Method for detecting content of amino acids and glycyl glutamine in compound amino acid (15) dipeptide (2) injection solution
A technology of glycylglutamine and compound amino acid, which is applied to measurement devices, instruments, scientific instruments and other directions, can solve the problems of inability to detect amino acid content at the same time, difficult quantitative analysis, complicated detection methods, etc. Short analysis time and high feasibility
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Embodiment 1
[0022] 1. Measurement conditions
[0023] Instrument: S-433D amino acid analyzer from Sykam, Germany.
[0024] Chromatographic column: using cation exchange column LCAK06 / Na (4.6×150mm) sulfonic acid strong acid cation exchange resin
[0025] 2. Assay
[0026] S1. Preparation of mobile phase buffer, regeneration solution and derivatization reagents
[0027] A. The preparation of mobile phase buffer A is: 11.8g of trisodium citrate dihydrate, 6.0g of citric acid, 65ml of ethanol, 5.6ml of 37% hydrochloric acid, 0.1ml of octanoic acid are put in a 1000ml measuring bottle, and the volume is adjusted to the scale with water , adjust the pH to 2-4;
[0028]B. The preparation of mobile phase buffer B is: 19.6g of trisodium citrate dihydrate, 3.1g of sodium hydroxide, 5.0g of boric acid, and 0.1ml of octanoic acid are placed in a 1000ml measuring bottle, add water to the mark, and adjust the pH to 10~ 11;
[0029] C. The preparation of the regeneration solution is: put 20g of so...
Embodiment 2
[0046] Example 2: Amino Acid and Glycylglutamine Localization
[0047] 1. Experimental method
[0048] Weigh the reference substances aspartic acid 12.52mg, threonine 12.05mg, serine 12.45mg, glutamic acid 11.98mg, proline 12.02mg, alanine 12.07mg, valine 11.88mg, glycyl glutamic acid Aminoamide (GQ) 12.65mg, Methionine 12.05mg, Isoleucine 12.36mg, Leucine 12.22mg, Phenylalanine 12.56mg, Histidine 11.78mg, Lysine Acetate 12.05mg, Arginine Put 12.44mg of acid in 50ml volumetric flasks, add sample diluent to dissolve and dilute to the mark, and shake well. According to the determination conditions of Example 1, sample analysis was carried out.
[0049] 2. Experimental results
[0050] The peak sequence and retention time of amino acids are shown in Table 4.
[0051] Table 4: Amino Acid Assay Methodology - Amino Acid Mapping
[0052] Peak order
Embodiment 3
[0053] Embodiment 3: blank interference test
[0054] 1. Experimental method
[0055] Preparation of the blank solution: prepare according to the prescription amount (without the above 14 kinds of amino acids and glycylglutamine), prepare samples according to the preparation method of the test solution in Example 2, and get ready.
[0056] The sample diluent, blank solution, and reference solution were respectively taken for injection analysis according to the above analysis conditions.
[0057] 2. Experimental results
[0058] The results showed that the blank solution and the sample diluent did not produce peaks at various amino acid positions in the reference solution, and did not interfere with its determination, and the separation of various amino acid peaks in the reference solution met the requirements.
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