Investigation of the in vitro biological activities of polyethylene glycol-based thermally stable polyurethane elastomers.

The intense urge to replace conventional polymers with ecofriendly monomers is a step towards green products. The novelty of this study is the extraction of starch from the biowaste of wheat bran (WB) and banana peel (BP) for use as a monomer in the form of chain extenders. For the synthesis of polyurethane (PU) elastomers, polyethylene glycol (PEG) bearing an average molecular weight Mn = 1000 g mol-1 was used as a macrodiol, which was reacted with isophorone diisocyanate (IPDI) to develop NCO-terminated prepolymer chains. These prepolymer chains were terminated with chain extenders. Two series of linear PU elastomers were prepared by varying the concentration of chain extenders (0.5-2.5 mol%), inducing a variation of 40 to 70 wt% in the hard segment (HS). Fourier-transform infrared (FTIR) spectroscopy confirmed the formation of urethane linkages. Thermal gravimetric analysis (TGA) showed a thermal stability of up to 250 °C. Dynamic mechanical analysis (DMA) revealed a storage modulus (E') of up to 140 MPa. Furthermore, the hemolytic activities of up to 8.97 ± 0.1% were recorded. The inhibition of biofilm formation was investigated against E. coli and S. aureus (%), which was supported by phase contrast microscopy.

A review on the application of chitosan-based polymers in liver tissue engineering.

Chitosan-based polymers have enormous structural tendencies to build bioactive materials with novel characteristics, functions, and various applications, mainly in liver tissue engineering (LTE). The specific physicochemical, biological, mechanical, and biodegradation properties give the effective ways to blend these biopolymers with synthetic and natural polymers to fabricate scaffolds matrixes, sponges, and complexes. A variety of natural and synthetic biomaterials, including chitosan (CS), alginate (Alg), collagen (CN), gelatin (GL), hyaluronic acid (HA), hydroxyapatite (HAp), polyethylene glycol (PEG), polycaprolactone (PCL), poly(lactic-co-glycolic) acid (PGLA), polylactic acid (PLA), and silk fibroin gained considerable attention due to their structure-properties relationship. The incorporation of CS within the polymer matrix results in increased mechanical strength and also imparts biological behavior to the designed PU formulations. The significant and growing interest in the LTE sector, this review aims to be a detailed exploration of CS-based polymers biomaterials for LTE. A brief explanation of the sources and extraction, properties, structure, and scope of CS is described in the introduction. After that, a full overview of the liver, its anatomy, issues, hepatocyte transplantation, LTE, and CS LTE applications are discussed.

Novel enrichment in biobased monomers of waterborne polyurethane dispersions as a textile finishing agent for poly-cotton fabrics.

This study introduces a novel biobased textile finishing agent synthesized as waterborne polyurethane dispersions (FCCB-WPUDs), utilizing bio-based monomers like fenugreek oil-based polyol, corn oil-derived emulsifier, and cellulose acetate butyrate (CAB) chain extender. The FCCB-WPUDs were prepared through the prepolymer polymerization method and characterized using FTIR, TGA, DMA, SEM, DLS, and swelling tests. Their application to poly-cotton fabrics significantly improved various fabric properties. The enhancements included increased washing fastness (from 3/4 ± 0.01 to 4 ± 0.02 for dyed and 3 ± 0.02 to 4/5 ± 0.02 for printed fabrics), rubbing fastness (from 3 ± 0.02 to 4/5 ± 0.03 for dyed and 4 ± 0.02 to 4/5 ± 0.03 for printed fabrics), and perspiration fastness (from 3 ± 0.02 to 4 ± 0.03 for acidic dyed and 3/4 ± 0.02 to 4 ± 0.02 for alkaline printed fabrics). Additionally, tear strengths improved significantly (from 13.66 ± 0.04 N/m to 20.53 ± 0.06 N/m for warp dyed and 10.85 ± 0.06 N/m to 15.14 ± 0.06 N/m for warp printed fabrics), along with tensile strengths (from 327 ± 5.38 N/m to 361 ± 3.26 N/m for warp dyed and 357 ± 5.34 N/m to 449 ± 4.90 N/m for warp printed fabrics). These improvements correlated with increasing CAB moles as a chain extender. This research presents a cost-effective and simple biobased method for textile finishing, offering an alternative to petrochemical-based monomers in conventional WPUD preparation.

