Junk food: Polymer composition of macroplastic marine debris ingested by green and loggerhead sea turtles from the Gulf of Oman.

Pollution of the marine environment by plastic marine debris has become one of the most pervasive threats impacting marine environments. In this study, for the first time, we evaluate the polymer types of the plastic marine debris ingested by 49 green and 14 loggerhead sea turtle strandings in the Gulf of Oman. Plastic marine debris was ingested by 73.5% of green and 42.9% of loggerhead sea turtles in this study. Overall, evidence suggested that green sea turtles from the Gulf of Oman coast of the United Arab Emirates ingested high levels of plastic marine debris, predominantly Polypropylene (PP) & Polyethylene (PE), followed by Nylon, PP-PE mixture, Polystyrene (PS), Poly vinyl chloride (PVC) and Ethylene vinyl acetate (EVA), respectively. Loggerhead sea turtles also ingested high levels of plastic marine debris, which also predominantly consisted of PP & PE, followed by PP-PE mixture, Nylon and PS. While recent studies were directed into polymer characterization of micro-plastics in aquatic life, our study focuses on macro-plastics which impose significantly greater risks.

Lysozyme and Human Serum Albumin Proteins as Potential Nitric Oxide Cardiovascular Drug Carriers: Theoretical and Experimental Investigation.

Nitric oxide-containing drugs present a critical remedy for cardiovascular diseases. Nitroglycerin (NG, O-NO) and S-nitrosoglutathione (SNG, S-NO) are the most common nitric oxide drugs for cardiovascular diseases. Insights regarding the binding affinity of NO drugs with lysozyme and human serum albumin (HSA) proteins and their dissociation mechanism will provide inquisitive information regarding the potential of the proteins as drug carriers. For the first time, the binding interactions and affinities are investigated using molecular docking, conventional molecular dynamics, steered molecular dynamics, and umbrella sampling to explore the ability of both proteins to act as nitric oxide drug carriers. The molecular dynamics simulation results showed higher stability of lysozyme-drug complexes compared to HSA. For lysozyme, cardiovascular drugs were bound in the protein cavity mainly by the electrostatic and hydrogen bond interactions with residues ASP53, GLN58, ILE59, ARG62, TRP64, ASP102, and TRP109. For HSA, key binding residues were ARG410, TYR411, LYS414, ARG485, GLU450, ARG486, and SER489. The free energy profiles produced from umbrella sampling also suggest that lysozyme-drug complexes had better binding affinity than HSA-drug. Binding characteristics of nitric oxide-containing drugs NG and SNG to lysozyme and HSA proteins were studied using fluorescence and UV-vis absorption spectroscopy. The relative change in the fluorescence intensity as a function of drug concentrations was analyzed using Stern-Volmer calculations. This was also confirmed by the change in the UV-vis spectra. Fluorescence quenching results of both proteins with the drugs, based on the binding constant values, demonstrated significantly weak binding affinity to NG and strong binding affinity to SNG. Both computational and experimental studies provided important data for understanding protein-drug interactions and will aid in developing potential drug carrier systems in cardiovascular diseases.

FRET-based fluorescent probe for drug assay from amino acid@gold-carbon nanoparticles.

Biocompatible and luminescent nanostructures synthesized by capping gold-carbon nanoparticles (HOOC-4-C6H4-AuNPs) with amino acids tyrosine, tryptophan, and cysteine were used for the quantitative estimation of ranitidine (RNH), a peptic ulcer and gastroesophageal reflux drug. We applied a fluorescence quenching mechanism to investigate the viability of the energy transfer based on gold-carbon nanosensors. Förster resonance energy transfer (FRET) calculations showed a donor-acceptor distance of 1.69 nm (Tyr@AuNPs), 2.27 nm (Trp@AuNPs), and 2.32 nm (Cys@AuNPs). The constant time-resolved fluorescence lifetime measurements supported the static quenching nature. This method was successfully utilized in the detection and quantification of RNH, with a limit of detection (LOD) of 0.174, 0.56, and 0.332 µM for Tyr@AuNP, Trp@AuNP, and Cys@AuNP bioconjugates, respectively. This approach was also successful in the quantification of RNH in spiked serum samples.

Recent advances in gold and silver nanoparticles: synthesis and applications.

