Abstract: The disclosure provides a method of active immunotherapy for a cancer patient, comprising administering vaccines against Globo series antigens (i.e., Globo H, SSEA-3 and SSEA-4). Specifically, the method comprises administering Globo H-CRM197 (OBI-833/821) in patients with cancer. The disclosure also provides a method of selecting a cancer patient who is suitable as treatment candidate for immunotherapy. Exemplary immune response can be characterized by reduction of the severity of disease, including but not limited to, prevention of disease, delay in onset of disease, decreased severity of symptoms, decreased morbidity and delayed mortality.

Abstract: An acute kidney injury predicting system and a method thereof are proposed. A processor reads the data to be tested, the detection data, the machine learning algorithm and the risk probability comparison table from a main memory. The processor trains the detection data according to the machine learning algorithm to generate an acute kidney injury prediction model, and inputs the data to be tested into the acute kidney injury prediction model to generate an acute kidney injury characteristic risk probability and a data sequence table. The data sequence table lists the data to be tested in sequence according to a proportion of each of the data to be tested in the acute kidney injury characteristics. The processor selects one of the medical treatment data from the risk probability comparison table according to the acute kidney injury characteristic risk probability.

Abstract: A pressure buffering system includes a housing, a pump module, a pressure sensor and a pressure cylinder. The pump module, the pressure sensor and the pressure cylinder are disposed in the housing. The pressure cylinder is communicated between the pump module and the pressure sensor. A biological culture device is further provided.

Abstract: A pressure buffering system includes a housing, a pump module, a pressure sensor and a pressure cylinder. The pump module, the pressure sensor and the pressure cylinder are disposed in the housing. The pressure cylinder is communicated between the pump module and the pressure sensor. A biological culture device is further provided.

Abstract: A mask including patterned structures arranged sequentially along a predetermined direction and a peripheral area surrounding the patterned structures is provided. Each of the patterned structures includes an opening portion and a thinning portion surrounding the opening portion. The opening portion has through holes arranged in a matrix. An outline of the thinning portion has two side edges opposite to each other substantially parallel to the predetermined direction. The thinning portion is defined by an area demarked by the outline of the thinning portion and an outline of the opening portion. A thickness of the thinning portion is thinner than a thickness of the peripheral area.

Abstract: An X-ray emission device for emitting an integrated X-ray beam toward an object is disclosed. The X-ray emission device includes multiple X-ray emission tubes for respectively generating multiple X-rays, and a lens module for guiding the multiple X-rays toward the object to form the integrated X-ray beam.

Abstract: A method of analyzing biological particles for a biological particle analyzer includes outputting a first detection result when at least one particle has arrived at the first detection area, outputting a second detection result to the control module when the particles have arrived at the second detection area, and determining when to turn on or off the light emission source and outputting a control signal to turn on or off the light emission source according to the first detection result, wherein a control module is configured to calculate a turn-on time according to different particle characteristics and an average velocity of the at least one particle, and the light emission source is turned on only when the at least one particle is being tested during the turn-on time.

Abstract: An X-ray emission device for emitting an integrated X-ray beam toward an object is disclosed. The X-ray emission device includes multiple X-ray emission tubes for respectively generating multiple X-rays, and a lens module for guiding the multiple X-rays toward the object to form the integrated X-ray beam.

Abstract: A mask including patterned structures arranged sequentially along a predetermined direction and a peripheral area surrounding the patterned structures is provided. Each of the patterned structures includes an opening portion and a thinning portion surrounding the opening portion. The opening portion has through holes arranged in a matrix. An outline of the thinning portion has two side edges opposite to each other substantially parallel to the predetermined direction. The thinning portion is defined by an area demarked by the outline of the thinning portion and an outline of the opening portion. A thickness of the thinning portion is thinner than a thickness of the peripheral area.

Abstract: A method of analyzing biological particles for a biological particle analyzer includes outputting a first detection result when at least one particle has arrived at the first detection area, outputting a second detection result to the control module when the particles have arrived at the second detection area, and determining when to turn on or off the light emission source and outputting a control signal to turn on or off the light emission source according to the first detection result, wherein a control module is configured to calculate a turn-on time according to different particle characteristics and an average velocity of the at least one particle, and the light emission source is turned on only when the at least one particle is being tested during the turn-on time.

Abstract: A biological particle analyzer is disclosed and includes a microchannel including an end coupled to a first drive electrode, another end coupled to a second drive electrode, a first detection area at an upstream location and an excitation area at a downstream location for containing particles flowing from the upstream location to the downstream location inside the microchannel, a first detection circuit coupled to the first detection area for outputting a first detection result when at least one particle has arrived at the first detection area, a light emission source, and a control module coupled to the first detection circuit and the light emission source for determining when to turn on or off the light emission source according to the first detection result.

