Fracture Mechanics Model of Needle Cutting Tissue
Fracture Mechanics Model of Needle Cutting Tissue
Andrew C. Barnett
Department of Mechanical and Nuclear Engineering
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The Pennsylvania State University, University Park, PA
[email protected]
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Yuan-Shin Lee
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Department of Industrial and Systems Engineering
North Carolina State University, Raleigh, NC, USA
Jason Z. Moore1
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Department of Mechanical and Nuclear Engineering
The Pennsylvania State University, University Park, PA
[email protected]
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ABSTRACT
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This work develops a needle insertion force model based on fracture mechanics which
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incorporates the fracture toughness, shear modulus, and friction force of the needle and
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tissue. Ex vivo tissue experiments were performed to determine these mechanical tissue
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properties. A double insertion of the needle into the tissue was utilized to determine the
fracture toughness. The shear modulus was found by applying an Ogden Fit to the stress-
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strain curve of the tissue achieved through tension experiments. The frictional force was
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measured by inserting the needle through precut tissue. Results show the force model
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predicts within 0.2 N of experimental needle insertion force and the fracture toughness is
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primarily affected by the needle diameter and needle edge geometry. On average, the
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Corresponding Author
tearing force was found to account for 61% of the total insertion force, the spreading
force to account for 18%, and the friction force to account for the remaining 21%.
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1. INTRODUCTION
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Needles are a commonly used instrument in medicine. They are used to deliver
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drugs, biopsy tissue, draw blood, conduct brachytherapy radiation cancer treatment,
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and in many other medical procedures [1]. Low insertion force is critical in these
procedures for two reasons: first, a low insertion force has been shown to reduce the
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pain felt in patients [2]; second, lower insertion force allows for more accurate needle
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tip placement by reducing tissue deflection and needle bending [3].
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accuracy for the placement of radioactive seeds to kill cancer cells. The needle insertion
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force between the tissue and needle hinder placement accuracy. The insertion force
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causes the needle to bend, as seen in Figure 1(a). The insertion force also causes the
processes where the work piece is rigidly clamped, the tissue is free to move so the
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target can easily become displaced upon needle insertion. Lower insertion force has
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Work has been done to reduce the insertion force of needles by altering tip
geometries and reducing the gauge size. Needle geometries have been modelled in
order to define a more efficient cutting geometry [4-6]. This leads to different tip
geometries (bevel, lancet point, triangular, etc.) being created to reduce the insertion
force [7-9]. Smaller needles, including microneedles (needles that are sometimes only
100 μm in diameter) are now being used in procedures to drastically reduce the
insertion force [10]. However, microneedles cannot be used in all procedures. For
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example, vaccinations that require a large dose or have large particulates require a
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needle of sufficiently large diameter [11].
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The dynamic effects of insertion on cutting force have been briefly explored in
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tissue cutting literature. Work has been carried out exploring the effect of needle
rotation on insertion mechanics [12, 13]. Applied vibration has also been explored by
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researchers for cutting tissue [14-18]. Another dynamic method of insertion is to
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increase the needle insertion speed. Heverly et al. has shown that with increasing the
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insertion speed of the needle, the force needed to puncture the tissue is reduced in
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porcine heart [19]. Higher insertion speed has also been shown to reduce tissue
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deflection in porcine hearts [20], porcine liver samples [21], and turkey breast [22].