Fabrication and In Vitro Biological Assay of Thermo-Mechanically Tuned Chitosan Reinforced Polyurethane Composites.

The progressive trend of utilizing bioactive materials constitutes diverse materials exhibiting biocompatibility. The innovative aspect of this research is the tuning of the thermo-mechanical behavior of polyurethane (PU) composites with improved biocompatibility for vibrant applications. Polycaprolactone (CAPA) Mn = 2000 g-mol-1 was used as a macrodiol, along with toluene diisocyanate (TDI) and hexamethylene diisocyanate (HMDI), to develop prepolymer chains, which were terminated with 1,4 butane diol (BD). The matrix was reinforced with various concentrations of chitosan (1-5 wt %). Two series of PU composites (PUT/PUH) based on aromatic and aliphatic diisocyanate were prepared by varying the hard segment (HS) ratio from 5 to 30 (wt %). The Fourier-transformed infrared (FTIR) spectroscopy showed the absence of an NCO peak at 1730 cm-1 in order to confirm polymer chain termination. Thermal gravimetric analysis (TGA) showed optimum weight loss up to 500 °C. Dynamic mechanical analysis (DMA) showed the complex modulus (E*) ≥ 200 MPa. The scanning electron microscope (SEM) proved the ordered structure and uniform distribution of chain extender in PU. The hemolytic activities were recorded up to 15.8 ± 1.5% for the PUH series. The optimum values for the inhibition of biofilm formation were recorded as 46.3 ± 1.8% against E. coli and S. aureus (%), which was supported by phase contrast microscopy.

Fabrication, Thermo-Mechanical, and Morphological Characterization of Hydroxyapatite-Reinforced Polyurethane Biocomposites as Dye Adsorbent for Effluent.

Petrochemical costs, limited fossil fuel reserves, and concerns about greenhouse gas emissions have raised interest in developing renewable approaches for synthesizing biobased polyurethanes. This study aims to solve these problems by making nanocrystalline hydroxyapatite (HA) reinforcement from waste chicken eggshells and adding it to polyurethane synthesis through in situ polymerization. The novelty of the research lies in the utilization of HA as a reinforcement material and renewable resources for polyurethane production. The results confirm that HA was successfully added to the polyurethane backbone. Fourier transform infrared (FTIR) analysis confirmed that the NCO groups were changed to urethane linkages. TGA examination demonstrated that the samples exhibited thermal stability up to 457 °C with a mass loss of 61%, indicating enhanced thermal stability. DMA measurements showed improved mechanical properties of the synthesized polyurethanes, with storage modulus (E'), complex modulus (E*), and compliance complex (D*) values of 0.177, 22.522, and 0.660 MPa-1, respectively. SEM analysis confirmed the homogeneous surface and well-dispersed HA reinforcement. Swelling characteristics revealed an optimum absorption of 30% H2O, 35% CH3OH, and 45% CCl4. Polyurethane composites exhibited significant chemical resistance and hydrolytic stability in acidic and basic media. Additionally, the composites demonstrated efficient adsorption of methyl orange from wastewater, with the PUHCI series achieving a maximum adsorption capacity of 85.50 mg/g under optimal conditions of 0.030 g/mL dose, 45 °C temperature, 2.5 h contact time, and pH 6.0..

Development of biocompatible aqueous polyurethane dispersions using chitosan and curcumin to improve physicochemical properties of textile surfaces.

The present research work aims to synthesize a blend of chitosan (CSN) and curcumin (CRN) based aqueous polyurethane dispersions (CSN-CRN APUDs) for the modification of textile surfaces. A series of anionic CSN-CRN APUDs were prepared by the reaction of isophorone diisocyanate (IPDI) with polyethylene glycol (PEG) and extended with chain extenders (CSN and CRN). Structural characterizations of prepared materials were examined through a fourier transformed infrared (FTIR) spectrophotometer. The performances of coated CSN-CRN APUDs on the colorfastness properties (washing, rubbing and perspiration) and the mechanical properties like tensile strength and tearing strength of plain weaved poly/cellulosic textiles (dyed, printed and white) were examined before and after the application of CSN-CRN APUDs. The findings showed that the mechanical and colorfastness properties of all the CSN-CRN APUDs treated poly/cellulosic textile samples were improved significantly as compared with untreated poly/cellulosic textile samples. The newly synthesized CSN-CRN APUD coating materials are sustainable and greener products, particularly derivatized from bio-resources. These coating materials can be utilized as outstanding eco-friendly substitutes for poly/cellulosic textile coatings for surface modifications.

