Value of Hounsfield units measured by chest computed tomography for assessing bone density in the thoracolumbar segment of the thoracic spine.

STUDY DESIGN: A retrospective study. PURPOSE: To investigate the correlation between Hounsfield unit (HU) values measured by chest computed tomography (CT) and dual-energy Xray absorptiometry (DXA) T-scores. HU-based thoracolumbar (T11 and T12) cutoff thresholds were calculated for a cohort of Chinese patients. OVERVIEW OF LITERATURE: For patients with osteoporosis, the incidence of fractures in the thoracolumbar segment is significantly higher than that in other sites. However, most current clinical studies have focused on L1. METHODS: This retrospective study analyzed patients who underwent chest CT and DXA at our hospital between August 2021 and August 2022. Thoracic thoracolumbar segment HU values, lumbar T-scores, and hip T-scores were computed for comparison, and thoracic thoracolumbar segment HU thresholds suggestive of potential bone density abnormalities were established using receiver operating characteristic curves. RESULTS: In total, 470 patients (72.4% women; mean age, 65.5±12.3 years) were included in this study. DXA revealed that of the 470 patients, 90 (19%) had osteoporosis, 180 (38%) had reduced osteopenia, and 200 (43%) had normal bone mineral density (BMD). To differentiate osteoporosis from osteopenia, the HU threshold was established as 105.1 (sensitivity, 54.4%; specificity, 72.2%) for T11 and 85.7 (sensitivity, 69.4%; specificity, 61.1%) for T12. To differentiate between osteopenia and normal BMD, the HU threshold was 146.7 for T11 (sensitivity, 57.5%; specificity, 84.4%) and 135.7 for T12 (sensitivity, 59.5%; specificity, 80%). CONCLUSIONS: This study supports the significance of HU values from chest CT for BMD assessment. Chest CT provides a new method for clinical opportunistic screening of osteoporosis. When the T11 HU is >146.7 or the T12 HU is >135.7, additional osteoporosis testing is not needed unless a vertebral fracture is detected. If the T11 HU is <105.1 or the T12 HU is <85.7, further DXA testing is strongly advised. In addition, vertebral HU values that fall faster than those of the T11 and L1 vertebrae may explain the high incidence of T12 vertebral fractures.

Repair of buccal mucosa and floor of mouth defects using keystone design perforator island flap.

OBJECTIVE: To assess the feasibility of utilizing the keystone design perforator island flap (KDPIF) for the repair of small to medium-sized defects in the buccal mucosa and floor of mouth (cT1-2 stage tumor). STUDY DESIGN: We conducted a retrospective analysis of eight patients who underwent KDPIF to address oral defects at the Affiliated Hospital of Qingdao University between June 2021 and September 2022. Patient information, including medical history, defect site, flap size, operative time, hospital stay, complications, and postoperative recovery of oral function, was comprehensively evaluated. RESULTS: Eight patients (6 females and 2 males) underwent reconstruction using KDPIF. The mean operation time was 58.5 minutes (55-63 minutes), with an average length of stay of 3.5 days (3-5 days). None of the 8 cases (100%) exhibited flap splitting necrosis or infection. Moreover, no scar contracture was observed, and oral functions, including the degree of opening, type of opening, tongue mobility, speech function, and swallowing function, were successfully restored. One patient (12.5%) experienced bleeding from the incision on the first postoperative day, but following compression, hemostasis was achieved, and the incision healed well. CONCLUSIONS: KDPIF demonstrates technical feasibility and suitability for repairing small to medium-sized buccal mucosa and floor of mouth defects (cT1-2).

A graphitic C3N4 nanocomposite-based fluorescence platform for label-free analysis of trace mercury ions.

