Device for preparing human serum albumin

Abstract

The utility model discloses a device for preparing human serum albumin. The device comprises a liquid preparation bag, a three-way valve, a servo motor, a control system and a timing module, one end of the liquid dispensing bag is provided with an infusion connector, and the other end of the liquid dispensing bag is provided with a liquid dispensing connector which is connected with the human serum albumin tubing and the normal saline tubing through Luer tapers; the three-way valve is driven by the servo motor and operated by the control system, and the opening and closing time is accurately controlled by the timing module, so that accurate mixing of the human serum albumin and the normal saline is realized. According to the utility model, the traditional suction and injection configuration process can be effectively simplified, the pollution and pricking injury risks caused by repeated operation are reduced, and the configuration efficiency and safety are improved at the same time.

Description

TECHNICAL FIELD

[0001] The utility model belongs to the technical field of medical consumables relates to a device for configuring human albumin. BACKGROUND

[0002] At present, the configuration of human albumin in clinic mainly relies on manual operation, and the conventional method generally adopts 500ml physiological saline and 20g human albumin to mix. The specific operation process is as follows: first, use 20ml or 50ml empty needle to extract 200ml from 500ml physiological saline, and then use the empty needle to extract 20g human albumin and inject it into the remaining 300ml physiological saline, so that the two are fully mixed. This method has the following shortcomings:

[0003] 1. Complicated operation process and time-consuming: the traditional configuration method needs to be extracted and injected for many times, and each step requires the operator to accurately measure, which is complicated and time-consuming, and is easy to make mistakes or miss steps.

[0004] 2. High risk of pollution: in the process of repeated aspiration and injection, the operation interface is frequently exposed to the external environment, which is easy to introduce pollutants in the air or on the surface of the instrument, increase the risk of contaminated liquid, and may cause infection of the patient.

[0005] 3. Increased risk of needle stick injury: multiple use of empty needle for aspiration and injection, which is easy to cause needle stick injury due to careless operation or repeated use of needle, and poses a potential threat to the safety of medical staff and patients.

[0006] 4. Unstable mixing ratio control: complete reliance on manual operation can not guarantee the consistency of the mixing ratio of physiological saline and human albumin in each configuration, which is easy to cause mixing ratio deviation due to improper operation, and further affect the drug efficacy and treatment effect.

[0007] 5. Lack of automation and standardization: the existing method does not introduce automatic control equipment, lacks effective automation management of operation process, and cannot realize standardized production, resulting in uncertainty of the quality and effect of each configuration. UTILITY MODEL CONTENT

[0008] Therefore, the utility model aims to solve the problem of configuration of human albumin, and provides a device for configuring human albumin.

[0009] To achieve the above purpose, the utility model provides the following technical scheme:

[0010] The utility model relates to a device for configuring human blood albumin, including the liquid preparation bag, one end of the liquid preparation bag is equipped with infusion interface, the other end is equipped with liquid preparation interface, is connected with the three -way valve on the liquid preparation interface, and is connected human blood albumin pipe and normal saline pipe through the three -way valve respectively, and is connected through the luer joint between the three -way valve and liquid preparation interface, human blood albumin pipe and normal saline pipe.

[0011] Further, the three -way valve is connected with servo motor, and the three -way valve realizes switching action under the drive of servo motor, and the servo motor is connected with control system and is controlled through control system.

[0012] Further, the control system is equipped with timing module, and the on -time of three -way valve is controlled through timing module, thereby controlling the proportioning of human blood albumin and normal saline.

[0013] Further, the pipe diameter of human blood albumin pipe and normal saline pipe is same.

[0014] Further, the liquid preparation bag is equipped with scale line.

[0015] The utility model has the advantages of:

[0016] 1, traditional configuration method needs to suck and inject many times, and the step is complicated and requires higher to the operator, the utility model discloses through the integration of liquid preparation bag, three -way valve, servo motor and control system, and the mixing process of normal saline and human blood albumin realizes automatic operation, greatly simplifies the operation step.

[0017] 2, the utility model discloses through accurate control and full -enclosed design, ensures that each configuration process meets the standardization requirement, improves the quality and stability of final configuration solution, and reduces the incidence of medical accident.

[0018] The other advantages, objects and features of the utility model will be described in the subsequent specification to some extent, and to some extent, it will be obvious to those skilled in the art based on the study of the following text or can be taught from the practice of the utility model. The objects and other advantages of the utility model can be realized and obtained by the following specification. BRIEF DESCRIPTION OF DRAWINGS

[0019] In order to make the purpose, technical scheme and advantage of the utility model more clear, the preferred detailed description of the utility model will be described below in combination with the drawings, wherein:

[0020] Fig. 1The utility model discloses a whole schematic view for the device for configuring human blood albumin.

[0021] Fig. 2 The utility model discloses a structure schematic view of three -way valve.

[0022] Fig. 3 The utility model discloses the installation schematic view of servo motor.

