CN1398636A - Thymosin composition injection and its prepn - Google Patents
Thymosin composition injection and its prepn Download PDFInfo
- Publication number
- CN1398636A CN1398636A CN 02123538 CN02123538A CN1398636A CN 1398636 A CN1398636 A CN 1398636A CN 02123538 CN02123538 CN 02123538 CN 02123538 A CN02123538 A CN 02123538A CN 1398636 A CN1398636 A CN 1398636A
- Authority
- CN
- China
- Prior art keywords
- thymosin
- injection
- sodium chloride
- composition
- water
- 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.)
- Granted
Links
- 108010046075 Thymosin Proteins 0.000 title claims abstract description 32
- 102000007501 Thymosin Human genes 0.000 title claims abstract description 32
- LCJVIYPJPCBWKS-NXPQJCNCSA-N thymosin Chemical compound SC[C@@H](N)C(=O)N[C@H](CO)C(=O)N[C@H](CC(O)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](C)C(=O)N[C@H](C(C)C)C(=O)N[C@H](CC(O)=O)C(=O)N[C@H](C(C)C)C(=O)N[C@H](CO)C(=O)N[C@H](CO)C(=O)N[C@H](CCC(O)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@H]([C@H](C)O)C(=O)N[C@H](C(C)C)C(=O)N[C@H](CCCCN)C(=O)N[C@H](CC(O)=O)C(=O)N[C@H](CC(C)C)C(=O)N[C@H](CCCCN)C(=O)N[C@H](CCC(O)=O)C(=O)N[C@H](CCCCN)C(=O)N[C@H](CCCCN)C(=O)N[C@H](CCC(O)=O)C(=O)N[C@H](C(C)C)C(=O)N[C@H](C(C)C)C(=O)N[C@H](CCC(O)=O)C(=O)N[C@H](CCC(O)=O)C(=O)N[C@@H](C)C(=O)N[C@H](CCC(O)=O)C(O)=O LCJVIYPJPCBWKS-NXPQJCNCSA-N 0.000 title claims abstract description 32
- 238000002347 injection Methods 0.000 title claims abstract description 26
- 239000007924 injection Substances 0.000 title claims abstract description 26
- 239000000203 mixture Substances 0.000 title claims abstract description 25
- RWSXRVCMGQZWBV-WDSKDSINSA-N glutathione Chemical compound OC(=O)[C@@H](N)CCC(=O)N[C@@H](CS)C(=O)NCC(O)=O RWSXRVCMGQZWBV-WDSKDSINSA-N 0.000 claims abstract description 25
- 229960003180 glutathione Drugs 0.000 claims abstract description 20
- 230000002829 reductive effect Effects 0.000 claims abstract description 20
- 238000002360 preparation method Methods 0.000 claims abstract description 9
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 56
- 239000011780 sodium chloride Substances 0.000 claims description 26
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 20
- 235000003969 glutathione Nutrition 0.000 claims description 19
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 claims description 16
- 239000008215 water for injection Substances 0.000 claims description 15
- 239000000243 solution Substances 0.000 claims description 12
- 239000007788 liquid Substances 0.000 claims description 11
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 claims description 10
- 238000004659 sterilization and disinfection Methods 0.000 claims description 10
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 claims description 9
- 239000001110 calcium chloride Substances 0.000 claims description 8
- 229910001628 calcium chloride Inorganic materials 0.000 claims description 8
- 235000010265 sodium sulphite Nutrition 0.000 claims description 8
- 239000000463 material Substances 0.000 claims description 7
- 239000002994 raw material Substances 0.000 claims description 7
- 239000002158 endotoxin Substances 0.000 claims description 4
- 238000005374 membrane filtration Methods 0.000 claims description 4
- 238000003756 stirring Methods 0.000 claims description 4
- 210000001541 thymus gland Anatomy 0.000 claims description 4
- 238000004108 freeze drying Methods 0.000 claims description 3
- 108090000765 processed proteins & peptides Proteins 0.000 claims description 3
- 239000008176 lyophilized powder Substances 0.000 claims description 2
- 239000008354 sodium chloride injection Substances 0.000 claims description 2
