Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

In Vitro Drug Dissolution: Alternative Methods01:17

In Vitro Drug Dissolution: Alternative Methods

Alternative drug dissolution methods include the rotating bottle, intrinsic dissolution test, peristalsis, and the Franz diffusion cell method. The rotating bottle method involves meticulously rotating tightly capped controlled-release beads in a temperature-controlled bath. Periodic decanting of samples allows for residue assay, followed by refilling with fresh medium and testing at various pH levels to emulate the gastrointestinal tract conditions.In contrast, the intrinsic dissolution test...
In Vitro Drug Dissolution: Compendial Testing Models II01:09

In Vitro Drug Dissolution: Compendial Testing Models II

Various dissolution methods are utilized to assess a drug’s dissolution rate, including the flow-through cell, paddle-over-disk, cylinder, and reciprocating disk methods.The flow-through cell apparatus (USP (United States Pharmacopeia) method 4) comprises a reservoir for the dissolution medium and a pump that propels the medium through the cell containing the test sample. This method is crucial for assessing modified-release dosage forms with minimally soluble active ingredients, maintaining...
In Vitro Drug Dissolution: Compendial Testing Models I01:13

In Vitro Drug Dissolution: Compendial Testing Models I

Compendial dissolution methods are standardized procedures defined by pharmacopeias to evaluate the rate at which a drug dissolves in a specific medium. These methods ensure batch-to-batch consistency, enable quality control, and support the prediction of drug bioavailability. They are critical for both immediate and modified-release drug products.The apparatuses used for dissolution testing differ in their design and mechanical function, but all aim to simulate the physiological environment of...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Across-cities transportable <sup>13</sup>C hyperpolarization using UV-induced labile radicals.

Nature communications·2026
Same author

Suppressing loop current of shielded loops at fundamental resonance.

Scientific reports·2026
Same author

Optimal Variable Flip Angle Schemes for Hyperpolarized MR Kinetic Modeling Robust to RF Field Variations.

NMR in biomedicine·2025
Same author

Consensus recommendations for hyperpolarized [1-<sup>13</sup>C]pyruvate MRI multi-center human studies.

Magnetic resonance in medicine·2025
Same author

Consensus Recommendations for Hyperpolarized [1-<sup>13</sup>C]pyruvate MRI Multi-center Human Studies.

ArXiv·2025
Same author

First-in-Human: Simultaneous Hyperpolarized 1- 13 C-Pyruvate Magnetic Resonance Spectroscopy and 18 F-FDG PET (hyperPET) Imaging of a Patient With Lymphoma.

Clinical nuclear medicine·2024

Related Experiment Video

Updated: May 7, 2026

Dissolution Dynamic Nuclear Polarization Instrumentation for Real-time Enzymatic Reaction Rate Measurements by NMR
10:54

Dissolution Dynamic Nuclear Polarization Instrumentation for Real-time Enzymatic Reaction Rate Measurements by NMR

Published on: February 23, 2016

Formulation and utilization of choline based samples for dissolution dynamic nuclear polarization.

Sean Bowen1, Jan Henrik Ardenkjaer-Larsen

  • 1Technical University of Denmark, Department of Electrical Engineering, Kgs. Lyngby, Denmark.

Journal of Magnetic Resonance (San Diego, Calif. : 1997)
|September 17, 2013
PubMed
Summary
This summary is machine-generated.

Dissolution dynamic nuclear polarization (DNP) enables high spin polarization. Choline-based formulations offer stable, highly soluble samples for improved DNP performance and easier post-experiment processing.

Keywords:
Dynamic nuclear polarizationGlassing agentsHyperpolarizationNMR

More Related Videos

Hyperpolarized 13C Metabolic Magnetic Resonance Spectroscopy and Imaging
11:43

Hyperpolarized 13C Metabolic Magnetic Resonance Spectroscopy and Imaging

Published on: December 30, 2016

Use of a Multi-compartment Dynamic Single Enzyme Phantom for Studies of Hyperpolarized Magnetic Resonance Agents
08:59

Use of a Multi-compartment Dynamic Single Enzyme Phantom for Studies of Hyperpolarized Magnetic Resonance Agents

Published on: April 15, 2016

Related Experiment Videos

Last Updated: May 7, 2026

Dissolution Dynamic Nuclear Polarization Instrumentation for Real-time Enzymatic Reaction Rate Measurements by NMR
10:54

Dissolution Dynamic Nuclear Polarization Instrumentation for Real-time Enzymatic Reaction Rate Measurements by NMR

Published on: February 23, 2016

Hyperpolarized 13C Metabolic Magnetic Resonance Spectroscopy and Imaging
11:43

Hyperpolarized 13C Metabolic Magnetic Resonance Spectroscopy and Imaging

Published on: December 30, 2016

Use of a Multi-compartment Dynamic Single Enzyme Phantom for Studies of Hyperpolarized Magnetic Resonance Agents
08:59

Use of a Multi-compartment Dynamic Single Enzyme Phantom for Studies of Hyperpolarized Magnetic Resonance Agents

Published on: April 15, 2016

Area of Science:

  • Nuclear Magnetic Resonance (NMR) Spectroscopy
  • Chemical Engineering
  • Biophysics

Background:

  • Dissolution dynamic nuclear polarization (DNP) is a technique for enhancing NMR signal sensitivity.
  • Sample formulation for dissolution-DNP is challenging due to the need to balance concentration, viscosity, and polarization stability.
  • Traditional formulations often require complex optimization for successful dissolution-DNP experiments.

Purpose of the Study:

  • To explore choline and its derivatives as novel agents for dissolution-DNP sample formulation.
  • To compare the performance of choline-based formulations with traditional DNP sample matrices.
  • To assess the advantages of choline in terms of solubility, stability, and post-experiment processing.

Main Methods:

  • Formulation of choline-based salts and deep eutectic mixtures with carboxylic acids and urea.
  • Preparation and characterization of dissolution-DNP samples using choline-based matrices.
  • Comparison of polarization levels and sample stability against conventional DNP formulations.
  • Evaluation of choline removal and potential for experiments with hyperpolarized choline.

Main Results:

  • Choline enables the creation of highly soluble salts and deep eutectic mixtures suitable for dissolution-DNP.
  • Choline-based samples demonstrate exceptional polarization performance and stability during dissolution.
  • These formulations offer simpler handling and versatile options for post-experiment analysis, including the use of hyperpolarized choline.

Conclusions:

  • Choline is a highly effective component for developing robust and high-performance dissolution-DNP samples.
  • Choline-based formulations overcome key challenges in sample preparation for dissolution-DNP.
  • The use of choline provides significant advantages in terms of experimental flexibility and efficiency in DNP-NMR studies.