A kind of hou toujianwei ling capsule manufacturing equipment and process

Abstract

The present application relates to the technical field of medicine manufacturing, and particularly relates to a Hericium longi-ramosum stomach-healthy capsule manufacturing device and process, which comprises a supporting mechanism placed on the ground, the supporting mechanism is provided with a concentration mechanism for concentrating Hericium longi-ramosum, the concentration mechanism comprises a manufacturing tank, the inside of the manufacturing tank is three cavities, which are a premixing cavity, a concentration cavity and a scraper cavity, two separation mechanisms for separating the three cavities in the manufacturing tank are arranged in the concentration mechanism; the device integrates three processes of premixing, concentration and scraper concentration in the same manufacturing tank, realizes the automatic transfer of the medicinal liquid between different cavities through the adjustable-angle rotating seat and the separation mechanism, avoids the complicated operation of switching multiple devices in the traditional process, shortens the production cycle, and improves the production efficiency; the separation mechanism drives the manufacturing tank to rotate through an angle motor, and controls the start and stop of the separation mechanism through an opening and closing cylinder, realizes the automation of the medicinal liquid flow and the cavity switching, and improves the consistency and stability of the process.

Description

Technical Field

[0001] This invention relates to the field of pharmaceutical manufacturing technology, and in particular to a manufacturing equipment and process for Hou Tou Jian Wei Ling capsules. Background Technology

[0002] Hericium erinaceus (Hericium erinaceus) Jianweiling Capsules are a traditional Chinese medicine preparation with Hericium erinaceus culture as the main ingredient. They are effective in strengthening the stomach, aiding digestion, and improving gastrointestinal function. In traditional production processes, Hericium erinaceus culture undergoes multiple steps, including pulverization, mixing, concentration, and drying. The concentration step, in particular, has a significant impact on the retention of active ingredients and the final product quality.

[0003] Existing concentration equipment typically suffers from the following problems: Traditional processes require transferring the drug solution between different devices, such as premixing and concentration, which are carried out in separate equipment. This is not only cumbersome but also prone to drug solution contamination and loss of active ingredients. During concentration, uneven heating of the drug solution may lead to local overheating, damaging heat-sensitive components and affecting efficacy. Existing equipment often relies on manual adjustment of angles, switching of chambers, or control of valves, resulting in low production efficiency and difficulty in ensuring process consistency. Traditional partition structures may have leaks or residues, affecting the isolation effect between different chambers.

[0004] To address the aforementioned issues, there is an urgent need for a highly integrated and automated manufacturing equipment for Hericium erinaceus capsules, capable of continuous operation of premixing and concentration, while precisely controlling the flow of the liquid solution to improve production efficiency and product quality. Summary of the Invention

[0005] This invention proposes a manufacturing equipment and process for Hou Tou Jian Wei Ling capsules to solve the problems mentioned in the background art.

[0006] To address the aforementioned technical problems, the present invention adopts the following technical solution: a Hericium erinaceus (monkey head) stomach-strengthening capsule manufacturing equipment, comprising a support mechanism placed on the ground, the support mechanism including a base, a rotating seat rotatably mounted on the base, a concentration mechanism for concentrating Hericium erinaceus on the support mechanism, the concentration mechanism including a manufacturing tank, the manufacturing tank being divided into three chambers, namely a premixing chamber, a concentration chamber and a scraper chamber, the concentration mechanism being provided with two partitioning mechanisms for separating the three chambers inside the manufacturing tank, the partitioning mechanism including a closed frame fixedly installed inside the manufacturing tank;

[0007] The concentration mechanism includes a central shaft that is rotatably mounted inside the manufacturing tank, and the central shaft is rotatably mounted to the enclosure.

[0008] Furthermore, the support mechanism includes an angle motor fixedly installed inside the base, a motor gear fixedly installed on the motor shaft of the angle motor, and an arc-shaped rack fixedly installed on the rotating seat, the arc-shaped rack meshing with the motor gear.

[0009] Furthermore, a gas cylinder is fixedly installed inside the base, and an igniter is fixedly installed inside the rotating seat. The igniter is connected to the gas cylinder through a gas pipe.