- 230000000694 effects Effects 0.000 abstract description 16
- 108010024636 Glutathione Proteins 0.000 abstract description 5
- 238000004519 manufacturing process Methods 0.000 abstract description 5
- 239000002552 dosage form Substances 0.000 abstract description 3
- 206010020751 Hypersensitivity Diseases 0.000 abstract description 2
- 208000030961 allergic reaction Diseases 0.000 abstract 1
- 239000003814 drug Substances 0.000 description 8
- 238000005457 optimization Methods 0.000 description 7
- 230000001954 sterilising effect Effects 0.000 description 6
- 206010002198 Anaphylactic reaction Diseases 0.000 description 4
- 230000036783 anaphylactic response Effects 0.000 description 4
- 208000003455 anaphylaxis Diseases 0.000 description 4
- 238000012856 packing Methods 0.000 description 4
- 210000004185 liver Anatomy 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 208000002672 hepatitis B Diseases 0.000 description 2
- 239000008227 sterile water for injection Substances 0.000 description 2
- JGSARLDLIJGVTE-UHFFFAOYSA-N 3,3-dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid Chemical compound O=C1N2C(C(O)=O)C(C)(C)SC2C1NC(=O)CC1=CC=CC=C1 JGSARLDLIJGVTE-UHFFFAOYSA-N 0.000 description 1
- OBMZMSLWNNWEJA-XNCRXQDQSA-N C1=CC=2C(C[C@@H]3NC(=O)[C@@H](NC(=O)[C@H](NC(=O)N(CC#CCN(CCCC[C@H](NC(=O)[C@@H](CC4=CC=CC=C4)NC3=O)C(=O)N)CC=C)NC(=O)[C@@H](N)C)CC3=CNC4=C3C=CC=C4)C)=CNC=2C=C1 Chemical compound C1=CC=2C(C[C@@H]3NC(=O)[C@@H](NC(=O)[C@H](NC(=O)N(CC#CCN(CCCC[C@H](NC(=O)[C@@H](CC4=CC=CC=C4)NC3=O)C(=O)N)CC=C)NC(=O)[C@@H](N)C)CC3=CNC4=C3C=CC=C4)C)=CNC=2C=C1 OBMZMSLWNNWEJA-XNCRXQDQSA-N 0.000 description 1
- 101710176384 Peptide 1 Proteins 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- 241000700605 Viruses Species 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 208000026935 allergic disease Diseases 0.000 description 1
- 230000007815 allergy Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 208000006454 hepatitis Diseases 0.000 description 1
- 231100000283 hepatitis Toxicity 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 230000003612 virological effect Effects 0.000 description 1
Landscapes
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
The present invention is one kind of thymosin composition injection and its preparation. It consists of thymosin and reductive glutathione in the weight ratio of 1-10 to 2-120 as well as pharmaceutically acceptable supplementary material. It has perfect dosage form, reasonable production process, high purity, high stability, high curative effect, and less allergic reaction and side effect.
Description
Technical field
The present invention relates to a kind of thymus peptide medicament, do not relate to a kind of thymosin composition injection and preparation method thereof.
Technical background
Existing thymosin medicine is because of dosage form, component imperfection, and reason such as production technology is unreasonable makes that pharmaceutical purity is low, poor stability, curative effect be not high enough, and clinical anaphylaxis and side effect are big.
Summary of the invention
The objective of the invention is to overcome the above-mentioned shortcoming of prior art, a kind of stability, good effect are provided, the thymosin composition injection that clinical anaphylaxis and side effect are little; The present invention also aims to provide its preparation method of this invention medicine.
For achieving the above object, thymosin composition injection of the present invention is made by the following weight proportion raw material:
Thymus peptide 1-10
Reduced glutathion 2-120
Other auxiliary material of acceptable on the pharmaceutics.