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However, for tougher tissues such as skin, the reduction in insertion force is not seen
with higher velocities. Frick et al. showed no velocity dependence of insertion force on
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the insertion of suture needles into sheep skin [23]. In a skin like simulant, Koelmans et
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al. found that the insertion force increases 12% by increasing the insertion speed from
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100 µm/s to 500 µm/s [24]. A force model is needed to describe the velocity dependent
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Accurate models of needle force interaction can allow for the development of
more accurate needle insertion instruments. Several physics and nonphysics based
models have been developed to predict insertion forces. Many models have been
created to fit the insertion force profile without using any physical parameters in the
model [19, 25, 26]. Further, other models looked at incorporating mechanics of cutting
into the models by looking at the forces acting on the needle [8, 27, 28]. These models
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broaden the utilization across different medium and needle geometries; however they
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do not develop fundamental knowledge on how these forces are created. Shergold and
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Fleck developed a fracture mechanics based model to describe the forces acting on the
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needle for quasistatic insertion, and is the basis of the model presented in this work
[29]. Mirsa et al. utilized fracture mechanics concepts to determine the mechanics of
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steerable needles in tissues [30]. However, dynamic insertion models have only briefly
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been utilized. Mavash et al. developed a force model for dynamic insertion of needles
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by using the Modified Kelvin model to describe the tissue [31]. The work presented in
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this paper develops a fracture mechanics based model to describe dynamic needle
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insertion.
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and ceramic materials because of its ability to better predict when failure will occur [32,
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33]. In addition, fracture mechanics based models have been applied to cutting of
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materials [37-39]. By measuring the energy to fracture tissue and moving a needle
including fracture toughness and shear modulus of the tissue. Because of the
viscoelastic properties of the tissue, these factors are strain rate dependent, causing the
speed of insertion to vary the insertion force. In addition, the model developed
incorporates a frictional component. Researchers have found that the friction force
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between the needle and the tissue is dependent on insertion speed [8, 40].
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This study investigates the fracture mechanics of porcine skin and develops a
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physics based model to explain the dynamic needle-tissue interaction. This model
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explores the physical parameters of the tissue to determine how the velocity of
insertion affects their properties. Porcine skin was chosen as the testing medium for this
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work, as researchers in the past have used it as an appropriate analog to human skin
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[41]. Hypodermic needles of various sizes were used in this study, as they are commonly
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used in the medical field. This paper describes the mechanics of tissue cutting as well as
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the fracture mechanics model developed to describe the cutting. Experiments were
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conducted to determine the mechanical properties of the tissue as well as the needle-
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tissue interaction. For each parameter, a model was fit to the resultant data. Once all
the parameters were determined, they were incorporated into the final model and
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there are three phases, as shown in Figure 2. In Phase 1, the tissue deflects and the
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force gradually rises. In Phase 2 the tissue is cut; an initial crack is formed, the crack is
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widened by the needle geometry, and the needle passes through with friction acting
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between the needle and the tissue. In Phase 3 the needle continues to pass through the
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tissue and there is friction force between the outside of the needle and the tissue. If the
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needle was passing through a thicker tissue there may be multiple deflection and
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cutting phases before the needle reaches its target location. The maximum cutting force
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is reached in Phase 2 and is defined as the total cutting force, P as shown in Figure 2.
The three forces that make up P are the tearing force (Pt) that tears the tissue forming a
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crack, the force (Ps) needed to spread the tissue apart to allow the needle through, and
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the friction (PF) that acts between the needle and the tissue as shown in Figure 3 and
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P = Pt + Ps + PF (1)
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and insertion speed. As the needle inserts into tissue, work is performed equal to Pδl
where P is the force exerted and δl is a differential insertion length. The needle then
creates a crack in the tissue and spreads the tissue apart to accommodate the width of
the needle. During cutting, there is friction between the needle and tissue as well. The
work done by the needle is equal to the energy released by the creation of the crack
δWR, the strain energy stored by the tissue spreading around the needle δΛ, and the
work done by the friction on the needle PF (l) ∙ δl, where the friction is a function of
