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BACKGROUND CONTEXT: For patients with multilevel degenerative cervical myelopathy, laminectomy and posterior cervical fusions (PCFs) with instrumentation are widely accepted technique for symptom relief. However, hardware failure is not rare which results in neck pain or even permanent neurological leision. The prevalence of hardware-related complications of laminectomy and posterior cervical fusions (PCFs) with instrumentation are lack of in-depth study. PURPOSE: To investigate risk factors of hardware failure after laminectomy and posterior cervical fusions (PCFs) with instrumentation in patients with degenerative cervical myelopathy. STYDU DESIGN: single-center, retrospective study. METHODS: Fifty-six patients who underwent laminectomy and posterior cervical fusions (PCFs) with instrumentation between January 2019 and January 2021 were included in a single institution. Patients were divided into the hardware failure group (n = 14) and no hardware failure group (n = 42). The sex, age, screw density, end vertebra (C7 or T1), cervical sagittal alignment parameters (C2-C7 lordosis, C2-C7 sagittal vertical axis, T1 slope, CL correction), and regional Hounsfield units (HU) of screw trajectory, morbidity of osteoporosis were collected and compared between the two groups. RESULTS: The mean overall follow-up was 20.6 months (range, 12–30 months). There were no significant statistical differences in general information (age, gender, follow-up period) of patients between the two groups. The differences of fusion rate, fixation levels and screw density between the two groups were not statistically significant (p > 0.05). The failure rate of the fixation endpoint at T1 was lower than that at C7 (9% vs. 36.3%) (p 0.05). The hardware failure rate in cases without osteoporosis was lower than that in cases with osteoporosis (14.3% vs. 57.1%) (p CONCLUSION: Hardware failure was not uncommon after laminectomy and PCFs with instrumentation in patients with degenerative cervical myelopathy. Osteoporosis, fixation ended at C7, and low regional HU of screw trajectory were the independent risk factors.

Background Sarcopenia and osteoporosis are common diseases that predominantly affect older individuals. The interaction between muscle and skeleton exerts pivotal roles in bone remodeling. This study aimed to explore the function of myoblast-derived exosomal Prrx2 in osteogenic differentiation and its potential mechanisms. Methods Exosomes were isolated from myogenic differentiated C2C12 cells. qRT-PCR and Western blotting were used to determine target molecule expression. Osteogenic differentiation of BMSCs was evaluated by Alizarin red staining, ALP activity and levels of OCN, OPN, RUNX2, and BMP2. Dual-luciferase reporter assay, RIP, and ChIP assays were performed to verify the interaction between molecules. The nuclear translocation of YAP1 was observed by immunofluorescence staining. In vivo osteoporotic model was established by ovariectomy in mice. Bone loss was examined using HE staining. Results Prrx2 expression was elevated in myogenic differentiated C2C12 cells and their exosomes. Myoblast-derived exosomal Prrx2 enhanced osteogenic differentiation of BMSCs. Delivering exosomal Prrx2 directly bond to MIR22HG promoter and promoted its transcription and expression. MIR22HG enhanced expression and nuclear translocation of YAP via sponging miR-128, thus facilitating BMSC osteogenic differentiation. Knockdown of exosomal Prrx2 suppressed osteogenic differentiation, which could be abolished by MIR22HG overexpression. Similarly, miR-128 inhibitor or YAP overexpression reversed the inhibitory effect of MIR22HG depletion or miR-128 mimics on osteogenic differentiation. Finally, myoblast-derived exosomal Prrx2 alleviated osteoporosis in mice via up-regulating MIR22HG and activating the Hippo pathway. Conclusion Myoblast-derived exosomal Prrx2 contributes to transcriptional activation of MIR22HG to activate YAP pathway via sponging miR-128, thereby facilitating osteogenic differentiation of BMSCs.

