Fabrication and growth mechanism of t-selenium nanorods during laser ablation and fragmentation in organic liquids.

Introduction: The process of forming selenium nanoparticles with various shapes and structures through laser ablation and fragmentation in various solvents has been explored. Methods: Laser ablation and laser fragmentation techniques were employed using nanosecond Nd:YAG second harmonic laser irradiation in 9 different working fluids, including water. The characteristics of the resulting nanoparticles were assessed using transmission electron microscopy (TEM), dynamic light scattering (DLS), spectroscopy, and X-ray diffraction (XRD) methods. Results: Laser ablation and subsequent laser fragmentation of some organic solvents, such as ethanol, propanol-2, isobutanol, polyethylene glycol, and diethanolamine, have been found to produce trigonal selenium in the form of elongated nanorods approximately 1 µm long and 200 nm thick, with a well-defined crystal structure. In contrast, the use of deionized water, acetone, glycerol, and benzene as solvents results in the formation of spherical amorphous nanoparticles approximately 100 nm in diameter. Discussion: The polarity of the solvent molecules has been shown to influence the growth of crystalline selenium nanorods in solution during laser ablation and laser fragmentation. Generally, polar solvents hinder the growth of crystalline nanorods, due to interactions between selenium and solvent molecules. Nonpolar solvents, on the other hand, allow for laser fragmentation to reduce particle size and initiate the epitaxial growth of elongated, crystalline selenium nanorods.

The complete nucleotide sequence of Alternanthera mosaic virus infecting Portulaca grandiflora represents a new strain distinct from phlox isolates.

A southeastern European isolate of Alternanthera mosaic virus (AltMV-MU) of the genus Potexvirus (family Flexiviridae) was purified from the ornamental plant Portulaca grandiflora. The complete nucleotide sequence (6606 nucleotides) of AltMV-MU genomic RNA was defined. The AltMV-MU genome is different from those of all isolates described earlier and is most closely related to genomes of partly sequenced portulaca isolates AltMV-Po (America) and AltMV-It (Italy). Phylogenetic analysis supports the view that AltMV-MU belongs to a new "portulaca" genotype distinguishable from the "phlox" genotype.

Peroral endoscopic myotomy in a pregnant woman diagnosed with mitochondrial disease: A case report.

BACKGROUND: Achalasia is a primary esophageal motility disease characterized by impairment of normal esophageal peristalsis and absence of relaxation of the lower esophageal sphincter. Sometimes is can be a part of some genetic disorders. One of the causes of gastrointestinal motility disorders, including achalasia, is mitochondrial defects. CASE SUMMARY: We report about a pregnant woman with a history of symptoms associated with inherited mitochondrial disease, which was confirmed by genetic tests, and who was treated via peroral endoscopic myotomy. CONCLUSION: Peroral endoscopic myotomy is possible treatment option for a pregnant woman with achalasia caused by mitochondrial disease.

Peroral Endoscopic Myotomy in Diffuse Thickened Esophageal Wall in an Adolescent.

Achalasia is an extremely rare pathology in children. Peroral endoscopic myotomy (POEM) is the gold standard for the surgical treatment of achalasia in adults, but only a limited number of cases of achalasia treatment using POEM in children have been published in the literature. Sometimes, high-resolution manometry signs of achalasia can mimic diffuse esophageal leiomyoma. This case report represents the first known successful performance of POEM on a 15-year-old female with diffuse thickening of the esophagus with signs and symptoms of achalasia and suspicion for Alport syndrome associated with diffuse esophageal leiomyoma.

Characterization of Alternanthera mosaic virus and its Coat Protein.

A new isolate of Alternantheramosaic virus (AltMV-MU) was purified from Portulaca grandiflora plants. It has been shown that the AltMV-MU coat protein (CP) can be efficiently reassembled in vitro under different conditions into helical RNA-free virus-like particles (VLPs) antigenically related to native virus. The AltMV-MU and VLPs were examined by atomic force and transmission electron microscopies. The encapsidated AltMV-MU RNA is nontranslatable in vitro. However, it can be translationally activated by CP phosphorylation or by binding to the TGB1protein from the virus-coded movement triple gene block.