Sensor
Development for Measuring Capsule Contracture
Introduction
The
objective of our research is
to find a method to prevent capsule contracture around surgically
implanted objects in the body. Currently, our short-term task is
to develop a quantitative scale that measures the degree of contracture
around the object in vivo. Once we can obtain accurate
measurements of capsule contracture, we can begin to experiment with
variables to determine their effect on the contracture process and the
body's reaction.
Background
Whenever a foreign object enters the body, the body’s immune response
triggers a capsule to form around it. The same response occurs
for surgically implanted objects. The capsule tries to protect
the body against the possibly harmful effects of the implanted
object. Sometimes, the capsule will contract in an effort to
either eject or destroy the implant. Capsule contracture can be
painful for the host and cause deformation, migration, and/or hardening
of the implant. The consequences can only be corrected with
another surgery. The cause for capsule contracture is unclear,
but it is hypothesized that the amount of contracture is proportional
to the strength of the immune response. Many inconclusive
histological studies of capsule contracture have been published, but
there are no engineering solutions to the problem yet.
Research Team
Due to the interdisciplinary
nature of our area of research, our research team is a collaboration of
the University of South Carolina School of Medicine (Departments of
Surgery and of Cellular and Developmental Biology and Anatomy), College
of Engineering and Information Technology (Departments of Chemical and
of Mechanical Engineering). The following people have been
involved:
Sensor Concepts
Two
different concepts for this sensor have been explored. Initially,
Piezoelectric Wafer Active Sensors (PWAS) were adapted for use in
vivo. Dr. Victor Giurgiutiu and the Labratory of Adaptive
Materials and Smart Strucures (LAMSS) have a great amount of experience
using PWAS for structural health monitoring purposes. Since this
project is interested in monitoring the structural properties of the
collagen capsule, PWAS seemed to be a feasible solution. PWAS
operate on the basis of the piezoelectric effect. Piezoelectric
effect means that a mechanical input to the system will yield an
electrical output and vice versa. In order to exhibit this
behavior, the asymmetrical crystalline structure of the material must
cause a dipole. In the 7mm diameter PWAS used for our sensors,
the dipole produces thickness and radial vibrations as shown in the
figure below. Piezoelectric materials are extremely sensitive to
mass changes and are therefore applicable to a variety of fields,
especially the medical field.
Since
the trial run of PWAS did not yield conclusive results, it was
necessary to redesign the PWAS and look into another sensor
concept. Recently, attempts to use strain gauges have been made.
Experiments
Numerous experiments have been
conducted both in vivo and in vitro with both sensor concepts. A
list of experiments peformed and a brief description are below.
For more information and results obtained follow the
particular link.
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In Vivo
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In Vivo 1: The trial
run of PWAS were implanted into
rats and impedance measurements were taken frequently until failure.
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In Vivo 2: Newly
designed PWAS and the trial run of
strain gauges were implanted into rats (one PWAS and one strain gauge
in each rat). Measurements were taken initially inside the rat
and after 2, 4, 8, 12, and 16 weeks. (This experiment is still
underway, so there are no actual results yet)
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In Vitro
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Meat Loading: A PWAS was inserted into a slab of
muscular meat. Readings were taken initially and after an
increasing load was applied.
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Fluid Viscosity: A
PWAS was inserted into 10 fluids of
varying viscosities. Readings were taken in air and in the fluid.
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Coatings: Different coatings were applied to the PWAS
and readings in air were compared to see how the coating affects the
measurement.
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Curing: PWAS were inserted
into materials that cured to
varying hardness. Readings were taken hourly.
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Collagen Gel: PWAS
and strain gauges were placed into
Fibroblast Populated Collagen Gels (FPCG) and incubated so that they
contract around the sensors.