Zr-MOFs are characterized by their high thermal and chemical stability which may facilitate their application in heterogeneous catalysis. However, these applications could be restricted if large reactants exceed the MOF pore sizes leading to unavailable surface areas. In this work, we study the effect of acetic acid concentration, used as a modulator, on the formation of micro/mesoporous materials. This inclusion of a modulator during synthesis and its removal by an activation process generate materials with missing linker defects. We show that an increase in the concentration of modulator leads to an improvement of the calculated apparent surface area and to a modification of the MOF-808 pore structure by producing mesopores at the expense of micropores. Furthermore, we perform a post-synthetic modification (PSM) of MOF-808. We observe the expected sulfation of the zirconium oxo-cluster but also the sulfonation of the organic ligand. Also, we find that only the families of mesopores and the larger micropores are interconnected within the material, and the ultramicropores seem to be isolated from the porous structure. The PSM process led to the addition of Lewis and Brønsted acid sites to MOF-808. Experimental results are complemented by theoretical calculations using density functional theory and ab initio molecular dynamics simulations. The rationalization of the effect of synthesis conditions and the post-synthetic sulfation process on the final properties presented in this paper can serve as a basis for engineering of defects towards the synthesis of solid acid catalysts from MOF-808.

Growth factors (GF) are critical cytokines in wound healing. However, the direct delivery of these biochemical cues into a wound site significantly increases the cost of wound dressings and can lead to a strong immunological response due to the introduction of a foreign source of GFs. To overcome this challenge, we designed a poly(ethylene glycol) diacrylate (PEGDA) hydrogel with the potential capacity to sequester autologous GFs directly from the wound site. We demonstrated that synthetic peptide sequences covalently tethered to PEGDA hydrogels physically retained human transforming growth factor beta 1 (hTGFβ1) and human vascular endothelial growth factor (hVEGF) at 3.2 and 0.6 ng/mm², respectively. In addition, we demonstrated that retained hTGFβ1 and hVEGF enhanced human dermal fibroblasts (HDFa) average cell surface area and proliferation, respectively, and that exposure to both GFs resulted in up to 1.9-fold higher fraction of area covered relative to the control. After five days in culture, relative to the control surface, non-covalently bound hTGFβ1 significantly increased the expression of collagen type I and hTGFβ1 and downregulated vimentin and matrix metalloproteinase 1 expression. Cumulatively, the response of HDFa to hTGFβ1 aligns well with the expected response of fibroblasts during the early stages of wound healing.

The repair of neuronal tissue is a challenging process due to the limited proliferative capacity of neurons. Neural stem cells (NSCs) can aid in the regeneration process of neural tissue due to their high proliferation potential and capacity to differentiate into neurons. The therapeutic potential of these cells can only be achieved if sufficient cells are obtained without losing their differentiation potential. Toward this end, an astrocyte-derived coating (HAc) was evaluated as a promising substrate to promote the proliferation of NSCs. Mass spectroscopy and scanning electron microscopy were used to characterize the HAc. The proliferation rate and the expression of stemness and differentiation markers in NSCs cultured on the HAc were evaluated and compared to the responses of these cells to commonly used coating materials including Poly-L-Ornithine (PLO), and a Human Induced Pluripotent Stem Cell (HiPSC)-based coating. The use of the HAc promotes the in vitro cell growth of NSCs. The expression of the stemness markers Sox2 and Nestin, and the differentiation marker DCX in the HAc group was akin to the expression of these markers in the controls. In summary, HAc supported the proliferation of NSCs while maintaining their stemness and neural differentiation potential.

Multicomponent interpenetrating polymer network (mIPN) hydrogels are promising tissue-engineering scaffolds that could closely resemble key characteristics of native tissues. The mechanical and biochemical properties of mIPNs can be finely controlled to mimic key features of target cellular microenvironments, regulating cell-matrix interactions. In this work, we fabricated hydrogels made of collagen type I (Col I), fibrin, hyaluronic acid (HA), and poly (ethylene glycol) diacrylate (PEGDA) using a network-by-network fabrication approach. With these mIPNs, we aimed to develop a biomaterial platform that supports the in vitro culture of human astrocytes and potentially serves to assess the effects of the abnormal deposition of fibrin in cortex tissue and simulate key aspects in the progression of neuroinflammation typically found in human pathologies such as Alzheimer’s disease (AD), Parkinson’s disease (PD), and tissue trauma. Our resulting hydrogels closely resembled the complex modulus of AD human brain cortex tissue (~7.35 kPa), promoting cell spreading while allowing for the modulation of fibrin and hyaluronic acid levels. The individual networks and their microarchitecture were evaluated using confocal laser scanning microscopy (CLSM) and scanning electron microscopy (SEM). Human astrocytes were encapsulated in mIPNs, and negligible cytotoxicity was observed 24 h after the cell encapsulation.

Polymer and surfactant flooding are widely applied processes in enhanced oil recovery (EOR) in which viscous polymers or surfactants aqueous solutions are introduced in oil reservoirs to rise the recovery of the remaining oil. In this regard, one of the challenges of EOR practices is the use of efficient but low-cost viscosifier and surfactant polymers. This work is aimed at synthesizing a polyglycerol derived from the biodegradable and nontoxic monomer, glycerol, and evaluating the effect of its copolymerization on rheological and interfacial properties, which were tested in water and brine for the former and in the water/oil system for the last properties. The copolymers were synthesized using a polyglycerol backbone, acrylic acid, lactic acid, and oleic acid. The chemical structure of copolymers was characterized by Fourier transform infrared spectroscopy (FT-IR), thermogravimetry (TG), and differential scanning calorimetry (DSC). The viscosity and the interfacial tension (IFT) of polymeric solutions were tested. Thus, the viscosity and surface performance of the prepared polymer solutions in distilled water and brine were analyzed according to the structure of the synthesized polymers. The results showed that the synthesized polymers modified water viscosity and surface tension between water and oil. The developed polymers could be candidates for applications in enhanced oil recovery and related applications.