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Synthesis of an In vivo MRI-detectable Apoptosis Probe
Published on: July 31, 2012
Investigation of apoptotic events at molecular level induced by SERS guided targeted theranostic nanoprobe
Nisha Narayanan1, Lakshmi V Nair2, Varsha Karunakaran1
1CSIR-National Institute for Interdisciplinary Science & Technology (NIIST), Chemical Science & Technology Division (CSTD), Organic chemistry section, Industrial Estate, Thiruvananthapuram 695019, Kerala, India. kkmaiti@niist.res.in and Academy of Scientific and Innovative Research (AcSIR) - CSIR-NIIST, Thiruvananthapuram, India.
Abstract:
Herein, we have examined distinctive structural and functional variations of cellular components during apoptotic cell death induced by a targeted theranostic nanoprobe, MMP-SQ@GNR@LAH-DOX, which acted as a SERS "on/off" probe in the presence of a MMP protease and executed synergistic photothermal chemotherapy, as reflected by the SERS fingerprinting, corresponding to the phosphodiester backbone of DNA.
Insights
This study reveals how cellular components change during apoptosis, monitored by a smart nanoprobe. The probe uses SERS fingerprinting to track DNA damage during combined photothermal and chemotherapy.
Area of Science:
- Biomedical Engineering
- Nanotechnology
- Molecular Biology
Background:
- Apoptotic cell death is a critical biological process.
- Targeted drug delivery systems offer potential for cancer therapy.
- Developing theranostic nanoprobes can enable simultaneous diagnosis and treatment.
Purpose of the Study:
- To investigate cellular component alterations during apoptosis induced by a novel theranostic nanoprobe.
- To evaluate the nanoprobe's function as a Surface-Enhanced Raman Spectroscopy (SERS) "on/off" probe.
- To assess the efficacy of synergistic photothermal chemotherapy delivered by the nanoprobe.
Main Methods:
- Utilized a targeted theranostic nanoprobe (MMP-SQ@GNR@LAH-DOX).
- Employed SERS fingerprinting to monitor cellular changes.
- Investigated apoptosis and DNA structural integrity.
Main Results:
- Observed distinct structural and functional variations in cellular components during apoptosis.
- Demonstrated the nanoprobe's capability as a SERS "on/off" sensor for matrix metalloproteinase (MMP) protease activity.
- Confirmed synergistic photothermal chemotherapy effects via SERS analysis of DNA's phosphodiester backbone.
Conclusions:
- The theranostic nanoprobe effectively induces and monitors apoptosis.
- SERS fingerprinting provides insights into DNA damage during treatment.
- This approach shows promise for advanced cancer theranostics.
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