Authors: Wan Jin Cho, Jun Ho Kim, Se Heang Oh, Jin Ho Lee
Abstract: Electrospinning is a fabrication process that can produce highly porous nano-scale fiber-based
matrices using an electrostatically driven jet of polymer solution. This method represents an attractive
approach for polymeric biomaterial processing which provides the membrane structure that may retain
mechanical strengths, flexibility, and high surface area. In this study, we prepared a guided bone
regeneration (GBR) membrane with selective permeability, hydrophilicity, good mechanical strength and
adhesiveness with bone using polycaprolactone (PCL) and Tween 80 by the electrospinning method. The
prepared PCL and PCL/Tween 80 electrospun sheets were characterized via morphology observation,
mechanical property, water absorbability, and model nutrient permeability. It was observed that the
PCL/Tween 80 (3 wt%) electrospun sheet have an effective permeation of nutrients as well as the good
mechanical strength to maintain a secluded space for the bone regeneration. From the results, the
hydrophilized PCL/Tween 80 (3 wt%) electrospun sheet seem to be a good candidate as a GBR
membrane.
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Authors: Sung Mook Lim, Se Heang Oh, Il Kyu Park, Jin Ho Lee
Abstract: Chitosan cylindrical scaffolds with gradually increasing pore size along the longitudinal
direction were fabricated by a novel centrifugation method to investigate pore size effect on cell
interactions. The scaffold was fabricated by the centrifugation of a cylindrical mold containing fibril-like
chitosans. The pore size ranges of the scaffold could be controlled by adjusting the centrifugal speed: the
scaffold with gradually increasing pore size (from ~80 #m to ~400 #m) and porosity (from ~82 % to
~93 %) along the cylindrical axis was obtained by applying the centrifugal speed, 3,000 rpm. The scaffold
sections were examined for their in vitro cell interactions using different kinds of cells (fibroblasts,
chondrocytes, and osteoblasts) in terms of scaffold pore sizes. It was observed that different kinds of cells
were shown to have different pore size ranges in the scaffold for effective cell growth. The chitosan
scaffold section with ~400 #m pore size showed better cell growth for chondrocytes and osteoblasts,
while the scaffold section with ~190 #m pore size was better for fibroblast growth. The pore size gradient
scaffolds fabricated by the centrifugation method can be a good tool for the systematic studies of the
interactions between cells or tissues and scaffolds with different pore size.
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Authors: Kwang Joon Cho, Dae Keun Song, Se Heang Oh, Young Joo Koh, Sahng Hoon Lee, Myung Chul Lee, Jin Ho Lee
Abstract: Porous polydioxanone (PDO)/polyvinyl alcohol (PVA) scaffolds were fabricated by
blending PDO with a small amount of PVA to improve the hydrophilicity and cell/tissue
compatibility of the scaffolds for tissue engineering applications. PDO/PVA scaffolds with different
PVA compositions up to 10 wt% were fabricated by a melt-molding particulate-leaching method
(non-solvent method). The prepared scaffolds exhibited highly porous, uniform open-cellular pore
structures. The PDO/PVA scaffolds with PVA compositions more than 5 % were easily wetted in
cell culture medium. The hydrophilized PDO/PVA (5 wt%) scaffold showed better cell adhesion
and growth than the control hydrophobic PDO scaffold. The PDO/PVA (5 wt%) scaffold also
showed faster tissue infiltration into the scaffold than the PDO scaffold. It seems that 5 wt%
addition of PVA to PDO to fabricate PDO/PVA scaffolds is enough for improving the
hydrophilicity and cell/tissue compatibility of the scaffolds.