[0010] Furthermore, the concentration mechanism includes a mixing motor fixedly mounted on the manufacturing tank, a feed hopper provided on the manufacturing tank, a central shaft fixedly mounted to the motor shaft of the mixing motor, a switch plate rotatably mounted at the end of the manufacturing tank, an outlet hole provided on the switch plate, and a discharge hole provided at the end of the manufacturing tank.

[0011] Furthermore, a premixing frame, a scraper frame, and two mixing frames are fixedly installed on the central shaft. Three premixing blades are fixedly installed on the premixing frame, two mixing blades are fixedly installed on the mixing frame, and three scrapers are fixedly installed on the scraper frame.

[0012] Furthermore, the separation mechanism includes a closed frame fixedly installed inside the manufacturing tank, two switch-closed plates rotatably mounted on a central shaft, the switch-closed plates sliding along the inner wall of the closed frame, an arc-shaped rotating rod rotatably mounted on the switch-closed plates, and a lifting block rotatably mounted on the arc-shaped rotating rod.

[0013] Furthermore, a column is fixedly installed inside the manufacturing tank, and a connecting sleeve is fixedly installed on the column. The connecting sleeve is rotatably installed with the central shaft, and a lifting block is slidably installed on the column. A column spring is provided between the lifting block and the column.

[0014] Furthermore, an opening and closing electric cylinder is fixedly installed on the manufacturing tank, and a top head is fixedly installed on the output end of the opening and closing electric cylinder. A cross frame is slidably installed inside the connecting sleeve. A long groove for the central shaft to pass through is provided on the cross frame. An opening and closing rotating rod is rotatably installed on the cross frame. The opening and closing rotating rod is rotatably installed with the lifting block, and the cross frame is in contact with the top head.

[0015] A manufacturing process for Monkey Head Stomach-Strengthening Capsules includes the following steps:

[0016] S1. Weigh out 24.5wt% wheat bran, 3.5wt% rice bran, 3.5wt% corn, 3.15wt% corn fiber, 0.35wt% gypsum, and 65wt% water, mix them to prepare a culture medium, and then culture Hericium erinaceus in the culture medium.

[0017] S2. Remove the Hericium erinaceus cultured in the culture medium from the container, freeze-dry and dry to obtain Hericium erinaceus culture;

[0018] S3. Take the Hericium erinaceus culture, crush it into fine powder, set aside 15-25wt% of the Hericium erinaceus culture fine powder, put the remaining Hericium erinaceus culture fine powder into a manufacturing tank, add 8-12 times the amount of water of Hericium erinaceus culture fine powder, and initially form a medicinal solution.

[0019] S4. The pharmaceutical solution is initially mixed in the premixing chamber of the manufacturing tank;

[0020] S5. The solution is then heated and extracted in the concentration chamber for 2-6 hours, until the relative density is 0.8-1.1;

[0021] S6. The medicine then enters the scraper chamber and is heated and concentrated to a clear paste with a relative density of 1.2-1.3;

[0022] S7. Add 15-25wt% of the prepared Hericium erinaceus culture powder to the clear extract, mix well and dry to obtain Hericium erinaceus culture clear extract.

[0023] The beneficial effects of this invention compared to the prior art are:

[0024] (1) This equipment integrates the three processes of premixing, concentration and scraper concentration into the same manufacturing tank. The automatic transfer of the liquid medicine between different chambers is achieved through the adjustable angle rotating seat and the separation mechanism, which avoids the cumbersome operation of switching multiple equipment in the traditional process, significantly shortens the production cycle and improves production efficiency.

[0025] (2) The separation mechanism set in this invention drives the manufacturing tank to rotate by an angle motor, and controls the start and stop of the separation mechanism in conjunction with the opening and closing electric cylinder, so as to realize the automation of liquid flow and chamber switching, reduce manual operation error, and improve the consistency and stability of the process;

[0026] (3) The separation mechanism of the present invention adopts the sliding cooperation of the switch sealing plate and the sealing frame to ensure effective isolation between chambers and reduce drug residue. At the same time, the overall equipment structure is compact, easy to disassemble and clean, and meets the hygiene requirements of pharmaceutical production. Attached Figure Description

[0027] Figure 1 This is a schematic diagram of the overall structure of the present invention;

