Main-chain water-soluble polyphosphoesters: multi-functional polymers as degradable PEG-alternatives for biomedical applications

Polyphosphoesters (PPEs) are a class of (bio)degradable polymers with high chemical versatility and functionality. In particular, water-soluble PPEs with the phosphoester group in the polymer backbone are currently discussed as a potential alternative to poly(ethylene glycol) (PEG). Ring-opening polymerization of typically 5-membered cyclic phosphoesters gives straightforward access to various well-defined PPEs. Several PPE candidates have proven their biocompatibility in vitro in terms of cytocompatibility, antifouling properties, “stealth effect”, degradability (hydrolytic and enzymatic), and some promising in vivo results in drug delivery vehicles. The possibility to control the properties with the appropriate tuning of the lateral chain makes PPEs especially appealing. This review summarizes recent developments of such PPEs for biomedical applications, e.g. in protein-polymer conjugates, hydrogels for tissue engineering, or nanocarriers for drug and gene delivery. We summarize the progress made over the years, highlighting the strengths and the shortcomings of PPEs for these applications to date. We critically evaluate the current state of the art, try to assess their potential and to predict future perspectives, shedding light on the pathway that needs to be followed to translate into clinics

A versatile method to fingerprint and compare the oxidative behaviour of lipids beyond their oxidative stability

: In this work we propose the use of isothermal thermogravimetry to evaluate the oxidative stability of a lipid and to evaluate how the glyceride composition affects the entire oxidative process, to quantify the oxidation undertaken by the lipid, and numerically compare the oxidative behaviour of different lipids. The innovative aspect of the present method lies in the acquisition of a prolonged "oxygen uptake" curve (4000-10,000 min) of a lipid under oxygen and in the development of a semi-empirical fitting equation for the experimental data. This provides the induction period (oxidative stability), and allows to evaluate the rate of oxidation, the rate and the magnitude of oxidative degradation, the overall mass loss and the mass of oxygen taken by the lipid upon time. The proposed approach is used to characterize the oxidation of different edible oils with different degrees of unsaturation (linseed oil, sunflower oil, and olive oil) as well as chemically simpler compounds used in the literature to model the autoxidation of vegetable oils and lipids in general: triglycerides (glyceryl trilinolenate, glyceryl trilinoleate and glyceryl trioleate) and methyl esters (methyl linoleate and methyl linolenate). The approach proves very robust and very sensitive to changes in the sample composition

Geopolymers as a potential material for preservation and restoration of Urban Build Heritage: an overview

Since the introduction of the term 'geopolymer' by Davidovits in 1978, many works have been published, sometimes providing clear and concise indications, and other times creating confusion about what are a geopolymer. What seems interesting beyond the terminology discourse is the advantage of low CO2 emissions, the use of waste industrial byproducts in their implementation and the resistance to air pollution and aggressive agents. Playing on the combination of the different precursors and alkaline activators, geopolymers can reach competitive mechanical properties and significant environmental benefits. The materials, with specially designed formulations, can be fireproof, breathable, resistant to rising salts and acid rain, as well as products with low emission of carbon dioxide. Furthermore, a further advantage is the ability to imitate natural, artificial and stone materials. There are hundreds of papers about characteristics, properties both of precursors and final product, but only a few of them about the Cultural Heritage Application. Despite this, the data shown by the few publications present to date give hope for a use of these materials for the consolidation, conservation and restoration of the heritage built within the historical centres, where the low CO2 emissions and the characteristics shown by the geopolymers could bring a huge benefit to the environment and the protection of the structures themselves. In this work, we briefly review the bibliography available on the applications of these materials to Cultural Heritage, hypothesising future uses aimed at specific urban contexts, where the application could play a key role in the future projects to restore the built heritage

Structural and thermoanalytical characterization of 3D porous PDMS foam materials: The effect of impurities derived from a sugar templating process

Polydimethylsiloxane (PDMS) polymers are extensively used in a wide range of research and industrial fields, due to their highly versatile chemical, physical, and biological properties. Besides the different two-dimensional PDMS formulations available, three-dimensional PDMS foams have attracted increased attention. However, as-prepared PDMS foams contain residual unreacted low molecular weight species that need to be removed in order to obtain a standard and chemically stable material for use as a scaffold for different decorating agents. We propose a cleaning procedure for PDMS foams obtained using a sugar templating process, based on the use of two different solvents (hexane and ethanol) as cleaning agents. Thermogravimetry coupled with Fourier Transform Infrared Spectroscopy (TG-FTIR) for the analysis of the evolved gasses was used to characterize the thermal stability and decomposition pathway of the PDMS foams, before and after the cleaning procedure. The results were compared with those obtained on non-porous PDMS bulk as a reference. Micro-CT microtomography and scanning electron microscopy (SEM) analyses were employed to study the morphology of the PDMS foam. The thermogravimetric analysis (TGA) revealed a different thermal behaviour and crosslinking pathway between bulk PDMS and porous PDMS foam, which was also influenced by the washing process. This information was not apparent from spectroscopic or morphological studies and it would be very useful for planning the use of such complex and very reactive systems