Development of amylopectin based polyurethanes for sustained drug release studies.

In this research work, the crosslinked structure of polyurethane has been exploited for sustained drug delivery. Polyurethane composites have been prepared by the reaction of isophorone diisocyanate (IPDI) and polycaprolactone diol (PCL), which were further extended by varying the mole ratios of amylopectin (AMP) and 1,4-butane diol (1,4-BDO) chain extenders. The progress and completion of the reaction of polyurethane (PU) were confirmed using Fourier Transform infrared (FTIR) and nuclear magnetic resonance (1H NMR) spectroscopic techniques. Gel permeation chromatography (GPC) analysis showed that the molecular weights of prepared polymers were increased with the addition of amylopectin into the PU matrix. The molecular weight of AS-4 (Mw ≈ 99,367) was found threefold as compared to amylopectin-free PU (Mw ≈ 37,968). Thermal degradation analysis was done using thermal gravimetric analysis (TGA) and inferred that AS-5 showed stability up to 600 °C which was the maximum among all PUs because AMP has a large number of -OH units for linking with prepolymer resulting in a more cross-linked structure which improved the thermal stability of the AS-5 sample. The samples prepared with AMP showed less drug release (<53 %) as compared to the PU sample prepared without AMP (AS-1).

Biocompatibility and Hemolytic Activity Studies of Synthesized Alginate-Based Polyurethanes.

Many investigators have focused on the development of biocompatible polyurethanes by chemical reaction of functional groups contained in a spacer and introduced in the PU backbone or by a grafting method on graft polymerization of functional groups. In this study, alginate-based polyurethane (PU) composites were synthesized via step-growth polymerization by the reaction of hydroxyl-terminated polybutadiene (HTPB) and hexamethylene diisocyanate (HMDI). The polymer chains were further extended with blends of 1,4-butanediol (1,4-BDO) and alginate (ALG) with different mole ratios. The structures of the prepared PU samples were elucidated with FTIR and 1H NMR spectroscopy. The crystallinity of the prepared samples was evaluated with the help of X-ray diffraction (XRD). The XRD results reveal that the crystallinity of the PU samples increases when the concentration of alginate increases. Thermogravimetric (TGA) results show that samples containing a higher amount of alginate possess higher thermal stability. ALG-based PU composite samples show more biocompatibility and less hemolytic activity. Mechanical properties, contact angle, and water absorption (%) were also greatly affected.

Antimicrobial, selective antibiofilm, and antioxidant properties of plasticized PMMA/PVC and zinc oxide nano filler for biomedical applications.

The PMMA/PVC/ZnO-nanocomposites with zinc oxide nanoparticle (particle size < 50nm) was synthesized by solution casting technique. Morphology of the synthesized nano composites have been investigated by FT-IR and XRD techniques. After characterization, synthesized composites were applied for antibacterial, selective antibiofilm and free radical scavenging screening. Antibacterial studies were measured against different bacterial strains. Antibiofilms activities were studied against those bacterial model pathogenic strains which showed highest and minimum sensitivity as a (~94 and ~88 at 160 µg/ml). Antioxidant activity of synthesized nanocomposites were measured by DPPH and showed scavenging capacity with IC50, 110 to > 200 µg/mL. Thus PMMA/PVC/ZnO nanocomposite showed promising antimicrobial activity and antioxidant activity that can be used for biomedical applications.

Preparation and characterization of thermoplastic polyurethanes blended with chitosan and starch processed through extrusion.

