Synthesis, properties and biomedical applications of poly(glycerol sebacate) (PGS): A review

Poly(glycerol sebacate) (PGS) is a biodegradable polymer increasingly used in a variety of biomedical applications. This polyester is prepared by polycondensation of glycerol and sebacic acid. PGS exhibits biocompatibility and biodegradability, both highly relevant properties in biomedical applications. PGS also involves cost effective production with the possibility of up scaling to industrial production. In addition, the mechanical properties and degradation kinetics of PGS can be tailored to match the requirements of intended applications by controlling curing time, curing temperature, reactants concentration and the degree of acrylation in acrylated PGS. Because of the flexible and elastomeric nature of PGS, its biomedical applications have mainly targeted soft tissue replacement and the engineering of soft tissues, such as cardiac muscle, blood, nerve, cartilage and retina. However, applications of PGS are being expanded to include drug delivery, tissue adhesive and hard tissue (i.e., bone) regeneration. The design and fabrication of PGS based devices for applications that mimic native physiological conditions are also being pursued. Novel designs range from accordion-like honeycomb structures for cardiac patches, gecko-like surfaces for tissue adhesives to PGS (nano) fibers for extra cellular matrix (ECM) like constructs; new design avenues are being investigated to meet the ever growing demand for replacement tissues and organs. In less than a decade PGS has become a material of great scrutiny and interest by the biomedical research community. In this review we consolidate the valuable existing knowledge in the fields of synthesis, properties and biomedical applications of PGS and PGS-related biomaterials and devices.     

Green synthesis of silver nanoparticles using Zea mays and exploration of its biological applications

The biosynthesis of silver nanoparticles (AgNPs) has been proved to be a cost effective and environmental friendly approach toward chemical and physical methods. In the present study, biosynthesis of AgNPs was carried out using aqueous extract of Zea mays (Zm) husk. The initial colour change from golden yellow to orange was observed between 410 and 450 nm which confirmed the synthesis of AgNPs. Also, dynamic light scattering‐particle size analysis confirmed the average size to be 113 nm and zeta potential value of −28 kV. The morphology of synthesised Zm AgNPs displayed flower‐shaped structure, X‐ray diffraction pattern revealed the strongest peaks at 2θ = 38.6° and 64° which proved that the nanoparticle has the face centred crystalline structure. The Fourier transform infrared spectroscopy results showed strong absorption bands at 1394.53, 2980.02 and 2980.02 cm⁻¹ due to the presence of alkynes, carboxylic acids, alcoholic and phenolic groups. The maximum zone of inhibition was observed against Salmonella typhi (22 mm) and Candida albicans (18 mm). The synthesised nanoparticles exhibited more free radical scavenging activity than the aqueous plant extract. This is the first report on the synthesis of AgNP from Zm husk, delivers the efficient and stable Zm AgNPs through simple feasible approach toward green biotechnology.Inspec keywords: silver, nanoparticles, nanofabrication, light scattering, particle size, X‐ray diffraction, crystal structure, Fourier transform infrared spectra, absorption coefficients, free radicalsOther keywords: green synthesis, silver nanoparticles, biosynthesis, environmental friendly approach, aqueous extract, Zea mays husk, colour change, golden yellow, dynamic light scattering‐particle size analysis, average size, zeta potential value, flower‐shaped structure, X‐ray diffraction pattern, face centred crystalline structure, Fourier transform infrared spectroscopy, absorption bands, alkynes, carboxylic acids, alcoholic groups, phenolic groups, Salmonella typhi, Candida albicans, free radical scavenging activity, aqueous plant extraction, green biotechnology, size 113 nm, wavelength 410 nm to 450 nm     

Larvicidal activity of green synthesized silver nanoparticles using Excoecaria agallocha L. (Euphorbiaceae) leaf extract against Aedes aegypti

