Thursday, November 17, 2016 11:00 am
-
12:00 pm
EST (GMT -05:00)
The Waterloo Institute for Nanotechnology (WIN) presents a seminar by Professor Gang Zheng, from the Department of Medical Biophysics, University of Toronto – Ontario, Canada
Abstract
Porphyrins
are
aromatic,
organic,
light-absorbing
molecules
that
occur
abundantly
in
nature,
especially
in
the
form
of
molecular
self-assemblies.
In
2011,
we
first
discovered
‘porphysomes’,
the
self-assembled
porphyrin-lipid
nanoparticles
with
intrinsic
multimodal
photonic
properties
(Nature
Materials
2011).
The
high-density
porphyrin
packing
in
bilayers
enables
the
absorption
and
conversion
of
light
energy
to
heat
with
extremely
high
efficiency,
making
them
ideal
candidates
for
photothermal
therapy
and
photoacoustic
imaging.
Upon
nanostructure
dissociation,
fluorescence
and
photodynamic
activity
of
porphyrin
monomers
are
restored.
In
addition,
metal
ions
can
be
directly
incorporated
into
the
porphyrin
building
blocks
of
the
preformed
porphysomes
thus
unlocking
their
potential
for
PET
and
MRI.
By
changing
the
way
porphyrin-lipid
assembles,
we
developed
HDL-like
porphyrin
nanoparticles
(<20nm),
porphyrin
microbubbles
(~2um),
giant
porphyrin
vesicle
(~100um),
hybrid
porphyrin-gold
nanoparticles
and
metal
chelating
nanotexaphyrins.
By
mimicking
light
harvest
systems
in
photosynthetic
bacteria,
we
introduced
high-ordered
porphyrin
aggregates
into
supramolecular
assemblies,
resulting
unprecedented
photonic
properties
(e.g.,
reversible
photoacoustic
nanosensors).
Such
optical
properties
are
also
responsible
for
our
discovery
of
the
ultrasound-induced
microbubbles-to-nanoparticle
conversion
phenomenon
(Nature
Nano
2015),
which
may
open
the
door
to
bypass
the
enhanced
permeability
and
retention
effect
when
delivering
drugs
to
tumors.
We
have
now
validated
porphysome’s
multimodal
theranostic
utilities
in
different
cancer
types
(head
&
neck,
lung,
pancreatic,
prostate,
brain
and
ovarian
cancers,
as
well
as
lymph
node
and
bone
metastases),
different
tumor
models
(subcutaneous,
orthotopic,
chemically-induced
and
human
primary
xenografts)
as
well
as
different
animal
species
(mice,
rats,
hamsters
and
rabbits).
The
effort
of
moving
porphysomes
towards
first-in-human
use
is
on
the
way.
In
summary,
the
simple
yet
intrinsic
multimodal
nature
of
porphysomes
represents
a
new
nanomedicine
paradigm
and
also
confers
its
high
clinical
translation
potential.