of the kinetics of HDN generation from DN by CypExpress2C9: To address whether comparable amounts of HDN may produced simply by incubation DN with CypExpress for longer periods (vs. multiple cycles) the kinetics of HDN production in a single 400 ml (one cycle) were investigated. Aliquots of the suspension were removed at 0, 0.5, 1, 1.5 and 1.8 hr, extracted with HPLC Mobile Phase containing 15% (v/v) Methanol, 84.5% (v/v) Water, and 0.5% (v/v) Acetic acid, and subjected to RP- HPLC. Results are presented in figure 3. Discussion: These results clearly show the rapid production of HDN is hour of the, and slower production thereafter as the DN substrate (peak at 8 min) is depleted. Discussion: These results clearly show the rapid production of HDN is hour of the, and slower production thereafter as the DN substrate (peak at 8 min) is depleted. 2015 Oxford Biomedical Research, Inc. All Rights Reserved. Page 5 Page 5

CypExpress CypExpress 1A2 1A2 Conversion Conversion of of Phenacetin Phenacetin to Acetaminophen to Acetaminophen Yield: The AC AC yields obtained following the first and and second second cycles cycles are are shown shown in in table 2. 2. Reaction Sample μm of PH Reaction hrs. μm of AC ± SD C- 1 Supernatant 200 4 **36.53 ± 3.97 C- 1 Supernatant 500 4 **43.60 ± 0.87 C- 2 Cell Suspension 200 in Cycle- 1 No addition in C- 2 4 18.18 ± 0.17 C- 2 Cell Suspension 500 in Cycle- 1 No addition in C- 2 4 28.16 ± 0.03 *After Cycle- 1, cell pellet was stored at 4 C over night before start of Cycle- 2 **One unknown peak was partially co- eluted with AC peak. Hence, determination of the peak area was done by manually splitting of the partially overlapped peak. Summary: For 200 µm PH, two cycles effected 27.4% conversion to AC. For 500 µm PH, two cycles effected 14.4% conversion to AC. 2015 Sigma-Aldrich Co. LLC. All rights reserved. SIGMA-ALDRICH is a trademark of Sigma-Aldrich Co. LLC, registered in the US and other countries.