CN211847958U - Full-automatic device for simulating human gastrointestinal tract digestion glycolysis - Google Patents

Full-automatic device for simulating human gastrointestinal tract digestion glycolysis Download PDF

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CN211847958U
CN211847958U CN202020049545.2U CN202020049545U CN211847958U CN 211847958 U CN211847958 U CN 211847958U CN 202020049545 U CN202020049545 U CN 202020049545U CN 211847958 U CN211847958 U CN 211847958U
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digestion
tank
digestion tank
glycolysis
sampling
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聂少平
胡婕伦
嵇海华
张珊珊
聂启兴
谢明勇
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Nanchang University
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Nanchang University
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Priority to CN202022495312.8U priority patent/CN214654939U/en
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Abstract

The utility model discloses a device of full-automatic simulation human gastrointestinal tract digestion glycolysis, the device include equipment frame, equipment electrical control box and install in the equipment frame, be used for simulating human gastrointestinal tract digestion glycolysis, and consecutive oral cavity digester, stomach digester, duodenum digester, jejunum digester, ileum digester, rise colon digester, horizontal colon digester and fall colon digester. The full-automatic simulation device for the whole components of the gastrointestinal tract of the human body is explained in detail for the first time, and the structure and design of each part are explained in detail for the first time.

Description

Full-automatic device for simulating human gastrointestinal tract digestion glycolysis
Technical Field
The utility model belongs to the technical field of bionics, human physiology, microbiology, nutriology, organic chemistry and analysis and test, accurate saying so relates to a device of full-automatic simulation human gastrointestinal tract digestion glycolysis.
Background
The digestion and absorption of food by the human body is a very complex process, and after being ingested, the food is converted into nutrients for the body to grow. During the human digestive process, two main processes occur almost simultaneously: (1) reducing the size of the particle size of the food during mechanical transport in the digestive tract; (2) the macromolecules in the food are hydrolyzed into micromolecules which are absorbed into the blood. The food crushing process mainly takes place in the oral cavity and stomach, while the enzymatic hydrolysis and absorption of nutrients and water mainly take place in the small and large intestine.
Currently, the digestive system has become a focus of research in various fields (such as nutrition, toxicology, physiology, microbiology, etc.) in connection with various problems during research by researchers. Unfortunately, the development of this complex multi-stage process of human digestion presents economic and technical difficulties and is subject to ethical constraints when potentially toxic and harmful substances are involved in the development process. Therefore, a set of flexible, accurate and repeatable models simulating the physiological processes of human body such as digestion and absorption in vitro is urgently needed.
Scientists have tried to model the gastrointestinal tract over time, but most in vitro models are static, contain only a few simulation parameters, and are directed to specific organs. For example, the digestive juices of the gastrointestinal tract developed by the dutch scientist a.g. oomen et al in 2002 contain only saliva, gastric juice, pancreatic juice and bile. However, in the process of simulating the complex physiological, biochemical and physicochemical characteristics of the digestive tract, it is important to be able to simulate the time, pH, enzymatic hydrolysis conditions, etc. when food or a substance to be studied passes through the digestive tract during the digestion process. Therefore, several dynamic multiple digestive organ models were developed and applied to studies, such as the Human Gastric Simulator (HGS) developed by american scientists Kong F and Singh PR in 2010 for simulating the digestion of food in the stomach. A simulated human intestinal micro-ecosystem (SHIME) reactor developed and developed to date in 1993 by belgium scientist k.
For the research on the establishment and the method of the human gastrointestinal tract bionic system, the initiation is early abroad, the attention degree is higher, while the research in China is relatively lagged, and the research on the device and the method is carried out by a few organizations at present. For example, the utility model discloses a small-size fermentation device of simulation intestinal environment is disclosed to patent No. CN201634678U, and the device can be used for micro-fermentation such as laboratory good oxygen, anaerobism, gas production not, can accurately collect and measure the produced gas volume of fermentation. The invention patent No. CN102533543B discloses a device for intestinal microorganism culture, which can simulate the human intestinal environment, and can provide and maintain relatively constant temperature and humidity, and can oscillate to achieve the effect of simulating the intestinal environment. Utility model patent No. CN202658158U discloses an intelligent simulation control device for gastrointestinal tract digestive system, which can simulate gastrointestinal tract digestive system by computer control. The invention patent No. CN101482460B discloses a unit animal bionic digestion system and a method for simulating unit animal digestion based on the system, and the system and the method realize the process of simulating animal gastrointestinal tract digestion and feed absorption under in vitro conditions. The invention patent No. CN101665758B discloses a simulation test method for reproducing human gastrointestinal tract and microecological system under in vitro condition, which is based on a human intestinal tract microecological system simulation device introduced by the university of Gente in Belgium, and carries out technical improvement aiming at the living habits of oriental population to reproduce the human gastrointestinal tract system under in vitro condition.
These patent documents greatly enrich the devices and methods of use suitable for digestive glycolysis, but to date, these patents do not describe in detail the simulation of specific digestion in the oral cavity; secondly, these patents do not provide detailed simulation and description of gastric emptying process in stomach simulation; meanwhile, the specifications of the patents on parameters in a small intestine simulation system and a large intestine glycolysis system are not detailed; some of these patents are based only on animal-related parameters and are not very relevant to humans.
