Polymer Additives Research Articles

Kinetic and Thermodynamic Interplay of Polymer-Mediated Liquid-Liquid Phase Separation for Poorly Water-Soluble Drugs.

Understanding the interplay between kinetics and thermodynamics of polymer-mediated liquid-liquid phase separation is crucial for designing and implementing an amorphous solid dispersion formulation strategy for poorly water-soluble drugs. This work investigates the phase behaviors of a poorly water-soluble model drug, celecoxib (CXB), in a supersaturated aqueous solution with and without polymeric additives (PVP, PVPVA, HPMCAS, and HPMCP). Drug-polymer-water ternary phase diagrams were also constructed to estimate the thermodynamic behaviors of the mixtures at room temperature. The liquid-liquid phase separation onset point for CXB was detected using an inline UV/vis spectrometer equipped with a fiber optic probe. Varying CXB concentrations were achieved using an accurate syringe pump throughout this study. The appearance of the transient nanodroplets was verified by cryo-EM and total internal reflection fluoresence microscopic techniques. The impacts of various factors, such as polymer composition, drug stock solution pumping rates, and the types of drug-polymer interactions, are tested against the onset points of the CXB liquid-liquid phase separation (LLPS). It was found that the types of drug-polymer interactions, i.e., hydrogen bonding and hydrophobic interactions, are vital to the position and shapes of LLPS in the supersaturation drug solution. A relation between the behaviors of LLPS and its location in the CXB-polymer-water ternary phase diagram was drawn from the findings.

Colyophilized Sugar-Polymer Dispersions for Enhanced Processing and Storage Stability.

Sucrose and trehalose pharmaceutical excipients are employed to stabilize protein therapeutics in a dried state. The mechanism of therapeutic protein stabilization is dependent on the sugars being present in an amorphous solid-state. Colyophilization of sugars with high glass transition polymers, polyvinylpyrrolidone (PVP), and poly(vinylpyrrolidone vinyl acetate) (PVPVA), enhances amorphous sugar stability. This study investigates the stability of colyophilized sugar-polymer systems in the frozen solution state, dried state postlyophilization, and upon exposure to elevated humidity. Binary systems of sucrose or trehalose with PVP or PVPVA were lyophilized with sugar/polymer ratios ranging from 2:8 to 8:2. Frozen sugar-PVPVA solutions exhibited a higher glass transition temperature of the maximally freeze-concentrated amorphous phase (Tg') compared to sugar-PVP solutions, despite the glass transition temperature (Tg) of PVPVA being lower than PVP. Tg values of all colyophilized systems were in a similar temperature range irrespective of polymer type. Greater hydrogen bonding between sugars and PVP and the lower hygroscopicity of PVPVA influenced polymer antiplasticization effects and the plasticization effects of residual water. Plasticization due to water sorption was investigated in a dynamic vapor sorption humidity ramping experiment. Lyophilized sucrose systems exhibited increased amorphous stability compared to trehalose upon exposure to the humidity. Recrystallization of trehalose was observed and stabilized by polymer addition. Lower concentrations of PVP inhibited trehalose recrystallization compared to PVPVA. These stabilizing effects were attributed to the increased hydrogen bonding between trehalose and PVP compared to trehalose and PVPVA. Overall, the study demonstrated how differences in polymer hygroscopicity and hydrogen bonding with sugars influence the stability of colyophilized amorphous dispersions. These insights into excipient solid-state stability are relevant to the development of stabilized biopharmaceutical solid-state formulations.

Chemical and Physical Architecture of Macromolecular Gels for Fracturing Fluid Applications in the Oil and Gas Industry; Current Status, Challenges, and Prospects.

Hydraulic fracturing is vital in recovering hydrocarbons from oil and gas reservoirs. It involves injecting a fluid under high pressure into reservoir rock. A significant part of fracturing fluids is the addition of polymers that become gels or gel-like under reservoir conditions. Polymers are employed as viscosifiers and friction reducers to provide proppants in fracturing fluids as a transport medium. There are numerous systems for fracturing fluids based on macromolecules. The employment of natural and man-made linear polymers, and also, to a lesser extent, synthetic hyperbranched polymers, as additives in fracturing fluids in the past one to two decades has shown great promise in enhancing the stability of fracturing fluids under various challenging reservoir conditions. Modern innovations demonstrate the importance of developing chemical structures and properties to improve performance. Key challenges include maintaining viscosity under reservoir conditions and achieving suitable shear-thinning behavior. The physical architecture of macromolecules and novel crosslinking processes are essential in addressing these issues. The effect of macromolecule interactions on reservoir conditions is very critical in regard to efficient fluid qualities and successful fracturing operations. In future, there is the potential for ongoing studies to produce specialized macromolecular solutions for increased efficiency and sustainability in oil and gas applications.

