Natural Polymer Encapsulated Zeolitic Imidazolate Framework-12 Composite toward Electrochemical Sensing of Antitumor Agent.

Encapsulation of natural polymer pectin (Pec) into a zeolitic imidazolate framework-12 (ZIF-12) matrix via a simple chemical method toward anticancer agent gallic acid (GA) detection is reported in this work. GA, a natural phenol found in many food sources, has gained attention by its biological effects on the human body, such as an antioxidant and anti-inflammatory. Therefore, it is crucial to accurately and rapidly determine the GA level in humans. The encapsulation of Pec inside the ZIF-12 has been successfully confirmed from the physiochemical studies such as XRD, Raman, FTIR, and XPS spectroscopy along with morphological FESEM, BET, and HRTEM characterization. Under optimized conditions, the Pec@ZIF-12 composite exhibits wide linear range of 20 nM-250 µM with a detection limit of 2.2 nM; also, it showed excellent selectivity, stability, and reproducibility. Furthermore, the real sample analysis of food samples including tea, coffee, grape, and pomegranate samples shows exceptional recovery percentage in an unspiked manner. So far, there is little literature for encapsulating proteins, enzymes, metals, etc., that have been reported; here, we successfully encapsulated a natural polymer Pec inside the ZIF-12 cage. This encapsulation significantly enhanced the composite electrochemical performance, which could be seen from the overall results. All of these strongly suggest that the proposed Pec@ZIF-12 composite could be used for miniaturized device fabrication for the evaluation of GA in both home and industrial applications.

Molecular Diagnosis and Cancer Prognosis-A Concise Review.

Cancer is a complicated disease. Globally, it is one of the major causes for morbidity and mortality. A critical challenge associated with it is the difficulty to accurately diagnose it at an early stage. The malignancy due to multistage and heterogeneity that result from genetic and epigenetic modifications poses critical challenge to diagnose and monitor the progress at an early stage. Current diagnostic techniques normally suggest invasive biopsy procedure that can cause further infections and bleeding. Therefore, noninvasive diagnostic methods with high accuracy, safety and earliest detection are the needs of the hour. Herein, we provide a detailed review on the advanced methodologies and protocols developed for the detection of cancer biomarkers based on proteins, nucleic acids and extracellular vesicles. Furthermore, existing challenges and the improvements essential for the rapid, sensitive and noninvasive detection have also been discussed.

Biogenic Synthesis of Silver Nanoparticles Using Pantoea stewartii and Priestia aryabhattai and Their Antimicrobial, Larvicidal, Histopathological, and Biotoxicity Potential.

In recent years, green nanotechnology has gained considerable importance for the synthesis of nanoparticles due to its economic viability and biosafety. In the current study, silver nanoparticles were synthesized using two bacterial isolates, H2 and H3, which were isolated from soil samples collected from the Western Ghats, Tamil Nadu, and identified at the species level as Pantoeastewartii (H2) and Priestiaaryabhattai (H3) by sequencing their 16s rRNA genes. Intracellularly synthesized silver nanoparticles were characterized by UV-visible spectroscopy, Fourier transform infrared spectroscopy, atomic force microscopy, and particle size analysis. AFM studies show that both of the bacterial synthesized Ag NPs were circular-shaped and disaggregated, with an average size distribution of 4 nm for Pantoeastewartii and 3.6 nm for Priestiaaryabhattai. Furthermore, their larvicidal activity, antimicrobial, histopathological, and biotoxicity effects were determined. The synthesized Ag NPs exhibited potent larvicidal activity against fourth instars of Ae.aegypti, An.stephensi, and Cx.quinquefasciatus exposed to a 50 µg/mL concentration for 24 h based on their LC50 and LC90 values. Histopathological studies of the affected mosquito larvae clearly show damage to the epithelial cells, food bolus, basement membrane, muscles, and midgut parts. The maximum antimicrobial activity of Priestiaaryabhattai-synthesized Ag NPs was observed for Streptomyces varsoviensis MTCC-1537, and that of Pantoea stewartii-synthesized Ag NPs was against Escherichia coli MTCC-43. The toxicity test on non-target organisms such as Artemia nauplii and zebrafish embryos indicates no visible abnormalities or mortality after their exposure for 48h. It is concluded that silver nanoparticles can easily be synthesized using Pantoea stewartii (H2) and Priestia aryabhattai (H3) as capping and reducing agents. Silver nanoparticles showed potent larvicidal activities and could potentially be used in integrated vector control programs because they are safe for other inhabitants of the same aquatic environment as mosquito larvae.

Novel Electrochemical Sensing of Catechins in Raw Green Tea Extract via a Trimetallic Zeolitic Imidazolate Fibrous Framework.

