Novel whey protein isolate-based highly porous scaffolds modified with therapeutic ion-releasing bioactive glasses

In this work, for the first time, a material derived from food industry waste – whey protein isolate – and a material commonly used in bone regeneration – bioactive glasses – were combined to obtain novel composite biomaterials with potential applications in bone tissue engineering (BTE). Additionally, to obtain pro-angiogenic properties, sol–gel-derived BGs doped with Cu2+ and Co2+ ions were used. Using a simple gas foaming method, ready-to-use (sterile), bioactive scaffolds with high porosity (above 70%), fully connected pore networks, and pore size suitable for BTE applications (80–350 μm) were obtained. Furthermore, scaffolds showed additional functionalities – calcium phosphate-forming ability and gradual release of therapeutic ions. Porous WPI/BG composites showed great potential for use as novel bone substitutes

Poly(2-isopropenyl-2-oxazoline) hydrogels for biomedical applications

Synthetic polymers have had a major impact on the biomedical field. However, all polymers have their advantages and disadvantages, so that the selection of a certain polymeric material always is a compromise with regard to many properties, such as synthetic accessibility, solubility, thermal properties, biocompatibility, and degradability. The development of novel polymers with superior properties for medical applications is the focus of many research groups. The present study highlights the use of poly(2-isopropenyl-2-oxazoline) (PiPOx), as biocompatible functional polymer to develop synthetic hydrogel materials using a simple straightforward synthesis protocol. A library of hydrogels was obtained by chemical cross-linking of PiPO(x), using eight different nontoxic and bio-based dicarboxylic acids. The equilibrium swelling degree of the final material can be modulated by simple modification of the composition of the reaction mixture, including the polymer concentration in the feed ratio between the 2-oxazoline pendent groups and the carboxylic acid groups as well as the cross-linker length. The hydrogels with the highest water uptake were selected for further investigations regarding their potential use as biomaterials. We evaluated the thermoresponsiveness, the pH degradability under physiological conditions, and demonstrated proof-of-concept drug delivery experiments. The in vitro cellular studies demonstrated the noncytotoxic character of the PiPOx hydrogels, and their protein repellent properties, while mineralization studies revealed that such scaffolds do not promote mineralization/calcification phenomena. In view of these results, these hydrogels show potential use as ophthalmologic materials or in drug delivery applications

Newly crosslinked chitosan- and chitosan-pectin-based hydrogels with high antioxidant and potential anticancer activity

Monoaldehydes, due to natural origin and therapeutic activity, have attracted great attention for their ability to crosslink chitosan hydrogels for biomedical applications. However, most studies have focused on single-component hydrogels. In this work, chitosan-based hydrogels, crosslinked for the first time with 2,3,4-trihydroxybenzaldehyde (THBA), were modified with pectin (PC), bioactive glass (BG), and rosmarinic acid (RA). All of these were not only involved in the crosslinking, but also modulated properties or imparted completely new ones. THBA functioned as a crosslinker, resulting in improved mechanical properties, high swelling capacity and delayed degradation and also imparted high antioxidant activity and antiproliferative effect on cancer cells without cytotoxicity for normal cells. Hydrogels containing PC showed enhanced mechanical strength, while the combination with BG gave improved stability in PBS. All hydrogels modified with BG exhibited the ability to mineralise in SBF. The addition of RA enhanced antioxidant and anticancer activities and promoting the mineralisation process

Computed Tomography as a Characterization Tool for Engineered Scaffolds with Biomedical Applications

The ever-growing field of materials with applications in the biomedical field holds great promise regarding the design and fabrication of devices with specific characteristics, especially scaffolds with personalized geometry and architecture. The continuous technological development pushes the limits of innovation in obtaining adequate scaffolds and establishing their characteristics and performance. To this end, computed tomography (CT) proved to be a reliable, nondestructive, high-performance machine, enabling visualization and structure analysis at submicronic resolutions. CT allows both qualitative and quantitative data of the 3D model, offering an overall image of its specific architectural features and reliable numerical data for rigorous analyses. The precise engineering of scaffolds consists in the fabrication of objects with well-defined morphometric parameters (e.g., shape, porosity, wall thickness) and in their performance validation through thorough control over their behavior (in situ visualization, degradation, new tissue formation, wear, etc.). This review is focused on the use of CT in biomaterial science with the aim of qualitatively and quantitatively assessing the scaffolds’ features and monitoring their behavior following in vivo or in vitro experiments. Furthermore, the paper presents the benefits and limitations regarding the employment of this technique when engineering materials with applications in the biomedical field