This patent application will go on according to human digestion glycolysis process and physiological environment completely to the digestion glycolysis simulation of each position for the first time, has carried out the detailed description to each digestion glycolysis position, and the process at each digestion glycolysis position has realized full-automatic, dynamic simulation simultaneously, the physiological environment of the true people of laminating more.
SUMMERY OF THE UTILITY MODEL
In order to solve the problems, the utility model provides a full-automatic device for simulating the digestive glycolysis of the gastrointestinal tract of a human body. The utility model discloses will explain in detail the full-automatic analogue means of human whole component parts of intestines and stomach and method for the first time to carry out detailed simulation explanation to each partial structure and design for the first time, the device and implementation method can be surveyd the condition of the digestion glycolysis after various food, activity or nutrient substance got into the human body, and the help is explored the digestion and the glycolysis condition after various food, activity or nutrient substance got into the human body.
The utility model provides a technical scheme that its technical problem adopted does:
a full-automatic device for simulating human gastrointestinal tract digestion glycolysis comprises an equipment frame, an equipment electrical control box and an oral cavity digestion tank, a stomach digestion tank, a duodenum digestion tank, a jejunum digestion tank, an ileum digestion tank, a colon ascending digestion tank, a transverse colon digestion tank and a colon descending digestion tank which are arranged in the equipment frame and used for simulating human gastrointestinal tract digestion glycolysis and are sequentially connected, wherein the digestion tanks are connected through transfer pipelines, and the jejunum digestion tank, the ileum digestion tank, the colon ascending digestion tank and the transverse colon digestion tank are connected with a membrane absorption device;
each digestion tank comprises a tank cover, a tank cover flange, a tank body inner layer, a cleaning ball arranged in the tank body inner layer, a liquid transfer interface and a blow-down valve arranged at the lower end of the tank body inner layer and a tank body outer layer jacket, wherein the tank cover is provided with a digestion liquid port, a digestion sample port, a liquid discharge port, a sampling port, a seed receiving port, an acid liquid port, an alkali liquid port, an air inlet, an air outlet and a cleaning ball interface;
the membrane absorption device comprises a clamp fixing base, a front clamp and a rear clamp which are arranged on the clamp fixing base, a flat membrane is arranged between the front clamp and the rear clamp, a digestive juice/glycolysis juice inlet is formed in the lower end of the front clamp, a concentrated solution return port is formed in the upper end of the front clamp, the digestive juice/glycolysis juice inlet and the concentrated solution return port are both connected with corresponding digestion tanks through transfer pipelines, and the flat membrane is connected with a dialysis bag through a membrane absorption pipeline;
each digestion tank sampling port is connected with the sample pipeline, the sample pipeline end is provided with the sample needle, the sample needle is installed in automatic sampling equipment top.
As above-mentioned technical scheme's improvement, automatic sampling equipment includes the sampling bottle revolving stage, a plurality of sampling bottles are installed to sampling bottle revolving stage up end, be provided with sample needle slider and slide rail directly over the sampling bottle revolving stage, the sample needle carries out the ration sample in electronic or manual horizontal longitudinal movement inserts the sampling bottle under the cooperation of sample needle slider and slide rail, install ethanol needle slider on the slide rail, the ethanol needle is installed to ethanol needle slider front end.
As an improvement of the technical scheme, the cover of the digestion tank is also provided with a dissolved oxygen electrode interface, a pH electrode interface and a tank temperature electrode interface.
As an improvement of the technical scheme, the outer jacket of the digester tank body is connected with a tank jacket water inlet and a tank jacket water outlet.
As an improvement of the technical scheme, the front clamp and the rear clamp of the membrane absorption device are fixed through membrane fastening screws.
As an improvement of the technical scheme, the dialysis bag of the membrane absorption device is connected with the corresponding digestion tank through a transfer pipeline.
As an improvement of the technical scheme, the transfer pipeline, the membrane absorption pipeline and the sampling pipeline are all provided with peristaltic pumps.
The utility model discloses the beneficial effect who brings has:
the core of the full-automatic simulation human gastrointestinal tract digestion glycolysis device of the utility model is that the device and the implementation method thereof firstly describe the full-automatic simulation of all the components of the human gastrointestinal tract in detail, and firstly describe the design of each part structure and the corresponding function in detail.
The full-automatic human gastrointestinal tract digestion and glycolysis simulation device can observe the digestion and glycolysis conditions of various foods, activities or nutrient substances after entering the human body, and helps to explore the digestion and glycolysis conditions of various foods, activities or nutrient substances after entering the human body.
Drawings
The invention will be further explained with reference to the drawings and the specific embodiments,
FIG. 1 is a block diagram of the system flow of the full-automatic human gastrointestinal tract digestive glycolysis simulation device of the present invention;
FIG. 2 is a side view of the structure of the digestion tank of the present invention;
FIG. 3 is a top view of the structure of the middle digestion tank of the present invention;
FIG. 4 is a perspective view of the structure of the middle digestion tank of the present invention;
FIG. 5 is a simplified structural view of the middle membrane absorbent device of the present invention;
FIG. 6 is a schematic diagram of the structure and the membrane absorption principle of the present invention, which is taken from the jejunum digestion tank to the ileum digestion tank as an example;
fig. 7 is a schematic structural diagram of the automatic sampling device of the present invention.
