4 research outputs found
Site-Specific Amphiphilic Magnetic Copolymer Nanoaggregates for Dual Imaging
Molecular
imaging along with combinations of imaging modalities
can provide a thorough understanding of disease, in particular, tumors.
Magnetic resonance imaging (MRI) offers exceptional tissue contrast
and resolution; whereas optical imaging provides high sensitivity.
Hence a norbornene based copolymer (<b>Nor-Cob-Py-Fol</b>) is
reported in this paper as a dual-imaging agent. <b>Nor-Cob-Py-Fol</b> having Co<sup>2+</sup> complex, pyrene and poly(ethylene glycol)
derived folate, have been synthesized using ring-opening metathesis
polymerization (<b>ROMP</b>). All the monomers and polymers
are characterized by <sup>1</sup>H NMR, IR, GPC, and TGA techniques.
The morphology of the copolymer nanoaggregates has been evaluated
with DLS, TEM, and SEM techniques. The functionalization of Co<sup>2+</sup> to the polymer is monitored by FTIR, <sup>1</sup>H NMR,
and <sup>13</sup>C NMR spectroscopy. Furthermore, the presence of
Co<sup>2+</sup> in the nanoaggregates is confirmed by the EDX (SEM)
technique. To prove the MRI capabilities nature of copolymer nanoaggregates,
NMR experiment is performed at room temperature. Cell viability studies
suggest the biocompatibility nature of the copolymer. Flow cytometry
as well as epifluoroscence microscope experiments clearly demonstrate
the dual-imaging ability of the newly designed copolymer. The much
higher relaxivity ratio (<i>r</i><sub>2</sub>/<i>r</i><sub>1</sub>) of the present method clearly establishes the superiority
of our system as one of the best contrast agents known to the practitioners
of magnetic resonance imaging
Site-Specific Amphiphilic Magnetic Copolymer Nanoaggregates for Dual Imaging
Molecular
imaging along with combinations of imaging modalities
can provide a thorough understanding of disease, in particular, tumors.
Magnetic resonance imaging (MRI) offers exceptional tissue contrast
and resolution; whereas optical imaging provides high sensitivity.
Hence a norbornene based copolymer (<b>Nor-Cob-Py-Fol</b>) is
reported in this paper as a dual-imaging agent. <b>Nor-Cob-Py-Fol</b> having Co<sup>2+</sup> complex, pyrene and poly(ethylene glycol)
derived folate, have been synthesized using ring-opening metathesis
polymerization (<b>ROMP</b>). All the monomers and polymers
are characterized by <sup>1</sup>H NMR, IR, GPC, and TGA techniques.
The morphology of the copolymer nanoaggregates has been evaluated
with DLS, TEM, and SEM techniques. The functionalization of Co<sup>2+</sup> to the polymer is monitored by FTIR, <sup>1</sup>H NMR,
and <sup>13</sup>C NMR spectroscopy. Furthermore, the presence of
Co<sup>2+</sup> in the nanoaggregates is confirmed by the EDX (SEM)
technique. To prove the MRI capabilities nature of copolymer nanoaggregates,
NMR experiment is performed at room temperature. Cell viability studies
suggest the biocompatibility nature of the copolymer. Flow cytometry
as well as epifluoroscence microscope experiments clearly demonstrate
the dual-imaging ability of the newly designed copolymer. The much
higher relaxivity ratio (<i>r</i><sub>2</sub>/<i>r</i><sub>1</sub>) of the present method clearly establishes the superiority
of our system as one of the best contrast agents known to the practitioners
of magnetic resonance imaging
Site-Specific Amphiphilic Magnetic Copolymer Nanoaggregates for Dual Imaging
Molecular
imaging along with combinations of imaging modalities
can provide a thorough understanding of disease, in particular, tumors.
Magnetic resonance imaging (MRI) offers exceptional tissue contrast
and resolution; whereas optical imaging provides high sensitivity.
Hence a norbornene based copolymer (<b>Nor-Cob-Py-Fol</b>) is
reported in this paper as a dual-imaging agent. <b>Nor-Cob-Py-Fol</b> having Co<sup>2+</sup> complex, pyrene and poly(ethylene glycol)
derived folate, have been synthesized using ring-opening metathesis
polymerization (<b>ROMP</b>). All the monomers and polymers
are characterized by <sup>1</sup>H NMR, IR, GPC, and TGA techniques.
The morphology of the copolymer nanoaggregates has been evaluated
with DLS, TEM, and SEM techniques. The functionalization of Co<sup>2+</sup> to the polymer is monitored by FTIR, <sup>1</sup>H NMR,
and <sup>13</sup>C NMR spectroscopy. Furthermore, the presence of
Co<sup>2+</sup> in the nanoaggregates is confirmed by the EDX (SEM)
technique. To prove the MRI capabilities nature of copolymer nanoaggregates,
NMR experiment is performed at room temperature. Cell viability studies
suggest the biocompatibility nature of the copolymer. Flow cytometry
as well as epifluoroscence microscope experiments clearly demonstrate
the dual-imaging ability of the newly designed copolymer. The much
higher relaxivity ratio (<i>r</i><sub>2</sub>/<i>r</i><sub>1</sub>) of the present method clearly establishes the superiority
of our system as one of the best contrast agents known to the practitioners
of magnetic resonance imaging
Super paramagnetic Norbornene Copolymer Functionalized with Biotin and Doxorubicin: A Potential Unique Site-Specific Theranostic Agent
Polymer-based
nanosystems have been extensively explored either as therapeutic agents
or bioimaging probes in the cancer diagnosis. However, very few systems
are successful in combining both therapy and imaging. Herein, a new
class of norbornene based copolymer, <b>Nor-Dox-Cob-Btn</b> is
proposed as potential theranostics agent for tumor diagonosis. The
copolymer (<b>Nor-Dox-Cob-Btn</b>) with doxorubicin, cobalt
carbonyl complex, and biotin as pendent functionalized group is synthesized,
using ring opening metathesis polymerization (ROMP). The cell viability,
drug release, NMR relaxation, NMR 1-D image and Epi fluorescence microscopy
studies on <b>Nor-Dox-Cob-Btn</b> nanocarrier are thoroughly
studied. The effect of nanocarrier on transverse relaxation (<i>T</i><sub>2</sub>) of water molecule and NMR 1-D image suggest
that the nanocarrier has the potential application in magnetic resonance
imaging agent. The <i>T</i><sub>2</sub>-weighted MRI agent,
along with biotin receptor assisted pH responsive doxorubicin release
from <b>Nor-Dox-Cob-Btn</b>, prompts us to envision this newly
developed polymer for future application in theranostics
