CN114304053A - Construction method of rabbit aneurysm model - Google Patents

Construction method of rabbit aneurysm model Download PDF

Info

Publication number
CN114304053A
CN114304053A CN202111510794.2A CN202111510794A CN114304053A CN 114304053 A CN114304053 A CN 114304053A CN 202111510794 A CN202111510794 A CN 202111510794A CN 114304053 A CN114304053 A CN 114304053A
Authority
CN
China
Prior art keywords
rabbit
aneurysm
artery
closed cavity
model
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN202111510794.2A
Other languages
Chinese (zh)
Inventor
汪鹏丽
李扬
李朝辉
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Guangdong Jinshi Medical Technology Service Co ltd
Original Assignee
Guangdong Jinshi Medical Technology Service Co ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Guangdong Jinshi Medical Technology Service Co ltd filed Critical Guangdong Jinshi Medical Technology Service Co ltd
Priority to CN202111510794.2A priority Critical patent/CN114304053A/en
Publication of CN114304053A publication Critical patent/CN114304053A/en
Pending legal-status Critical Current

Links

Images

Landscapes

  • Investigating Or Analysing Biological Materials (AREA)

Abstract

The invention discloses a construction method of a rabbit aneurysm model, which comprises the following steps: s1: n different rabbit aneurysm model building methods are selected to build N groups of rabbit aneurysm models, wherein N is an integer greater than or equal to 2, and each model building method corresponds to one group of rabbit aneurysm models; s2: measuring the N groups of rabbit aneurysm models obtained in the step S1 by adopting DSA equipment to obtain the short diameter of the rabbit aneurysm bodies of each group; s3: and D, performing comparative analysis on the N groups of rabbit aneurysm body short diameter data obtained in the step S2, and selecting a construction method corresponding to the rabbit aneurysm model with the largest tumor body short diameter to obtain the rabbit aneurysm. The method for constructing the aneurysm model has the advantages of high success rate, convenience in research and the like.

