Related Experiment Video
Updated: Jun 4, 2026

09:09
Synthesis of Aptamer-PEI-g-PEG Modified Gold Nanoparticles Loaded with Doxorubicin for Targeted Drug Delivery
Published on: June 23, 2020
DNA-capped nanoparticles designed for doxorubicin drug delivery
Colleen M Alexander1, Mathew M Maye, James C Dabrowiak
1Department of Chemistry, Syracuse University, 111 College Pl., Syracuse, NY 13244-4100, USA.
Summary
Anticancer drug doxorubicin was loaded onto gold nanoparticles capped with DNA. This drug delivery system was confirmed to bind and release the drug effectively for targeted cancer therapy.
Area of Science:
- Biomedical Engineering
- Nanotechnology
- Pharmacology
Background:
- Gold nanoparticles (AuNP) offer a versatile platform for drug delivery.
- DNA serves as a biocompatible and programmable capping agent for nanoparticles.
- Targeted delivery of chemotherapeutic agents like doxorubicin (DOX) can improve efficacy and reduce side effects.
Purpose of the Study:
- To load the anticancer drug doxorubicin (DOX) onto DNA-capped gold nanoparticles (AuNP).
- To characterize the DOX-DNA-AuNP interaction and drug loading efficiency.
- To confirm the drug release capacity of the nanocarrier for potential targeted delivery.
Main Methods:
- Synthesis of DNA-capped gold nanoparticles (AuNP).
- Loading of doxorubicin (DOX) onto the DNA-AuNP constructs.
- Characterization of drug loading using DNA melting temperature, AuNP plasmon resonance, and hydrodynamic radius measurements.
- Assessment of drug release capability.
Main Results:
- Successful loading of doxorubicin onto DNA-capped gold nanoparticles was achieved.
- Drug binding was quantitatively confirmed by shifts in DNA melting temperature, AuNP plasmon resonance maximum, and hydrodynamic radius.
- The [DOX]/[DNA] ratio was optimized to maximize drug loading.
- The capacity for drug release to target DNA was validated.
Conclusions:
- DNA-capped gold nanoparticles provide an effective platform for doxorubicin (DOX) loading.
- The characterized nanocarrier demonstrates potential for targeted cancer drug delivery.
- Further in vivo studies are warranted to evaluate therapeutic efficacy and safety.

