Degradation Of PLA Research Articles

Quantitative analysis of factors determining the enzymatic degradation of poly(lactic acid)

The enzymatic degradation of poly(lactic acid) was catalyzed with Proteinase K and the effect of various factors on the rate of degradation was analyzed quantitatively with the help of appropriate kinetic models. The Michaelis-Menten model was modified for the purpose by considering the heterogeneous nature of the reaction and the denaturation of the enzyme. The results proved that Proteinase K degrades the polymer very efficiently. The rate of degradation increases considerably up to 0.1 mg/ml enzyme concentration, but remains constant at larger values. Temperature has an optimum at around 50 °C that is somewhat higher than the 37 °C extensively used in the literature as the most advantageous temperature. If degradation occurs in the same medium throughout the process, the formation of lactic acid results in the rapid decrease of pH and finally in the denaturation of the enzyme. The dropping of pH below 5 slows down and finally stops degradation completely. The daily change of the medium results in degradation with a constant rate and the entire amount of the polymer can be decomposed mainly into monomer or smaller oligomer fragments. Degradation rate decreases slightly with increasing molecular weight and increasing d-lactide content. The use of appropriate kinetic models allows quantitative analysis and the prediction of the rate of enzymatic degradation of PLA.

Earthworms' Degradable Bioplastic Diet of Polylactic Acid: Easy to Break Down and Slow to Excrete.

Microplastics (MPs) in soils may be ingested by terrestrial animals. While the application of bioplastics is increasing, the ingestion and excretion characteristics of bio-MPs by terrestrial animals are poorly understood as compared to fossil-MPs. Here, the approach-avoidance behavior of adult earthworms Eisenia fetida to MP-contaminated soil was assessed. Fossil-based poly(ethylene terephthalate) (PET) and bio-based poly(lactic acid) (PLA) MPs were found to be preferred by the earthworms, which might be due to the odor of polymer monomers. MPs in earthworm casts were analyzed by microscopy counting and liquid chromatography-tandem mass spectrometry. The amount of microscopically recognizable excreted PET and PLA was 553 and 261 items/g, respectively, while a higher proportion of smaller PLA particles also presented. Bio-based PLA is much easy to break down by earthworms than fossil-based PET. Submicron and nanocron PLA accounted for 57 and 13% of the excreted PLA on the 10th day of excretion. MP excretion was well described with the first-order kinetic model, and the elimination half-life was 9.3 (for PET) and 45 h (for PLA). A longer excretion period of PLA may be related to its potential to break down in the earthworms' digestive tract. This not only promotes the environmental degradation of PLA but also suggests the ecological risk caused by nanoparticles.

Use of oil palm frond waste to reinforce poly(lactic acid) based composites with the improvement of interfacial adhesion by alkali treatment

Oil palm frond waste was used as reinforcing fibers for biodegradable poly(lactic acid) or PLA in order to produce green composites that increased the value of agricultural waste. The alkali-treated oil palm frond (OPF) fibers of 30 wt% or 40 wt% were compounded with PLA and moulded into specimens. The alkali treatment was 0 wt%, 1 wt%, 3 wt%, and 5 wt% of the fibers for compatibility improvement with PLA matrix. It was found that the alkali-treated PLA/OPF composites adding 30 wt% and 40 wt% had the flexural modulus to be about 55% and 75% higher than those without the treatment, respectively. Tensile modulus of the composites was also increased. Nevertheless, the higher rigidity composites became more brittle as evident by the fracture toughness testing. The increase of total breaking energy confirmed the better interfacial adhesion between phases as shown in SEM micrographs. The glass transition temperature (Tg) of PLA matrix in the composites was shifted to lower temperature attributed to the thermal degradation of PLA during the melt compounding confirmed by the lower degradation temperature. Increasing the alkali concentration for surface treatment caused the Tg of PLA composites to be higher, supporting that the improvement of interfacial adhesion was achieved.

