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The rapid evolution of clinical medicine, materials science, and regenerative medicine has rendered traditional implantable scaffolds inadequate for addressing the complex therapeutic demands of various diseases. Currently, implantable scaffolds in clinical practice are mainly made of metal, with the disadvantages of high stiffness, poor toughness, and low deformation. This paper offers a thorough review of shape memory scaffolds (SMSs), emphasizing their distinctive self‐recovery and adaptive functionalities that enhance compatibility with injured tissues, surpassing the capabilities of conventional metallic biomaterials. It delves into the limitations of current clinical scaffolds and the requisite performance metrics for effective implants and outlines the essential materials and fabrication methods for SMSs. Moreover, we enumerate the biomedical applications of SMMs with different response types, including thermology‐responsive, water‐responsive, and light‐responsive. The discussion extends to the burgeoning applications of SMSs in biomedical engineering, including their utility in bone tissue engineering, cardiovascular stenting, tubular structures, and cardiac patches, which underscore their potential in minimally invasive procedures and dynamic tissue interactions. This review concludes with an analysis of current challenges and prospects, providing valuable insights for developing and applying SMSs in the biomedical sector. [ABSTRACT FROM AUTHOR]

Combining metal–organic frameworks (MOFs) with other functional materials can effectively improve the third‐order nonlinear optical (NLO) performances of MOFs. In this study, two distinct functional materials are selected and a PANI@MIL‐101(Cr)@CeO2 composite is successfully synthesized. The test results of third‐order NLO indicate that introducing PANI regulates the distribution of π electron clouds within the structure of the composite. Additionally, the core@shell structure formed by PANI@MIL‐101(Cr) and CeO2 promotes charge transfer and improves charge transfer efficiency under the weak heterojunction interaction, thereby enhancing nonlinear absorption and refractive signals. Under the double synergistic action of interior and exterior, a new charge transfer occurs between the components of the composite, resulting in excellent third‐order NLO performances. This study indicates that encapsulating polymer and loading metal oxides can effectively improve the NLO response of MOFs, which offers a new idea for more research on multiphase NLO materials. [ABSTRACT FROM AUTHOR]

Methicillin‐resistant Staphylococcus aureus (MRSA) biofilm infection, caused by impaired glucose metabolism in diabetic foot patients, poses a significant obstacle to the healing process and carries a high risk of being life‐threatening. Due to microvascular occlusion and the entrenchment of MRSA biofilms in diabetic foot, controlling and effectively treating MRSA infection remains challenging. Traditional hydrogels suffer from swelling‐related mechanical issues and inadequate drug release control, limiting their applications as biomimetic extracellular matrices for wound healing. Herein, a double‐network hydrogel composed of polyvinyl alcohol, sodium alginate, and gelatin (PSG) loaded with tea polyphenol self‐assembled magnesium nanoparticles (TP‐Mg NPs) with antibacterial and angiogenic properties for treating MRSA‐infected diabetic foot wounds under hyperglycemic conditions is constructed. TP‐Mg@PSG exhibits enhanced mechanical strength and toughness for wound attachment and recovery movement torsion. In the acidic infection microenvironment representative of MRSA‐infected wounds, the TP‐Mg@PSG hydrogel degrades to release TP‐Mg NPs, showing excellent anti‐MRSA biofilm effect and high biocompatibility. Such localized controlled release enhances the inhibition of MRSA infection and reduces the inflammatory response in rats, promoting cell proliferation and rapid wound repair. Therefore, this study presents a multifunctional biomaterial system for managing diabetic foot conditions, highlighting its potential for clinical applications. [ABSTRACT FROM AUTHOR]

The endometrium is a unique human tissue with an extraordinary ability to undergo a hormone‐regulated cycle encompassing shedding, bleeding, scarless repair, and regeneration throughout the female reproductive cycle. The cyclical repair and regeneration of the endometrium manifest as changes in endometrial epithelialization, glandular regeneration, and vascularization. The mechanisms encompass inflammation, coagulation, and fibrinolytic system balance. However, specific conditions such as endometriosis or TCRA treatment can disrupt the process of cyclical endometrial repair and regeneration. There is uncertainty about traditional clinical treatments' efficacy and side effects, and finding new therapeutic interventions is essential. Researchers have made substantial progress in the perspective of regenerative medicine toward maintaining cyclical endometrial repair and regeneration in recent years. Such progress encompasses the integration of biomaterials, tissue‐engineered scaffolds, stem cell therapies, and 3D printing. This review analyzes the mechanisms, diseases, and interventions associated with cyclical endometrial repair and regeneration. The review discusses the advantages and disadvantages of the regenerative interventions currently employed in clinical practice. Additionally, it highlights the significant advantages of regenerative medicine in this domain. Finally, we review stem cells and biologics among the available interventions in regenerative medicine, providing insights into future therapeutic strategies. [ABSTRACT FROM AUTHOR]

Rare earth oxyfluorides (REOF) have potential applications in luminescent devices and energy storage and are important for synthesis and properties of RE‐doped oxyfluoride glasses. This study evaluates the thermodynamic properties of stoichiometric REOF with varying RE (RE = La, Nd, Gd, Ho, Y, and Yb) elements using high temperature oxide melt solution calorimetry and investigates the phase transitions of YbOF by differential scanning calorimetry. The formation enthalpies from binary oxides and fluorides are exothermic and become less exothermic with the decrease of ionic radius of RE3+, showing that REOF compounds are energetically stable relative to equal molar mixtures of RE2O3 and REF3 and the RE–O interactions contribute to most of their thermodynamic stabilities. Different from REOF with large RE ions (La–Er and Y) having the rhombohedral phase, REOF with small cations (e.g., Yb) possesses the monoclinic structure as the more energetically stable phase at room temperature. However, the slow transition between the monoclinic and cubic phases easily generates the rhombohedral phase, which is favored by kinetics. [ABSTRACT FROM AUTHOR]

Porous organic polymers (POPs), with features of permanent nanopores and designable frameworks, show great promise as sulfur host materials to restrain the shuttling of polysulfides, one of the main obstacles in the development of lithium–sulfur batteries. However, the simple physical entrapment from weak intermolecular interactions via a typical melt‐diffusion method results in the diffusive loss of polysulfides that has thus far restricted their potential. Herein, a facile strategy for introducing chemical covalent interactions between POPs and sulfur via the regulation of sulfur infiltration temperature is reported. The results show that increasing the temperature to a suitable value, e.g., 400 °C, for a fluorinated triazine‐based framework (FCTF), enables chemical bonding between the sulfur and aromatic FCTF backbone. Benefitting from the synergetic chemical and physical confinement effect, the shuttling of polysulfides can be efficiently restrained. As a result, the sample features superior sulfur utilization, high‐rate performances, and good cycle stability, as compared with the sample with only physical confinement. The proposed strategy can also be extended to other POPs, such as the boroxine‐linked covalent organic framework, by judiciously tailoring the infiltration temperatures. The findings disclose the important role of infiltration temperatures in developing efficient cathode host materials for lithium–sulfur batteries. [ABSTRACT FROM AUTHOR]