scholarly journals Mechanical Properties of Membranes of Poly(L-co-DL-lactic acid) with Poly(caprolactone triol) and StudyIn Vivo

2014 ◽  
Vol 2014 ◽  
pp. 1-9 ◽  
Author(s):  
Marcia Adriana Tomaz Duarte ◽  
Adriana Cristina Motta ◽  
Eliana Aparecida de Rezende Duek
Keyword(s):  
Lactic Acid ◽  
Subcutaneous Tissue ◽  
Mechanical Analysis ◽  
Initial Time ◽  
Scanning Calorimetry ◽  
Time Intervals ◽  
Aliphatic Polyesters ◽  
Potential Applications ◽  
Poly Caprolactone

There is increasing interest in aliphatic polyesters from lactones and lactides because of their biodegradability and biocompatibility. Among these compounds, poly(lactide), and poly(glycolide), poly(ε-caprolactone) and their copolymers are especially interesting because of their potential applications as biomedical materials. The aim of this study was to examine the properties of membranes of poly(L-co-D,L lactic acid) (PLDLA) with poly(caprolactone triol) (PCL-T) obtained by solvent evaporation. The blends were characterized by differential scanning calorimetry, dynamic mechanical analysis, Fourier transform infrared spectroscopy, and tensile strength tests. Based on the results ofin vitrostudies, PLDLA/PCL-T blends of 100/0 and 90/10 were implanted in subcutaneous tissue of Wistar rats for 1, 3, 7, 15, and 60 days to evaluate their biocompatibility. Histological analysis indicated that, although PCL-T-containing membranes caused a more prominent inflammatory reaction in the initial time intervals, by 60 days after implantation, the material was surrounded by dense, organized collagen with almost no inflammatory infiltrate.

scholarly journals Relationship between the Stereocomplex Crystallization Behavior and Mechanical Properties of PLLA/PDLA Blends

Polymers ◽  
2021 ◽  
Vol 13 (11) ◽  
pp. 1851
Author(s):  
Hye-Seon Park ◽  
Chang-Kook Hong
Keyword(s):  
Mechanical Properties ◽  
Lactic Acid ◽  
Crystallization Behavior ◽  
Mechanical Analysis ◽  
X Ray Diffraction ◽  
Nucleation Agent ◽  
Scanning Calorimetry ◽  
Nucleation Sites ◽  
Wide Range ◽  
Degree Of Crystallization

Poly (l-lactic acid) (PLLA) is a promising biomedical polymer material with a wide range of applications. The diverse enantiomeric forms of PLLA provide great opportunities for thermal and mechanical enhancement through stereocomplex formation. The addition of poly (d-lactic acid) (PDLA) as a nucleation agent and the formation of stereocomplex crystallization (SC) have been proven to be an effective method to improve the crystallization and mechanical properties of the PLLA. In this study, PLLA was blended with different amounts of PDLA through a melt blending process and their properties were calculated. The effect of the PDLA on the crystallization behavior, thermal, and mechanical properties of PLLA were investigated systematically by thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), X-ray diffraction (XRD), polarized optical microscopy (POM), dynamic mechanical analysis (DMA), and tensile test. Based on our findings, SC formed easily when PDLA content was increased, and acts as nucleation sites. Both SC and homo crystals (HC) were observed in the PLLA/PDLA blends. As the content of PDLA increased, the degree of crystallization increased, and the mechanical strength also increased.

Full biodegradable elastomeric nanocomposites fabricated by chitin nanocrystal and poly(caprolactone-diol citrate) elastomer

2019 ◽  
Vol 34 (6) ◽  
pp. 453-463
Author(s):  
Kai Liang ◽  
Yajing Zhou ◽  
Yali Ji
Keyword(s):  
Tensile Modulus ◽  
Mechanical Analysis ◽  
Biological Properties ◽  
Uniaxial Tensile ◽  
Uniaxial Tensile Test ◽  
Melt Polycondensation ◽  
Biodegradable Poly ◽  
Poly Caprolactone ◽  
Phosphate Buffered Saline

