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Development and Validation of an Ultrasensitive Single Molecule Array Digital Enzyme-linked Immunosorbent Assay for Human Interferon-α
Published on: June 14, 2018
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Enzyme-Linked Immunosorbent Assay to Quantify Targeting Molecules on Nanoparticles
Rachel S Riley1, Jilian R Melamed1, Emily S Day2
1University of Delaware Biomedical Engineering, Newark, DE, USA.
Methods in Molecular Biology (Clifton, N.J.)
|July 28, 2018
Summary
This study details a method for attaching targeting antibodies to silica-gold nanoshells and quantifying them using ELISA. This technique enhances nanoparticle cancer therapy specificity and efficacy.
Area of Science:
- Biomedical Engineering
- Nanotechnology
- Cancer Therapeutics
Background:
- Molecular targeting improves cancer therapeutic specificity and reduces off-target effects.
- Nanoparticle-based treatments can be enhanced by targeting strategies for improved anticancer efficacy.
Purpose of the Study:
- To describe methods for conjugating antibodies to silica-gold nanoshells.
- To establish a quantitative assay for measuring antibody content on these nanoparticles.
- To provide a versatile method for enhancing nanoparticle drug delivery systems.
Main Methods:
- Conjugation of antibodies (e.g., anti-EGFR) to silica-gold nanoshells.
- Quantification of conjugated antibodies using a solution-based enzyme-linked immunosorbent assay (ELISA).
- Utilized anti-EGFR antibodies and gold-silica nanoshells as a model system.
Main Results:
- Successful conjugation of antibodies to silica-gold nanoshells was achieved.
- An ELISA method was developed to accurately quantify the amount of antibody on the nanoparticles.
- The described methodology is adaptable for various targeting antibodies and nanoparticle types.
Conclusions:
- The developed method enables precise quantification of antibody-conjugated nanoparticles.
- This approach is crucial for optimizing nanoparticle-based cancer therapies.
- The technique offers broad applicability for enhancing targeted drug delivery systems.
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