Biodegradation Of PLA Research Articles

Degradation of polylactic acid/polybutylene adipate-co-terephthalate blend by Papiliotrema laurentii S2P4P isolated from agricultural soils

Polylactic acid/polybutylene adipate-co-terephthalate blend (PLA/PBAT) has been widely used due to their good biodegradation. Recently, the biodegradation of PLA and PBAT has received increasing attention. However, PLA/PBAT blend-degrading strains have been rarely reported in comparison to that for pure PLA and PBAT. A fungus strain, Papiliotrema laurentii S2P4P, was isolated from agricultural soils and identified. S2P4P can efficiently degrade commercial PLA/PBAT films at 30°C in mineral salt medium (MSM) and obtained about 14% of weight loss within 30 days of incubation. Additionally, rough and uneven surface of PLA/PBAT film with cracks and creases, increased hydrophilicity, changes in mechanical property, and decreased intensity of C=O and C-O bonds were observed after S2P4P treatments. The strain secreted esterase to catalyze the degradation of the ester bonds in PLA/PBAT blend, resulting in the production of degradation products such as butanediol, adipic acid, lactic acid and terephthalic acid as well as their oligomers. Furthermore, as carbon and energy sources, the degradation products could participate in the metabolism of S2P4P and then accelerate degradation of PLA/PBAT blend. The advantages of P. laurentii S2P4P in simultaneous degradation of PLA and PBAT indicated that the strain has potential value for the bioremediation of PLA/PBAT blend in the actual environment.

Stability and Composting Behaviour of PLA-Starch Laminates Containing Active Extracts and Cellulose Fibres from Rice Straw.

The stability and composting behaviour of monolayers and laminates of poly (lactic acid) (PLA) and starch with and without active extracts and cellulose fibres from rice straw (RS) were evaluated. The retrogradation of the starch throughout storage (1, 5, and 10 weeks) gave rise to stiffer and less extensible monolayers with lower water vapour barrier capacity. In contrast, the PLA monolayers, with or without extract, did not show marked changes with storage. However, these changes were more attenuated in the bilayers that gained water vapour and oxygen barrier capacity during storage, maintaining the values of the different properties close to the initial range. The bioactivity of the active films exhibited a slight decrease during storage, so the antioxidant capacity is better preserved in the bilayers. All monolayer and bilayer films were fully composted within 90 days but with different behaviour. The bilayer assembly enhanced the biodegradation of PLA, whose monolayer exhibited a lag period of about 35 days. The active extract reduced the biodegradation rate of both mono- and bilayers but did not limit the material biodegradation within the time established in the Standard. Therefore, PLA-starch laminates, with or without the valorised fractions from RS, can be considered as biodegradable and stable materials for food packaging applications.

Biopolymeric Blends of Thermoplastic Starch and Polylactide as Sustainable Packaging Materials.

The improper disposal of plastics is a growing concern due to increasing global environmental problems such as the rise of CO2 emissions, diminishing petroleum sources, and pollution, which necessitates the research and development of biodegradable materials as an alternative to conventional packaging materials. The purpose of this research was to analyse the properties of biodegradable polymer blends of thermoplastic potato starch (TPS) and polylactide, (PLA) without and with the addition of citric acid (CA) as a potential compatibilizer and plasticizer. The prepared blends were subjected to a comprehensive physicochemical characterization, which included: FTIR-ATR spectroscopy, morphological analysis by scanning electron microscopy (SEM), determination of thermal and mechanical properties by differential scanning calorimetry (DSC), water vapour permeability (WVP), as well as biodegradation testing in soil. The obtained results indicate an improvement in adhesion between the TPS and PLA phases due to the addition of citric acid, better homogeneity of the structure, and greater compatibility of the polymer blends, leading to better thermal, mechanical and barrier properties of the studied biodegradable TPS/PLA polymer blends. After conducting the comprehensive research outlined in this paper, it has been determined that the addition of 5 wt.% of citric acid serves as an effective compatibilizer and plasticizer. This supplementation achieves an optimal equilibrium across thermal, mechanical, morphological, and barrier properties, while also promoting material sustainability through biodegradation. In conclusion, it can be stated that the use of thermoplastic starch in TPS/PLA blends accelerates the biodegradation of PLA as a slowly biodegradable polymer. While the addition of citric acid offers significant advantages for TPS/PLA blends, further research is needed to optimize the formulation and processing parameters to achieve the desired balance between mechanical strength, thermal and barrier properties and biodegradability.

