4 research outputs found
Hybrid Graphene Oxide Based Ultrasensitive SERS Probe for Label-Free Biosensing
A metal
nanoparticle attached to graphene oxide has the ability
to open a new avenue of research with significant opportunities in
the biomedical field. In this Letter, we report graphene oxide attached
to a popcorn-shaped gold nanoparticle based hybrid SERS probe with
ultrasensitive label-free sensing of HIV DNA and bacteria and provide
its chemical fingerprint. Our SERS data with the hybrid material shows
that it can be used for label-free detection of HIV DNA on the femto-molar
level without any labeling. Experimental data with a novel SERS substrate
show excellent reproducibility of the SERS signal. The current Letter
demonstrates that the label-free SERS detection limit using a hybrid
material can be as low as 10 CFU/mL for MRSA bacteria. The possible
mechanism for very high sensitivity has been discussed
Hybrid Graphene Oxide Based Plasmonic-Magnetic Multifunctional Nanoplatform for Selective Separation and Label-Free Identification of Alzheimer’s Disease Biomarkers
Despite
intense efforts, Alzheimer’s disease (AD) is one of the top
public health crisis for society even at 21st century. Since presently
there is no cure for AD, early diagnosis of possible AD biomarkers
is crucial for the society. Driven by the need, the current manuscript
reports the development of magnetic core-plasmonic shell nanoparticle
attached hybrid graphene oxide based multifunctional nanoplatform
which has the capability for highly selective separation of AD biomarkers
from whole blood sample, followed by label-free surface enhanced Raman
spectroscopy (SERS) identification in femto gram level. Experimental
ELISA data show that antibody-conjugated nanoplatform has the capability
to capture more than 98% AD biomarkers from the whole blood sample.
Reported result shows that nanoplatform can be used for SERS “fingerprint”
identification of β-amyloid and tau protein after magnetic separation
even at 100 fg/mL level. Experimental results indicate that very high
sensitivity achieved is mainly due to the strong plasmon-coupling
which generates huge amplified electromagnetic fields at the “hot
spot”. Experimental results with nontargeted HSA protein, which
is one of the most abundant protein components in cerebrospinal fluid
(CSF), show that multifunctional nanoplatform based AD biomarkers
separation and identification is highly selective
Hybrid Theranostic Platform for Second Near-IR Window Light Triggered Selective Two-Photon Imaging and Photothermal Killing of Targeted Melanoma Cells
Despite
advances in the medical field, even in the 21st century
cancer is one of the leading causes of death for men and women in
the world. Since the second near-infrared (NIR) biological window
light between 950 and 1350 nm offers highly efficient tissue penetration,
the current article reports the development of hybrid theranostic
platform using anti-GD2 antibody attached gold nanoparticle (GNP)
conjugated, single-wall carbon nanotube (SWCNT) for second near-IR
light triggered selective imaging and efficient photothermal therapy
of human melanoma cancer cell. Reported results demonstrate that due
to strong plasmon-coupling, two-photon luminescence (TPL) intensity
from theranostic GNP attached SWCNT materials is 6 orders of magnitude
higher than GNP or SWCNT alone. Experimental and FDTD simulation data
indicate that the huge enhancement of TPL intensity is mainly due
to strong resonance enhancement coupled with the stronger electric
field enhancement. Due to plasmon coupling, the theranostic material
serves as a local nanoantennae to enhance the photothermal capability
via strong optical energy absorption. Reported data show that theranostic
SWCNT can be used for selective two-photon imaging of melanoma UACC903
cell using 1100 nm light. Photothermal killing experiment with 1.0
W/cm<sup>2</sup> 980 nm laser light demonstrates that 100% of melanoma
UACC903 cells can be killed using theranostic SWCNT bind melanoma
cells after just 8 min of exposure. These results demonstrate that
due to plasmon coupling, the theranostic GNP attached SWCNT material
serves as a two-photon imaging and photothermal source for cancer
cells in biological window II
Accurate Identification and Selective Removal of Rotavirus Using a Plasmonic–Magnetic 3D Graphene Oxide Architecture
According
to the World Health Organization, even in the 21st century,
more than one million children die each year due to the rotavirus
contamination of drinking water. Therefore, accurate identification
and removal of rotavirus are very important to save childrens’
lives. Driven by the need, in this Letter, we report for the first
time highly selective identification and removal of rotavirus from
infected water using a bioconjugated hybrid graphene oxide based three-dimensional
(3D) solid architecture. Experimental results show that due to the
presence of a high intensity of “hot spots” in the 3D
network, an antibody-attached 3D plasmonic–magnetic architecture
can be used for accurate identification of rotavirus using surface-enhanced
Raman spectroscopy (SERS). Reported data demonstrate that the antibody-attached
3D network binds strongly with rotavirus and is capable of highly
efficient removal of rotavirus, which has been confirmed by SERS,
fluorescence imaging, and enzyme-linked immunosorbent assay (ELISA)
data. We discuss a possible mechanism for accurate identification
and efficient removal of rotavirus from infected drinking water