The label names corresponding to the sequence numbers in the figure are as follows:
101-inner layer of tank, 102-cleaning ball, 103-outer layer jacket of tank, 104-liquid-transfer interface, 105-blow-down valve, 106-digestive juice port, 107-digestive sample port, 108-liquid discharge port, 109-sampling port, 110-inoculation port, 111-acid liquid port, 112-alkali liquid port, 113-gas inlet, 114-gas outlet, 115-cleaning ball interface, 116-dissolved oxygen electrode interface, 117-pH electrode interface, 118-tank temperature electrode interface, 119-tank jacket water inlet, 120-tank jacket water outlet;
201-a clamp fixing base, 202-a front clamp, 203-a flat membrane, 204-a rear clamp, 205-a digestive fluid/glycolysis fluid inlet, 206-a concentrated fluid reflux port, 207-a small molecule permeation port and 208-a membrane fastening screw;
301-sample bottle rotating platform, 302-sample needle sliding block, 303-sliding rail and 304-ethanol needle sliding block.
Detailed Description
Example 1
This embodiment will be described with reference to the accompanying drawings for a fully automatic device for simulating human gastrointestinal tract digestive glycolysis.
The device comprises an equipment frame, an equipment electrical control box and an oral cavity digestion tank, a stomach digestion tank, a duodenum digestion tank, a jejunum digestion tank, an ileum digestion tank, a ascending colon digestion tank, a transverse colon digestion tank and a descending colon digestion tank which are arranged in the equipment frame and used for simulating the human gastrointestinal tract digestion glycolysis and are sequentially connected. Referring to the attached figure 1, the digestion tanks are connected in sequence through transfer pipelines, and the jejunum digestion tank, the ileum digestion tank, the ascending colon digestion tank and the transverse colon digestion tank are connected with a membrane absorption device. The sample connection 109 of each digester is connected with the sample pipeline, and the sample pipeline end is provided with the sampling needle, and the sampling needle is installed in automatic sampling equipment top.
Referring to fig. 2 to 4, each digestion tank includes a tank cover, a tank cover flange, a tank inner layer 101, a cleaning ball 102 disposed in the tank inner layer 101, a liquid transfer port 104 and a blow-off valve 105 disposed at a lower end of the tank inner layer 101, and a tank outer layer jacket 103, and the tank cover is provided with a digestion solution port 106, a digestion sample port 107, a liquid discharge port 108, a sampling port 109, a seed receiving port 110, an acid solution port 111, an alkali solution port 112, an air inlet 113, an air outlet 114, and a cleaning ball port 115.
Meanwhile, the cover of the digestion tank is also provided with a dissolved oxygen electrode interface 116, a pH electrode interface 117 and a tank temperature electrode interface 118. The outer layer jacket 103 of the digestion tank body is connected with a tank jacket water inlet 119 and a tank jacket water outlet 120.
Referring to fig. 5, the film adsorbing device includes a jig fixing base 201, and a front jig 202, a rear jig 204, a front jig 202, the rear clamp 204 is fixed through a membrane fastening screw 208, a flat membrane 203 is arranged between the front clamp 202 and the rear clamp 204, a digestive juice/glycolysis solution inlet 205 is arranged at the lower end of the front clamp 202, a concentrated solution return port 206 is arranged at the upper end of the front clamp, the digestive juice/glycolysis solution inlet 205 is connected to a sampling port 109 of the digestion tank through a transfer pipeline, the concentrated solution return port 206 is connected to a liquid discharge port 108 of the digestion tank through a transfer pipeline, the flat membrane 203 is connected to a dialysis bag through a small molecule permeation port 207 and a membrane absorption pipeline, and the dialysis bag adds a small amount of physiological saline to absorbed water molecules to return to the corresponding digestion tank through the transfer pipeline (the ascending, transverse and descending colon digestion tanks can be filled with nutrient solution selectively) and is in butt joint with a seed-grafting port.
Referring to fig. 6, a schematic diagram of a tank body connection structure and a schematic diagram of a membrane absorption principle are shown by taking a jejunum digestion tank to an ileum digestion tank as an example. After digestion (fermentation) of the jejunum digestion tank is finished and sampling is finished, starting a transfer peristaltic pump, transferring a digestion sample to a membrane absorption device, completing absorption (flow rate is 50-100mL/min) under the action of the peristaltic pump, absorbing small molecules (less than or equal to 5.8-6.0KDa) as much as possible, allowing the small molecules to enter a dialysis bag, then refluxing the absorbed water molecules to the digestion tank, refluxing concentrated solution to the jejunum digestion tank under the pressure of the peristaltic pump, circularly absorbing for 15-30min, and absorbing 55-60% of the total absorption volume. When the fermentation liquor is separated to meet the process requirement, the membrane absorption procedure is ended, the transfer peristaltic pump is started, and the digestion sample is sent into the ileum digestion tank to continue the next step of digestion.