Biodegradability and Water Absorption of Macadamia Nutshell Powder-Reinforced Poly(lactic Acid) Biocomposites

This study investigates the biodegradability and water absorption properties of Macadamia nutshell powder and poly(lactic acid) (PLA) biocomposites using a Design of Experiments (DOE) approach. The influences of processing methods, the Macadamia nutshell powder’s weight content, and the powder’s condition are studied. A biodegradability test is performed in accordance with the American Society for Testing and Materials (ASTM) D5338-11 by burying the test specimens in wet garden soil at a controlled temperature of 50 °C and 100% humidity. The specimens obtained by counter-rotating processing exhibit varying weight loss patterns with an increasing powder weight content, while the specimens obtained by co-rotating processing demonstrate consistent behaviour. This study highlights the complex nature of PLA biodegradation, which is affected by diverse factors such as test conditions and environments, thereby contributing to a deeper understanding of the sustainability implications. A water absorption test is carried out in accordance with ASTM D570-98. It is shown that the water absorption characteristics are predominantly determined by the hydrophilic nature of Macadamia nutshells, with an increased powder weight content leading to higher absorption. Pure PLA, due to its hydrophobic nature, exhibits minimal water absorption. By unravelling the complexities of PLA biodegradation and water absorption in Macadamia nutshell and PLA biocomposites, this study not only advances the understanding of materials’ behaviour but also underscores the potential sustainability implications of utilizing natural resources in composite materials. This research contributes valuable insights to the broader discourse on environmentally friendly materials and their role in promoting sustainable practices.

Biodegradation behavior of poly (lactic acid) samples obtained by three‐dimensional printing: Influence of temperature and pigment presence

AbstractIn this study, the biodegradation behavior in the soil of natural and pigmented poly (lactic acid) (PLA) plates obtained by three‐dimensional (3D) printing or by compression molding was evaluated by the respirometry method at three different temperatures: 21, 28, and 35°C. PLA samples before and after aerobic biodegradation tests were characterized by Fourier transform infrared spectroscopy, differential scanning calorimetry (DSC), thermogravimetric analysis (TG), and size exclusion chromatography analysis. The increase in test temperature enhanced the biodegradation process. At a test temperature of 35°C, the maximum biodegradation rates of natural PLA and pigmented PLA were 65% and 68% higher, respectively, compared to the maximum biodegradation rate observed at 21°C. DSC and TG analysis indicate that pigmented PLA samples were more susceptible to degradation by hydrolysis. However, the rate of biodegradation efficiency was lower in pigmented PLA samples, with a decrease of 16%, 24%, and 14% at 21, 28, and 35°C, respectively, compared to natural PLA. This behavior indicated that pigment hindered the hydrolysis by‐products absorption by microorganisms. Additionally, the presence of micro voids in PLA samples obtained through 3D printing accelerated the rate of biodegradation efficiency by 32% at 28°C compared to pressed samples.Highlights Poly (lactic acid) (PLA) plate biodegradation in soil was analyzed using respirometry method. Temperature, pigment presence, and sample preparation method were considered. Higher temperatures enhanced both natural and pigmented PLA biodegradation. Pigments appeared to act as antimicrobial agents, slowing down the process. Water presence in the micro voids accelerated hydrolysis and biodegradation.

