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US4147767A Expired / Lapsed US ⏱️ 0.0 years remaining

Albumin medicament carrier system

Assignee: 3M Co
•
Filing: 1977-09-30
•
Granted: 1979-04-03
•
Expires: 1997-09-30
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Abstract

Abstract Solid serum albumin spherules having 5 to 30 percent by weight of an organic medicament homogeneously entrapped therein are disclosed. These spherules are especially suited for intravascular injection into the body wherein the drug is released from the spherule in a biphasic manner having an initial fast release phase followed by a slow release phase.

Inventors

  • 👤 Anthony F. Yapel, Jr.

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-23 17:15
CPC Classifications
A; A61; A61K; A61K9/00; A61K9/14; A61K9/16; A61K9/1605; A61K9/1629; A61K9/1658; A61P; A61P35/00; Y; Y10; Y10T; Y10T428/00; Y10T428/29; Y10T428/2982; Y10T428/2989

Claims Analysis

Total Claims: 22
Claim 1
Independent Claim 128 words
A therapeutic composition for controlling the release of drugs comprising solid spherules of serum albumin having homogeneously entrapped therein from 5 to 30 percent by weight of the spherule of an organic medicament which is at least 0.01 percent water soluble at 37° C., which spherules have been crosslinked by a process selected from the group consisting of: (a) heating at 110° to 180° C. for at least twenty minutes and (b) exposing to at least one chemical crosslinking agent which does not substantially affect the activity of said medicament for sufficient time to crosslink the albumin to a degree equivalent to heating at 110° to 180° C. for at least twenty minutes, and when placed in an aqueous medium, said medicament is released in a biphasic manner.
Claim 2
Dependent Claim 128 words
A therapeutic composition for controlling the release of drugs comprising solid spherules of serum albumin having homogeneously entrapped therein from 5 to 30 percent by weight of the spherule of an organic medicament which is at least 0.01 percent water soluble at 37° C., which spherules have been crosslinked by a process selected from the group consisting of: (a) heating at 110° to 180° C. for at least twenty minutes and (b) exposing to at least one chemical crosslinking agent which does not substantially affect the activity of said medicament for sufficient time to crosslink the albumin to a degree equivalent to heating at 110° to 180° C. for at least twenty minutes, and when placed in an aqueous medium, said medicament is released in a biphasic manner.
Claim 3
Dependent Claim 13 words
A composition according to claim 1 wherein the medicament is an antitumor agent.
Claim 4
Dependent Claim 11 words
A composition according to claim 2 wherein the medicament is 6-mercaptopurine.
Claim 5
Dependent Claim 11 words
A composition according to claim 2 wherein the medicament is 5-fluorouracil.
Claim 6
Dependent Claim 11 words
A composition according to claim 2 wherein the medicament is 6-thioguanine.
Claim 7
Dependent Claim 11 words
A composition according to claim 2 wherein the medicament is hydroxyurea.
Claim 8
Dependent Claim 11 words
A composition according to claim 2 wherein the medicament is colchicine.
Claim 9
Dependent Claim 11 words
A composition according to claim 2 wherein the medicament is chlorambucil.
Claim 10
Dependent Claim 11 words
A composition according to claim 2 wherein the medicament is busulfan.
Claim 11
Dependent Claim 12 words
A composition according to claim 1 wherein the medicament is a bronchodilator.
Claim 12
Dependent Claim 11 words
A composition according to claim 10 wherein the medicament is epinephrine.
Claim 13
Dependent Claim 11 words
A composition according to claim 10 wherein the medicament is salbutamol.
Claim 14
Dependent Claim 11 words
A composition according to claim 10 wherein the medicament is terbutaline.
Claim 15
Dependent Claim 16 words
A composition according to claim 1 dispersed in pharmaceutically acceptable extending medium suitable for intravascular injection.
Claim 16
Dependent Claim 21 words
A method of treating a disease state in an animal by intravascular injection of a therapeutic composition according to claim 1.
Claim 17
Dependent Claim 61 words
A process for preparing solid serum albumin spherules having a medicament homogeneously entrapped therein comprising injecting an aqueous solution of said albumin having said medicament dispersed therein into an agitated vegetable oil bath containing a lipophilic drying alcohol and a crosslinking agent which does not substantially affect the activity of said medicament selected from the group consisting of glutaraldehyde and formaldehyde.
Claim 18
Dependent Claim 61 words
A process for preparing solid serum albumin spherules having a medicament homogeneously entrapped therein comprising injecting an aqueous solution of said albumin having said medicament dispersed therein into an agitated vegetable oil bath containing a lipophilic drying alcohol and a crosslinking agent which does not substantially affect the activity of said medicament selected from the group consisting of glutaraldehyde and formaldehyde.
Claim 19
Dependent Claim 85 words
A therapeutic composition for controlling the release of drugs comprising solid spherules of serum albumin having homogeneously entrapped therein from 5 to 30 percent by weight of the spherule of an organic medicament which is at least 0.01 percent water soluble at 37° C., which spherules have been crosslinked by heating at 110° to 180° C. for at least twenty minutes during preparation to crosslink the albumin, and when placed in an aqueous medium, said medicament is released from said spherules in a biphasic manner.
Claim 20
Dependent Claim 85 words
A therapeutic composition for controlling the release of drugs comprising solid spherules of serum albumin having homogeneously entrapped therein from 5 to 30 percent by weight of the spherule of an organic medicament which is at least 0.01 percent water soluble at 37° C., which spherules have been crosslinked by heating at 110° to 180° C. for at least twenty minutes during preparation to crosslink the albumin, and when placed in an aqueous medium, said medicament is released from said spherules in a biphasic manner.
Claim 21
Dependent Claim 107 words
A therapeutic composition for controlling the release of drugs comprising solid spherules of serum albumin having homogeneously entrapped therein from 5 to 30 percent by weight of the spherule of an organic medicament which is at least 0.01 percent water soluble at 37° C., which spherules have been exposed to at least one chemical crosslinking agent which does not substantially affect the activity of the medicament to crosslink the albumin to a degree equivalent to that achieved by heating at 110° to 180° C. for at least twenty minutes, and when placed in an aqueous medium, said medicament is released from said spherules in a biphasic manner.
Claim 22
Dependent Claim 107 words
A therapeutic composition for controlling the release of drugs comprising solid spherules of serum albumin having homogeneously entrapped therein from 5 to 30 percent by weight of the spherule of an organic medicament which is at least 0.01 percent water soluble at 37° C., which spherules have been exposed to at least one chemical crosslinking agent which does not substantially affect the activity of the medicament to crosslink the albumin to a degree equivalent to that achieved by heating at 110° to 180° C. for at least twenty minutes, and when placed in an aqueous medium, said medicament is released from said spherules in a biphasic manner.

References Cited (Backward Citations)

US3043782A Cited
US3265630A Cited
US3265629A Cited
US3533958A Cited
US3663685A Cited
US3663686A Cited
US3663687A Cited
US3541201A Cited
US3937668A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1982-04-02 1982-10-02 1983-04-03 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1986-04-02 1986-10-02 1987-04-03 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1990-04-02 1990-10-02 1991-04-03 $7700.00 Window Closed / Lapsed

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