Neat PCL Research Articles

Poly(ε-caprolactone)-grafted-chitosan copolymers: Synthesis and use as tunable and biodegradable coating for water soluble fertilizers

The urgent need for efficient agriculture to increase crop and food has fueled the development of coated fertilizers with a slow-release kinetics, water economy and full degradability to avoid negative environmental impact. In this context, we herein report the synthesis of poly(ε-caprolactone) (PCL) grafted from chitosan (CS) as a new class of biodegradable coating materials. The CS-g-PCL were prepared following a one-pot, two-step strategy, in which the primary amines of CS first react with ε-caprolactone (CL) to form CL-oligomers linked to CS via amide bonds terminated with hydroxyls, which together with the native hydroxyls of CS initiate the ring-opening polymerization of CL after addition of Sn(C ≡ CPh)4 as catalyst. Owing to the great stability of the used catalyst, the high molar mass of PCL grafted onto CS was successfully obtained under trivial open-air conditions. Different copolymers (CS-g-PCL) were prepared by varying the CS content. The structural characterization of CS-g-PCL was carried out using FTIR, 1H NMR, X-ray diffraction, contact angle and size exclusion chromatography (SEC) while the thermal and mechanical characterization of the prepared CS-g-PCL were compared to the neat PCL. Next, using a laboratory rotary drum, CS-g-PCL was implemented to uniformly coat granular diammonium phosphate fertilizer (DAP). Consequently, the kinetic releases of nitrogen and phosphorus were significantly delayed compared to that observed from uncoated DAP (conventional fertilizers). Finally, the degradation of CS-g-PCL was examined under aerobic conditions and showed a significant increase in their biodegradability with respect to neat PCL.

Modified cellulose nanocrystals enhanced polycaprolactone multifunctional films with barrier, UV-blocking and antimicrobial properties for food packaging

The packaging industry demands improved eco-friendly materials with new and enhanced properties. In this context, bio-nanocomposite films with antimicrobial and UV-shielding properties based on modified cellulose nanocrystals/polycaprolactone (MCNC/PCL) were fabricated via solution casting method, and then food packaging simulation was carried out. CNCs were obtained by acid hydrolysis followed by successful functionalization with Quaternary ammonium surfactant, confirmed by FTIR, XPS, XRD, TEM, and DLS analyses. Furthermore, the morphological, physical, antibacterial, and food packaging properties of all prepared films were investigated. Results showed that the mechanical, UV blocking, barrier properties, and antibacterial activity of all composite films were remarkably improved. Particularly, the addition of 3 wt% MCNC increased the tensile strength and elongation at break by 27.5 % and 20.0 %, respectively. Moreover, the permeability of O2, CO2, and water vapor dramatically reduced by 97.6 %, 96.7 %, and 49.8% compared to the Neat PCL. Further, the UV-blocking properties of the composite films were significantly improved. The antimicrobial properties of MCNC/PCL films showed good antimicrobial properties against S. aureus. Finally, cherry packaged with 1 and 3 wt% MCNC films exhibited satisfactory freshness after 22 days of preservation. Overall, the fabricated PCL nanocomposite films can be utilized in the food packaging industry.

Effect of Gelatin Coating and GO Incorporation on the Properties and Degradability of Electrospun PCL Scaffolds for Bone Tissue Regeneration.

Polymer-based nanocomposites such as polycaprolactone/graphene oxide (PCL/GO) have emerged as alternatives for bone tissue engineering (BTE) applications. The objective of this research was to investigate the impact of a gelatin (Gt) coating on the degradability and different properties of PCL nanofibrous scaffolds fabricated by an electrospinning technique with 1 and 2 wt% GO. Uniform PCL/GO fibers were obtained with a beadless structure and rough surface. PCL/GO scaffolds exhibited an increase in their crystallization temperature (Tc), attributed to GO, which acted as a nucleation agent. Young's modulus increased by 32 and 63% for the incorporation of 1 and 2 wt% GO, respectively, in comparison with neat PCL. A homogeneous Gt coating was further applied to these fibers, with incorporations as high as 24.7 wt%. The introduction of the Gt coating improved the hydrophilicity and degradability of the scaffolds. Bioactivity analysis revealed that the hydroxyapatite crystals were deposited on the Gt-coated scaffolds, which made them different from their uncoated counterparts. Our results showed the synergic effect of Gt and GO in enhancing the multifunctionality of the PCL, in particular the degradability rate, bioactivity, and cell adhesion and proliferation of hGMSC cells, making it an interesting biomaterial for BTE.