Featuring a combination of size-tunable emission wavelengths, high thermal stability, and low cytotoxicity, carbon quantum dots (CQDs) have opened up a new possibility for next-generation displays. However, the theoretically highest external quantum efficiency (EQE) limit of electroluminescent light-emitting diodes (LEDs) based on fluorescent CQDs is 5% due to the spin-forbidden nature of triplet state transitions. Comparatively, phosphorescent or delayed fluorescence CQDs are expected to overcome this limitation and allow the EQE of the devices to reach nearly 25%. At present, the preparation of CQDs with good solution processability, narrow bandwidth emission, and full-color phosphorescence or delayed fluorescence still faces great challenges. Herein, this review aims to offer a materials-chemistry perspective to tailor highly efficient phosphorescent or delayed fluorescence CQDs and present their applications in electroluminescent LEDs for the display technology. The mechanism and design principle of pure organic phosphorescence and delayed fluorescence as well as their recent advances in electroluminescent devices are summarized. Furthermore, we focus on the prospects and challenges for phosphorescent and delayed fluorescence CQDs in displays. We hope that this review will further stimulate the development of high-performance CQD-based electroluminescent displays with a combined effort from different disciplines.

Background: Osteosarcoma (OS) is the most common malignant bone tumor in the pediatric population. The main goal of this study is to investigate the role of circPARD3 and the underlying signaling pathway involved in OS.Methods: Cell proliferation was measured using a CCK-8 assay kit and clone formation assay. Cell migration and invasion was measured using transwell assay kit and wound-healing assay. Change of RNA and protein expression was determined using RNA extract and quantitative real time PCR (RT-qPCR) assay and Western blotting, respectively. RNA immune precipitation and Luciferase assay was used to confirm the predicted results. The xenograft model was established to evaluate the function of circPARD3 in vivo.Results: Expression of circPARD3 was upregulated in both OS tissues and cell lines. Silencing circPARD3 repressed OS cell proliferation and metastasis, while overexpression of circPARD3 promote OS cell tumorigenesis in vitro. Furthermore, up-regulation of circPARD3 significantly promoted the growth of OS cells in vivo. Moreover, circPARD3 directly and negatively modulated the expression of miR-1294 and positively regulated the expression of SKIL. Conclusion: Abnormally high expression of circPARD3 may promote the proliferation, migration, and invasion of OS cells through up-regulating SKIL by sponging miR-1294. These results provide insight into therapeutic targets for preventing and treating OS.

Localized surface plasmon resonance (LSPR) is well known for its unique ability to tune the reactivity of plasmonic materials via photoexcitation; however, it is still an open question as to whether plasmonic holes can be directly extracted to drive valuable chemical reactions. Herein we give an affirmative answer by reporting an illumination-enhanced oxygen evolution reaction (OER) using CuS nanodisks (NDs) alone as the electrocatalyst. Impressively, under 1221 nm laser or xenon lamp illumination, an unprecedented reduction of OER overpotential was observed on the CuS ND-coated electrodes. Transient absorption combined with Mott-Schottky measurements disclosed that near-infrared (NIR) irradiation generated abundant hot holes from LSPR damping in the CuS NDs accounting for the remarkable OER performance enhancement. This is the first report on the direct utilization of plasmonic hot holes in CuS nanomaterials for boosting OER performance, opening up a new route to designing NIR-active photocatalysts/electrocatalysts by exploiting the unique LSPR properties.

Previous studies only investigated the simple linear relationships of global tilt (GT) with thoracic kyphosis (TK), lumbar lordosis (LL) and pelvic incidence (PI). This study aimed to establish multiple linear regressions of GT based on individual TK, LL and PI in patients with degenerative spines. Four hundred sixty-nine adult patients aged older than 35 years with various degenerative spinal diseases were enrolled in this two-centre study between January 2017 and December 2020. Full-spine X-rays were performed for all the subjects in a standing position. The following regional and global parameters were measured in the sagittal plane: TK, LL, PI, pelvic tilt (PT), sagittal vertical axis (SVA) and GT. The correlations of the GT, PT and SVA with the TK, LL and PI were analysed, and then multiple linear regressions were constructed. GT was statistically correlated with TK, LL and PI. Additionally, TK, LL and PI were significant predictors for the GT, PT and SVA models. The relevant predictive formulae were as follows: GT = -9.60 + 1.09*PI + 0.89*LL + 0.42*TK (R2 = 0.935), PT = -4.49 + 0.81*PI + 0.56*LL + 0.24*TK (R2 = 0.792) and SVA = -25.68 + 2.98*LL + 2.37*PI + 1.67*TK (R2 = 0.416). The specific sagittal spinopelvic morphology, evaluated by GT parameters, should be determined by individual TK, LL and PI values in the degenerative spine. Surgeons can utilize such predictive models to better understand the degenerative evolution of sagittal alignment and recognize the relationships between regional parameters and global sagittal alignment to customize a precise correction strategy.

