US4397995A
Expired / Lapsed
US
⏱️ 0.0 years remaining
Polymeric anti-tumor agent and method of preparation
Assignee: Monsanto Co
•
Filing: 1980-12-29
•
Granted: 1983-08-09
•
Expires: 2000-12-29
Abstract
Abstract An improved pharmaceutically active derivative of a copolymer of olefin monomer and alpha , beta -unsaturated polycarboxylic anhydride is prepared by reacting the copolymer with aqueous ammonia, spray drying the resulting aqueous solution of half-amide, half-ammonium salt and thermally imidating the resulting substantially dry, solid particulate product by simultaneous treatment with elevated temperature and removal of water until 5-40% of the derivative half-amide, half-ammonium salt groups are converted to imide groups.
Inventors
- 👤 Marvin L. Oftedahl
- 👤 Howard M. Solomon
- 👤 James A. Webster
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-05 16:42
CPC Classifications
A; A61; A61K; A61K31/00; A61K31/74; A61K31/785; A61P; A61P1/00; A61P1/04; A61P35/00; C; C08; C08F; C08F8/00; C08F8/44; C08F8/48
Claims Analysis
Total Claims: 8
Claim 1
Independent Claim
131 words
The method of making an improved pharmaceutically active derivative of a copolymer of an olefin monomer having from 2 to about 4 carbon atoms and an α,β-unsaturated polycarboxylic anhydride having from 4 to about 6 carbon atoms, said copolymer having a number average molecular weight of from about 300 to about 1500, comprising reaction said copolymer with aqueous ammonia in an amount sufficient to form an aqueous solution of a copolymer derivative having half-amide, half-ammonium salt groups, spray drying said aqueous solution to provide a substantially dry particulate solid form of said copolymer derivative, and then thermally imidating said substantially dry copolymer derivative by simultaneous treatment with elevated temperature and removal of water until from about 5% to about 40% by weight of said derivative groups are converted to imide groups.
Claim 2
Independent Claim
131 words
The method of making an improved pharmaceutically active derivative of a copolymer of an olefin monomer having from 2 to about 4 carbon atoms and an α,β-unsaturated polycarboxylic anhydride having from 4 to about 6 carbon atoms, said copolymer having a number average molecular weight of from about 300 to about 1500, comprising reaction said copolymer with aqueous ammonia in an amount sufficient to form an aqueous solution of a copolymer derivative having half-amide, half-ammonium salt groups, spray drying said aqueous solution to provide a substantially dry particulate solid form of said copolymer derivative, and then thermally imidating said substantially dry copolymer derivative by simultaneous treatment with elevated temperature and removal of water until from about 5% to about 40% by weight of said derivative groups are converted to imide groups.
Claim 3
Dependent Claim
38 words
The method of claim 1 in which the aqueous solution of the half-amide, half-ammonium salt copolymer derivative is vacuum distilled to remove from about 1% to about 2% by volume of a distillate prior to said spray drying.
Claim 4
Dependent Claim
43 words
The method of claim 1 in which a small but effective amount of a water soluble bisulfite salt is incorporated in the aqueous solution of the half-amide, half-ammonium salt copolymer derivative prior to spray drying to prevent peroxide formation during said spray drying.
Claim 5
Dependent Claim
17 words
The method of claim 1 in which the copolymer is a copolymer of ethylene and maleic anhydride.
Claim 6
Dependent Claim
23 words
The method of claim 1 in which the imide groups comprise from about 10% to about 25% by weight of said derivatized groups.
Claim 7
Dependent Claim
17 words
The method of claim 1 in which the copolymer has an average molecular weight of about 850.
Claim 8
Dependent Claim
32 words
The method of claim 4 in which the imide groups comprise about 18% by weight of said derivatized groups and in which the copolymer has an average molecular weight of about 850.
References Cited (Backward Citations)
CA664326A
Cited
US2854357A
Cited
US2892736A
Cited
US2883287A
Cited
US2957767A
Cited
US2930775A
Cited
US3157595A
Cited
US3282879A
Cited
US3261798A
Cited
US3651171A
Cited
US3840499A
Cited
US4255537A
Cited
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1986-08-08 | 1987-02-07 | 1987-08-09 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1990-08-08 | 1991-02-07 | 1991-08-09 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1994-08-08 | 1995-02-07 | 1995-08-09 | $7700.00 | Window Closed / Lapsed |