Carbohydrate/protein hydrogels as responsive scaffolds in controlling inorganic crystallization

<p>The strategies that both invertebrate and vertebrate organism use to produce organic-inorganic composite materials for different purposes such as mechanical support and protection for the body are fascinating. While extensive research has been done on understanding the basic principles of biomineral formation, mimicking the critical principles of the mechanisms of biomineralization in vitro and fully capturing the structural information and characteristics remain challenging issues for scientists. Calcium is an essential element in biological systems. It plays a central role in the mineralization and maintenance of the skeleton as well as in fundamental physiological processes including growth and development in vertebrates. Within a biological organism calcium ions are stored, delivered, or released in the presence of different anions such as phosphate, carbonate and citrate. Competition between the different anions which interact with calcium ions in different hydrogel matrices leads to manipulation of the various composite materials produced such as bone and nacre. Soluble anionic acidic macromolecules associated with biominerals play a vital role in modulating the mineral morphology and hierarchy of the organized composite. Understanding the interaction between the constituent ions and the organic matrix is crucial if we are to make synthetic materials, the structure and properties of which replicate those of native biominerals, or materials that have the storage and/or release characteristics of foods, for example. Carbohydrate-based hydrogels versus protein-based hydrogels are used here as scaffolds for the synthesis of calcium carbonate and calcium phosphate biominerals. Water soluble acidic additives are used to modulate the nucleation and growth of the minerals. In particular chitosan and gelatin hydrogel templates were used as the mineralization scaffolds. Three different mineralization methods were used: the Kitano, alternate soaking and McGrath methods. Monomeric vs. polymeric additives (acrylic acid, glutamic acid, aspartic acid and their corresponding polymers) were introduced into all systems in order to control the nucleation and growth of the so-formed minerals. The morphology, crystallinity, polymorphism and composition of the synthesized organic-inorganic composites were investigated. Analyses were carried out using a number of techniques including Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM), X-ray Diffraction (XRD), micro-Raman spectroscopy and solid-sate NMR. In the case of calcium carbonate the morphology and crystallinity were more affected by the use of polymeric additives compared with their monomeric equivalents. In particular the calcium carbonate preferentially grew laterally within and on the periphery of the chitosan or gelatin hydrogel scaffold. This results from the formation of a polyelectrolyte complex between the chitosan or gelatin hydrogels and the added polymer. The presence of the polyelectrolyte complex modifies the nucleation of the mineral. Nanoparticles are preferentially formed which then aggregate together maintaining a lateral perspective with the scaffold. In the case of calcium phosphate mostly spherical and platelet-shaped morphologies composed of amorphous calcium phosphate and poorly crystalline hydroxylapatite respectively were always formed within both chitosan and gelatin hydrogel scaffolds. pH was also found to be a key factor in controlling which polymorph of calcium phosphate precipitates. The crystallinity is influenced by the presence of additives for chitosan scaffold. For systems with added aspartic or polyaspartic acid platelet-shaped CaP forms. These crystals are more highly crystalline compared to those where predominately the porous spherical calcium phosphate morphology is observed which form when L-glutamic acid is added. In the presence of polymeric additives nanoparticles form which then aggregate to yield larger crystals. Such aggregation was preferentially observed for gelatin scaffolds. Citrate anions are particularly important in calcium phosphate precipitation in bone. Biomimetic hydroxylapatite-chitosan and hydroxylapatite-gelatin nanocomposite were synthesized where citrate ions were used to control the size and crystallinity of the hydroxylapatite crystals. TEM data show that the size of the hydroxylapatite crystals decreases upon introducing citrate ions into the systems. Solid-state NMR dipolar dephasing data indicate the hydroxylapatite precipitation can be stabilized with 2.5 wt% sodium citrate with respect to the chitosan and gelatin mass. The data included within this thesis illustrate that both gelatin and chitosan hydrogel scaffolds display similar ability in modulating calcium carbonate or calcium phosphate crystallization in the absence and presence of additives. The role of soluble acidic additives is significant in the formation of biominerals. These results reveal therefore the possibility that carbohydrate-based systems, which have many advantages over protein-based systems, could be used to provide more options for fabricating new implantable materials for humans and animals. The results from the combination of techniques used including XRD, SSNMR and TEM showed the possibility of in vitro synthesis of a bio-nanocomposite material in the presence of citrate similar to that of natural bone (in terms of composition and morphology). The achievement of this work demonstrates that new advanced materials with various composite structures and morphologies can be synthesized through a biomimetic biomineralization mechanism under ambient conditions similar to natural materials such as bone and nacre. These advancements have potential application in biomedical research and more specifically in fabrication of implantable materials.</p>