Role of acrylate terpolymers in flow assurance studies of crude oil

Paraffinic crude oil causes deposition in the pipeline at low temperatures which hinders the flow during pipeline transportation. The primary technique for mitigation of paraffin deposition is chemical treatment. Polymeric chemical additives have gained considerable attention as flow improvers for waxy crude oil. Terpolymer application for flow assurance is a novel approach since terpolymers are seldom used as chemical additives for crude oil. Current research aims to synthesize four acrylate terpolymers with different alkyl pendant chains and study their effect on the rheological behavior of crude oil. The structure of additives was validated and their depression effect was investigated. The results of the investigation revealed that the additives showed significant decrease in pour point (ΔPP = 21 °C for CO-1 and 15 °C for CO-2) at a dose of 1000 ppm for CO-1 and 2000 ppm for CO-2. These results were also supported by rheological data which exhibited a significant reduction in viscosity (>75%) of both the crude oils which showed the efficiency of additives as flow improvers. Moreover, the cold finger test displayed excellent paraffin inhibition efficiency of synthesized additives (66 and 52% for CO-1 and CO-2, respectively). The investigation demonstrated a promising role of terpolymers as flow improvers for waxy crude oil.

Multi-criteria optimization of SBR-modified mortar incorporating polyethylene terephthalate waste

Thermosetting post-consumer plastics like polyethylene terephthalate (PET) raise serious recycling challenges, leading frequently to disposal through incineration or landfilling. This study assesses the feasibility of cementitious materials containing PET additions including the influence of cement content, water-to-cement ratio (w/c), styrene-butadiene rubber (SBR) polymer additions, and PET volume on the fresh and hardened properties. The mixture proportioning followed the Taguchi methodology, which entailed the utilization of four factors, each possessing three different levels to create an L9 orthogonal matrix. The assessment included diverse performance indicators such as flow, compressive strength, flexural strength, bond strength, water absorption, and resistance to carbonation. Test results revealed that the incorporation of SBR and PET degraded the compressive strength, albeit this can be restored by increasing the cement content and/or reducing w/c. The addition of SBR significantly improved the flexural and bond strengths yet curtailed the water absorption and resistance to carbonation due to increased closed porosity that facilitated the transport properties. The multi-criteria optimization approach (TOPSIS) indicated that superior performance can be achieved using a cement content of 525 kg/m3, w/c of 0.55, SBR of 3.5 %, and PET incorporation of 4.5 %. These parameters were subsequently employed in the development of multivariate regression models, allowing for the prediction of fresh and hardened properties in SBR-PET mortar.

Transfer of a rational formulation and process development approach for 2D inks for pharmaceutical 2D and 3D printing

The field of pharmaceutical 3D printing is growing over the past year, with Spitam® as the first 3D printed dosage form on the market. Showing the suitability of a binder jetting process for dosage forms. Although the development of inks for pharmaceutical field is more trail and error based, focusing on the Z-number as key parameter to judge the printability of an ink. To generate a more knowledgeable based ink development an approach from electronics printing was transferred to the field of pharmaceutical binder jetting. Therefore, a dimensionless space was used to investigate the limits of printability for the used Spectra S Class SL-128 piezo print head using solvent based inks. The jettability of inks could now be judged based on the capillary and weber number. Addition of different polymers into the ink narrowed the printable space and showed, that the ink development purely based on Z-numbers is not suitable to predict printability. Two possible ink candidates were developed based on the droplet momentum which showed huge differences in process stability, indicating that the used polymer type and concentration has a high influence on printability and process stability. Based on the study a more knowledgeable based ink design for the field of pharmaceutical binder jetting is proposed, to shift the ink design to a more knowledgeable based and process-oriented approach.