Thermodynamic stability of myoglobin-poly(ethylene glycol) bioconjugates: A calorimetric study

PEGylated proteins are widely used for therapeutic applications, therefore a fundamental understanding of the conjugates’ structure and their behaviour in solution is essential to promote new developments in this field. In the present work, myoglobin-poly(ethylene glycol) conjugates were synthesized and studied by differential scanning calorimetry and UV–vis spectroscopy to obtain information on the bioconjugates’ thermodynamic stability, also focusing on PEG’s role on the solvent-protein surface interaction. The overall results of this study indicated a thermal destabilization of the protein that follows the extent of the bioconjugation without, however, compromising the native structure which remains functional. Moreover, the myoglobin PEGylation prevented the post-denaturation aggregation phenomena and enhanced the protein thermal reversibility. The thermodynamic interpretation of the data indicated that the bioconjugation influences the solvent-exposed protein surface difference between native and denatured state, contributing to the interpretation of the overall protein modification and functionality

A circular dichroism study of the protective role of polyphosphoesters polymer chains in polyphosphoester‐myoglobin conjugates

Protein-polymer conjugates are a blooming class of hybrid systems with high biomedical potential. Despite a plethora of papers on their biomedical properties, the physical–chemical characterization of many protein-polymer conjugates is missing. Here, we evaluated the thermal stability of a set of fully-degradable polyphosphoester-protein conjugates by variable temperature circular dichroism, a common but powerful technique. We extensively describe their thermodynamic stability in different environments (in physiological buffer or in presence of chemical denaturants, e.g., acid or urea), highlighting the protective role of the polymer in preserving the protein from denaturation. For the first time, we propose a simple but effective protocol to achieve useful information on these systems in vitro, useful to screen new samples in their early stages

An investigation into the curing of urushi and tung oil films by thermoanalytical and mass spectrometric techniques

Urushi is the oldest and most precious lacquer used since antiquity in East Asia. For artistic purposes, in order to obtain suitable rheological properties, the lacquer is usually mixed with a vegetable oil. In this work we investigated the curing process of urushi/tung oil mixtures in order to highlight the chemical interactions at the molecular level between the two materials. A multi-analytical approach was adopted, based on thermogravimetry (TG), differential scanning calorimetry (DSC), gas chromatography-mass spectrometry (GC-MS), evolved gas analysis mass spectrometry (EGA-MS), analytical pyrolysis coupled with gas chromatography and mass spectrometry (Py-GC-MS) and high performance liquid chromatography-mass spectrometry (HPLC-MS). Fresh and aged mixtures were analysed and the results were compared with those obtained from the analysis of the individual materials. The data highlighted that different polymerization and oxidation mechanisms take place in oil/urushi mixtures compared to the pure materials. Py-GC-MS and GC-MS showed that the profile of aliphatic mono- and di-carboxylic acids was drastically different for the aged film of pure tung oil compared to the mixtures. The ratio between the relative content of azelaic and palmitic acids was much lower in the mixtures than in the pure oil, highlighting a lower level of oxidation. On the other hand, the relative content of short chain carboxylic acids, which are produced by pyrolysis of the cross-linked oil network, increased as the concentration of urushi in the mixtures increased, thus indicating an increasing level of reticulation. HPLC-MS showed a relatively higher amount of triglycerides with hydroxylated fatty acids – the intermediate oxidation product of polyunsaturated fatty acids - in the mixtures with respect to pure tung oil

A Complex Case of Pulmonary Silico-Tuberculosis and Review of Literature

Silicosis caused by the inhalation/deposition of free silica particles is characterized by pulmonary inflammation/fibrosis. Among the clinical disorders associated with silicosis, tuberculosis is by far the most prominent. A 66-year-old male non-smoker, originally from North Africa, reported a dry cough and significant weight loss. He was a foundry worker. He had a medical history of bladder carcinoma associated with schistosomiasis. Computed tomography (CT) and positron emission tomography (PET)/CT showed bilateral multiple hypermetabolic lung nodules, some with cavitation. The patient underwent surgical resection of the largest nodule, which was highly suspicious of lung metastasis. The histological examination revealed multiple nodular formations. Several lesions showed the characteristic features of silicotic nodules. There were also adjacent well-formed granulomas, some with central caseous necrosis. A real-time polymerase chain reaction, performed for the identification and quantification of the DNA of the Mycobacterium tuberculosis complex, was positive. Pulmonary silico-tuberculosis is often encountered in patients with a history of silica exposure in tuberculosis-endemic areas. This case serves as a reminder to never underestimate patient occupational exposure and geographic origin. A careful histological diagnosis and molecular investigation are mandatory when approaching difficult cases, especially patients with a prior cancer history and clinical/radiological features suggestive of tumour recurrence/metastasis