Description

Construction method of rabbit aneurysm model
Technical Field
The invention relates to the field of animal tumor models, in particular to a construction method of a rabbit aneurysm model.
Background
Aneurysm is a manifestation of localized or diffuse expansion or bulging of an artery wall due to lesion or injury of the artery wall, mainly manifested by a swelling or pulsating mass, and serious patients may suffer from arterial embolism, organ ischemia or necrosis, etc., thereby causing serious damage to human bodies. Since human aneurysms are found in a substantially advanced stage, it is difficult to deeply study the mechanism of aneurysm formation and treatment. Therefore, establishing a feasible aneurysm model with good repeatability is a precondition for research on aneurysm pathology, treatment method and the like. For this reason, a series of studies have been conducted, but how to obtain an effective and easy-to-study aneurysm model remains to be studied.
Disclosure of Invention
The invention aims to overcome the defects in the prior art and provide a construction method for effectively obtaining a rabbit aneurysm model with high success rate and convenient research.
In order to achieve the purpose, the invention adopts the following technical scheme:
a construction method of a rabbit aneurysm model comprises the following steps:
s1: n different rabbit aneurysm model building methods are selected to build N groups of rabbit aneurysm models, wherein N is an integer greater than or equal to 2, and each model building method corresponds to one group of rabbit aneurysm models;
s2: measuring the N groups of rabbit aneurysm models obtained in the step S1 by adopting DSA equipment to obtain short diameter data of rabbit aneurysm bodies of each group (as the whole aneurysm body is in an ellipsoid shape, the long diameter and the short diameter exist, and the short diameter data are obtained in the invention);
s3: and D, performing comparative analysis on the N groups of rabbit aneurysm body short diameter data obtained in the step S2, and selecting a construction method corresponding to the rabbit aneurysm model with the largest tumor body short diameter to obtain the rabbit aneurysm.
In the present invention, a further preferred embodiment is that the rabbit aneurysm model establishing method includes the following steps: constructing a closed sac at the root of the right common carotid artery of the rabbit, injecting an aneurysm inducer into the sac, cleaning the aneurysm inducer in the sac of the rabbit arterial artery after 20-30min, and then recovering the smoothness of the rabbit artery to obtain the rabbit aneurysm model.
In a more preferred embodiment of the present invention, the aneurysm-inducing agent is one or a combination of two or more of elastase, papain, calcium chloride, and collagenase.
In the present invention, a further preferred scheme is that the specific steps of constructing the closed capsule cavity are as follows: clamping or tightening two ends of one section of the middle part of the rabbit artery to form a rabbit artery closed cavity, pumping blood in the rabbit artery closed cavity, and cleaning the blood in the rabbit artery closed cavity by using normal saline containing heparin sodium to obtain the closed sac cavity.
In the present invention, it is further preferable that the rabbit aneurysm model is a rabbit carotid aneurysm model.
In the present invention, it is further preferable that the number of effective rabbit aneurysm models in each group in step S1 is at least 2, and the short diameter data of rabbit aneurysm body of each group in step S2 is an average of the short diameter data of effective rabbit aneurysm models of each group; the effective rabbit aneurysm model is a model of aneurysm.
In the present invention, a further preferred scheme is that, in step S1, 3 different rabbit aneurysm model establishment methods are selected to construct 3 groups of rabbit aneurysm models, wherein:
the method for establishing the first group of rabbit aneurysm models specifically comprises the following steps: constructing a rabbit artery closed cavity of 1.9-2.1cm at the root of the right carotid artery of the rabbit, cleaning the closed cavity by using normal saline containing heparin sodium until no blood residue exists, injecting 0.1ml of elastase solution containing 70U into the rabbit artery closed cavity, keeping the peripheral tissues of the rabbit carotid artery moist by using the normal saline, further ligating the far end of the carotid artery after 20-30min, recovering the artery to be smooth, and feeding for more than 28 days (the invention contains the original number), thus obtaining the rabbit arterial closed cavity;
the method for establishing the second group of rabbit aneurysm models comprises the following steps: constructing a rabbit artery closed cavity of 1.9-2.1cm at the root of the right carotid artery of a rabbit, cleaning the closed cavity by normal saline containing heparin sodium until no blood residue exists, injecting 0.1ml of elastase solution containing 200U into the rabbit artery closed cavity, keeping the closed cavity in an inflated state, keeping the peripheral tissues of the rabbit carotid artery moist by normal saline, further ligating the distal end of the carotid artery after 20-30min, recovering the artery unobstructed, and feeding for more than 28 days to obtain the rabbit arterial closed cavity;
the method for establishing the third group of rabbit aneurysm models comprises the following specific steps: constructing a rabbit artery closed cavity of 1.9-2.1cm at the root of the right carotid artery of a rabbit, cleaning the closed cavity by normal saline containing heparin sodium until no blood remains, injecting 0.1ml of elastase solution containing 200U into the rabbit artery closed cavity, keeping the closed cavity in an inflated state, keeping the peripheral tissues of the rabbit carotid artery moist by normal saline, further ligating the distal end of the carotid artery after 20-30min, recovering the smoothness of the artery, feeding for more than 28 days, and feeding the animal with double antibodies every day during feeding to obtain the rabbit.
In the present invention, it is further preferable that the rabbit aneurysm model building method in step S1 is implemented by using one or a combination of two or more of an elastase induction method, a papain induction method, a calcium chloride induction method, an elastase + collagenase induction method, and an adenovirus induction method.
In the present invention, it is further preferable that the time for measuring the tumor body minor diameter of the rabbit aneurysm model using the DSA apparatus in step S2 is 28 days or more after the rabbit aneurysm model is established in step S1.
Compared with the prior art, the invention has the following beneficial effects:
