Growth Of Hydroxyapatite Research Articles

Improving hydroxyapatite coating ability on biodegradable metal through laser-induced hydrothermal coating in liquid precursor: Application in orthopedic implants.

During the past decade, there has been extensive research toward the possibility of exploring magnesium and its alloys as biocompatible and biodegradable materials for implantable applications. Its practical medical application, however, has been limited to specific areas owing to rapid corrosion in the initial stage and the consequent complications. Surface coatings can significantly reduce the initial corrosion of Mg alloys, and several studies have been carried out to improve the adhesion strength of the coating to the surfaces of the alloys. The composition of hydroxyapatite (HAp) is very similar to that of bone tissue; it is one of the most commonly used coating materials for bone-related implants owing to favorable osseointegration post-implantation. In this study, HAp was coated on Mg using nanosecond laser coating, combining the advantages of chemical and physical treatments. Photothermal heat generated in the liquid precursor by the laser improved the adhesion of the coating through the precipitation and growth of HAp at the localized nanosecond laser focal area and increased the corrosion resistance and cell adhesion of Mg. The physical, crystallographic, and chemical bondings were analyzed to explore the mechanism through which the surface adhesion between Mg and the HAp coating layer increased. The applicability of the coating to Mg screws used for clinical devices and improvement in its corrosion property were confirmed. The liquid environment-based laser surface coating technique offers a simple and quick process that does not require any chemical ligands, and therefore, overcomes a potential obstacle in its clinical use.

Picosecond laser-induced hybrid groove structures on Ti-6Al-4V bio-alloy to accelerate osseointegration.

Regulating cell growth, extracellular matrix deposition and mineralization of artificial implants are some important parameters that decide the longevity of implants in the body. Picosecond laser-induced hybrid groove structures have been shown to improve these properties of the Ti-6Al-4V bio-alloy. Two hybrid structures containing groove patterns with periodic and non-periodic substructures therein were generated on Ti-6Al-4V by varying the extent of laser pulse overlapping on sample surface. Laser-induced alteration in surface topography, chemical composition and wettability of Ti-6Al-4V resulted in 3-fold increase in the rate of hydroxyapatite growth, 2.5-fold increment in protein adsorption and 2-fold enhancement in cell adhesion in comparison to pristine sample. While the periodic substructure was found to guide cell growth, the nonperiodic sub structure offered homogenous growth leading to higher overall cell density on the substrate surface.

Antibacterial 3D-Printed Silver Nanoparticle/Poly Lactic-Co-Glycolic Acid (PLGA) Scaffolds for Bone Tissue Engineering.

Infectious bone defects present a major challenge in the clinical setting currently. In order to address this issue, it is imperative to explore the development of bone tissue engineering scaffolds that are equipped with both antibacterial and bone regenerative capabilities. In this study, we fabricated antibacterial scaffolds using a silver nanoparticle/poly lactic-co-glycolic acid (AgNP/PLGA) material via a direct ink writing (DIW) 3D printing technique. The scaffolds' microstructure, mechanical properties, and biological attributes were rigorously assessed to determine their fitness for repairing bone defects. The surface pores of the AgNPs/PLGA scaffolds were uniform, and the AgNPs were evenly distributed within the scaffolds, as confirmed via scanning electron microscopy (SEM). Tensile testing confirmed that the addition of AgNPs enhanced the mechanical strength of the scaffolds. The release curves of the silver ions confirmed that the AgNPs/PLGA scaffolds released them continuously after an initial burst. The growth of hydroxyapatite (HAP) was characterized via SEM and X-ray diffraction (XRD). The results showed that HAP was deposited on the scaffolds, and also confirmed that the scaffolds had mixed with the AgNPs. All scaffolds containing AgNPs exhibited antibacterial properties against Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli). A cytotoxicity assay using mouse embryo osteoblast precursor cells (MC3T3-E1) showed that the scaffolds had excellent biocompatibility and could be used for repairing bone tissue. The study shows that the AgNPs/PLGA scaffolds have exceptional mechanical properties and biocompatibility, effectively inhibiting the growth of S. aureus and E. coli. These results demonstrate the potential application of 3D-printed AgNPs/PLGA scaffolds in bone tissue engineering.

Three-Dimensional-Bioprinted Bioactive Glass/Cellulose Composite Scaffolds with Porous Structure towards Bone Tissue Engineering.