Design of silver containing mesoporous bioactive glass-embedded polycaprolactone substrates with antimicrobial and bone regenerative properties

ObjectivesThe aim of the present study was to design, produce and characterize composite substrates consisting of different formulations of poly(ε-caprolactone) (PCL), as a polymer matrix, and silver-containing mesoporous bioactive glasses (Ag-MBGs) with improved properties for bone tissue engineering. MethodsAg-MBGs were synthesized by an evaporation-induced self-assembly process. Different polymer-to-particles weight ratios were considered (90/10, 80/20, 70/30 wt%). PCL/Ag-MBGs composites substrates were manufactured by melting and molding technique. The effect of Ag-MBGs embedded in the polymer matrix was investigated by morphological (field emission scanning electron microscopy (FE-SEM), SEM and contact angle measurement), structural/functional (small punch and tensile tests), antimicrobial, and in vitro biological analyses. ResultsThe obtained results highlighted that the inclusion of 10% by weight of Ag-MBGs improved the punching performances as well as the tensile Young’s modulus (from 350.3 ± 32.0 MPa for PCL to 473.5 ± 41.0 MPa), without negatively altering the tensile strength of the neat PCL. Indeed, small punch test findings indicated that, over a threshold concentration (10% by weight), the Ag-MBGs acted as "weak points", rather than reinforcement, because the mechanical properties of the composite substrates decreased. The bacterial growth monitoring showed a clear antimicrobial effect against both Gram-negative and Gram-positive, confirmed by reduced cell viability registered after 24 h (2 ×105 CFU/mL for P. aeruginosa and 2.3 ×105 CFU/mL for S. aureus). The results were confirmed in terms of adhesion and adherent growth, reduced at day 3 on PCL samples with 10% of Ag/MBGs. Furthermore, this formulation induced a significant inhibition zone (21 mm for P. aeruginosa, 23 mm for S. aureus). In vitro biological assays confirmed that all formulations of PCL/Ag-MBGs supported periodontal ligament stem cells’ viability and differentiation over time. Particularly, substrates with Ag-MBGs at a concentration of 10% and 20% by weight of Ag-MBGs provided higher values of the percentage of Alamar Blue reduction meanwhile, the highest Ag-MBGs concentration induced a higher expression of alkaline phosphatase activity. SignificanceAg-MBGs proved to be suitable candidates as filler at a specific threshold concentration (10% by weight), considering a compromise among physicochemical, antimicrobial, and pro-regenerative features. These findings provide useful data for the design and development of improved biomaterials with optimized properties, suggesting a potential application in maxillofacial bone and/or periodontal tissue repair.

Sustainable Integration of Zinc Oxide Nanoparticles: Enhancing Properties of Poly(ε-Caprolactone) Electrospun Nanofibers and Cast Films

This study investigated the impact of adding zinc oxide nanoparticles (ZnO-NPs) to electrospun membranes and cast films made of poly(ε-caprolactone) (PCL). The physicochemical, mechanical, and morphological properties of the samples were analyzed. Physicochemical parameters included water contact angle (WCA), water vapor transmission rate (WVTR), permeance, water vapor permeability (WVP), light transmission (T600), and transparency (T). Mechanical properties, such as maximum stress (Ϭmax), elongation (εmax), and Young’s modulus (MPa), were also evaluated. Morphological properties were analyzed in terms of thickness, dispersion, and surface roughness (measured by the arithmetic (Ra) and quadratic (Rq) averages). The crystallinity and melting point, as well as the functional DPPH• scavenging percentage (SP%), were also studied. The results showed that adding 1 wt% ZnO-NPs improved the water barrier properties of PCL membranes and films, increasing WCA by 1%–6% and decreasing WVTR by 11%–19%, permeance by 34%–20%, and WVP by 4%–11%, respectively. The T600 values of PCL/ZnO-NPs membranes and films were 2–3 times lower than those of neat PCL samples, indicating improved optical properties. The mechanical properties of the composite membranes and films also improved, with Ϭmax increasing by 56%–32% and Young’s modulus increasing by 91%–95%, while εmax decreased by 79%–57%. The incorporation of ZnO-NPs also increased the thickness and surface roughness of the samples. The SP% of PCL/ZnO-NPs increased by almost 69%, demonstrating the beneficial effects of ZnO-NPs on the system. These findings suggest that incorporating ZnO-NPs into PCL membranes and films can enhance their properties, making them well suited for various applications, such as those within the realm of materials science and nanotechnology.

