Antibiotic formulation and method of treatment

Abstract

A formulation comprised of particles which may be in groups and are comprised of a biocompatible polymer and an antimicrobial drug for controlled release of the drug is disclosed. The particles may be in an aqueous solution comprising thrombin and be dispersed in a gel. The formulation is administered to an area such as an open wound having an orthopedic implant therein and provides a therapeutically effective level of drug to the patient over therapeutically effective period of time.

Description

CROSS-REFERENCES [0001] This application claims the benefit of priority of earlier filed U.S. Provisional Patent Application Ser. No. 60 / 821,668 filed Aug. 7, 2006 and of earlier filed U.S. Provisional Patent Application Ser. No. 60 / 805,267 filed Jun. 20, 2006 and is a continuation-in-part of U.S. application Ser. No. 11 / 383,562 filed May 16, 2006 which is a continuation-in-part of earlier filed U.S. application Ser. No. 10 / 618,255 filed Jul. 10, 2003 (now abandoned) which is a continuation-in-part of earlier filed U.S. application Ser. No. 10 / 195,046 filed Jul. 12, 2002 (now abandoned) which claims priority to provisional Application Ser. No. 60 / 326,675 filed Oct. 2, 2001 and provisional Application Ser. No. 60 / 305,364 filed Jul. 13, 2001 all of which applications are incorporated herein by reference and to which application priority is claimed.FIELD OF THE INVENTION [0002] The invention relates to a formulation of controlled release particles which may be dispersed in a gel and / or...

AI Technical Summary

Benefits of technology

[0012] In one embodiment the groups of particles of the antimicrobial are put into an aqueous solution of thrombin (e.g. 5 cc providing 20,000 units thrombin / cc ±20%) and this aqueous solution is then combined with a biocompatible gel such as Floseal™. As the release rate of one group of particles is decreasing (or the drug released from the group is being metabolized out of the system) the release rate of another group of particles is increasing (or drug from one group is being added to the system) so that the combined groups of particles making up the formulation provide a substantially constant level of drug (30 mcg / ml ±25 mcg / ml) over a therapeutically effective period of time (1-7 days). The concentrations of antimicrobial drug and BMP obtained at a wound and the release rate of these drugs may be varied with different antimicrobial drugs and patient conditions to obtain a desired end result.

[0042] Another aspect of an embodiment of this invention is to provide orthopedic hardware with antimicrobial maximized for its delivery of the antibiotic to the clinically relevant zone without exposing the patient to chronic, systemic doses of antimicrobial

Problems solved by technology

If the level of the antimicrobial drug drops too low then the antimicrobial effect is lost.

However, if the level is raised too high the drug becomes toxic to surrounding tissue such as hindering bone growth.

Still further, if the therapeutic level of the drug is not maintained for a sufficiently long period of time infection can occur.

If the therapeutic level of the antimicrobial level is maintained for too long of a period of time there may also be undesirable results such as the development of microbes which are resistant to the drug being used.

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