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The development of 3D non-random porous structures for eral efforts to produce scaffolds with 3D pore inter-connectivity
biomedical applications has been of interest for many years. for tissue-engineered implants using different processing tech-
Processing of these 3D non-random porous structures using niques, such as, fibre bonding, solvent casting, particulate
the fused deposition modelling (FDM) process is presented in leaching, melt moulding, and membrane lamination [2–5].
this paper. The FDM built structures were evaluated to deter- Unfortunately, most of these processes generate scaffolds with
mine their suitability for use in the area of tissue engineering. unpredictable pore sizes and arrangements owing to their lim-
The influence of process parameters on the porosity, pore ited flexibility in controlling the pore volume and distribution.
diameter and compressive strength of the porous structures Moreover, the generated scaffolds lack structural stability and
was investigated. The FDM process was found to be able to have poor mechanical strength. With the introduction of rapid
provide good control and reproducibility of the desired degree prototyping (RP) technology [6], scaffolds suitable for tissue
of porosity and 3D microstructure. This technology also offers engineering can be produced with 3D microstructures contain-
flexibility and ease of varying the microstructure to meet ing consistent pore sizes and arrangements [7–12]. In addition,
specific structural and functional requirements for tissue engin- RP technology offers the ease and flexibility to meet scaffold
eering. characteristics in terms of the structural and functional require-
ments specified for use in different applications of tissue engin-
Keywords: Biomedical application; Fused deposition model- eering.
ling (FDM); Porous structure; Rapid prototyping (RP); Raster
Fused deposition modelling (FDM), developed by Stratasys
gap; 3D microstructure
[13], is among one of the most popular RP processes. It creates
physical objects directly from CAD 3D solid models via
computer-controlled robotic extrusion of a small polymeric
1. Introduction road in an additive layer-by-layer material deposition process
[14,15]. This polymeric material is vertically stacked layer-by-
The development of specially designed porous structures (i.e. layer and consists of material “roads” or “raster lines” with
scaffolds) for biomedical application in the area of tissue pre-defined voids called raster gaps. The ability of the FDM
engineering, has been a major focus in current biomedical process to pre-define the raster gap enables it to create a non-
research. Among the most important features required in scaf- random porous 3D object with a predictable and intended
folds built for tissue engineering purposes, are porosity, pore microstructure for a specific parameter setting.
diameter, and mechanical strength. The regeneration of specific This paper studies the feasibility of employing the FDM
tissue cells seeded on a scaffold is shown to be dependent on technique in scaffold building. Fundamental studies were car-
the porosity and the pore size of its structure. A large pore ried out on the microstructure of FDM parts to determine
volume is required to accommodate and deliver the cells for their conformity to scaffold requirements. Initial studies were
tissue repair, whereas a high surface area favours cell attach- conducted to investigate the influence of the raster gap process
ment and growth. For scaffold designs, appropriate pore sizes parameter for the porosity, pore diameter, and strength of the
must be incorporated for the delivery of a large number of FDM parts. These studies will determine the suitability of the
cells to accelerate bone-remodelling [1]. There have been sev- FDM process for providing an effective and high degree of
control over the sizes of the pores generated, and the uniformity
of their arrangement within the part. A mathematical model to
Correspondence and offprint requests to: Dr C. K. Chua, School
of Mechanical and Production Engineering, Nanyang Technological predict the porosity of FDM built structures with prespecified
University, Nanyang Avenue, 639798, 2263, Singapore. E-mail: process parameter settings is presented.
mckchua얀ntu.edu.sg
218 M. H. Too et al.
2. Experimental Method All the test specimens were built in cube form with edge
dimensions of 10 mm. The test specimens were built with
An FDM system, Stratasys FDM1650 Modeller, was employed varying raster gap, RG, settings from 0 mm to 0.5 mm in
to build all the test specimens. Under the FDM process, as increments of 0.05 mm. RW and ST were set at 0.315 mm
shown in Fig. 1, spooled filaments of 0.070 in or 1.778 mm and 0.254 mm, respectively, for all the specimens built. Based
nominal diameter are fed into a liquefier head using computer- on the built test specimens, several measurements were car-
driven counter-rotating rollers. The filament softens and melts ried out.
inside the liquefier at a temperature just above its melting The 3D pore interconnectivity of the test specimens was
point. This molten material is extruded from a nozzle at the investigated using micrographs taken of their microstructure
end of the liquefier, where it is controlled to move in the with a JEOL 5600 scanning electron microscope (SEM). The
horizontal X,Y–plane. A fixtureless build platform moves in effect of the variation of RG setting on the porosity, pore
the Z-direction to provide the third axis of motion, which size, and mechanical strength of the test specimens were
reproduces the height of the model. The process starts with a also investigated.
road of material of defined road width, RW, and slice thickness, To calculate the porosity, Pcalc, within the specimens, weight
ST, being deposited onto the part bed to recreate the slice measurements were taken using a microscale and used as a
data. All test specimens were fabricated from acrylonitrile- variable for the calculation. The value of Pcalc was then determ-
butadiene-styrene (ABS) material under the brand name ABS ined using Eq. (1), which is an established equation for the
(P400) marketed by Stratasys [13]. calculation of porosity for open structures.