Referring to fig. 7, the automatic sampling device comprises a sampling bottle rotating platform 301, wherein a plurality of sampling bottles are mounted on the upper end face of the sampling bottle rotating platform 301, samples are stored at low temperature of about 0-2 ℃, at least 80-100 sampling bottles are reserved, each sampling bottle corresponds to a number, and the sampled bottles can be used for distinguishing which digestion tank sample through colors, so that confusion is avoided. A sampling needle slider 302 and a slide rail 303 are arranged right above the sampling bottle rotating platform 301, the sampling needle moves transversely and longitudinally under the matching of the sampling needle slider 302 and the slide rail 303 electrically or manually, quantitative sampling is carried out after the sampling needle is inserted downwards into the sampling bottle, and the sampling needle is connected to a sampling port 109 of the digestion tank through a sampling pipeline.
Meanwhile, an ethanol needle sliding block 304 is arranged on the sliding rail 303, an ethanol needle is arranged at the front end of the ethanol needle sliding block 304, and after sampling is finished, a sample is added with ethanol for enzyme deactivation and preservation.
The sampling system is provided with a set of independent control system, industrial Ethernet communication is established with the main program of the electrical control box of the digestion glycolysis system, the corresponding sampling time of the digestion tank is set by the control system, and automatic sampling is carried out after the control program detects a sampling command.
After sampling, the simulated digestion and glycolysis process is repeated three times, and the digestion and glycolysis conditions of the substance to be detected are detected by adopting corresponding detection methods such as liquid phase and gas phase.
The PLC electric control system part related in the embodiment applies the prior art, and the application does not relate to the improvement of the PLC electric control system part; to realize the functions of each unit, for example: the contents of the sample bottle rotating platform control, the electric matching of the sliding block and the sliding rail and the like which are not described in detail in the embodiment can be applied to the prior art.
Example 2
This example describes the method of the present application for fully automated simulation of human gastrointestinal digestion glycolysis.
The method is applied to the device for fully automatically simulating human gastrointestinal tract digestive glycolysis in the embodiment 1, and specifically comprises the following steps:
step 1: connecting each digestion tank, the matched pipeline, the supply pipeline and the detection electrode;
step 2: empty can sterilization
Starting each digestion tank for magnetic stirring, entering high-pressure pure water for cleaning, discharging residues from a blow-down valve 105 at the bottom of each digestion tank, simultaneously washing each transfer peristaltic pump pipeline and a sampling pipeline with pure water for 3-10min, entering steam for high-temperature disinfection of each digestion tank after the washing, wherein the disinfection time is 25-30min, introducing nitrogen after the disinfection, then entering 80-100mL of ethanol to each transfer peristaltic pump pipeline and sampling pipeline for disinfection, introducing 200-300mL of pure water for cleaning each digestion tank, each transfer peristaltic pump pipeline and sampling pipeline after the disinfection, introducing high-temperature nitrogen for drying each digestion tank after the disinfection, introducing normal-temperature nitrogen after the disinfection, and ensuring the positive pressure and anaerobic environment of each digestion tank at the flow rate of 1-10 mL/min;
step 3: simulated digestion
Simulated digestion was performed in the following order:
buccal digestion → gastric digestion → duodenal digestion → jejunal digestion → ileal digestion;
oral digestion: connecting each sterilized supplementary liquid to an oral cavity digestion tank, starting magnetic stirring, circulating temperature control, pumping 15-20mL of oral cavity digestion liquid before digestion, pumping a digestion sample into the oral cavity digestion tank by using a transfer peristaltic pump, pumping 80-100mL of the digestion sample at a flow rate of 80-100mL/min, and respectively pumping 70-80mL of the oral cavity digestion liquid at a flow rate of 80-100mL/min and CaCl20.3-0.5mL of solution, flow rate 0.8-1.0mL/min, pH 6.8-7.0, temperature 37 ℃, digestion 3-5min, sampling time point: magnetic stirring is carried out for 0min and 3-5 min; when the oral cavity digestion is finished and the oral cavity digestive juice transfer peristaltic pump stops working, the gastric digestion is started, and meanwhile, the pre-cleaning is automatically carried out: firstly, automatically opening a blowdown valve 105 of an oral digestion tank, cleaning the tank body through a shower head above the tank body of the oral digestion tank, closing the blowdown valve 105 of the oral digestion tank after cleaning for 3-10min, then soaking in pure water with the volume of 80-90% of the tank body, starting pre-cleaning of a sampling pipeline of the oral digestion tank, cleaning for 1-2min, waiting for cleaning of a transfer pipeline, and automatically cleaning and sterilizing;