The basic aim of the research work is to expand the application range of biomaterials in the field of medical by increasing antibacterial and biocompatible behavior of thermoplastic polyurethanes. Blends of thermoplastic polyurethanes with chitosan and starch were prepared through extrusion process. The effect of polysaccharides (corn starch and chitosan) incorporation in thermoplastic polyurethane matrix and polymers interaction on thermal and morphological aspects was investigated. Possible interaction among chitosan and starch within TPU matrix individually and together in a blend were assessed by Fourier Transform Infrared Spectroscopy (FTIR) and X-ray Diffractometer (XRD). The results indicated that thermoplastic polyurethanes were semi crystalline in nature whereas hydrophilicity of prepared thermoplastic polyurethanes was determined by contact angle. Biological properties endowed that TPU blended with chitosan and starch possessed antibacterial and hemolytic potential. Hence, it can be a suitable candidate for biomedical applications.

Preparation and characterization of guar gum based polyurethanes.

Guar gum (plant-based polysaccharide) is a promising candidate with immense potential. It is used as emulsifier, thickener, stabilizer, and as binding agent in many industries. In the present project, it was planned to synthesize guar gum based polyurethanes by varying the amount of guar gum. Guar gum (GG) was used along with hydroxyl-terminated polybutadiene (HTPB) as soft segment, which was then reacted with isophorone diisocyanate (IPDI) to form PU pre-polymers. In last step, these -NCO terminated pre-polymers were extended with 1,4 butane diol as chain extender. The prepared polyurethane samples were then characterized by using FTIR, solid-state 1HNMR and X-ray diffraction (XRD). Thermal behavior of the samples was studied by thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). Results indicated that the incorporation of guar gum in PU backbone improved its thermal behavior and crystallinity.

Synthesis and characterization of hydroxyethyl cellulose copolymer modified polyurethane bionanocomposites.

Bio based polyurethane nanocomposites (renewable thermosets) show a diverse range in properties, processing components and production of smart materials for health, food, and energy sectors. In this work, polyurethane nanocomposites based on isophorone diisocyanate (IPDI), and hydroxyl terminated-polybutadiene (HTPB) incorporating clay were modified using hydroxyethyl cellulose (HLAC) to be further assessed for thermal and mechanical properties. Elastomers samples were prepared by blending clay suspension and PU prepolymer to attain clay contents of 0.3, 0.5, and 1% (weight on dry basis) along with butane diol and HLAC chain extenders. Effect of nanofiller aggregation and dispersion on the thermal degradation and surface morphology of the bionanocomposites were studied. Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), scanning electron microscopy/energy dispersive X-ray (SEM/EDX) and thermal gravimetric (TG) techniques were used to investigate the interactions among PU matrix, clay nanofillers, and HLAC. Mechanical testing indicated an increase in tensile strength and a decrease in elongation at break (%) by just adding 0.3 wt% clay. The thermal stability of the bionanocomposites was improved with the addition of clay. The results of the thermal and mechanical studies demonstrated the feasibility of the bionanocomposites as strong and thermally stable elastomers with low filler loading.

Synthesis and molecular characterization of chitosan/alginate blends based polyurethanes biocomposites.

The present work aims to examine the structural properties of polyurethanes bio-composites with mole ratios of alginate and chitosan. For this concern, a two-step reaction mechanism was carried out; in the first step isocyanate (-NCO) terminated pre-polymer was synthesized by the reaction of hexamethylene diisocyanate (HMDI) and hydroxyl-terminated polybutadiene (HTPB). The pre-polymer was further extended with 1,4-butanediol (BDO), chitosan (CS) and alginate (ALG) in the second step. Structural and functional group elucidation was done by using Fourier Transform Infra-red (FT-IR) and proton nuclear magnetic resonance (1H NMR) spectroscopy. The crystallinity of the prepared samples was investigated by using X-ray diffraction (XRD) method, the maximum observed intensity was 7704 a.u. The thermal properties of polyurethane composites were carried out using thermogravimetric analysis (TGA) and differential scanning calorimeter (DSC). The TGA results showed that thermal stability of RPU-5 was 20 °C more than RPU-1 at each corresponding degradation temperature. It is observed all physical parameters like crystallinity, glass transition temperature, melting point are much dependent on ratio of chain extenders. Overall, CS based samples along with small amount of ALG showed better thermal properties.

Influence of Graphene Oxide Contents on Mechanical Behavior of Polyurethane Composites Fabricated with Different Diisocyanates.

