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Chemical Shift: Internal References and Solvent Effects01:17

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In an NMR sample, precise measurement of the absolute absorption frequencies of nuclei is difficult. A standard internal reference compound is added, and the frequency difference between the reference signal and sample signals is measured.
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Higher molecular weight biomolecules are nonvolatile compounds that may decompose before ionizing or vaporizing during mass analysis with conventional electron impact ionization methods. Accordingly, electrospray ionization (ESI) is the favored method for vaporizing and ionizing biomolecules as it circumvents rapid fragmentation and enables the recording of mass signals for the entire biomolecule.
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The axial and equatorial protons in cyclohexane can be distinguished by performing a variable-temperature NMR experiment. In this process, except for one proton, the remaining eleven protons are replaced by deuterium. The deuterium substitution avoids the possible peak splitting caused by the spin-spin coupling between the adjacent protons. The remaining proton flips between the axial and equatorial positions.
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Updated: Jul 5, 2025

Preparation of Binary and Ternary Deep Eutectic Systems
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A solid-state NMR method for characterization of pharmaceutical eutectics.

Chaithanya Hareendran1,2, Parth S Shaligram2,3, Rajesh Gonnade2,3

  • 1Central NMR facility and Physical/Materials Chemistry Division, CSIR-National Chemical Laboratory, Pune 411008, India. tg.ajithkumar@ncl.res.in.

Physical Chemistry Chemical Physics : PCCP
|January 19, 2024
PubMed
Summary

This study shows that 1H fast magic angle spinning solid-state NMR can confirm pharmaceutical eutectic formation by detecting intermolecular hydrogen bonds, offering a new analytical method beyond differential scanning calorimetry.

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Area of Science:

  • Pharmaceutical Science
  • Solid-State Chemistry
  • Analytical Chemistry

Background:

  • Pharmaceutical eutectics are crucial for drug formulation development.
  • Currently, differential scanning calorimetry (DSC) is the primary method for confirming eutectic formation.
  • A need exists for alternative or complementary techniques to verify eutectic structures.

Purpose of the Study:

  • To demonstrate the utility of 1H fast magic angle spinning (MAS) solid-state NMR (SSNMR) for confirming pharmaceutical eutectic formation.
  • To identify intermolecular hydrogen bonding as a key indicator of eutectic formation using SSNMR.
  • To provide an alternative or supplementary method to DSC for eutectic analysis.

Main Methods:

  • Utilized 1H fast magic angle spinning (MAS) solid-state NMR (SSNMR) spectroscopy.
  • Focused on detecting intermolecular hydrogen bonding interactions within pharmaceutical eutectic mixtures.
  • Compared SSNMR findings with traditional methods like DSC.

Main Results:

  • Successfully confirmed the formation of pharmaceutical eutectics using 1H MAS SSNMR.
  • Demonstrated that SSNMR can directly detect the intermolecular hydrogen bonds characteristic of eutectics.
  • Provided evidence that SSNMR is a viable technique for analyzing eutectic systems.

Conclusions:

  • 1H MAS SSNMR is a powerful technique for confirming pharmaceutical eutectic formation.
  • The detection of intermolecular hydrogen bonding by SSNMR serves as a reliable indicator of eutectics.
  • This study expands the analytical toolkit for pharmaceutical formulation scientists.