1) different rabbit aneurysm models are established by selecting different aneurysm model establishing methods, then DSA image measurement is carried out, comparison is carried out, and the establishing method corresponding to the rabbit aneurysm model with the largest tumor body minor diameter is screened out, so that the rabbit aneurysm model with high success rate, good aneurysm forming effect and convenience in research can be obtained, and the subsequent research on the aneurysm can be better guided;
2) through analysis, a model construction method for optimizing the concentration of elastase is determined, the intima of the blood vessel is fully destroyed, and the success rate of forming aneurysm is improved;
3) through analysis, a model construction method of the continuous feeding double antibody is screened out, thrombosis at the distal end of the aneurysm is reduced, the possibility of self-occlusion of the aneurysm is reduced, and therefore the aneurysm model is obtained.
Drawings
FIG. 1 is an angiogram of a rabbit aneurysm model obtained by DSA device testing according to the first rabbit aneurysm model building method in example 1;
FIG. 2 is a angiogram obtained by DSA equipment testing of a rabbit aneurysm model obtained by the first rabbit aneurysm model establishing method in example 1;
FIG. 3 is an angiogram obtained by DSA equipment testing of a rabbit aneurysm model obtained by the establishing method of the second group of rabbit aneurysm models in embodiment 1;
FIG. 4 is a angiogram obtained by DSA equipment testing of a rabbit aneurysm model obtained by the establishing method of the second group of rabbit aneurysm models in embodiment 1;
FIG. 5 is a angiogram obtained by DSA equipment testing of a rabbit aneurysm model obtained by the method for establishing a third group of rabbit aneurysm models in example 1;
fig. 6 is an angiogram obtained by DSA device test of a rabbit aneurysm model obtained by the method for establishing a rabbit aneurysm model of the third group in example 1.
Detailed Description
The present invention is further described below with reference to the following detailed description and the accompanying drawings, and it should be noted that, in the present invention, various embodiments or technical features described below may be arbitrarily combined to form a new embodiment without conflict. Except as specifically noted, the materials and equipment used in this example are commercially available. The specific embodiments are merely illustrative and are not to be construed as limiting the scope of the invention.
A construction method of a rabbit aneurysm model comprises the following steps:
s1: n different rabbit aneurysm model building methods are selected to build N groups of rabbit aneurysm models, wherein N is an integer greater than or equal to 2, and each model building method corresponds to one group of rabbit aneurysm models;
s2: measuring the N groups of rabbit aneurysm models obtained in the step S1 by adopting DSA equipment to obtain short diameter data of rabbit aneurysm bodies of each group (as the whole aneurysm body is in an ellipsoid shape, the long diameter and the short diameter exist, and the short diameter data are obtained in the invention);
s3: and D, performing comparative analysis on the N groups of rabbit aneurysm body short diameter data obtained in the step S2, and selecting a construction method corresponding to the rabbit aneurysm model with the largest tumor body short diameter to obtain the rabbit aneurysm.
Different rabbit aneurysm models are established by selecting different aneurysm model establishing methods, then DSA image measurement is carried out, comparison is carried out, and the establishing method corresponding to the rabbit aneurysm model with the largest tumor body minor diameter is screened out, so that the rabbit aneurysm model with high success rate, good aneurysm forming effect and convenience in research can be obtained, and follow-up research on aneurysms can be better guided.
The method for establishing the rabbit aneurysm model can be obtained by the following method, and specifically comprises the following steps: constructing a closed sac at the root of the right common carotid artery of the rabbit, injecting an aneurysm inducer into the sac, cleaning the aneurysm inducer in the sac of the rabbit arterial artery after 20-30min, recovering the smoothness of the rabbit artery, and obtaining the rabbit aneurysm model after at least 28 days.
The aneurysm inducer may be one or a combination of two or more of elastase, papain, calcium chloride, and collagenase; by means of the aneurysm-inducing agent, damage can be caused to the arterial wall, thereby inducing aneurysm.
For the method for constructing the closed sac cavity, a section of artery is generally clamped or fastened at two ends to form a sac cavity; the specific steps for constructing the rabbit artery sac cavity can be exemplified by: clamping or tightening two ends of one section of the middle part of the rabbit artery to form a rabbit artery closed cavity, pumping blood in the rabbit artery closed cavity, and cleaning the blood in the rabbit artery closed cavity by using normal saline containing heparin sodium to obtain the closed sac cavity.
The types of rabbit aneurysm models can be selected according to positions or research requirements, such as celiac arteries, lower limbs and the like; the rabbit common carotid artery is selected, so that the operation and the research are more convenient.
In order to reduce errors or accidental factors of a single experiment, the number of effective rabbit aneurysm models in each group in the step S1 is at least 2, and the short diameter data of the rabbit aneurysm body of each group in the step 2 is the average of the short diameter data of the effective rabbit aneurysm models of each group; the effective rabbit aneurysm model is a model in which an aneurysm is formed; the reliability of the related data can be further improved by averaging a plurality of data, and the model construction method can be better determined.
As for the method for establishing the rabbit aneurysm model, various existing rabbit aneurysm model establishing methods can be selected, and for example, 3 different rabbit aneurysm model establishing methods are selected in step S1 to establish 3 groups of rabbit aneurysm models, where:
the method for establishing the first group of rabbit aneurysm models specifically comprises the following steps: constructing a rabbit artery closed cavity of 1.9-2.1cm at the root of the right carotid artery of the rabbit, cleaning the closed cavity by using normal saline containing heparin sodium until no blood residue exists, injecting 0.1ml of elastase solution containing 70U into the rabbit artery closed cavity, keeping the peripheral tissues of the rabbit carotid artery moist by using the normal saline, further ligating the far end of the carotid artery after 20-30min, recovering the artery to be smooth, and feeding for more than 28 days (the invention contains the original number), thus obtaining the rabbit arterial closed cavity;
