Professional Documents
Culture Documents
MID02181115
Semester; 8th
Section; B
CONTRAST MEDIA;
Contrast media are used to improve the inside images of the body produced by
ultrasound, MRI , X-ray, and CT scans. It allows radiologists to distinguish between normal and
abnormal tissues. They are not dyes that discolor the internal organs permanently.
contrast agents, and better than radiocontrast agents used in contrast CT scans.
1. MICROBUBBLE SHELL;
Selection of shell material determines how easily the microbubble is taken up by the
immune system. A more hydrophilic material tends to be taken up more easily, which
reduces the microbubble residence time in the circulation. This reduces the time available
for contrast imaging. The shell material also affects microbubble mechanical elasticity.
Microbubble shell are composed of albumin, lipid, galactose or polymer.
The gas core is the most important part of the ultrasound contrast microbubble
because it determines the echogenicity. When gas bubbles are caught in an ultrasonic
frequency field, they compress, oscillate, and reflect a characteristic echo- this generates
the strong and unique sonogram in contrast-enhanced ultrasound. Gas cores can be
composed of air, or heavy gases like perfluorocarbon, or nitrogen.
UNTARGETED CEUS;
TARGETED CEUS;
ADVANTAGES OF CEUS;
The body is 73% water, and therefore, acoustically homogeneous. Blood and
surrounding tissues have similar echogenicities, so it is also difficult to clearly
discern the degree of blood flow, perfusion, or the interface between the tissue
and blood using traditional ultrasound.
Ultrasound imaging allows real-time evaluation of blood flow.
Destruction of microbubbles by ultrasound in the image plane allows absolute
quantification of tissue perfusion.
Ultrasonic molecular imaging is safer than molecular imaging modalities such as
radionuclide imaging because it does not involve radiation.
Alternative molecular imaging modalities, such as MRI, PET, and SPECT are
very costly. Ultrasound, on the other hand, is very cost-efficient and widely
available.
Since microbubbles can generate such strong signals, a lower intravenous dosage
is needed, micrograms of microbubbles are needed compared to milligrams for
other molecular imaging modalities such as MRI contrast agents.
Targeting strategies for microbubbles are versatile and modular. Targeting a new
area only entails conjugating a new ligand.
Active targeting can be increased (enhanced microbubbles adhesion) by
Acoustic radiation force using a clinical ultrasound imaging system in 2D-mode
and 3D-mode.
DISADVANTAGES OF CEUS;
Microbubbles don't last very long in circulation. They have low circulation residence
times because they either get taken up by immune system cells or get taken up by the
liver or spleen even when they are coated with PEG.
Ultrasound produces more heat as the frequency increases, so the ultrasonic frequency
must be carefully monitored.
Microbubbles burst at low ultrasound frequencies and at high mechanical indices (MI),
which is the measure of the negative acoustic pressure of the ultrasound imaging system.
Increasing MI increases image quality, but there are tradeoffs with microbubble
destruction. Microbubble destruction could cause local microvasculature ruptures and
hemolysis.
Targeting ligands can be immunogenic, since current targeting ligands used in preclinical
experiments are derived from animal culture.
Low targeted microbubble adhesion efficiency, which means a small fraction of injected
microbubbles bind to the area of interest. This is one of the main reasons that targeted
contrast-enhanced ultrasound remains in the preclinical development stages.
Contrast-enhanced ultrasound can be used to image blood perfusion in organs, measure blood
flow rate in the heart and other organs, and for other applications.