Probucol-Ursodeoxycholic Acid Otic Formulations: Stability and In Vitro Assessments for Hearing Loss Treatment

Targeted drug delivery is an ongoing aspect of scientific research that is expanding through the design of micro- and nanoparticles. In this paper, we focus on spray dried microparticles as carriers for a repurposed lipophilic antioxidant (probucol). We characterise the microparticles and quantify probucol prior to assessing cytotoxicity on both control and cisplatin treated hair cells (known as House Ear Institute-Organ of Corti 1; HEI-OC1). The addition of water-soluble polymers to 2% β-cyclodextrin resulted in a stable probucol formulation. Ursodeoxycholic acid (UDCA) used as formulation excipient increases probucol miscibility and microparticle drug content. Formulation characterisations reveals spray drying results in spherical UDCA-drug microparticles with a mean size distribution of ∼5–12 μm. Probucol microparticles show stable short-term storage conditions accounting for only ∼10% loss over seven days. By mimicking cell culture conditions, both UDCA-probucol (67%) and probucol only (82%) microparticles show drug release in the initial two hours. Furthermore, probucol formulations with or without UDCA preserve cell viability and reduce cisplatin-induced oxidative stress. Mitochondrial bioenergetics results in lower basal respiration and non-mitochondrial respiration, with higher maximal respiration, spare capacity, ATP production and proton leak within cisplatin challenged UDCA-probucol groups. Overall, we present a facile method for incorporating lipophilic antioxidant carriers in polymer-based particles that are tolerated by HEI-OC1 cells and show stable drug release, sufficient in reducing cisplatin-induced reactive oxygen species accumulation.

Fabrication of Loose Nanofiltration Membrane by Crosslinking TEMPO-Oxidized Cellulose Nanofibers for Effective Dye/Salt Separation.

Dye/salt separation has gained increasing attention in recent years, prompting the quest to find cost-effective and environmentally friendly raw materials for synthesizing high performance nanofiltration (NF) membrane for effective dye/salt separation. Herein, a high-performance loose-structured NF membrane was fabricated via a simple vacuum filtration method using a green nanomaterial, 2,2,6,6-tetramethylpiperidine-1-oxide radical (TEMPO)-oxidized cellulose nanofiber (TOCNF), by sequentially filtrating larger-sized and finer-sized TOCNFs on a microporous substrate, followed by crosslinking with trimesoyl chloride. The resulting TCM membrane possessed a separating layer composed entirely of pure TOCNF, eliminating the need for other polymer or nanomaterial additives. TCM membranes exhibit high performance and effective dye/salt selectivity. Scanning Electron Microscope (SEM) analysis shows that the TCM membrane with the Fine-TOCNF layer has a tight layered structure. Further characterizations via Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD) confirmed the presence of functional groups and chemical bonds of the crosslinked membrane. Notably, the optimized TCM-5 membrane exhibits a rejection rate of over 99% for various dyes (Congo red and orange yellow) and 14.2% for NaCl, showcasing a potential candidate for efficient dye wastewater treatment.

Electrolyte design for zinc dynamic windows with fast switching that cycle more than 11,000 times with high optical contrast

The widespread adoption of electronically adjustable dynamic windows promises to significantly improve the energy efficiency of buildings. In this manuscript, we develop robust dynamic windows based on the reversible metal electrodeposition (RME) of Zn from DMSO electrolytes. We systematically interrogate the role of anions, cations, and polymer additives on electrolyte properties and develop design rules to increase the electrochemical and optical reversibility of these systems. This fundamental understanding allows us to develop an electrolyte that facilitates reversible Zn electrodeposition with unprecedented speed and reversibility with a Coulombic efficiency of 99.5%. We implement this electrolyte into practical two-electrode 25 cm2 dynamic windows and demonstrate that these devices switch more than 11,000 times without degradation in optical performance and without altering the switching speed or voltage profile. This outstanding durability is unprecedented in the field of RME windows and brings metal-based dynamic windows substantially closer to successful commercialization.