Green synthesis of silver nanoparticles (AgNPs) using plant extracts has been achieved by eco‐friendly reducing and capping agents. The present study was conducted to evaluate the larvicidal efficacies of AgNPs synthesized using aqueous leaf extracts of Excoecaria agallocha against dengue vector, Aedes aegypti. The 3^rd and 4^th instar larvae of A. aegypti were exposed to various concentrations of aqueous extracts of E. agallocha, synthesized AgNPs and also crude solvent extracts (methanol and chloroform) for 24 h. The formation of AgNPs using aqueous leaf extracts was observed after 30 min with a characteristic colour change. The results recorded from UV‐Vis spectrum, XRD, FTIR, EDX, SEM and HR‐TEM were used to characterize and confirm the biosynthesis of AgNPs. The highest larvicidal efficacy of synthesized AgNPs was observed against 3^rd instar larvae at LC₅₀ 4.65 mg/L, LC₉₀ 14.17 mg/L and 4^th instar larvae with a concentration of LC₅₀ 6.10 mg/L, LC₉₀ 15.64 mg/L. A significant larvicidal activity was also observed with crude methanolic extracts against 3^rd instar larvae at a concentration LC₅₀ 41.74 mg/L, LC₉₀ 123.61 mg/L and 4^th instar larvae at a concentration of LC₅₀ 52.06 mg/L, LC₉₀ 166.40 mg/L as compared to the chloroform extract.Inspec keywords: silver, nanoparticles, nanofabrication, microorganisms, cellular biophysics, organic compounds, ultraviolet spectra, visible spectra, X‐ray diffraction, Fourier transform infrared spectra, X‐ray chemical analysis, scanning electron microscopy, transmission electron microscopyOther keywords: larvicidal activity, green synthesised silver nanoparticles, Excoecaria agallocha L. leaf extract, Aedes aegypti, plant extracts, capping agents, larvicidal efficacies, aqueous leaf extracts, excoecaria agallocha, dengue vector, Aedes aegypti, aegypti, aqueous extraction, E. agallocha, crude solvent extracts, methanol, chloroform, characteristic colour change, ultraviolet‐visible spectrum, X‐ray diffraction, Fourier‐transform infrared spectroscopy, EDX, scanning electron microscopy, high‐resolution transmission electron microscopy, AgNP biosynthesis, larvicidal efficacy, third instar larvae, instar larvae, crude methanolic extracts, chloroform extraction, time 24 h     

Blends of cardanol-based epoxidized novolac resin and CTBN for application in surface coating: a study on thermal,mechanical, chemical,and morphological characteristics

Blend samples of cardanol-based epoxidized novolac resin and different weight percentages of carboxyl-terminated butadiene acrylonitrile (CTBN) were developed and cured with stoichiometric amounts of aliphatic amine. The formation of various products during the curing of blend samples has been studied by Fourier-transform infrared spectroscopy. The dynamic differential scanning calorimeter scans showed that the pure epoxies and their blend samples with CTBN cured in the temperature range of 100–150°C. The blend sample containing 15 wt% CTBN showed the least cure time (at 120°C) among all other blend samples. Upon evaluation, it was found that blend samples exhibit better properties compared to pure epoxy resin in terms of increase in impact strength and elongation-at-break of the casting and gloss, scratch hardness, adhesion, and flexibility of the film. The improvement in these properties indicates that the rubber modified resin would be more durable than the epoxy based on cardanol. Chemical and morphological properties of the formulated resins were also determined. The thermal stability of the blend samples containing 15 wt% CTBN in epoxy resin was the highest among all other prepared systems. The blend morphology, studied by scanning electron microscope, showed the presence of precipitated discrete rubber particles, which dispersed throughout the epoxy matrix—i.e., they revealed the presence of two-phase morphological features.     

A green chemistry approach for the synthesis and characterization of bioactive gold nanoparticles using Azolla microphylla methanol extract

This article reports the environmentally benign synthesis of gold nanoparticles （GNPs） using methanol extract of Azolla microphylla as the stabilizing and reducing agent. The GNPs were characterized by UV-vis spectrophotometry and FTIR, and the morphological characteristics were analyzed by XRD, FESEM-EDX and HRTEM. The GNPs could be formed in very short time, even in less than 30 min. The nanoparticles measured by UV-spectrophotometer demonstrated a peak at 540 nm corresponding to surface plasmon resonance spectra, and the peaks showed by FTIR suggested the presence of organic biomolecules on the surface of the GNPs. XRD results confirmed the crystalline nature of the GNPs, and FESEM-EDX and HRTEM analyses had been performed in the size ranges of 17-40nm and 1.25-17.5nm respectively. The synthesized GNPs showed excellent antioxidant activity. This study shows the feasibility of using plant sources for the biosynthesis of GNPs.     

Proton Nuclear Magnetic Resonance-Based Method for the Quantification of Epoxidized Methyl Oleate

Epoxidized methyl esters (EMO) with their high oxirane ring reactivity, acts as a raw material in the synthesis of various industrial chemicals including polymers, stabilizers, plasticizers, glycols, polyols, carbonyl compounds, biolubricants etc. EMO has been generally quantified by the gas chromatography (GC) and high-performance liquid chromatography (HPLC) techniques. Taking into the account of the limitations of these techniques, two qHNMR-based equations have been proposed for the quantification of EMO in the mixture of EMO and methylesters (MO). The validity of the proposed method was determined using standard mixtures of MO and EMO having different molar concentrations. The developed equations have been applied on the samples of EMO prepared from oleic acid in two-step process viz., esterification followed by epoxidation. The qHNMR-based EMO quantification showed acceptable agreement with the results obtained from HPLC analysis.     

