Infusion preparation for dialysis patient
A technology for patients and uses, applied in blood diseases, drug delivery, extracellular fluid diseases, etc., to achieve the effect of reducing the dosage and frequency of occurrence
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Embodiment 1
[0090] Embodiment 1: Preparation of anti-anemia preparation (amino acid infusion)
[0091] The ingredients shown in the following Table 1 were dissolved in water for injection according to the amounts shown in the table. The solution was sterile filtered and placed in a glass bottle. The bottle was sealed and autoclaved to prepare an anti-anemia preparation (amino acid infusion).
[0092] The pH value of the preparation is 6.6-7.6, and the osmotic pressure ratio is about 2.
[0093] Table 1:
[0094] Element
[0095] The amino acid infusion prepared according to Example 1 is also used as the following purposes: a pharmaceutical preparation for reducing the dosage of erythropoietin (second aspect of the present invention), a pharmaceutical preparation for controlling serum phosphorus levels (third aspect of the present invention) and Pharmaceutical preparations for inhibiting protein catabolism (fourth aspect of the invention).
Embodiment 2
[0096] Example 2. Determination of the ability of pharmaceutical preparations to improve anemia and reduce the dosage of erythropoietin
[0097] Exemplary anti-anemia preparation of the present invention was administered to 18 chronic renal failure patients receiving hemodialysis (HD: 9 cases) or hemodiafiltration (HFD: 9 cases) to examine that the preparation improves anemia and reduces erythropoietin administration Quantitative capacity.
[0098] [method]
[0099] A commercially available amino acid infusion solution "NEOAMYU (registered trademark)" (200 mL formulation, Ajinomoto Pharma Co., Ltd.) prepared according to Example 1 was used.
[0100] In the week before the administration period, the necessary diagnosis, examination and detection were carried out on the first dialysis day (week 1 or week 2). The "NEOAMYU" preparation was continuously administered from 1 week after the diagnosis to 12 weeks and 1 day (the 37th dialysis). Specifically, 1 vial (200 mL) of the pr...
Embodiment 3
[0107] Example 3: Determination of the ability of the above pharmaceutical formulations to control serum phosphorus levels
[0108] The exemplary serum phosphorus control preparation of the present invention was administered to 8 chronic renal failure patients receiving hemodialysis (HD) to examine changes in serum phosphorus levels.
[0109] [method]
[0110] The commercially available amino acid infusion solution "NEOAMYU" (200 mL formulation, Ajinomoto Pharma Co., Ltd.) prepared according to Example 1 was used.
[0111] In the week before the administration period, the necessary diagnosis, examination and detection were carried out on the first dialysis day (week 1 or week 2). The "NEOAMYU" preparation was continuously administered from 1 week after the diagnosis to 12 weeks and 1 day (the 37th dialysis). Specifically, 1 vial (200 mL) of the preparation was infused into the venous side of the dialysis circuit each time of dialysis. The formulation was infused throughout ...
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