In this study, a nanocomposite consisting of graphitic carbon nitride nanosheets loaded with graphitic carbon nitride quantum dots (CNQDs/CNNNs) was synthesized via a one-step pyrolysis method. This nanocomposite exhibited excellent thermal stability, photobleaching and salt resistance. Then a new fluorescence sensing platform based on CNQDs/CNNNs was constructed, which showed high sensitivity and selectivity towards trace mercury ions (Hg2+). By using X-ray photoelectron spectroscopy, UV-vis diffuse reflectance spectra and density functional theory, the fluorescence response mechanism was elucidated where Hg2+ could interact with CNQDs/CNNNs, causing a structural change in the nanocomposite, further affecting its bandgap structure, and finally leading to fluorescence quenching. The linear range for detecting Hg2+ was found to be 0.025-4.0 µmol L-1, with a detection limit of 7.82 nmol L-1. This strategy provided the advantages of a rapid response and a broad detection range, making it suitable for quantitative detection of Hg2+ in environmental water.

Diffuse Large B-cell Lymphoma (Leg Type) Originating in the Skin of the Right Cheek Region: A Case Report and Literature Review.

Primary diffuse cutaneous large B-cell lymphoma, leg type (PCDLBCL-LT), usually affecting one or both lower legs, with a 5-year disease-free survival rate of less than 60%. Solitary facial lesions are extremely rare. Our report is about a 93-year-old woman whose clinical examination revealed a 4 cm × 5 cm × 3 cm mass with a soft texture and smooth margins on the right side of her cheek. Immunohistochemical analyses were consistent with a diagnosis of PCDLBCL-LT. The surgical method for this patient was: extensive resection of the tumor and repair of the defect with an adjacent flap. Neither local recurrence nor systemic invasion was observed during postoperative follow-up (8 months). The clinician must be very careful when making a correct diagnosis based on the clinical and immunohistochemical findings of PCDLBCL-LT. For this type of PCDLBCL-LT isolated in 1 site without invasion of the rest of the body, extensive surgical resection may result in a favorable prognosis.

Gold Nanoparticles: Construction for Drug Delivery and Application in Cancer Immunotherapy.

Cancer immunotherapy is an innovative treatment strategy to enhance the ability of the immune system to recognize and eliminate cancer cells. However, dose limitations, low response rates, and adverse immune events pose significant challenges. To address these limitations, gold nanoparticles (AuNPs) have been explored as immunotherapeutic drug carriers owing to their stability, surface versatility, and excellent optical properties. This review provides an overview of the advanced synthesis routes for AuNPs and their utilization as drug carriers to improve precision therapies. The review also emphasises various aspects of AuNP-based immunotherapy, including drug loading, targeting strategies, and drug release mechanisms. The application of AuNPs combined with cancer immunotherapy and their therapeutic efficacy are briefly discussed. Overall, we aimed to provide a recent understanding of the advances, challenges, and prospects of AuNPs for anticancer applications.

Novel electrochemical sensing platform basing on di-functional stimuli-responsive imprinted polymers for simultaneous extraction and determination of metronidazole.

A novel magnetic-controlled electrochemical sensor has been fabricated by combined photo-responsive surface molecular imprinted polymers (P-SMIPs) and electrochemical sensor. In particular, the P-SMIPs were obtained by living radical polymerization of photo-responsive functional monomer onto the magnetic Fe3O4 modified multi-walled carbon nanotubes nanocomposites. The magnetic glassy carbon electrode was introduced to make the anchoring and removal of P-SMIPs onto the magnetic-controlled glassy carbon electrode easy to manipulate. Driven by UV/vis light, the platform performs releasing and absorption of metronidazole basing on conformational variations of the photo-responsive monomer at the receptor sites part in the P-SMIPs. This process can be tested by the photo-responsive variations of metronidazole electrochemical signal. As the consequence, extracting of P-SMIPs sensor can be conveniently triggered by the controllable UV light intervention measure, leading to effectively improve in both analytes mass transfer rate to the receiving media and extraction efficiency. The experimental result indicated that the excellent recoveries of metronidazole were varied between 77.9% and 89.9% with RSDs ≤4.87% in the biological samples. Therefore, the P-SMIPs sensor shows satisfactory potential in reusable extractions that can be recycled several times with no significant loss of activity, and this utilization strategy can be extended to other analytes, achieving manifold applications of pharmaceutical and environmental.