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insertion depth l. This relationship produces Equation 2:
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Pδl = δWR + δΛ + PF(l) ∙ δl (2)
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The work released by the generation of a crack in the tissue, δWR, is:
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δWR(d,v) = JIC(d,v) a(d) δl (3)
Where a(d) is the length of the crack generated in m, JIC(d,v)is the mode-I fracture
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toughness of the tissue in J/m2, d is the outer diameter of the needle in m, and v is the
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insertion speed of the needle in m/s. Kinetic energy was neglected in the development
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of the model due to its contribution in the work-energy equation being in the range of
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The strain energy δΛ associated with the spreading of the tissue can be modelled
as spreading a circle with an initial radius r = 0 to final radius r = R. With a plane strain
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δΛ = ½ π µ(v) R2 δl (4)
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However, the crack around the needle is not completely circular [37]. Because of this, a
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nondimensional contact factor f(d) needs to be added into the δΛ term. Absorbing the
The goal of this work is to be able to describe the maximum insertion force of the
needle into tissue. The friction occurring at the maximum insertion force is the puncture
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friction force PFP. This friction force is substituted into Equation 6. Assuming the tissue
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parameters do not change with depth and describing only the maximum insertion force,
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Equation 6 becomes:
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P(d,v) = JIC(d,v) a(d) + µ(v) R2 f(d) + PFP(d,v) (7)
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shear modulus μ, as well as the needle-tissue interaction components crack length a and
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puncture friction force PFP, experiments were conducted as discussed in Section 4. The
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contact factor f(d) is determined by fitting the model to the experimental data as
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discussed in Section 6. For this model, only the diameter of the needle and the insertion
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speed were explored. The needles were inserted into the same tissue under the same
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conditions. Other factors such as type of tissue, temperature of the tissue, and pre-
3. EXPERIMENTAL PROCEDURES
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force, and crack length were found by inserting a needle into tissue as discussed in
Sections 3.1 and shown in Table 1. Experiments used four different needle gauge sizes
(16, 18, 21, and 25) and 4 different speeds (1, 20, 40, and 80 mm/s) with each
parameter set run at 5 trials for a total of 80 trials. In experimental procedure 2 the
shear modulus was determined by stretching the porcine skin at 4 different strain rates
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3.1 Needle Insertion Experiment
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The fracture toughness, friction force, and crack length of the tissue were
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experimentally determined utilizing the needle insertion setup shown in Figure 4. The
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setup uses a linear motor (Dunkermotoren) to insert the needle into the porcine skin.
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The porcine skin is mounted between two plates to have consistent boundary
conditions across trials. A six-axis force sensor (ATI Industries) records the force on the
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tissue. Position data was acquired from an encoder located on the linear motor.
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For each trial the needle was inserted through the porcine skin, tearing a hole
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into the skin, and then reinserted through the same hole in the skin. During the initial
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needle insertion, the total insertion force at puncture, P, is due to the fracturing of the
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tissue, the spreading of the tissue, and friction. In the second insertion the needle is
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inserted into the exact hole as before producing a force P′. Since the crack has already
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been formed in the first insertion, only the force from spreading the tissue and the
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friction remain. These forces are equal to the spreading and friction forces of the first
insertion. The difference between P′ and P is therefore the fracture force. Therefore
P’δl = δΛ + PF δl (8)
Utilizing Azar and Hayward’s method using two insertions, the fracture toughness is able
to be extracted when the needle is under steady penetration during a portion of Phase
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2, from x to x′ [37]. The region begins after the drop off in force after the initial puncture
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and ends before the relaxation of the tissue begins. An example plot of the double
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insertion can be seen in Figure 5(a). The fracture work, the integral of the difference in
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force P-P’ with respect to insertion depth, can be seen plotted against the fracture area
in Figure 5(b). The crack area was calculated with the crack width results shown later in
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Section 4.3. The slope of this line yields the fracture toughness JIC, as shown in Figure
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5(b).
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The puncture friction force PFP was acquired during the needle insertion trials.
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Because the porcine skin has no tissue backing, after the fracture the force drops and
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levels off. The force occurring in Phase 3, as can be seen in Figure 2, is comprised only of
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friction force acting on the surface area of the needle along the thickness of the tissue.
