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Co-Culturing Cancer Cells and Normal Cells in a Biochip under Electrical Stimulation
Kin Fong Lei,Shao-Chieh Hsieh,Rei-Lin Kuo,Ngan-Ming Tsang 한국바이오칩학회 2018 BioChip Journal Vol.12 No.3
The ideal cancer therapeutic strategy is to inhibit the tumor with minimal influence on the normal tissue. Recently, applying an alternating electric field for inhibiting tumor was developed; but, it has not been adopted to be one of the regular therapeutic options. More basic scientific evidence is needed to clarify the efficacy and safety. In the current study, co-culturing cancer cells and normal cells under the electrical stimulation was conducted to provide evidence of this novel cancer therapy. A microfluidic cell culture biochip has been developed and consisted of nine culture chambers incorporating with stimulating electrodes. Cells cultured in the chamber received uniform electric field and cell viability was studied during the culture course. The electric field perturbs cell division and the correlation between cell proliferation rate and inhibition effect was studied among five cell lines, i.e., Huh7, HeLa, TW06, BM1, and HEL299. The results confirmed that cells with higher proliferation rate responded to a higher inhibition. In addition, co-culturing cancer cells and normal cells was conducted to mimic in vivo microenvironment that consists of both cancer and stromal cells. The cancer cells and normal cells were respectively transduced with green fluorescent protein and red fluorescent protein in order to differentiate the cells in a same culture chamber. During the culture course, the electric field was applied to the culture chamber and both cells simultaneously received the field. The results indicated that the growth of the cancer cells were inhibited while the normal cells were maintained. These results provided the evidence of the therapeutic efficacy and safety. Moreover, the microfluidic cell culture biochip could be used for the systematic and precise investigations of the cellular responses under the electrical stimulation.
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Kin Fong Lei,Jun-Liang Liu,Chia-Hao Huang,Rei-Lin Kuo,Ngan-Ming Tsang 한국바이오칩학회 2016 BioChip Journal Vol.10 No.1
Development of effective disease screening method is the best approach for the control of infectious diseases. However, conventional screening methods require to operate in well-equipped laboratory. That makes the screening operation expensive and time-consuming. In this work, a reagent-ready-on-chip microfluidic immunoassay system was developed and rapid detection of influenza A H1N1 and H3N2 viruses was demonstrated to show its simplicity and rapidity. The microfluidic system integrated 4 single-stroke thermopneumatic actuators and a reaction chamber. All related reagents were pre-installed in the system and manipulated automatically for indirect immunoassay. Detection of influenza A H1N1 and H3N2 viruses based on its internal structure protein, i.e., nucleoprotein (NP), was demonstrated using the system. Result was represented by colorimetric signal in the reaction chamber. The use of thermopneumatic actuation could achieve fluid manipulation without external assistive equipment and colorimetric result could be observed directly without the need of external dedicated detector. Influenza virus screening could be completed around 1 hour with less sample volume (20 μL) and reagent volume (50 μL). The system achieved one-step operation of immunoassay. It is highly integrated and has potential to be developed to portable devices to realize rapid diagnostics in remote environment and clinics without well-equipped facility. Development of effective disease screening method is the best approach for the control of infectious diseases. However, conventional screening methods require to operate in well-equipped laboratory. That makes the screening operation expensive and time-consuming. In this work, a reagent-ready-on-chip microfluidic immunoassay system was developed and rapid detection of influenza A H1N1 and H3N2 viruses was demonstrated to show its simplicity and rapidity. The microfluidic system integrated 4 single-stroke thermopneumatic actuators and a reaction chamber. All related reagents were pre-installed in the system and manipulated automatically for indirect immunoassay. Detection of influenza A H1N1 and H3N2 viruses based on its internal structure protein, i.e., nucleoprotein (NP), was demonstrated using the system. Result was represented by colorimetric signal in the reaction chamber. The use of thermopneumatic actuation could achieve fluid manipulation without external assistive equipment and colorimetric result could be observed directly without the need of external dedicated detector. Influenza virus screening could be completed around 1 hour with less sample volume (20 μL) and reagent volume (50 μL). The system achieved one-step operation of immunoassay. It is highly integrated and has potential to be developed to portable devices to realize rapid diagnostics in remote environment and clinics without well-equipped facility.
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( Daniel Balbachevsky ),( Robinson Esteves Pires ),( Rodrigo Guerra Sabongi ),( Theophilo Asfora Lins ),( Geiser De Souza Carvalho ),( Helio Jorge Alvachian Fernandes ),( Fernando Baldy Dos Reis ) 대한외상학회 2019 大韓外傷學會誌 Vol.32 No.1
Unstable pelvic ring lesions are usually treated with internal fixation. In patients presenting clinical instability or soft tissue complication risk, external fixation is a safe treatment option. However, pin tract infection, insufficient biomechanical properties, difficulty sitting and changing decubitus are important drawbacks related to the treatment. The present study reports the association of anterior and posterior subcutaneous internal fixation by applying spine-designed implants on the pelvic ring disruption: supra- acetabular pedicle screws with an interconnecting rod (Infix), plus posterior transiliac fixation with the same system, which the authors have named the “Hula Hoop Technique”.
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