PLA/Hydroxyapatite scaffolds exhibit in vitro immunological inertness and promote robust osteogenic differentiation of human mesenchymal stem cells without osteogenic stimuli

Bone defects stand out as one of the greatest challenges of reconstructive surgery. Fused deposition modelling (FDM) allows for the printing of 3D scaffolds tailored to the morphology and size of bone damage in a patient-specific and high-precision manner. However, FDM still suffers from the lack of materials capable of efficiently supporting osteogenesis. In this study, we developed 3D-printed porous scaffolds composed of polylactic acid/hydroxyapatite (PLA/HA) composites with high ceramic contents (above 20%, w/w) by FDM. The mechanical properties of the PLA/HA scaffolds were compatible with those of trabecular bone. In vitro degradation tests revealed that HA can neutralize the acidification effect caused by PLA degradation, while simultaneously releasing calcium and phosphate ions. Importantly, 3D-printed PLA/HA did not induce the upregulation of activation markers nor the expression of inflammatory cytokines in dendritic cells thus exhibiting no immune-stimulatory properties in vitro. Evaluations using human mesenchymal stem cells (MSC) showed that pure PLA scaffolds exerted an osteoconductive effect, whereas PLA/HA scaffolds efficiently induced osteogenic differentiation of MSC even in the absence of any classical osteogenic stimuli. Our findings indicate that 3D-printed PLA scaffolds loaded with high concentrations of HA are most suitable for future applications in bone tissue engineering.

Degradation of wheat straw/polylactic acid composites by Aspergillus niger

AbstractPolylactic acid has good biodegradability and it is dosage is increasing. Therefore, the degradation of PLA has become a new problem that needs serious management. In this study, the spores of Aspergillus niger were inoculated onto wheat straw/PLA composites containing different contents of sodium alginate, and the mass loss and characterization (microstructure, fourier transform infrared spectroscopy, thermal properties, and X‐ray diffraction) of the composites were detected. The objective was to explore the possibility of degradation of PLA composites by A. niger and the effect of sodium alginate on the degradability of PLA composites. The results showed that when the amount of sodium alginate was 3% and 6%, the mass loss rate of the composites only increased at the initial stage of degradation. However, when the amount of sodium alginate was 9%, the mass loss rate of the composites was significantly increased. It was found that A. niger could colonize the surface of the composites and cause cracks and depressions on the surface by morphological observation. The infrared spectral curve showed that the number of hydroxyl and carbonyl groups in the composites increased after degradation. According to the thermogravimetric curve of the composites, the pyrolysis temperature of the composites with sodium alginate content of 9% increased and the residual mass decreased after degradation. When the amount of sodium alginate was 9%, the crystallinity of the composites was greatly reduced, and it is crystallization zone was easier to degrade compared with other treatments. The results would provide a theoretical support for the rapid degradation of PLA composites.

N‐Heterocyclic Phosphines as Precatalysts for the Highly Selective Degradation of Poly(lactic acid)

AbstractAn N‐heterocyclic phosphine (NHP) has been investigated as a catalyst for transesterification of a range of commercial polymer samples. NHP catalysed degradation of poly(lactic acid) with methanol provides access to methyl lactate (MeLA) in high yields over the course of days. In situ NMR spectroscopy and kinetic analysis has provided quantitative assessment of the catalyst, and a solvent screen is reported. Surprisingly attempts to depolymerise polycaprolactone (PCL) and polyethylene terephthalate (PET) were unsuccessful, and reactions mixed PLA/PCL and PLA/PET provided completely specific degradation of the PLA alone. NMR analysis of the catalyst provides insight into its solution speciation, indicating that the NHP does not remain intact under the transesterification conditions. The enediamine, tBuN(H)CH=CHN(H)tBu, was shown to be formed via methanolysis of the NHP and proved to be a selective catalyst for PLA degradation. Assessment of the depolymerisation activity of by‐products of the NHP methanolysis suggest this is the active catalyst.

Characterization of Potential Pollutants from Poly(lactic acid) after the Degradation Process in Soil under Simulated Environmental Conditions

In recent years, the amount of produced petrochemical plastic waste has been growing at an alarming rate. According to the Plastics Europe Market Research Group (PEMRG)/Conversio Market & Strategy GmbH, in 2018 the global production of plastics amounts to 359 million tons, and in Europe—61.8 million tons. More than 80% of all marine litter is plastic, which accumulates in the environment due to its durability. Due to the growing problem, biodegradable polymer products are introduced to the market. Therefore, it is necessary to conduct research on degradation products in order to estimate the risk arising from their presence in the environment. This paper discusses research on compounds that may potentially remain in the soil after the degradation of the double green PLA polymer. The aim of the research was to prove whether products made of PLA, e.g., packaging, films and other waste can release substances harmful to the environment. Therefore, soil was selected as a medium to characterize the substances potentially released from the polymer under conditions simulating the degradation process in the environment. The soil was always used from the same producer. Before the polymer biodegradation process, it was additionally checked for pH, C and N content, number of microorganisms, etc. PLA degradation in soil was carried out in a laboratory accredited by the Polish Accreditation Center (PCA). During the research, soil samples at various stages of the degradation process under laboratory conditions were subjected to both extraction in an aqueous environment and organic solvent extraction The studies used the gas chromatography coupled with mass spectrometry (GC/MS), as well as pyrolysis gas chromatography (Py-GC/MS). In addition, the study used the gel permeation chromatography (GPC/SEC) allowing to determine the distribution of molar masses, average molar masses and polydispersity, and the infrared spectroscopy (FTIR).

