HyperSense® - the in-vitro DNP Polariser

HyperSense DNP Polariser

Oxford Instruments is currently focusing on commercialisation activities and will continue to sell, promote and support the HyperSense instrument.

HyperSense allows the user to drive NMR sensitivity to levels never seen before. The sensitivity improvements attainable with 13C, 15N, 29Si and 31P have the potential to increase the breadth of Nuclear Magnetic Resonance (NMR) experiments and your applications.

Examples are:

  • Shorter data collection times and/or the use of much smaller amounts of sample material
  • Benefits of quaternary carbons that will improve structure confirmation and elucidation. This could provide more reliable NMR spectral assignments in a shorter time
  • The ability using direct detection of ¹³C to identify complex biomixtures in metabonomics
  • Using the enhanced signal to carry out chemical kinetic experiments
  • HyperSense configures easily with your laboratory and existing spectrometer
  • Applications Library 
  • Performance 
  • Services 
  • Specification 
  • Publications 

Applications Library

Click here to link to Applications Library - Downloadable applications notes, posters, articles and more ...

Nuclei available:

13C, 15N, 29Si, 31P and other spin 1/2 nuclei 

Sample polarisation times:

Typically 15 minutes to 6 hours

NMR spectrometer compatibility:

All current spectrometer platforms

NMR RF probe requirements:

Operation with 5 and 10mm probes

Dissolution solvents:  

Water and methanol

Polarising agent:

‘Trityl radical’, typical usage 0.2-5mg per sample

Compressed air/nitrogen:

6 bar min

Helium gas:

6 bar min, grade 99.999% pure from cylinder

Exhaust line: Vacuum exhaust line or suitable safety compliant filter

Electrical:

Europe: 230V, 50Hz, 2.5A single phase and 415V, 50Hz 20A three phase

USA: 110V, 60Hz, 3A single phase and 208V, 60Hz, 20A three phase

Japan: 100V, 50-60Hz, 3A single phase and 200V,

50-60Hz, 20A three phase

Microwave source:

Integrated 94GHz with 0.5GHz sweep (user selectable) up to 100mW

Magnetic field strength:

3.35T actively shielded

Sample temperature:

Selectable < 3.9K,  1.4K1

Helium refill volume:

65L from minimum level

Nitrogen refill volume:

60L from minimum level

Helium consumption during dissolutions:

Typical <2L per dissolution2

Minimun operating ceiling height:

<3.0m

System weight including cryogens:

~ 600kg

Trigger output for NMR spectrometer:

5V signal

Dimensions

Footprint:

W 1668mm (~ 66") x D 1038mm (~ 41")

Height:

2860mm (~ 113")

 

 (1) As measured by instrument control system with 65% helium insert level at microwave power 100mW over 30 minutes
 (2) Averaged over 10 repeatable runs with a temperature of 1.4K over a 6 hour polarisation and dissolution, 100mW microwave power with helium level at 65%

 Author  Journal  Reference  Title
Bowen S.; Zeng H.; Hilty C. Anal. Chem. 2008, 80, 5794-5798 Chemical Shift Correlations from Hyperpolarized NMR by Off-Resonance Decoupling
Bowen S.;Hilty C. Angew. Chem. Int. Ed. 2008, 47, 5235-5237 Time-Resolved Dynamic Nuclear Polarization Enhanced NMR Spectroscopy
Reynolds S.; Patel H. Applied Magnetic Resonance 2008, 34, 495-508 Monitoring the Solid-State Polarization of 13C, 15N, 2H, 29Si and 31P
Day I. J.; Mitchell J. C.; Snowden M. J.; Davis A. L. Applied Magnetic Resonance 2008, 34, 453-460 Investigation of the Potential of the Dissolution Dynamic Nuclear Polarization Method for General Sensitivity Enhancement in Small-Molecule NMR Spectroscopy
Emwas A.-H.; Saunders M.; Ludwig C.; Günther U. L. Applied Magnetic Resonance 2008, 34, 483-494  Determinants for Optimal Enhancement in Ex Situ DNP Experiments
Mishkovsky M.; Frydman L. ChemPhysChem 2008, 9, 2340-2348 Progress in Hyperpolarized Ultrafast 2D NMR Spectroscopy
Gabellieri C.; Reynolds S.; Lavie A.; Payne G. S.; Leach M. O.; Eykyn T. R. J. Am. Chem. Soc.  2008,130, 4598-4599 Therapeutic Target Metabolism Observed Using Hyperpolarized 15N Choline
Saunders M. G.; Ludwig C.;Günther U. L. J. Am. Chem. Soc.  2008, 130, 6914-6915  Optimising the Signal Enhancements In Cryogenic ex situ DNP-NMR Spectroscopy
Merritt M. E.; Harrison C.; Kovacs Z.; Kshirsagar P.; Malloy C. R.; Sherry A. D.  J. Am. Chem. Soc.  2007, 129, 12942-12943 Hyperpolarized 89Y Offers the Potential of Direct Imaging of Metal Ions in Biological Systems by Magnetic Resonance
Merritt M. E.; Harrison C.; Mander W.; Malloy C. R.; Sherry A. D. Journal of Magnetic Resonance  2007, 189 (2), 280 - 285 Dipolar cross-relaxation modulates signal amplitudes in the 1H NMR spectrum of hyperpolarized [13C]formate
Day I. J.; Mitchell J. C.; Snowden M. J.; Davis A. L. Journal of Magnetic Resonance 2007, 187(2), 216 - 224  Applications of DNP-NMR for the measurement of heteronuclear T1 relaxation times

Masafumi Harada; Hitoshi Kubo; Takamasa Abe; Hiroshi Maezawa; Hideki Otsuka

Jpn J Radiol 2010, 28, 173 - 179 Selection of endogenous 13C substrates for observation of intracellular metabolism using the dynamic nuclear polarization technique
Day I. J.; Mitchell J. C.; Snowden M. J.; Davis A. L. Magn Reson. Chem.  2007, 45, 1018-1021 Co-acquisition of hyperpolarised 13C and 15N NMR spectra
Frydman L.; Blazina D. Nature Physics 2007, 3, 415-419 Ultra fast two-dimensional nuclear magnetic resonance spectroscopy of hyperpolarized solutions
Merritt M. E.; Harrison C.; Storey C.; Jeffrey F. M.; Sherry A. D.; Malloy C. R.  PNAS 2007, 104, no. 50, 19773-19777 Hyperpolarized 13C allows a direct measure of flux through a single enzyme-catalyzed step by NMR
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