Modification of poly(lactate) via polymer blending with microbially produced poly[(R)-lactate-co-(R)-3-hydroxybutyrate] copolymers

This study investigated the effect of polymer blending of microbially produced poly[(R)-lactate-co-(R)-3-hydroxybutyrate] copolymers (LAHB) with poly(lactate) (PLA) on their mechanical, thermal, and biodegradable properties. Blending of high lactate (LA) content and high molecular weight LAHB significantly improved the tensile elongation of PLA up to more than 250 % at optimal LAHB composition of 20–30 wt%. Temperature-modulated differential scanning calorimetry and dynamic mechanical analysis revealed that PLA and LAHB were immiscible but interacted with each other, as indicated by the mutual plasticization effect. Detailed morphological characterization using scanning probe microscopy, small-angle X-ray scattering, and solid-state NMR confirmed that PLA and LAHB formed a two-phase structure with a characteristic length scale as small as 20 nm. Because of mixing in this order, the polymer blends were optically transparent. The biological oxygen demand test of the polymer blends in seawater indicated an enhancement of PLA biodegradation during biodegradation of the polymer blends.

Accelerating Biodegradation: Enhancing Poly(lactic acid) Breakdown at Mesophilic Environmental Conditions with Biostimulants.

Poly(lactic acid) (PLA) has garnered interest due to its low environmental footprint and ability to replace conventional polymers and be disposed of in industrial composting environments. Although PLA is compostable when subjected to a suitable set of conditions, its broader acceptance in industrial composting facilities has been affected adversely due to longer degradation timeframes than the readily biodegradable organic waste fraction. PLA must be fully exposed to thermophilic conditions for prolonged periods to biodegrade, which has restricted its adoption and hindered its acceptance in industrial composting facilities, negating its home composting potential. Thus, enhancing PLA biodegradation is crucial to expand its acceptance. PLA's biodegradability is investigated in a compost matrix under mesophilic conditions at 37 °C for 180 days by biostimulating the compost environment with skim milk, gelatin, and ethyl lactate to enhance the different stages of PLA biodegradation. The evolved CO2, number average molecular weight (Mn), and crystallinity evolution are tracked. To achieve a Mn ≲ 10kDa for PLA, the biodegradation rate is accelerated by 15% by adding skim milk, 25% by adding gelatin, and 22% by adding ethyl lactate. This work shows potential techniques to help biodegrade PLA in home composting setting by adding biostimulants.

Cheap organocatalyst diphenyl phosphate for efficient chemical recycling of poly(lactic acid), other polyesters and polycarbonates

Bioplastics are regarded as a sustainable alternative to traditional petroleum-based plastics, particularly poly(lactic acid) (PLA). However, due to the slow biodegradation of PLA and the lack of an overall recycling strategy, its large-scale use could make it an acute source of future plastic pollution. Herein, we find that diphenyl phosphate (DPP), a cheap organocatalyst, can efficiently catalyze PLA hydrolysis into valuable oligomers/lactic acid. Without pressure and organic solvents, under mild conditions with 3.5 wt% DPP and a little water (160 °C, 1.5 h), commercial PLA pellets/products are rapidly converted into oligomers with molecular weight below 500 g/mol by random hydrolysis. DPP can catalyze at least 10 batches of PLA without compromising its catalytic performance, and kilogram-scale PLA degradation is facilely achieved. The DPP-containing oligomers can be used directly to synthesize lactide, and subsequently high-quality PLA is obtained using a well-established industrial route to achieve closed-loop recycling. Meanwhile, an aqueous lactic acid solution with comparable commercial quality and intact configuration retention is harvested. Moreover, DPP can also effectively catalyze the hydrolysis of other polyesters and polycarbonates. Overall, this study is expected to address the environmental and engineering challenges associated with plastic waste disposal, in particular fostering a PLA-based green circular bio-economy.