Carbohydrate/protein hydrogels as responsive scaffolds in controlling inorganic crystallization

<p>The strategies that both invertebrate and vertebrate organism use to produce organic-inorganic composite materials for different purposes such as mechanical support and protection for the body are fascinating. While extensive research has been done on understanding the basic principles of biomineral formation, mimicking the critical principles of the mechanisms of biomineralization in vitro and fully capturing the structural information and characteristics remain challenging issues for scientists. Calcium is an essential element in biological systems. It plays a central role in the mineralization and maintenance of the skeleton as well as in fundamental physiological processes including growth and development in vertebrates. Within a biological organism calcium ions are stored, delivered, or released in the presence of different anions such as phosphate, carbonate and citrate. Competition between the different anions which interact with calcium ions in different hydrogel matrices leads to manipulation of the various composite materials produced such as bone and nacre. Soluble anionic acidic macromolecules associated with biominerals play a vital role in modulating the mineral morphology and hierarchy of the organized composite. Understanding the interaction between the constituent ions and the organic matrix is crucial if we are to make synthetic materials, the structure and properties of which replicate those of native biominerals, or materials that have the storage and/or release characteristics of foods, for example. Carbohydrate-based hydrogels versus protein-based hydrogels are used here as scaffolds for the synthesis of calcium carbonate and calcium phosphate biominerals. Water soluble acidic additives are used to modulate the nucleation and growth of the minerals. In particular chitosan and gelatin hydrogel templates were used as the mineralization scaffolds. Three different mineralization methods were used: the Kitano, alternate soaking and McGrath methods. Monomeric vs. polymeric additives (acrylic acid, glutamic acid, aspartic acid and their corresponding polymers) were introduced into all systems in order to control the nucleation and growth of the so-formed minerals. The morphology, crystallinity, polymorphism and composition of the synthesized organic-inorganic composites were investigated. Analyses were carried out using a number of techniques including Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM), X-ray Diffraction (XRD), micro-Raman spectroscopy and solid-sate NMR. In the case of calcium carbonate the morphology and crystallinity were more affected by the use of polymeric additives compared with their monomeric equivalents. In particular the calcium carbonate preferentially grew laterally within and on the periphery of the chitosan or gelatin hydrogel scaffold. This results from the formation of a polyelectrolyte complex between the chitosan or gelatin hydrogels and the added polymer. The presence of the polyelectrolyte complex modifies the nucleation of the mineral. Nanoparticles are preferentially formed which then aggregate together maintaining a lateral perspective with the scaffold. In the case of calcium phosphate mostly spherical and platelet-shaped morphologies composed of amorphous calcium phosphate and poorly crystalline hydroxylapatite respectively were always formed within both chitosan and gelatin hydrogel scaffolds. pH was also found to be a key factor in controlling which polymorph of calcium phosphate precipitates. The crystallinity is influenced by the presence of additives for chitosan scaffold. For systems with added aspartic or polyaspartic acid platelet-shaped CaP forms. These crystals are more highly crystalline compared to those where predominately the porous spherical calcium phosphate morphology is observed which form when L-glutamic acid is added. In the presence of polymeric additives nanoparticles form which then aggregate to yield larger crystals. Such aggregation was preferentially observed for gelatin scaffolds. Citrate anions are particularly important in calcium phosphate precipitation in bone. Biomimetic hydroxylapatite-chitosan and hydroxylapatite-gelatin nanocomposite were synthesized where citrate ions were used to control the size and crystallinity of the hydroxylapatite crystals. TEM data show that the size of the hydroxylapatite crystals decreases upon introducing citrate ions into the systems. Solid-state NMR dipolar dephasing data indicate the hydroxylapatite precipitation can be stabilized with 2.5 wt% sodium citrate with respect to the chitosan and gelatin mass. The data included within this thesis illustrate that both gelatin and chitosan hydrogel scaffolds display similar ability in modulating calcium carbonate or calcium phosphate crystallization in the absence and presence of additives. The role of soluble acidic additives is significant in the formation of biominerals. These results reveal therefore the possibility that carbohydrate-based systems, which have many advantages over protein-based systems, could be used to provide more options for fabricating new implantable materials for humans and animals. The results from the combination of techniques used including XRD, SSNMR and TEM showed the possibility of in vitro synthesis of a bio-nanocomposite material in the presence of citrate similar to that of natural bone (in terms of composition and morphology). The achievement of this work demonstrates that new advanced materials with various composite structures and morphologies can be synthesized through a biomimetic biomineralization mechanism under ambient conditions similar to natural materials such as bone and nacre. These advancements have potential application in biomedical research and more specifically in fabrication of implantable materials.</p>