The negative impact of rare-earth elements (REEs) on the environment, limited supply and high cost prompt the need for REE-free phosphor-converted white light-emitting diodes (LEDs). Here, we report the gram-scale synthesis of red/green/blue solid-state bandgap fluorescent carbon quantum rings (R/G/B-SBF-CQRs) with high quantum yields up to 30-46 %. This was achieved using cyano-group-bearing p-phenyldiacetonitrile as precursor and forming carbon quantum rings of different diameters through the linkage of curved carbon quantum ribbons of different lengths. The results show the role of cyano groups in inducing the curvature of the carbon quantum ribbons for CQR formation and emission of stable solid-state bandgap fluorescence. R/G/B-SBF-CQRs-phosphor-based LEDs emitted warm white light with low CCT (3576 K), high CRI (96.6), and high luminous efficiency (48.7 lm W-1 ), comparable to REE-phosphor-based LEDs.

The preparation of high-value biochar as a supercapacitor is a promising way for biomass utilization. In this work, a self-activation method was proposed to prepare nitrogen and sulfur co-doping hi...

Pyrolysis has created many (and will open more) possibilities for high-value utilization of biomass. To obtain the optimal amount of desired pyrolysis products, especially high-quality bio-oil, a g...

Background Wheat is one of three major food crops in China. Alternaria species can cause spoilage of wheat with consequent mycotoxin accumulation. Alternariol (AOH), alternariol monomethyl ether (AME), and tenuazonic acid (TeA) are the most common and frequently studied mycotoxins. There are limited regulations placed on Alternaria mycotoxin concentrations worldwide due to the lack of toxicity data available. More data on the levels of mycotoxin contamination are also needed. It is also important to reduce the risks of Alternaria mycotoxins. Results One hundred and thirty-two wheat samples were collected from Hebei Province, China, and analyzed for AOH, AME, and TeA. Tenuazonic acid was found to be the predominant Alternaria mycotoxin, especially in flour samples. Studying Alternaria species that cause black-point disease of wheat indicated that Alternaria alternata and Alternaria tenuissima were the dominant species. Most of the Alternaria strains studied produced more than one mycotoxin and TeA was produced at the highest concentration, which may have resulted in the high level of TeA contamination in the wheat samples. Furthermore, magnolol displayed obvious antifungal and antimycotoxigenic activity against Alternaria. This is the first report on the antimycotoxigenic activity of magnolol against Alternaria species. Conclusion The Alternaria mycotoxin contamination levels in wheat and wheat products from Hebei Province, China, were correlated with the toxigenic capacity of the Alternaria strains colonizing the wheat. Considering its safety, magnolol could be developed as a natural fungicide in wheat, or as a natural alternative food preservative based on its strong antifungal and antimycotoxigenic activity against Alternaria strains. © 2020 Society of Chemical Industry.

Nitrogen doping is a promising method for the preparation of functional carbon materials. In this study, a nitrogen-doped porous coral biochar was prepared by using bamboo as raw material, urea as nitrogen source, and KHCO3 as green activator through in-situ pyrolysis. The structure of the obtained biochar was characterized by various techniques including nitrogen adsorption and desorption, Raman spectroscopy, X-ray photoelectron spectrometer, and etc. The adsorption properties of nitrogen-doped biochar were evaluated with phenol and methylene blue probes. The results showed that the nitrogen source ratio had a significant effect on the evolution of pore structure of biochar. Low urea addition ratio was beneficial to the development of pore structures. The optimum specific surface area of nitrogen-doped biochar could be up to 1693 m2·g-1. Nitrogen doping can effectively improve the adsorption capacity of biochar to phenol and methylene blue. Biochar prepared at 973.15 K with low urea addition ratio exhibited the highest adsorption capacity for phenol and methylene blue, and the equilibrium adsorption capacity was 169.0 mg·g-1 and 499.3 mg·g-1, respectively. By comparing the adsorption capacity of various adsorbents in related fields, it is proved that the nitrogen-doped biochar prepared in this study has a good adsorption effect.