At this point, no fracture or spreading of tissue is occurring. For this study, the friction
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maximum insertion force during puncture. This approximation was made because the
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friction during puncture is at its maximum value when it is in contact with the entire
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thickness of tissue, just as in Phase 3. Although the geometry of the needle in contact
with the tissue varies between Phase 2 and Phase 3, the identical tissue thickness will
make this an accurate approximation. Separating the friction force during puncture from
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the spreading force is a difficult task as they occur simultaneously. The speed
dependence of PFP was determined through the needle insertion experiments run at
varying speeds.
After needle insertion experiments were performed, the skin was inspected
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under an optical microscope. The crack length was then measured. An example tissue
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crack can be seen in Figure 6. Black ink was applied to the needle before insertion to
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allow for easier visual inspection of the crack length.
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3.2 Tissue Tension Experiment
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The shear modulus was found by performing tension experiments on porcine
skin. The experiment utilized the test setup shown in Figure 7. The skin was pulled at
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strain rates of 0.25, 1, 10, and 25 % mm/mm-s. The results of this experiment were
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analyzed with an Ogden model to determine the shear modulus and strain hardening
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Porcine skin is viscoelastic and anisotropic. These properties come from the
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structure of the skin. The skin consists of stiffer collagen fibers and softer more flexible
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elastin. The collagen fibers are naturally oriented in a specific direction, along Langer
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lines, due to the natural pretension of skin. When tensioned, the Young’s modulus of
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the tissue is low to begin because the collagen fibers are moving about each other. Most
of the initial stress occurs in the elastin fibers. At higher strains, the fibers become
aligned and the tissue stiffens. This creates a J-shape stress-strain curve. As can be seen
in Figure 8, the shape of the curve is dependent on the direction the skin is pulled. These
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mechanics are strain rate sensitive as well [42]. It has been seen that most biological
materials experience shear thinning, thus making it easier to deform them at high strain
rates [43].
A sample response of the material with an Ogden fit can be seen in Figure 8. For
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this study, the shear modulus of the porcine skin is perpendicular to the Langer lines. It
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is easier for a crack to travel along the collagen fibers than through them, similar to
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what occurs in bone tissue [44]. Thus, the tissue spreads perpendicular to the Langer
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lines upon needle insertion. The response can be described by the Ogden model for
incompressible, isotropic, hyper-elastic solids. The Ogden fit is used to determine the
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shear modulus and strain hardening of the skin [45]. The Ogden fit can be written as:
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2
2 3 3
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ϕ (10)
2
1
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Where ϕ is the strain energy density, μ is the shear modulus, α is the strain hardening,
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and λi are the principle stretch ratios. The one term, one dimension Ogden fit is utilized
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to determine μ and α:
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1 1 / 2
z 2 z z (11)
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Where σz and λz are the stress and stretch ratio in the pull direction respectively. The
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Ogden equation is fit to the tension test data using least square regression to determine
the shear modulus and strain hardening. The one dimensional Ogden fit can closely
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The results of the fracture toughness trials are shown in Figure 9. As can be seen
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in the figure, the velocity of the insertion has little effect on the value. The diameter of
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the needle plays a major role in determining the fracture toughness. A third-degree
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multivariable (d and v) polynomial was fit to the data with an R2 value of 0.95. The fit
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was third ordered across the needle diameters and first ordered across the speeds. The
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equation for the fitted surface is:
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JIC(d,v) = 1.305x107d + 1.52x104v + 3.389x1010d2 – 2.222x107dv
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– 1.003x1013d3 + 8.006x109d2v (12)
The fracture toughness found in this study for hypodermic needles has a
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complex shape; the 21 gauge needle has the lowest fracture toughness while the 25
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gauge needle has the highest. Gokgol et al. found that the measured fracture toughness
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of round sharp punches decreases linearly with increased diameter [46]. The possibility
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for difference with our needles is the hypodermic needle is more complex than a round
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sharp punch. Hypodermic needles have three angles that define their geometry: ξ1, ξ2,
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and β, as can be seen in Figure 10 [6]. The three angles were measured for all for needle
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gauges used in this study and the results are shown in Table 2. It has been seen that
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results [47, 48]. The different angled bevels of the different diameter needles could be
affecting the fracture toughness and causing the 21 gauge needle have lower fracture
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toughness than the 16 gauge needle. As seen in Table 2, both bevel angles, ξ1 and ξ2, are
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The puncture friction force was recorded and the results are shown in Figure 11.
