Bismuth-Based Nano- and Microparticles in X-Ray Contrast, Radiation Therapy, and Radiation Shielding Applications

Bismuth has gained attention in preclinical research because of its ability to attenuate X-rays and high biocompatibility, which make it an excellent element for use in a biomedical agent or in radiation shielding. Developments in the synthesis of elemental bismuth nano- and microparticles, their X-radiation interactions, and their biological interactions will be reviewed in this chapter. The chapter will pay special focus to emerging medical applications of elemental bismuth nano- and microparticles, including the possibility of targeted molecular X-ray imaging, photo-thermal and X-radiation dose enhancing therapies for cancer treatment, and the construction of flexible radiation shielding materials and X-ray opaque devices

Notes on the diet and reproduction of the bark scorpion \u3cem\u3eCentruroides gracilis\u3c/em\u3e (Scorpiones: Buthidae) on Utila Island, Honduras

The brown bark scorpion Centruroides gracilis (Latreille, 1804) (Buthidae) is an abundant and widespread species, however, fairly little is known about its ecology and natural history. We include several observations from Utila Island, Honduras, that expand on the known literature regarding the diet and reproductive behavior of C. gracilis. We report several prey items for this opportunistic species, which include invertebrates such as spiders (including tarantulas), centipedes, katydids, and crickets; as well as a case of cannibalism between two adult females C. gracilis. We suggest that such cannibalism may be driven by high population densities and/or strong intraspecific competition for prey sources on the island. Additionally, we observed a courtship dance involving a female that still carried second-instar offspring, a common behavior within the Buthidae family, although, to our knowledge, not previously reported for C. gracilis

Aerobic Method for the Synthesis of Nearly Size-Monodisperse Bismuth Nanoparticles from a Redox Non-Innocent Precursor

Herein, we report an aerobic synthesis method to produce bismuth nanoparticles (Bi NPs) with average diameters in the range 40-80 nm using commercially available bismuth triiodide (BiI3) as starting material; the method uses only readily available chemicals and conventional laboratory equipment. Furthermore, size data from replicates of the synthesis under standard reaction conditions indicate that this method is highly reproducible in achieving Bi NP populations with low standard deviations in the mean diameters. We also investigated the mechanism of the reaction, which we determined results from the reduction of a soluble alkylammonium iodobismuthate precursor species formed in situ. Under appropriate concentration conditions of iodobismuthate anion, we demonstrate that burst nucleation of Bi NPs results from reduction of Bi3+ by the coordinated, redox non-innocent iodide ligands when a threshold temperature is exceeded. Finally, we demonstrate phase transfer and silica coating of the Bi NPs, which results in stable aqueous colloids with retention of size, morphology, and colloidal stability. The resultant, high atomic number, hydrophilic Bi NPs prepared using this synthesis method have potential for application in emerging X-ray contrast and X-ray therapeutic applications

Redox Regulation, Rather than Stress-Induced Phosphorylation, of a Hog1 Mitogen-Activated Protein Kinase Modulates Its Nitrosative-Stress-Specific Outputs

Data availability. The RNA sequencing dataset is available at EBI (www.ebi.ac.uk/arrayexpress/) under accession number E-MTAB-5990. Other data that support the findings of this study are available from the corresponding author upon reasonable request. ACKNOWLEDGMENTS We thank Debbie Smith for constructing the strains JC41 and JC310, Arnab Pradhan for help with DHE control experiments, and our colleagues in the Aberdeen Fungal Group and Newcastle Yeast Group for insightful discussions. We are also grateful to Mike Gustin for his advice. We are grateful to the Centre for Genome Enabled Biology and Medicine, Aberdeen Proteomics, the Iain Fraser Cytometry Centre, the Microscopy and Histology Facility, and the qPCR facility at the University of Aberdeen for their help, advice, and support. This work was funded by the UK Biotechnology and Biological Research Council (http://www.bbsrc.ac.uk) (grants BB/K017365/1 and BB/F00513X/1 to A.J.P.B. and grant BB/K016393/1 to J.Q.). This work was also supported by the European Research Council (http://erc.europa.eu/) (STRIFE advanced grant C-2009-AdG-249793 to A.J.P.B.), the UK Medical Research Council (http://www.mrc.ac.uk) (grant MR/M026663/1 to A.J.P.B. and grant MR/M000923/1 to P.S.S.), the Wellcome Trust (https://wellcome.ac.uk) (grant 097377 to A.J.P.B. and J.Q.), the MRC Centre for Medical Mycology and the University of Aberdeen (grant MR/M026663/1 to A.J.P.B.). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.Peer reviewedPublisher PD