The exceptional behavior of graphene has not yet been entirely implicit in the polymer matrix. To explore this fact in the present work, two series of Polyurethan (PU) composites were synthesized. The structural modification was observed by the use of two different diisocyanate of methylene diisocyanate (MDI) and hexamethylene diisocyanate (HMDI) in hydroxylterminated polybutadiene (HTPB) by using I,4 Butane diol (BD) as the chain extender. The variation in hard segment up to 25 (wt.%) in both series led to significant changes in the mechanical behavior of graphene oxide (GO) induced composites. Both series were prepared by an in situ polymerization process. Fourier transform infrared (FTIR) analysis showed a peak in the region of 1700 cm-1, which confirmed the conversion of the NCO group into urethane linkages. Thermal gravimetric analysis (TGA) revealed a thermal stability up to 450 °C @ 90% weight loss. The swelling behavior showed the optimum uptake of 30% of water and 40% of dimethyl sulfoxide (DMSO) with aliphatic diisocyanate. The values of storage modulus (E'), complex modulus (E*), and compliance complex (D*) were observed up to 7 MPa, 8 Mpa, and 0.7 MPa-1, respectively. The degree of entanglement (N) values were calculated from DMA and were found in the range of 1.7 × 10-4 (mol/m3). Phase segregation of PU was observed by scanning electron microscopy (SEM), elucidating the morphology of composites.

Polyvinylidene fluoride nanocomposite super hydrophilic membrane integrated with Polyaniline-Graphene oxide nano fillers for treatment of textile effluents.

Water pollution from the fashion industries containing dyes has become a major source of water pollution. These anthropogenic contaminated waters directly enter irrigation and drinking water systems, causing irreversible environmental damage to human health. Nanomembrane technology has attracted extensive attention to remove these toxic chemicals but new approaches are still required for improving removal efficiency and control the channel size. The work deals with the fabrication of a novel hybrid polyvinylidene fluoride (PVDF)-polyaniline (PANI) membrane with graphene oxide (GO). Incorporation of PANI-GO as a nanofiller has significantly improved antifouling properties and a solvent content of the fabricated membrane. Besides, pure water flux also increases from 112 to 454 L m-2 h-1 indicating the hydrophilic nature of the nanocomposite membrane. Among various compositions, the nanocomposites membrane with 0.1 %w/v GO demonstrated a maximum of 98 % dye rejection at 0.1 MPa operating pressure. After multiple testing of the membrane, the flux recovery ratio reached about 94 % and dyes rejection improved with the addition of PANI-GO. The removal efficiency of the composite membrane for Allura red is 98 % and for methyl orange is 95 %. Based on the above results the PVDF/PANI/GO membranes are recommended for practical use in wastewater treatment, particularly for anionic dyes removal from textile effluents.

Synthesis and characterization of graphene nanoplatelets-hydroxyethyl cellulose copolymer-based polyurethane bionanocomposite system.

Bionanocomposites is an emerging class of biohybrid materials, have a significant impact in environmental and biomedical fields owing to their high performance, lightweight, unique, and ecofriendly properties. A major challenge in the multiphase bionanocomposites system is to subtle control over the performance by managing the individual properties of reacting components. Herein, we presented the preliminary investigation on bionanocomposite system based on graphene nanoplatelets (GNPs) and hydroxyethyl cellulose graft poly(lactic acid) copolymer-polyurethane (HLAC-PU) with the aim to understand the structure property correlation for proposed applications in electronics and medical areas. The HLAC was fabricated by graft copolymerization of hydroxyethyl cellulose (HEC) and lactic acid (LA) with dibutyltin dilaurate. The HLAC was used to get a bio-functionalized PU matrix reinforced with GNPs by step-growth polymerization method. The structural, surface, and thermal properties of the HLAC and GNPs-HLAC-PU bionanocomposites were studied. The spectroscopic techniques confirmed the structure of bionanocomposites by the identification of related bands. The SEM/EDX results demonstrated that the 0.3 wt% of GNPs dispersed well in the HLAC-PU matrix and offered higher crystallinity. The reinforcement of the 0.3 wt% of GNPs has meaningfully enhanced the thermal stability producing higher residue contents. The reinforced GNPs filler increased the water resistance of bionanocomposites by reducing their water vapor permeability.

