Use of thymulin on preparing protective medicine of antineoplastic agent, tumour physiatry and chemotherapeutic medicine
A technology for serum thymus factor and chemotherapeutic drugs, which is applied in the field of application of serum thymus factor in the preparation of anti-tumor drugs, protective drugs for tumor physics and chemotherapeutic drugs
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Example Embodiment
[0050] Example 1
[0051] This example relates to the EAC ascites tumor group results
[0052] Subcutaneous injection was administered, animals were inoculated on day 0, and culture conditions were checked on day 1. If there was no contamination, the animals were weighed and randomized into groups to start administration. The tumor model mice were randomly divided into 5 groups, namely the high-dose group, the middle-dose group, the low-dose group, the positive control group and the blank group, with the high-dose 0.25 mg·kg respectively. -1 , medium dose 0.125mg·kg -1 , low dose 0.0625mg·kg -1 , except the positive drug group, administered once a day for 14 consecutive days; the positive drug group, 5-fluorouracil, once every other day, three times in total. The results are shown in Table 1:
[0053] Table 1 Results of FTS used for anti-EAC ascites tumor drugs (x±s, n=10)
[0054] group
[0055] △△ P △△△ P<0.001 compared with blank group; life extension rate w...
Example Embodiment
[0057] Embodiment 2
[0058] This example involves the results of the H22 solid tumor group
[0059] Subcutaneous injection was administered, animals were inoculated on day 0, and culture conditions were checked on day 1. If there was no contamination, the animals were weighed and randomized into groups to start administration. The tumor model mice were randomly divided into 5 groups, namely the high-dose group, the middle-dose group, the low-dose group, the positive control group and the blank group, with the high-dose 0.25 mg·kg respectively. -1 , medium dose 0.125mg·kg -1 , low dose 0.0625mg·kg -1 , except for the positive drug group, administered once a day for 14 consecutive days; cyclophosphamide was administered once. The results are shown in Table 2.
[0060] Table 2. Results of FTS for anti-H22 solid tumor drugs (x±s, n=10)
[0061] group
[0062] △△ P △△△ P<0.001 compared with blank group; tumor inhibition rate was compared with blank group.
[0063]...
Example Embodiment
[0064] Embodiment 3
[0065] This example relates to the Walker-256 tumor group results
[0066] Subcutaneous injection was administered, animals were inoculated on day 0, and culture conditions were checked on day 1. If there was no contamination, the animals were weighed and randomized into groups to start administration. The tumor model rats were randomly divided into 5 groups, namely the high-dose group, the middle-dose group, the low-dose group, the positive control group and the blank group, with the high-dose 2.2 mg·kg respectively. -1 , medium dose 1.1mg·kg -1 , low dose 0.55mg·kg -1 , except for the positive drug group, administered once a day for 14 consecutive days; cyclophosphamide was administered once. The results are shown in Table 3.
[0067] The solid tumors in the administration group were dissected out and weighed the next day after the last administration, and the tumor inhibition rate was calculated. The tumor inhibition rates in the administration gr...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap