IP Library Granted Patent US 8,075,907
Granted Patent B2
US 8,075,907 · App. 12/017,499 · Granted Dec 13, 2011

Polymethylmethacrylate revision bone cement

Assignee: Heraeus Kulzer GmbH
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,075,907
App. No.
12/017,499
Granted
Dec 13, 2011
Kind
B2
Abstract

The invention relates to a PMMA revision bone cement having powder and liquid component, in which the powder component contains two or more granular antibiotics whose grain size distribution is equal in that the main screening fraction each of the individual antibiotics is in the same grain size range, in particular in the range of 100-250 μm or 150-250 μm.

Claims (9)

1. A polymethylmethacrylate (PMMA) revision bone cement having powder and liquid components, wherein the powder component comprises two or more granular individual antibiotics whose grain size distribution is equal in that a main screening fraction of each of the individual antibiotics is in the same grain size range, wherein the main screening fraction of the antibiotics each comprises at least 50 weight percent of each antibiotic, and wherein the grain size range of the main screening fraction of the individual antibiotics is 100 to 250 gm.

2. PMMA revision bone cement according to claim 1 , wherein the grain size range of the main screening fraction of the individual antibiotics is 150 to 250 μm.

3. PMMA revision bone cement according to claim 1 , wherein the granular antibiotics are one or more members selected from the group consisting of gentamicin sulfate, gentamicin hydrochloride, amikacin sulfate, amikacin hydrochloride, tobramycin sulfate, tobramycin hydrochloride, clindamycin hydrochloride, lincosamine hydrochloride, moxifloxacin, ciprofloxacin, teicoplanin, vancomycin, ramoplanin, dalbavancin, daptomycin, tigecyglin, metronidazole, tinidazole, and omidazole.

4. PMMA revision bone cement according to claim 1 , wherein the granular antibiotics are selected from the group consisting of sparingly water-soluble salt forms of antibiotics from the group of antibiotics flavone phosphates, antibiotics palmitates, antibiotics myristates, and antibiotics laurates.

5. PMMA revision bone cement according to claim 1 , wherein the granular antibiotics are selected from the group consisting of oxazolidones.

6. PMMA revision bone cement according to claim 1 , wherein the granular antibiotics component further comprises at least one excipient selected from the group consisting of polyvinylpyrrolidone, polyethyleneglycol, polyethyleneoxide, maltose, sorbitol, and mannitol.

7. PMMA revision bone cement according to claim 1 , wherein the granular antibiotics component further comprises at least one excipient selected from the group consisting of the toxicologically acceptable polymers, gelatin, collagen, and dextran.

8. PMMA revision bone cement according to claim 1 , wherein at least a part of the granular antibiotics is glued or cemented by adhesive excipients into antibiotics granulates having particle sizes in the range of 63-900 μm.

9. A polymethylmethacrylate (PMMA) revision bone cement having powder and liquid components, wherein the powder component comprises granules of a first antibiotic and granules of a second antibiotic, wherein the granules of said first antibiotic are present in said powder component in a plurality of grain size fractions, and the granules of said second antibiotic are also present in said powder component in a plurality of grain size fractions; wherein one of said grain size fractions of said first antibiotic is designated as a main screening fraction of said first antibiotic, and one of said grain size fractions of said second antibiotic is designated as a main screening fraction of said second antibiotic; wherein the main screening fraction of said first antibiotic is present in an amount of at least 50 percent by weight based on a total weight of the first antibiotic in the powder component, and the main screening fraction of said second antibiotic is also present in an amount of at least 50 percent by weight based on a total weight of the second antibiotic in the powder component; and wherein the grain size of the main screening fraction of said first antibiotic is 100 to 250 μm, and the grain size of the main screening fraction of said second antibiotic is also 100 to 250 μm.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 7, 2014
From: HERAEUS KULZER GMBH
To: HERAEUS MEDICAL GMBH
Reel/Frame 031905/0674 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 28, 2008
From: KUHN, KLAUS-DIETER, DR.; VOGT, SEBASTIAN, DR.; BUCHNER, HUBERT, DR.
To: HERAEUS KULZER GMBH
Reel/Frame 020864/0014 →
Priority Claims (1)
DE 10 2007 004 968 · Jan 26, 2007 · national
Continuity (1)
Related Publication 20080213336A1 · Sep 4, 2008