As optimization, other auxiliary material of acceptable comprises on the described pharmaceutics: sodium sulfite, sodium chloride and water for injection.
As optimization, the content of other auxiliary material of acceptable is on the aforementioned pharmaceutics:
The concentration of sodium sulfite is 0.05mol
Sodium chloride accounts for 0.9% of overall solution volume
The water for injection surplus.
As optimization, it is a lyophilized powder injection, its water content≤2%.
As optimization, it is made by following steps:
(1) other raw material mix homogeneously that will be except that reduced glutathion and sodium chloride;
(2) feeding ozone carries out disinfection;
(3) adding calcium chloride handles;
(4) filter the back and add reduced glutathion and water for injection and sodium chloride standardize solution.
The preparation method of thymosin composition injection of the present invention may further comprise the steps:
(1) other raw material mix homogeneously that will be except that reduced glutathion and sodium chloride;
(2) feeding ozone carries out disinfection;
(3) adding calcium chloride handles;
(4) filter the back and add reduced glutathion and water for injection and sodium chloride standardize solution.
As optimization, described (2) step is to make vector gas with aseptic, dustless compressed air, feeds the 5-20ppm concentration of ozone 30 ± 10min that sterilizes;
The calcium chloride purity that described (3) step adds is that top grade is pure, and its addition is 0.05mol;
Described (4) step is with the product of step (3) the two-stage membrane filtration with 0.45 μ m and 0.22 μ m, the reduced glutathion and the water for injection standardize solution that add ormal weight again, be stirred to dissolving fully, stir that to add concentration down be 15% sodium chloride, make that the concentration of sodium chloride reaches 0.9% in the medicinal liquid.
As optimization, also comprise after described (4) step: measure thymosin and sodium chloride content, bacterial endotoxin.
As optimization, also comprise after described (4) step and carrying out the step that lyophilization makes moisture≤2%
After adopting technique scheme, the indication of medicine of the present invention is mainly: hepatitis.
The composition principle of medicine of the present invention is: reduced glutathion is used to protect that thymosin is not oxidized loses activity as antioxidant, in addition its also have with thymosin collaborative protect the liver, the treating the liver effect; Reduced glutathion also has micro-M-band in the anti-thymosin, viral allergy effect reaches the detrimental effect to liver.
The inventive method adopt sodium sulfite can ozone to the medicinal liquid sterilization process in protection thymosin is not oxidized loses activity; After sulfurous acid is oxidized to sodium sulfate, adds calcium chloride solution and generate calcium sulfate precipitation after filtering; Sodium chloride concentration in the solution is 0.9%, is for medicinal liquid and blood of human body etc. are oozed; Medicinal liquid adopts the room temperature sterilization to replace high temperature sterilize, can prevent that thymosin and active ingredient thereof are subjected to thermal change and lose curative effect, prevents that anaphylaxis from increasing; Tu Chu advantage is that tradition adopts 121 ℃/20min of moist heat sterilization more, it can not remove bacterial endotoxin, and ozone sterilization both killing microorganisms, spore, virus, and can thoroughly destroy bacterial endotoxin in the medicinal liquid, make medicinal liquid not have heat source response, very favourable to making this medicine.
Medical instrument of the present invention has dosage form, component perfect, and production technology is reasonable, purity height, good stability, curative effect height, the advantage that clinical anaphylaxis and side effect are little.