Tuning organic crystal chirality by the molar masses of tailored polymeric additives

Hierarchically ordered chiral crystals have attracted intense research efforts for their huge potential in optical devices, asymmetric catalysis and pharmaceutical crystal engineering. Major barriers to the application have been the use of costly enantiomerically pure building blocks and the difficulty in precise control of chirality transfer from molecular to macroscopic level. Herein, we describe a strategy that offers not only the preferred formation of one enantiomorph from racemic solution but also the subsequent enantiomer-specific oriented attachment of this enantiomorph by balancing stereoselective and non-stereoselective interactions. It is demonstrated by on-demand switching the sign of fan-shaped crystal aggregates and the configuration of their components only by changing the molar mass of tailored polymeric additives. Owing to the simplicity and wide scope of application, this methodology opens an immediate opportunity for facile and efficient fabrication of one-handed macroscopic aggregates of homochiral organic crystals from racemic starting materials.

Solution Blow Spun Silica Nanofibers: Influence of Polymeric Additives on the Physical Properties and Dye Adsorption Capacity

The physical properties of porous silica nanofibers are an important factor that impacts their performance in various applications. In this study, porous silica nanofibers were produced via solution blow spinning (SBS) from a silica precursor/polymer solution. Two polyvinylpyrrolidone (PVP, Mw = 360,000 and 1,300,000) were chosen as spinning aids in order to create different pore properties. The effect of their physical properties on the adsorption of methylene blue (MB) in an aqueous solution was explored. After forming, the nanofibers were calcined to remove the organic phase and create pores. The calcined nanofibers had a large amount of micro and mesopores without the use of additional surfactants. The molecular weight of the PVP impacted the growth of silica particles and consequently the pore size. High Mw PVP inhibited the growth of silica particles, resulting in a large volume of micropores. On the other hand, silica nanofibers with a high fraction of mesopores were obtained using the lower Mw PVP. These results demonstrate a simple method of producing blow spun silica nanofibers with defined variations of pore sizes by varying only the molecular weight of the PVP. In the adsorption process, the accessible mesopores improved the adsorption performance of large MB molecules.

Optimisation of reaction parameters for a novel polymeric additives as flow improvers of crude oil using response surface methodology

In recent years, polymeric additives have received considerable attention as a wax control approach to enhance the flowability of waxy crude oil. Furthermore, the satisfactory model for predicting maximum yield in free radical polymerisation has been challenging due to the complexity and rigours of classic kinetic models. This study investigated the influence of operating parameters on a novel synthesised polymer used as a wax deposition inhibitor in a crude oil pipeline. Response surface methodology (RSM) was used to develop a polynomial regression model and investigate the effect of reaction temperature, reaction time, and initiator concentration on the polymerisation yield of behenyl acrylate-co-stearyl methacrylate-co-maleic anhydride (BA-co-SMA-co-MA) polymer by using central composite design (CCD) approach. The modelled optimisation conditions were reaction time of 8.1 h, reaction temperature of 102 °C, and initiator concentration of 1.57 wt%, with the corresponding yield of 93.75%. The regression model analysis (ANOVA) detected an R2 value of 0.9696, indicating that the model can clarify 96.96% of the variation in data variation and does not clarify only 3% of the total differences. Three experimental validation runs were carried out using the optimal conditions, and the highest average yield is 93.20%. An error of about 0.55% was observed compared with the expected value. Therefore, the proposed model is reliable and can predict yield response accurately. Furthermore, the regression model is highly significant, indicating a strong agreement between the expected and experimental values of BA-co-SMA-co-MA yield. Consequently, this study’s findings can help provide a robust model for predicting maximum polymerisation yield to reduce the cost and processing time associated with the polymerisation process.

Concrete Strengthening by Introducing Polymer-Based Additives into the Cement Matrix—A Mini Review

The modern types of concrete are a mixture of aggregates, cement, water and optional additives and admixtures. In particular, polymer additives seem to be a promising type of component that can significantly change concrete and mortar properties. Currently, the most popular polymer additives include superplasticizers, latexes and redispersible powders. Moreover, in order to improve the properties of concrete-based composite admixtures, which enhance the resistance to cracking, polymer fibres and recycled polymers have been researched. All the types of polymeric materials mentioned above are broadly used in the construction industry. This work summarizes the current knowledge on the different types of popular polymeric additives. Moreover, it describes the correlation between the chemical structure of additives and the macro-behaviour of the obtained concrete.