In this study, three-dimensional (3D) bioactive glass/lignocellulose (BG/cellulose) composite scaffolds were successfully fabricated by the 3D-bioprinting technique with N-methylmorpholine-N-oxide (NMMO) as the ink solvent. The physical structure, morphology, mechanical properties, hydroxyapatite growth and cell response to the prepared BG/cellulose scaffolds were investigated. Scanning electron microscopy (SEM) images showed that the BG/cellulose scaffolds had uniform macropores of less than 400 μm with very rough surfaces. Such BG/cellulose scaffolds have excellent mechanical performance to resist compressive force in comparison with pure cellulose scaffolds and satisfy the strength requirement of human trabecular bone (2-12 MPa). Furthermore, BG significantly increased the excellent hydroxyapatite-forming capability of the cellulose scaffolds as indicated by the mineralization of the scaffolds in simulated body fluid (SBF). The BG/cellulose scaffolds showed low cytotoxicity to human bone marrow mesenchymal stem cells (hBMSCs) in the CCK8 assay. The cell viability reached maximum (percent of the control group) when the weight ratio of cellulose to BG was 2 in the scaffold. Therefore, the 3D-printed BG/cellulose scaffolds show a potential application in the field of bone tissue engineering.

DNA hydrogels for bone regeneration

DNA-based biomaterials have been proposed for tissue engineering approaches due to their predictable assembly into complex morphologies and ease of functionalization. For bone tissue regeneration, the ability to bind Ca2+ and promote hydroxyapatite (HAP) growth along the DNA backbone combined with their degradation and release of extracellular phosphate, a known promoter of osteogenic differentiation, make DNA-based biomaterials unlike other currently used materials. However, their use as biodegradable scaffolds for bone repair remains scarce. Here, we describe the design and synthesis of DNA hydrogels, gels composed of DNA that swell in water, their interactions invitro with the osteogenic cell lines MC3T3-E1 and mouse calvarial osteoblast, and their promotion of new bone formation in rat calvarial wounds. We found that DNA hydrogels can be readily synthesized at room temperature, and they promote HAP growth invitro, as characterized by Fourier transform infrared spectroscopy, X-ray diffraction, scanning electron microscopy, atomic force microscopy, and transmission electron microscopy. Osteogenic cells remain viable when seeded on DNA hydrogels invitro, as characterized by fluorescence microscopy. Invivo, DNA hydrogels promote the formation of new bone in rat calvarial critical size defects, as characterized by micro-computed tomography and histology. This study uses DNA hydrogels as a potential therapeutic biomaterial for regenerating lost bone.

Effect of pectin on the crystallization of strontium substituted HA for bone reconstruction application

The biomacropolymers of bone extracellular matrix (ECM) guide the growth of hydroxyapatite (HA) with various ionic substitutions. Pectin, a plant polysaccharide with chemical similarities to ECM, was investigated for its potential to promote the crystallization of strontium-substituted HA (SH). The influence of pectin (0.5 and 1.0 wt%) on the in situ mineralization of SH (10 and 30 mol% calcium substitution with strontium) was studied. The preferential affinity of pectin to strontium over calcium favoured the incorporation of strontium in apatite, decreased crystal size (18.85–26.22 nm) and retained more pectin residues (8–16%). The residual pectin strongly interacted with small SH particles, resulting in high microhardness (0.43–0.85 GPa) and high surface charge (−32.1 to −30.3 mV), while weak interaction with large HA particles resulted in low microhardness (0.15–0.25 GPa) and low surface charge (−35.4 to −34.6 mV). The in vitro cellular study using human osteoblast-like MG-63 cells demonstrated that inorganic size and material crystallinity play a vital role in regulating osteogenesis. The study suggests that the synchronization of low pectin concentration (0.5 wt%) and high strontium substitution in HA (30 mol%) offers the desired microhardness and in vitro osteogenic properties to emulate natural bone.

Piezoelectric signals of HAp and collagen with different glucose concentrations: A method for diabetes detection.

