Bjerring Briggs (zoosalt89)

Conventional photodynamic therapy (PDT) has proved effective in the management of primary tumors and individual metastases. However, most cancer mortality arises from wide-spread multiple metastases. The latter has thus become the principal target in oncology, and X-ray induced photodynamic therapy (XPDT or PDTX) offers a great solution for adapting the PDT principle to deep tumors and scattered metastases. Developing agents capable of being excited by X-rays and emitting visible light to excite photosensitizers is based on challenging physical and chemical technologies, but there are fundamental biological limitations that are to be accounted for as well. see more In the present review, we have established eight major groups of safety determinants of NPs encompassing 22 parameters of clinical applicability of XPDT nanoparticulate formulations. Most, if not all, of these parameters can be accounted for and optimized during the design and development of novel XPDT nanoparticles.Cell metabonomics focuses on discovering metabolic biomarkers and pathway changes in cells from biological systems to obtain the cell properties and functional information under different conditions. Baicalin possesses various pharmacological activities, and plays a vital role in the oncology research field. However, the detailed mechanism of its action is still unclear. In this work, we employed ultra-high performance liquid chromatography-mass spectrometry (UPLC-MS) based non-targeted metabolomics method associated with chemometrics analysis to explore metabolic pathways and biomarkers for investigating the efficacy and pharmacological targets of baicalin against thyroid cancer cells. In addition, morphological observation, parameter calculation of cell proliferation and apoptosis were carried out, which assisted in elucidation of pharmacological activity of baicalin on the human thyroid cancer cells. The results showed that baicalin possesses an intense stimulative apoptosis and inhibits proliferation activity on SW579 human thyroid cancer cells, and partially reversed the cell metabolite abnormalities. A total of nineteen differentiated metabolites in SW579 cells were identified and deemed as potential biomarkers after the baicalin treatment, involving nine metabolic pathways, such as taurine and hypotaurine metabolism, pyrimidine metabolism, fructose and mannose metabolism, steroid hormone biosynthesis and sphingolipid metabolism. High-throughput non-targeted metabolomics provide an insight into specialized mechanism of baicalin against thyroid cancer and contributes to novel drug discovery and thyroid cancer management in clinical practice.Using the density functional theory, we investigated the geometric, electronic structure, phase stability and electrochemical properties of a potential P2 layer orthorhombic cathode material NaxMnO2 (0 ≤ x ≤ 1) applied for sodium-ion batteries. Herein, we shed the light on the undeniable effect of the polaron formation and polaron migration on the diffusion of Na+ ions in the orthorhombic P2 layered oxides. Both GGA+U and HSE06 methods agree that, when a Na+ ion is removed from the fully charged state of NaMnO2, the accompanying polaron preferably forms at one of the third nearest Mn (3NN) octahedra to the Na vacancy, implying the oxidization of the Mn3+ ion at one of these 3NN sites to Mn4+. The positive polaron migrates simultaneously with the Na vacancy and would hinder the diffusion of Na ions. Two kinds of elementary diffusion processes, named parallel and crossing, have been explored which required almost same activation energy of about 423 meV (518 meV) by GGA+U (HSE06). In the fully discharged state, GGA+U and HSE06 methods indicate that the negative polaron forms at one of the second nearest Mn neighbours (2NN). The activation energy of 273 meV (327 meV) is needed for diffusion in a structure with a low Na concentration, which is much lower than that required for diffusion in the Na-rich regime. Cons