Biological Reactions Research Articles

Exploring the Biomedical Frontiers of Plant-Derived Nanoparticles: Synthesis and Biological Reactions.

As contemporary technology advances, scientists are striving to identify new approaches to managing several diseases. Compared to the more popular physiochemical synthesis, the plant-derived combination of metallic nanoparticles using plant secondary metabolites as a precursor has a number of benefits, including low expenses, low energy consumption, biocompatibility, and medicinal usefulness. This study intends to explore the impacts of using plant-derived synthetic materials including metallic nanoparticles (NPs), emphasizing the benefits of their broad use in next-generation treatments for cancer, diabetes, Alzheimer's, and vector diseases. This comprehensive analysis investigates the potential of plant-derived remedies for diseases and looks at cutting-edge nanoformulation techniques aimed at addressing the function of the nanoparticles that accompany these organic substances. The purpose of the current review is to determine how plant extracts contribute to the synthesis of Silver nanoparticles (AgNPs), Gold nanoparticles (GtNPs), and platinum nanoparticles (PtNPs). It provides an overview of the many phytocompounds and their functions in biomedicine, including antibacterial, antioxidant, anticancer, and anti-inflammatory properties. Furthermore, this study placed a special focus on a range of applications, including drug delivery systems, diagnostics and therapy, the present benefits of nanoparticles (NPs), their biomedical uses in medical technology, and their toxicities.

Technologies for investigating single-molecule chemical reactions

Abstract Single molecules, the smallest independently stable units in the material world, serve as the fundamental building blocks of matters. Among different branches of single-molecule sciences, single-molecule chemical reactions, by revealing the behavior and properties of individual molecules at the molecular scale, are particularly attractive because they can advance the understanding of chemical reaction mechanisms and help to address key scientific problems in broad fields such as physics, chemistry, biology, and materials science. This review provides a timely, comprehensive overview of single-molecule chemical reactions based on various technical platforms such as scanning probe microscopy, single-molecule junction, single nanostructure, single-molecule fluorescence detection, and crossed molecular beam. We present multidimensional analyses of single-molecule chemical reactions, offering new perspectives for research in different areas like photocatalysis/electrocatalysis, organic reactions, surface reactions, and biological reactions. Finally, we discuss the opportunities and challenges in this thriving field of single-molecule chemical reaction.

A signal-amplified electrochemical immunosensor for the detection of sulfadimidine in crayfish using COOH-MWCNTs-Fe3O4-GO nanohybrids modified working electrode

The label-free immunosensing technique is highly valued for its sensitivity and specificity, and advantages of simple preparation, fast detection (one-step), and rapid signal response. However, the sensitivity, stability, and specificity of this technique not only depend on the performance of antibodies, but also on the immunosensing interface of the bare glassy carbon electrode (GCE). This includes factors such as electrical conductivity, biocompatibility, and antibody loading capacity. In this study, carboxyl multiwalled carbon nanotubes-ferrosoferric oxide-graphene oxide (COOH-MWCNTs-Fe3O4-GO) was screened as the modified material of GCE to create an ideal immunosensing interface for the biological reaction between antibody-sulfadimidine (anti-SM2) and SM2. The structure of both nanomaterials and the immunosensor were characterized. The nanohybrid exhibited a uniform interwoven structure of laminar and tubular components. This unique structure allows for a higher capacity for antibody loading. Based on this, a novel electrochemical immunosensor was constructed using COOH-MWCNTs-Fe3O4-GO/GCE, which exhibited a high anti-SM2 loading capacity and a rapid detection time of 30 min. The immunosensor exhibited a linear detection range of 0.01–100 ng/mL for SM2, with a limit of detection (LOD) of 0.003 ng/mL and a limit of quantification (LOQ) of 0.01 ng/mL. Additionally, satisfactory recoveries ranging from 94.40% to 109.00% were achieved in crayfish samples, with a relative standard deviation (RSD) of 4.97–8.64%. A novel immunosensors for highly sensitive detection of SM2 has been developed, which may provide an alternative idea for determination of SM2 in crayfish and other seafood.