Bi-phasic bio-conversion of sulfur present in model organo-sulfur compounds and hydro-treated diesel

Bacterial strain of Rhodococcus sp. (JUBT1) isolated from petrol/diesel station has been used for the desulfurization of different model organo-sulfur compounds like DBT, substituted DBT, etc. which are difficult to remove in the conventional hydro-desulfurization of diesel fraction. The initial concentration of organo-sulfur compounds has been varied in the range of 100–1000 mg/dm³. Under the present experimental range, the bacterial growth has been observed to follow Haldane-type kinetics characterizing the presence of substrate inhibition. The extent of inhibition by the substrate has been observed to increase with the number of substituents in the same range of initial concentration of different organo-sulfur compounds. The values of intrinsic kinetic parameters, like maximum desulfurization rate, v_max, half saturation constant, K_S, inhibition constant, K_Si and the maximum substrate concentration, C_Smax, corresponding to the maximum uninhibited rate of desulfurization, have been determined using each organo-sulfur compound having different number of substituents as limiting substrate. Relative changes in the values of the kinetic parameters have been correlated to the number of substitutions. Separate studies have also been conducted to determine the kinetics of bio-desulfurization of a hydro-treated diesel fraction. The concentration of sulfur in diesel was selected in the range of 100–500 mg/dm³.

The effect of aqueous to non-aqueous ratio on the rate of specific desulfurization of hydro-treated diesel fraction in the range from 1:9 to 9:1 has also been studied in the present investigation. Mathematical models have been developed to predict the conversion of sulfur during batch-type bio-desulfurization of model compounds as well as diesel having known distribution of organo-sulfur compounds. The predictions of the model satisfactorily compare with the experimental results.     

Thermal and mechanical properties of nano-titanium dioxide-doped polyvinyl alcohol

Organic polymers exhibit poor thermal stability and inferior mechanical properties. Significant improvement in mechanical and thermal properties of polymers can be achieved by homogeneous distribution of inorganic materials preferably in nano size. In this study, these properties of polyvinyl alcohol were found to improve by addition of nano-titanium dioxide. Microwave irradiation method was used to prepare nano-titanium dioxide and doped in polyvinyl alcohol matrix to formulate the composite film. The spectral and morphological characterizations of the composites were carried out by the conventional techniques. Various mechanical properties were determined by Tinus Oisen universal testing machine. Thermal gravimetric analysis and differential scanning calorimetry were used for studying the thermal properties of the composites. Shift in decomposition temperature of polyvinyl alcohol indicated the enhanced thermal stability of polyvinyl alcohol. The composite also exhibited significant improvement in all the mechanical properties.     

Indian black rice: A brewing raw material with novel functionality

Indian black rice (Chakhao Poireiton) is a pigmented variety, rich in anthocyanins and other phytonutrients. With growing interest in the use of local raw materials in brewing, it was of interest to develop protocols for malting and brewing with Chakhao Poireiton to see whether the antioxidant capacity of anthocyanins could be delivered into finished beer. Protocols for brewing with 100% malted rice were developed and the performance of Indian black rice compared with that of an Italian white rice cultivar suited to brewing. The apparent fermentabilities of rice worts were 69.5% (black) and 67.3% (white), yielding beers of 3.28 and 3.19% ABV respectively. Black rice worts were deficient in free amino nitrogen (83.5 mg/L relative to 137 mg/L for white rice) and would need nitrogen supplementation to avoid issues with fermentation, e.g. elevated diacetyl. Black rice beer had an orange-red hue as a result of extraction of anthocyanin pigments (2.84 mg/L). The oxidative stability of 100% rice beers was measured using electron spin resonance spectroscopy and both samples were found to be unusually stable. Interestingly, when rice beers were blended with a control barley malt derived lager in varying proportions (10, 25, 50%), the oxidative stability was improved, relative to the control lager, particularly so in the case of black rice beer, which contained an antioxidant capacity over and above that of the white rice beer. Future studies are required to determine whether the noted oxidative stability of 100% rice malt beers results in a more flavour-stable beer. © 2019 The Institute of Brewing & Distilling