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A two-dimensional fit was applied to the data with an R2 value of 0.90. The equation of
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the fit is:
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PFP (d, v)= 0.1493 + 365.7d + 0.4463 ln(v) (13)
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As in previous studies [8, 21], the experiments show an increase in frictional force with
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increasing speed. The puncture friction force also increases with increasing needle
diameter which is to be expected. A larger needle size has more contact surface area
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and there is more pressure pushing the needle and tissue together.
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The results of the crack length showed a linear trend of increasing crack length
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Where a is the crack length and d is the diameter of the needle in millimeters. The data
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is plotted in Figure 12 along with the standard deviation. The smaller crack size than
needle diameter occurs because as the needle moves forward, the skin deflects and is
stretched before the needle begins to cut. The crack does not run and keep enlarging
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because there are many mechanisms found in biological tissues to increase the amount
of energy needed to continue fracturing material once a crack is formed, such as the
fibers being stretched and therefore helping to round the edge of the crack [43].
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4.4 Shear Modulus
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The shear modulus was measured at four different speeds using the Ogden fit
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described in Section 4.2. The shear modulus results and standard deviation are plotted
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in Figure 13. An equation was fit to the data:
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Where μ is in MPa and ε is strain rate of insertion in mm/mm-s. The shear modulus
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decreased as the strain rate increased, confirming that the porcine skin shows shear
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thinning. The shear modulus was reduced by 36.4% from the 1 mm/s insertion speed to
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the 80 mm/s speed. The shear modulus values are similar to others in literature [42, 49].
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To determine the strain rate induced by the needle insertion, it was assumed
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that the tissue strained perpendicular to the insertion direction. The strain rate of the
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tissue is proportional to the insertion speed of the needle by the following equation:
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v ta n( )
(16)
Rs
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Where β is the major bevel angle of the needle and Rs is the radius of the hole in the
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back plate holding the skin, as shown in Figure 4(b). Combining Equation 15 and 16 gives
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The contact factor f was found by fitting the insertion force model, Equation 7, to
the experimental force results. The contact factor was found for each needle gauge size
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separately using a best fit least-squares regression. The results for the contact factor are
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shown in Figure 14 and were shown to decrease with increasing diameter based on
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Equation 17.
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f = 17.534 d -0.542 (17)
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5. Force Model and Validation tN
The completed force model, Equation 7, with the values of JIC(d,v) (Equation 12),
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a(d) (Equation 14), μ(v) (Equations 15 and 16), f(d) (Equation 17), and PFP(d,v) (Equation
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13) is formed and shown in Figure 15 with the experimental results. The model for each
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needle gauge is within one standard deviation of the experimental data with the largest
error being 0.2 N. Equation 7 can be used to determine the portion of the total insertion
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force represented by each of the three forces acting on the needle as given by
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Equation 1. The tearing force is given by JIC(d,v)a(d), the spreading force is given by
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µ(v)R2f(d), and the puncture friction force is PFP. On average across the four needle sizes,
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the tearing force accounts for 61% of the total insertion force, the spreading force
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accounts for 18%, and the friction force accounts for the remaining 21%.
To validate the force model, a 27 gauge hypodermic needle was tested. The
needle’s outer diameter is 0.41 mm as can be seen in Table 1. The experimental data
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was plotted in Figure 16 along with the model’s prediction. The over prediction of the
model is caused by the complex third degree fit of the fracture toughness
overestimating the fracture toughness outside the range of needles tested. However,
the model is still within one standard deviation for each data point with all the errors
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less than the 0.2 N maximum error of the trials used to create the model.