Photoelectrochemical sensor consisting of sulfhydryl-borate ester modified A1/B1 type Pillar[5]arene-functionalized gold NPs

Recognition of mitochondrial reactive oxygen species (ROS) in cells is essential for understanding the critical roles of different ROS in biology reaction processes. In this study, an ultrasensitive and specific photoelectrochemical (PEC) sensor is constructed and applied for the capture and identification of H2O2 in cells. For the targeted detection of H2O2 in cells containing similar groups, such as •OH and O2•-, a new sulfhydryl-borate ester modified A1/B1 type pillar[5]arene (BP5) with a specific borate group is designed as a specific recognition molecule, and Au nanoparticles (Au NPs) are synthesized as the photoactive material. Specifically, the localized surface plasmon resonance (LSPR) of the Au NPs and host-guest interaction between BP5 and H2O2 increase the photocurrent signal. At the same time, specific groups on BP5 react with H2O2 to specifically recognize it. The Au@BP5/GCE shows strong photoelectrochemical response for the detection of H2O2 with limit of detection (0.33 pM, S/N=3), an extended linear range (1–60 pM), high specificity, good stability and excellent reproducibility.

A carbon-carbon composite implant with a bioceramic coating: assessment of biological reactions using histological and tomographic methods

A carbon-carbon composite implant with a bioceramic coating: assessment of biological reactions using histological and tomographic methods

Co-composting of dewatered sludge and wheat straw with newly isolated Xenophilus azovorans: Carbon dynamics, humification, and driving pathways

Composting is a biological reaction caused by microorganisms. Composting efficiency can be adequately increased by adding biochar and/or by inoculating with exogenous microorganisms. In this study, we looked at four methods for dewatered sludge waste (DSW) and wheat straw (WS) aerobic co-composting: T1 (no additive), T2 (5% biochar), T3 (5% of a newly isolated strain, Xenophilus azovorans (XPA)), and T4 (5% of biochar-immobilized XPA (BCI-XPA)). Throughout the course of the 42-day composting period, we looked into the carbon dynamics, humification, microbial community succession, and modifications to the driving pathways. Compared to T1 and T2, the addition of XPA (T3) and BCI-XPA (T4) extended the thermophilic phase of composting without negatively affecting compost maturation. Notably, T4 exhibited a higher seed germination index (132.14%). Different from T1 and T2 treatments, T3 and T4 treatments increased CO2 and CH4 emissions in the composting process, in which the cumulative CO2 emissions increased by 18.61–47.16%, and T3 and T4 treatments also promoted the formation of humic acid. Moreover, T4 treatment with BCI-XPA addition showed relatively higher activities of urease, polyphenol oxidase, and laccase, as well as a higher diversity of microorganisms compared to other processes. The Functional Annotation of Prokaryotic Taxa (FAPROTAX) analysis showed that microorganisms involved in the carbon cycle dominated the entire composting process in all treatments, with chemoheterotrophy and aerobic chemoheterotrophy being the main pathways of organic materials degradation. Moreover, the presence of XPA accelerated the breakdown of organic materials by catabolism of aromatic compounds and intracellular parasite pathways. On the other hand, the xylanolysis pathway was aided in the conversion of organic materials to dissolved organics by the addition of BCI-XPA. These findings indicate that XPA and BCI-XPA have potential as additives to improve the efficiency of dewatered sludge and wheat straw co-composting.

Effects of handheld nonthermal plasma on the biological responses, mineralization, and inflammatory reactions of polyaryletherketone implant materials