Bio-inspired, biodegradable, and fluffy 3D PLA fibrous sponges with dynamic fractal nano-sweepers for on-demand oil/water separation

Frequent oil leakage results in a huge waste of fossil fuel resources and severely threatens the global water-waste-energy nexus. Membrane separation technology is a promising effective and energy-saving approach for recycling waste oil resources and oily-environment remediation. Despite many bioinspired materials with the mitigated selectivity/permeability trade-off having been developed, a significant issue has been ignored, that is, most of the membranes are non-biodegradable and could cause secondary environmental pollution. In this work, inspired by the natural 3D coral organisms with sustainable fiber tentacles; we propose a biomimetic crystal-engineering strategy of space-confined solvent-induced recrystallization to prepare a 3D biodegradable PLA fibrous sponge with coral-like nanoflower/honeycomb sweeper arrays. By virtue of the coral-like nanoporous fractal arrays with superhydrophobicity and proactive fouling resistance, the resulting PLA sponge exhibits excellent separation performance of immiscible oil–water mixtures (ultrahigh permeation flux of up to 27,908 L m-2h−1) and water-in-oil emulsions (high separation efficiency of up to 99.9 %). Significantly, with the advantage of biodegradability and recyclability of PLA, we envision such environmentally friendly PLA fibrous sponges would show promising potential in the fields of environmental remediation, oil recovery, self-cleaning, etc.

Biodegradable poly(lactic acid) and polycaprolactone alternating multiblock copolymers with controllable mechanical properties

As the environmental pollution problems caused by plastic waste and the dependence on petroleum resources become more serious, the need for biodegradable plastics and bioplastics is increasing. Recently, poly(lactic acid) (PLA), one of the leading biodegradable plastics, has been widely used as a biomass plastic to replace petroleum-based materials. However, PLA is brittle and does not decompose easily in real environments, limiting its use. In this study, PLA was copolymerized with polycaprolactone (PCL) to obtain triblock copolymers PLA-PCL-PLA, and then chain-extended by hexamethylene diisocyanate to obtain PLA-PCL alternating multiblock copolymers based on PLA. By varying the chain lengths of PLA in the alternating multiblock copolymers, the mechanical properties could be easily controlled, and the toughness was significantly improved compared to PLA-PCL random copolymers. Evaluation of biodegradability in compost showed improved CO2 production and biodegradation rate in the initial stage of the test, suggesting high biodegradability. The change in molecular weight of the copolymer films in seawater did not prove marine biodegradability, but it was assumed that the copolymer's regularly arranged structure and low Tg contributed to its low molecular weight, one of the key factors in PLA biodegradation.

Assessing the Effect of Cellulose Nanocrystal Content on the Biodegradation Kinetics of Multiscale Polylactic Acid Composites under Controlled Thermophilic Composting Conditions.

This work studied the effect of cellulose nanocrystal (NCC) content on the biodegradation kinetics of PLA-based multiscale cellulosic biocomposites (PLAMCBs). To facilitate biodegradation, the materials were subjected to thermo-oxidation before composting. Biodegradation was carried out for 180 days under controlled thermophilic composting conditions according to the ASTM D 5338 standard. A first-order model based on Monod's kinetics under limiting substrate conditions was used to study the effect of cellulose nanocrystal (NCC) content on the biodegradation kinetics of multiscale composite materials. It was found that thermo-oxidation at 70 °C for 160 h increased the biodegradability of PLA. Also, it was found that the incorporation of cellulosic fibrous reinforcements increased the biodegradability of PLA by promoting hydrolysis during the first stage of composting. Likewise, it was found that partial substitution of micro cellulose (MFC) by cellulose nanocrystals (NCCs) increased the biodegradability of the biocomposite. This increase was more evident as the NCC content increased, which was attributed to the fact that the incorporation of cellulose nanocrystals facilitated the entry of water into the material and therefore promoted the hydrolytic degradation of the most recalcitrant fraction of PLA from the bulk and not only by surface erosion.

Novel Epoxidized Brazil Nut Oil as a Promising Plasticizing Agent for PLA.