[0028] Figure 2 This is a schematic diagram of the support mechanism in this invention. Figure One ;

[0029] Figure 3 This is a schematic diagram of the support mechanism in this invention. Figure Two ;

[0030] Figure 4 This is a schematic diagram of the support mechanism in this invention. Figure Three ;

[0031] Figure 5 This is a schematic diagram of the concentration mechanism in the present invention. Figure One ;

[0032] Figure 6 This is a schematic diagram of the concentration mechanism in the present invention. Figure Two ;

[0033] Figure SevenThis is a schematic diagram of the concentration mechanism in the present invention. Figure Three ;

[0034] Figure Eight This is a schematic diagram of the separation mechanism in the present invention. Figure One ;

[0035] Figure Nine This is a schematic diagram of the separation mechanism in the present invention. Figure Two ;

[0036] Figure Ten This is a schematic diagram of the separation mechanism in the present invention. Figure Three ;

[0037] Figure Eleven This is a schematic diagram of the separation mechanism in the present invention. Figure Four .

[0038] Reference numerals: 101, Base; 102, Rotating seat; 103, Gas cylinder; 104, Angle motor; 105, Motor gear; 106, Gas pipe; 107, Igniter; 108, Arc-shaped rack; 201, Manufacturing tank; 202, Mixing motor; 203, Feed hopper; 204, Central shaft; 205, Premixing frame; 206, Mixing frame; 207, Premixing blade; 208, Mixing plate; 209, Scraper frame; 210, Scraper; 211, Switch plate; 212, Outlet hole; 301, Sealing frame; 302, Opening / closing electric cylinder; 303, Top head; 304, Horizontal frame; 305, Opening / closing rotating rod; 306, Connecting sleeve; 307, Column; 308, Column spring; 309, Lifting block; 310, Arc-shaped rotating rod; 311, Switch sealing plate. Detailed Implementation

[0039] The technical solution of the present invention will be further described below with reference to the accompanying drawings and specific embodiments.

[0040] The accompanying drawings are for illustrative purposes only and are schematic diagrams, not actual images. They should not be construed as limiting the scope of this patent. To better illustrate the embodiments of the present invention, some parts in the drawings may be omitted, enlarged, or reduced, and do not represent the actual dimensions of the product. It is understandable to those skilled in the art that some well-known structures and their descriptions may be omitted in the drawings.

[0041] like Figures 1-11As shown, a monkey head stomach-strengthening capsule manufacturing equipment includes a support mechanism placed on the ground. The support mechanism includes a base 101, on which a rotating seat 102 is rotatably mounted. The support mechanism is provided with a concentration mechanism for concentrating monkey head fungus. The concentration mechanism includes a manufacturing tank 201, which is divided into three chambers: a premixing chamber, a concentration chamber, and a scraper chamber. The concentration mechanism is provided with two partitioning mechanisms for separating the three chambers inside the manufacturing tank 201. The partitioning mechanism includes a sealing frame 301 fixedly installed inside the manufacturing tank 201.

[0042] The concentration mechanism includes a central shaft 204 rotatably mounted inside the manufacturing tank 201, and the central shaft 204 is rotatably mounted to the enclosure 301.

[0043] like Figures 2-4 As shown, the support mechanism includes an angle motor 104 fixedly installed in the base 101, a motor gear 105 fixedly installed on the motor shaft of the angle motor 104, and an arc-shaped rack 108 fixedly installed on the rotating seat 102, the arc-shaped rack 108 meshing with the motor gear 105.

[0044] like Figures 2-4 As shown, a gas cylinder 103 is fixedly installed inside the base 101, and an igniter 107 is fixedly installed inside the rotating seat 102. The igniter 107 and the gas cylinder 103 are connected through a gas pipe 106.

[0045] The rotation of the angle motor 104 drives the motor gear 105 to rotate. Through the meshing of the motor gear 105 and the arc rack 108, the rotating seat 102 can be driven to rotate relative to the base 101, thereby adjusting the angle of the manufacturing tank 201, so as to facilitate the flow of the liquid medicine in the manufacturing tank 201 between the three chambers in the manufacturing tank 201.

[0046] Gas cylinder 103 contains gas, which is supplied to igniter 107 through gas pipe 106. Igniter 107 ignites and heats the gas to heat the liquid in the concentration chamber and scraper chamber of manufacturing tank 201.