Background/purposeThe handheld nonthermal plasma (HNP) treatment may alter the surface properties, bone metabolism, and inflammatory reactions of polyaryletherketone (PAEK) dental implant materials. This study tested whether the HNP treatment might increase the biocompatibility, surface hydrophilicity, surface free energies (SFEs), and the cell adhesion and mineralization capability of PAEK materials. Materials and methodsDisk-shaped samples of titanium (Ti), zirconia (Zr), polyetheretherketone (PEEK [PE]), and polyetherketoneketone (PEKK [PK]) were subjected to HNP treatment and termed as TiPL, ZrPL, PEPL, and PKPL, respectively. Water-surface reactions were examined using a goniometer. MG-63 cells were cultured on all samples to assess the cell viability, cytotoxicity, cell attachment, and mineralization characteristics. The expression of pro-inflammatory cytokines (tumor necrosis factor-alpha and interleukin-6) and key mineralization markers (alkaline phosphatase [ALKP], osteopontin [OPN], and dentin matrix protein 1 [DMP1]) was measured using enzyme-linked immunosorbent assay kits. ResultsThe HNP-treated samples exhibited significantly enhanced surface hydrophilicities and SFEs compared to the untreated samples. The cell viability remained high across all samples, indicating no cytotoxic effects. The HNP treatment significantly enhanced MG-63 cell adherence and proliferation. Elevated levels of ALKP and OPN were observed for the plasma-treated PEPL and PKPL specimens, while DMP1 levels increased significantly only in the PKPL specimen. Pro-inflammatory cytokine levels were low across all samples, suggesting no inflammatory response. ConclusionThe HNP-treated PAEKs have enhanced the surface hydrophilicity and SFEs as well as superior cell adhesion and mineralization capability, and thus may be good clinical dental implant materials.

Recent Advances in Fluorescent Biosensor: A Comprehensive Review

Herein, short review paper investigated the rapidly progress in fluorescent biosensors field and their significant influences on analytical chemistry applications. An electrical signal can be produced from a biological reaction using an integrated receptor-transducer device called a biosensor. Because there are so many uses for biosensors in the medical field, including medication delivery, environmental monitoring, water and food quality monitoring, and illness detection, biosensor design and development have become a top priority for scientists and researchers in the last ten years. In the beginning, we started to explain the basic principles of fluorescence. Then, we moved to discuss about the current advancements, creative sensor designs, and the fusion of materials science and nanotechnology. The paper highlighted the sensitivity of fluorescent biosensors by addressing a wide range of applications, including biological research, environmental monitoring, and medical diagnostics. This review paper censoriously assessed the present difficulties, such as interference and constrained dynamic range, and provided explanations into ongoing research. Advanced material and nanotechnology integration is emerging as a force that improves biosensor performance and broadens their uses. This study also discussed the future possible breakthroughs in biosensor technology and its broad use in a variety of scientific and societal fields.

A novel cascade catalysis for one-pot enzymatically modified isoquercitrin (EMIQ) conversion from rutin and sucrose using rationally designed gradient temperature control

Enzymatically modified isoquercitrin (EMIQ) is a glyco-chemically modified flavonoid exhibiting notably high biological activity, such as antioxidant, anti-inflammatory and anti-allergic properties. However, the utilization of expensive substrates such as isoquercitrin and cyclodextrin in the conventional approach has hindered the industrial-scale production of EMIQ due to high cost and low yields. Hence, the development of a cost-effective and efficient method is crucial for the biological synthesis of EMIQ. In this study, a natural cascade catalytic reaction system was constructed with α-L-rhamnosidase and amylosucrase using the inexpensive substrates rutin and sucrose. Additionally, a novel approach integrating gradient temperature regulation into biological cascade reactions was implemented. Under the optimal conditions, the rutin conversion reached a remarkable 95.39% at 24 h. Meanwhile, the productivity of quercetin-3-O-tetraglucoside with the best bioavailability reached an impressive 41.69%. This study presents promising prospects for future mass production of EMIQ directly prepared from rutin and sucrose.

Dual detection of tryptophan and S2O82− by a simple yet rapid fluorometric half-salamo-based chemodosimeter in actual water samples

Tryptophan (Trp) and persulfate (S2O82−) are attracting extensive attention because they have significant influence on biological reactions and the natural environment. Thus, developing a novel method for simultaneous detection of Trp and S2O82− is significant and challenging. Herein, a new type of fluorescent chemodosimeter HL based on a half-salamo was synthesized, which has specific recognition for Trp and S2O82−. The chemodosimeter HL showed high selectivity and rapid detection for Trp and S2O82− over various interfering analytes, and the limits of detection of the HL for Trp and S2O82− were 1.2 × 10−7 and 9.8 × 10−7 M, respectively. The response mechanism of HL for Trp and S2O82− was confirmed by ESI-MS, Job′s plot, 1H NMR titration & DFT calculations. Additionally, the applicability of HL for the detection of Trp and S2O82− was investigated in actual water samples, indicating its potential for usefulness.