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6. CONCLUSIONS
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A dynamic physics-based model was constructed and shown to accurately
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predict insertion forces upon needle insertion into porcine skin for four different gauge
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hypodermic needles. The model shows that on average, 61% of the total insertion force
comes from creating the crack. Friction contributes 21% of the total force and the
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spreading of the tissue contributes 18% of the force. For porcine skin, increasing the
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insertion speed did not lower the insertion force. From the experimental results, it is
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evident that fracture toughness is relatively constant across different insertion speeds. It
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was also shown that increasing insertion speed increases the frictional force on the
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needle. Increasing speeds were shown to benefit in reducing the spreading force of the
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ACKNOWLEDGMENT
This material is based upon work supported by the National Science Foundation under
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[25] Crouch, J. R., Schneider, C. M., Wainer, J., and Okamura, A. M., 2005, "A Velocity-
Dependent Model for Needle Insertion in Soft Tissue," Medical Image Computing and
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Computer-Assisted Intervention - Miccai 2005, Pt 2, 3750, pp. 624-632.
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ot
Needle–Tissue Interaction Modeling with Depth-Varying Mean Parameter: Preliminary Study,"
Biomedical Engineering, IEEE Transactions on, 56(2), pp. 255-262.
tN
ip
[27] Dehghan, E., Wen, X., Zahiri-Azar, R., Marchal, M., and Salcudean, S. E., 2007, "Modeling of
Needle-Tissue Interaction Using Ultrasound-Based Motion Estimation," Medical Image
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709-716.
nu
[28] Roesthuis, R. J., Van Veen, Y. R., Jahya, A., and Misra, S., 2011, "Mechanics of Needle-Tissue
Interaction," eds., pp. 2557-2563.
Ma
[29] Shergold, O. A., and Fleck, N. A., 2004, "Mechanisms of Deep Penetration of Soft Solids,
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with Application to the Injection and Wounding of Skin," Proceedings of the Royal Society a-
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[30] Misra, S., Reed, K. B., Schafer, B. W., Ramesh, K. T., and Okamura, A. M., 2010, "Mechanics
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of Flexible Needles Robotically Steered through Soft Tissue," International Journal of Robotics
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Ac
[31] Mahvash, M., and Dupont, P. E., 2010, "Mechanics of Dynamic Needle Insertion into a
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[35] Liu, J., Bai, Y. L., and Xu, C. Y., 2014, "Evaluation of Ductile Fracture Models in Finite Element
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[36] Orlowski, K. A., Ochrymiuk, T., Atkins, A., and Chuchala, D., 2013, "Application of Fracture
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Co
[37] Azar, T., and Hayward, V., 2008, "Estimation of the Fracture Toughness of Soft Tissue from
ot
Needle Insertion," Biomedical Simulation, Proceedings, 5104, pp. 166-175.