WFDC21P promotes triple-negative breast cancer proliferation and migration through WFDC21P/miR-628/SMAD3 axis.

Long non-coding RNAs (lncRNAs) modulate cell proliferation, cycle, and apoptosis. However, the role of lncRNA-WFDC21P in the tumorigenesis of triple-negative breast cancer (TNBC) remains unclear. Results of this study demonstrated that WFDC21P levels significantly increased in TNBC, which was associated with the poor survival of patients. WFDC21P overexpression significantly promoted TNBC cell proliferation and metastasis. WFDC21P interacted with miR-628-5p, which further suppressed cell proliferation and metastasis by negatively regulating Smad3-related gene expression. Recovery of miR-628-5p weakened the roles of WFDC21P in promoting the growth and metastasis of TNBC cells. Moreover,N6-methyladenosine (m6A) modification upregulated WFDC21P expression in the TNBC cells. WFDC21P and its m6A levels were increased after methyltransferase like 3 (METTL3) overexpression but reduced after METTL3 silencing. The proliferation and metastasis of TNBC cells were promoted by METTL3 overexpression but suppressed by METTL3 silencing. This study demonstrated the vital roles of WFDC21P and its m6A in regulating the proliferation and metastasis of TNBC cells via the WFDC21P/miR-628/SMAD3 axis.

MiR-205-5p promotes lung cancer progression and is valuable for the diagnosis of lung cancer.

BACKGROUND: MicroRNAs (miRNAs) function as potential diagnostic biomarkers in various cancers. This study aimed to evaluate the roles of miR-205-5p in lung cancer progression and diagnosis. MATERIALS AND METHODS: MiR-205-5p was detected by quantitative real-time PCR. The effect of miR-205-5p on cell proliferation and metastasis was estimated by MTT and flow cytometry. The expression of TP53INP1 and related genes was analyzed by immunoblotting. The diagnostic value of miR-205-5p was analyzed using receiver operating characteristic (ROC) curve analysis, sensitivity, and specificity. RESULTS: The miR-205-5p was increased in lung cancer tissues. MiR-205-5p mimics were promoted but its inhibitor suppressed cell proliferation and metastasis compared with control treatment in vitro and in vivo. By regulating the 3' untranslated region, miR-205-5p could negatively regulate TP53INP1 expression, which further inhibited the expression of RB1 and P21, but increased that of cyclinD1. Moreover, the serum miR-205-5p levels of patients with lung cancer were significantly higher than those of normal controls, and they were correlated with patients' gender, drinking status, and clinical stage. The area under the ROC curve of serum miR-205-5p in the diagnosis of non-small-cell lung cancer was 0.8250, respectively. The finding supported its possession of high diagnostic efficiency for lung cancer. CONCLUSIONS: MiR-205-5p promoted lung cancer cell proliferation and metastasis by negatively regulating the novel target TP53INP1, which further affected the expression of P21, RB1, and cyclin D1. Serum miR-205-5p is a novel and valuable biomarker for lung cancer diagnosis.

Self-cleaning electrochemical protein-imprinting biosensor with a dual-driven switchable affinity for sensing bovine serum albumin.

