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121.
A novel torsion sensor is proposed, which is composed of one long period fibre grating and one asymmetrically corrugated long period fibre grating based on the high-frequency CO2 laser pulses technology and burning fibre coating and etching cladding technology, respectively. By combing the advantages of the two aforementioned elements, a sensitivity of 331.7 and 310.3 pm/(rad/m) towards clockwise and anticlockwise direction, respectively, is reached in the experiments. 相似文献
122.
123.
Chen J Luo Y Hong L Ling Y Pang J Fang Y Wei K Gao X 《Journal of materials science. Materials in medicine》2011,22(3):547-555
A superior drug controlled release system capable of achieving efficient osteogenesis is in imperative demand because of limited
bone substitute tissue for the treatment of bone defect. In the present study, we investigated the potential of using poly(ε-caprolactone)–hydroxyapatite
(PCL–HA) composite microspheres as an injectable bone repair vehicle by controlled release of alendronate (AL), a medicine
that belongs to the bisphosphonates family. The PCL/HA–AL microspheres were prepared with solid/oil/water emulsion technique,
which included two processes: (1) AL was loaded on the hydroxyapatite nanoparticles; (2) the HA–AL complex was built in the
PCL matrix. The spherical PCL/HA–AL microspheres were characterized with its significantly improved encapsulation efficiency
of hydrophilic AL and better sustained release. Human bone mesenchymal stem cells (hMSCs) were cultured on the surface of
these microspheres and exhibited high proliferative profile. Specifically, in osteogenic medium, hMSCs on the surface of PCL/HA–AL
microspheres displayed superior osteogenic differentiation which was verified by alkaline phosphatase activity assay. In conclusion,
by presenting strong osteogenic commitment of hMSCs in vitro, the PCL/HA–AL microspheres have the potential to be used as
an injectable vehicle for local therapy of bone defect. 相似文献
124.
125.
Zicheng Li Yifeng Gao Zhihao Zhang Qiu Xiong Longhui Deng Xiaochun Li Qin Zhou Yuanxing Fang Peng Gao 《纳微快报(英文)》2021,(7):12-27
Efficient electron transport layers(ETLs)not only play a crucial role in promoting carrier separation and electron extraction in perovskite solar cells(PSCs)but... 相似文献
126.
Rapid global population growth has caused an increasing need for products containing protein.Meat products are the most common high-protein food source,but impa... 相似文献
127.
128.
Po Hu Zhi-Guo Ma Kai Zhao Guo-Qiang Zhang De-Qing Fang Bao-Ren Wei Chang-Bo Fu Yu-Gang Ma 《核技术(英文版)》2021,32(6):84-92
With the development of laser technologies,nuclear reactions can happen in high-temperature plasma environments induced by lasers and have attracted a lot of at... 相似文献
129.
130.
Ke Fang Yuki Murakami Seiji Kanda Takaki Shimono Anh Tuan Dang Mitsuaki Ono Toshimasa Nishiyama 《International journal of molecular sciences》2022,23(14)
Osteoporosis is a common bone disease, particularly in menopausal women. Herein, we screened four Kampo medicines (Unkeito (UKT), Kamishoyosan (KSS), Kamikihito (KKT), and Ninjinyoeito (NYT)), frequently used to treat menopausal syndromes, for their effects on receptor activator of nuclear factor-kappaB ligand (RANKL)-induced osteoclast differentiation in RAW 264 cells. Considering that UKT exhibited the most potent effect, we examined its effect on RANKL-induced osteoclastogenesis, the induction of osteoclast apoptosis, and the mechanisms underlying its effects. UKT inhibits RANKL-induced osteoclast differentiation in the early stage and decreases osteoclast-related genes, including tartrate-resistant acid phosphatase (Trap), dendritic cell-specific transmembrane protein (Dcstamp), matrix metalloproteinase-9 (Mmp9), and cathepsin K (Ctsk). Specifically, UKT inhibits the nuclear factor of activated T cells 1 (NFATc1), which is essential for osteoclastogenesis. UKT increases Bcl6, which antagonizes NFATc1 and Dc-stamp, thereby blocking the progression of osteoclasts to maturation. UKT also decreased nuclear translocation by downregulating the activity of p65/NF-κB. In addition, UKT enhances mononuclear osteoclast apoptosis via activation of caspase-3. Herein, we demonstrate that UKT suppresses RANKL-mediated osteoclastogenesis via the Blimp1–Bcl6 and NF-κB signaling pathways and enhances mononuclear osteoclast apoptosis. Furthermore, UKT prevents bone loss in OVX mice. Thus, UKT might be a potential therapeutic agent for postmenopausal osteoporosis. 相似文献