Clinical efficacy
(1) thymosin composition treatment hepatitis B observation of curative effect of the present invention
Case sum produce effects has several total effective rate thymosin composition injection 35 45% 46% 91% thymosin one-component injections 35 36% 35% 77%
(2) thymosin composition treatment hepatitis B of the present invention side effect is observed
The highest 38.9 ℃ of 2% slight thymosin one pack system injection of the irritated thymosin composition injection of case sum heating 35 5% 35 15% the highest 39.5 ℃ 7% obvious
Specific embodiment embodiment one small-volume injection
L, component are:
Thymosin 20000mg
Reduced form glutathione 20000mg
Sodium chloride (injection is used) 45g
Water for injection adds to 5000ml
Concentration of sodium sulfite is 0.05mol
Above medicine is packed as 1000
2, small-volume injection production craft step
(1) making into 4500ml except that the said components reduced form glutathione and the sodium chloride adds water for injection;
(2) feed contain ozone concentration be the aseptic dustless compressed air of 12PPm in above-mentioned medicinal liquid, stir sterilization 30min by the vector gas air-flow;
(3) add the pure calcium chloride crystal of top grade, making its concentration is 0.05mol;
(4) medicinal liquid is through 0.45 μ m and 0.22 μ m two-stage membrane filtration mistake;
(5) set up volume 5000ml with sterile water for injection, add 15% sodium chloride solution setting sodium chloride concentration 0.9%;
(6) with the doubly bottle packing of 5ml peace, seal, lamp inspection is up to the standards, the packing warehouse-in.
Embodiment two lyophilized injectable powders
1, component is:
Thymosin 20000mg
Reduced form glutathione 20000mg
Sodium chloride (injection is used) 18g
Water for injection adds to 2000ml
Concentration of sodium sulfite is 0.05mol
Above medicine is packed as 1000
2, production craft step
(1) said components except that reduced form glutathione and sodium chloride is added water for injection;
(2) feed contain ozone concentration be the aseptic dustless compressed air of 12PPm in above-mentioned medicinal liquid, stir sterilization 30min by the vector gas air-flow;
(3) add the pure calcium chloride crystal of top grade, making its concentration is 0.05mol;
(4) medicinal liquid is through 0.45 μ m and 0.22 μ m two-stage membrane filtration mistake;
(5) set up volume 2000ml with sterile water for injection, add 15% the sodium chloride solution of preparing with 18 gram sodium chloride;
(6) with the packing of 7ml cillin bottle, the false add plug, lyophilization is handled and is made water content≤2%, tamponade, Zha Gai detects, packing, warehouse-in.The above-mentioned raw materials proportioning also can be: the content of other auxiliary material of acceptable is on thymus peptide 1 0g, 50g, 100g reduced glutathion 20g, 600g, the 1200g pharmaceutics: the concentration of sodium sulfite accounts for 0.9% water for injection surplus of overall solution volume for 0.05mol sodium chloride.
Claims (9)
1, a kind of thymosin composition injection is characterized in that being made by the following weight proportion raw material:
Thymus peptide 1-10
Reduced glutathion 2-120
Other auxiliary material of acceptable on the pharmaceutics.
2, thymosin composition injection according to claim 1 is characterized in that other auxiliary material of acceptable comprises on the described pharmaceutics: sodium sulfite, sodium chloride and water for injection.
3, thymosin composition injection according to claim 2 is characterized in that the content of other auxiliary material of acceptable on the aforementioned pharmaceutics is:
The concentration of sodium sulfite is 0.05mol
Sodium chloride accounts for 0.9% of overall solution volume
The water for injection surplus.
4,, it is characterized in that it is a lyophilized powder injection, its water content≤2% according to claim 1,2 or 3 described thymosin composition injections.
5,, it is characterized in that it is made by following steps according to claim 1,2 or 3 described thymosin composition injections:
(1) other raw material mix homogeneously that will be except that reduced glutathion and sodium chloride;
(2) feeding ozone carries out disinfection;
(3) adding calcium chloride handles;
(4) filter the back and add reduced glutathion and water for injection and sodium chloride standardize solution.
6, the preparation method of thymosin composition injection of the present invention is characterized in that may further comprise the steps:
(1) other raw material mix homogeneously that will be except that reduced glutathion and sodium chloride;
(2) feeding ozone carries out disinfection;
(3) adding calcium chloride handles;
(4) filter the back and add reduced glutathion and water for injection and sodium chloride standardize solution.