The possible association of mitochondrial fusion and fission in copper deficiency-induced oxidative damage and mitochondrial dysfunction of the heart

IntroductionAs an essential trace element, Copper (Cu) participates in numerous physiological and biological reactions in the body. Cu is closely related to heart health, and an imbalance of Cu will cause cardiac dysfunction. The research aims to examine how Cu deficiency affects the heart, assess mitochondrial function in the hearts, and disclose possible mechanisms of its influence. MethodsWeaned mice were fed Cu-deficient diets and intraperitoneally given copper sulfate (CuSO4) to correct the Cu deficiency. The pathological change of the heart was assessed using histological inspection. Cardiac function and oxidative stress levels were evaluated by biochemical assay kits. ELISA and ATP detection kits were used to detect the levels of complexes I-IV in the mitochondrial respiratory chain (MRC) and ATP, respectively. Real time PCR was utilized to determine mRNA expressions, and Western blotting was adopted to determine protein expressions, of molecules related to mitochondrial fission and fusion. ResultsCu deficiency gave rise to elevated heart index, cardiac histological alterations and oxidation injury, increased serum levels of creatine kinase (CK), lactic dehydrogenase (LDH), and creatine kinase isoenzyme MB (CK-MB) together with increased malondialdehyde (MDA) production, decreased the glutathione (GSH), Superoxide Dismutase (SOD), and Catalase (CAT) activities or contents. Besides, Cu deficiency caused mitochondrial damage characterized by decreased contents of complexes I-IV in the MRC and ATP in the heart. In the meantime, Cu deficiency also reduced protein and mRNA expressions of factors associated with mitochondrial fusion, including Mfn1 and Mfn2, while significantly increased factors Drip1 and Fis1 related to mitochondrial fission. However, adding CuSO4 improved the above changes significantly. ConclusionAccording to research results, Cu deficiency can cause heart damage in mice, along with oxidative damage and mitochondrial dysfunction, which are closely related to mitochondrial fusion and fission disorders.

Mixed rare earth metals production from surface soil in Idaho, USA: Techno-economic analysis and greenhouse gas emission assessment

Rare earth elements are crucial for the development of cutting-edge technologies in various sectors, such as energy, transportation, and health care. Traditional extraction of rare earth elements from soil and ore deposits primarily involves chemical leaching and solvent extraction. Environmental-based biological rare earth element extraction, such as bioleaching, can be a promising alternative to mitigate pollution and hazardous wastes. We investigated the sustainability aspects (techno-economic and environmental impact) of mixed rare earth metals production from soil in Idaho, USA. We focused on the bioleaching of surface soil using techno-economic analysis and “cradle-to-gate” life cycle assessment. The system boundary included collection, transportation, bioleaching, and molten salt electrolysis. Our results revealed that the mixed rare earth metals (including Nd, Ce, and La) production costs approximately $10,851 per metric ton and generates 1.9 × 106 kg CO2 eq./ton. Our results showed that most emissions are due to energy consumption during bioleaching. Over a 100-year time horizon ultrasound-assisted bioleaching can reduce greenhouse gas emissions by approximately 91 % compared to the traditional bioleaching process by decreasing the organic acid leaching process time and energy consumption. Our work demonstrates that higher solids loading in leaching with biological reactions can promote economic feasibility and reduce chemical wastes.