Kinetics of the Thermal Degradation of Poly(lactic acid) and Polyamide Bioblends.

Poly(lactic acid) (PLA) and biosourced polyamide (PA) bioblends, with a variable PA weight content of 10–50%, were prepared by melt blending in order to overcome the high brittleness of PLA. During processing, the properties of the melt were stabilized and enhanced by the addition of a styrene-acrylic multi-functional-epoxide oligomeric reactive agent (SAmfE). The general analytical equation (GAE) was used to evaluate the kinetic parameters of the thermal degradation of PLA within bioblends. Various empirical and theoretical solid-state mechanisms were tested to find the best kinetic model. In order to study the effect of PA on the PLA matrix, only the first stage of the thermal degradation was taken into consideration in the kinetic analysis (α < 0.4). On the other hand, standardized conversion functions were evaluated. Given that it is not easy to visualize the best accordance between experimental and theoretical values of standardized conversion functions, an index, based on the integral mean error, was evaluated to quantitatively support our findings relative to the best reaction mechanism. It was demonstrated that the most probable mechanism for the thermal degradation of PLA is the random scission of macromolecular chains. Moreover, y(α) master plots, which are independent of activation energy values, were used to confirm that the selected reaction mechanism was the most adequate. Activation energy values were calculated as a function of PA content. Moreover, the onset thermal stability of PLA was also determined.

Hydrolytic Degradation of 3D-Printed Poly (Lactic Acid) Structures

Hydrolytic degradation of commercially available 3D printing filament, i.e. poly (lactic acid) with broad molecular weight distribution was induced by incubating 3D-printed parts in deionized water at 3 temperatures. Small changes in orthogonal dimensions occurred due to relaxation of printing stresses, but no mass or volume loss were detected over the time-frame of the experiments. Molecular weight decreased while polydispersity remained constant. The most sensitive measure of degradation was found to be nondestructive, small-amplitude oscillatory tensile measurements. A rapid decay of tensile storage modulus was found with an exponential decay time constant of about an hour. This work demonstrates that practical monitoring of commercially available PLA degradation can be achieve with linear viscoelastic measurements of modulus.

Development of Bio-Composites with Enhanced Antioxidant Activity Based on Poly(lactic acid) with Thymol, Carvacrol, Limonene, or Cinnamaldehyde for Active Food Packaging.

The new trend in food packaging films is to use biodegradable or bio-based polymers, such as poly(lactic acid), PLA with additives such as thymol, carvacrol, limonene or cinnamaldehyde coming from natural resources (i.e., thyme, oregano, citrus fruits and cinnamon) in order to extent foodstuff shelf-life and improve consumers’ safety. Single, triple and quadruple blends of these active compounds in PLA were prepared and studied using the solvent-casting technique. The successful incorporation of the active ingredients into the polymer matrix was verified by FTIR spectroscopy. XRD and DSC data revealed that the crystallinity of PLA was not significantly affected. However, the Tg of the polymer decreased, verifying the plasticization effect of all additives. Multicomponent mixtures resulted in more intense plasticization. Cinnamaldehyde was found to play a catalytic role in the thermal degradation of PLA shifting curves to slightly lower temperatures. Release of thymol or carvacrol from the composites takes place at low rates at temperatures below 100 °C. A combined diffusion-model was found to simulate the experimental release profiles very well. Higher antioxidant activity was noticed when carvacrol was added, followed by thymol and then cinnamaldehyde and limonene. From the triple-component composites, higher antioxidant activity measured in the materials with thymol, carvacrol and cinnamaldehyde.