A facile, universal and highly efficient approach for producing a self-cleaning electrochemical protein-imprinting biosensor based on dual stimuli-responsive memory hydrogels via free-radical polymerisation is described. As confirmed by static contact angle and scanning electron microscopy results, the imprinted hydrogels exhibited reversible conformational changes after being simulated by an external electric field and temperature. By exploring the properties of imprinted hydrogels for sensing applications, the electrochemical protein-imprinting biosensor was originally fabricated on a glassy carbon electrode using the drop-casting method. Because of the trigger gates of the temperature and electric field, the biosensor demonstrated excellent self-cleaning behaviours compared with other corresponding electric-field or thermo-responsive imprinting biosensors. Moreover, the prepared biosensor exhibited satisfactory selectivity, good biocompatibility, comparable limits of detection and linearity ranges as well as acceptable stability toward bovine serum albumin. Consequently, the biosensor was successfully employed to simultaneously enrich, detect and extract bovine serum albumin from complex biological samples; the process was dynamic, controllable and harmless to the template under the dual external stimuli. Thus, the proposed biosensor exhibited considerable potential in controlled drug/chemical delivery and smart sensing for bioanalyses involving dual stimuli-responsive behaviours.

Anticancer roles of let-7f-1-3p in non-small cell lung cancer via direct targeting of integrin ß1.

Lung cancer is one of the most common types of cancer, with the highest mortality rate worldwide. MicroRNAs play notable roles in the chemotherapeutic effects of anticancer drugs. The present study used reverse transcription-quantitative PCR, western blotting and cell migration and invasion assays to reveal the role of let-7f-1-3p in non-small cell lung cancer (NSCLC) and explore the effect of let-7f-1-3p on doxorubicin (DOX) treatment. It was demonstrated that the levels of let-7f-1-3p in carcinoma tissues were lower compared with those in paracarcinoma tissues. Thus, let-7f-1-3p may act as a suppressor gene. The present study also explored the role of let-7f-1-3p in A549 and NCI-H1975 cells. Results revealed that let-7f-1-3p could inhibit the viability, migration and invasion of NSCLC cells and induce their apoptosis. Integrin ß1 acted as a target gene regulated by let-7f-1-3p. This suggested that let-7f-1-3p could enhance DOX-inhibited cell viability, migration and invasion in vitro. Overall, the present study demonstrated that let-7f-1-3p may act as a target for drug design and lung cancer therapy.

Chemoprotective Effects of Geraniin against Azoxymethane Induced Colorectal Cancer by Reduction of Inflammatory Reaction.

The leading cause of cancer-related death is colorectal cancer, and inflammatory bowel disease is a risk factor for this disease. Azoxymethane (AOM) is a potent cancer inducer widely used in rats for colon cancer. The current study was scrutinizing the chemo-protective effect of geraniin against AOM induced colorectal cancer via alteration of oxidative stress and inflammatory cytokines. The rats were divided into different groups such as Group I: normal control, Group II geraniin (20 mg/kg), Group III: received AOM, Group IV-VI: AOM + geraniin (5, 10 and 20 mg/kg), respectively. All group of rats were received treatment for 16 weeks. At the end of the experimental study, the hepatic, biochemical, phase II antioxidant, antioxidant enzymes, cytokines, apoptosis and inflammatory mediators were estimated. Geraniin treatment significantly reduced tumor weight and enhanced body weight. Geraniin administration also altered the level of antioxidant parameters-superoxide dismutase (SOD), glutathione peroxidase (GPx), glutathione reductase (GR); phase I enzymes - cytochrome B5, cytochrome P450; phase II enzymes - Glutathione-S-Transferase (GST), UDP-Glucuronyl transferase (UDP-GT) respectively. Obtained results also demonstrate that geraniin treatment reduced the level of pro-inflammatory cytokines such as IL-2, IL-1α, IL-10, IL-1ß, IL-4, IL-6, IL-12, IL-17A, IFN-γ, tumor necrosis factor-α, G-CSF, and GM-CSF. Geraniin also reduced the expression of IL-1α, IL-1ß, IL-6, IFN-γ, G-CSF, and GM-CSF. On the basis of result we can conclude that geraniin reduced the colorectal cancer via inflammatory pathway.

Preparation of Gas-Responsive Imprinting Hydrogel and Their Gas-Driven Switchable Affinity for Target Protein Recognition.