Piezoelectric signals were obtained from samples based on hydroxyapatite (HAp) and collagen (C) containing different glucose (G) concentrations. HAp was obtained by coprecipitation using Ca2+ and HPO42- as precursor ions in solution. C and G were added at the beginning of the coprecipitation method during the HAp growth. The presence of glucose in HAp and collagen samples drastically reduces the voltage amplitudes and considerably increases the relaxation times of the piezoelectric signals. HAp and collagen are the main constituents of bone, muscle, etc., then, it is possible to use piezoelectric technology for local and early detection of high glucose concentrations: small pressures applied by electrodes or by actuators placed in appropriate places on the body to establish a background concentration and, from this, to determine regions of the body with high local glucose concentrations: weak signals and large relaxation times are associated with a diminishing in the sensitivity, and are indicative of the presence of regions of abnormally high glucose concentrations.

The study of hydroxyapatite growth kinetics on CP – Ti and Ti65Zr treated by Plasma electrolytic oxidation process

The kinetics of hydroxyapatite growth on titanium alloys (CP–Ti and Ti65Zr) was studied. Specimens were treated by Plasma Electrolytic Oxidation (PEO) and immersed into the Hanks' solution. The PEO method was performed at AC mode with the current density of 4 A/dm2 in an electrolyte containing calcium acetate and calcium glycerophosphate, allowing the inclusion of calcium and phosphorus in the obtained oxide layer, which promotes the osseointegration when applied to bone tissue. The treated specimens were immersed in the Hanks’ solution with different exposure times, followed by studying changes in morphology, chemical, and phase composition. In addition, the surface wettability was tested, and the corrosion behavior of the treated samples was investigated. Tiny HA crystals can be seen on the surface of CP-Ti samples treated by PEO for 5 and 30 min. The morphology with a distinct layer of HA was obtained for the Ti65Zr sample after 5 min of PEO treatment. As for the immersion times, the highest crystal growth velocity was observed for the Ti65Zr of 5 min of PEO and 14 days of immersion. The change in morphology and EIS analysis confirms the observed behavior. Finally, based on the XRD analysis for the Ti65Zr of 5 min PEO treatment samples, the Srilankite phase in an amount of 60% is responsible for the crystal growth, resulting in the best crystal growth velocity and good corrosion properties (Rp = 0.732 MΩ cm2).

Mussel-Inspired Caries Management Strategy: Constructing a Tribioactive Tooth Surface with Remineralization, Antibiofilm, and Anti-inflammation Activity.

Dental caries is a common chronic oral disease in humans resulting from tooth demineralization caused by acid production of bacterial plaque, which leads to the destruction of enamel and dentin and oral inflammation. However, it is still a challenge that the function of natural active ingredients in currently available oral care products is not comprehensive, especially the lack of remineralization. Here, inspired by the strong biological adhesion ability of mussels and ancient oral disease plant therapy, a multifunctional strategy is proposed to construct a bioactive tooth surface to treat dental caries. It has been demonstrated that the Turkish gall extract (TGE) can inhibit adhesion of cariogenic bacteria Streptococcus mutans and Actinomyces viscosus and destroy biofilms on the tooth surface. Meanwhile, TGE can reduce the expression of inflammatory factors. Notably, the TGE coating can induce the growth of hydroxyapatite (HAP) crystals in vivo and in vitro, recovering the enamel mechanical properties under normal oral conditions. MD simulations interpreted the adsorption mechanism by which the hydroxyl groups in TGE bind to phosphate group (PO43-) on the tooth surface, attracting calcium ions (Ca2+) as nucleation sites for remineralization. This work underlines the importance of TGE coating in remineralization, antibiofilm, and anti-inflammation activity as a promising strategy for dental caries.

Biomimetic Growth of Hydroxyapatite in Hybrid Polycaprolactone/Graphene Oxide Ultra-Porous Scaffolds.

This paper reports the preparation and characterization of hybrid scaffolds composed of polycaprolactone (PCL) and different graphene oxide (GO) amounts, intending to incorporate the intrinsic characteristics of their constituents, such as bioactivity and biocidal effect. These materials were fabricated by a solvent-casting/particulate leaching technique showing a bimodal porosity (macro and micro) that was around 90%. The highly interconnected scaffolds were immersed in a simulated body fluid, promoting the growth of a hydroxyapatite (HAp) layer, making them ideal candidates for bone tissue engineering. The growth kinetics of the HAp layer was influenced by the GO content, a remarkable result. Furthermore, as expected, the addition of GO neither significantly improves nor reduces the compressive modulus of PCL scaffolds. The thermal behavior of composites was investigated by differential scanning calorimetry, showing an increase in crystallinity as the addition of GO raised, which implies that GO nanosheets can act as seeds to induce the crystallization of PCL. The improved bioactivity was demonstrated by the deposition of an HAp layer on the surface of the scaffold with GO, especially with a 0.1% GO content.