The perimeter and contour fill patterns provided in the
“QuickSlice” software of the FDM system, are not employed
in these studies to avoid blocking the interconnectivity of the
Pcalc ⫽ 1 ⫺ 冉 Wspecimen/Vspecimen
material 冊 (1)
pores within the structure in both the X- and Y-directions. The where Wspecimen and Vspecimen represent the measured weight and
use of such fill patterns will create closed-loop road patterns the volume of the specimens, respectively, and material is the
with a start and end-point, which will eventually negate the density of the ABS (P400) material.
through and interconnected pore concept required for tissue- A mercury porosimeter, Autopore III, Micromeritics, was
engineering purposes. Therefore, only the raster fill pattern is also used in the measurement of porosity, Pmeasured, within the
used, in which the liquefier head is controlled to move back test specimens. The mercury porosimeter is able to measure the
and forth over the entire predefined regions to be built for value of the pore diameter, Pdia, achieved in each test specimen.
each single layer. The advantage of using this pattern is the To determine the mechanical strength of the specimens, a
ability to change the direction of the raster motion in adjacent tensile machine, Instron 5569, fitted with a 10 kN load cell,
layers, which results in a matrix-like structure, which is favour- was used. The specimens were compressed at a rate of 0.5
able for use in tissue engineering. The raster angle used is mm s⫺1. The compression tests were carried out with loading
0°/90°, so that every successive layer is built orthogonal to applied in the Z-direction of the specimens.
the previously generated layer. This design, because of its
simplicity, allows a better understanding of the FDM process
in terms of its porosity, pore sizes, and mechanical strength. 3. Results and Discussion
3.1 Microstructure Examination
Fig. 3. Micrographs for specimens built with (a) 0 mm, (b) 0.1 mm, (c) 0.2 mm, (d) 0.3 mm, (e) 0.4 mm, (f) 0.5 mm RG settings.
3D Non-Random Porous Structures 221
⫽ 0 exp(⫺bPcalc) (2)
where, and 0 are the compressive stresses on the porous
and non-porous structure, respectively, b is a constant and Pcalc
is the porosity calculated using Eq. (1).
that the raster gap size has a profound effect on the porosity, 4. D. J. Mooney, D. F. Baldwin, N. P. Suh, J. P. Vacanti and R.
pore diameter, and compressive strength of the FDM built part. Langer, “Novel approach to fabricate porous sponges of poly
(D,L-lactic-Co-glycolic acid) without the use of organic solvents”,
An equation was formulated to predict the effect of raster gap Biomaterials, 17(14), pp. 1417–1422, July 1996.
size on the porosity of the structure. Although the equation 5. M. C. Peters and D. J. Mooney, “Synthetic extracellular matrices
predicts the trend of the porosity with respect to the raster gap for cell transplantation”, Materials Science Forum : Porous
size accurately, more detailed investigation into controlling and Materials for Tissue Engineering, 250, pp. 43–52, 1997.
6. C. K. Chua and K. F. Leong, Rapid Prototyping : Principles and
determination of the cross-section of the extruded roads is Applications in Manufacturing, John Wiley, 1997.
required in order to use the equation effectively. Since the FDM 7. I. Zein, D. W. Hutmacher, J. T. Schantz et al., “Processing of
process allows flexibility in the control of other parameters 3D Scaffolds by Fused Deposition Modelling”, The International
such as road width, slice thickness, and raster angle, different Workshop on Advances in Materials Science and Technology,
combinations of these parameters can be optimised to produce Singapore, pp. 48, 3–6 April 2000.
8. J. T. Schantz, D. W. Hutmacher, I. Zein, K. W. Ng and T. C. Lim,
porous scaffold structures suitable for use with different appli- “A study of human osteoblasts on poly(caprolactone) scaffolds”,
cations in tissue engineering. International Workshop on Advances in Materials Science and
Technology, Singapore, pp. 27, 3–6 April 2000.
9. A. Hattiangadi and A. Bandyopadhyay, “Modelling of multiple
Acknowledgements
pore ceramic materials fabricated via fused deposition process”,
Scripta Materialia, 42, pp. 581–588, 2000.
The authors express their appreciation to Singapore Polytechnic 10. S. Bose, M. Avila and A. Bandyopadhyay, ”Processing of biocer-
for the use of its facilities for this research. They acknowledge amic implants via fused deposition process”, Proceedings of the
Solid Freeform Fabrication Symposium, vol. 1998, pp. 629–636,
the financial support of this project by the Ministry of Edu- 1998.
cation, Singapore. 11. A. Hattiangadi and A. Bandyopadhyay, “Processing, characteris-
ation and modelling of non-random porous ceramic structures”,
Proceedings of the Solid Freeform Fabrication Symposium, vol.
1999, pp. 319–326, 1999.
References 12. S. F. Yang, K. F. Leong, Z. H. Du and C. K. Chua, State of the
Art Report : Tissue Engineering Using RP Techniques, Tissue
1. D. Baksh and J. E. Davies, “Three-dimensional matrices of calcium Engineering, accepted, 2001.
phosphates support bone growth in-vitro and in-vivo”, Journal of 13. Stratasys Incorporate website : http://www.stratasys.com/, 2000.
Materials Science : Materials in Medicine 9, pp. 743–748, 1998. 14. “QuickSlice Users Manual”, Stratasys, 1997.
2. A. G. Mikos, G. Sarakinos et al., Biocompatible Polymer Mem- 15. M. K. Agarwala, V. R. Jamalabad, N. A. Langrana et al., “Struc-
branes and Methods of Preparation of Three Dimensional Mem- tural quality of parts processed by fused deposition”, Rapid Proto-
brane Structures, US Patent 5, 514 378, 7 May 1996. typing Journal, 2(4), pp. 4–19, 1996.
3. L. Lu, Mikos and G. Antonios, “Importance of new processing 16. E. Ryshkewitch, “Compression strength of porous sintered alumina
techniques in tissue engineering”, MRS Bulletin, 21(11), pp. 28– and zirconia”, Journal of the American Ceramic Society, 36(2),
32, November 1996. pp. 65–68, 1953.