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Authors: Se Heang Oh, Jun Ho Kim, Ji Youl Lee, Sung Ho Ghil, Soon Hong Yuk, Jin Ho Lee
Abstract: In this study, muscle-derived stem cell (MDSC)/Pluronics/polycaprolactone (PCL)
microparticle hybrid mixture was prepared as a potential injectable urethral bulking agent for the
treatment of urinary incontinence. The MDSCs were isolated from the gastrocnemius muscles of
SD rats by a modified preplate method and characterized through FACS analysis using various
primary antibodies (CD34, Sca-1, CD45 and desmin). The hybrid mixture was prepared by the
mixing of PCL microparticles (diameter, 100~200 μm) and MDSCs-containing thermo-sensitive
Pluronic (F127/F68 mixture) solution (4.5/5.5, w/v). The hybrid mixture was easily injected
through 18G needle into the body and stably remained in the applied site without initial volume
decrease, owing to a well-packed structure of PCL particles exhibited in the hybrid mixture. It was
observed that the MDSCs were stably grown in the hybrid mixture without severe inflammation and
immune reaction. From the results, we recognized that the hybrid mixture can be a good candidate
as an injectable bulking agent for the treatment of urinary incontinence, due to their good
injectability, volume retention and biocompatibility.
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Authors: Sahng Hoon Lee, Sang Cheol Seong, Jin Ho Lee, Il Kyu Han, Se Heang Oh, Kwang Joon Cho, Hyuk Soo Han, Myung Chul Lee
Abstract: Meniscus is the most commonly injured structure in the knee joint. Resection of the
meniscus as well as the torn menisci is known to induce the degeneration of the articular cartilage.
Replacement of the resected meniscus by allograft is limited by its availability and potential disease
transmission. Artificial prostheses are being tried in an attempt to regenerate the meniscal tissue and
we developed the biodegradable porous polycaprolactone(PCL) scaffold, which acts as a temporary
scaffold to enable the regeneration of a new tissue in time. We report the results of rabbit
implantation model. Biodegradable PCL scaffold coated with type I collagen with pores sized
100~150 +m and with compression modulus 400 kpa were fabricated by melt-molding particulate-
leaching method. The molds were made using the native meniscus of the rabbit. Medial meniscus of
right knee was partially removed through arthrotomy, leaving anterior 1/5 of the meniscus, after
sectioning medial collateral ligament. The implant was attached to the peripheral capsule and
remnant anterior meniscus with sutures. The medial meniscus of the left knee was removed and
served as a control without replacement. The regenerated meniscus was harvested at 4 & 12wks
after implantation. In addition to the routine histology of the tissue regenerated and remnant
scaffold, junction between the normal meniscus and the regenerated tissue, and cartilage surface
degeneration was observed. After 4 and 12 weeks the scaffolds, although considerable amount of
the materials remained, were largely filled and covered with fibrous tissue which was assumed to be
derived from synovial tissue of peripheral capsule. The tissue grossly resembling the native
meniscus was maintained and spindle shaped cells with extracellular matrices were observed
histologically. Neither cells with chondrocytic phenotype nor distinct cartilage matrices were
observed until 12 weeks. The bonding between the regenerated tissue and the peripheral synovial
capsule was firm and solid in all cases. The tissue bridges between the native meniscus and the
regenerated tissue were found in 9/10 operated knees. Articular surface degeneration was not
different between experimental and control groups except one case. More or less, the extrusion of
the meniscus was found in almost all knees. This study revealed that meniscal replacement with
PCL polymer prosthesis was feasible and led to adequate tissue formation. Long term studies on
adaptive remodeling will be required.
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Authors: A.K. Go, J.K. Kim, Se Heang Oh, Soon Hong Yuk, Jin Ho Lee
Abstract: This study was designed to evaluate the effect of polyethylene glycol (PEG) and
nonsteroidal anti-inflammatory drug (ibuprofen) on the prevention of postoperative tissue adhesion. For this, we synthesized poly(L-lactic acid)-PEG diblock copolymers and used them to prepare ibuprofen-loaded films as tissue adhesion barrier films. We also prepared lower critical solution temperature (LCST)-controllable Pluronic F127/F68 mixtures including mildly crosslinked alginate and ibuprofen as tissue adhesion barrier gels. The prepared films and gels with/without ibuprofen were evaluated by the observations of peritoneal tissue adhesion via animal study using a rat model.
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