Nanofibrous hybrid scaffolds based on PCL-borosilicate system by a green sol-gel process

Tissue regeneration is yet a critical issue, and to mimic the natural extracellular matrix (ECM) innovative scaffolds need to be developed to ensure the functional and safe repair of the damaged organs or tissues. Hybrid biomaterials based on the combination of a biodegradable polymer and bioactive glasses (BGs) are potential candidates for tissue engineering (TE), since they exhibit tailored physical, biological, and mechanical properties, as well as controlled degradation behavior. Thus, the main purpose of this research was to develop by electrospinning (ES) a hybrid nanofibrous membrane composed of a synthetic polymeric matrix (PCL) and a boron and calcium silicate glass, formed via in situ sol-gel, and based on a non-aqueous and green fabrication route. Formic acid (FA) and glacial acetic acid (AA) were used as green solvents to dissolve the PCL. Different compositions were prepared: neat PCL and PCL/SiO2–B2O3–CaO with different sol-gel aging times and green solvent systems. All prepared hybrid solutions, except the composition with only AA, were spinnable. Structural features of the hybrids were assessed by ATR-FTIR spectroscopy, which confirmed the presence of siloxane (Si–O–Si) bonds of silica and carbonyl (CO) bonds characteristic of PCL polymer as well as intermolecular hydrogen-bonding interactions between the carbonyls of PCL and the silanol hydroxyls (Si–OH) of silica networks. Boron (B–O–B) and borosiloxane (B–O–Si) bonds were not visible due to the overlapping of PCL bands in the spectra. Only the solid state 11B NMR technique allowed to find peaks assigned to trigonal BO3 and tetrahedral BO4 groups, which evidence the boron linkages to silica. Thermal analysis showed a change in the crystallinity of PCL with the incorporation of inorganic domains, confirming the formation of chemical interactions between the polymer and the inorganic part. Microstructure and chemical analysis, by SEM/EDS, showed a homogenous distribution of Ca and Si elements into the fibers, as well as an increase of the fiber diameter with the incorporation of boron and calcium silicate glass in the PCL. The developed compositions of PCL/boron and calcium-containing silicate were feasible to electrospin into fibrous meshes, proving its potential for further design of multicomponent nanofibrous microstructures closer to extra cellular matrix architectures.

Hydrolytic Degradation and Bioactivity of Electrospun PCL-Mg-NPs Fibrous Mats.

In this work, the in vitro degradation behavior of nanofibers was investigated in phosphate buffer solution (PBS) and simulated body fluid (SBF) to study their degradation behavior, as well as their bioactivity. The degradation was studied at different immersion times in order to evaluate how the presence of Mg-based nanoparticles can affect the degradation in terms of morphology, crystallinity, degradation rate and pH changes, and finally to evaluate the bioactivity of PCL-based electrospun nanofibers. We found that the degradation of the materials takes more than 3 months; however, the presence of nanoparticles seems to have an accelerating effect on the degradation of the electrospun nanofibers based on PCL. In fact, a reduction in diameter of almost 50% was observed with the highest content of both types of nanoparticles and an increase in crystallinity after 296 days of immersion in PBS. Moreover, the carbonyl index was calculated from an FTIR analysis, and a reduction of 20-30% was observed due to the degradation effect. Additionally, the bioactivity of PCL-based electrospun nanofibers was studied and the formation of crystals on the nanofibers surface was detected, except for neat electrospun PCL related to the formation of NaCl and apatites, depending on the amount and type of nanoparticles. The presence of apatites was confirmed by an XRD analysis and FT-IR analysis observing the characteristic peaks; furthermore, the EDX analysis demonstrated the formation of apatites than can be reconducted to the presence of HA when 20 wt% of nanoparticles is added to the PCL electrospun fibers.

