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Use of tumor caryon single-antibody in physical therapeutic tumor as synergist

A technique of physical therapy and cell nucleus, applied in the field of biomedicine, can solve the problems of esophageal cancer treatment only relying on surgery and radiotherapy, misembolization of other organs, catheter can not be superselective intubation, etc., to achieve the effect of eliminating immune rejection

Inactive Publication Date: 2007-09-05
SHANGHAI MEDIPHARM BIOTECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0069] 3) Unsolved problems in radiofrequency ablation
[0111] ② Misembolization and ectopic embolization: Catheters cannot be super-selectively intubated, improper selection of embolic agent, high pressure of injection contrast agent and other reasons may cause embolic agent reflux and misembolization of other organs
And because the vast majority of patients with esophageal cancer are already in the advanced stage when they are diagnosed, not only the local lesions have been extensively infiltrated, but also the distant spread of subclinical lesions or lymph node metastasis have been found. Autopsy found that many cases that were considered to be locally early died at the time of death. More than half of them have distant metastasis, more than 70% have extensive lymph node invasion, and less than 1 / 3 of the cases can be curatively resected. The 5-year survival rate of conventional radiotherapy is only 13%. The main cause of failure accounts for more than 80%. It can be seen that the treatment of esophageal cancer is far from enough by surgery and radiotherapy alone.
However, so far, there has been no report on the new use of tumor cell nuclear monoclonal antibody as a synergist in physical therapy of various solid tumors

Method used

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  • Use of tumor caryon single-antibody in physical therapeutic tumor as synergist

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0293] Example 1, Determination of Pharmacodynamic Activity of Labeled Tumor Cell Nuclear Monoclonal Antibody

[0294] (1) Drugs: 131 I-chTNT-MAb injection, 2ml / bottle, radioactive concentration 50mCi / ml, radiochemical purity > 95%, immune activity > 50%, sterile, qualified for pyrogen inspection. Dilute to the required concentration with 4% human albumin normal saline solution when used.

[0295] (2) Animals: tumor-bearing nude mice.

[0296] Each tumor-bearing nude mice were randomly divided into 6 groups.

[0297] (3) Method: In this experiment, the nude mouse animal model bearing human colon cancer, the nude mouse animal model bearing human liver cancer and the nude mouse animal model bearing human cervical cancer were selected as the research objects. The nude mouse animal models were intraperitoneally injected with different doses of 131 After I-chTNT-MAb injection, use the SPECT instrument to observe the localization and concentration of the drug in the tumor, and ob...

Embodiment 2

[0303] Example 2, Determination of Pharmacodynamic Activity of Labeled Tumor Cell Nuclear Monoclonal Antibody

[0304] (1) Drugs: 90 Y-chTNT-MAb injection, 2ml / bottle, radioactive concentration 50mCi / ml, radiochemical purity > 95%, immune activity > 50%, sterile, qualified for pyrogen inspection. Dilute to the required concentration with 4% human albumin normal saline solution when used.

[0305] (2) Animals: tumor-bearing nude mice.

[0306] Each tumor-bearing nude mice were randomly divided into 6 groups.

[0307] (3) Method: In this experiment, the nude mouse animal model bearing human colon cancer, the nude mouse animal model bearing human liver cancer and the nude mouse animal model bearing human cervical cancer were selected as the research objects. The nude mouse animal models were intraperitoneally injected with different doses of 90 After Y-chTNT-MAb injection, use the SPECT instrument to observe the localization and concentration of the drug in the tumor, and obse...

Embodiment 3

[0313] Example 3, Acute Toxicity Study of Labeled Tumor Cell Nuclear Monoclonal Antibody

[0314] (1) Drugs: 131 I-chTNT-MAb injection, radioactive concentration 2mCi / ml, radiochemical purity > 95%, immune activity > 50%, sterile, pyrogen inspection qualified. Dilute to the required concentration with 4% human albumin normal saline solution when used.

[0315] (2) Animals: Kunming mice were randomly divided into 4 groups, 5 mice per group, 20 mice in total, half male and half male.

[0316] (3) Method: Inject three doses into the tail vein of mice respectively, that is, 0.25mCi 131 I-chTNT-MAb / 0.25mgchTNT-MAb / piece, 0.5mCi 131 I-chTNT-MAb / 0.5mg chTNT-MAb / piece, 1mCi 131 I-chTNT-MAb / 1mgchTNT-MAb / monkey, observed for 48 hours.

[0317] (4) Results: 131When the dosage unit weight of I-chTNT-MAb was 20 times of the human dose, and the unit weight of the chTNT-MAb dosage was 200 times of the human dosage, no mouse died after 48 hours of observation, indicating that the drug h...

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Abstract

An application of the tumor cell nucleus monoantibody as the synergist in physically treating solid tumor by directionally combining with the necrotic tissue of tumor specifically and killing the tumor cells by the nuclein carried by it is disclosed. It features that the normal tissue can not be damaged.

Description

technical field [0001] The present invention relates to the technical field of biomedicine, in particular to the new use of tumor cell nuclear monoclonal antibody, and more specifically to the new use of tumor cell nuclear monoclonal antibody as a synergist in physical therapy of various solid tumors. Background technique [0002] (1) Molecular targeted therapy of tumors [0003] 1 Overview [0004] Molecular targeted therapy of tumors is the most dynamic field that has attracted much attention in recent years. It is a tumor-specific treatment in the fundamental sense. Molecular binding. An ideal targeting molecule should have the following characteristics: ① Highly specific target antigen binding; ② Appropriate molecular weight range to facilitate the penetration of the targeting molecule in tumor tissue; ③ High affinity when binding to the target molecule; ④The molecular structure is beneficial for stability and reduces clearance; ⑤Has biological homology with the treat...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A61K51/00A61K31/395A61P35/00A61K101/00A61K103/32A61K103/30
Inventor 鞠佃文张昕泂陶群叶丹杨建军
Owner SHANGHAI MEDIPHARM BIOTECH
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