CH652306A5 - Verfahren zur herstellung einer pharmazeutischen, parenteralen dosiseinheit des natriumsalzes von piperacillin. - Google Patents
Verfahren zur herstellung einer pharmazeutischen, parenteralen dosiseinheit des natriumsalzes von piperacillin. Download PDFInfo
- Publication number
- CH652306A5 CH652306A5 CH1857/82A CH185782A CH652306A5 CH 652306 A5 CH652306 A5 CH 652306A5 CH 1857/82 A CH1857/82 A CH 1857/82A CH 185782 A CH185782 A CH 185782A CH 652306 A5 CH652306 A5 CH 652306A5
- Authority
- CH
- Switzerland
- Prior art keywords
- concentration
- piperacillin
- pharmaceutical
- lyophilized
- solution
- Prior art date
Links
- 159000000000 sodium salts Chemical class 0.000 title claims description 6
- 229960002292 piperacillin Drugs 0.000 title description 5
- 238000004519 manufacturing process Methods 0.000 title description 2
- IVBHGBMCVLDMKU-GXNBUGAJSA-N piperacillin Chemical class O=C1C(=O)N(CC)CCN1C(=O)N[C@H](C=1C=CC=CC=1)C(=O)N[C@@H]1C(=O)N2[C@@H](C(O)=O)C(C)(C)S[C@@H]21 IVBHGBMCVLDMKU-GXNBUGAJSA-N 0.000 title 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 17
- 239000003085 diluting agent Substances 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 5
- 238000002360 preparation method Methods 0.000 claims description 4
- IVBHGBMCVLDMKU-UHFFFAOYSA-N 6-[[2-[(4-ethyl-2,3-dioxopiperazine-1-carbonyl)amino]-2-phenylacetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid Chemical compound O=C1C(=O)N(CC)CCN1C(=O)NC(C=1C=CC=CC=1)C(=O)NC1C(=O)N2C(C(O)=O)C(C)(C)SC21 IVBHGBMCVLDMKU-UHFFFAOYSA-N 0.000 claims description 2
- 230000008014 freezing Effects 0.000 claims 1
- 238000007710 freezing Methods 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- WCMIIGXFCMNQDS-IDYPWDAWSA-M piperacillin sodium Chemical compound [Na+].O=C1C(=O)N(CC)CCN1C(=O)N[C@H](C=1C=CC=CC=1)C(=O)N[C@@H]1C(=O)N2[C@@H](C([O-])=O)C(C)(C)S[C@@H]21 WCMIIGXFCMNQDS-IDYPWDAWSA-M 0.000 description 21
- 239000003708 ampul Substances 0.000 description 16
- 239000007788 liquid Substances 0.000 description 12
- 239000000243 solution Substances 0.000 description 12
- 238000002347 injection Methods 0.000 description 11
- 239000007924 injection Substances 0.000 description 11
- 238000004108 freeze drying Methods 0.000 description 7
- 239000007795 chemical reaction product Substances 0.000 description 6
- 239000012467 final product Substances 0.000 description 5
- 150000002960 penicillins Chemical class 0.000 description 5
- 239000000047 product Substances 0.000 description 4
- 230000007928 solubilization Effects 0.000 description 4
- 238000005063 solubilization Methods 0.000 description 4
- 238000010561 standard procedure Methods 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 101100065885 Caenorhabditis elegans sec-15 gene Proteins 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 210000001217 buttock Anatomy 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- DKAGJZJALZXOOV-UHFFFAOYSA-N hydrate;hydrochloride Chemical compound O.Cl DKAGJZJALZXOOV-UHFFFAOYSA-N 0.000 description 1
- 238000002372 labelling Methods 0.000 description 1
- 229960004393 lidocaine hydrochloride Drugs 0.000 description 1
- YECIFGHRMFEPJK-UHFFFAOYSA-N lidocaine hydrochloride monohydrate Chemical compound O.[Cl-].CC[NH+](CC)CC(=O)NC1=C(C)C=CC=C1C YECIFGHRMFEPJK-UHFFFAOYSA-N 0.000 description 1
- 239000003589 local anesthetic agent Substances 0.000 description 1
- 238000012792 lyophilization process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 210000003205 muscle Anatomy 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/19—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles lyophilised, i.e. freeze-dried, solutions or dispersions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/429—Thiazoles condensed with heterocyclic ring systems
- A61K31/43—Compounds containing 4-thia-1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula, e.g. penicillins, penems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US24758681A | 1981-03-26 | 1981-03-26 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH652306A5 true CH652306A5 (de) | 1985-11-15 |