In situ measurements of dissolved gases in xylem sap as tracers in plant physiology

Abstract Trees transport gases from the ground into the atmosphere through the process of transpiration. Tracing gases transported through this mechanism continuously and under field conditions remains an experimental challenge. Here we measured gases dissolved in the tree sap in situ and in real time, aiming to simultaneously analyse the transport of several gases (He, Ar, Kr, N2, O2 and CO2) from the soil, through the trees, into the atmosphere. We constructed and inserted custom-made semi-permeable membrane probes in the xylem of a fir tree and measured gas abundances at different heights using a portable gas equilibrium membrane-inlet mass spectrometer (‘miniRUEDI’). With this method, we were able to continuously measure the abundances of He, Ar, Kr, N2, O2 and CO2 in sap over several weeks. We observed diurnal variations of CO2 and O2 concentrations that reflected tree physiological activities. As a proof of the concept that trees do uptake dissolved gases in soil water, we irrigated the tree with He-enriched water in a tracer experiment and were able to determine upward sap flow velocity. Measurements of inert gases together with reactive species, such as CO2 and O2, allowed separation of the physical transport and exchange of gases derived from the soil or atmosphere from biological reactions. We discuss the opportunities that our technique provides for continuous in situ measurements of gases in the tree sap.

Enhancement of titanium surfaces using different acid solutions at room temperature to improve bone cell responses

Background/purposeEarly osseointegration of titanium (Ti) dental implants relies on the surface topography. Surface modification of Ti seeks to enhance bone regeneration around implants. Acid etching is the simple, less technique sensitive and cost-effective technique for surface treatment. The purpose of this study was to elucidate the simplified acid etching technique at room temperature lies in its capacity to enhance both physical properties and biological reactions relevant to bone. Materials and methodsUtilizing sulfuric acid (H2SO4) and hydrochloric acid (HCl), five distinct acid solutions were prepared, and the acid etching process was executed at five different time points at room temperature. The surface characterization of nanoscale modified titanium disks encompassed surface characteristics analysis, wettability and roughness tests. The biocompatibility evaluation involves tests that assess cell attachment, proliferation, alkaline phosphatase activity (ALP), and mineralization. ResultsThe surface modified by HCl exhibited the most significant alterations, characterized by an elevated roughness value and reduced hydrophilicity properties. The surface treated with a mixture of HCl and H2SO4 for 24 h (TH5) displayed a hydrophilic surface and high surface energy. Acid etched surfaces showed the greater cell attachment with long pseudopodia. The cell proliferation rate and ALP reaction rate of TH5 is the highest at day 7. Cells mineralization of Ti surface treated with 37% HCl for 24 h (TC5) shows the lowest and TH5 shows the greatest on day 21. ConclusionThe proposed acid etching at room temperature utilizing a combination of H2SO4 and HCl demonstrated improved physical properties while fostering favorable biological responses.

Effect of SlSAHH2 on metabolites in over-expressed and wild-type tomato fruit.

Tomato (Solanum lycopersicum) is an annual or perennial herb that occupies an important position in daily agricultural production. It is an essential food crop for humans and its ripening process is regulated by a number of genes. S-adenosyl-l-homocysteine hydrolase (AdoHcyase, EC 3.3.1.1) is widespread in organisms and plays an important role in regulating biological methylation reactions. Previous studies have revealed that transgenic tomato that over-express SlSAHH2 ripen earlier than the wild-type (WT). However, the differences in metabolites and the mechanisms driving how these differences affect the ripening cycle are unclear. To investigate the effects of SlSAHH2 on metabolites in over-expressed tomato and WT tomato. SlSAHH2 over-expressed tomato fruit (OE-5# and OE-6#) and WT tomato fruit at the breaker stage (Br) were selected for non-targeted metabolome analysis. A total of 733 metabolites were identified by mass spectrometry using the Kyoto Encyclopedia of Genes and Genomes (KEGG) database and the Human Metabolome database (HMDB). The metabolites were divided into 12 categories based on the superclass results and a comparison with the HMDB. The differences between the two databases were analyzed by PLS-DA. Based on a variable important in projection value >1 and P < 0.05, 103 differential metabolites were found between tomato variety OE-5# and WT and 63 differential metabolites were found between OE-6# and WT. These included dehydrotomatine, L-serine, and gallic acid amongst others. Many metabolites are associated with fruit ripening and eight common metabolites were found between the OE-5# vs. WT and OE-6# vs. WT comparison groups. The low L-tryptophan expression in OE-5# and OE-6# is consistent with previous reports that its content decreases with fruit ripening. A KEGG pathway enrichment analysis of the significantly different metabolites revealed that in the OE-5# and WT groups, up-regulated metabolites were enriched in 23 metabolic pathways and down-regulated metabolites were enriched in 11 metabolic pathways. In the OE-6# and WT groups, up-regulated metabolites were enriched in 29 pathways and down-regulated metabolites were enriched in six metabolic pathways. In addition, the differential metabolite changes in the L-serine to flavonoid transformation metabolic pathway also provide evidence that there is a phenotypic explanation for the changes in transgenic tomato. The metabolomic mechanism controlling SlSAHH2 promotion of tomato fruit ripening has been further elucidated.