Study on the characteristics of glass fiber‐reinforced polymers from recycled wind turbine blades as reinforcement in particleboard

AbstractGlass fiber‐reinforced polymer (GFRP), extensively employed in diverse industries, generates considerable waste, especially from decommissioned wind turbine blades. Our research group has developed a new method of mechanical recovery for GFRP from wind turbine blades. In this study, waste GFRP was processed into a mixed particle size of 0.9–6 mm using a crusher and a screening machine, and then added as reinforcement materials to particleboards. The effects of different levels of four factors (GFRP addition, hot pressing temperature, hot pressing time, and binder dosage) on the properties of GFRP particleboards were evaluated by orthogonal experiments. The study results showed that the particleboards with 30 wt% GFRP improved modulus of rupture (MOR), modulus of elasticity (MOE), and internal bonding strength (IB) by 74.94%, 42.28%, and 92.05%, respectively, compared to pure poplar particleboards. Moreover, GFRP particleboards demonstrated better water resistance and dimensional stability than commercial particleboards and excelled in thermal stability. Recycling GFRP waste from decommissioned wind turbine blades and incorporating it into particleboard production can reduce environmental pollution, increase the resource recovery utilization rate, and contribute to sustainable manufacturing practices.Highlights Low‐cost and efficient methods of recycling wind turbine blades were proposed. Recycled GFRP from wind turbine blades can be used as reinforcement for particleboard. The prepared particleboards have excellent physical and mechanical properties and are thermally stable. Determination of the optimal glass fiber‐reinforced polymer addition level in particleboard at 30 wt%.

Electrospinning Nonspinnable Sols to Ceramic Fibers and Springs.

Electrospinning has been applied to produce ceramic fibers using sol gel-based spinning solutions consisting of ceramic precursors, a solvent, and a polymer to control the viscosity of the solution. However, the addition of polymers to the spinning solution makes the process more complex, increases the processing time, and results in porous mechanically weak ceramic fibers. Herein, we develop a coelectrospinning technique, where a nonspinnable sol (<10 mPa s) consisting of only the ceramic precursor(s) and solvent(s) is encapsulated inside a polymeric shell, forming core-shell precursor fibers that are further calcined into ceramic fibers with reduced porosity, decreased surface defects, uniform crystal packing, and controlled diameters. We demonstrate the versatility of this method by applying it to a series of nonspinnable sols and creating high-quality ceramic fibers containing TiO2, ZrO2, SiO2, and Al2O3. The polycrystalline TiO2 fibers possess excellent flexibility and a high Young's modulus reaching 54.3 MPa, solving the extreme brittleness problem of the previously reported TiO2 fibers. The single-component ZrO2 fibers exhibit a Young's modulus and toughness of 130.5 MPa and 11.9 KJ/m3, respectively, significantly superior to the counterparts prepared by conventional sol-gel electrospinning. We also report the creation of ceramic fibers in micro- and nanospring morphologies and examine the formation mechanisms using thermomechanical simulations. The fiber assemblies constructed by the helical fibers exhibit a density-normalized toughness of 3.5-5 times that of the straight fibers due to improved fracture strain. This work expands the selection of the electrospinning solution and enables the development of ceramic fibers with more attractive properties.

Implications of Low-concentration Polymer on the Physical Stability of Glassy Griseofulvin: Role of the Segmental Mobility.

Crystallization of amorphous pharmaceutical solids are widely reported to be affected by the addition of polymer, while the underlying mechanism require deep study. Herein, crystal growth behaviors of glassy griseofulvin (GSF) doped with various 1% w/w polymer were systematically studied. From the molecular structure, GSF cannot form the hydrogen bonding interactions with the selected polymer poly(vinyl acetate), polyvinyl pyrrolidone (PVP), 60:40 vinyl pyrrolidone-vinyl acetate copolymer (PVP/VA 64), and poly(ethylene oxide) (PEO). 1% w/w polymer exhibited weak or no detectable effects on the glass transition temperature (Tg) of GSF. However, crystal growth rates of GSF was altered from 4.27-fold increase to 2.57-fold decrease at 8 ℃ below Tg of GSF. Interestingly, the ability to accelerate and inhibit the growth rates of GSF crystals correlated well with Tg of polymer, indicating the controlling role of segmental mobility of polymer. Moreover, ring-banded growth of GSF was observed in the polymer-doped systems. Normal compact bulk and ring-banded crystals of GSF were both characterized as the thermodynamically stable form I. More importantly, formation of ring-banded crystals of GSF can significantly weaken the inhibitory effects of polymer on the crystallization of glassy GSF.