A PRELIMINARY STUDY EXAMINING THE BURST STRENGTH OF VASCULAR TUBULAR SCAFFOLDS

In this study, neat PCL, neat PLA and PLA/PCL (50/50) based tubular surfaces are produced by electrospinning to simulate the native blood vessel structure and to investigate the effects of both graft material and fiber orientation on burst strength. The burst pressure values of these vascular graft structures that designed with both randomly oriented fibers and oriented fibers, measured by a custom- burst pressure tester, and the results are compared. The results show that fiber orientation have a great influence on burst pressure, regardless of the type of biomaterial. It is determined that grafts with oriented fibers have at least twice the burst strength than those with random fibers. The findings indicate that changing the graft material has also an effect on burst strength. When the results are analyzed by polymer type, although the PLA100_O sample has the highest burst strength among all oriented fiber sample groups, it is better to determine the vascular graft candidate by taking into account radial elasticity.

Polycaprolactone/epoxide-functionalized silica composite microparticles for long-term controlled release of trans-chalcone

Abstract In this study, controlled release of trans-chalcone was achieved by using a polycaprolactone-based hybrid system as the drug carrier material. Encapsulation efficiency was obtained in the range of 70–75% for various formulations and in vitro release studies, conducted at 37 °C and pH 7.4, revealed slow profile reaching 60% cumulative release. As interpreted from kinetic modelling, drug release was controlled mainly by Fickian diffusion; polymer erosion did not contribute to the TC release. Difference in drug loading efficiencies of the hybrid and neat PCL microparticles was observed such that PCL microparticles had lower loading efficiency than the hybrid microparticles whereas the release profiles were similar. pH of the release medium had affected release profiles; acidic medium enhanced drug release. Characterization of the microparticles were realized by FT-IR, TGA, DSC, SEM and WCA which revealed key properties such as molecular dispersion state and hydrophilicity. With the results obtained, we concluded that our hybrid system has a significant potential for long term release of trans-chalcone.

Crystallization Behavior of Poly(ε-Caprolactone)-Hollow Glass Microspheres Composites for Rotational Molding Technology

Composites suitable for rotational molding technology based on poly(ε-caprolactone) (PCL) and filled with hollow glass microspheres (HGM) or functionalized hollow glass microspheres (HGMf) were prepared via melt-compounding. The functionalization of glass microspheres was carried out by a silanization treatment in order to improve the compatibility between the inorganic particles and the polymer matrix and achieve a good dispersion of glass microspheres in the matrix and an enhanced filler–polymer adhesion. The crystallization behavior of materials was studied by DSC under isothermal and non-isothermal conditions and the nucleating effect of the glass microspheres was proven. In particular, the presence of silanized glass microspheres promoted faster crystallization rates and higher nucleation activity, which are enhanced by 75% and 50%, respectively, comparing neat PCL and the composite filled with 20 wt% HGMf. The crystalline and supermolecular structure of PCL and composites crystallized from the melt was evaluated by WAXD and SAXS, highlighting differences in terms of crystallinity index and structural parameters as a function of the adopted crystallization conditions.

Fabrication and Characterization of Hybrid Bio-Composites Using Braided Natural Fibers and Aligned Thermoplastic Filaments

The composite group investigates endlessly the features of natural fiber/thermoplastic matrix composite materials to improve recyclability, use of renewable sources, and reduce material costs. In this context, the development and use of biodegradable polymers for composites is considered one of the important strategies for reducing environmental challenges. Here, axially oriented fibers incorporated in conforming matrices make up fiber-reinforced composites. Due to the high viscosity of molten Poly(ε-caprolactone) (PCL), impregnating into reinforced fiber strands is challenging. So, continuous hybrid flax and hemp fibers were produced using a braiding technique by considering the fiber aspect ratio (AR). The resulting braided yarns were parallel aligned with PCL filaments before being compression molded into unidirectional composite laminates. The flax and PCL blend had better mechanical properties than the other produced composites. Temperatures for the glass transition, melting, and crystallization, were much greater than for neat PCL. However, mechanical properties were barely altered due to the ductile nature of PCL.