7, the preparation method of thymosin composition injection according to claim 6 is characterized in that described (2) step is to make vector gas with aseptic, dustless compressed air, feeds the 5-20ppm concentration of ozone 30 ± 10min that sterilizes;
The calcium chloride purity that described (3) step adds is that top grade is pure, and its addition is 0.05mol;
Described (4) step is with the product of step (3) the two-stage membrane filtration with 0.45 μ m and 0.22 μ m, the reduced glutathion and the water for injection standardize solution that add ormal weight again, be stirred to dissolving fully, stir that to add concentration down be 15% sodium chloride, make that the concentration of sodium chloride reaches 0.9% in the medicinal liquid.
8, the preparation method of thymosin composition injection according to claim 7 is characterized in that also comprising after described (4) step: measure thymosin and sodium chloride content, bacterial endotoxin.
9,, it is characterized in that also comprising after described (4) step and carry out the step that lyophilization makes moisture≤2% according to the preparation method of claim 6 or 7 described thymosin composition injections.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 02123538 CN1193790C (en) | 2002-07-01 | 2002-07-01 | Thymosin composition injection and its prepn |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 02123538 CN1193790C (en) | 2002-07-01 | 2002-07-01 | Thymosin composition injection and its prepn |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1398636A true CN1398636A (en) | 2003-02-26 |
| CN1193790C CN1193790C (en) | 2005-03-23 |
Family
ID=4745153
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN 02123538 Expired - Fee Related CN1193790C (en) | 2002-07-01 | 2002-07-01 | Thymosin composition injection and its prepn |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN1193790C (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1840177B (en) * | 2006-01-11 | 2011-04-06 | 成都圣诺科技发展有限公司 | Injection liquid of thymic peptide alpha 1 and preparation method thereof |
| CN102579347A (en) * | 2012-03-02 | 2012-07-18 | 海南灵康制药有限公司 | Thymalfasin liposome preparation for injecting |
| CN104840418A (en) * | 2015-06-11 | 2015-08-19 | 山东新时代药业有限公司 | Fasudil hydrochloride injection composition and preparation method thereof |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101380461B (en) * | 2008-09-27 | 2011-09-07 | 吴建中 | Efficient thymosin enteric-coated tablets and thymosin for injection |
-
2002
- 2002-07-01 CN CN 02123538 patent/CN1193790C/en not_active Expired - Fee Related
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1840177B (en) * | 2006-01-11 | 2011-04-06 | 成都圣诺科技发展有限公司 | Injection liquid of thymic peptide alpha 1 and preparation method thereof |
| CN102579347A (en) * | 2012-03-02 | 2012-07-18 | 海南灵康制药有限公司 | Thymalfasin liposome preparation for injecting |
| CN102579347B (en) * | 2012-03-02 | 2013-03-06 | 海南灵康制药有限公司 | Thymalfasin liposome preparation for injecting |
| CN104840418A (en) * | 2015-06-11 | 2015-08-19 | 山东新时代药业有限公司 | Fasudil hydrochloride injection composition and preparation method thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1193790C (en) | 2005-03-23 |
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Assignee: Hunan Kangyuan Pharmacy Co., Ltd. Assignor: Cai Haide Contract record no.: 2011430000207 Denomination of invention: Thymosin composition injection and its prepn Granted publication date: 20050323 License type: Exclusive License Open date: 20030226 Record date: 20111008 |
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Owner name: HUNAN KANGYUAN PHARMACY CO., LTD. Free format text: FORMER OWNER: CAI HAIDE Effective date: 20120306 |
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Effective date of registration: 20120306 Address after: 410329 No. 36, link road, A District, Liuyang biomedical industry park, Hunan Patentee after: Hunan Kangyuan Pharmacy Co., Ltd. Address before: 330009, room 11, 201 Bai Yi lane, Xiangshan South Road, Nanchang, Jiangxi Patentee before: Cai Haide |
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