tN
[38] Mahvash, M., and Hayward, V., 2001, "Haptic Rendering of Cutting: A Fracture Mechanics
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r ip
[39] Shergold, O. A., and Fleck, N. A., 2005, "Experimental Investigation into the Deep
sc
Penetration of Soft Solids by Sharp and Blunt Punches, with Application to the Piercing of Skin,"
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[40] Asadian, A., Patel, R. V., and Kermani, M. R., 2011, "A Distributed Model for Needle-Tissue
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Mammalian Soft Tissues Using the Scissors Cutting Test," Journal of Biomechanics, 30(1), pp. 91-
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Co
[48] Purslow, P. P., 1983, "Measurement of the Fracture-Toughness of Extensible Connective
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ot
tN
[49] Shergold, O. A., Fleck, N. A., and Radford, D., 2006, "The Uniaxial Stress Versus Strain
Response of Pig Skin and Silicone Rubber at Low and High Strain Rates," International Journal of
ip
23
NOMENCLATURE
d
ite
d Outer diameter of the needle
ed
Strain rate of the tissue
f Contact factor
py
JIC Mode I fracture toughness of the tissue
Co
l Insertion depth of the needle
ot
Λ Strain energy stored in tissue
tN
λi Principle stretch ratios
Pt Tearing Force
ed
PF Friction Force
pt
Ps Spreading Force
Ac
24
d
ite
x’ Position of end of steady needle penetration
ed
ξ2 Secondary bevel angle of the needle
py
y Axis initially normal to major bevel angle
Co
y’ Axis normal to major bevel after rotation
ot
tN
r ip
sc
nu
Ma
ed
pt
ce
Ac
25
d
FIGURE 3. Forces that compose total cutting force
ite
FIGURE 4. (a) Experimental setup for needle insertion and (b) porcine skin
ed
mounting
FIGURE 5. (a) Graph of 1st and 2nd needle insertion and (b) graph of fracture work
py
performed to determine JIC
Co
FIGURE 6. Measured needle crack length in porcine skin
ot
modulus tN
FIGURE 8. Stress-strain curve of the porcine skin parallel, at a 45° angle, and
perpendicular (including Ogden Fit) to the Langer lines
ip
FIGURE 10. Definition of the three angles that define hypodermic needle geometry
nu
FIGURE 11. Two-dimensional fit of friction data where the points are the
experimental data and the surface is the best fit
Ma
FIGURE 15. Completed force model (lines) plotted against experimental needle
insertion force results (points)
Ac
FIGURE 16. Completed force model (line) plotted against experimental needle
insertion force result (point) for 27 gauge needle
26
d
ite
ed
py
Co
ot
tN
r ip
sc
nu
Ma
ed
pt
ce
Ac
27
TISSUE
Intended Path
Needle Trajectory
(a)
Final Target Initial Target
d
Position Position
ite
Needle
ed
(b)
py
FIGURE 1. Needle position inaccuracy due to (a) the needle bending and
(b) target position movement
Co
ot
tN
r ip
sc
nu
Ma
ed
pt
ce
Ac
28
TISSUE
Needle
d
Phase 1 Phase 2 Phase 3
ite
1.2 Delfection Cutting Friction Force
ed
1 Point of
Total cutting
needle
py
force (P)
0.8 exiting
Force (N)
Point of tissue
Co
intial
0.6
crack
formed
ot
0.4 tN
0.2
ip
0
r
sc
0 1 2 3 4 5 6 7 8
Needle Displacement (mm)
nu
29
TISSUE
Spreading Force, Ps
d
ite
Tearing Force, Pt Needle
ed
Friction Force, PF