Chitin nanocrystal is a biocompatible and biodegradable nanofiller, with great potential in enhancing the mechanical and biological properties of polymers. Poly(caprolactone-diol citrate) is a kind of citrate-based biodegradable elastomer prepared by an additive-free melt polycondensation of polycaprolactone-diol and citric acid coupled with subsequent thermocuring. Here, a facile casting/evaporation method was utilized to prepare full biodegradable poly(caprolactone-diol citrate)/chitin nanocrystal nanocomposites, and their structure and properties were characterized by Fourier transform infrared spectroscopy, scanning electron microscopy, uniaxial tensile test, dynamic mechanical analysis, surface wettability and swelling analysis, thermogravimetric analysis, in vitro degradation, and cytocompatibility test. The results showed the chitin nanocrystals were uniformly distributed in the poly(caprolactone-diol citrate) matrix; with increasing chitin nanocrystal loading, the tensile modulus and strength significantly increased; furthermore, the incorporation of chitin nanocrystals endowed the poly(caprolactone-diol citrate) with more hydrophilicity, lower swelling in phosphate buffered saline solution, slow degradation rate, and greatly improved cytocompatibility. Thus, the chitin nanocrystal was a good bio-based nanofiller that could be used to tune the properties of poly(caprolactone-diol citrate) degradable bioelastomer.

Novel shape-memory polyurethane fibers for textile applications

2018 ◽  
Vol 89 (6) ◽  
pp. 1027-1037 ◽  
Author(s):  
Míriam Sáenz-Pérez ◽  
Tariq Bashir ◽  
José Manuel Laza ◽  
Jorge García-Barrasa ◽  
José Luis Vilas ◽  
...  
Keyword(s):  
Differential Scanning Calorimetry ◽  
Shape Memory ◽  
Tensile Testing ◽  
Melt Spinning ◽  
Mechanical Analysis ◽  
Knitted Fabric ◽  
Scanning Calorimetry ◽  
Moisture Management ◽  
Potential Applications ◽  
Shape Memory Polyurethane

In this work, thermoresponsive shape-memory polyurethane (SMPU) fibers were produced by melt spinning from different SMPU pellets. Afterwards, the knitted fabric samples were prepared by the obtained fibers. Some of the SMPUs used were synthesized previously in our laboratory whereas a commercial one, named DIAPLEX MM4520, was also evaluated in order to carry out comparative studies. All the SMPUs were characterized by different techniques, such as thermogravimetric analysis, differential scanning calorimetry, dynamic mechanical analysis and tensile testing. Moreover, the shape-memory capabilities of the fabrics were measured by thermo-mechanical analysis. The obtained results show that the synthesized SMPUs could be attractive candidates for potential applications such as breathable fabrics or moisture-management textiles.

scholarly journals Polydopamine-Coated Paraffin Microcapsules as a Multifunctional Filler Enhancing Thermal and Mechanical Performance of a Flexible Epoxy Resin

2020 ◽  
Vol 4 (4) ◽  
pp. 174
Author(s):  
Giulia Fredi ◽  
Cordelia Zimmerer ◽  
Christina Scheffler ◽  
Alessandro Pegoretti
Keyword(s):  
Phase Change ◽  
Storage Modulus ◽  
Mechanical Performance ◽  
Value Added ◽  
Mechanical Analysis ◽  
Scanning Calorimetry ◽  
Management Capability ◽  
Deposition Parameters ◽  
Potential Applications ◽  
Ep Matrix

This work focuses on flexible epoxy (EP) composites containing various amounts of neat and polydopamine (PDA)-coated paraffin microcapsules as a phase change material (PCM), which have potential applications as adhesives or flexible interfaces with thermal management capability for electronics or other high-value-added fields. After PDA modification, the surface of PDA-coated capsules (MC-PDA) becomes rough with a globular appearance, and the PDA layer enhances the adhesion with the surrounding epoxy matrix, as shown by scanning electron microscopy. PDA deposition parameters have been successfully tuned to obtain a PDA layer with a thickness of 53 ± 8 nm, and the total PDA mass in MC-PDA is only 2.2 wt %, considerably lower than previous results. This accounts for the fact that the phase change enthalpy of MC-PDA is only marginally lower than that of neat microcapsules (MC), being 221.1 J/g and 227.7 J/g, respectively. Differential scanning calorimetry shows that the phase change enthalpy of the prepared composites increases with the capsule content (up to 87.8 J/g) and that the enthalpy of the composites containing MC-PDA is comparable to that of the composites with MC. Dynamic mechanical analysis evidences a decreasing step in the storage modulus of all composites at the glass transition of the EP phase, but no additional signals are detected at the PCM melting. PCM addition positively contributes to the storage modulus both at room temperature and above Tg of the EP phase, and this effect is more evident for composites containing MC-PDA. As the capsule content increases, the mechanical properties of the host EP matrix also increase in terms of elastic modulus (up to +195%), tensile strength (up to +42%), Shore D hardness (up to +36%), and creep compliance (down to −54% at 60 min). These effects are more evident for composites containing MC-PDA due to the enhanced interfacial adhesion.