Suitable conditions and reduction mechanisms of Cr(VI) contaminated groundwater by in-situ bioremediation with molasses

Molasses is an inexpensive and efficient biological carbon source for Cr(VI) remediation. This study explored the application of molasses in the remediation of contaminated aquifers. Under the conditions of 10–30 °C and pH > 6, molasses was effective for the bioremediation of 50 mg L−1 Cr(VI). Under these conditions, Cr(VI) had a faster remediation rate, and the generated Cr(III) had a lower migration risk. The average removal rate of Cr(VI) doubled when the temperature increased from 10 °C to 20 °C. Considering the remediation efficiency of Cr(VI) and total chromium in groundwater, a concentration limit of injected molasses (<5 g L−1) was proposed. When the molasses concentration exceeded 5 g L−1, >40 % of Cr(III) existed in the form of a complex colloid in the solution, which hindered the precipitation removal of Cr(III). Reduction of Cr(VI) by indigenous microorganisms mainly occurs extracellularly. The results of the simulated tank study showed that molasses can rapidly create in-situ biological reaction zones in the aquifer. Molasses migrated faster in deep aquifers thereby enabling a quicker removal of Cr(VI). In addition, it also has a good removal effect on NO3−. This study is of great significance for the application of molasses to reduce Cr(VI).

Engineering Biomimetic Protein Camouflage for Delivering Peptide/siRNA Nanocomplexes.

For cationic nanoparticles, the spontaneous nanoparticle-protein corona formation and aggregation in biofluids can trigger unexpected biological reactions. Herein, we present a biomimetic strategy for camouflaging the cationic peptide/siRNA nanocomplex (P/Si) with single or dual proteins, which exploits the unique properties of endogenous proteins and stabilizes the cationic P/Si complex for safe and targeted delivery. An in-depth study of the P/Si protein corona (P/Si-PC) formation and protein binding was conducted. The results provided insights into the biochemical and toxicological properties of cationic nanocomplexes and the rationales for engineering biomimetic protein camouflages. Based on this, the human serum albumin (HSA) and apolipoprotein AI (Apo-AI) ranked within the top 20 abundant protein species of P/Si-PC were selected to construct biomimetic HSA-dressed P/Si (P/Si@HSA) and dual protein (HSA and Apo-AI)-dressed P/Si (P/Si@HSA_Apo), given that the dual-protein camouflage plays complementary roles in efficient delivery. A branched cationic peptide (b-HKR) was tailored for siRNA delivery, and their nanocomplexes, including the cationic P/Si and biomimetic protein-dressed P/Si, were produced by a precise microfluidic technology. The biomimetic anionic protein camouflage greatly enhanced P/Si biostability and biocompatibility, which offers a reliable strategy for overcoming the limitation of applying cationic nanoparticles in biofluids and systemic delivery.

Identification and validation of a platelet-related signature for predicting survival and drug sensitivity in multiple myeloma.