py
Co
ot
FIGURE 3. Forces that compose total cutting force
tN
r ip
sc
nu
Ma
ed
pt
ce
Ac
30
Skin Plates
Rs
Force Sensor
d
Needle
ite
Porcine
ed
Linear Motor Skin
py
(a) (b)
Co
FIGURE 4. (a) Experimental setup for needle insertion and (b) porcine skin mounting
ot
tN
r ip
sc
nu
Ma
ed
pt
ce
Ac
31
Phase 1 Phase 2
1.2 x x'
P
1
Insertion Forec (N)
0.8
d
0.6
ite
P-P'
0.4
ed
0.2 P'
0
py
0 1 2 3 4 5
Needle Displacement (mm)
(a)
Co
0.18
0.16
Fracture Work ∫(P-P')δl
ot
0.14
0.12
tN
0.1
JIC
0.08
ip
0.06
r
0.04
sc
0.02
0
nu
FIGURE 5. (a) Graph of 1st and 2nd needle insertion and (b) graph of fracture work
performed to determine JIC
ed
pt
ce
Ac
32
Porcine skin
1.847 mm
d
ite
ed
Crack formed by needle
insertion
py
1 mm
Co
FIGURE 6. Measured needle crack length in porcine skin
ot
tN
r ip
sc
nu
Ma
ed
pt
ce
Ac
33
Porcine Skin
d
Force Sensor
ite
ed
Linear Motor
py
Co
FIGURE 7. Experimental setup for stretching porcine skin to determine shear modulus
ot
tN
r ip
sc
nu
Ma
ed
pt
ce
Ac
34
3.5
Parallel
3
Ogden Fit
Stress σz (MPa)
2.5
2 45o Angle
d
1.5
ite
1 Perpendicular
ed
0.5
0
py
1 1.2 1.4 1.6 1.8 2
Stretch Ratio λz
Co
FIGURE 8. Stress-strain curve of the porcine skin parallel, at a 45° angle, and
ot
perpendicular (including Ogden Fit) to the Langer lines
tN
r ip
sc
nu
Ma
ed
pt
ce
Ac
35
4
Fracture Toughness (kJ/m2) 3.5
3
25g
2.5
d
ite
2
18g
ed
1.5
16g
py
1 21g
0.5
Co
0
0 20 40 60 80 100
ot
Insertion Speed (mm/s)
tN
FIGURE 9. Fracture toughness of varying gauge needles from 1 to 80 mm/s
r ip
sc
nu
Ma
ed
pt
ce
Ac
36
d
ite
ed
ξ2
y = y’
py
ξ1 y’
y
β
Co
ot
FIGURE 10. Definition of the three angles that define hypodermic needle geometry
tN
r ip
sc
nu
Ma
ed
pt
ce
Ac
37
0.8
d
0.7
ite
Friction Force (N)
0.6
ed
0.5
0.4
py
0.3
Co
0.2
0.1 1.2
ot
m
0.0 tN 1.0
70 60 50 0.6
40 30 20 10
ip
FIGURE 11. Two-dimensional fit of friction data where the points are the experimental
r
sc
38
1.2
d
0.8 a = 0.9052 d
ite
0.4
ed
0
0 0.5 1 1.5 2
py
Needle Diameter (mm)
Co
FIGURE 12. Tissue crack length results with linear fit
ot
tN
r ip
sc
nu
Ma
ed
pt
ce
Ac
39
0.12
0.08
d
ite
0.04
ed
0.02
py
0
0 5 10 15 20 25 30
Strain Rate (%mm/mm-s)
Co
FIGURE 13. Measured shear modulus compared to strain rate
ot
tN
r ip
sc
nu
Ma
ed
pt
ce
Ac
40
30
25
Contact Factor f
f = 17.534 d -0.542
20
15
d
10
ite
5
ed
0
py
0 0.5 1 1.5 2
Needle Outer Diameter (mm)
Co
Figure 14. Contact factor f compared to needle outer diameter
ot
tN
r ip
sc
nu
Ma
ed
pt
ce
Ac
41
4
3.5
3 16g
Insertion Force (N)
2.5 18g
d
ite
2
21g
ed
1.5
25g
py
1
0.5
Co
0
0 20 40 60 80 100
ot
Insertion Speed (mm/s)
tN
FIGURE 15.
Completed force model (lines) plotted against experimental needle insertion force
ip
results (points)
r
sc
nu
Ma
ed
pt
ce
Ac
42
2
1.8
d
0.8
ite
0.6
0.4
ed
0.2
0
py
0 20 40 60 80 100
Co
Insertion Speed (mm/s)
FIGURE 16. Completed force model (line) plotted against experimental needle insertion
ot
force result (point) for 27 gauge needle
tN
r ip
sc
nu
Ma
ed
pt
ce
Ac
43
d
80
25 0.51
ite
27 0.41
ed
py
Co
ot
tN
r ip
sc
nu
Ma
ed
pt
ce
Ac
44
Needle Gauge ξ1 ξ2 β
16 9.9° 17.5° 53.0°
18 10.6° 21.5° 48.5°
21 9.4° 16.0° 46.5°
d
25 9.6° 18.5° 43.0°
ite
ed
py
Co
ot
tN
r ip
sc
nu
Ma
ed
pt
ce
Ac
45