An economic and facilely prepared dopamine ( DA) sensor have been successfully fabricated by the electrodeposition of copper on single-walled carbon nanotubes ( SWNTs )/Nafion-modified glassy carbon electrode. The morphology of the material was observed by scanning electron microscopy ( SEM) and element composition of the material was investigated by energy dispersive X-ray spectroscopy ( EDX ) . Tests with various scan rates and pH conditions indicated that an adsorption-controlled process occured in the electrochemical system. The mechanism of the electrode reaction of dopamine involved a two-electron process which was accompanied by a deprotonation step. Electrochemical parameters were calculated with the electron transfer number as 2 . 67 , the charge transfer coefficients as 0 . 6 , the apparent heterogeneous electron transfer rate constant as 1. 38 s-1 . Under the optimal conditions with differential pulse voltammetric measurement, the linear equation was Ipa(μA)=-0. 054c (μmol/L)-3. 82(R2=0. 9988), with linear range of 5-100 μmol/L and detection limit of 0 . 0135 μmol/L ( S/N=3 ) . The main advantages of sensor included facile fabrication approach, high sensitivity, good stability and high reproducibility. The sensor was applied to the detection of DA in volunteer urine by differential pulse voltammetry with favorable recoveries of 96 . 5%-100 . 4% and relative standard deviations (RSDs) of 1. 2%-2. 4%.

Objective To investigate the radiotherapy curative effects on pains of bone metastases of breast cancer. Methods To analysis 32 patients retrospectively, in which 22 patients received radiotherapy(17 moderate pain, 5 severe pain, 6 dysfunction). Result 16 patients obtained complete remission with 6 cases partial response to radiation. Karnorfsky's score was improved and malfunction disappeared. Conclusion Radiotherapy is a simple and effective treatment on bone metastases of breast cancer with quick and persistent pain relieves.

Bone regeneration remains a great clinical challenge. Low intensity near-infrared (NIR) light showed strong potential to promote tissue regeneration, offering a promising strategy for bone defect regeneration. However, the effect and underlying mechanism of NIR on bone regeneration remain unclear. We demonstrated that bone regeneration in the rat skull defect model was significantly accelerated with low-intensity NIR stimulation. In vitro studies showed that NIR stimulation could promote the osteoblast differentiation in bone mesenchymal stem cells (BMSCs) and MC3T3-E1 cells, which was associated with increased ubiquitination of the core circadian clock protein Cryptochrome 1 (CRY1) in the nucleus. We found that the reduction of CRY1 induced by NIR light activated the bone morphogenetic protein (BMP) signaling pathways, promoting SMAD1/5/9 phosphorylation and increasing the expression levels of Runx2 and Osterix. NIR light treatment may act through sodium voltage-gated channel Scn4a, which may be a potential responder of NIR light to accelerate bone regeneration. Together, these findings suggest that low-intensity NIR light may promote in situ bone regeneration in a CRY1-dependent manner, providing a novel, efficient and non-invasive strategy to promote bone regeneration for clinical bone defects.
Animals ; Rats ; Bone Morphogenetic Protein 2/metabolism* ; Bone Regeneration ; Cell Differentiation ; Circadian Clocks ; Cryptochromes/metabolism* ; Osteoblasts/metabolism* ; Osteogenesis ; Transcription Factors/metabolism*