[0023] Fig. 1 - liquid preparation bag;2 - infusion interface;3 - three -way valve;4 - physiological saline pipe;5 - human blood albumin pipe;6 - servo motor;7 - control system. DETAILED DESCRIPTION

[0024] The following through specific concrete example explains the embodiment of the utility model, and the person skilled in the art can easily understand the other advantages and functions of the utility model from the content disclosed in the specification. The utility model can also be implemented or applied through another different specific embodiment, and each detail in the specification can be modified or changed based on different viewpoints and applications without departing from the spirit of the utility model. It should be noted that the drawings provided in the following examples only illustrate the basic concept of the utility model in a schematic manner, and the following examples and features in the examples can be combined with each other without conflict.

[0025] Among them, the drawing is only used for example for illustration, and the representation is only a schematic drawing, and cannot be understood as the restriction of the utility model; In order to better illustrate the embodiment of the utility model, some components of the drawing will be omitted, enlarged or reduced, and the size of the actual product is not represented; For those skilled in the art, it is understandable that some well-known structures and their descriptions in the drawing can be omitted.

[0026] The same or similar signs in the drawings of the embodiments of the utility model correspond to the same or similar parts; In the description of the utility model, it should be understood that if the orientation or positional relationship indicated by the terms "upper", "lower", "left", "right", "front", "back" and the like is based on the orientation or positional relationship shown in the drawing, only for the convenience of describing the utility model and simplifying the description, and not indicating or implying that the device or element indicated must have a particular orientation, structure and operation, therefore the positional relationship of the terms described in the drawing is only used for example for illustration, and cannot be understood as the restriction of the utility model, for the ordinary skilled in the art, the specific meaning of the above terms can be understood according to the specific situation.

[0027] Please refer to Figs. 1-3The utility model provides a device for configuring human serum albumin, which comprises a liquid preparation bag, one end of the liquid preparation bag is provided with an infusion interface, the other end is provided with a liquid preparation interface, a three-way valve is connected to the liquid preparation interface, and a human serum albumin pipe and a physiological saline pipe are connected to the three-way valve respectively; the three-way valve, the liquid preparation interface, the human serum albumin pipe and the physiological saline pipe are connected by luer connectors.

[0028] A servo motor is connected to the three-way valve, and the three-way valve is driven to realize switching operation under the servo motor; the servo motor is connected to a control system and is controlled by the control system.

[0029] The pipe diameter of the human serum albumin pipe and the physiological saline pipe is the same. A timing module is arranged in the control system, and the switching time of the three-way valve is controlled by the timing module, so that the mixing ratio of human serum albumin and physiological saline is controlled. The timing module calculates the valve opening time according to the formula t=Q / (k·d 2 ), which ensures that the liquid preparation accuracy error is less than or equal to 2%.

[0030] In the embodiment, the liquid preparation bag is made of medical PVC material, has a volume of 300ml, and the surface is printed with interval scale lines of 10ml. The liquid preparation interface is connected to the inlet end of the three-way valve through a luer connector, and the two outlet ends of the three-way valve are connected to a 500ml physiological saline bag (outlet A) and a 20g human serum albumin bottle (outlet B) respectively.

[0031] Operation process:

[0032] 1. Initial state: the three-way valve connects the physiological saline bag and the liquid preparation bag;

[0033] 2. After the control system is started, the servo motor drives the three-way valve to open outlet A, and the physiological saline flows into the liquid preparation bag to the 200ml scale line and then automatically closes;

[0034] 3. The three-way valve is switched to outlet B, and the human serum albumin flows into the remaining 300ml physiological saline under the action of gravity, and the valve is closed after the mixing is completed;

[0035] 4. The infusion device can be connected to the infusion interface for clinical infusion.

[0036] Finally, it should be pointed out that the above embodiments are only used to illustrate the technical solutions of the utility model and are not limited. Although the utility model has been described in detail with reference to the preferred embodiments, those skilled in the art should understand that the technical solutions of the utility model can be modified or replaced equivalently without departing from the purpose and scope of the technical solutions, and all of them should be covered in the claim scope of the utility model.

Claims

1. An apparatus for configuring human serum albumin, characterized by: The liquid preparation bag is provided with an infusion interface at one end and a liquid preparation interface at the other end, the liquid preparation interface is connected with a three-way valve, and a human albumin pipe and a physiological saline pipe are connected with the three-way valve respectively; the three-way valve, the liquid preparation interface, the human albumin pipe and the physiological saline pipe are connected through luer connectors.

2. A device for configuring human serum albumin according to claim 1, characterized in that: The three-way valve is connected with a servo motor, and the three-way valve is driven to realize switching operation under the servo motor; the servo motor is connected with a control system, and is controlled through the control system.

3. A device for configuring human serum albumin according to claim 2, characterized in that: A timing module is arranged in the control system, the switching time of the three-way valve is controlled through the timing module, so that the mixing ratio of the human albumin and the physiological saline is controlled.

4. The apparatus for configuring human serum albumin according to claim 1, wherein: The pipe diameter of the human albumin pipe and the physiological saline pipe is the same.

5. The apparatus for configuring human serum albumin according to claim 1, wherein: The liquid preparation bag is provided with a scale line.

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