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

Simple and sensitive enzyme-linked immunosorbent assay for ivermectin

Y Mitsui1, H Tanimori, T Kitagawa

  • 1Department of Parasitology, Institute of Tropical Medicine, Nagasaki University, Japan.

The American Journal of Tropical Medicine and Hygiene
|March 1, 1996
PubMed
Summary

A new enzyme-linked immunosorbent assay (ELISA) accurately measures ivermectin (IVM) in biological fluids. This sensitive method allows for easy determination of ivermectin serum levels in animal studies.

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

Development and application of a sandwich enzyme immunoassay for Glycyrrhizae Radix protein (GRP) using monoclonal antibodies.

Biological & pharmaceutical bulletin·1998
Same author

Determination of urinary acetylpolyamines by a monoclonal antibody-based enzyme-linked immunosorbent assay (ELISA).

Journal of biochemistry·1995
Same author

Clonal growth of hepatitis B virus-integrated hepatocytes in cirrhotic liver nodules.

Cancer research·1992
Same author

Intraarterial lymphocyte-injection therapy for lymphedema of the leg: an examination using indium-111 oxine labeled autologous lymphocytes.

The Tokushima journal of experimental medicine·1992
Same author

[A case report of Lucas-Schmidt IIA type Cor triatriatum in neonate].

[Zasshi] [Journal]. Nihon Kyobu Geka Gakkai·1992
Same author

Capillary gas chromatographic method for the determination of the thromboxane A2 receptor antagonist S-1452 and its metabolites in human plasma.

Journal of chromatography·1992

Area of Science:

  • Analytical Chemistry
  • Pharmacology
  • Veterinary Medicine

Background:

  • Accurate quantification of ivermectin (IVM) in biological samples is crucial for pharmacokinetic and efficacy studies.
  • Existing methods may lack the sensitivity or reproducibility required for precise IVM determination.
  • Development of a robust assay is needed to support research involving ivermectin.

Purpose of the Study:

  • To develop and validate a sensitive and reproducible enzyme-linked immunosorbent assay (ELISA) for quantifying ivermectin (IVM) in biological fluids.
  • To establish the assay's performance characteristics, including sensitivity, precision, and specificity.
  • To demonstrate the utility of the developed ELISA in a relevant animal model.

Main Methods:

  • A competitive ELISA format was employed using an ivermectin-biotin conjugate and specific antibodies.

Related Experiment Videos

  • Antibodies were generated in rabbits against an ivermectin-bovine serum albumin conjugate.
  • The assay involved simultaneous incubation of sample IVM and conjugate, followed by detection using avidin-peroxidase.
  • Main Results:

    • The developed ELISA demonstrated high sensitivity with a limit of detection of 0.1 ng/ml and a working range of 0.3-10 ng/ml.
    • The assay exhibited excellent reproducibility, with a coefficient of variation less than 10%.
    • Negligible cross-reactivity was observed with other anthelmintic drugs, indicating high specificity.

    Conclusions:

    • A sensitive, reproducible, and specific competitive ELISA for ivermectin determination in biological fluids has been successfully developed.
    • This assay enables accurate measurement of ivermectin serum levels in animal models, facilitating pharmacokinetic research.
    • The established ELISA provides a valuable tool for research requiring precise quantification of ivermectin concentrations.