stomach digestion: connecting each sterilized supply liquid to a gastric digestion tank, starting magnetic stirring, pumping 50-60mL of gastric digestion liquid in the gastric digestion tank before digestion, transferring 180-200mL of oral digestion sample to the gastric digestion tank, and respectively pumping 130-150mL of gastric digestion liquid through a peristaltic pump at the flow rate of 80-100mL/min and CaCl after the transfer is finished20.3-0.5mL of the solution, 0.8-1.0mL/min of flow rate, 0.0005t of pH20.079t +4.47, digestion 120-150min, sampling time points 0, 10, 20, 30, 60, 120 and 150min, and magnetic stirring is carried out for three times per minute, wherein the duration of each time is 10-15 s; when the gastric digestion is finished and the gastric digestive juice transfer peristaltic pump stops working, the duodenal digestion is started, and meanwhile, the pre-cleaning is automatically carried out: firstly, automatically opening a blowdown valve 105 of a gastric digestion tank, opening a transfer peristaltic pump between the oral digestion tank and the gastric digestion tank, rapidly transferring pure water in the oral digestion tank for 1-2min, completing pre-cleaning of a transfer pipeline between the oral digestion tank and the gastric digestion tank, cleaning the tank body through a shower head above the tank body of the gastric digestion tank, closing the blowdown valve 105 of the gastric digestion tank after cleaning for 3-10min, then soaking in pure water with the volume of 80-90% of the tank, opening the pre-cleaning of a sampling pipeline of the gastric digestion tank, cleaning for 1-2min, waiting for cleaning of the transfer pipeline, and automatically cleaning and sterilizing;
digestion of duodenum: connecting each sterilized supply liquid to a duodenum digestion tank, starting magnetic stirring, transferring 400mL of a gastric digestion sample to the duodenum digestion tank by a transfer peristaltic pump, and after the transfer is finished, respectively pumping 400mL of 380-400mL intestinal electrolytes by the peristaltic pump at the flow rate of 80-100mL/min and 0.6-0.8mL of CaCl2Digesting the solution at the flow rate of 0.8-1.0mL/min and the pH value of 6.1-6.2 for 45-50min, and sampling at the sampling time points of 0, 10, 20 and 45-50min, and magnetically stirring the solution for a long time; when the digestion of the duodenum is finished and the duodenum digestive fluid transfer peristaltic pump stops working, the jejunum digestion is started, and meanwhile, the precleaning is automatically carried out: firstly, automatically opening a drain valve 105 of a duodenal digestion tank, opening a transfer peristaltic pump between the gastric digestion tank and the duodenal digestion tank, rapidly transferring pure water in the gastric digestion tank for 1-2min, completing pre-cleaning of a transfer pipeline between the gastric digestion tank and the duodenal digestion tank, cleaning the tank body through a shower head above the duodenal digestion tank body, closing the drain valve 105 of the duodenal digestion tank after cleaning for 3-10min, then soaking in pure water with the volume of 80-90% of the tank, opening pre-cleaning of a sampling pipeline of the duodenal digestion tank, cleaning for 1-2min, waiting for cleaning of the transfer pipeline, and performing automatic cleaning and sterilization operation;
jejunal digestion: connecting each sterilized supply liquid to a jejunum digestion tank, starting magnetic stirring, transferring all duodenum digestion samples to the jejunum digestion tank through a transfer peristaltic pump, wherein the total volume is 700-800mL, the pH value is 6.4-6.5, the digestion time is 45-50min, the sampling time points are 0, 10, 20 and 45-50min, the magnetic stirring is continuously operated, the absorption is finished through the peristaltic pump after the sampling is finished, the flow rate is 50-100mL/min, the absorbed water molecules are pumped back to the jejunum digestion tank in the absorption process, the cyclic absorption is carried out, the small molecules are absorbed as much as possible for 15-30min until 55-60% of the total volume is absorbed, and the remaining volume is 300-320 mL; when jejunum digestion is finished and the jejunum digestive juice transfer peristaltic pump stops working, the ileum digestion is started, and meanwhile, pre-cleaning is automatically carried out: firstly, automatically opening a drain valve 105 of a jejunum digestion tank, opening a transfer peristaltic pump between a duodenum digestion tank and the jejunum digestion tank, quickly transferring pure water in the duodenum digestion tank for 1-2min, completing pre-cleaning of a transfer pipeline between the duodenum digestion tank and the jejunum digestion tank, cleaning the tank body through a shower head above the jejunum digestion tank, closing the drain valve 105 of the jejunum digestion tank after cleaning for 3-10min, then soaking in 80-90% of the pure water in the tank volume, opening the pre-cleaning of a sampling pipeline of the jejunum digestion tank, cleaning for 1-2min, then opening the cleaning of a membrane absorption pipeline of the jejunum digestion tank, circularly cleaning for 3-5min, waiting for cleaning of the transfer pipeline, and automatically cleaning and sterilizing;
ileum digestion: connecting each sterilized supplement liquid to an ileum digestion tank, starting magnetic stirring, transferring the residual digestion sample in the jejunum digestion tank to the ileum digestion tank by a transfer peristaltic pump, wherein the flow rate is 80-100mL/min, the pH value is 7.4-7.5, the digestion time is 90-100min, the sampling time points are 0, 10, 20, 30, 60 and 90-100min, the magnetic stirring is continuously operated, the absorption is finished by the peristaltic pump after the sampling is finished, the absorbed water molecules are pumped back to the ileum digestion tank in the absorption process, the cyclic absorption is carried out, the small molecules are absorbed as much as possible for 15-30min until the total absorption volume is 55-60%, and the residual volume is 120-130 mL; when the ileum digestion is finished and the ileum digestive juice transfer peristaltic pump stops working, starting colon ascending digestion, and automatically pre-cleaning: firstly, automatically opening a drain valve 105 of an ileum digestion tank, opening a transfer peristaltic pump between the jejunum digestion tank and the ileum digestion tank, rapidly transferring pure water in the jejunum digestion tank for 1-2min, completing the pre-cleaning of a transfer pipeline between the jejunum digestion tank and the ileum digestion tank, cleaning the tank body through a shower head above the tank body of the ileum digestion tank, closing the drain valve 105 of the ileum digestion tank after cleaning for 3-10min, then soaking in pure water with the volume of 80-90% of the tank, opening the pre-cleaning of a sampling pipeline of the ileum digestion tank, cleaning for 1-2min, then opening the cleaning of a membrane absorption pipeline of the ileum digestion tank, circularly cleaning for 3-5min, waiting for the cleaning of the transfer pipeline, and automatically cleaning and sterilizing;