the method for establishing the second group of rabbit aneurysm models comprises the following steps: constructing a rabbit artery closed cavity of 1.9-2.1cm at the root of the right carotid artery of a rabbit, cleaning the closed cavity by normal saline containing heparin sodium until no blood residue exists, injecting 0.1ml of elastase solution containing 200U into the rabbit artery closed cavity, keeping the closed cavity in an inflated state, keeping the peripheral tissues of the rabbit carotid artery moist by normal saline, further ligating the distal end of the carotid artery after 20-30min, recovering the artery unobstructed, and feeding for more than 28 days to obtain the rabbit arterial closed cavity;
the method for establishing the third group of rabbit aneurysm models comprises the following specific steps: constructing a rabbit artery closed cavity of 1.9-2.1cm at the root of the right carotid artery of a rabbit, cleaning the closed cavity by normal saline containing heparin sodium until no blood remains, injecting 0.1ml of elastase solution containing 200U into the rabbit artery closed cavity, keeping the closed cavity in an inflated state, keeping the peripheral tissues of the rabbit carotid artery moist by normal saline, further ligating the distal end of the carotid artery after 20-30min, recovering the smoothness of the artery, feeding for more than 28 days, and feeding the animal with double antibodies every day during feeding to obtain the rabbit.
For the constructed rabbit aneurysm model, after DSA tumor body short diameter is measured, relevant tumor body short diameter data can be stored, then a relevant database is established, different rabbit aneurysm models can be continuously added subsequently, and more model data corresponding to different construction methods can be obtained; furthermore, the training can be carried out through a convolutional neural network, and a better method can be obtained through model data of multiple samples.
As for the method for establishing the rabbit aneurysm model in step S1, one or a combination of two or more of an elastase induction method, a papain induction method, a calcium chloride induction method, an elastase + collagenase induction method, and an adenovirus induction method may be selected.
For better measurement of DSA data of the rabbit tumor model, the time for measuring the tumor body short diameter of the rabbit aneurysm model by using a DSA device in the step S2 is more than 28 days after the rabbit aneurysm model is established in the step S1.
Example 1
A construction method of a rabbit aneurysm model is characterized by comprising the following steps:
s1: n different rabbit aneurysm model building methods are selected to build N groups of rabbit aneurysm models, wherein N is an integer greater than or equal to 2, and each model building method corresponds to one group of rabbit aneurysm models;
s2: measuring the N groups of rabbit aneurysm models obtained in the step S1 by adopting DSA equipment to obtain short diameter data of rabbit aneurysm bodies of all groups;
s3: performing comparative analysis on the N groups of rabbit aneurysm body short diameter data obtained in the step S2, and selecting a construction method corresponding to the rabbit aneurysm model with the largest tumor body short diameter to obtain the rabbit aneurysm model;
in the step S1, 3 different rabbit aneurysm model building methods are selected to build 3 groups of rabbit aneurysm models, wherein:
the method for establishing the first group of rabbit aneurysm models specifically comprises the following steps: constructing a rabbit artery closed cavity of 1.9-2.1cm at the root of the right carotid artery of the rabbit, cleaning the closed cavity by using normal saline containing heparin sodium until no blood residue exists, injecting 0.1ml of elastase solution containing 70U into the rabbit artery closed cavity, keeping the peripheral tissues of the rabbit carotid artery moist by using normal saline, further ligating the far end of the carotid artery after 20-30min, recovering the artery to be smooth, and feeding for 28 days to obtain the rabbit arterial closed cavity;
the method for establishing the second group of rabbit aneurysm models comprises the following steps: constructing a rabbit artery closed cavity of 1.9-2.1cm at the root of the right carotid artery of a rabbit, cleaning the closed cavity by normal saline containing heparin sodium until no blood residue exists, injecting 0.1ml of elastase solution containing 200U into the rabbit artery closed cavity, keeping the closed cavity in an inflated state, keeping the peripheral tissues of the rabbit carotid artery moist by normal saline, further ligating the distal end of the carotid artery after 20-30min, recovering the artery unobstructed, and feeding for 28 days to obtain the rabbit arterial closed cavity;
the method for establishing the third group of rabbit aneurysm models comprises the following specific steps: constructing a rabbit artery closed cavity of 1.9-2.1cm at the root of the right carotid artery of a rabbit, cleaning the closed cavity by normal saline containing heparin sodium until no blood remains, injecting 0.1ml of elastase solution containing 200U into the rabbit artery closed cavity, keeping the closed cavity in an inflated state, keeping the peripheral tissues of the rabbit carotid artery moist by normal saline, further ligating the distal end of the carotid artery after 20-30min, recovering the smoothness of the artery, feeding for 28 days, and feeding animals with double antibodies every day during feeding to obtain the rabbit arterial occlusive cavity;
then, DSA image measurement is carried out on rabbit aneurysm models (carotid arteries) of different groups, and specific test results are shown in figures 1-6; through analysis and comparison, the data of the third group of models is more optimal, and the corresponding model building method of the group is determined to be a rabbit aneurysm model building method; subsequent experiments show that the method has high tumor formation rate and good reproducibility, and is convenient for researching pathological mechanism, treatment and the like of the aneurysm.
Finally, it should be noted that: the above embodiments are only preferred embodiments of the present invention, and the protection scope of the present invention should not be limited thereby, and any insubstantial changes and substitutions made by those skilled in the art based on the present invention are within the protection scope of the present invention.