Preparation of hydroxyethyl cellulose/halloysite nanotubes graft polylactic acid-based polyurethane bionanocomposites.

2-Hydroxyethyl cellulose graft polylactic acid copolymer (HLAC) was prepared by graft copolymerization of lactic acid (LA) and 2-hydroxyethyl cellulose (2-HEC), initiated by dibutyltin dilaurate (DBTDL) catalyst in aqueous media. Halloysite nanotubes (HNTs)/polyurethane (PU) bionanocomposites were prepared using the HLAC as chain extender in the step-growth polymerization. HNTs were dispersed in HLAC based PU matrix at different weight ratios of 0.30, 0.50, 1.00, and 3.00. Chemical structure and morphology of the graft copolymer and bionanocomposite elastomers were characterized using solid state 1H NMR, ATR-FTIR, XRD, and SEM-EDX, while thermal degradation behavior was studied by TGA and DSC techniques. Surface morphology of the HNTs reinforced HLAC/PU bio-nanocomposites demonstrated the homogeneous dispersion of HNTs with little wavy rough surface at low contents which turned to be brittle at higher contents due to agglomerated HNTs. It is observed that the lower contents of HNTs were completely exfoliated in the HLAC/PU matrix. Crystalline pattern of the elastomers improved at lower contents of HNTs that enhanced the thermal stability of the bionanocomposites. The mechanical testing suggested that HNTs/HLAC/PU bionanocomposites have higher values of tensile strength and % elongation with only 0.3-0.5 wt% contents of HNTs that suggested the potential applications of elastomers at economic cost.

Structural elucidation and biological aptitude of modified hydroxyethylcellulose-polydimethyl siloxane based polyurethanes.

The main aim of this research work was to incorporate modified hydroxyethylcellulose (HEC) into PDMS based polyurethanes. In the first part, modification of hydroxyethylcellulose was carried out by polymerizing lactic acid (LA) with HEC using ammonia water to prepare poly(lactic acid) grafted hydroxyethylcellulose (HEC-g-PLA). The maximum degree of grafting (59.5%) was achieved at: 1:9 mole ratio of HEC/LA, 2 h, 80 °C (for activation) and 4 h, 90 °C (for reaction) with 0.74 degree of substitution. In the second part, hydroxyl terminated polybutadiene (HTPB) was reacted with isophorone diisocyanate to produce NCO-terminated polyurethane prepolymer which in turn extended by chain extender to synthesize polydimethyl siloxane hydroxyl terminated (PDMS) based polyurethanes. Effect of incorporation of HEC-g-PLA as a chain extender was studied by varying its mole ratio in PDMS based PUs. Characterization of HEC-g-PLA and all PDMS/HEC-g-PLA based polyurethane samples was carried out by using Fourier Transform Infrared (FTIR) and proton solid-state NMR (1H SS NMR). Biological behavior of synthesized samples was also tested by various biological activities and results indicated that incorporation of HEC-g-PLA in to PDMS based polyurethanes leads to improvement in antibacterial activity, anti-biofilm inhibition, biocompatibility and non-mutagenicity. Therefore, HEC-g-PLA/PDMS blended polyurethanes are promising biomaterials that have potential for various biomedical applications.

A review on grafting of hydroxyethylcellulose for versatile applications.

Hydroxyethylcellulose (HEC) is a biocompatible, biodegradable, nontoxic, hydrophilic, non- ionic water soluble derivative of cellulose. It is broadly used in biomedical field, paint industry, as a soil amendment in agriculture, coal dewatering, cosmetics, absorbent pads, wastewater treatment and gel electrolyte membranes. Industrial uses of HEC can be extended by the its grafting with different polymers including poly acrylic acid, polyacrylamide, polylactic acid, polyethyleneglycol, polydimethyleamide, polycaprolactone, polylactic acid and dimethylamino ethylmethacrylate. This permits the formation of new biomaterials with improved properties and versatile applications. In this article, a comprehensive overview of graft copolymers of HEC with other polymers/compounds and their applications in drug delivery, stimuli sensitive hydrogels, super absorbents, personal hygiene products and coal dewatering is presented.