step 4: simulated glycolysis
The simulated glycolysis was performed in the following order:
ascending colon glycolysis → transverse colon glycolysis → descending colon glycolysis;
ascending colon glycolysis: connecting each sterilized supply liquid to a colon ascending digestion tank, starting magnetic stirring, transferring a peristaltic pump to transfer all ileum digestion liquid into the colon ascending digestion tank, feeding 120 mL of colon ascending culture liquid through the peristaltic pump, keeping the flow rate at 80-100mL/min, keeping the pH at 5.5-6.0, fermenting for 6-8h, sampling time points at 0, 3 and 6h or 0, 4 and 8h, running the magnetic stirring, completing absorption through the peristaltic pump after sampling, pumping absorbed water molecules back into the colon digestion tank in the absorption process, circularly absorbing small molecules to the greatest extent, absorbing for 15-30min until 55-60% of the total absorption volume and the rest volume is 90-100 mL; after the ascending colon glycolysis is finished and the ascending colon glycolysis liquid transfer peristaltic pump stops working, the transverse colon glycolysis is started, and meanwhile, pre-cleaning is automatically carried out: firstly, automatically opening a blowdown valve 105 of a colon ascending digestion tank, opening a transfer peristaltic pump between the ileum digestion tank and the colon ascending digestion tank, quickly transferring pure water in the ileum digestion tank for 1-2min, completing pre-cleaning of a transfer pipeline between the ileum digestion tank and the colon ascending digestion tank, cleaning the tank body through a shower head above the tank body of the colon ascending digestion tank, closing the blowdown valve 105 of the colon ascending digestion tank after cleaning for 3-10min, then soaking in pure water with the volume of 80-90% of the tank, opening the pre-cleaning of a sampling pipeline of the colon ascending digestion tank, cleaning for 1-2min, then opening the cleaning of a membrane absorption pipeline of the colon ascending digestion tank, circularly cleaning for 3-5min, waiting for cleaning of the transfer pipeline, and automatically cleaning and sterilizing;
performing zymolysis on the transverse colon: connecting each sterilized supply solution to a transverse colon digestion tank, starting magnetic stirring, transferring a peristaltic pump to completely transfer the ascending colon zymolysis solution to the transverse colon digestion tank, feeding 90-100mL of ascending colon culture solution through the peristaltic pump, keeping the flow rate at 80-100mL/min, keeping the pH at 6.0-6.4, carrying out glycolysis for 12-16h, sampling time points at 0, 4, 8, 12 and 16h, continuously carrying out magnetic stirring, completing absorption through the peristaltic pump after sampling is completed, pumping absorbed water molecules back to the transverse colon digestion tank in the absorption process, circularly absorbing the small molecules for 15-30min to the greatest extent until 55-60% of the total absorption volume is obtained, and keeping the volume at 60-70 mL; after the transverse colon zymolysis is finished and the transverse colon zymolysis liquid transfer peristaltic pump stops working, the colon degradation zymolysis is started, and meanwhile, pre-cleaning is automatically carried out: firstly, automatically opening a blowdown valve 105 of a transverse colon digestion tank, starting a transfer peristaltic pump between a ascending colon digestion tank and the transverse colon digestion tank, quickly transferring pure water in the ascending colon digestion tank for 1-2min, completing pre-cleaning of a transfer pipeline between the ascending colon digestion tank and the transverse colon digestion tank, cleaning the tank body through a shower head above the tank body of the transverse colon digestion tank, closing the blowdown valve 105 of the transverse colon digestion tank after cleaning for 3-10min, then soaking in pure water with 90% of the tank volume, starting pre-cleaning of a sampling pipeline of the transverse colon digestion tank, cleaning for 1-2min, then starting cleaning of a membrane absorption pipeline of the transverse colon digestion tank, circularly cleaning for 3-5min, waiting for cleaning of the transfer pipeline, and automatically cleaning and sterilizing;
colon degradation: connecting each sterilized supply solution to a descending colon digestion tank, starting magnetic stirring, transferring a peristaltic pump to transfer all the transverse colon zymolysis solution to the descending colon, feeding 60-70mL of ascending colon culture solution through the peristaltic pump, allowing the flow rate to be 80-100mL/min, allowing the pH to be 6.5-6.9, allowing the zymolysis time to be 6-8h, and sampling time points to be 0, 3, 6 or 0, 4, 8h, allowing the magnetic stirring to be operated all the time, and transferring the sample to a waste liquid barrel through the transfer peristaltic pump after sampling; when the degradation colon fermentation is finished and the degradation colon fermentation liquid transfer peristaltic pump stops working, pre-cleaning is automatically carried out: firstly, automatically opening a blow-off valve 105 of a colon descending digestion tank, opening a transfer peristaltic pump between a transverse colon digestion tank and the colon descending digestion tank, rapidly transferring pure water in the colon descending digestion tank for 1-2min, completing the pre-cleaning of a transfer pipeline between the transverse colon digestion tank and the colon descending digestion tank, cleaning the tank body through a shower head above the colon descending digestion tank, closing the blow-off valve 105 of the colon descending digestion tank after cleaning for 3-10min, then soaking in pure water with the volume of 80-90% of the tank, simultaneously opening the pre-cleaning of a colon descending sampling pipeline, the transfer pipeline and a waste discharge pipeline, cleaning for 1-2min, and waiting for automatic cleaning and sterilization operation.
