The largest database of trusted experimental protocols

1 13c pyruvate

Manufactured by Cambridge Isotopes
Sourced in United Kingdom

[1-13C]pyruvate is a stable isotope-labeled compound used for various research and analytical applications. It serves as a precursor molecule for metabolic studies and can be utilized in techniques such as nuclear magnetic resonance (NMR) spectroscopy and mass spectrometry. The [1-13C] designation indicates the location of the 13C isotope within the pyruvate molecule.

Automatically generated - may contain errors

4 protocols using 1 13c pyruvate

1

Dynamic Nuclear Polarization of 1-13C-Pyruvate

Check if the same lab product or an alternative is used in the 5 most similar protocols
Dynamic Nuclear Polarization of 1-13C-pyruvate was performed using a HyperSense DNP polarizer (Oxford Instruments, Abingdon, UK) at an excitation frequency of 94.080 GHz and temperature of ~1.4 K. DNP was performed on a stock mixture of 14 M [1-13C]-pyruvate (Cambridge Isotopes, Tewksbury, MA), 15 mM OX063 radical (GE Healthcare) and 1.5 mM of Dotarem (Guerbet LLC, Princeton, NJ). 22 μL of stock solution were melted in 4 mL or 8 mL of dissolution buffer (80 mM NaOH, 40 mM Trizma (pH = 7.6), 50 mM NaCl and 0.42 mM EDTA), for in vivo or in vitro experiments for in vivo or in vitro experiments respectively, at 10-bar pressure and 180 °C to yield 80 mM isotonic, neutral hyperpolarized 1-13C-pyruvate. For in vitro experiments, 6.3 mL of hyperpolarized 1-13C-pyruvate was pumped into the cell mass at 7 mL/min. For in vivo studies, 6.7 mL/kg of the sample was administered through a tail vein catheter over 13 seconds by hand injection, followed by administration of 300-μL saline over 2 seconds to flush the pyruvate from the catheter’s dead volume.
+ Open protocol
+ Expand
2

Hyperpolarized [1-13C] Pyruvate Production

Check if the same lab product or an alternative is used in the 5 most similar protocols
Pyruvate samples were prepared by mixing 14 M [1-13C] pyruvate (Cambridge Isotopes), 15 mM OX063 radical (GE Healthcare) and 1.5 mM of Dotarem (Guerbet LLC). 22 µL aliquots were polarized using a commercial HyperSense DNP polarizer (Oxford Instruments) for approximately one hour at ~1.4 K temperature. Samples were melted with 4 mL dissolution buffer (80 mM NaOH, 40 mM Trizma buffer, 50 mM NaCl and 0.1 mg/L EDTA) at 10-bar pressure and 180 °C to yield 80 mM isotonic neutral polarized [1-13C] pyruvate at 37 °C. Solid-state polarization was estimated to be 28 ± 3% for the studies based on the solid-state build-up curve and separate measurements. 4 ml/kg of the sample was administered through the tail vein over 6 seconds, followed by a 300-µL saline dose over 2 seconds to flush the pyruvate from the catheter’s dead volume. To minimize respiratory motion during data acquisition, a 12-second breath-hold was applied using the ventilator and data acquisition was initiated 18 seconds after the start of injection.
+ Open protocol
+ Expand
3

Hyperpolarized 13C-Pyruvate Injection Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols
DNP (HyperSense, Oxford Instruments, UK) was used to polarize 40-μL samples of [1-13C]pyruvate (Cambridge Isotope Laboratories Inc., Tewksbury, MA) doped with 15 mM trityl radical (Oxford Instruments, Concord, MA). Following DNP, the sample was rapidly heated with 1.5 mL of 426 mM NaOH, 2.3 mL of 400 mM Tris base, and 2.2 mL of 250 mg/L EDTA. 10 μL/g of sample was injected into the tail vein over ~20 s after the start of imaging [14 (link),22 (link)]. Liquid-state polarizations ranged from 16 – 20% at the time of injection.
+ Open protocol
+ Expand
4

Hyperpolarized 13C-Substrate Preparation

Check if the same lab product or an alternative is used in the 5 most similar protocols
Solutions of [1-13C]pyruvate (Cambridge Isotope Laboratories, MA, USA) and [1,3-13C]AcAc (Cambridge Isotope Laboratories, MA, USA) were prepared separately for polarization as previously described32 (link), 43 (link). Briefly, neat [1-13C]pyruvate was mixed with OX063 (15 mM) and gadoteridol ([Gd3+] = 2 mM)32 (link). A [1,3-13C2]AcAc solution, prepared by hydrolysis of ethyl [1,3-13C2]AcAc with 5 M NaOH at 45 °C for 45 min, was mixed with an equal volume of glycerol and added OX063 (15 mM) and gadoteridol ([Gd3+] = 2mM)43 (link). To be polarized, the 13C-pyruvate (4 µL) and 13C-acetoacetate (36 µL) solutions were sequentially added into a polarization sample cup placed in liquid nitrogen forming separate layers of the 13C-enriched substrates. The frozen solutions were then loaded into a 3.35T HyperSense polarizer (Oxford Instruments, UK) and polarized for 2 h at ~1.4 K with ~94.1 GHz microwave irradiation. The polarized sample was quickly dissolved in the superheated KH buffer (4 mL). Three milliliters of the co-polarized solution was mixed with additional KH buffer (20 mL) and injected directly into the perfused heart through a polyethylene catheter. Final concentrations for both 13C-pyruvate and 13C-acetoacetate injected into the heart were 2 mM.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!