Novel gas-responsive imprinting hydrogels were fabricated by combining N,N'-dimethylaminoethyl methacrylate gas-sensitive monomers, N,N'-methylenebis(acrylamide) cross-linkers, and human serum albumin (HSA) template proteins via a free radical polymerization. The hydrogel exhibited a reversible gas-responsive property upon N2/CO2 exchange. This result was supported by the evidences from hydrogen nuclear magnetic resonance spectroscopy and scanning electron microscopy. By applying this property to sensing application, a CO2-responsive imprinted biosensor was originally designed on the surface of a glassy carbon electrode. The biosensor exhibited unique self-clean and self-recognition properties toward HSA proteins based on reversible conformational changes driven by N2/CO2 stimuli. Moreover, the proposed imprinted biosensor favored HSA proteins by showing satisfactory sensitivity and selectivity and a wider detection range with a low detection limit. As a rare example in imprint sensing, the biosensor was successfully applied to the HSA extraction from complex serum samples. With gas stimuli, the whole process was efficient, controllable, and harmless to the proteins. Thus, the developed biosensor may provide a new prospect in molecularly imprinted sensing applications.

Roles of HOTAIR in lung cancer susceptibility and prognosis.

BACKGROUND: Long noncoding (lncRNA) single-nucleotide polymorphisms (SNPs) are associated with the susceptibility to the development of various malignant tumors. The aim of this study was to investigate the roles of HOX transcript antisense intergenic RNA (HOTAIR) and its SNPs in lung cancer. METHODS: Initially, the expression of HOTAIR in different tumors was investigated using the online Gene Expression Profiling Interactive Analysis (GEPIA) resource. Three SNPs (rs920778, rs1899663, and rs4759314) of HOTAIR were identified using the MassArray system. Following this, the relationship between these SNPs and susceptibility to lung cancer was investigated. RESULTS: Expression of HOTAIR was found to increase in a variety of cancers, including nonsmall cell lung cancer (NSCLC). We found that the genotypes of these SNPs (rs920778, rs1899663, and rs4759314) were not significantly associated with lung cancer type, family history, lymph node metastasis, or lung cancer stage. In gender stratification, the results of rs920778 genotypes showed that, compared to genotype AA, the AG (OR = 0.344, 95% CI: 0.133-0.893, p = .028) and AG + GG (OR = 0.378, 95% CI: 0.153-0.932, p = .035) genotypes of rs920778 are protective factors against NSCLC in females. In smoking stratification, compared with AA of rs920778, the genotype AG + GG (OR = 0.507, 95% CI: 0.263-0.975, p = .042) was a protective factor against NSCLC in nonsmoking people. No statistical differences were observed in the classifications of rs1899663 and rs4759314 genotypes. Linkage disequilibrium analysis revealed a high linkage disequilibrium between the rs920778 and rs1899663 (D' = 0.99, r2  = .74), rs920778 and rs4759314 (D' = 0.85, r2  = .13), and rs1899663 and rs4759314 (D' = 0.79, r2  = .00). CONCLUSION: Our study demonstrated that HOTAIR expression increased in NSCLC, and that the genotypes of rs920778 could be useful in the diagnosis and prognosis of lung cancer.

Fast and selective detection of mercury ions in environmental water by paper-based fluorescent sensor using boronic acid functionalized MoS2 quantum dots.

In this study, the B-MoS2 QDs, boronic acid functionalized MoS2 quantum dots, are synthesized by a simple aminoacylation reaction between MoS2 QDs and 3-aminobenzeneboronic acid (APBA). It not only exhibits excellent thermo-stability, photo-stability and good salt tolerance, but shows excellent fluorescence stability even under industrial wastewater with high concentration. These good characters can be used to construct a new fluorescence sensor for sensitive and selective detection of mercury ions (Hg2+). The fluorescence intensity of B-MoS2 QDs linearly decreases with the increase of Hg2+ concentration ranging from 0.005 to 41 µmol L-1, and the limit of detection as low as 1.8 nmol L-1. Due to the mercury ion-promoted transmetalation reaction of aryl boronic acid, this proposed method exhibits fast response, ultra-sensitivity and high selectivity for analysis of Hg2+ in different environmental water, and which also uses to online monitoring of Hg2+. The B-MoS2 QDs-based test paper can be used to detect the trace amounts of Hg2+ under UV lamp by naked eyes, suggesting that the proposed method has potential application in on-site monitoring of environmental Hg2+.

