Changes in the structure of the amorphous alloy Fe73.5Cu1Nb3Si13.5B9 were investigated after annealing for 1 h in a temperature range from 450-800 degrees C using X-ray diffraction scattering and Mossbauer effect spectroscopy. Between 520 and 550 degrees C nanocrystalline Fe80Si20 grains with the DO3 structure (diameter of about 10 nm) are embedded in an amorphous grain boundary phase. Above 650 degrees C the grain size increases and the amorphous grain boundary phase disappears. The Fe-B phases form and a new paramagnetic phase is observed. Furthermore the kinetics of the amorphous-to-nanocrystalline phase transition of this alloy was examined by X-ray diffraction observing the development of crystallization with time at a fixed annealing temperature of 520 degrees C. The beginning of crystallization appears at times less than 2 min, most grains developing in the first 10 to 20 min while after about 5 min the grain size remains constant with a diameter of about 10 nm.
Peptidic ligands selectively targeting distinct G protein-coupled receptors that are highly expressed in tumor tissue represent a promising approach in drug delivery. Receptor-preferring analogues of neuropeptide Y (NPY) bind and activate the human Y1 receptor subtype (hY1 receptor), which is found in 90% of breast cancer tissue and in all breast-cancer-derived metastases. Herein, novel highly boron-loaded Y1 -receptor-preferring peptide analogues are described as smart shuttle systems for carbaboranes as (10) B-containing moieties. Various positions in the peptide were screened for their susceptibility to carbaborane modification, and the most promising positions were chosen to create a multi-carbaborane peptide containing 30 boron atoms per peptide with excellent activation and internalization patterns at the hY1 receptor. Boron uptake studies by inductively coupled plasma mass spectrometry revealed successful uptake of the multi-carbaborane peptide into hY1 -receptor-expressing cells, exceeding the required amount of 10(9) boron atoms per cell. This result demonstrates that the NPY/hY receptor system can act as an effective transport system for boron-containing moieties.
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