Purpose Precise vehicle localization is a basic and critical technique for various intelligent transportation system (ITS) applications. It also needs to adapt to the complex road environments in real-time. The global positioning system and the strap-down inertial navigation system are two common techniques in the field of vehicle localization. However, the localization accuracy, reliability and real-time performance of these two techniques can not satisfy the requirement of some critical ITS applications such as collision avoiding, vision enhancement and automatic parking. Aiming at the problems above, this paper aims to propose a precise vehicle ego-localization method based on image matching. Design/methodology/approach This study included three steps, Step 1, extraction of feature points. After getting the image, the local features in the pavement images were extracted using an improved speeded up robust features algorithm. Step 2, eliminate mismatch points. Using a random sample consensus algorithm to eliminate mismatched points of road image and make match point pairs more robust. Step 3, matching of feature points and trajectory generation. Findings Through the matching and validation of the extracted local feature points, the relative translation and rotation offsets between two consecutive pavement images were calculated, eventually, the trajectory of the vehicle was generated. Originality/value The experimental results show that the studied algorithm has an accuracy at decimeter-level and it fully meets the demand of the lane-level positioning in some critical ITS applications.

In terms of how the signal varies in response to increased concentration of an analyte, sensors can be classified as either "signal-on" or "signal-off" format. While both types hold potentials to be sensitive, selective, and reusable, in many situations "signal-on" sensors are preferred for their low background signal and better selectivity. In this study, with the detection of lysozyme using its DNA aptamer as a trial system, for the first time we demonstrated that such an aptamer-based electrochemical biosensor can be converted from intrinsically "signal-off" to "signal-on" with the aid of a DNA exonuclease. The fact that the stepwise cleavage of antilysozyme aptamer catalyzed by Exonuclease I (Exo I) is entirely inhibited upon binding lysozyme leads to the selective removal of unbound DNA probes (thiolate anti-lysozyme DNA aptamer strands immobilized on gold electrode) upon the introduction of Exo I to the sensor. With the aid of electrostatically bound redox cations ([Ru(NH3)6]3+), we were able to quantitate the number of aptamer strands that are bound with lysozymes via conventional cyclic voltammetry (CV) measurements. We demonstrated that Exo I-assisted signal-on conversion protocol not only improves the sensing performance (10 times better limit of detection) but also promises a versatile strategy for DNA-based biosensor design, i.e., it can be readily adapted to other aptamer-protein binding systems (thrombin, as another example).

Strategies for selectively imaging and delivering drugs to tumours typically leverage differentially upregulated surface molecules on cancer cells. Here, we show that intravenously injected carbon quantum dots, functionalized with multiple paired α-carboxyl and amino groups that bind to the large neutral amino acid transporter 1 (which is expressed in most tumours), selectively accumulate in human tumour xenografts in mice and in an orthotopic mouse model of human glioma. The functionalized quantum dots, which structurally mimic large amino acids and can be loaded with aromatic drugs through π–π stacking interactions, enabled—in the absence of detectable toxicity—near-infrared fluorescence and photoacoustic imaging of the tumours and a reduction in tumour burden after the targeted delivery of chemotherapeutics to the tumours. The versatility of functionalization and high tumour selectivity of the quantum dots make them broadly suitable for tumour-specific imaging and drug delivery., Intravenously injected functionalized carbon quantum dots that bind to the large neutral amino acid transporter 1 and that structurally mimic large amino acids selectively accumulate in human tumours in mice, facilitating targeted theranostics.

Large doses of anticancer drugs entering cancer cell nuclei are found to be effective at killing cancer cells and increasing chemotherapeutic effectiveness. Here we report red-emissive carbon quantum dots, which can enter into the nuclei of not only cancer cells but also cancer stem cells. After doxorubicin was loaded at the concentration of 30 μg/mL on the surfaces of carbon quantum dots, the average cell viability of HeLa cells was decreased to only 21%, while it was decreased to 50% for free doxorubicin. The doxorubicin-loaded carbon quantum dots also exhibited a good therapeutic effect by eliminating cancer stem cells. This work provides a potential strategy for developing carbon quantum-dot-based anticancer drug carriers for effective eradication of cancers.

Co-based metal organic frameworks (ZIF-67), working as an oxidase-mimicking nanozyme, can simultaneously catalyze the oxidation of 3,3',5,5'-tetramethylbenzidine, 2,2'-azino-bis(3-ethylbenzthiazoline-6-sulfonic acid) and Amplex red, exhibiting a high catalytic activity. For Amplex red, two consecutive redox reactions are reported, which is specifically applied for fluorescence "turn-on" detection of biothiols.

