Journal of Radioanalytical and Nuclear Chemistry - There is an urgent need to develop more specific targeted therapies for lung cancer treatment due to the its low survival rate. EGFR is a... 相似文献
Gastrin releasing peptide receptors (GRPRs) are one of the most interesting targets over expressed in various tumors. Due to the superior potential of the GRPR antagonist analogs, they have been studied in the tumor radio imaging and therapy field. However, typical antagonists suffered the shortcomings of no internalization and poor binding affinity which hampered their applications in radiotherapy. Therefore, we attempted to introduce Oligoarginines (cell penetrating peptides) to RM26, aiming to increase the binding affinity or even trigger the internalization of the peptides on cells. The results showed Arg6 as the most potent CPP, significantly enhanced the binding avidity of RM26 to the GRPR.
We study an infinite-server fork–join queueing system with dependent services, which experiences alternating renewal service disruptions. Jobs are forked into a fixed number of parallel tasks upon arrival and processed at the corresponding parallel service stations with multiple servers. Synchronization of a job occurs when its parallel tasks are completed, i.e., non-exchangeable. Service times of the parallel tasks of each job can be correlated, having a general continuous joint distribution function, and moreover, the service vectors of consecutive jobs form a stationary dependent sequence satisfying the strong mixing (\(\alpha \)-mixing) condition. The system experiences renewal alternating service disruptions with up and down periods. In each up period, the system operates normally, but in each down period, jobs continue to enter the system, while all the servers will stop working, and services received will be conserved and resume at the beginning of the next up period. We study the impact of both the dependence among service times and these down times upon the service dynamics, the unsynchronized queueing dynamics, and the synchronized process, assuming that the down times are asymptotically negligible. We prove FWLLN and FCLT for these processes, where the limit processes in the FCLT possess a stochastic decomposition property and the convergence requires the Skorohod \(M_1\) topology. 相似文献
The achievement of significant photoluminescence (PL) in lanthanide ions (Ln3+) has primarily relied on host sensitization, where energy is transferred from the excited host material to the Ln3+ ions. However, this luminous mechanism involves only one optical antenna, namely the host material, which limits the accessibility of excitation wavelength-dependent (Ex-De) PL. Consequently, the wider application of Ln3+ ions in light-emitting devices is hindered. In this study, we present an organic–inorganic compound, (DMA)4LnCl7 (DMA+=[CH3NH2CH3]+, Ln3+=Ce3+, Tb3+), which serves as an independent host lattice material for efficient Ex-De emission by doping it with trivalent antimony (Sb3+). The pristine (DMA)4LnCl7 compounds exhibit high luminescence, maintaining the characteristic sharp emission bands of Ln3+ and demonstrating a high PL quantum yield of 90–100 %. Upon Sb3+ doping, the compound exhibits noticeable Ex-De emission with switchable colors. Through a detailed spectral study, we observe that the prominent energy transfer process observed in traditional host-sensitized systems is absent in these materials. Instead, they exhibit two independent emission centers from Ln3+ and Sb3+, each displaying distinct features in luminous color and radiative lifetime. These findings open up new possibilities for designing Ex-De emitters based on Ln3+ ions. 相似文献
Microchimica Acta - The authors report on a chromogenic system based MnO2 nanosheet and the chomgenic substrate 3,3′,5,5′-tetramethylbenzidine (TMB). The MnO2 nanosheet can oxidize TMB... 相似文献
Journal of Radioanalytical and Nuclear Chemistry - Death receptor 5 (DR5) is overexpressed in many tumors. Combination of the anti-DR5 antibody with radionuclides such as lutetium-177 (177Lu) could... 相似文献