Improving the flame retardancy and accelerating the degradation of poly (lactic acid) in soil by introducing fully bio-based additives

In this study, a novel bio-based flame retardant LC-PA is prepared by the Mannich reaction between phytic acid (PA) and L-citrulline (LC). LC-PA is combined with tannic acid (TA) and introduced into PLA to improve fire performance and accelerate biodegradability. Compared with control PLA, the PLA composite containing 10% LC-PA/TA increases the LOI value to 26.9%, reaches a V-0 rating in the UL-94 test, and reduces the peak heat release rate and total heat release by 24.5% and 21.1%, respectively. More importantly, the introduction of LC-PA/TA accelerates the degradation rate of PLA in soil, which is of significance for biodegradable materials. The addition of LC-PA/TA can attract water and provide a suitable energy source for microbial proliferation, accelerating the hydrolysis and microbial degradation of PLA. This work provides a practical approach for high flame retardancy and rapid biodegradability in the soil to the bio-based polymer.

Effects of compost, cover crops, and local conditions on degradation of two agricultural mulches in soil

AbstractBiobased and biodegradable mulches (BDM) are a potentially sustainable alternative to polyethylene plastic mulch because they can be tilled into the soil at the end of the growing season. However, their degradation rate in the soil is uncertain, limiting their on-farm adoption. The objective of this study was to determine whether organic soil management practices could be leveraged to speed degradation of two potentially BDM across two diverse agroecoregions [Lincoln (LNK) and Scottsbluff (SBF), NE, USA]. Management treatments included compost, compost extract, cover crops, all three of these practices combined and a control. The two mulch types studied were a nonwoven polylactic acid fabric with embedded wood particles (PLA), and a starch-polyester mulch film (BLK). Mulches were applied in spring 2017 for vegetable production and removed in fall after harvest. Recovered mulch was sectioned into squares 10 cm2and buried in mesh bags for 22 months. Mulch degradation, and soil chemical, physical and biological properties were measured at four times over 2 years. Management treatments applied seasonally across 2 years led to expected changes in soil properties, yet they had no effect on mulch degradation. Instead, mulch degradation was driven by the interaction of location and mulch type. The BLK mulch had degraded by 98% at LNK after 12 months, but only by half after 22 months at SBF. Degradation of PLA after 22 months was similar between locations with 29 ± 4% mulch mass remaining at SBF and 33 ± 4% remaining at LNK. Climate and soil characteristics at each location were strong determinants of mulch degradation. Specifically, soils at LNK were finer textured, lower in pH, higher in soil water content, organic matter and nitrates, and with greater bacterial abundance compared to SBF. The strong location by mulch type interaction observed could inform the development of regionally specific predictive models of degradation.

A new strategy to prepare fully bio-based poly(lactic acid) composite with high flame retardancy, UV resistance, and rapid degradation in soil

Despite the advantages of biological compatibility and high transparency, there are still some drawbacks for Poly(lactic acid) (PLA) such as highly flammability and poor ultraviolet resistance. Herein, a fully bio-based additive (PA@CHTM) with a core–shell structure is synthesized by chitosan microspheres and phytic acids. The introduction of PA@CHTM simultaneously improves the mechanical properties, flame retardancy, and UV-blocking performance of PLA, accompanied by an accelerated degradation capacity in soil. By the presence of 9 wt% PA@CHTM in the PLA composite sample, the limiting oxygen index value is increased from 18.2% to 29.6%, and the UL-94 test grade is improved to V-0. The tensile strength is well maintained and Young's modulus is sharply increased for PLA/PA@CHTM composites. Moreover, the photoaging process of PLA can be significantly delayed due to the excellent free radical quenching capacity of PA@CHTM. Only less than 10% UV light can be penetrated for the PLA/9%PA@CHTM sample, and the ultraviolet protection factor is increased from 0.77 of control PLA to 30.07. More importantly, the addition of PA@CHTM can accelerate the degradation of PLA, which is of significance for biodegradable materials. This work firstly provides a green strategy to fabricate fully bio-based polymer composites with high performance, long service life, and rapid degradation in soil.