A Comparative Study on the Addition of MgO and Mg(OH)2 Nanoparticles into PCL Electrospun Fibers

AbstractIn this work, a comparative study between the morphology, the thermal and the mechanical properties of poly(ɛ‐caprolactone) (PCL)‐based electrospun fiber mats reinforced with both MgO and Mg(OH)2 nanoparticles, is carried out. Both MgO and Mg(OH)2 nanoparticles have been added in a range of concentrations such as 0.5, 1, 5, 10, 20 wt% with respect to the PCL matrix, with the aim of improving their mechanical properties in comparison with neat PCL electrospun fibers. From the morphological point of view, electrospun fibers are randomly collected and an increase in the average fiber diameter with the addition of nanoparticles is observed. The addition of both types of nanoparticles lower the onset degradation temperature as well as the maximum degradation temperature of neat ePCL of about 50 °C with the higher content of nanoparticles. Furthermore, PCL electrospun nanofiber mats show a degree of crystallinity of 53%, which is quite high. However, the addition of 20 wt% of both MgO and Mg(OH)2 lowers the crystallinity of the reinforced electrospun fibers to 50% and 43% for PCL + MgO 20 wt% and Mg(OH)2 20 wt%, respectively.

Blends Based on Poly(ε-Caprolactone) with Addition of Poly(Lactic Acid) and Coconut Fibers: Thermal Analysis, Ageing Behavior and Application for Embossing Process.

In this research a biodegradable blend of poly(ɛ-caprolactone) (PCL) and poly(lactic acid) (PLA) is proposed as a new material for the production of a relief printing plate used for special applications on packaging materials, i.e., the embossing process. Coconut fibers (CFs) were added as a natural filler to PCL/PLA blends to improve the functional properties of the prepared blends. Thermal, mechanical and surface analyses were performed on the unaged and artificially aged blends. The results showed that CF has been proven to optimize the hardness of the blend, which is crucial for the production of relief plate for embossing applications. The lowest hardness was measured on neat PCL (53.30° Sh D) and the highest value on PCL/PLA/CF 70/30/3.0 blend (60.13° Sh D). Stronger interfacial interactions were present at the PLA/CF interface because the interfacial free energy is closer to zero and the work of adhesion and spreading coefficient are higher than for the PCL/CF interface. The results of thermal analysis of unaged and aged blends showed that ageing for 3 weeks resulted in significantly lower thermal stability, especially for neat PCL and PCL/PLA 80/20 blends. Blends with a higher content of PLA and CF showed a slightly increased ageing resistance, which is attributed to the increased crystallinity of PLA after ageing due to the addition of CF showed in the DSC diagrams.

Antibacterial and antioxidant phenolic compounds loadedPCLbiocomposites for active food packaging application

AbstractActive food packages must not only act as a protective food barrier but also exhibit radical scavenging activity, antibacterial and controlled release properties that can have a positive effect on food quality, safety and shelf life. In this study, poly(ε‐caprolactone) (PCL)/ferulic acid (FA) and PCL/gallic acid (GA) biocomposites were prepared by melt blending method to use in active food packaging applications. The physicochemical properties of the prepared biocomposites were investigated by FTIR‐ATR, SEM, and DMA. In addition, antioxidant and antibacterial activities, water contact angle, oscillation test and water vapor transmission rate of biocomposites were also investigated. FTIR‐ATR and SEM results showed that both fillers were well dispersed in the PCL matrix. Dynamic mechanical analysis was performed to examine the mechanical behavior of the samples and to determine theirTgtemperatures. The biocomposites exhibited a higher storage modulus and loss modulus than pure PCL. Especially, the glass transition temperature of the PCL/FA sample containing 5 wt.% FA increased 17°C compared to the neat PCL. They exhibited high‐scavenging activity against DPPH and ABTS radicals, and showed high‐antibacterial activity against bothE. coliandS. aureusbacteria.

