Thin layer detection method for quickly identifying honeysuckle and mountain honeysuckle
A technology of thin-layer detection and honeysuckle, which is applied in the field of plant identification, can solve the problems of long time, high cost, and low reliability, and achieve the effect of simple method, obvious contrast, and strong specificity
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Embodiment 1
[0075] A thin-layer detection method for rapidly distinguishing honeysuckle and mountain silver flower, comprising the following steps:
[0076] 1) Prepare reference substance solution and sample solution
[0077] 1.1) Take an appropriate amount of chlorogenic acid, luteolin, honeysuckle saponin B and Dipsacus saponin B, dissolve in methanol to make a reference solution with a concentration of 1 mg / ml, and number them in sequence as No. 1, No. 2, No. 3, No. 4.
[0078] 1.2) Take appropriate amount of honeysuckle (including honeysuckle reference medicinal material and honeysuckle test sample) and mountain silver flower (including mountain silver flower control medicinal material and mountain silver flower test sample), crush them and pass through an 80-mesh sieve, and place them in a Daisy triangular flask Among them, there are four groups, and they are numbered: No. 5 is honeysuckle control medicinal material, No. 6 is mountain silver flower control medicinal material, No. 7 ...
Embodiment 2
[0098] The difference with Embodiment 1 is:
[0099] 1.1) Take appropriate amount of chlorogenic acid, luteolin, Lonicerae saponin B and Dipsapacea saponin B respectively, and dissolve them in methanol to make a 0.8 mg / ml reference solution;
[0100] In step 1.3), add respectively to the four groups of Erlenmeyer flasks in Step 1.2) the amount of 8 times the amount of the sample in the bottle, and the mass concentration is 70% ethanol, and perform ultrasonic treatment for 45 minutes, take out the Erlenmeyer flask and put it at room temperature;
[0101] In step 2), the distance between the origin of sample application and the lower edge of the silica gel G thin-layer plate is 1.5cm;
[0102] In step 3), the specification of the double-slot expanded steel is 10×20cm; and the developing agent is presaturated in the expanding cylinder for 20 minutes;
[0103] In step 4), when the leading edge of the developing agent goes up to the edge of the silica gel G thin-layer plate and is...
Embodiment 3
[0107] The difference with Embodiment 1 is:
[0108] 1.1) Take an appropriate amount of chlorogenic acid, luteolin, Lonicerae saponin B and Dipsacus saponin B respectively, and dissolve them in methanol to make a 2 mg / ml reference solution;
[0109] In step 1.3), add ethanol with 10 times the sample mass and a mass concentration of 95% to the four groups of conical flasks in step 1.2), perform ultrasonic treatment for 30 minutes, take out the conical flask and place it at room temperature;
[0110] In step 2), the distance between the origin of sample application and the lower edge of the silica gel G thin-layer plate is 1.2cm;
[0111] In step 4), when the leading edge of the developing agent goes up to the edge of the silica gel G thin-layer plate and is 15 cm away from the origin of sample application, take out the silica gel G thin-layer plate;
[0112] In step 5.1), after spraying with a natural color developer, place it on an electric heating plate, heat it at 105°C for...
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