Hydroxyapatite nucleation and growth modulated by amino acid-capped gold nanoparticles: An in vitro study

Surface modification of biomaterials significantly influences implantable materials' surface reactivity to induce an apatite-like layer formation. This study observed the bioactivity and surface reactivity of modified biomaterials (calcium-deficient hydroxyapatite [CDHA] on amino acid-capped AuNPs [AA-AuNPs]) through immersion in simulated body fluid (SBF). AuNPs capped with eight different amino acids (AA)—both charged and polar uncharged AAs—showed the ability to induce the biomimetic hydroxyapatite formation. The presence of a hydroxyapatite peak in the X-ray powder diffraction (XRD) pattern indicated hydroxyapatite formation after all samples’ immersion in SBF. Moreover, longer immersion time in SBF contributed to the nucleation and growth of hydroxyapatite shown by the changing of the crystal structure including lattice parameters, crystallinity index, and crystallite size. The XRD results confirmed that surface modification using AA-AuNPs significantly affected the orientation of the hydroxyapatite crystal, where AAs served as a binding site for Ca2+ and PO43− ions. Furthermore, grayscale analysis based on scanning electron microscope images showed that charged AAs exhibited a role in hydroxyapatite nucleation and growth while polar uncharged AAs only contributed to hydroxyapatite growth. The calculated Ca/P ratio also confirmed the formation of hydroxyapatite from CDHA. XRD and scanning electron microscopy/energy-dispersive X-ray spectroscopy results signify the bioactivity of CDHA-modulated AA-AuNPs in hydroxyapatite formation for new bone tissue regeneration.

Cooperative Calcium Phosphate Deposition on Collagen-Inspired Short Peptide Nanofibers for Application in Bone Tissue Engineering.

In recent years, immense attention has been devoted over the production of osteoinductive materials. To this direction, collagen has a dominant role in developing hard tissues and plays a crucial role in the biomineralization of these tissues. Here, we demonstrated for the first time the potential of the shortest molecular pentapeptide domain inspired from collagen toward mineralizing hydroxyapatite on peptide fibers to develop bone-filling material. Our simplistic approach adapted the easy and facile route of introducing the metal ions onto the peptide nanofibers, displaying adsorbed glutamate onto the surface. This negatively charged surface further induces the nucleation of the crystalline growth of hydroxyapatite. Interestingly, nucleation and growth of the hydroxyapatite crystals lead to the formation of a self-supporting hydrogel to construct a suitable interface for cellular interactions. Furthermore, microscopic and spectroscopic investigations revealed the crystalline growth of the hydroxyapatite onto peptide fibers. The physical properties were also influenced by this crystalline deposition, as evident from the hierarchical organization leading to hydrogels with enhanced mechanical stiffness and improved thermal stability of the scaffold. Furthermore, the mineralized peptide fibers were highly compatible with osteoblast cells and showed increased cellular biomarkers production, which further reinforced the potential application toward effectively fabricating the grafts for bone tissue engineering.

Regulation of recombinant humanized collagen on HAP growth and its molecule simulation.

Hydroxyapatite (HAP) in natural bone is formed under the regulation of natural collagen I. Here, we report how recombinant humanized collagen I (rhCol I) regulates the growth of HAP nanocrystals in a long belt shape 100-150 nm in width and 200-300 nm in length. MD simulation results showed that the interactions between rhCol I and the (001), (100), and (211) planes of HAP mainly contributed to the electrostatic force and van der Waals forces via COO⋯Ca, -NH⋯Ca, CH⋯OPO3, and NH⋯OPO3 bonds, respectively. On the (001) plane, the interaction between -COO- and Ca was stronger than on the (100) and (211) planes, resulting in a large electrostatic force, which inhibited the growth of the (001) plane. The lowest energy of adsorption to the (211) plane resulted in the preferential growth of the (211) plane due to the weakest interaction with rhCol I. The detailed correlation between HAP and rhCol I could explain HAP growth under regulation by rhCol I. This study provides a reference for the bio-application of recombinant collagen.