One-pot synthesis of superabsorbant hybrid hydrogels based on methacrylamide gelatin and polyacrylamide: effortless control of hydrogel properties through composition design

BiocompatibLe methacryLamide-modified geLatin (GELMA) hydrogeLs with tuned characteristics, obtained through network-forming photopoLymerization, have recenty attracted increasing attention due to their wide range of possibLe appLications such as drug reLease, tissue regeneration and generation of bioartificiaL impLants. Due to the controlled number of C=C bonds, GELMA may simuLtaneousLy act as macromonomer and crossLinker Leading through poLymerization to hydrogeLs with rationally designed performances. This study provides effortess one-pot synthesis of hybrid hydrogeLs based on covaLenty Linked GELMA and poLyacryLamide (PM), using photo-induced network-forming poLymerization. ConventionaL synthesis of simiLar hydrogeLs Leads to interpenetrating geLatin and PAA networks, usually invoLving muLtistep crossLinking of the components and the use of toxic crossLinkers. Through the described one-pot chemistry, the synthetic water superabsorbent PM with its well-recognized advantages can rationally benefit from the high biocompatibiLity and cell-adherence of GELMA in a simpLe covaLent way. This work provides a correLation between the composition and the corresponding hydrogeL properties (incLuding swelling, pH influence, mechanicaL behaviour, abiLity to generate porous scaffoLds, enzymatic degradation). The addition of PM moduLated the network density and the water affinity allowing the controL of eLasticity and degradabiLity. SuppLementary crossLinking of the synthetic component provided additionaL controL over hydrophiLicity. The capacity of such hydrogeLs to generate porous scaffoLds was proved; interesting morphoLogies were deveLoped onLy by varying the composition. In vitro ceLLuLar studies indicated that the presence of GELMA conferred controlled cell-affinity properties to the bicomponent hydrogeLs. NevertheLess, the drug reLease potentiaL of such hydrogeLs was preLiminarlly investigated using sodium nafcillin. GELMA PM hydrogeLs may be usefuL for tissue regeneration due to effortess synthesis, compositionaL flexibiLity and variabLe properties

Fibronectin influences cell–gelatin/PHEMA hydrogel interactions

Hydrogels based on natural or/and synthetic (co)polymers are promising materials for tissue engineering and regenerative medicine. The aim of this study was to evaluate the influence of fibronectin on the behaviour of human foreskin fibroblasts (HFF-1) immobilized on gelatin-PHEMA based hydrogels

Double-Cross-Linked Networks Based on Methacryloyl Mucin

Mucin is a glycoprotein with proven potential in the biomaterials field, but its use is still underexploited for such applications. The present work aims to produce a synthesis of methacryloyl mucin single-network (SN) hydrogels and their double-cross-linked-network (DCN) counterparts. Following the synthesis of the mucin methacryloyl derivative, various SN hydrogels are prepared through the photopolymerization of methacrylate bonds, using reaction media with different pH values. The SN hydrogels are converted into DCN systems via supplementary cross-linking in tannic acid aqueous solution. The chemical modification of mucin is described, and the obtained product is characterized; the structural modification of mucin is assessed through FTIR spectroscopy, and the circular dichroism and the isoelectric point of methacryloyl mucin is evaluated. The affinity for aqueous media of both SN and DCN hydrogels is estimated, and the mechanical properties of the systems are assessed, both at macroscale through uniaxial compression and rheology tests and also at microscale through nanoindentation tests

The potential of NDPs-loaded fish gelatin fibers as reinforcing agent for fish gelatin hydrogels

In this work we report the potential of nanostructured fibers consisting of nanodiamond particles (NDPs) and fish gelatin (FG) to modulate the mechanical properties of fish gelatin hydrogels, in the aim of developing bioinspired ECM analogues. NDPs-loaded FG fibers were obtained by electrospinning. The biocomposites were obtained through the enzymatic crosslinking of gelatin in the presence of NDPs-loaded FG fibers. The mechanical behavior was assessed at different preparative stages (precursors, fibrous mesh, biocomposite scaffolds)