[0047] like Figures 5-7 As shown, the concentration mechanism includes a mixing motor 202 fixedly installed on the manufacturing tank 201, a feed hopper 203 provided on the manufacturing tank 201, a central shaft 204 fixedly installed with the motor shaft of the mixing motor 202, a switch plate 211 rotatably installed at the end of the manufacturing tank 201, an outlet hole 212 provided on the switch plate 211, and a discharge hole provided at the end of the manufacturing tank 201.

[0048] like Figures 5-7As shown, a premixing frame 205, a scraper frame 209, and two mixing frames 206 are fixedly installed on the central shaft 204. Three premixing blades 207 are fixedly installed on the premixing frame 205, two mixing blades 208 are fixedly installed on the mixing frame 206, and three scrapers 210 are fixedly installed on the scraper frame 209.

[0049] Initially, one separating mechanism separates the premixing chamber and the concentration chamber, while another separating mechanism separates the concentration chamber from the scraper chamber. The mixing motor 202 drives the central shaft 204 to rotate, thereby rotating the premixing frame 205 and premixing blades 207, the mixing frame 206 and mixing blades 208, and the scraper frame 209 and scraper 210. The rotating seat 102 rotates to a state parallel to the horizontal plane, allowing the Hericium erinaceus culture powder to be fed from the feed hopper 203 into the premixing chamber of the manufacturing tank 201. Then, 8-12 times the amount of water is added. The liquid in the premixing chamber is mixed and stirred by the premixing blade 207 to mix the Hericium erinaceus culture with the water. The separation mechanism between the premixing chamber and the concentration chamber is then opened, and the manufacturing tank 201 and the rotating seat 102 rotate relative to the base 101, allowing the liquid in the premixing chamber to enter the concentration chamber. The separation mechanism between the premixing chamber and the concentration chamber is then closed, and the rotating seat 102 rotates to a state parallel to the horizontal plane. The liquid in the concentration chamber is stirred by the mixing plate 208, and the liquid in the concentration chamber is heated to 70°C by the igniter 107. Extraction is performed for 2-6 hours, concentrating the liquid to a relative density of 0.8-1.1. The separation mechanism between the concentration chamber and the scraper chamber is then opened, and the manufacturing tank 201 and the rotating seat 102 rotate relative to the base 101, allowing the liquid in the concentration chamber to enter the scraper chamber. The separation mechanism between the concentration chamber and the scraper chamber is then closed, and the rotating seat 102 rotates to a state parallel to the horizontal plane. The liquid in the scraper chamber is stirred by the scraper 210. Stirring is performed, and the liquid in the scraper chamber is heated to 70°C by igniter 107, concentrating it to a clear paste with a relative density of 1.2-1.3. After completion, the switch plate 211 is rotated so that the outlet hole 212 is aligned with the discharge hole at the end of the manufacturing tank 201. Then, the rotating seat 102 and the manufacturing tank 201 are rotated relative to the base 101, and the clear paste in the scraper chamber of the manufacturing tank 201 is discharged through the outlet hole 212. Then, the prepared Hericium erinaceus culture fine powder is added, mixed and dried to obtain Hericium erinaceus culture clear paste.

[0050] like Figures 8-11 As shown, the separation mechanism includes a closed frame 301 fixedly installed inside the manufacturing tank 201. Two switch-closed plates 311 are rotatably mounted on the central shaft 204. The switch-closed plates 311 slide along the inner wall of the closed frame 301. An arc-shaped rotating rod 310 is rotatably mounted on the switch-closed plates 311. A lifting block 309 is rotatably mounted on the arc-shaped rotating rod 310.

[0051] like Figures 8-11As shown, a column 307 is fixedly installed inside the manufacturing tank 201, and a connecting sleeve 306 is fixedly installed on the column 307. The connecting sleeve 306 is rotatably installed with the central shaft 204. A lifting block 309 is slidably installed on the column 307, and a column spring 308 is provided between the lifting block 309 and the column 307.