This work evaluates for the first time the potential of an environmentally friendly plasticizer derived from epoxidized Brazil nut oil (EBNO) for biopolymers, such as poly(lactic acid) (PLA). EBNO was used due to its high epoxy content, reaching an oxirane oxygen content of 4.22% after 8 h of epoxidation for a peroxide/oil ratio of 2:1. Melt extrusion was used to plasticize PLA formulations with different EBNO contents in the range of 0-10 phr. The effects of different amounts of EBNO in the PLA matrix were studied by performing mechanical, thermal, thermomechanical, and morphological characterizations. The tensile test demonstrated the feasibility of EBNO as a plasticizer for PLA by increasing the elongation at break by 70.9% for the plasticized PLA with 7.5 phr of EBNO content in comparison to the unplasticized PLA. The field-emission scanning electron microscopy (FESEM) of the fractured surfaces from the impact tests showed an increase in porosity and roughness in the areas with EBNO addition, which was characteristic of ductile failure. In addition, a disintegration test was performed, and no influence on the PLA biodegradation process was observed. The overall results demonstrate the ability of EBNO to compete with other commercial plasticizers in improving the ductile properties of PLA.

Microbes drive metabolism, community diversity, and interactions in response to microplastic-induced nutrient imbalance

The impact of conventional and biodegradable microplastics on soil nutrients (carbon and nitrogen) has been widely examined, and the alteration of nutrient conditions further influences microbial biosynthesis processes. Nonetheless, the influence of microplastic-induced nutrient imbalances on soil microorganisms (from metabolism to community interactions) is still not well understood. We hypothesized that conventional and biodegradable microplastic could alter soil nutrients and microbial processes. To fill this knowledge gap, we conducted soil microcosms with polyethylene (PE, new and aged) and polylactic acid (PLA, new and aged) microplastics to evaluate their effects on the soil enzymatic stoichiometry, co-occurrence interactions, and success patterns of soil bacterial communities. New and aged PLA induced soil N immobilization, which decreased soil mineral N by 91–141 %. The biodegradation of PLA led to a higher bioavailable C and wider bioavailable C:N ratio, which further filtered out specific microbial species. Both new and aged PLA had a higher abundance of copiotrophic members (Proteobacteria, 35–51 % in PLA, 26–34 % in CK/PE treatments) and rrn copy number. The addition of PLA resulted in a lower alpha diversity and reduced network complexity. Conversely, because of the chemically stable hydrocarbon structure of PE polymers, the new and aged PE microplastics had a minor effect on soil mineral N, bacterial community composition, and network complexity, but led to microbial C limitation. Collectively, all microplastics increased soil C-, N-, and P -acquiring enzyme activities and reduced the number of keystone species and the robustness of the co-occurrence network. The PLA treatment enhanced nitrogen fixation and ureolysis, whereas the PE treatment increased the degradation of recalcitrant carbon. Overall, the alteration of soil nutrient conditions by microplastics affected the microbial metabolism and community interactions, although the effects of PE and PLA microplastics were distinct.

Multi-faceted analysis of thermophilic anaerobic biodegradation of poly(lactic acid)-based material

Currently, the production of bio-based polymeric materials, of which poly(lactic acid) (PLA) is the most popular, has been increasing, causing the growth of PLA waste in municipal waste. Thus, it is necessary to develop sustainable methods for treating it. Methane production, resulting from anaerobic digestion (AD), is a potential end-of-life scenario for PLA waste that needs to be investigated. To obtain high efficiency of AD, thermophilic fermentation was applied, and to overcome low rates of biodegradation, hydrothermal (HT) and alkaline (A) pretreatments were used. For a deep insight into the process, differential scanning calorimetry (DSC), Fourier-transform infrared spectroscopy (FTIR), and microscopic and microbial analyses (based on 16S rDNA) were applied. For both untreated (PLA) and pretreated (PLAHT, PLAA) samples a high maximal methane production (MP) of 453 L/kg volatile solids (VS) was obtained, almost 100 % of the theoretical methane yield from PLA. The use of pretreatment allowed shortening of the time for obtaining maximal MP, especially the hydrothermal pretreatment, which shortened the overall time of MP 1.3-fold, and methane was produced at an almost 10 % higher rate (8.35 vs 7.79 L/(kg VS·d)). However, DSC and microscopic analyses revealed that, in all cases, methane was intensively produced i) after the reduction of the molecular mass of the PLA material and ii) also when PLA pieces were not visible. This should be considered when designing the operational time for the AD process. Parallel to the gradual biodegradation of PLA, the abundances of Firmicutes, Thermotogae, and Euryarcheota increased. With PLAHT, Syntrophobacteraceae, Thermoanaerobacteraceae, and methanogens were identified as potential key thermophilic PLA biodegraders.

