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Antimicrobial polymer conjugates

a polymer and antimicrobial technology, applied in the field of conjugates of antimicrobial agents, can solve the problems of small proteins (less than about 70 kda), significant morbidity and mortality, and high lethal death, and achieve the effects of reducing antibody binding, increasing circulating half-life, and retaining antimicrobial activity

Inactive Publication Date: 2009-03-26
BIOSYNEXUS INC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The conjugation extends the serum half-life of antimicrobial agents, allowing for less frequent dosing and reduced immunogenicity, thereby enhancing their therapeutic effectiveness and safety.

Problems solved by technology

Lysostaphin is a bacterial endopeptidase capable of cleaving the specific cross-linking polyglycine bridges in the cell walls of staphylococci, and is therefore highly lethal thereto.
Staphylococcal infections, such as those caused by S. aureus, are a significant cause of morbidity and mortality, particularly in settings such as hospitals, schools, and infirmaries.
However, small proteins (less than about 70 kDa), such as lysostaphin, have a relatively short half-life in blood after intravenous injection.
Lysostaphin's rapid clearance from circulation may reduce its efficacy.
Thus, lysostaphin's short circulating half-life cannot be effectively countered by increasing the amount or frequency of dosage.
When multiple conjugation sites are employed, this can result in the loss of bioactivity.

Method used

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  • Antimicrobial polymer conjugates
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Examples

Experimental program
Comparison scheme
Effect test

example 1

Study of PEGylated Lysostaphin

Lysostaphin PEGylation

[0058]Lysostaphin at 0.27, 1, or 5 mg / mL was dissolved in either 0.2M borate buffer (pH 8.5) or DMSO. The mPEG2-NHS esters were prepared in DMSO and added to the lysostaphin solution in molar excess at ratios of 40, 20, 10, 5 or 2.5:1. PEGylation was performed with three different buffer conditions, all at room temperature for 1, 2, or 3 hours: borate buffer (with <10% DMSO contributed by adding PEG), 50% borate / 50% DMSO, and 100% DMSO. All reactions were quenched by added glycine to 25 mM and vortexing.

[0059]PEG conjugation to lysostaphin was evaluated by SDS-PAGE with the NuPage Electrophoresis System. Non-reduced samples (300 ng) were run on a Novex 4-12% Bis-Tris gel at 115V and stained with colloidal blue. PEGylated lysostaphin was separated from unreached lysostaphin by running the reaction mixture over a SEPHACRYL S-100HR column. Purified PEG-lysostaphin was concentrated and saved for activity assays.

[0060]Alternatively, unc...

example 2

Fractionation of 40 kD PEG Lysostaphin Conjugates

[0073]Fractionation of the various 40 kD PEG-lysostaphin conjugate species of Example 1 was performed by ion-exchange chromatography as a means to test enzyme activity as a function of PEG conjugation number. Although perfect resolution was not achieved, fractions tended to be enriched in just one specific band. The mono-PEGylated form was purified to greater than 99% 1-mer, while the di-PEGylated form was purified to 93% 2-mer with the remainder contributed mostly by the 1-mer, as determined by size-exclusion chromatography HPLC.

[0074]Killing Assay for Activity: The ability of lysostaphin to kill SA in saline was tested with varying concentrations of the enzyme. The bacteria were streaked onto blood agar plates after a 1-2 hour incubation with lysostaphin and surviving colonies were counted the next day. The data is reported in FIG. 5 as surviving colonies of SA so that the lower value on the graph, the more effective the killing of ...

example 3

Fractionation of 30 kD PEG-Lysostaphin Conjugates

[0079]Example 2 was repeated substituting 30 kD PEG for 40 kD PEG and 1-mers and 2-mers of mPEG 30 kD lysostaphin conjugates were isolated in separate fractions having the following properties:

[0080]OD drop assay: The OD at 280 nm of a high innoculum of S. aureus (SA, about 109 / mL) in saline is monitored over time. When bacteria are lysed, the OD drops and thus is a measure of lysostaphin activity. The faster the OD drops, the greater the enzyme activity. A typical standard takes 6-7 minutes to reach 50% of starting OD. The 1-mer has greater activity than the 2-mer, but both have significantly reduced activity compared to unconjugated lysostaphin (FIGS. 8 and 9).

[0081]Killing Assay for Activity: The ability of lysostaphin to kill SA in saline was tested with varying concentrations of the enzyme. The bacteria were streaked onto blood agar plates after a 1-2 hour incubation with lysostaphin and surviving colonies were counted the next d...

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Abstract

Water-soluble polymer conjugates of antimicrobial agents retaining at least a portion of the antimicrobial activity of the agent, pharmaceutical compositions containing the polymer conjugates, and methods for treating microbial infections with the pharmaceutical compositions.

Description

CROSS-REFERENCE TO RELATED APPLICATION[0001]This application is a continuation of pending U.S. patent application Ser. No. 10 / 403,223 filed Mar. 26, 2003, which claims priority benefit under 35 U.S.C. § 119(e) to U.S. Provisional Application Ser. No. 60 / 368,112 filed on Mar. 26, 2002, each of which is hereby incorporated by reference in its entirety.FIELD OF THE INVENTION[0002]The present invention relates to the conjugation of antimicrobial agents to water-soluble polymers to improve their clinical properties in terms of their pharmacokinetics, pharmacodynamics, and reduced immunogenicity. More specifically, the present invention relates to the conjugation of antimicrobial agents such as lysostaphin to poly(alkylene oxides), such as poly(ethylene glycol) (PEG).BACKGROUND ARTA. Lysostaphin[0003]Lysostaphin is a potent antimicrobial agent first identified in Staphylococcus simulans (formerly known as S. staphylolyticus). Lysostaphin is a bacterial endopeptidase capable of cleaving th...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K38/48C12N9/52A61K38/00A61K38/43A61K45/00A61K47/34A61K47/48A61P31/04A61P43/00C08F2/00
CPCA61K47/48215A61K38/00A61K47/60A61P31/04A61P43/00
Inventor WALSH, SCOTT M.SHAH, ANJALI G.MOND, JAMES J.LEES, ANDREWDRABICK, JOSEPH J.
Owner BIOSYNEXUS INC
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