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Compound formula mannitol injection liquid

A technology of mannitol and injection, which is applied in the formulation field of compound mannitol injection, can solve problems such as easy crystallization and precipitation, and achieve the effects of reducing crystallization and precipitation, reducing infusion reactions, and convenient clinical use

Inactive Publication Date: 2006-08-30
夏运岳
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] The invention provides a medical compound mannitol injection, which aims to replace the existing medical mannitol injection, so as to solve the problem that the current mannitol injection is easy to crystallize and precipitate in a low temperature environment (when the room temperature is low), which leads to infusion reactions. and other adverse consequences, providing convenience for clinical use

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0025] (1), formula

[0026] Mannitol 10% by weight;

[0027] Sorbitol 12.5% ​​by weight;

[0028] The balance of water for injection.

[0029] (2), preparation method

[0030] According to the conventional mannitol production method. The conventional mannitol production method refers to the production method of 20% mannitol injection described in the prior art.

Embodiment 2

[0032] (1), formula

[0033] Mannitol 15% by weight;

[0034] Sorbitol 6.25% by weight;

[0035] The balance of water for injection.

[0036] (2), preparation method

[0037] According to the conventional mannitol production method. The conventional mannitol production method refers to the production method of 20% mannitol injection described in the prior art.

Embodiment 3

[0039] (1), formula

[0040] Mannitol 16% by weight;

[0041] Sorbitol 5% by weight;

[0042] The balance of water for injection.

[0043] (2), preparation method

[0044] According to the conventional mannitol production method, the conventional mannitol production method refers to the production method of 20% mannitol injection described in the prior art.

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PUM

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Abstract

A compound mannitol injection without crystal eduction is prepared from mannitol (5-18 Wt%), sorbitol (2-20), and the water for injection (rest).

Description

technical field [0001] The invention relates to the field of medical drugs, in particular to a formula of compound mannitol injection. This formula contains both Mannitol and Sorbitol. The compound mannitol injection has no crystallization at low room temperature, solves the crystallization problem of the mannitol injection, and is an ideal mannitol preparation with convenient clinical use and few adverse reactions. Background technique [0002] 20% Mannitol Injection is widely used in clinical neurosurgery as an agent to reduce intracranial pressure and free radical scavenger. At present, mannitol is the first choice for the treatment of cerebral edema and lowering intracranial pressure. It has a significant effect in reducing intracranial pressure, and there is no obvious "rebound phenomenon". Since the 20% mannitol solution is a supersaturated solution, during clinical use, the crystallization of mannitol injection has brought great inconvenience to clinical use. In us...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A61K31/047A61K9/08A61P7/10A61P43/00
Inventor 夏运岳
Owner 夏运岳
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