[0052] like Figures 8-11 As shown, an electric cylinder 302 is fixedly installed on the manufacturing tank 201. A top head 303 is fixedly installed on the output end of the electric cylinder 302. A cross frame 304 is slidably installed inside the connecting sleeve 306. A long groove for the central shaft 204 to pass through is provided on the cross frame 304. An opening and closing rotating rod 305 is rotatably installed on the cross frame 304. The opening and closing rotating rod 305 is rotatably installed with the lifting block 309. The cross frame 304 is in contact with the top head 303.

[0053] In the initial state, the two switch-closed plates 311 and the closing frame 301 separate the cavity. When the switch-closed plates 311 need to be opened, the opening and closing electric cylinder 302 extends, causing the top head 303 to extend. The top head 303 pushes the cross frame 304 to slide inside the connecting sleeve 306. The cross frame 304 drives the lifting block 309 to slide upward along the column 307 through the opening and closing rotating rod 305. The column spring 308 is compressed, and the lifting block 309 rises, causing the two switch-closed plates 311 to rotate relative to the central axis 204 through the arc-shaped rotating rod 310. This causes the two switch-closed plates 311 to rotate upward, opening the bottom of the closing frame 301. At this time, the liquid can flow from the premixing chamber to the concentration chamber, and from the concentration chamber to the scraper chamber. The opening and closing electric cylinders 302 of the two separating mechanisms are controlled independently.

[0054] When the separation mechanism needs to be closed, the opening and closing electric cylinder 302 retracts, the column spring 308 rebounds, and the lifting block 309 descends. The lifting block 309 drives the two switch sealing plates 311 to rotate downwards through the arc-shaped rotating rod 310, and closes again. The descent of the lifting block 309 drives the cross frame 304 to slide outwards and reset through the opening and closing rotating rod 305.

[0055] like Figures 1-11 As shown, a manufacturing process for Hou Tou Jian Wei Ling capsules includes the following steps:

[0056] S1. Weigh 24.5wt% wheat bran, 3.5wt% rice bran, 3.5wt% corn, 3.15wt% corn fiber, 0.35wt% gypsum, and 65wt% water, mix them to prepare a culture medium, and culture Hericium erinaceus in the culture medium;

[0057] S2. Remove the Hericium erinaceus cultured in the culture medium from the container, freeze-dry and dry to obtain Hericium erinaceus culture;

[0058] S3. Take the Hericium erinaceus culture, crush it into fine powder, set aside 15-25 wt% of the Hericium erinaceus culture fine powder, and put the remaining Hericium erinaceus culture fine powder into manufacturing tank 201, add water 8-12 times the amount of Hericium erinaceus culture fine powder to initially form a medicinal solution.

[0059] S4. The liquid medicine is initially mixed in the premixing chamber of manufacturing tank 201;

[0060] S5. The solution is then heated and extracted in the concentration chamber for 2-6 hours, until the relative density is 0.8-1.1;

[0061] S6. The medicine then enters the scraper chamber and is heated and concentrated to a clear paste with a relative density of 1.2-1.3;

[0062] S7. Add 15-25wt% of the prepared Hericium erinaceus culture powder to the clear extract, mix well and dry to obtain Hericium erinaceus culture clear extract.

[0063] The working principle of the monkey head stomach-strengthening capsule manufacturing equipment disclosed in this invention is as follows:

[0064] Angle motor 104 rotates, driving motor gear 105 to rotate. Motor gear 105 meshes with arc-shaped rack 108, causing rotating seat 102 to rotate relative to base 101, thereby adjusting the angle of manufacturing tank 201. This facilitates the flow of the liquid medicine within manufacturing tank 201 between its three chambers. Gas tank 103 contains gas, which is supplied to igniter 107 via gas pipe 106. Igniter 107 ignites and heats the gas, heating the liquid medicine in the concentration chamber and scraper chamber of manufacturing tank 201. Initially, a separating mechanism separates the premixing chamber and concentration chamber, and another separating mechanism separates the concentration chamber and scraper chamber. Two switch-closed plates 311 and a closing frame 301 separate the chambers. Mixing motor 202 drives the central shaft. Rotation of 204 causes the premixing frame 205 and premixing blades 207 to rotate, which in turn causes the mixing frame 206 and mixing blades 208 to rotate, and the scraper frame 209 and scraper 210 to rotate. The rotating seat 102 rotates to a state parallel to the horizontal plane, and the fine powder of Hericium erinaceus culture is put into the premixing chamber of the manufacturing tank 201 from the feed hopper 203. Then, 8-12 times the amount of water is added. The liquid in the premixing chamber is mixed and stirred by the premixing blades 207 to mix the Hericium erinaceus culture with the water. Then, the separation mechanism between the premixing chamber and the concentration chamber is opened, and the opening and closing electric cylinder 302 extends, causing the top head 303 to extend. The top head 303 pushes the cross frame 304 to slide in the connecting sleeve 306. The cross frame 304 drives the lifting block 309 along the opening and closing rotating rod 305. The column 307 slides upward, compressing the column spring 308. The lifting block 309 rises, driving the two switch-closing plates 311 to rotate relative to the central axis 204 via the arc-shaped rotating rod 310. This causes the two switch-closing plates 311 to rotate upward, opening the lower part of the sealing frame 301. Simultaneously, the manufacturing tank 201 and the rotating seat 102 rotate relative to the base 101, allowing the liquid medicine in the premixing chamber to enter the concentration chamber. Subsequently, the separation mechanism between the premixing chamber and the concentration chamber closes, the opening and closing electric cylinder 302 retracts, and the column spring 308 rebounds, driving the lifting block 309 to descend. The lifting block 309, via the arc-shaped rotating rod 310, drives the two switch-closing plates 311 to rotate downward, closing them again. The descent of the lifting block 309, via the opening and closing rotating rod 305, causes the horizontal frame 304 to slide outward and reset. The rotating seat 102 rotates to a state parallel to the horizontal plane, and the liquid medicine in the concentration chamber is stirred by the mixing plate 208. The liquid medicine in the concentration chamber is heated to 70°C by the igniter 107 and extracted for 2-6 hours to concentrate the liquid medicine to a relative density of 0.8-1.1. Then, the separation mechanism between the concentration chamber and the scraper chamber is opened, and the manufacturing tank 201 and the rotating seat 102 rotate relative to the base 101. The liquid medicine in the concentration chamber enters the scraper chamber. Then, the separation mechanism between the concentration chamber and the scraper chamber is closed, and the rotating seat 102 rotates to a state parallel to the horizontal plane. The liquid medicine in the scraper chamber is stirred by the scraper 210 and heated to 70°C by the igniter 107 to concentrate the liquid medicine to a relative density of 1.2-1.After the paste is cleared (step 3), rotate switch plate 211 to align outlet hole 212 with discharge hole at the end of manufacturing tank 201. Then, rotate base 102 and manufacturing tank 201 relative to base 101 to discharge the clear paste from scraper cavity of manufacturing tank 201 through outlet hole 212. Then, add prepared Hericium erinaceus culture powder, mix well, and dry to obtain Hericium erinaceus culture clear paste.

[0065] This invention is not limited to the specific embodiments described above. Any modifications made by those skilled in the art based on the above concept without creative effort are within the protection scope of this invention.

Claims

1. A manufacturing device for monkey head stomach-strengthening capsules, comprising a support mechanism placed on the ground, characterized in that: The support mechanism includes a base (101), on which a rotating seat (102) is rotatably mounted. The support mechanism is provided with a concentration mechanism for concentrating Hericium erinaceus. The concentration mechanism includes a manufacturing tank (201). The manufacturing tank (201) is divided into three chambers, namely a premixing chamber, a concentration chamber, and a scraper chamber. The concentration mechanism is provided with two partitioning mechanisms for separating the three chambers inside the manufacturing tank (201). The partitioning mechanism includes a closed frame (301) fixedly installed inside the manufacturing tank (201). The concentration mechanism includes a central shaft (204) rotatably mounted inside the manufacturing tank (201), and the central shaft (204) is rotatably mounted to the enclosure (301); The separation mechanism includes a closed frame (301) fixedly installed inside the manufacturing tank (201), two switch-closed plates (311) rotatably mounted on a central shaft (204), the switch-closed plates (311) sliding along the inner wall of the closed frame (301), an arc-shaped rotating rod (310) rotatably mounted on the switch-closed plate (311), and a lifting block (309) rotatably mounted on the arc-shaped rotating rod (310). The support mechanism includes an angle motor (104) fixedly installed in the base (101), a motor gear (105) fixedly installed on the motor shaft of the angle motor (104), and an arc rack (108) fixedly installed on the rotating seat (102), the arc rack (108) meshing with the motor gear (105); The angle motor (104) rotates to drive the motor gear (105) to rotate. Through the meshing of the motor gear (105) and the arc rack (108), the rotating seat (102) can be driven to rotate relative to the base (101), thereby adjusting the angle of the manufacturing tank (201) so that the liquid medicine in the manufacturing tank (201) can flow between the three chambers in the manufacturing tank (201).