Cisplatin decreases cyclin D2 expression via upregulating miR­93 to inhibit lung adenocarcinoma cell growth.

MicroRNAs (miRNAs/miRs) serve important roles in the chemotherapeutic effect of anticancer drugs. To investigate the roles of miRNAs in cisplatin­induced suppression of lung adenocarcinoma cell proliferation, A549 cells were treated with different concentrations of cisplatin. An MTT assay demonstrated that cisplatin inhibited A549 cell proliferation in a dose­dependent manner. Cisplatin induced cell apoptosis and inhibited cell migration by increasing the levels of miR­93, miR­26a and miR­26b. Furthermore, as an upstream factor, miR­93 was proposed to regulate cyclin D2 expression in miR­93­transfected A549 cells. Cisplatin also induced Bcl­2­associated X protein expression, and decreased that of Bcl­2 and c­Myc in lung adenocarcinoma cells. In vivo analysis further supported that cisplatin inhibited lung adenocarcinoma cell growth by regulating cyclin D2 and miR­93 expression. In conclusion, our findings demonstrated that cisplatin could effectively inhibit lung adenocarcinoma cell proliferation by decreasing cyclin D2 expression via miR­93.

Near-infrared light-responsive electrochemical protein imprinting biosensor based on a shape memory conducting hydrogel.

Herein, a near-infrared (NIR) light-responsive imprinting biosensor with excellent conductivity and tensibility was designed by incorporation graphene oxide/polyaniline (GO/PANI) with thermo-responsive poly(N-isopropylacrylamide) hydrogel (PNiPAAm) on a glassy carbon electrode (GCE). In this design, polyaniline (PANI) nanofiber modifies with graphene oxide (GO) acts as a physically cross-linker, providing hydrogen bond interaction with amide groups in the PNiPAAm. It is functioned to enhance the strength of imprinted hydrogel networks. Thus, the imprinted hydrogel biosensor incorporation of GO/PANI nanocomposite exhibited excellent mechanical performance and NIR light-responsive characteristic. As a NIR radiation trigger gate, the obtained biosensor not only has a function of IR-based cleaning toward bovine serum albumin (BSA) in the absence of elution solution, but also a function of proteins releasing and uptaking, basing on reversibly conformational changes with 808 nm NIR light. Simultaneously, the responsive processes were electronically monitored by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) and verified by scanning electron microscopy (SEM). Moreover, the proposed GO/PANI nanocomposite imprinted biosensor exhibited excellent characteristics along with high conductivity and tensibility, long-term stability, and wide linear range, performing great promising for preparing remote NIR light-driven extraction protein smart devices.

A photoresponsive molecularly imprinted polymer with rapid visible-light-induced photoswitching for 4-ethylphenol in red wine.