scholarly journals Bio-composites for Fused Filament Fabrication. Effects of Maleic Anhydride Grafting on Poly(Lactic Acid) and Microcellulose

2021 ◽  
Author(s):  
Daniele Rigotti ◽  
Luca Fambri ◽  
Alessandro Pegoretti
Keyword(s):  
Lactic Acid ◽  
Maleic Anhydride ◽  
Nucleating Agent ◽  
Mechanical Analysis ◽  
Poly Lactic Acid ◽  
Crystalline Cellulose ◽  
Fused Filament Fabrication ◽  
Scanning Calorimetry ◽  
Electron Microscopy Analysis ◽  
Reactive Mixing

Abstract Composite filaments consisting of poly(lactic acid) (PLA) and micro crystalline cellulose (MCC) were successfully used for additive manufacturing (AM) by fused filament fabrication (FFF). PLA and MCC bio-composites were obtained by direct mixing in a melt compounder; maleic anhydride (MAH) was also grafted onto PLA in reactive mixing stage to evaluate its effect on the final properties of the printed material. Filaments with various concentrations of MCC (up to a maximum content of 10 wt%) were produced with a single screw extruder and used to feed a commercial desktop FFF printer. Upon grafting of PLA with MAH, a more coherent interfacial morphology between PLA and MCC was detected by electron microscopy analysis. The thermal degradation of the PLA was unaffected by the presence of MCC and MAH. According to differential scanning calorimetry and dynamic mechanical analysis results, micro-cellulose acted as nucleating agent for PLA. In fact, the crystallization peak shifted towards lowers temperature and a synergistic effect when MCC was added to PLA grafted with MAH was observed possibly due to the increase of the chain mobility. Micro cellulose led to an increase in the stiffness of the material in both filaments and 3D printed specimen, however, a different fracture behavior was observed due to the peculiar structure of printed samples.

scholarly journals Influence of the Lignin Content on the Properties of Poly(Lactic Acid)/lignin-Containing Cellulose Nanofibrils Composite Films

Polymers ◽  
2018 ◽  
Vol 10 (9) ◽  
pp. 1013 ◽  
Author(s):  
Xuan Wang ◽  
Yuan Jia ◽  
Zhen Liu ◽  
Jiaojiao Miao
Keyword(s):  
Lactic Acid ◽  
Lignin Content ◽  
Cellulose Nanofibrils ◽  
Composite Films ◽  
Tensile Tests ◽  
Nucleating Agent ◽  
Mechanical Analysis ◽  
Degree Of Crystallinity ◽  
Poly Lactic Acid ◽  
Scanning Calorimetry

Poly(lactic acid) (PLA)/lignin-containing cellulose nanofibrils (L-CNFs) composite films with different lignin contents were produced bythe solution casting method. The effect of the lignin content on the mechanical, thermal, and crystallinity properties, and PLA/LCNFs interfacial adhesion wereinvestigated by tensile tests, thermogravimetric analysis, differential scanning calorimetry (DSC), dynamic mechanical analysis, Fourier transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM). The tensile strength and modulus of the PLA/9-LCNFs (9 wt % lignin LCNFs) composites are 37% and 61% higher than those of pure PLA, respectively. The glass transition temperature (Tg) decreases from 61.2 for pure PLA to 52.6 °C for the PLA/14-LCNFs (14 wt % lignin LCNFs) composite, and the composites have higher thermal stability below 380 °C than pure PLA. The DSC results indicate that the LCNFs, containing different lignin contents, act as a nucleating agent to increase the degree of crystallinity of PLA. The effect of the LCNFs lignin content on the PLA/LCNFs compatibility/adhesion was confirmed by the FTIR, SEM, and Tg results. Increasing the LCNFs lignin content increases the storage modulus of the PLA/LCNFs composites to a maximum for the PLA/9-LCNFs composite. This study shows that the lignin content has a considerable effect on the strength and flexibility of PLA/LCNFs composites.

