Microplastics - A major contaminant in marine macro algal population: Review.

Microplastics (MPs) are a significant concern in this modern environment, and the marine environment is a sink for them now. Researchers have taken an interest in marine microplastic studies recently, which has opened the door to research in macroalgae and microalgae. Macroalgae are the primary producers in maritime ecosystems and are economically significant. This review aimed to identify the microplastic interactions with marine macroalgae and the impacts of microplastics on macroalgae based on existing literature while also recognizing knowledge gaps. MPs were mostly fibers and polymers with notable production and application levels; their abundance differed among species. More MPs were found in filamentous species than in other types. The results of this study indicated that, in maritime environments, macroalgae contribute to MP biomagnification and bioaccumulation. Adequate studies are needed to fill the research gaps in this area of MPs in macroalgae and their effects.

Hemoprotein bioconjugates of gold and silver nanoparticles and gold nanorods: structure-function correlations.

Bioconjugates of the hemoproteins, myoglobin, and hemoglobin have been synthesized by their adsorption on spherical gold and silver nanoparticles and gold nanorods. The adsorption of hemoproteins on the nanoparticle surface was confirmed by their molecular ion signatures in matrix assisted laser desorption ionization mass spectrometry and specific Raman features of the prosthetic heme b units. High-resolution transmission electron microscopy (HRTEM) and UV-visible spectroscopy showed that the particles retain their morphology and show aggregation only in the case of silver. The binding of azide ion to the Fe(III) center of the prosthetic heme b moiety caused a red shift of the Soret band, both in the case of the bioconjugates and in free hemoproteins. This was further confirmed by the characteristic signature at 2050 cm-1 in the Fourier-transform infrared spectra, which corresponds to the asymmetric stretching of the Fe(III) bound azide. The retention of the chemical behavior of the prosthetic heme group after adsorption on the nanoparticle is interesting due to its implications in nanoparticle supported enzyme catalysis. The absence of morphology changes after the reaction of bioconjugates with azide ion observed in HRTEM studies implies the stability of nanoparticles under the reaction conditions. All these studies indicate the retention of protein structure after adsorption on the nanoparticle surface.

Interaction of azide ion with hemin and cytochrome c immobilized on Au and Ag nanoparticles.

This paper presents a set of investigations on the binding of a metabolic inhibitor, azide with prosthetic heme group of biomolecules, hemin chloride (Hem) and cytochrome c (Cyt c) immobilized on Au and Ag nanoparticles. A variety of spectroscopic tools have been used to understand the chemistry occurring on the nanoparticle surface. While the nature of binding of the model system, hemin has been investigated by UV-visible, fluorescence, FTIR, and Raman spectroscopies, the azide binding has been studied in detail by MALDI-TOF MS. Hemin binding on the nanoparticle surface occurs through the carboxylic acid groups. The hemin-N(3) adduct on the nanoparticle surface has been detected by mass spectrometry and its fragments have been studied by post source decay analysis. The chemistry of hemin on the nanoparticle surface has been compared with that of the protein, Cyt c. Azide binding of Cyt c requires thermal activation due to reduced accessibility of the heme center, unlike in the case of hemin. The binding chemistry is similar for free Cyt c and Cyt c bound to the nanoparticles.

Ciprofloxacin-protected gold nanoparticles.

The antibacterial drug ciprofloxacin (cfH) has been used to protect gold nanoparticles of two different mean diameters, 4 and 20 nm. The protection is complete with about 65 and 585 cfH molecules covering 4 and 15 nm particles, respectively. The nature of binding has been investigated by several analytical techniques. The nitrogen atom of the NH moiety of piperazine group binds on the gold surface, as revealed by voltammetric and spectroscopic studies. The cfH-adsorbed particles are stable in the dry state as well as at room temperature, and as a result, redispersion is possible. The rate of release of the drug molecule from the nanoparticles is more in the basic medium than in pure water, and the kinetics depend on the size of the particle; faster desorption is seen in smaller particles. The bound cfH is fluorescent, and this property could be used in biological investigations. This study shows that metal nanoparticles could be useful carriers for cfH and fluoroquinolone molecules. Most of the bound molecules could be released over an extended period of time.

Detection and extraction of endosulfan by metal nanoparticles.

One of the most common pesticides in the developing world, endosulfan, can be detected in ppm levels using gold nanoparticles. Endosulfan adsorbs on the nanoparticle surface and upon interaction for a long time, the nanoparticles precipitate from the solution. Interaction with silver is weak, yet adsorption occurs leading to removal of endosulfan from the solution. A multilayer assembly of gold nanoparticles prepared on a glass substrate shows excellent spectrophotometric response suggesting potential applications.