Family
ID=22935482
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH1857/82A CH652306A5 (de) | 1981-03-26 | 1982-03-25 | Verfahren zur herstellung einer pharmazeutischen, parenteralen dosiseinheit des natriumsalzes von piperacillin. |
Country Status (23)
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6207661B1 (en) * | 1999-02-22 | 2001-03-27 | Baxter International Inc. | Premixed formulation of piperacillin sodium and tazobactam sodium injection |
| SI1675573T2 (sl) | 2003-10-23 | 2012-08-31 | Otsuka Pharma Co Ltd | Sterilna injektibilna aripiprazolna formulacija z nadzorovanim sproščanjem in postopek |
| ITMI20051630A1 (it) * | 2005-09-02 | 2007-03-03 | Acs Dobfar Spa | Formulazione farmaceutica sterile iniettabile contenente almeno due principi attivi |
| KR101546106B1 (ko) | 2007-07-31 | 2015-08-20 | 오쓰까 세이야꾸 가부시키가이샤 | 아리피프라졸 현탁액 및 냉동건조 제형의 제조 방법 |
| CN114200057A (zh) * | 2021-12-14 | 2022-03-18 | 坛墨质检科技股份有限公司 | 一种可替代标准溶液的抗生素类药物固体混合标准物质的制备方法 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2608507A (en) * | 1949-08-20 | 1952-08-26 | Sharp & Dohme Inc | Dialkyl sulfamyl benzoic acids |
| CH546783A (de) * | 1971-03-11 | 1974-03-15 | Hoffmann La Roche | Verfahren zur herstellung von penicilloinsaeurederivate. |
| JPS5817728B2 (ja) * | 1973-11-20 | 1983-04-09 | 山之内製薬株式会社 | アンピシリンナトリウムエン ノ セイホウ |
| IL47168A (en) * | 1974-05-09 | 1979-07-25 | Toyama Chemical Co Ltd | Mono or dioxo piperazino(thio)carbonylamino derivatives ofpenicillins and cephalosporins and process for producing the same |
| JPS52143221A (en) * | 1976-05-22 | 1977-11-29 | Yamanouchi Pharmaceut Co Ltd | Novel preparations for rectal administration |
| DE2623835C2 (de) * | 1976-05-28 | 1978-03-02 | C.H. Boehringer Sohn, 6507 Ingelheim | Verfahren zur Herstellung von Natriumampicillin |
| JPS542337A (en) * | 1977-06-08 | 1979-01-09 | Toyama Chem Co Ltd | Bactericidal composition for medical use |
| FR2403078A1 (fr) * | 1977-09-19 | 1979-04-13 | Lafon Labor | Nouveau procede de preparation de formes pharmaceutiques, cosmetiques ou de diagnostic |
| JPS54147917A (en) * | 1978-05-08 | 1979-11-19 | Sumitomo Chem Co Ltd | Ferrze-drying method |
| PT70225A (en) * | 1978-10-03 | 1979-10-01 | Gist Brocades Nv | Process for the preparation of sodium amoxicillin preparations |
| DE2925009A1 (de) * | 1979-06-21 | 1981-01-08 | Basf Ag | Zubereitung fuer substanzen, verfahren zu deren herstellung und deren verwendung |
-
1982
- 1982-01-26 CA CA000394904A patent/CA1209477A/en not_active Expired
- 1982-01-27 AU AU79865/82A patent/AU549784B2/en not_active Expired
- 1982-01-28 GB GB8202414A patent/GB2095551B/en not_active Expired
- 1982-01-29 ZA ZA82605A patent/ZA82605B/xx unknown
- 1982-02-01 ES ES509234A patent/ES8302455A1/es not_active Expired
- 1982-02-02 NZ NZ199632A patent/NZ199632A/en unknown
- 1982-02-02 SE SE8200591A patent/SE453153B/sv not_active IP Right Cessation
- 1982-02-03 GR GR67200A patent/GR78386B/el unknown
- 1982-02-03 IL IL64924A patent/IL64924A/xx unknown
- 1982-02-04 DK DK048382A patent/DK157976C/da active
- 1982-02-22 JP JP57026172A patent/JPS57159708A/ja active Granted
- 1982-03-09 DE DE19823208505 patent/DE3208505A1/de active Granted
- 1982-03-09 DE DE1993175106 patent/DE19375106I2/de active Active
- 1982-03-09 AT AT0092982A patent/AT395533B/de not_active IP Right Cessation
- 1982-03-12 FR FR8204196A patent/FR2502624B1/fr not_active Expired
- 1982-03-18 BE BE0/207599A patent/BE892541A/fr not_active IP Right Cessation
- 1982-03-18 PL PL1982235509A patent/PL130564B1/pl unknown
- 1982-03-19 IT IT48034/82A patent/IT1147916B/it active
- 1982-03-24 LU LU84031A patent/LU84031A1/de unknown
- 1982-03-25 CH CH1857/82A patent/CH652306A5/de not_active IP Right Cessation
- 1982-03-25 IE IE703/82A patent/IE52936B1/en unknown
- 1982-03-25 HU HU82914A patent/HU186489B/hu unknown
- 1982-03-25 NL NL8201251A patent/NL192664C/nl not_active IP Right Cessation
-
1989
- 1989-05-11 HK HK391/89A patent/HK39189A/xx not_active IP Right Cessation
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PL | Patent ceased |