scholarly journals Multi-layer Scaffolds of Poly(caprolactone), Poly(glycerol sebacate) and Bioactive Glasses Manufactured by Combined 3D Printing and Electrospinning

Nanomaterials ◽  
2020 ◽  
Vol 10 (4) ◽  
pp. 626 ◽  
Author(s):  
Adja B. R. Touré ◽  
Elisa Mele ◽  
Jamieson K. Christie
Keyword(s):  
3D Printing ◽  
Three Dimensional ◽  
Bioactive Glasses ◽  
Multi Scale ◽  
Potential Applications ◽  
3D Printed ◽  
Excellent Adhesion ◽  
Poly Caprolactone ◽  
Hydrolysis Of

Three-dimensional (3D) printing has been combined with electrospinning to manufacture multi-layered polymer/glass scaffolds that possess multi-scale porosity, are mechanically robust, release bioactive compounds, degrade at a controlled rate and are biocompatible. Fibrous mats of poly (caprolactone) (PCL) and poly (glycerol sebacate) (PGS) have been directly electrospun on one side of 3D-printed grids of PCL-PGS blends containing bioactive glasses (BGs). The excellent adhesion between layers has resulted in composite scaffolds with a Young’s modulus of 240–310 MPa, higher than that of 3D-printed grids (125–280 MPa, without the electrospun layer). The scaffolds degraded in vitro by releasing PGS and BGs, reaching a weight loss of ~14% after 56 days of incubation. Although the hydrolysis of PGS resulted in the acidification of the buffer medium (to a pH of 5.3–5.4), the release of alkaline ions from the BGs balanced that out and brought the pH back to 6.0. Cytotoxicity tests performed on fibroblasts showed that the PCL-PGS-BGs constructs were biocompatible, with cell viability of above 125% at day 2. This study demonstrates the fabrication of systems with engineered properties by the synergy of diverse technologies and materials (organic and inorganic) for potential applications in tendon and ligament tissue engineering.

Structure and properties of poly(lactic acid)/poly(lactic acid)-α-cyclodextrin inclusion compound composites

2017 ◽  
Vol 37 (9) ◽  
pp. 897-909
Author(s):  
Li Zhang ◽  
Weijun Zhen ◽  
Yufang Zhou
Keyword(s):  
Lactic Acid ◽  
Average Molecular Weight ◽  
Gel Permeation Chromatography ◽  
Mechanical Analysis ◽  
Poly Lactic Acid ◽  
Polymerization Temperature ◽  
Scanning Calorimetry ◽  
Synthesis Conditions ◽  
Cyclodextrin Inclusion ◽  
Comprehensive Performance

Abstract Poly(lactic acid) (PLA) was synthesized using a green catalyst, nano-zinc oxide (ZnO). The optimum synthesis conditions of PLA were as follows: a stoichiometric amount of 0.5 wt% of nano-ZnO, polymerization time of 14 h, and polymerization temperature of 170°C. Gel permeation chromatography results showed that the weight-average molecular weight (Mw) of PLA was 13,072 g/mol with a polydispersity index (PDI) of 1.7. Furthermore, PLA-α-cyclodextrin inclusion compounds (PLA-CD-ICs) were prepared by ultrasonic co-precipitation techniques. X-ray diffraction analysis and Fourier transform infrared spectroscopy demonstrated the change in lattice of α-CD from a cage configuration to a tunnel structure and the existence of some physical interactions between α-CD and PLA in the PLA-CD-ICs. To enhance the crystallization properties of PLA, PLA/PLA-CD-IC composites were blended with different contents of PLA-CD-ICs as nucleating agents. The crystallization behavior and comprehensive performance were investigated by differential scanning calorimetry, polarized optical microscopy, tensile testing, dynamic mechanical analysis, and scanning electron microscopy. Compared to PLA, the crystallinities of PLA/PLA-CD-IC composites were increased by 24.0%, 26.3%, 27.3%, and 31.8%. The results of all the analyses proved that PLA-CD-ICs were useful as green organic nucleators and improved the comprehensive performance of PLA materials.