The above method further comprises the steps of:
step 5: automatic cleaning and sterilizing
After all digestion and glycolysis are finished, waiting for formal cleaning and sterilization of each digestion tank, the transfer pipeline, the membrane absorption pipeline and the sampling pipeline:
automatically opening a bottom blow-down valve 105 of each digestion tank of the oral cavity, the stomach, the duodenum, the jejunum, the ileum, the ascending colon, the transverse colon and the descending colon, discharging waste water in the tanks, cleaning each digestion tank by high-pressure pure water again, discharging residues by the tank bottom blow-down valve 105, simultaneously flushing pure water at the tank side of a transfer peristaltic pump pipeline, after cleaning for 3-10min, closing the bottom blow-down valve 105 by the tank body without the membrane absorption device, and performing membrane regeneration cleaning;
membrane regeneration and cleaning: pumping 400 plus 500mL of pure water into a corresponding tank, cleaning for 5-10min, discharging the wastewater, pumping 400 plus 500mL of membrane cleaning agent, cleaning for 30-40min, pumping 400 plus 500mL of pure water, cleaning for 5-10min, discharging the wastewater, then the corresponding tank enters steam for high-temperature disinfection, air is introduced after the disinfection, the bottom blowoff valve 105 is closed, the corresponding tank enters 250-300mL of pure water, all the transfer peristaltic pumps are opened to clean the transfer pipeline, and simultaneously cleaning the sampling pipeline, discharging wastewater after cleaning for 3-5min, adding 250 plus 300mL of ethanol to each corresponding tank to disinfect the membrane absorption device, the transfer pipeline and the sampling pipeline, adding 400 plus 500mL of pure water to clean the tank, the membrane absorption device, the transfer pipeline and the sampling pipeline after finishing, introducing high-temperature nitrogen to dry the tank and each pipeline after finishing, and introducing normal-temperature nitrogen after finishing.
Others need to be specifically mentioned:
(1) automatic sampling is carried out in each step of digestion/glycolysis process:
the control mode of the sampling system is as follows: the sample bottle rotating platform 301 can automatically rotate, samples are stored at low temperature of about 0-2 ℃, at least 80-100 sample bottles are reserved, and the corresponding number of each sample bottle can distinguish which digestion tank the sample is in through color in the sampled bottle program, so that disorder is prevented; the sampling system is provided with a set of independent control system, industrial Ethernet communication is established with the main program of the electrical control box of the digestion glycolysis system, the corresponding sampling time of the digestion tank is set by the control system, automatic sampling is carried out after the control program detects a sampling command, and ethanol is added for inactivating enzyme and storing.
A sampling needle and a sampling pipeline are disinfected: for guaranteeing that the sample does not have the residue (easily lead to mixed pollution), the sample pipeline leans on the sample needle side pipeline all to carry out cleaning and disinfecting before the sample with after the sample to let in and heat nitrogen and weather, to at every turn taking out the sample after, the sample pipeline is close to remaining digestion appearance in the pipeline of digestion (glycolysis) jar side, adopts nitrogen gas to push back the mode, with remaining sample in the sample pipeline push back the digestion jar in continue digestion (or glycolysis), and then make the sample have more the representative.
After sampling, the digestion and glycolysis simulation process is repeated three times, and the digestion and glycolysis condition of the substance to be detected is detected by a corresponding detection method, such as liquid phase and gas phase.
(2) In each step, when the transfer peristaltic pump transfers the digestion sample, the transfer time is prolonged by 1-2min, the digestion sample at the previous position is completely transferred as much as possible, and meanwhile, the residue of a transfer pipeline is reduced.
(3) In each step, the supply liquid is provided with a water bath heating device with the temperature of 37 ℃; at least two sets of glass tanks for containing digestion samples, supply liquid, simulated absorption liquid and the like and corresponding rubber pipelines are provided.