Modification of Poly(lactic acid) with Orange Peel Powder as Biodegradable Composite.

Traditional fossil-based plastic usage and disposal has been one of the largest environmental concerns due to its non-biodegradable nature and high energy consumption during the manufacturing process. Poly(lactic acid) (PLA) as a renewable polymer derived from natural sources with properties comparable to classical plastics and low environmental cost has gained much attention as a safer alternative. Abundantly generated orange peel waste is rich in valuable components and there is still limited study on the potential uses of orange peel waste in reinforcing the PLA matrix. In this study, orange peel fine powder (OPP) synthesized from dried orange peel waste was added into PLA solution. PLA/OPP solutions at different OPP loadings, i.e., 0, 10, 20, 40, and 60 wt% were then casted out as thin films through solution casting method. Fourier-transform infrared spectroscopy (FTIR) analysis has shown that the OPP is incorporated into the PLA matrix, with OH groups and C=C stretching from OPP can be observed in the spectra. Tensile test results have reviewed that the addition of OPP has decreased the tensile strength and Young’s modulus of PLA, but significantly improve the elongation at break by 49 to 737%. Water contact angle analysis shows that hydrophilic OPP has modified the surface hydrophobicity of PLA with a contact angle ranging from 70.12° to 88.18°, but higher loadings lead to decrease of surface energy. It is proven that addition of OPP improves the biodegradability of PLA, where PLA/60 wt% OPP composite shows the best biodegradation performance after 28 days with 60.43% weight loss. Lastly, all PLA/OPP composites have better absorption in alkaline solution.

Achieving high flame retardancy, crystallization and biodegradability PLA based on 1 wt% addition of novel fully bio-based flame retardant

In this paper, a bio-based flame retardant PA-AR is synthesized, which endows PLA with good flame retardant and crystallization properties, and at the same time promotes the biodegradability of PLA. Only 1 wt% PA-AR makes the LOI value of PLA reach 26.8% and reaches UL-94 V-0 level. In addition, 1 wt% PA-AR increases the crystallinity of PLA to 23.4%, which increased by 460% compared with PLA. Further, due to the increase of crystallinity, the tensile strength is also improved. Besides, the addition of PA-AR can greatly promote the degradation performance of PLA under specific biological conditions. This work proposed a novel method to obtain completely biodegradable flame retardant composites.

Rapid Solvent-Free Microcrystalline Cellulose Melt Functionalization withl-Lactide for the Fabrication of Green Poly(lactic acid) Biocomposites

A green approach is proposed to achieve a rapid surface functionalization of microcrystalline cellulose (MCC) in 30 min by a solvent-free "grafting from" reaction of l-lactide through compression molding without the need for an inert atmosphere. A sufficient hydrophobization of the MCC surface is achieved with an amount of grafted poly(l-lactic acid) (PLLA) oligomers of 7 wt % with respect to MCC. The obtained MCC-g-PLLA is subsequently melt-compounded with poly(lactic acid) (PLA) through extrusion and injection molding. As a result of higher compatibility and interfacial adhesion of the functionalized filler with PLA, PLA/MCC-g-PLLA biocomposites with a cellulose content ranging from 4 to 20 wt % exhibit an enhancement in important physicochemical properties (i.e., water vapor barrier, crystallinity, stiffness) compared to both pure PLA and formulations containing an equal or higher amount of nonfunctionalized MCC. At the same time, the materials retain the mechanical strength and resistance to thermal degradation of PLA. The physicochemical characteristics, excellent biocompatibility, and biodegradability of PLA and cellulose and the simplicity, rapidity, and cost-effectiveness of the grafting process render these biocomposites suitable for several applications within the plastics domain including packaging, agriculture, automotive, consumer goods, and household appliances.

