Friday, May 27, 2022

Intelligent hydroponic machine m0.8s

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Conflicts of Interest

The authors have declared no conflict of interests.

2. Materials and Methods

Data Availability

The data used to support the findings of this study are available from the corresponding author upon request.

2.3. High-Performance Liquid Chromatography (HPLC) Determination

Take 2.0 g of medicinal powder (passing through 100-mesh sieve) and accurately weigh it. Put it into a 150 ml Soxhlet extractor, add 40 ml methanol, soak it overnight (12 h), add 20 ml methanol, and heat and reflux at 85°C for 4 h. The solvent was recovered and concentrated to dryness. The residue was dissolved with 10 ml water and shaken with water-saturated n-butanol for 4 times, 40 ml each time. Wash thoroughly with ammonia test solution for 2 times, 40 ml each time. Discard ammonia solution, and evaporate with n-butanol solution. The residue was dissolved with 5 ml water and cooled down. The residue was washed off with 50 ml water and then eluted with 30 ml 40% ethanol. The eluent was continued to be eluted with 80 ml 70% ethanol. The eluate was collected and evaporated to dryness. The residue was dissolved in methanol and transferred to 5 ml volumetric flask; add methanol to volume to the scale, shake well, filter with 0.45 μm microporous membrane, and set aside.

For the chromatographic column, Agilent Zorbax sb-c18 column () was used. The mobile phase was acetonitrile water (32 : 68); the flow rate was 1.0 ml·min-1; the column temperature was 27°C; the ELSD parameters are as follows: evaporator temperature: 112°C, nebulizer temperature: 85°C, gas flow rate: 1.5 SLM, data rate: 80 Hz, led intensity: 100%, smoothing: 50 (5.0 seconds), and PMT gain: 10.0; the theoretical number of astragaloside IV was not less than 4 μl, 10 μl, 20 μl, and 10 μl of the reference solution, and the test solution was, respectively, injected into the liquid chromatograph. The determination was carried out according to the above chromatographic conditions, and the HPLC liquid chromatograms were recorded.

2.1. A. membranaceus Cultivation Conditions

Seeds of A. membranaceus were collected in Chifeng City, Inner Mongolia, China, and then, seeds were sown in nutrient soils (vermiculite and nutrient soil ratio was 1 : 3). The seeds were planted with sufficient water. Then, the seedlings were cultured under 16 h light/8 h darkness and 25°C for 30 days. Watered every two days. Then, the one-month plants were cultivated in a hydroponic device. The root of these plants was harvested in one, two, and four weeks, respectively.

For Field conditions, the seeds of A. membranaceus were planted directly in the field, and the plants grew for one and two years in Hohhot, Baotou, and Chifeng, Inner Mongolia. The root of A. membranaceus in the field was harvested with four-week hydroponic plants. Collect these roots, dry them in an oven at 45°C, weigh, and count 10 roots. These roots were used in HPLC.

3.2. The Biomass and Astragaloside IV Contents between Hydroponic Culture and Cultivation

In order to further study whether the selected cultivation has the representativeness of astragaloside IV content in the root of A. membranaceus in Inner Mongolia, three different production areas cultivation were selected for comparison. The results show that the content of astragaloside IV in hydroponic root is significantly higher than that in other areas (Figure 2(a)). At the same time, in order to understand the biomass difference between hydroponics and cultivation, their biomass was statistically analyzed. The results showed that there was significant difference between hydroponic culture, annual cultivation, and biennial cultivation (Figure 2(b)). Therefore, A. membranaceus used in this study is universal. The nutrient solution is changed every 2 weeks in the intelligent hydroponic device which can be grown continuously for 2 months of A. membranaceus.

2.2. Structure of Designed Hydroponic Device

The intelligent hydroponic device is designed according to the needs of A. membranaceus growth. It has hydroponic tank, support seat, and support leg, which are bolted with each other; the surface of the support leg is bolted with a water pump. The water outlet end of the water pump is connected with a water injection pipe and a water extraction pipe. The water extraction pipe far away from the end of the water pump is connected with a three-way water valve. The water inlet ends at the top and bottom of the right side of the three-way water valve are, respectively, connected with a nutrition pipe and a water supply pipe. The water supply pipe away from the three-way water valve is connected with a special water pipe. Both sides of the top of the hydroponic tank are bolted with a support plate. The gap inside the support frame is penetrated with a moisture discharge pipe which is connected with a moisture discharge cover. The inner part of the fixing frame is bolted with a moisture exhaust fan. The pump operates 24 hours every work day, at 25°C, humidity 30%; the cultivate medium was modified Hoagland nutrient solution (Table 1).

MacroelementsFinal concentration (mM)Stock solution concentration (mM)
KNO351000
Ca(NO3)2·4H2O51000
MgSO4·7H2O2400
KH2PO41200
MicroelementFinal concentration (μM)Stock solution concentration (mM)
H3BO346.146.1
MnCl2·4H2O9.19.1
ZnSO4·7H2O0.760.76
CuSO4·5H2O0.320.32
Na2MoO4·2H2O0.240.24
Fe2+Final concentration (μM)
EDTA-Fe-Na50

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