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 Experiment Videos

[Methyl-D3]2hypericin as internal standard for quantification in human plasma.

Georgios Piperopoulos1, Andrea Kiehne, Arnd Ingendoh

  • 1Institut für Organische Chemie, Eberhard-Karls Universität Tübingen, Auf der Morgenstelle 18, 72076 Tübingen, Germany.

Analytical and Bioanalytical Chemistry
|March 29, 2003
PubMed
Summary

A new deuterated hypericin (1-D(6)) was synthesized for quantifying hypericin in human plasma. This isotope-dilution liquid chromatography-mass spectrometry method enables accurate measurements in the ng/mL range.

Related Concept Videos

You might also read

Related Articles

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

Sort by
Same author

Comparability of Steroid Collision Cross Sections Using Three Different IM-HRMS Technologies: An Interplatform Study.

Journal of the American Society for Mass Spectrometry·2022
Same author

An unusual family of glycosylated peptides isolated from Dendroaspis angusticeps venom and characterized by combination of collision induced and electron transfer dissociation.

Journal of the American Society for Mass Spectrometry·2011
Same author

Concerning the deprotonation of the trimethylsulfonium ion by the dimethylsulfinyl anion.

Organic & biomolecular chemistry·2011
Same author

Targeted analysis of protein citrullination using chemical modification and tandem mass spectrometry.

Rapid communications in mass spectrometry : RCM·2009
Same author

Heterocycles [h]fused onto 4-oxoquinoline-3-carboxylic acid, part IV. Convenient synthesis of substituted hexahydro [1,4]thiazepino[2,3-h]quinoline-9-carboxylic acid and its tetrahydroquino[7,8-b]benzothiazepine homolog.

Molecules (Basel, Switzerland)·2007
Same author

A novel approach for ganglioside structural analysis based on electrospray multiple-stage mass spectrometry.

Journal of biomolecular techniques : JBT·2007

Area of Science:

  • Analytical Chemistry
  • Pharmacology
  • Organic Synthesis

Background:

  • Hypericin is a natural compound with potential therapeutic applications.
  • Accurate quantification of hypericin in biological matrices is crucial for pharmacokinetic and pharmacodynamic studies.
  • Existing quantification methods may lack the sensitivity or specificity required for low concentrations.

Purpose of the Study:

  • To describe the synthesis and fragmentation of deuterated hypericin ([methyl-D(3)](2)hypericin, 1-D(6)).
  • To demonstrate the utility of 1-D(6) as an internal standard for hypericin quantification in human plasma.
  • To establish a reliable isotope-dilution liquid chromatography-mass spectrometry (LC-MS) method for hypericin analysis.

Main Methods:

  • Multistep synthesis of [methyl-D(3)](2)hypericin (1-D(6)).

Related Experiment Videos

  • Negative ion-electrospray ionization (ESI) mass spectrometry for fragmentation analysis.
  • Isotope-dilution LC-MS with an ion-trap system for quantification in human plasma.
  • Main Results:

    • Successful synthesis and characterization of 1-D(6) with its fragmentation pattern elucidated.
    • Demonstration of 1-D(6) as an effective internal standard for hypericin quantification.
    • Establishment of linear standard curves from 1 to 10 ng/mL in human plasma with high accuracy, precision, and recovery.

    Conclusions:

    • Deuterated hypericin (1-D(6)) is a suitable internal standard for hypericin quantification.
    • Isotope-dilution LC-MS provides an accurate and sensitive method for measuring hypericin in human plasma.
    • The developed method supports further research into hypericin's biological activity and therapeutic potential.