My family has a different
presentation style.

He worked in that around this life and

the Good morning.

Morehouse College and this summer I
was given an opportunity to work it

what I've been doing
the Sounders working on target.

Cancer therapy and basically working
with nanoparticles for the liver and

the tumor drugs to two sides
going over what cancer

is give me a little background
information on the drug

my purpose my goals my spirits
My met my results and steps.

What is cancer cancer is
a disease is there characterized

by basically the uncontrolled
growth of cells.

So what happens in the cells become
mutated in the beginning of the world

tended to be there to
put there's more respect

in the year two thousand over one point
five million in the visions were diagnosed

cancer in the state of Georgia alone
over forty four thousand were diagnosed.

So there are different types
of cancer prostate pancreas

liver I said and
also there is type different types there

surgery chemotherapy radiation but

the problem with their cells other
than actually trying to rid of and

this are these to many sites
such as pain hair loss and

little clouds which is basically short to
last a short time with even more time.

So the overall goal is to work
with targeted treatment to

target the tumor cells without
affecting any other cells and

the way to do this is using now
particles to deliver an answer to answer

to the tumor size by the way the enhanced
probability and attention effect.

Now what the D.V.R. effect is is when
you begin the world they grow so

rapidly that they get as
an amount of blood flow so

they have to create their
own blood vessels and

these gloves are you know are wrong or
made.

So I know more that they're
only large enough to allow

these nano particles to come through and
make it through.

So this is where we get this large but
I'm out of base.

Now part of the way around to
the nano particles around where

our lives on these artificial mail.

Here's a picture of it here you see
a living by layer right here and

in this region right here is
where we hope to load and

how to treat

treat it accumulated so

on a video it shows you the pretty picture
of the your face and as you see I got so

large it creates own blood vessels which
allow for these nano particles to get

around to suck the drug
down with zones with

you maybe familiar with every meal you
drug originally used to treat can't I mean

depression anxiety disorder is
actually a modification of that.

Drugs which is to basically inhibit
the growth of brain tumors.

So the overall objective
is to load this into

the transport to do so.

The purpose of my LOT of Tory
investigation is to test and

compare the type system
of the real drug and

I think when I react with so

I want to see how tight it
is to the tumor cells and

also I would like to see how
toxic that I'll be there

are comparisons and

what I hope to see is that they
show the same toxicity levels that

I'll be over a long period of
time because when you inject

something to the body the national
ballot is to reject it.

So we want to see this.

I'll be drug.

We want to see that it's like time
span over a long amount of town so

it can actually reach into sight
was out there rejected by some

other methods in order to make
the best kind of like the S.T.C.

cholesterol and put them in ethanol and

people yesterday said we are living

together purified them
up on the street now

the storage basically uses pressure
to force the dollars filters and

these filters are set of different sizes
so I can shape the certain size I want

to basically filter out the P.B.S.

that we use to basically purify
the base of my liver and then.

I couldn't do a deal filtration which
basically is access another filter to

really experience it now myself cause
because I work with you every seven

human tumor cells and I needed about one
million cells to complete this process.

Once I had one million cells
to twenty four plates and

in each individual Well I placed twenty
thousand cells and then I went back and

I took my ideal exams I may just be and
I didn't do them

at different concentrations five my mother
being highest in the zero in the lower

one sided this L.M.C. it for
about two days and then I'll round do a C.

see Kate as it now looks easy is basically

a process where I can count how many
cells I have on the license I was

a C C K is added to the cell
Veyron it is metabolized by live.

Cells produces does Darkhorse die.

So the more guy I have seen in
the spectrometer the more alive cells

are so from these results.

I was able to see the trials of
the time in that the free I.V.

is indeed more toxic then I did with if
you look at the castration of the micro.

You'll see that they have
less numbers even at two and

you see that throughout
no matter what trial you.

This was seen what I was really

interested in words were what
these cells begin to look like.

So I begin the image
from up to seventy two

hours twenty four hours forty hours in
the seventies and twenty four hours.

There we look at the control the control
was composed of no concentrations of I.V.

I.V. with his own because
sometimes a well.

Plates the cells tend in my programming so
I want to measure my social role correctly

they were extreme in our screening out
there on actual cell your matrix is

just dividing wrong and
we look at the free

idea of five Michael Moeller we see
that there are indications of toxicity.

It appears into the troll control
we all seem or if so images and

ourselves are becoming while
when the cells become brown.

That means that they have
been targeted tax again

on a comparison might be with zones of
five by the way you see that they're not

showing it as much toxicity as the free
I.V. but you do have some level

of toxicity see right here you
have around so that contacts.

We have someone that actually cellular
measures is not as I find it as a control.

We are starting to show some
signs of toxicity at the free

the free idea to Michael Moore will
be seen of more levels inside me but

not as much as suspect that forty hours.

The great intro the cells are on
the way there from the free I.V.

we start to see even
more levels of toxicity.

Actually the cells of the become detached
on the dial is going to be seen by

the Blur images those blurred images
are actually the cells that have became

a detached from the wells and are just
floating around in the like a mole with

more toxicity levels of every cell in
matrices become even more degraded and

also to my family style see this process

where taxes where was are increasing
on current Seymour's or so the Missus.

And then it's seventy two hours

we started to see the stars ourselves.

Diving with even more taxes.

Michael let's say there's

so many that I drove

to Texas it was also the free world.

So this place into the bloodstream.

We can almost guarantee our I.V.

drug because of the slower this
factor because of this bill on drugs.

If you study this we have found out that

it does work against brain
cells to see how that affects

the brain cancer cells.

I like that in itself.

I think it's probably done a Christian for

helping me out around the laboratory for

guidance in everything I do
is advise me that question.

Cool.

Great.

So

you can actually look at

our

life guys

back off and control their ourselves.

But what if when they are in the crease
that's when they begin to detach.

Much that we

did see that day was just
that there was a slow crisis.

I guess the question.

That's a.

Yes yes definitely.

You can see here right here if you
can see right there right here you

see that the cells are becoming
more well so they are have a town

they are they have no

control like this.

I mean there is something right here.

And so maybe if I had done this over
the last number of cells because there is

the specter of I presentation.

Because it just

has to be so if

something were to do with it.