Silver nanowire loaded poly(ε-caprolactone) nanocomposite fibers as electroactive scaffolds for skeletal muscle regeneration

Volumetric muscle loss (VML) due to trauma and tumor removal operations affects millions of people every year. Although skeletal muscle has a natural repair mechanism, it cannot provide self-healing above a critical level of VML. In this study, nanocomposite aligned fiber scaffolds as support materials were developed for volumetric skeletal muscle regeneration. For this purpose, silver nanowire (Ag NW) loaded poly(ε-caprolactone) (PCL) nanocomposite fiber scaffolds (PCL-Ag NW) were prepared to mimic the aligned electroactive structure of skeletal muscle and provide topographic and conductive environment to modulate cellular behavior and orientation. A computer-aided rotational wet spinning (RWS) system was designed to produce high-yield fiber scaffolds. Nanocomposite fiber bundles with lengths of 50 cm were fabricated via this computer-aided RWS system. The morphological, chemical, thermal properties and biodegradation profiles of PCL and PCL-Ag NW nanocomposite fibers were characterized in detail. The proliferation behavior and morphology of C2C12 mouse myoblasts were investigated on PCL and PCL-Ag NW nanocomposite fibrous scaffolds with and without electrical stimulation. Significantly enhanced cell proliferation was observed on PCL-Ag NW nanocomposite fibers compared to neat PCL fibers with electrical stimulations of 1.5 V, 3 V and without electrical stimulation.

Effect of kaolin waste annealing on the structural and thermal behavior of poly(ε−caprolactone)

The heat treatment effect on kaolin waste from mining was evaluated on the structural and thermal behavior of poly(ε-caprolactone) (PCL). The PCL/KW (kaolin waste) and PCL/HTKW (heat-treated kaolin waste) composites were processed in an internal mixer and subsequently characterized by X-ray diffraction (XRD) and differential scanning calorimetry (DSC). The kaolin waste showed kaolinite and quartz in its composition, while the heat treatment at 1200°C modified it to mullite, quartz and silica-rich amorphous phase. By XRD, there was an increase in the intensity of the peak 2θ = 23.9° of the PCL/KW composites compared to neat PCL. In contrast, PCL/HTKW composites tended to reduce the intensity of the peak 2θ = 23.9°, especially at 5% HTKW. The crystalline melting temperature and the degree of crystallinity of PCL/KW and PCL/HTKW composites were practically unchanged, compared to PCL. However, the crystallization process was more effective with the kaolin waste (KW) without heat treatment, indicating that the HTKW amorphous phase inhibited crystallization. The PCL/KW development promoted an increase in crystallization temperature, relative crystallinity, and crystallization rate, surpassing PCL and the PCL/HTKW system. In view of this, kaolin waste has the potential to accelerate the PCL crystallization process, contributing to add value to a material that would otherwise be discarded and minimizing environmental impacts.

Preparation of a sustainable bio-copolymer based on Luffa cylindrica cellulose and poly(ɛ-caprolactone) for bioplastic applications

In this research, a bio-based graft copolymer (LCC-g-PCL) based on the cellulose of Luffa cylindrica (LCC) main chain possessing poly(ɛ-caprolactone) (PCL) pendant groups is synthesized through a grafting from approach via ring-opening polymerization (ROP). For this purpose, LCC, extracted from luffa sponges by combined method, is utilized for ROP of ɛ-caprolactone (ɛ-CL) as a macro-initiator in the presence of stannous octoate as a catalyst. Fourier transform infrared (FT-IR), proton and carbon nuclear magnetic resonance (1H NMR and 13C NMR) spectroscopies are utilized to structurally indicate the success of ROP, while the achieved graft copolymer is analyzed in detail by comparing with LCC and neat PCL in terms of wettability, thermal and degradation behaviors by conducting water contact angle (WCA) measurements, thermogravimetric and differential scanning calorimetry analyses (TGA and DSC) and in vitro both hydrolytic and enzymatic biodegradation tests, respectively. The results of conducted tests show that the incorporation of PCL groups on LCC provide the increasing hydrophobicity. In addition, the degradation behavior of the LCC-g-PCL copolymer is found to be more pronounced under enzymatic medium rather than hydrolytic conditions. It is anticipated from the results that LCC-g-PCL can be a potential eco-friendly material particularly in bioplastic industry.