Background: Significant progress has been achieved in the management of multiple myeloma (MM) by implementing high-dose therapy and stem cell transplantation. Moreover, the prognosis of patients has been enhanced due to the introduction of novel immunomodulatory drugs and the emergence of new targeted therapies. However, predicting the survival rates of patients with multiple myeloma is still tricky. According to recent researches, platelets have a significant impact in affecting the biological activity of tumors and are essential parts of the tumor microenvironment. Nonetheless, it is still unclear how platelet-related genes (PRGs) connect to the prognosis of multiple myeloma. Methods: We analyzed the expression of platelet-related genes and their prognostic value in multiple myeloma patients in this study. We also created a nomogram combining clinical metrics. Furthermore, we investigated disparities in the biological characteristics, immunological microenvironment, and reaction to immunotherapy, along with analyzing the drug susceptibility within diverse risk groups. Results: By using the platelet-related risk model, we were able to predict patients' prognosis more accurately. Subjects in the high-risk cohort exhibited inferior survival outcomes, both in the training and validation datasets, as compared to those in the low-risk cohort (p < 0.05). Moreover, there were differences in the immunological microenvironments, biological processes, clinical features, and chemotherapeutic drug sensitivity between the groups at high and low risk. Using multivariable Cox regression analyses, platelet-related risk score was shown to be an independent prognostic influence in MM (p < 0.001, hazard ratio (HR) = 2.001%, 95% confidence interval (CI): 1.467-2.730). Furthermore, the capacity to predict survival was further improved when a combined nomogram was utilized. In training cohort, this outperformed the predictive value of International staging system (ISS) alone from a 5-years area under curve (AUC) = 0.668 (95% CI: 0.611-0.725) to an AUC = 0.721 (95% CI: 0.665-0.778). Conclusion: Our study revealed the potential benefits of PRGs in terms of survival prognosis of MM patients. Furthermore, we verified its potential as a drug target for MM patients. These findings open up novel possibilities for prognostic evaluation and treatment choices for MM.

Janus Membrane-Based Wearable pH Sensor with Sweat Absorption, Gas Permeability, and Self-Adhesiveness.

Wearable biomedical sensors have enabled noninvasive and continuous physiological monitoring for daily health management and early detection of chronic diseases. Among biomedical sensors, wearable pH sensors attracted significant interest, as pH influences most biological reactions. However, conformable pH sensors that have sweat absorption ability, are self-adhesive to the skin, and are gas permeable remain largely unexplored. In this study, we present a pioneering approach to this problem by developing a Janus membrane-based pH sensor with self-adhesiveness on the skin. The sensor is composed of a hydrophobic polyurethane-polydimethylsiloxane porous hundreds nanometer-thick substrate and a hydrophilic poly(vinyl alcohol)-poly(acrylic acid) porous nanofiber layer. This Janus membrane exhibits a thickness of around 10 μm, providing a conformable adhesion to the skin. The simultaneous realization of solution absorption, gas permeability, and self-adhesiveness makes it suitable for long-term continuous monitoring without compromising the comfort of the wearer. The pH sensor was tested successfully for continuous monitoring for 7.5 h, demonstrating its potential for stable analysis of skin health conditions. The Janus membrane-based pH sensor holds significant promise for comprehensive skin health monitoring and wearable biomedical applications.

Construction of multi(iron)porphyrin array multilayers on quartz surface as peroxidase mimetics for H2O2 and glucose colorimetric, fluorometric and color-read detection

Multi(metallo)porphyrin arrays are important artificial biomimetics for mimicking the biological catalytic reactions in nature. Here, we report construction of multi(iron)porphyrin array ultrathin films on the quartz surface by coordination-driven layer-by-layer (LBL) assembling method with the Pd(II) ion as a connector and iron(III) tetrapyridylporphyrin (FeTPyP) as a linker. It is revealed that the (Pd-FeTPyP)n LBL multilayers can catalyze oxidation of 3,3′,5,5′-tetramethylbenzidine (TMB) in the presence of H2O2 with peroxidase-like activity, resulting in the formation of the blue-colored oxidized TMB (oxTMB). Coupled with glucose oxidase, three sensitive probes based on the colorimetric, fluorometric and color-read methods have been developed by using modified quartz plates as the heterogenous catalyst, with a glucose detection limit of about 0.89, 1.5 and 0.65 μM, respectively. Mechanism studies confirm an enhanced affinity between (Pd-FeTPyP)n and H2O2/TMB molecules and an improved catalytic performance, which are attributed to the reason that the FeTPyP macrocycles are well-dispersed and arranged on the two-dimensional quartz surface. Furthermore, owing to chemically anchored on the transparent quartz surface, the (Pd-FeTPyP)n films exhibit good stability with naked-eye observation of color change under moderate conditions, thus providing a potential candidate for developing colorimetric, fluorometric and color-read glucose biosensors.