Administration method and administration device for experimental animal brain

A technology for experimental animals and drug delivery devices, applied in the field of medicine, can solve the problems of death of experimental animals, affecting experimental results, and increasing damage, and achieves the effects of avoiding influence, convenient injection, and strong practicability.

Inactive Publication Date: 2015-01-14
SHENYANG PHARMA UNIVERSITY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, many problems are also encountered in the application of the intracerebroventricular injection method. For example, in the process of some drug screening, multiple administrations are required. Due to the fact that physical damage is easily caused during the administration of the brain, the experimental animals are caused by multiple injections. If the damage increases, it may affect the experimental results, and in severe cases, it will cause the death of the experimental animals.

Method used

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  • Administration method and administration device for experimental animal brain
  • Administration method and administration device for experimental animal brain
  • Administration method and administration device for experimental animal brain

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0024] Experimental materials: Take 20 Alzheimer's mice (AD mice) that have been successfully modeled, weighing 30-35g. in

[0025] 10 rats were used for hippocampus injection of donepezil; 10 rats were used for blank experiment (injection of normal saline). Donepezil was produced by Dalian Meilun Biopharmaceutical Co., Ltd., and normal saline was produced by Jilin Dubang Pharmaceutical Co., Ltd.

[0026] drug delivery device see figure 1 , including a drug delivery catheter 1, which is a stainless steel catheter with a length of 12 mm cut from a No. 12 scalp needle. A collar 2 that can be fixed on the catheter, the position of the collar on the catheter is shown in 3, and the height on the catheter is 5mm.

[0027] Steps: 1. Anesthetize the experimental mouse with 30% chloral hydrate, fix it on the mouse brain locator, and determine the position of the hippocampus.

[0028] 2. Obtain the positioning coordinates of the embedding tube according to the above steps, a...

Embodiment 2

[0033] In this embodiment, the difference from Example 1 is only: the drug injected into the mice of the administration group is 2 μl of a solution of 2 mg / ml huperzine A, administered continuously for 5 days, and injected with the huperzine A solution by this method to achieve Anti-senile dementia effect.

Embodiment 3

[0035] The difference from Example 1 in this example is only: the medicine injected into the mouse ventricle of the administration group is 2 μ l of Edaravone solution of 3 mg / ml, administered continuously for 5 days, and the Edaravone solution is injected by this method to achieve Sedative-hypnotic effect.

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Abstract

The invention discloses an administration method for an experimental animal brain; by adopting a method for burying a catheter into the experimental animal brain, injection to the experimental animal brain is more convenient. According to the administration method, a special successive administration device is adopted, and a mouse or a rat is taken as an experimental animal, and the administration method comprises the following steps: 1, narcotizing the experimental animal with 30 percent of chloral hydrate, fixing the experimental animal on a mouse brain locator, and determining the position of a paracele; 2, burying an administration catheter into the paracele of the experimental animal according to the step, and fixing the catheter to the head of the experimental animal by dental cement when cerebrospinal fluid overflows from the catheter; 3, in 4 days after the catheter is buried successfully, performing successive intramuscular injection every day with 0.2ml of 0.8 million units of penicillin sodium, and diminishing inflammation of the experimental animal; 4, performing administration: sucking up a right amount of to-be-experimented drug solution by a 10mul microinjector, and partially inserting the syringe needle of a microsyringe into the catheter buried into the experimental animal brain, wherein the insertion depth is 0.5-2.0cm, and successive administration can be performed on the mice brain from the catheter.

Description

technical field [0001] The invention belongs to the technical field of medicine, relates to a method for administering medicine to mice and rats, and relates to a method and a device for administering medicine to the brain of experimental animals. [0002] and drug delivery devices. Background technique [0003] In the process of modern drug research and development, drug activity screening is one of the important links. The existing drug activity screening mostly adopts in vitro screening method and in vivo screening method. Among them, the in vivo screening method can more directly reflect the effect of the drug in the in vivo environment, and this method plays an important role in the drug screening process. [0004] The use of in vivo drug screening methods must first establish a suitable animal model, and secondly requires a suitable drug delivery method. Drug researchers have established many effective animal models in various ways, such as hypertension models, senil...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A61D7/00A61K31/43
CPCA61D7/00A01K2267/0393A61D7/04
Inventor 贾英赵旭毛歆许璇吴博毕开顺
Owner SHENYANG PHARMA UNIVERSITY
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