Abstract: A measurement device with electroencephalography (EEG) and electrocardiography (ECG) functionalities includes a shell and a turning structure. The shell includes a first contact and a second contact located at a first side of the shell; and a third contact. The turning structure, disposed on the shell, is utilized for adjusting the third contact to be located at the first side when the measurement device is in an EEG mode, and adjusting the third contact to be located at a second side of the shell when the measurement device is in an ECG mode, wherein the second side is substantially opposite to the first side.

Abstract: A biochip detecting device for detecting a biochip is provided. The biochip receives an incident light to produce an excitation light. Both the incident light and the excitation light include a specific wavelength. The biochip detecting device includes a light source producing the incident light, an optical attenuator, a filter, a sensor, and a control module electrically connected to the light source and the sensor. Light with the specific wavelength passes through the filter. The optical attenuator disposed between the light source and the filter attenuates an intensity of the incident light, and replaces the biochip. The sensor detects an intensity of the light with the specific wavelength attenuated by the optical attenuator, and generates an intensity signal. The control module adjusts the intensity of the incident light according to whether the intensity signal is complied with a predetermined requirement. A detection method for the light source is provided.

Abstract: A measurement device with electroencephalography (EEG) and electrocardiography (ECG) functionalities includes a shell and a turning structure. The shell includes a first contact and a second contact located at a first side of the shell; and a third contact. The turning structure, disposed on the shell, is utilized for adjusting the third contact to be located at the first side when the measurement device is in an EEG mode, and adjusting the third contact to be located at a second side of the shell when the measurement device is in an ECG mode, wherein the second side is substantially opposite to the first side.

Abstract: A measurement device with electroencephalography (EEG) and electrocardiography (ECG) functionalities includes a shell and a turning structure. The shell includes a first contact and a second contact located at a first side of the shell; and a third contact. The turning structure, disposed on the shell, is utilized for adjusting the third contact to be located at the first side when the measurement device is in an EEG mode, and adjusting the third contact to be located at a second side of the shell when the measurement device his in an ECG mode, wherein the second side is substantially opposite to the first side.

Abstract: A measurement device with electroencephalography (EEG) and electrocardiography (ECG) functionalities includes a first shell having ECG functionality and a second shell. The first shell includes a first contact and a second contact located at a first side of the first shell; and a third contact located at a second side of the first shell, wherein the second side of the first shell is substantially opposite to the first side of the first shell. The second shell includes a fixing device, for connecting with and fixing on the first shell; and a fourth contact, a fifth contact and a sixth contact, located at a first side of the second shell, for electrically connecting with the first contact, the second contact and the third contact respectively when the first shell is connected to and fixed on the fixing device, in order to perform EEG measurement.

Abstract: A measurement device with electroencephalography (EEG) and electrocardiography (ECG) functionalities includes a first shell having ECG functionality and a second shell. The first shell includes a first contact and a second contact located at a first side of the first shell; and a third contact located at a second side of the first shell, wherein the second side of the first shell is substantially opposite to the first side of the first shell. The second shell includes a fixing device, for connecting with and fixing on the first shell; and a fourth contact, a fifth contact and a sixth contact, located at a first side of the second shell, for electrically connecting with the first contact, the second contact and the third contact respectively when the first shell is connected to and fixed on the fixing device, in order to perform EEG measurement.

Abstract: A measurement device with electroencephalography (EEG) and electrocardiography (ECG) functionalities includes a shell and a turning structure. The shell includes a first contact and a second contact located at a first side of the shell; and a third contact. The turning structure, disposed on the shell, is utilized for adjusting the third contact to be located at the first side when the measurement device is in an EEG mode, and adjusting the third contact to be located at a second side of the shell when the measurement device his in an ECG mode, wherein the second side is substantially opposite to the first side.

Abstract: A biochip detecting device for detecting a biochip is provided. The biochip receives an incident light to produce an excitation light. Both the incident light and the excitation light include a specific wavelength. The biochip detecting device includes a light source producing the incident light, an optical attenuator, a filter, a sensor, and a control module electrically connected to the light source and the sensor. Light with the specific wavelength passes through the filter. The optical attenuator disposed between the light source and the filter attenuates an intensity of the incident light, and replaces the biochip. The sensor detects an intensity of the light with the specific wavelength attenuated by the optical attenuator, and generates an intensity signal. The control module adjusts the intensity of the incident light according to whether the intensity signal is complied with a predetermined requirement. A detection method for the light source is provided.

Abstract: A biological particle analyzer is disclosed and includes a microchannel including an end coupled to a first drive electrode, another end coupled to a second drive electrode, a first detection area at an upstream location and an excitation area at a downstream location for containing particles flowing from the upstream location to the downstream location inside the microchannel, a first detection circuit coupled to the first detection area for outputting a first detection result when at least one particle has arrived at the first detection area, a light emission source, and a control module coupled to the first detection circuit and the light emission source for determining when to turn on or off the light emission source according to the first detection result.