We propose a fiber optic single-unit but dual-mode optical imaging system that can provide fast cross-sectional imaging capabilities of swept-source optical coherence tomography (SS-OCT) and functional capabilities of fluorescence spectroscopy (FS). By adopting a fiber optic FS system into a fiber-based SS-OCT system, a compact and effective multimodal single-unit SSOCT-FS system is achieved. Here, the key element of the proposed multimodal imaging system is a specially designed fiber coupler based on double-clad fiber (DCF), which has only cladding-mode coupling capability. The DCF couplers are fabricated with home-drawn DCF by several fabrication methods; a twisting method, a side-polishing method and a fused biconical tapered (FBT) method. Experimentally, the FBT method provides rather flat cladding mode coupling efficiency over 40% in a wide wavelength range. With this specially designed DCF coupler, the OCT signal and the fluorescence signal is measured independently but with a single-unit system. The performance of the SSOCT-FS system is confirmed by measuring the cross-sectional image and the fluorescence signal of a photosensitizer chlorin e6 injected in-vivo rat tumor model. 相似文献
The effects of the Pt catalyst sputter deposited on the patterned ITO glass (SD-Pt/pITO) on the photovoltaic properties and charge-transfer characteristics at the Pt/electrolyte interface of dye-sensitized solar cells (DSSCs) are studied and compared with those of a conventional Pt counter electrode deposited by thermal reduction on fluorine-doped tin oxide (FTO) glass (TD-Pt/FTO). The DSSC with the SD-Pt/pITO (sample cell) shows a lower charge-transfer resistance than that of the DSSC with the TD-Pt/FTO (reference cell), which leads to an improvement of its fill factor by about 7.6%. The long-term durability test performed for 1000 h at room temperature reveals that the sample cell retains up to 99% of its energy conversion efficiency, while that of the reference cell is degraded by about 7.2%. 相似文献
Molecular emitters simultaneously generating light at different wavelengths have wide applications. With a small molecule, however, it is challenging to realize two independent radiative pathways. We invented the first examples of dual-emissive single-benzene fluorophores (SBFs). Two emissive tautomers are generated by synthetic modulation of the hydrogen bond acidity, which opens up pathways for excited-state proton transfer. White light is produced by a delicate balance between the energy and intensity of the emission from each tautomer. We show that the excited-state antiaromaticity of the benzene core itself dictates the proton movements driving the tautomer equilibrium. Using this simple benzene platform, a fluorinated SBF was synthesized with a record high solubility in perfluorocarbon solvents. White light-emitting devices and multicolor imaging of perfluorocarbon nanodroplets in live cells demonstrate the practical utility of these molecules. 相似文献
Summary: We have prepared hexa‐p‐phenylene based rod‐coil molecules with identical coil volume fractions, but different poly(propylene oxide) (PPO) coil architectures (linear versus dibranched), and investigated their self‐assembling behavior in the solid state by small angle X‐ray scattering (SAXS) and transmission electron microscopy (TEM) techniques. Rod‐coil molecules with a linear PPO coil showed a honeycomb‐like lamellar assembly of rod segments with hexagonally arrayed PPO coil perforations. In contrast, the rod‐coil molecules with dibranched PPO coils self‐organized into rod bundles with a body centered tetragonal symmetry surrounded by a PPO coil matrix. These results demonstrate that the steric hindrance at the rod/coil interface arising from coil architectural variation is a dominant parameter governing supramolecular rod assembly in the rod‐coil system.
TEM images and schematic illustrations of the self‐assembled structures of rod‐coil molecules with linear (left) and dibranched (right) PPO coils, respectively. 相似文献
Macromolecules are large, complex molecules composed of smaller subunits known as monomers. The four primary categories of macromolecules found in living organisms are carbohydrates, lipids, proteins, and nucleic acids; they also encompass a broad range of natural and synthetic polymers. Recent studies have shown that biologically active macromolecules can help regenerate hair, providing a potential solution for current hair regeneration therapies. This review examines the latest developments in the use of macromolecules for the treatment of hair loss. The fundamental principles of hair follicle (HF) morphogenesis, hair shaft (HS) development, hair cycle regulation, and alopecia have been introduced. Microneedle (MN) and nanoparticle (NP) delivery systems are innovative treatments for hair loss. Additionally, the application of macromolecule-based tissue-engineered scaffolds for the in vitro and in vivo neogenesis of HFs is discussed. Furthermore, a new research direction is explored wherein artificial skin platforms are adopted as a promising screening method for hair loss treatment drugs. Through these multifaceted approaches, promising aspects of macromolecules for future hair loss treatments are identified. 相似文献