The trans to cis isomerization of the azobenzene chromophore in most azobenzene-based photoresponsive molecularly imprinted polymers (MIPs) is initiated by UV irradiation. This limits the application of these materials in cases where UV light toxicity is an issue, such as in biological systems, food monitoring, and drug delivery. Herein we report a tetra-ortho-methyl substituted azobenzene, (4-[(4-methacryloyloxy)-2,6-dimethyl phenylazo]-3,5-dimethyl benzenesulfonic acid (MADPADSA). The photoswitching of MADPADSA could be induced by visible-light irradiation (550 nm for trans to cis and 475 nm for cis to trans) in 4-hydroxyethylpiperazineethanesulfonic acid (HEPES) buffer-ethanol (4:1, v/v) at pH 7.0, however, the photoisomerization was slow. With the use of MADPADSA as a functional monomer, NaYF4:Yb3+,Er3+ as a substrate, 4-ethylphenol (4-EP) as a template, a novel photoresponsive surface molecularly imprinted polymer NaYF4:Yb3+,Er3+@MIP was obtained. The NaYF4:Yb3+,Er3+@MIP displayed rapid visible-light-induced photoswitching. The NaYF4:Yb3+,Er3+ substrate could efficiently increase the trans to cis isomerization rate of the photoresponsive MIP on its surface, which was faster than that of the corresponding azobenzene monomer MADPADSA. Possible reasons for this effect were investigated by fluorescence spectroscopy. NaYF4:Yb3+,Er3+@MIP displayed good specificity toward 4-EP with a specific binding constant (Kd) of 3.67 × 10-6 mol L-1 and an apparent maximum adsorption capacity (Qmax) of 10.73 µmol g-1, respectively. NaYF4:Yb3+,Er3+@MIP was applied to determine the concentration of 4-EP in red wine with good efficiency and a limit of detection lower than the value that could cause an unpleasant off-flavor.

Boronic acid-functionalized molybdenum disulfide quantum dots for the ultrasensitive analysis of dopamine based on synergistic quenching effects from IFE and aggregation.

Herein, a novel fluorescent material, boronic acid-functionalized molybdenum disulfide quantum dots (B-MoS2 QDs) produced by an amidation reaction between 3-aminobenzeneboronic acid and previously prepared molybdenum disulfide quantum dots (MoS2 QDs), was prepared to fabricate a rapid and sensitive platform for the quantitative analysis of dopamine. This material exhibits strong fluorescence, excellent salt tolerance and light fastness. In particular, the quantum yield of this material is about 21.1 times that of its fundamental material, MoS2 QDs. Notably, owing to an interesting synergistic effect between the inner filter effect and the aggregation quenching effect, this material was successfully applied for the determination of dopamine in the linear range 0.25-35 µmol L-1 with the detection limit of 0.087 µmol L-1; moreover, B-MoS2 QDs manifested better selectivity in the presence of multiple interferences due to their inert surface. As expected, this proposed material shows satisfactory performance in human serum; thus, the present study exploits a new avenue for the application of functionalized MoS2 QDs in fluorescence sensing.

A photoresponsive surface molecularly imprinted polymer shell for determination of trace griseofulvin in milk.

A new photoresponsive surface molecularly imprinted polymer shell (PMIPS) was developed for determination of trace griseofulvin from milk. The PMIPS was prepared by surface imprinting technique using poly(styrene-co-methacrylic acid) (PS-co-PMMA) microspheres as the sacrificial substrate, griseofulvin as the template, a photoresponsive azobenzene derivative 4-((4-(methacryloyloxy)phenyl)diazenyl)-3,5-dimethyl benzenesulfonic acid as the functional monomer, and triethanolamine trimethacrylate as the cross-linker. The PMIPS was obtained after the removal of the sacrificial PS-co-PMMA core from the surface imprinted core-shell microspheres, PS-co-PMAA@PMIP. Compared with PS-co-PMAA@PMIP, PMIPS displayed better properties such as higher surface area and pore volume, rapid photo-isomerization rate, and higher adsorption capacities, specific binding constant and binding density. The PMIPS could efficiently detect griseofulvin in complex samples such as milk.

An electro-responsive imprinted biosensor with switchable affinity toward proteins.

We combined electro-responsive materials with molecular imprinted polymers (MIPs) to develop an electro-responsive imprinted biosensor for the first time. As an electric field controlled gate, the biosensor exhibits a novel self-cleaning ability, as well as switchable affinity toward proteins in aqueous media, based on a reversible structure change.