Plastic breath: Quantification of microplastics and polymer additives in airborne particles

The widespread extensive use of synthetic polymers has led to a substantial environmental crisis caused by plastic pollution, with microplastics detected in various environments and posing risks to both human health and ecosystems.The possibility of plastic fragments to be dispersed in the air as particles and inhaled by humans may cause damage to the respiratory and other body systems. Therefore, there is a particular need to study microplastics as air pollutants. In this study, we tested a combination of analytical pyrolysis, gas chromatography–mass spectrometry, and gas and liquid chromatography-mass spectrometry to identify and quantify both microplastics and their additives in airborne particulate matter and settled dust within a workplace environment: a WEEE treatment plant. Using this combined approach, we were able to accurately quantify ten synthetic polymers and eight classes of polymer additives.The identified additives include phthalates, adipates, citrates, sebacates, trimellitates, benzoates, organophosphates, and newly developed brominated flame retardants.

Development and In Vitro Evaluation of Aceclofenac Buccal Film.

This study aimed to formulate and characterize aceclofenac buccal film formulations made of different polymers and evaluate the effects of polymer type on buccal film properties. Five polymer types, namely hydroxypropyl methylcellulose (HPMC), sodium carboxymethylcellulose (SCMC), polyvinyl alcohol (PVA), Eudragit S100, and Eudragit SR100, were used to prepare aceclofenac buccal film formulation either separately or combined by solvent-casting method. These formulations were evaluated in terms of physical appearance, folding test, film weight and thickness, drug content, percentage of elongation, moisture uptake, water vapor permeability, and in vitro drug release. The addition of Eudragit polymer in most of the produced buccal films was unacceptable with low folding endurance. However, the dissolution profile of buccal films made from PVA and Eudragit SR100 provided a controlled drug release profile. Buccal films can be formulated using different polymers either individually or in combination to obtain the drug release profile required to achieve a desired treatment goal. Furthermore, the property of the buccal films depends on the type and concentration of the polymer used.

Mitigating autogenous shrinkage of cement with carbon nanotube sponge

Autogenous shrinkage can be mitigated by the addition of superabsorbent polymer (SAP), however, typically at the cost of a significant strength loss. To overcome such dilemma, hydrophilic carbon nanotube sponge (H-CNTSP) was proposed in this study as a novel internal curing agent. Due to the high porosity and enriched hydrophilic functional groups, H-CNTSP can absorb pore solution at 72 g/g driven by the capillary force, which is 176%–620 % higher than the commercial SAPs. The autogenous shrinkage of cement can be reduced or mitigated with the addition of 0.05–0.2 wt% H-CNTSP due to the continuous water release after final setting. Interestingly, the compressive strength loss resulting from the addition of H-CNTSP can be greatly diminished and even be overcompensated by the formation of CNT/hydrate nanocomposite shell with a higher modulus. This study illustrates the great potential to optimize concrete performance through proper design of assembly structures with chemically functionalized nanomaterials.

Physical property comparison of polymeric KCl sludge composition and polyamine at different temperatures

Drilling mud is a fluid used to assist the drilling process. The composition and physical properties of the mud greatly influence a drilling operation. Drilling operations that penetrate formations with shale content have the potential to experience drilling problems related to shale hydration. To get a good ability to prevent shale hydration, mud is added with polymeric and polyamine KCl additives (shale inhibitors) with the aim of stabilizing shale in contact with drilling fluid, as well as preventing drill cuttings from forming colloids. The results obtained in the KCl polymer mud composition at temperatures of 80°F, 250°F, and 300°F for mud weight were 9.3 ppg, 9.1 ppg, and 9 ppg, respectively. Funnel viscosity was 40 sec/qt, 36 sec/qt, and 34 sec/qt. Tap rates were 4.8 cc, 6 cc, and 6.6 cc. Mud cake remained at 1 mm and pH also remained at 9. While the results obtained on polyamine mud composition at temperatures of 80°F, 250°F, and 300°F for mud weight were 9.2 ppg, 8.9 ppg, and 8.8 ppg, respectively. Funnel viscosity was 26 sec/qt, 20 sec/qt, and 17 sec/qt. Tap rate of 10 cc, 13.8 cc, and 15 cc. Mud cake of 1 mm, 2 mm, and 2 mm. pH remains at 9. The data obtained shows that the results of the physical properties of polymeric KCl mud are better than polyamine mud.