In the last decade, gold and silver nanomaterials have received considerable attention due to their attractive electronic and chemical properties and their potential applications in the development of new technologies. Recent advances in the study of various gold and silver nanomaterials have led to their utilization in a number of very important applications including biosensing, diagnostic imaging, and cancer diagnosis and therapy. This review surveys the various synthetic methods of gold and silver nanomaterials. Recent experimental studies focusing on the use of gold and silver nanomaterials in catalysis, food industry, and environmental conservation are also reviewed. This review also highlights the advantages of gold and silver nanomaterials in the development of fluorescence biosensors, glucose biosensors, nucleic acids-based biosensors, and protein-based biosensors. Moreover, the potent in vitro and in vivo anti-microbial and cyto-genotoxic effects of various gold and silver nanomaterials are underlined. Finally, recent advances in the employment of gold and silver nanomaterials as effective drug delivery vehicles and promising cancer therapeutic agents are summarized. Despite their use in remediating numerous medical and health-related conditions, the efficacy and safety of many gold and silver nanomaterials is still under some scrutiny. Needless to say, researchers are facing many challenges and obstacles in their ample attempts to synthesize nanomaterials that are relatively easy to design, inexpensive to fabricate, and effective in treating various diseases, but at the same time display a very low, if any, toxicity to the body. Future investigations should aim at overcoming such challenges in an attempt to design nanomaterials that will prove to be useful in diagnosing and treating life-threatening diseases while ensuring a high degree of efficacy and safety.

Carbon nanotube-ionic liquid composite sensors and biosensors.

A new composite electrode has been fabricated using multiwall carbon nanotubes (MWCNT) and the ionic liquid n-octylpyridinum hexafluorophosphate (OPFP). This electrode shows very attractive electrochemical performances compared to other conventional electrodes using graphite and mineral oil, notably improved sensitivity and stability. One major advantage of this electrode compared to other electrodes using carbon nanotubes and other ionic liquids is its extremely low capacitance and background currents. A 10% (w/w) loading of MWCNT was selected as the optimal composition based on voltammetric results, as well as the stability of the background response in solution. The new composite electrode showed good activity toward hydrogen peroxide and NADH, with the possibility of fabricating a sensitive biosensor for glucose and alcohol using glucose oxidase and alcohol dehydrogenase, respectively, by simply incorporating the specific enzyme within the composite matrix. The marked electrode stability and antifouling features toward NADH oxidation was much higher for this composite compared to a bare glassy carbon electrode. While a loading of 2% MWCNT showed very poor electrochemical behavior, a large enhancement was observed upon gentle heating to 70 degrees C, which gave a response similar to the optimum composition of 10%. The ease of preparation, low background current, high sensitivity, stability, and small loading of nanotubes using this composite can create new novel avenues and applications for fabricating robust sensors and biosensors for many important species.

Semiconducting metal oxide based sensors for selective gas pollutant detection.

A review of some papers published in the last fifty years that focus on the semiconducting metal oxide (SMO) based sensors for the selective and sensitive detection of various environmental pollutants is presented.

Dual WO(3) based sensors to selectively detect DMMP in the presence of alcohols.

A size selective approach to improving selectivity in semiconducting metal oxides (SMO) sensors was obtained by tailoring the architecture of WO(3) powders. The key for achieving high selectivity is based on using a dual sensor configuration where the response on a porous WO(3) powder sensor was compared to the response on a nonporous WO(3) powder sensor. Detection selectivity between methanol and dimethyl methylphosphonate (DMMP) is obtained because the access of a gas molecule in the interior pore structure of WO(3) is size dependent leading to a size dependant magnitude change in the conductivity of SMO sensor.

Photodecomposition of carbaryl in the presence of silver-doped zeolite Y and Suwannee River natural organic matter.

The synthesis and characterization of a novel catalyst for the photodecomposition of carbaryl (1-naphthyl, N-methylcarbamate) is reported. In the absence of a catalyst, but in the presence of UV light a 30 ppm solution of carbaryl decomposes with a first-order rate constant of (5.6 +/- 0.3) x 10(-5) s(-1) (298 K) and a quantum efficiency of 4.8 x 10(-3) molecules/photon. In the presence of the Ag-zeolite Y catalyst with 2.42% Ag by weight, the photodecomposition rate becomes 80 times faster. The addition of Suwannee River natural organic matter (NOM), which can inactivate photocatalysts, has a minimal effect on this system. In the presence of three different concentrations of NOM and 30 ppm carbaryl, our results indicate that the NOM increases or decreases the catalytic photodecomposition rate by only a factor of 3 at most.