Degradation mechanisms and acceleration strategies of poly (lactic acid) scaffold for bone regeneration

Poly (lactic acid) (PLA) with good biodegradability, biocompatibility and processability has a wide application prospect in bone tissue engineering. However, PLA exhibits a very slow degradation rate, hindering the regeneration of new bone. In this study, the degradation mechanisms of PLA bone scaffold, including autocatalysis and non-catalysis, end-chain and random chain breaking, surface degradation and bulk degradation, were analyzed systematically, and the influence factors including crystallinity, molecular weight, pH, and so on, were introduced. On this basis, the strategies including blending, copolymerization, compounding and surface modification to accelerate the degradation of PLA were summarized, and the accelerating mechanisms were analyzed and discussed detailedly. In addition, rapid prototyping technologies with unique advantages on the structure and shape of scaffold were introduced. The mechanical properties (strength and modulus) and biological properties (in vivo and in vitro) of PLA scaffold were reviewed and discussed. Finally, the present problem of research including the simultaneous improvement of mechanical and degradation properties was put forward, and four-dimensional printing (4D printing) as an advanced technique which might bring new ideas to improve and extend the properties of PLA scaffold was mentioned.

Genome Annotation of Poly(lactic acid) Degrading Pseudomonas aeruginosa, Sphingobacterium sp. and Geobacillus sp.

Pseudomonas aeruginosa and Sphingobacterium sp. are well known for their ability to decontaminate many environmental pollutants while Geobacillus sp. have been exploited for their thermostable enzymes. This study reports the annotation of genomes of P. aeruginosa S3, Sphingobacterium S2 and Geobacillus EC-3 that were isolated from compost, based on their ability to degrade poly(lactic acid), PLA. Draft genomes of the strains were assembled from Illumina reads, annotated and viewed with the aim of gaining insight into the genetic elements involved in degradation of PLA. The draft genome of Sphinogobacterium strain S2 (435 contigs) was estimated at 5,604,691 bp and the draft genome of P. aeruginosa strain S3 (303 contigs) was estimated at 6,631,638 bp. The draft genome of the thermophile Geobacillus strain EC-3 (111 contigs) was estimated at 3,397,712 bp. A total of 5385 (60% with annotation), 6437 (80% with annotation) and 3790 (74% with annotation) protein-coding genes were predicted for strains S2, S3 and EC-3, respectively. Catabolic genes for the biodegradation of xenobiotics, aromatic compounds and lactic acid as well as the genes attributable to the establishment and regulation of biofilm were identified in all three draft genomes. Our results reveal essential genetic elements that facilitate PLA metabolism at mesophilic and thermophilic temperatures in these three isolates.

Effect of poly(ε‐caprolactone) and titanium (IV) dioxide content on the UV and hydrolytic degradation of poly(lactic acid)/poly(ε‐caprolactone) blends

AbstractThe effect of accelerated weathering degradation on the properties of poly(lactic acid) (PLA)/poly(ε‐caprolactone) (PCL) blends and PLA/PCL/titanium (IV) dioxide (TiO2) nanocomposites are presented in this paper. The results show that both polymers are susceptible to weathering degradation, but their degradation rates are different and are also influenced by the presence of TiO2 in the samples. Visual, microscopic and atomic force microsocpy observations of the surface after accelerated weathering tests confirmed that degradation occurred faster in the PLA/PCL blends than in the PLA/PCL/TiO2 nanocomposites. The X‐ray diffraction results showed the degradation of PCL in the disappearance of its characteristic peaks over weathering time, and also confirmed that PLA lost its amorphous character and developed crystals from the shorter chains formed as a result of degradative chain scission. It was further observed that the presence of TiO2 retarded the degradation of both PLA and PCL. These results were supported by the differential scanning calorimetry results. The thermogravimetric analysis results confirmed that that PLA and PCL respectively influenced each other's thermal degradation, and that TiO2 played a role in the thermal degradation of both PLA and PCL. The tensile properties of both PLA/PCL and PLA/PCL/TiO2 were significantly reduced through weathering exposure and the incorporation of TiO2.

A Slow-Release Fertilizer of Urea Prepared via Melt Blending with Degradable Poly(lactic acid): Formulation and Release Mechanisms.

In this research, a low molecular weight poly(lactic acid) (or PLA) synthesized from direct polycondensation was melt compounded with urea to formulate slow-release fertilizer (SRF). We studied the influence of the molecular weight (MW) of PLA as a matrix and the urea composition of SRF towards release kinetics in water at 30 °C. The physical appearance of solid samples, the change in urea concentration, and acidity (pH) of water were monitored periodically during the release test. Three studied empirical models exhibited that diffusion within the matrix dominated the urea release process, especially when the release level was less than 60%. Thus, a lower MW of PLA and a higher urea content of SRF showed a faster release rate. For the entire length of the release experiment, a combination of diffusion and degradation mechanisms exhibited the best agreement with the experimental data. The hydrolytic degradation of PLA may begin after 96 h of immersion (around 60% release level), followed by the appearance of some micro-holes and cracks on the surface of the SRF samples. Generally, this research revealed the good release performance of urea without residues that damage the soil structure and nutrient balance.

