SPRi/SERS dual-mode biosensor based on ployA-DNA/ miRNA/AuNPs-enhanced probe sandwich structure for the detection of multiple miRNA biomarkers.

MicroRNA (miRNA) has broad application prospects in the early detection of various cancers. In this work, a SPRi/SERS dual-mode biosensor was developed on the same gold chip by AuNPs as the reinforcing medium. High throughput and sensitivity detection of three typical cervical cancer markers miRNA21, miRNA124 and miRNA143 were achieved based on the sandwich structure of polyA blocks-DNA capture probe/target miRNA/AuNPs-assistant probe or SERS nanoprobes. AuNPs greatly improved the SPR response due to mass increase and more sensitive refractive index changes. Meanwhile, due to the LSPR effect of AuNPs, the signal of SERS nanoprobe can be amplified. The miRNAs were detected in serum to verify its practicality. SPRi achieved detection of three miRNAs simultaneously. LODs were 6.3 fM, 5.3 fM and 4.6 fM, respectively, and wide dynamic response range of 500 pM-10 nM. While SERS assay ensured high sensitivity with LODs as low as 1 fM, 0.8 fM and 1.2 fM, respectively, and with the recoveries in the range of 90.0 %-100.2 %. The redundant detection signals of the two modes can provide more reliable data to prevent false positive or false negative detection, and have great application prospects in detection of cancer-related nucleic acids in early stage of disease.

Efficient interfacial self-assembled MXene/Ag NPs film nanocarriers for SERS-traceable drug delivery.

Combining the unique advantages of two-dimensional transition metal carbon/nitrogen compounds (MXene) and the excellent surface-enhanced Raman scattering (SERS) performance of noble metal materials, MXene/Ag NPs films were proposed as nanocarriers for SERS-traceable drug delivery. The films were prepared by two-step self-assembly on positively charged silicon wafers using virtue of the high evaporation of ethyl acetate, the Marangoni effect, and an oil/water/oil three-phase system. With 4-mercaptobenzoic acid (4-MBA) as the probe molecule, the SERS detection limit was 10-8 M and had shown a good linear relationship in the range of 10-8-10-3 M. Simultaneously, the film had good uniformity, repeatability, and stability. When Ti3C2Tx/Ag NPs films were used as nanocarriers, the anticancer drug doxorubicin (DOX) was loaded onto the surface through 4-MBA, and the tracking and monitoring were realized by SERS. The addition of glutathione (GSH) triggered the thiol exchange reaction, resulting in the shedding of 4-MBA from the surface of the film, which indirectly achieved the efficient release of DOX. Furthermore, the loading of DOX and the drug release effect triggered by GSH maintained a certain stability in serum, which provided a potential possibility for the subsequent loading and release of drugs by films with three-dimensional structures as scaffolds in biological therapy. Self-assembled MXene/Ag NPs film nanocarriers for SERS-traceable drug delivery and GSH-triggered high-efficiency drug release.

Self-Assembled MXene-Au Multifunctional Nanomaterials with Various Shapes for Label-free SERS Detection of Pathogenic Bacteria and Photothermal Sterilization.

Early diagnosis of pathogenic bacteria and treatment are essential to prevent further infection. Photothermal therapy (PTT) is a promising sterilization method with advantages of minimal invasiveness and high efficiency. The effect of PTT depends on the performance of photothermal materials. Herein, Ti3C2-Au nanomaterials were prepared by the electrostatic self-assembly method, and the absorption characteristics were modulated by changing the morphology of Ti3C2-Au to achieve high photothermal conversion efficiency and sensitive label-free SERS bacterial detection. The results showed that the prepared Ti3C2-Au had better SERS performance than Au and achieved direct and sensitive detection of Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus). Under 808 nm laser irradiation, the photothermal conversion efficiency of Ti3C2-Au nanobipyramids (NBPs) was increased to 50.41% compared with the other two composites. The bactericidal rates of Ti3C2-Au NBPs against E. coli and S. aureus were 95.11 and 99.80% in 8 min, respectively, and the killing rates of nine other bacteria were all above 95%, showing broad-spectrum antibacterial properties. Cell viability studies showed that the Ti3C2-Au NBP had significantly improved biocompatibility compared with the Au NBP and was suitable for biological applications. It can simultaneously realize sensitive bacterial detection and photothermal sterilization and is important for the detection and inhibition of pathogenic bacteria.

