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Synthesis of 68Ga Core-doped Iron Oxide Nanoparticles for Dual Positron Emission Tomography /(T1)Magnetic Resonance Imaging
Published on: November 20, 2018
Gadolinium-encapsulating iron oxide nanoprobe as activatable NMR/MRI contrast agent
Santimukul Santra1, Samuel D Jativa, Charalambos Kaittanis
1Nanoscience Technology Center and Chemistry Department, University of Central Florida, 12424 Research Parkway, Suite 400, Orlando, Florida 32826, USA.
ACS Nano
|July 20, 2012
Summary
This study introduces an activatable MRI nanoprobe that signals acidic tumor environments. The probe releases a contrast agent in acidic conditions, enhancing MRI signals and enabling drug release monitoring.
Area of Science:
- Biomedical Engineering
- Nanotechnology
- Medical Imaging
Background:
- Developing novel contrast agents for Magnetic Resonance Imaging (MRI) is crucial for early disease detection.
- Acidic tumor microenvironments present unique challenges and opportunities for targeted therapies.
- Superparamagnetic iron oxide nanoparticles (SPIONs) offer versatile platforms for theranostic applications.
Purpose of the Study:
- To develop an activatable, gadolinium-encapsulating iron oxide nanoparticle-based nanoprobe for MRI.
- To investigate the nanoprobe's T(1) relaxation properties and MRI signal changes in response to acidic conditions.
- To evaluate the nanoprobe's potential for cancer cell targeting, drug delivery assessment, and detection of acidic tumors.
Main Methods:
- Synthesis of a composite magnetic nanoprobe (IO-PAA-Gd-DTPA) by encapsulating gadolinium-diethylenetriaminepentaacetic acid (Gd-DTPA) within poly(acrylic acid) (PAA)-coated iron oxide nanoparticles (IO-PAA).
- Assessment of T(1) relaxation rate changes upon release of Gd-DTPA in acidic media.
- Incubation of folate-conjugated nanoprobe with HeLa cells to evaluate receptor-mediated internalization and lysosomal degradation.
- Co-encapsulation of an anticancer drug (Taxol) with Gd-DTPA for simultaneous drug release monitoring and cytotoxic effect evaluation.
Main Results:
- The nanoprobe exhibited quenched T(1) relaxation, which was activated (de-quenched) in acidic conditions, leading to an increased T(1)-weighted MRI signal.
- Folate-conjugated nanoprobe showed increased signal in HeLa cells, indicating successful receptor-mediated uptake and acidic lysosomal degradation.
- T(1) activation correlated with the release rate of co-encapsulated Taxol and its cytotoxic effect in cell culture.
Conclusions:
- The developed activatable T(1) nanoprobe can effectively detect acidic tumor environments through MRI signal changes.
- The nanoprobe holds significant potential for monitoring targeted drug delivery and release in cancer therapy.
- This nanoagent represents a promising tool for theranostic applications in oncology.
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