(4) Annular hollowed-out rings attached to the wall need to be added inside all the tank bodies so as to better simulate the secretion of digestive juice and acid-base liquid; a1-2 mm screen is additionally arranged on the stomach to simulate the stomach screening function.
The above detailed description of the embodiments of the present invention is only for the preferred embodiments of the present invention, and should not be considered as limiting the scope of the present invention. All the equivalent changes and improvements made according to the application scope of the present invention should still fall within the patent coverage of the present invention.
It should also be understood that although the present description has been described in terms of embodiments, not every embodiment includes only a single embodiment, and such description is for clarity purposes only, and those skilled in the art will recognize that the embodiments described herein may be combined as a whole to form other embodiments as would be understood by those skilled in the art.

Claims (7)

1. A full-automatic device for simulating human gastrointestinal tract digestion glycolysis is characterized in that: the device comprises an equipment frame, an equipment electrical control box and an oral cavity digestion tank, a stomach digestion tank, a duodenum digestion tank, a jejunum digestion tank, an ileum digestion tank, a ascending colon digestion tank, a transverse colon digestion tank and a descending colon digestion tank which are arranged in the equipment frame and used for simulating digestion and glycolysis of the gastrointestinal tract of a human body and are sequentially connected, wherein the digestion tanks are connected through transfer pipelines, and the jejunum digestion tank, the ileum digestion tank, the ascending colon digestion tank and the transverse colon digestion tank are connected with a membrane absorption device;
each digestion tank comprises a tank cover, a tank cover flange, a tank body inner layer, a cleaning ball arranged in the tank body inner layer, a liquid transfer interface and a blow-down valve arranged at the lower end of the tank body inner layer and a tank body outer layer jacket, wherein the tank cover is provided with a digestion liquid port, a digestion sample port, a liquid discharge port, a sampling port, a seed receiving port, an acid liquid port, an alkali liquid port, an air inlet, an air outlet and a cleaning ball interface;
the membrane absorption device comprises a clamp fixing base, a front clamp and a rear clamp which are arranged on the clamp fixing base, a flat membrane is arranged between the front clamp and the rear clamp, a digestive juice/glycolysis juice inlet is formed in the lower end of the front clamp, a concentrated solution return port is formed in the upper end of the front clamp, the digestive juice/glycolysis juice inlet and the concentrated solution return port are both connected with corresponding digestion tanks through transfer pipelines, and the flat membrane is connected with a dialysis bag through a membrane absorption pipeline;
each digestion tank sampling port is connected with the sample pipeline, the sample pipeline end is provided with the sample needle, the sample needle is installed in automatic sampling equipment top.
2. The fully automatic human gastrointestinal tract digestion glycolysis simulation apparatus of claim 1, wherein: automatic sampling equipment includes the sampling bottle revolving stage, a plurality of sampling bottles are installed to sampling bottle revolving stage up end, be provided with sample needle slider and slide rail directly over the sampling bottle revolving stage, the sample needle carries out the ration sample in electronic or manual horizontal longitudinal movement inserts the sampling bottle under the cooperation of sample needle slider and slide rail, install ethanol needle slider on the slide rail, the ethanol needle is installed to ethanol needle slider front end.
3. The fully automatic human gastrointestinal tract digestion glycolysis simulation apparatus of claim 1, wherein: the digestion tank cover is also provided with a dissolved oxygen electrode interface, a pH electrode interface and a tank temperature electrode interface.
4. The fully automatic human gastrointestinal tract digestive glycolysis simulation apparatus of claim 3, wherein: the outer jacket of the digestion tank body is connected with a tank jacket water inlet and a tank jacket water outlet.
5. The fully automatic human gastrointestinal tract digestion glycolysis simulation apparatus of claim 1, wherein: and the front clamp and the rear clamp of the membrane absorption device are fixed by membrane fastening screws.
6. The fully automatic human gastrointestinal tract digestive glycolysis simulation apparatus of claim 5, wherein: the dialysis bag of the membrane absorption device is connected with the corresponding digestion tank through a transfer pipeline.
7. The fully automatic human gastrointestinal tract digestion glycolysis simulation apparatus of claim 1, wherein: the transfer pipeline, the membrane absorption pipeline and the sampling pipeline are all provided with peristaltic pumps.
CN202020049545.2U 2020-01-10 2020-01-10 Full-automatic device for simulating human gastrointestinal tract digestion glycolysis Active CN211847958U (en)

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CN202022495287.3U CN214654938U (en) 2020-01-10 2020-01-10 Membrane absorption device for simulating human gastrointestinal tract digestive glycolysis
CN202020049545.2U CN211847958U (en) 2020-01-10 2020-01-10 Full-automatic device for simulating human gastrointestinal tract digestion glycolysis
CN202022496884.8U CN214654940U (en) 2020-01-10 2020-01-10 Automatic sampling device for simulating human gastrointestinal tract digestive glycolysis
CN202022495312.8U CN214654939U (en) 2020-01-10 2020-01-10 Digestion tank for simulating digestion glycolysis of human gastrointestinal tract

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CN202020049545.2U Active CN211847958U (en) 2020-01-10 2020-01-10 Full-automatic device for simulating human gastrointestinal tract digestion glycolysis
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