Flexible SERS platform based on Ti3C2Tx-modified filter paper: preparation and SERS application.

A novel, simple, and inexpensive flexible surface-enhanced Raman-scattering (SERS) platform based on common laboratory filter paper modified with Ti3C2Tx flakes was reported. Ti3C2Tx synthesized from a Ti3AlC2 phase with a mixture of HCl and LiF and Ti3C2Tx nanosheets were characterized by the TEM, XRD, UV-Vis spectrum, and Raman spectrum. Paper-based substrate has been proven to sample on rough and irregular surfaces. Thus, Ti3C2Tx was further manufactured as paper substrate by the immersion method to transfer nanosheets to filter paper. SERS activity of prepared substrate was demonstrated using R6G by the same filter paper modified with and without Ti3C2Tx, and various concentrations of R6G were tested to prove the sensitivity of the substrates. Further detection of CV and MG certified the universality of paper substrate based on Ti3C2Tx nanosheets for detection of organic pollutants. The uniformity and stability were proved by CV and R6G molecules. This SERS platform combines the advantages of 2D material and flexible paper scaffolds, resulting in a highly sensitive, cost-efficient, and easy-to-manufacture large-scale flexible substrate and is expected to be used in practice.

Large-scale two-dimensional titanium carbide MXene as SERS-active substrate for reliable and sensitive detection of organic pollutants.

As a new class of two-dimensional material, MXene not only has the unique planar structure, electronic and optical properties, but also has a large surface area and hydrophilicity, which make them to build as potential SERS substrates with good sensitivity and stability. In this work, we reported a modified method by adjusting the ratio of HCl to LiF and reducing sonicate time to form large-sized monolayer Ti3C2Tx nanosheets. SERS performance of Ti3C2Tx was demonstrated by detecting dye molecules such as CV, R6G and MG. A remarkable enhanced effect was obtained, and Raman signals up to 10-8 M could be detected. Furthermore, the relationship between SERS effects and illumination laser wavelengths of different probe molecules has been studied, the results showed the selectivity between dye molecules and the excitation wavelengths. Besides, the uniformity and stability of the substrates have been proved by mapping experiments in a large area (80 × 80 µm2). The results demonstrated that Ti3C2Tx nanosheets can be built as lager-sized, uniform and stable sensor for ultra-sensitive detection of organic dye pollutant molecules.

Bacterial lactase genes diversity in intestinal mucosa of mice with dysbacterial diarrhea induced by antibiotics.

The current study aimed at exploring the diversity of bacterial lactase genes in the intestinal mucosa of mice with dysbacterial diarrhea induced by antibiotics and to provide experimental basis for antibiotics-induced diarrhea. Mice model of dysbacterial diarrhea was established by gastric perfusion with mixture of cephradine capsules and gentamicin sulfate (23.33 mL kg-1 d-1), twice a day and continuously for 5 days. Intestinal mucosa from jejunum to ileum was collected, and bacterial metagenomic DNA was extracted for Miseq metagenome sequencing to carry out diversity analysis. The results showed that specific operational taxonomic units (OTUs) were 45 in the control group and 159 in the model group. The Chao1, ACE, Shannon and Simpson indices in model group were significantly higher (P < 0.01 or P < 0.05) than control group. Principal component analysis (PCA) and box chart of the control group were relatively intensive, while in the model group, they were widely dispersed. Furthermore, the inter-group box area was higher than that in the intra-group. Compared with the model group, the abundance of bacterial lactase genes in Proteobacteria from the intestinal mucosa of the control group was higher, but lower in Actinobacteria and unclassified bacteria. At the genus level, the relative abundance of bacterial species and taxon units in model group was obviously increased (P < 0.05). Our results indicate that antibiotics increased the diversity and abundance of bacterial lactase genes in the intestinal mucosa, as the abundance of Betaproteobacteria, Cupriavidus, Ewingella, Methyloversatilis, Rhodocyclaceae and Rhodocyclales. In addition, antibiotics become an additional source for lactase genes of Ewingella, Methyloversatilis, Mycobacterium, Microbacterium, Beutenberqia and Actinomyces.