Claims (9)

1. A construction method of a rabbit aneurysm model is characterized by comprising the following steps:
s1: n different rabbit aneurysm model building methods are selected to build N groups of rabbit aneurysm models, wherein N is an integer greater than or equal to 2, and each model building method corresponds to one group of rabbit aneurysm models;
s2: measuring the N groups of rabbit aneurysm models obtained in the step S1 by adopting DSA equipment to obtain short diameter data of rabbit aneurysm bodies of all groups;
s3: and D, performing comparative analysis on the N groups of rabbit aneurysm body short diameter data obtained in the step S2, and selecting a construction method corresponding to the rabbit aneurysm model with the largest tumor body short diameter to obtain the rabbit aneurysm.
2. The construction method according to claim 1, wherein the rabbit aneurysm model building method comprises the following steps: constructing a closed sac at the root of the right common carotid artery of the rabbit, injecting an aneurysm inducer into the sac, cleaning the aneurysm inducer in the sac of the rabbit arterial artery after 20-30min, and then recovering the smoothness of the rabbit artery to obtain the rabbit aneurysm model.
3. The method according to claim 2, wherein the aneurysm induction agent is one or a combination of two or more of elastase, papain, calcium chloride, and collagenase.
4. The construction method according to claim 2, wherein the specific steps of constructing the closed capsule cavity are as follows: clamping or tightening two ends of one section of the middle part of the rabbit artery to form a rabbit artery closed cavity, pumping blood in the rabbit artery closed cavity, and cleaning the blood in the rabbit artery closed cavity by using normal saline to obtain the closed sac cavity.
5. The method of constructing according to claim 1, wherein the rabbit aneurysm model is a rabbit carotid aneurysm model.
6. The method according to claim 1, wherein the number of effective rabbit aneurysm models in each group in step S1 is at least 2, and the short diameter data of rabbit aneurysm body of each group in step S2 is an average of the short diameter data of the effective rabbit aneurysm models of each group; the effective rabbit aneurysm model is a model of aneurysm.
7. The method according to claim 1, wherein 3 different rabbit aneurysm model building methods are selected in step S1 to build 3 rabbit aneurysm models, wherein:
the method for establishing the first group of rabbit aneurysm models specifically comprises the following steps: constructing a rabbit artery closed cavity of 1.9-2.1cm at the root of the right carotid artery of the rabbit, cleaning the closed cavity by using normal saline containing heparin sodium until no blood residue exists, injecting 0.1ml of elastase solution containing 70U into the rabbit artery closed cavity, keeping the peripheral tissues of the rabbit carotid artery moist by using normal saline, further ligating the far end of the carotid artery after 20-30min, recovering the artery to be smooth, and feeding for more than 28 days to obtain the rabbit arterial closed cavity;
the method for establishing the second group of rabbit aneurysm models comprises the following steps: constructing a rabbit artery closed cavity of 1.9-2.1cm at the root of the right carotid artery of a rabbit, cleaning the closed cavity by normal saline containing heparin sodium until no blood residue exists, injecting 0.1ml of elastase solution containing 200U into the rabbit artery closed cavity, keeping the closed cavity in an inflated state, keeping the peripheral tissues of the rabbit carotid artery moist by normal saline, further ligating the distal end of the carotid artery after 20-30min, recovering the artery unobstructed, and feeding for more than 28 days to obtain the rabbit arterial closed cavity;
the method for establishing the third group of rabbit aneurysm models comprises the following specific steps: constructing a rabbit artery closed cavity of 1.9-2.1cm at the root of the right carotid artery of a rabbit, cleaning the closed cavity by normal saline containing heparin sodium until no blood remains, injecting 0.1ml of elastase solution containing 200U into the rabbit artery closed cavity, keeping the closed cavity in an inflated state all the time, keeping the peripheral tissues of the rabbit carotid artery moist by normal saline, further ligating the distal end of the carotid artery after 20-30min, recovering the smoothness of the artery, feeding for more than 28 days, and feeding the animal with double antibody every day during feeding to obtain the rabbit.
8. The constructing method according to claim 1, wherein the rabbit aneurysm model establishing method in step S1 is performed by using one or a combination of two or more of elastase induction, papain induction, calcium chloride induction, elastase + collagenase induction, and adenovirus induction.
9. The constructing method according to claim 1, wherein the time for measuring the tumor body minor diameter of the rabbit aneurysm model using a DSA apparatus in step S2 is 28 days or more after the rabbit aneurysm model is established in step S1.
CN202111510794.2A 2021-12-10 2021-12-10 Construction method of rabbit aneurysm model Pending CN114304053A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202111510794.2A CN114304053A (en) 2021-12-10 2021-12-10 Construction method of rabbit aneurysm model