20 - Peptide-DNA hybrid nanostructures as scaffolds for hydroxyapatite growth

20 - Peptide-DNA hybrid nanostructures as scaffolds for hydroxyapatite growth

Hydroxyapatite Growth on Activated Carbon Surface for Methylene Blue Adsorption: Effect of Oxidation Time and CaSiO3 Addition on Hydrothermal Incubation

Many adsorbent materials are now commercially available; however, studies have focused on modifying them to enhance their properties. In this study, an activated carbon (AC) and hydroxyapatite (HAp) composite was synthesized by the immersion of ACs in a simulated body fluid solution, varying the AC oxidation degree along with the addition of CaSiO3. The resulting composites were characterized by ash %, X-ray fluorescence (XRF), Fourier-transformed infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and point of zero charge (PZC). The characterization results indicated that the addition of CaSiO3 and the oxygenated functional groups in the AC surface are key factors for HAp growth. The composites were tested on methylene blue (MB) adsorption as a potential application for the synthesized materials. Adsorption isotherms were modeled with Langmuir and Freundlich isotherms, and the composites were fitted to a Langmuir model with the highest qmax value of 9.82. The kinetic results indicated that for the pseudo-second-order model, the composites fitted, with a contact time of 180 min to remove a 95.61% average of the MB. The results indicate that composite materials can be an efficient adsorbent for the removal of MB from aqueous solutions at low concentrations since the material with the highest amount of HAp growth removed 99.8% of the MB in 180 min.

Effect of tantalum interlayer on hydroxyapatite biointerface for orthopedic applications

Various attempts have been made during recent decades to improve the functionality, biocompatibility and osseointegration of metallic implants. With technological advancement, modifying superficial properties of orthopedic implants has undergone great evolution. Current efforts of scientists and the orthopedic industry have focused on modifying surface properties to achieve a specific biointerface that can reduce patient's healing time and prevent aseptic loosening. This study investigates the contribution of a protective tantalum interlayer deposited on titanium substrates on the growth of hydroxyapatite (HAp) crystals with hydrothermal synthesis method. We investigated the morphology and structure of the produced coatings, as well as in vitro bioactivity in simulated body fluid and biocompatibility in osteoblast-like cell culture. The hydrothermal method allows to synthesize coating with micro-sized HAp crystallites that exhibit rod-like hexagonal shape. The diameter of HAp crystallites may be controlled and driven by nature of the interlayer (tantalum, tantalum oxide or titanium oxide) previously formed on the titanium substrate. Coatings with smaller diameters of HAp crystals (between 0,3 μm and 0,6 μm) synthesized on tantalum-based films were found to be more favorable for cell viability and attachment. High bioactivity and positive effect on the osteoblast-like cells of the HAp biointerface with a tantalum intermediate layer was observed.

A novel borate-based 45S5 Bioglass®: In vitro assessment in phosphate-buffered saline solution

A novel borate-based 45S5 Bioglass® has been formulated and synthesized using the melt-quenching method. The in vitro assessment was performed to determine the bioactivity of the glasses using phosphate buffer saline (PBS) as an immersion solution. The pH measurement is performed using a pH meter, while ion dissolution is quantified using Inductively coupled plasma atomic emission spectrometer (ICP-OES). The immersion of borate-containing glass exhibits pH closes to human body fluid (≈7.40). The (Ca/P) atomic ratio was calculated and its value increased (1.7–4.0) along with borate contents, indicating improved bioactivity. The alteration of glass structure after the in vitro test is inspected using attenuated total reflectance sensor–Fourier transform infrared spectrophotometer (ATR-FTIR) and Raman spectrometer. The 45S5 Bioglass that comprised 40–80% of borate showed the appearance of HPO42− a vibration band which specifies the growth of hydroxyapatite (HPA) after the in vitro test. Relative to 45S5 Bioglass®, glass labeled 0.4B2O3 displayed the highest potential of HPA growth (248%), while dissolving BO3 and BO4 units at 57.36 and 8.48%, respectively. The new formulation technique offers an alternative path to control the degradation behavior of 45S5 Bioglass® glass by modifying the ratio of borate constituent. The prepared glass may find its potential in soft-bone tissue engineering applications.