scholarly journals Encapsulation of Diclofenac Molecules into Poly(-Caprolactone) Electrospun Fibers for Delivery Protection

2009 ◽  
Vol 2009 ◽  
pp. 1-8 ◽  
Author(s):  
Loredana Tammaro ◽  
Giuseppina Russo ◽  
Vittoria Vittoria
Keyword(s):  
Diclofenac Sodium ◽  
Composite Fibers ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Electrospinning Technique ◽  
In Vitro Drug Release ◽  
Good Thermal Stability ◽  
Fibrous Membranes ◽  
Poly Caprolactone

Mg-Al Hydrotalcite-like clay (LDH) intercalated with diclofenac anions (HTlc-DIC) was introduced into poly(-caprolactone) (PCL) in different concentrations by the electrospinning technique, and mats of nonwoven fibers were obtained and compared to the pristine pure electrospun PCL. The fibers, characterized by X-ray diffraction, thermogravimetric analysis, and differential scanning calorimetry, show an exfoliated clay structure up to 3 wt%, a good thermal stability of the diclofenac molecules and a crystallinity of PCL comparable to the pure polymer. The scanning electron microscopy revealed electrospun PCL and PCL composite fibers diameters ranging between 500 nm to 3.0 m and a generally uniform thickness along the fibers. As the results suggested the in vitro drug release from the composite fibers is remarkably slower than the release from the corresponding control spun solutions of PCL and diclofenac sodium salt. Thus, HTlc-DIC/PCL fibrous membranes can be used as an antinflammatory scaffold for tissue engineering.

scholarly journals Biodegradable 3D Printed Scaffolds of Modified Poly (Trimethylene Carbonate) Composite Materials with Poly (L-Lactic Acid) and Hydroxyapatite for Bone Regeneration

Nanomaterials ◽  
2021 ◽  
Vol 11 (12) ◽  
pp. 3215
Author(s):  
Honglei Kang ◽  
Xudong Jiang ◽  
Zhiwei Liu ◽  
Fan Liu ◽  
Guoping Yan ◽  
...  
Keyword(s):  
Lactic Acid ◽  
Composite Materials ◽  
Polymeric Materials ◽  
Bone Cell ◽  
Cell Multiplication ◽  
X Rays ◽  
Trimethylene Carbonate ◽  
Scanning Calorimetry

Biodegradable scaffolds based on biomedical polymeric materials have attracted wide interest in bone transplantation for clinical treatment for bone defects without a second operation. The composite materials of poly(trimethylene carbonate), poly(L-lactic acid), and hydroxyapatite (PTMC/PLA/HA and PTMC/HA) were prepared by the modification and blending of PTMC with PLA and HA, respectively. The PTMC/PLA/HA and PTMC/HA scaffolds were further prepared by additive manufacturing using the biological 3D printing method using the PTMC/PLA/HA and PTMC/HA composite materials, respectively. These scaffolds were also characterized by Fourier transform infrared spectroscopy (FT-IR), gel permeation chromatography (GPC), automatic contact-angle, scanning electronic micrographs (SEM), diffraction of X-rays (XRD), differential scanning calorimetry (DSC), and thermogravimetry (TG). Subsequently, their properties, such as mechanical, biodegradation, cell cytotoxicity, cell compatibility in vitro, and proliferation/differentiation assay in vivo, were also investigated. Experiment results indicated that PTMC/PLA/HA and PTMC/HA scaffolds possessed low toxicity, good biodegradability, and good biocompatibility and then enhanced the cell multiplication ability of osteoblast cells (MC3T3-E1). Moreover, PTMC/PLA/HA and PTMC/HA scaffolds enhanced the adhesion and proliferation of MC3T3-E1 cells and enabled the bone cell proliferation and induction of bone tissue formation. Therefore, these composite materials can be used as potential biomaterials for bone repatriation and tissue engineering.

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