As one of the most promising nanomaterials for biomedical applications, carbon dots (CDs) hold great potential in the field of bioimaging, biosensing and biotherapy due to their low cytotoxicity, high water solubility, favorable biocompatibility, good photostability, tunable fluorescence emission and excitation. In this review, we will provide an update on the latest research of CDs on the synthetic routes, chemical modifications, optical properties and biomedical applications. We will mainly discuss their applications in bioimaging of normal and cancer stem cells and tumour cells, two-photon fluorescence imaging, in vivo imaging, biosensing, and cancer therapy including photothermal therapy, photodynamic therapy and chemotherapy. At the end, current challenges and future perspectives of CDs in biomedical applications will also be discussed. We hope that this review will provide valuable insights to inspire new discoveries on CDs and draw a roadmap towards a broader range of biomedical applications.

Two-photon fluorescent (TPF) probes, which allow imaging of biological events in a high spatiotemporal resolution, are in great demand. Recently, carbon quantum dots (CQDs) have emerged as a promising class of TPF probes. Unfortunately, the use of the existing CQDs has been limited by their weak TPF capacities. Herein, we report the first facile and large-scale synthesis of nitrogen-rich CQDs (NRCQDs) based on a donor-π-acceptor (D-π-A) strategy. The resulting NRCQDs demonstrated a tremendous TPF capacity with a two-photon absorption cross section (TPACS) and quantum yield (QY) up to 61 200 Göppert-Mayer (GM) units and 63%, respectively, which is greater than those that could be achieved by the existing TPF carbon probes. Structural and optical analyses of NRCQDs revealed that the great TPF capacity is contributed by the nitrogen-rich D-π-A structure as well as the high crystallinity, large plane, rigid, graphitic nitrogen-doped π-conjugated system. We further demonstrated that NRCQDs allow imaging of live cells as well as live liver tissues at depths of up to 440 μm. Our results suggest NRCQDs as a robust TPF probe that can be potentially used for a variety of biological applications.

Laccase mimics are multicopper oxidase highly important for biotechnology and environmental evaluation/remediation. However, buffer species-dependent catalytic activity is rarely investigated. Herein, through Cu

Cation exchange has been a successful methodology for tuning the bandgaps of nanomaterials, while the most popular protocol in the toluene/methanol system lacks precise compositional control due to its inherent poor solvent compatibility. We herein report an alternative cation exchange route in N,N-dimethylformamide (DMF) solvent for converting preformed colloidal CdTe nanowires into CdxM1-xTe (M = Pb2+, Zn2+, Ag+, Hg2+) nanowires with good batch-to-batch reproducibility. The resulting CdxM1-xTe nanowires show a tunable bandgap from 2.26 to 0.63 eV, and the energy levels of these nanowires can be finely tuned. Furthermore, a comparative study for the cation exchange of CdTe nanowires with Pb2+ ions in toluene/methanol and DMF illustrated that the reduction of Cd2+ extraction and the Pb2+ introduction barrier accounts for precise compositional control. The cation exchange reaction in the DMF phase provides an efficient way to obtain nanomaterials with precise composition control. Moreover, these available high-quality colloidal semiconductor nanowires also pave the way for near-infrared device exploration.

N-doped biochar with a high nitrogen content and tuned pore structure was obtained from Pinus sylvestris by an in-situ pyrolysis process with simultaneous doping nitrogen and activation where urea was used as a nitrogen precursor and NaHCO3 was employed as the activator. To test the feasibility of N-doped biochars obtained under different pyrolysis temperatures as catalyst supports, a series of Ru catalysts were prepared for use in the methanation and the catalysts were labelled as Ru/N-ABC-x, where x represented the pretreatment temperatures(500, 600 and 700 °C). Besides, the catalytic test of Ru/ABC which was prepared under the same conditions without N modification was also conducted for comparison. The probe reaction test of CO2 methanation showed that the Ru/N-ABC-600 catalyst with the highest pyridinic-N (37.7%) content had superior or comparable catalytic performance to Ru/N-ABC-500 and Ru/N-ABC-700 prepared from N-doped biochar with different pyridinic-N content. A high CO2 conversion of 93.8% with a CH4 selectivity of 99.7% was achieved on Ru/N-ABC-600 under the optimum reaction conditions (380 °C, 1 MPa, n(H2)/n(CO2) of 4, with a gas hourly space velocity of 6000 mL·g-1·h-1). This work provides an effective strategy for the utilization of biochar to develop highly active catalysts for CO2 methanation.