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202111510794.2A CN114304053A (en) 2021-12-10 2021-12-10 Construction method of rabbit aneurysm model

Publications (1)

Publication Number Publication Date
CN114304053A true CN114304053A (en) 2022-04-12

Family

ID=81049819

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202111510794.2A Pending CN114304053A (en) 2021-12-10 2021-12-10 Construction method of rabbit aneurysm model

Country Status (1)

Country Link
CN (1) CN114304053A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN116058992A (en) * 2022-12-15 2023-05-05 中国人民解放军总医院第六医学中心 System and device for constructing near-end thoracic aortic aneurysm animal model

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003063911A1 (en) * 2002-02-01 2003-08-07 Anges Mg, Inc. Decoy-containing pharmaceutical compositions and method of using the same
CN101023893A (en) * 2005-10-06 2007-08-29 科迪斯公司 Endoluminal device for treating disease of aneurysm and combination of drugs
CN101351453A (en) * 2005-10-28 2009-01-21 武田药品工业株式会社 Heterocyclic amide compound and use thereof
US20100260726A1 (en) * 2007-11-02 2010-10-14 Inserm Methods for Producing a Non Human Model for Aortic Aneurysm
CN103491983A (en) * 2011-02-08 2014-01-01 伦敦王室学院 Materials and methods relating to cardiovascular imaging
CN105368975A (en) * 2015-12-18 2016-03-02 四川省人民医院 Intracranial aneurysm marker ODAM and application thereof
CN111388765A (en) * 2020-04-03 2020-07-10 北京臻溪谷医学研究中心(有限合伙) Composite polymer material and stem cell rack for treating aneurysm and vascular malformation and its prepn
CN111588510A (en) * 2020-05-25 2020-08-28 上海市第六人民医院 Method for constructing rabbit wide-neck aneurysm model by combining aneurysm clip and pancreatic elastase