Effect of Cellulose and Cellulose Nanocrystal Contents on the Biodegradation, under Composting Conditions, of Hierarchical PLA Biocomposites.

In this work, the effect of microfibrillated cellulose (MFC) and cellulose nanocrystals (CNCs) on the biodegradation, under composting conditions, of hierarchical PLA biocomposites (HBCs) was studied using a full 22 factorial experimental design. The HBCs were prepared by extrusion processing and were composted for 180 days. At certain time intervals, the specimens were removed from the compost for their chemical, thermal and morphological characterizations. An ANOVA analysis was carried out at different composting times to study MFC and CNCs’ effects on biodegradation. The specimen’s mass loss and molecular weight loss were selected as independent variables. The results show that the presence of MFC enhances the PLA biodegradation, while with CNCs it decreases. However, when both cellulosic fibers are present, a synergistic effect was evident—i.e., in the presence of the MFC, the inclusion of the CNCs accelerates the HBCs biodegradation. Analysis of the ANOVA results confirms the relevance of the synergistic role between both cellulosic fibers over the HBC biodegradation under composting conditions. The results also suggest that during the first 90 days of incubation, the hydrolytic PLA degradation prevails, whereas, beyond that, the enzymatic microbial biodegradation dominates. The SEM results show MFC’s presence enhances the surface biodeterioration to a greater extent than the CNCs and that their simultaneous presence enhances PLA biodegradation. The SEM results also indicate that the biodegradation process begins from hydrophilic cellulosic fibers and promotes PLA biodegradation.

Towards Controlled Degradation of Poly(lactic) Acid in Technical Applications

Environmental issues urge for the substitution of petrochemical-based raw materials with more environmentally friendly sources. The biggest advantages of PLA over non-biodegradable plastics are that it can be produced from natural sources (e.g., corn or sugarcane), and at the end of its lifetime it can be returned to the soil by being composted with microorganisms. PLA can easily substitute petroleum-based plastics in a wide range of applications in many commodity products, such as disposable tableware, packaging, films, and agricultural twines, partially contributing to limiting plastic waste accumulation. Unfortunately, the complete replacement of fossil fuel-based plastics such as polyethylene (PE) or poly(ethylene terephthalate) (PET) by PLA is hindered by its higher cost, and, more importantly, slower degradation as compared to other degradable polymers. Thus, to make PLA more commercially attractive, ways to accelerate its degradation are actively sought. Many good reviews deal with PLA production, applications, and degradation but only in the medical or pharmaceutical field. In this respect, the present review will focus on controlled PLA degradation and biodegradation in technical applications. The work will include the main degradation mechanisms of PLA, such as its biodegradation in water, soil, and compost, in addition to thermal- and photo-degradation. The topic is of particular interest to academia and industry, mainly because the wider application of PLA is mostly dependent on discovering effective ways of accelerating its biodegradation rate at the end of its service life without compromising its properties.

Biodegradable performance of PLA stents affected by geometrical parameters: The risk of fracture and fragment separation

Biodegradable endovascular stents have been claimed to be reliable candidates for implantation devices used in treating cardiovascular diseases since they reduce the long-term side effects on the human biological system. It is aimed in this study to investigate the effect of geometrical parameters on the degradation behavior of poly (lactic acid) stents in term of strut fracture and fragment separation. In this regard, various structural geometry of the PLA stents was simulated in a stenosed artery using finite element method. For predicting the PLA degradation, a computational model was prepared by which the influence of stents design on their radial strength and fracture was investigated. Using a laboratory-scale designed bioreactor, the PLA fibers degradation was evaluated to calibrate the material parameters and verify the simulation method. Simulation results demonstrated that the geometrical parameters, i.e., number of struts, curves radius and stent cells shape, strongly affect the degradation behavior. The results indicated that the smooth design leads to uniform degradation in the whole stent and decreases the danger of stent fragments separation. It was shown that the maximum degradation rate of the stents with rounded curves was one-third of the models with sharp corners.