A new strategy for the treatment of middle ear infection using ciprofloxacin/amoxicillin-loaded ethyl cellulose/polyhydroxybutyrate nanofibers

A middle ear infection occurs due to the presence of several microorganisms behind the eardrum (tympanic membrane) and is very challenging to treat due to its unique location and requires a well-designed treatment. If not treated properly, the infection can result in severe symptoms and unavoidable side effects. In this study, excellent biocompatible ethyl cellulose (EC) and biodegradable polyhydroxybutyrate (PHB) biopolymer were used to fabricate drug-loaded nanofiber scaffolds using an electrospinning technique to overcome antibiotic overdose and insufficient efficacy of drug release during treatment. PHB polymer was produced from Halomonas sp., and the purity of PHB was found to around be 90 %. Additionally, ciprofloxacin (CIP) and amoxicillin (AMX) are highly preferable since both drugs are highly effective against gram-negative and gram-positive bacteria to treat several infections. Obtained smooth nanofibers were between 116.24 and 171.82 nm in diameter and the addition of PHB polymer and antibiotics improved the morphology of the nanofiber scaffolds. Thermal properties of the nanofiber scaffolds were tested and the highest Tg temperature resulted at 229 °C. The mechanical properties of the scaffolds were tested, and the highest tensile strength resulted in 4.65 ± 6.33 MPa. Also, drug-loaded scaffolds were treated against the most common microorganisms that cause the infection, such as S.aureus, E.coli, and P.aeruginosa, and resulted in inhibition zones between 10 and 21 mm. MTT assay was performed by culturing human adipose-derived mesenchymal stem cells (hAD MSCs) on the scaffolds. The morphology of the hAD MSCs' attachment was tested with SEM analysis and hAD MSCs were able to attach, spread, and live on each scaffold even on the day of 7. The cumulative drug release kinetics of CIP and AMX from drug-loaded scaffolds were analysed in phosphate-buffered saline (pH: 7.4) within different time intervals of up to 14 days using a UV spectrophotometer. Furthermore, the drug release showed that the First-Order and Korsmeyer-Peppas models were the most suitable kinetic models. Animal testing was performed on SD rats, matrix and collagen deposition occurred on days 5 and 10, which were observed using Hematoxylin-eosin and Masson's trichrome staining. At the highest drug concentration, a better repair effect was observed. Results were promising and showed potential for novel treatment.

Controlling polymer degradation by addition of plant aromatic polymer, lignin

This study examined the accelerated degradation of poly(caprolactone) films using two types of lignin derivatives. The degradation of poly(caprolactone) films was unaffected by the lignin derivative capped hydroxy groups, indicating the participation of radicals from phenolic hydroxy groups in lignin derivatives for accelerating the degradation of films. Furthermore, the role of lignin radicals in relation to polymer degradation changed as per the mechanism of polymer decomposition, e.g., the degradation of poly(ethylene carbonate) films was suppressed by feeding lignin derivatives because of the back biting type decomposition nature of poly(ethylene carbonate), which differs from the radical-mediated addition/cleavage type decomposition nature of poly(caprolactone). These results provide an approach of designing bio-degradative materials from lignin, a natural phenolic polymer.

Inducing Microstrain in Electrodeposited Pt through Polymer Addition for Highly Active Oxygen Reduction Catalysis

Inducing Microstrain in Electrodeposited Pt through Polymer Addition for Highly Active Oxygen Reduction Catalysis

Characterization of Functional Biohybrid Materials Based on Saccharomyces Cerevisiae Biomass

Biohybrid materials and engineered living materials (ELMs) are a dynamic field of research at the interface of material science and synthetic biology. Recently, microorganisms have been described as both functional and structural building blocks of such materials. Dry materials with bacteria as structural building block have previously not been investigated for their ability to retain catalytic activity. Herein, it is shown that Saccharomyces cerevisiae biomass can act as a structural building block in dry, macroscopic materials while simultaneously providing functionality. A benign method for the preparation of both coatings and free‐standing, flexible films is presented. Notably, free‐standing films can be prepared solely from biomass and plasticizers without the need for other additives. During the process, the integrity of the cells and the catalytic activity within is preserved, which is demonstrated by biocatalytic H2O2 degradation. The film‐forming properties of S. cerevisiae biomass and the influence of plasticizing and polymeric additives on the mechanical properties are investigated in detail and compared to related materials. The work presented is a first step toward new, mechanically strong microorganism‐based functional coatings and films.