Evaluation of quaternization effect on chitosan-HAP composite for bone tissue engineering application

This study attempts to improve the aqueous solubility of chitosan and utilizes it in the fabrication of composites with hydroxyapatite (HAP). The composites were evaluated as a curcumin delivery vehicle for bone regeneration. The chitosan was modified by quaternization, with a quaternization degree of 5 % for low quaternized chitosan (LQC) and 11 % for high quaternized chitosan (HQC). The modified chitosan, at alkaline pH 11, facilitated in situ HAP growth and formed LQC-HAP and HQC-HAP composites. The quaternization weakens intermolecular hydrogen bonds, facilitates interaction with the apatite precursor ions and promotes the growth of HAP. The modification significantly improved drug encapsulation (2.6 fold) but at the cost of a slight decrease in mechanical strength and increase in drug release. The in vitro studies with human osteoblast-like MG-63 cells established that the curcumin-loaded composites, LQC-HAP-C and HQC-HAP-C are biocompatible, encourage proliferation and promote a 2-fold increase in calcium mineralization over drug-free composites. The study exemplifies the reciprocity between quaternization degree and drug load/release properties and also illustrates that the magnitude of the latter reflects bioactivity. Thus, the quaternized chitosan-based HAP composite with tailorable bio-physicochemical properties becomes an interesting drug delivery system in bone regeneration.

A novel flexible, conductive, and three-dimensional reduced graphene oxide/polyurethane scaffold for cell attachment and bone regeneration

Development of conductive and three-dimensional scaffolds with elastic properties and shape-recovery capability for bone regeneration within irregular bone cavities has been challenging. Polyurethanes (PUs) are intrinsically elastic polymers; however, their mechanical performance, biocompatibility, and functionality need to be improved for application as implants and biomedical devices. Herein, application of a novel flexible, conductive, and three-dimensional polyurethane scaffold (3DPU), fabricated through coating a commercial PU foam with graphene oxide (GO) and its subsequent reduction with ascorbic acid, described as 3DrGO/PU, is investigated for bone regeneration. The 3DrGO/PU scaffold supported the growth and proliferation of mouse osteoblast cells (MG-63) with strong mineralization and cell attachment. It is likely that the electrically conductive macro-porous 3DrGO/PU scaffold, provides bioactivity and promote nucleation and growth of hydroxyapatite (HA) in the simulated body fluid. Experiments assessing in vivo bone formation in rat calvarial skull defects provided clear evidence for efficacy of the 3D scaffold for treatment of irregular bone defects. The results of this study are promising, as they present easy production of a cost-effective green fabricated scaffold. It also offers a potential for cell attachment and capture, to be used in future tissue engineering and even biosensing applications.

Improved shape stability and ceramifiable properties of ceramifiable polyethylene composites by crystallization reaction

Wollastonite fiber (WF) was added to further improve shape stability and ceramifiable properties of polyethylene (PE)/ mica/ phosphate glass frits (PGF) composites. To evaluate shape stability property, the surface cracking of ceramic-like residues obtained by calcining at different temperatures were observed, and dimensional variation and self-supporting properties of the residues were measured. The ceramifiable properties (flexural strength and apparent porosity) of the PE composites were also investigated. Results showed that the addition of WF reduced surface cracking effectively, improved dimensional stability and self-supporting properties. Furthermore, at high temperatures, the flexural strength of the PE composites was enhanced by incorporation of WF, accompanying with the reduction of porosity. X-ray diffraction (XRD), scanning electron microscopy (SEM) and energy dispersive spectroscopy (EDS) were used to analyze the effect of WF on the performance of the PE composites. Results showed that there was a novel crystalline phase hydroxyapatite (HAP) was formed within the residues. During the heat treatment process, WF acted as the promoter to participate in a crystallization reaction with molten phosphate glassy phase by the way of ion diffusion to generate the HAP. The crystallization thermodynamics demonstrated that the reaction could occur spontaneously above 873 K. Crystallization reaction improved the crystallinity, which was beneficial to enhance the flexural strength. Moreover, crystallization kinetic analysis was investigated. The results indicated that the growth of crystal HAP was promoted with the increase of temperature and the flow of glassy phase was limited, which improved the shape stability. Therefore, it was inferred that crystallization reaction played an important role in the improvement of the shape stability and ceramifiable properties of PE composite simultaneously.