p53 represses human papillomavirus type 16 DNA replication via the viral E2 protein

<p>Abstract</p> <p>Background</p> <p>Human papillomavirus (HPV) DNA replication can be inhibited by the cellular tumour suppressor protein p53. However, the mechanism through which p53 inhibits viral replication and the role that this might play in the HPV life cycle are not known. The papillomavirus E2 protein is required for efficient HPV DNA replication and also regulates viral gene expression. E2 represses transcription of the HPV E6 and E7 oncogenes and can thereby modulate indirectly host cell proliferation and survival. In addition, the E2 protein from HPV 16 has been shown to bind p53 and to be capable of inducing apoptosis independently of E6 and E7.</p> <p>Results</p> <p>Here we use a panel of E2 mutants to confirm that mutations which block the induction of apoptosis via this E6/E7-independent pathway, have little or no effect on the induction of apoptosis by the E6/E7-dependent pathway. Although these mutations in E2 do not affect the ability of the protein to mediate HPV DNA replication, they do abrogate the repressive effects of p53 on the transcriptional activity of E2 and prevent the inhibition of E2-dependent HPV DNA replication by p53.</p> <p>Conclusion</p> <p>These data suggest that p53 down-regulates HPV 16 DNA replication via the E2 protein.</p

Contribution of Fdh3 and Glr1 to Glutathione Redox State, Stress Adaptation and Virulence in Candida albicans

Acknowledgments: We thank Aaron Mitchell and Dominique Sanglard for providing the C. albicans protein kinase and transposon mutant libraries, and Louise Walker for the strain CAMY203.Peer reviewedPublisher PD

Nurses\u27 Alumnae Association Bulletin - Volume 7 Number 11

Anna M. Shafer Barton Memorial Division Births Changes in the Ophthalmology Division Change of Address Clara Melville Fund Continental Tour Deceased Digest of Meetings Inter-County Hospitalization Plan Katherine Childs\u27 Letter Lost Members Marriages Miscellaneous Nursing Home Committee\u27s Report Physical Advantages President James L. Kauffman\u27s Letter President\u27s Greeting Private Duty Section Prizes Relief Fund School Nursing Silhouette of a Public Health Nurse Rooming-in of Infant with Mother Staff Activities The Student White Haven Divisio

Heavy Dynamical Fermions in Lattice QCD

It is expected that the only effect of heavy dynamical fermions in QCD is to renormalize the gauge coupling. We derive a simple expression for the shift in the gauge coupling induced by $N_f$ flavors of heavy fermions. We compare this formula to the shift in the gauge coupling at which the confinement-deconfinement phase transition occurs (at fixed lattice size) from numerical simulations as a function of quark mass and $N_f$. We find remarkable agreement with our expression down to a fairly light quark mass. However, simulations with eight heavy flavors and two light flavors show that the eight flavors do more than just shift the gauge coupling. We observe confinement-deconfinement transitions at $\beta=0$ induced by a large number of heavy quarks. We comment on the relevance of our results to contemporary simulations of QCD which include dynamical fermions.Comment: COLO-HEP-311, 26 pages and 6 postscript figures; file is a shar file and all macros are (hopefully) include