Human health-related issues are increasing in day to day life because of the modern and unhygienic food lifestyles. In recent times, green tea (GT) gains more attention due to its numerous health benefits. It contains more biologically active compounds that improve mental health, increase metabolism, reduce cancer risks, and serve as an anti-aging agent for the brain. As it is globally consumed, the evaluation of the compounds present in it is very important. Hence, an attempt has been performed to evaluate these components in GT by using a cobalt nickel iron-based trimetallic zeolitic imidazolate framework as microfibers (CoNiFe-ZIF-MFs) synthesized via an electrospinning technique. Interestingly, the synthesized CoNiFe-ZIF-MFs catalyst simultaneously detects three major catechin (CT) groups, namely, epigallocatechin-3-gallate (EGCG), epicatechin (EC), and epicatechingallate (ECG). Further, the square wave voltammetry findings showed that there is a wide linear range of 50 ng to 1 mg for all the three CTs with LODs 45, 8, and 4 ng for EGCG, EC, and ECG, respectively. These results confirm the excellent sensing behavior of the composite toward GT extracts, proposing its practical utility in real-time compound analysis in food sectors. Other results like stability and reproducibility also promote its usage in the biomedical field. This study mainly focuses on the direct sensing of CTs present in GT without spiking any commercially purchased sample, and the sensing was performed simultaneously for all the three analytes; thus, this work gains novelty from the existing ones.

Cobalt-iron zeolitic imidazolate frameworks (ZIFs) as microfibers for the effective detection of hydroquinone.

The monitoring of pollutants has received significant attention from researchers in recent years owing to their hazardous nature and their toxic effect on the environment. Among them, water pollution plays a major role and results in dominant diseases along with life-long health problems. Hydroquinone (HQ), the major metabolite of benzene, is an industrially used organic compound which causes symptoms associated with nervous related disorders, such as faintness, therefore the research community has been inspired to detect sources of this carcinogenic agent. In this work, cobalt-iron based zeolitic imidazolate framework microfibers (CoFe-ZIF-MFs) were used for the selective detection of HQ. Micro-structured CoFe-ZIF fibers were fabricated using the wet chemical and electrospinning method. The electrochemical response of the prepared composite revealed an excellent redox behavior towards HQ and does not suffer from interference resulting from other analytes. The proposed sensor exhibited a wide linear range of 1 µM-1 mM with a detection limit of 230 nM, resulting in a good stability of up to 88%, even after 250 cycles. The designed sensor showed an exquisite performance for real sample analysis which indicates the device mechanism is reliable for use in environmental monitoring, public health care, industrialized areas and waste water management systems.

Size controllable, pH triggered reduction of bovine serum albumin and its adsorption behavior with SnO2/SnS2 quantum dots for biosensing application.

The pH dependent size control of Bovine Serum Albumin (BSA) and its biosensing potential with Tin Oxide and Tin Sulfide Quantum Dots (SnO2/SnS2 QDs) is reported. The role of disulfide bond cleavage in BSA at acidic and circumneutral pH conditions (3 and 7.2) with sodium borohydride as reducing agent, makes changes in its stability, prone to aggregation and microcapsule formation respectively. Here, the structural reduction in BSA (r-BSA2) at pH 7.2 probed more -OH groups eventually creating adhesive surfaces for SnO2/SnS2 QDs due to electrostatic and hydrophobic forces, thus avoids the aggregation of SnO2/SnS2 QDs in composite formation. The accumulation of more active sites in SnO2/SnS2 QDs decorated r-BSA2 (SnO2/SnS2@r-BSA2) nanobiocomposite favored suitable orientation for Melatonin (Mel) detection. The designed SnO2/SnS2@r-BSA2 nanobiocomposite over the screen printing electrode exhibited electrochemical detection capabilities for the selective and sensitive recognition of Mel in the linear range of 0.2-1000 µM with a lower detection limit of 16 nM. Additionally, the fabricated biosensor was successfully validated for the determination of Mel in real samples.

Studies on electrochemical glucose sensing, antimicrobial activity and cytotoxicity of fabricated copper nanoparticle immobilized chitin nanostructure.

In this study, copper nanoparticle immobilized chitin nanocomposite (CNP/CuNP) was synthesized and used for the development of non-enzymatic electrochemical sensor. The CNP/CuNP was characterized by X-ray diffraction (XRD), fourier transform infra red (FTIR) spectroscopy and high resolution transmission electron microscopy (HRTEM) analysis. The glucose sensing property of CNP/CuNP was investigated by cyclic voltammetry (CV) and chronoamperometry (CA). As a result of the synergistic effect of CNP and CuNP, the modified electrode displayed effective electro-oxidation of glucose in 0.1M NaOH solution. At 0.45V potential the modified electrode showed response towards glucose in the linear range of 1-1000µM with a lowest detection limit of 0.776µM with better selectivity and stability. In addition, the antimicrobial activity of CNP/CuNP was evaluated against bacterial and fungal strains. CNP/CuNP displayed enhanced antimicrobial activity when compared to CNP and CuNP alone. Similarly, cytotoxicity of CNP/CuNP was tested against Artemia salina, which showed no toxic effect in the tested concentration.