Flexibly Controlling the Polycrystallinity and Improving the Foaming Behavior of Polylactic Acid via Three Strategies.

Controlling foamability plays the central role in preparing PLA foams with high performances. To achieve this, chain extension was often used to improve the rheological property of PLA resins; however, despite the availability of this approach, it often deteriorates the biodegradability of PLA and greatly increases the processing cost and complexity. Hence, we reported a special crystallization induction method to design PLA foams with a tunable cellular structure and a high expansion ratio. A novel crystallization-promoting agent combination (D-sorbitol, CO2, and phenylphosphonic acid zinc salt) was used to induce PLA to enhance the chain interaction force and chain mobility and to provide crystallization templets. A series of PLAs with tunable stereocomplex (Sc)/α crystallinity and rapid non-isothermal crystallization ability were obtained. The effect of various crystallization properties on the foaming behavior of PLA was studied. The results demonstrated that proper crystallization conditions (a small spherulite size, a crystallinity of 6%, and rapid crystallization ability) could virtually contribute to the optimized cellular structure with the highest cell density of 4.36 × 106 cell/cm3. When the Sc crystallinity was above 10%, PLA had a superior foamability, which thereby resulted in a high foaming expansion ratio of 16.2. A variety of cellular morphologies of PLA foams could be obtained by changing the foaming temperature and the crystallization property. The proposed crystallization-induced approach provided a useful method for controlling the cellular structure and the performances of the PLA foams.

Optimization of process parameters for 3D printing process using Taguchi based grey approach

Additive manufacturing (AM) is the method for fabricating the components effectively. The components fabricated by AM process has wider applications in various domains. Fusion deposition modeling is one of the AM methodology that has been used for fabricating the components. Biodegradability of PLA makes the material as best alternate for plastics and carbon nano particles has been addedwith PLA which has the possibility using this material for various engineering applications. Taguchi’s experimental design is concept used for devising the experimentation with the help of selected independent process variables. Single aspects optimization has been performed by Taguchi’s approach. Tensile strength, toughness and roughness of the fabricated samples are considered as performance measures. Grey system theory is the methodology engaged for adopting the multi aspects optimization. The best possible process variables are identified for multiple experimentation measures. The effect combinatorial variables were identified by using the interaction analysis.

Long-Term Evaluation of Poly(lactic acid) (PLA) Implants in a Horse: An Experimental Pilot Study.

In horses, there is an increasing interest in developing long-lasting drug formulations, with biopolymers as viable carrier alternatives in addition to their use as scaffolds, suture threads, screws, pins, and plates for orthopedic surgeries. This communication focuses on the prolonged biocompatibility and biodegradation of PLA, prepared by hot pressing at 180 °C. Six samples were implanted subcutaneously on the lateral surface of the neck of one horse. The polymers remained implanted for 24 to 57 weeks. Physical examination, plasma fibrinogen, and the mechanical nociceptive threshold (MNT) were performed. After 24, 28, 34, 38, and 57 weeks, the materials were removed for histochemical analysis using hematoxylin-eosin and scanning electron microscopy (SEM). There were no essential clinical changes. MNT decreased after the implantation procedure, returning to normal after 48 h. A foreign body response was observed by histopathologic evaluation up to 38 weeks. At 57 weeks, no polymer or fibrotic capsules were identified. SEM showed surface roughness suggesting a biodegradation process, with an increase in the median pore diameter. As in the histopathological evaluation, it was not possible to detect the polymer 57 weeks after implantation. PLA showed biocompatible degradation and these findings may contribute to future research in the biomedical area.