Enhancing the crystallization of biodegradable poly(ε-caprolactone) using a polyvinyl alcohol fiber favoring nucleation

In this study, biodegradable poly(ε-caprolactone) (PCL)/polyvinyl alcohol (PVA) fiber composites were prepared using melt processing techniques with different PVA fiber contents. The effect of PVA fiber on the non-isothermal and isothermal melt crystallization kinetics of PCL/PVA fiber composites was studied by using differential scanning calorimetry. Non-isothermal crystallization peak temperatures were enhanced significantly, as exemplified by about 20 K increase for the composite loaded with 5 wt% PVA fiber at a cooling rate of 20 K/min compared to that of neat PCL. The crystallization half-time decreased from 1.67 min for neat PCL to 0.80 min for composite with 5 wt% PVA fiber at a cooling rate of 5 K/min. PVA fiber was also found to dramatically accelerate the isothermal crystallization rate of PCL/PVA fiber composites. The crystallization half-time of composite containing 5 wt% PVA fiber was reduced by more than 10 times compared with neat PCL. Moreover, dynamic mechanical analysis results showed that PVA fiber had a strengthening effect on the PCL.

Regeneration of Bone Defects in a Rabbit Femoral Osteonecrosis Model Using 3D-Printed Poly (Epsilon-Caprolactone)/Nanoparticulate Willemite Composite Scaffolds.

Steroid-associated osteonecrosis (SAON) is a chronic disease that leads to the destruction and collapse of bone near the joint that is subjected to weight bearing, ultimately resulting in a loss of hip and knee function. Zn2+ ions, as an essential trace element, have functional roles in improving the immunophysiological cellular environment, accelerating bone regeneration, and inhibiting biofilm formation. In this study, we reconstruct SAON lesions with a three-dimensional (3D)-a printed composite made of poly (epsilon-caprolactone) (PCL) and nanoparticulate Willemite (npW). Rabbit bone marrow stem cells were used to evaluate the cytocompatibility and osteogenic differentiation capability of the PCL/npW composite scaffolds. The 2-month bone regeneration was assessed by a Micro-computed tomography (micro-CT) scan and the expression of bone regeneration proteins by Western blot. Compared with the neat PCL group, PCL/npW scaffolds exhibited significantly increased cytocompatibility and osteogenic activity. This finding reveals a new concept for the design of a 3D-printed PCL/npW composite-based bone substitute for the early treatment of osteonecrosis defects.

Improvement of Mechanical Strength of Tissue Engineering Scaffold Due to the Temperature Control of Polymer Blend Solution

Polymeric scaffolds made of PCL/PLCL (ratio 1:3, respectively) blends have been developed by using the Thermally Induced Phase Separation (TIPS) process. A new additional technique has been introduced in this study by applying pre-heat treatment to the blend solution before the TIPS process. The main objective of this study is to evaluate the influence of the pre-heat treatment on mechanical properties. The mechanical evaluation showed that the mechanical strength of the scaffolds (including tensile strength, elastic modulus, and strain) improved as the temperature of the polymer blend solution increased. The effects on the microstructure features were also observed, such as increasing strut size and differences in phase separation morphology. Those microstructure changes due to temperature control contributed to the increasing of mechanical strength. The in vitro cell study showed that the PCL/PLCL blend scaffold exhibited better cytocompatibility than the neat PCL scaffold, indicated by a higher proliferation at 4 and 7 days in culture. This study highlighted that the improvement of the mechanical strength of polymer blends scaffolds can be achieved using a very versatile way by controlling the temperature of the polymer blend solution before the TIPS process.