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003063911A1 (en) * 2002-02-01 2003-08-07 Anges Mg, Inc. Decoy-containing pharmaceutical compositions and method of using the same
CN101023893A (en) * 2005-10-06 2007-08-29 科迪斯公司 Endoluminal device for treating disease of aneurysm and combination of drugs
CN101351453A (en) * 2005-10-28 2009-01-21 武田药品工业株式会社 Heterocyclic amide compound and use thereof
US20100260726A1 (en) * 2007-11-02 2010-10-14 Inserm Methods for Producing a Non Human Model for Aortic Aneurysm
CN103491983A (en) * 2011-02-08 2014-01-01 伦敦王室学院 Materials and methods relating to cardiovascular imaging
CN105368975A (en) * 2015-12-18 2016-03-02 四川省人民医院 Intracranial aneurysm marker ODAM and application thereof
CN111388765A (en) * 2020-04-03 2020-07-10 北京臻溪谷医学研究中心(有限合伙) Composite polymer material and stem cell rack for treating aneurysm and vascular malformation and its prepn
CN111588510A (en) * 2020-05-25 2020-08-28 上海市第六人民医院 Method for constructing rabbit wide-neck aneurysm model by combining aneurysm clip and pancreatic elastase

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
王一镗等: "《心肺脑复苏 第3版》", 31 January 2020, 上海科学技术出版社 *
胡立英: "弹性蛋白酶诱导兔颈部分支动脉瘤模型建立", 《中国优秀硕士学位论文全文数据库(电子期刊),医药卫生科技辑》 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN116058992A (en) * 2022-12-15 2023-05-05 中国人民解放军总医院第六医学中心 System and device for constructing near-end thoracic aortic aneurysm animal model

Similar Documents

Publication Publication Date Title
Fujikawa et al. An experimental evaluation of microvenous grafts
Schneider et al. Hepatic arterial pulsatility index in cirrhosis: correlation with portal pressure
CN114304053A (en) Construction method of rabbit aneurysm model
CN108030550B (en) Virtual imaging-based aneurysm neck angle calculation method for aneurysm
Madding et al. Hepatoportal arteriovenous fistula
US4585010A (en) Process and apparatus for measurement of outflow resistance
Yalçin et al. Vascular anatomy of normal and undescended testes: surgical assessment of anastomotic channels between testicular and deferential arteries
Morris et al. Chronic portal vein occlusion and portal hypertension in the dog
Qiu et al. Mechanical and contractile properties of in situ localized mesenteric arteries in normotensive and spontaneously hypertensive rats
RU2231309C1 (en) Method for developing bilateral end-loop pancreatoenteroanastomosis after median pancreatic resection
RU2336831C2 (en) Pancreaticoduodenal resection method in case of locally advanced carcinoma of periampullary zone with major tumorous invasion of mesentricoportal system main veins
RU2311875C1 (en) Method for carrying out pancretaoduodenal resection in locally disseminated periampular carcinoma cases accompanied by tumor invasion of portal vein orifice
CN113143458A (en) Method and device for evaluating aortic dissection distal laceration occlusion treatment scheme
LaMuraglia et al. Angioscopic evaluation of unilateral aortic graft limb thrombectomy: Is it helpful?
RU2312608C1 (en) Method for pancreatoduodenal resection at local cancer of periampular area at extensive tumor invasion of the main veins in mesenterico-portal system
RU47201U1 (en) DEVICE FOR STUDYING HEMODYNAMICS OF INTERNAL BODIES
RU2796313C1 (en) Method for glomus-sparing carotid endarterectomy during surgical treatment of hemodynamicly significant internal carotid stenosis
Zeeman et al. The significance of resection length on the patency rate, and the histopathology, of experimentally avulsed and microsurgically repaired blood vessels
RU2664805C1 (en) Method of preparation autovein for shunting
Merrell et al. Cuffing techniques in microarterial surgery
RU2317018C1 (en) Method for pancreatoduodenal resection at locally-metastasing cancer of periampullar area at vast tumor invasion of the main veins of mesenterico-portal system and the presence of two main trunks of the superior mesenteric vein
RU2329771C1 (en) Method temporary vascular bypass within mesenterioportal great vessel resection
CN207734396U (en) Blood circulation Temporary access ensuring equipment in replantation of severed limb
RU2316270C1 (en) Method for pancreatoduodenal resection at local cancer of periampullar area along with tumor invasion of superior mesenteric vein
Speden et al. Constriction of ear arteries from normotensive and renal hypertensive rabbits against different transmural pressures

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20220412