2. The equipment for manufacturing monkey head stomach-strengthening capsules according to claim 1, characterized in that: A gas cylinder (103) is fixedly installed inside the base (101), and an igniter (107) is fixedly installed inside the rotating seat (102). The igniter (107) and the gas cylinder (103) are connected through a gas pipe (106).

3. The equipment for manufacturing monkey head stomach-strengthening capsules according to claim 1, characterized in that: The concentration mechanism includes a mixing motor (202) fixedly installed on the manufacturing tank (201), a feed hopper (203) provided on the manufacturing tank (201), a central shaft (204) fixedly installed with the motor shaft of the mixing motor (202), a switch plate (211) rotatably installed at the end of the manufacturing tank (201), an outlet hole (212) provided on the switch plate (211), and a discharge hole provided at the end of the manufacturing tank (201).

4. The equipment for manufacturing monkey head stomach-strengthening capsules according to claim 3, characterized in that: A premixing frame (205), a scraper frame (209) and two mixing frames (206) are fixedly installed on the central shaft (204). Three premixing blades (207) are fixedly installed on the premixing frame (205), two mixing blades (208) are fixedly installed on the mixing frame (206), and three scrapers (210) are fixedly installed on the scraper frame (209).

5. The equipment for manufacturing monkey head stomach-strengthening capsules according to claim 1, characterized in that: A column (307) is fixedly installed inside the manufacturing tank (201). A connecting sleeve (306) is fixedly installed on the column (307). The connecting sleeve (306) is rotatably installed with the central shaft (204). A lifting block (309) is slidably installed on the column (307). A column spring (308) is provided between the lifting block (309) and the column (307).

6. The equipment for manufacturing monkey head stomach-strengthening capsules according to claim 5, characterized in that: An electric cylinder (302) is fixedly installed on the manufacturing tank (201). A top head (303) is fixedly installed on the output end of the electric cylinder (302). A cross frame (304) is slidably installed inside the connecting sleeve (306). A long groove for the central shaft (204) to pass through is provided on the cross frame (304). An opening and closing rotating rod (305) is rotatably installed on the cross frame (304). The opening and closing rotating rod (305) is rotatably installed with the lifting block (309). The cross frame (304) is in contact with the top head (303).

7. A manufacturing process for Hou Tou Jian Wei Ling capsules, using the Hou Tou Jian Wei Ling capsule manufacturing equipment as described in claim 1, characterized in that, Includes the following steps: S1. Weigh 24.5wt% wheat bran, 3.5wt% rice bran, 3.5wt% corn, 3.15wt% corn fiber, 0.35wt% gypsum, and 65wt% water, mix them to prepare a culture medium, and culture Hericium erinaceus in the culture medium; S2. Remove the Hericium erinaceus cultured in the culture medium from the container, freeze-dry and dry to obtain Hericium erinaceus culture; S3. Take the Hericium erinaceus culture, crush it into fine powder, set aside 15-25wt% of the Hericium erinaceus culture fine powder, and put the remaining Hericium erinaceus culture fine powder into the manufacturing tank (201), add water 8-12 times the amount of Hericium erinaceus culture fine powder to initially form a medicinal solution; S4. The drug solution is initially mixed in the premixing chamber of the manufacturing tank (201); S5. The solution is then heated and extracted in the concentration chamber for 2-6 hours, until the relative density is 0.8-1.1; S6. The medicine then enters the scraper chamber and is heated and concentrated to a clear paste with a relative density of 1.2-1.3; S7. Add 15-25wt% of the prepared Hericium erinaceus culture powder to the clear extract, mix well and dry to obtain Hericium erinaceus culture clear extract.

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