LC-MS LC-MS NMR NMR LC-NMR [1] LC-NMR LC-NMR LC-NMR NMR [2] LC-NMR MHz NMR HPLC NMR LC-NMR LC-NMR LC-NMR WET water suppression enhanced through T1 eff

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Technical Review LC-NMR How do you use liquid chromatography-nuclear magnetic resonance (LC-NMR) effectively for structural determinations of pharmaceutical impurities and metabolites? Toray Research Center, Inc., Biological Science Labs. 10-1 Tebiro 6-chome, Kamakura-shi, Kanagawa-ken 248-0036, Japan Abstract Structural determinations of pharmaceutical impurities called as related substances and its metabolites are required in the process of new pharmaceuticals developments. Liquid chromatography-nuclear magnetic resonance (LC-NMR) is a powerful tool for the structural determinations in spite of its low sensitivity. In the case of low molecular weight compounds, amount of target sample needed for LC-NMR measurement using stop-flow method is 1-5 µg per a target peak. The amount is too small for NMR but too large for HPLC. To use LC-NMR effectively for the purpose, some points to keep in mind for selecting mobile phase will be provided besides those for injection of the large amount into column and analysis approach. Keywords: liquid chromatography-nuclear magnetic resonance (LC-NMR), structural determination, pharmaceutical impurity, related substance, metabolite, high performance liquid chromatography (HPLC) NMR TEL: FAX: E-mail: Ken_Kawaguchi@trc.toray.co.jp

LC-MS LC-MS NMR NMR LC-NMR [1] LC-NMR LC-NMR LC-NMR NMR [2] LC-NMR MHz NMR HPLC NMR LC-NMR LC-NMR LC-NMR WET water suppression enhanced through T1 effect [3] WET Figure WET WET Figure H Gz pulsed-field gradient pulse pulsed-field gradient pulse PFG Figure H Gz PFG H C pulse train PFG dephase WET pulse train [3,4] pulse version WET Figure 1 Solvent suppression by WET method. (Upper) Conventional 1 H NMR measurement. (Lower) 1 H NMR measurement by WET. WET pulse sequence is shown on the middle left-hand side (see text for details). Sample: 2 mg/ml peptide solution in 90% H2O, 10% D2O.

PFG PFG PFG [5]pulse version WET PFG PFG eddy-current effect NMR SLP [6] C C C HNMR LC-NMR HNMR C LC-NMR LC-NMR NMR HPLC LC-NMR PFG Figure LC- NMR LC-NMR HPLC NMR LC-NMR PFG H stop-flow HNMR NMR HSQC LC-NMR HPLC LC-NMR on-flow stop-flow on-flow on-flow LC NMR NMR NMR LC UV Figure 2 Schematic diagram of LC-NMR system (right) and a photograph of HPLC and magnet of LC-NMR apparatus (left).

HNMR LC-NMR stop-flow stop-flow stop-flow HPLC LC-NMR stop-flow on-flow stop-flow HNMR NMR on-flow stop-flow stop-flow HPLC UV LC-NMR HPLC UV NMR NMR HPLC NMR Figure stop-flow FigurePNMR P P NMR Figure NMR mm HPLC WET NMR ppm ppm stop-flow NMR NMR LC-NMR LC-NMR LC-MS LC-NMR LC-NMR MHz LC HNMR HPLC µg HNMR LC stop-flow H- H NMR Figure 3 LC-NMR (stop-flow method). (Left) HPLC chromatogram when LC-NMR was measured. Flow of mobile phase was stopped at position 1, 2, 3 and re-flow after NMR measurements. (Right) LC-NMR spectra by stop-flow method ( H NMR, 600MHz). P1: Phenol (14 µg), P2: N,N -diethyl-m-toluamide (12 µg), P3: toluene (80 µg).

µg LC-NMR HNMR HPLC µg NMR HPLC too small for NMR but too large for HPLC LC-NMR LC-NMR HNMR H NMR NMR HPLC HNMR LC-MS LC-NMR NMR LC-NMR µl NMR NMR LC-NMR HNMR HNMR LC-MS LC-NMR [1]HPLC stop-flow HNMR Figure LC-NMR NMR LC-MS NMR LC-MS Diclofenac sodium Diclofenac sodium LC-NMR Figure I LC-MS LC-MS/MS Figure NMR Diclofenac sodium MHz LC-NMR Figure LC-NMR LC-NMR LC-NMR MHz NMR [7] HPLC

Figure 4 LC-NMR analysis of an impurity found in Geranyl acetate. Figure 5 LC-NMR analysis of a photolyte of Diclofenac sodium. (Upper) LC-NMR spectrum of the photolyte and the estimated structure. (Lower) LC-NMR spectrum and the structure of Diclofenac sodium.

Figure 6 A trial measurement of a 0.05% content impurity by direct injection of alkaline thermal degradation products of Diclofenac sodium by using cryo-lc probe with 700 MHz NMR [7]. Long range COSY LC-NMR HMBC NMR Long range COSY HMBC HMBC NOESY LC-NMR pulse sequencefigure µg [8] HMBC NOESY LC-NMR-DOSY LC-NMR-DOSY LC-NMR DOSY [9] LC-NMR HPLC DOSY Diffusion Ordered Spectroscopy NMR [10,11] DOSY LC- NMR HPLC LC-NMR HPLC DOSY HPLC DOSY S/N LC-NMR- DOSY LC-NMR- DOSY HPLC LC-NMR-DOSY LC-NMR-DOSY [1] LC- NMR-DOSY LC-NMR DOSY WET BPPLED bipolar LED sequence [12] LC Figure LC-NMR-DOSY

Figure 7 Long range COSY spectrum of Inosine. The correlation between position 1 and 8 is observed by long range COSY, but can not by HMBC under small amount of sample. LC-NMR-DOSY LC-NMR HNMRµg/peak H- H NMR µg/peak LC-MS HNMR LC- MS [1] NMR 2011 p 130 [2] Watanabe, N.; Niki, E. Proc. Japan Acad. 1978, 54, Ser. B, 194. [3] Smallcombe, S. H.; Patt, S. L.; Keifer P. A. J. Magn. Reson. A 1995, 117, 295. [4] Ogg, R. J.; Kingsley, P. B.; Taylor, J. S. J. Magn. Reson. B 1995, 104, 1. [5] Moonen, C. T.; van Zijli, P. C. M. J. Magn. Reson. 1990, 88, 28. [6] Patt, S. L. J. Magn. Reson. 1992, 96, 94. [7] NMR [8] NMR 2008 p 270 [9], NMR 2000 p 202 [10] Morris, K. F.; Jonson, C. S. J. Am. Chem. 1993, 115, 4291. [11] Barjat, H.; Morris, G. A.; Smart, S.; Swanson, A. G.; Williams, S. C. R. J. Magn. Reson. B 1995, 108, 170. [12] Wu, D.; Chen, A.; Johnson, C. S. Jr. J. Magn. Reson. A 1995, 115, 260.

( /s) Figure 8 LC-NMR-DOSY. (Upper) Stop-flow LC-NMR spectrum measured from a single peak. (Lower) LC-NMR-DOSY spectrum measured from the upper spectrum. Vertical axis: diffusion coefficient, horizontal axis: NMR chemical shift. Two mixed components in the upper spectrum are separated in the lower one by difference of diffusion coefficient.