Carbon quantum dots (CQDs) have developed into prospective nanomaterials for next-generation lighting and displays due to their intrinsic advantages of high stability, low cost, and environmental friendliness. However, confined by the spin-forbidden nature of triplet state transitions, the highest theoretical value of external quantum efficiency (EQE) of fluorescent CQDs is merely 5%, which fundamentally limits their further application in electroluminescent light-emitting diodes (LEDs). Soluble phosphorescent CQDs offer a means of breaking the shackle to achieve efficient monochromatic electroluminescence, especially red emission, which is a pivotal constituent in full-color displays. Here, the synthesis of red (625 nm) phosphorescent carbon quantum dot organic frameworks (CDOFs) with a quantum yield of up to 42.3% and realization of high-efficiency red phosphorescent electroluminescent LEDs are reported. The LEDs based on the CDOFs exhibited a red emission with a maximum luminance of 1818 cd m-2 and an EQE of 5.6%. This work explores the possibility of a new perspective for developing high-performance CQD-based electroluminescent LEDs.

Metal-organic frameworks (MOFs) as a peroxidase mimic have been integrated with glucose oxidase (GOx) to achieve one-step glucose detection. However, limited by the loading amount of GOx, the performances of the developed glucose sensing assays still remain to be further improved to meet sensing requirements in diverse biological samples. Herein, with Fe3+ as the metal ion and 2-amino-benzenedicarboxylic acid as a ligand, a fluorescent Fe-based organic framework (NH2-MIL-101) with peroxidase-like activity was synthesized. Due to the large specific surface area (791.75 m2 g-1), 68 μg mg-1 GOx could be immobilized through the amidation coupling reaction, and the product was designated GOx@NH2-MIL-101. With OPD as the substrate, Gox@NH2-MIL-101 achieved highly efficient biomimetic cascade catalysis for one-step glucose detection through an inner filter effect: upon reacting with glucose, GOx@NH2-MIL-101 catalytically oxidized glucose using dissolved O2, and the produced H2O2 concurrently oxidized o-phenylenediamine (OPD) to oxidized OPD (oxOPD), accompanied by the fluorescence of GOx@NH2-MIL-101 at 456 nm being quenched and that of oxOPD at 565 nm being enhanced. With the fluorescent ratio F565/F456 used as a readout signal, a wide linear range of 0.1-600 μM was obtained, and the detection limit was 0.0428 μM. Based on the excellent selectivity and high stability of GOx@NH2-MIL-101, the developed assay was successfully applied to glucose detection in human serum and saliva, presenting potential applications in diverse biological samples and even medical diagnosis.

Nitrogen-doped hierarchical porous biochar has aroused great interest in energy storage and adsorption applications. In this study, nitrogen-doped hierarchical porous biochar was prepared from corn...

Due to severely overlapping emission and or/ excitation spectra of polycyclic aromatic hydrocarbons (PAHs), the specifically recognizing PAHs by the fluorescent technique is still a challenge. Here, synthesized Ag@SiO2 nanoparticles with 40 ± 4 nm Ag core and 7 ± 1 nm SiO2 shell performing as a nanoprobe could selectively recognize 2-aminoanthracene (2-AA) via metal-enhanced fluorescence (MEF) within 2 min. The sensing mechanism was based on the facts: (1) there was a perfect spectral overlap between the local surface plasmon resonance (LSPR) peak of Ag@SiO2 and the absorptive peak of 2-AA, and (2) 2-AA could interact with Ag@SiO2 nanoparticles through hydrogen bonds between –NH2 in 2-AA and –OH in SiO2 shell. As a result, with Ag@SiO2 nanoparticles as a nanoprobe, a fluorescent assay for detecting 2-AA was developed with a linear range from 1 nM to 800 nM, which exhibited an excellent selectivity over possible PAHs, dyes and metal ions. The detection limit was 1 nM. Finally, the developed assay was applied to analyse 2-AA in industrial wastewater samples, which were highly consistent with that of high performance liquid chromatography (HPLC). This study presents a feasible assay for detecting 2-AA for environmental monitoring and toxic evaluating.