Pure PEG-lipid conjugates

• US 20110040113A1
• Filed: 06/01/2010
• Published: 02/17/2011
• Est. Priority Date: 06/02/2009
• Status: Abandoned Application

• Current Assignee: Brian Charles Keller, Nian Wu
• Original Assignee: Brian Charles Keller, Nian Wu
• Inventors: Wu, Nian, Keller, Brian Charles
• Application Number:
  US12/802,197
• Publication Number:
  US 20110040113A1
• Time in Patent Office: Days
• US Class Current: 554/227
• CPC Class Codes: A61K 47/60 the organic macromolecular compound being a polyoxyalkylene oligomer, polymer or dendrimer, e.g. PEG, PPG, PEO or polyglycerol
• CPC Class Codes: A61K 47/6911 the form being a liposome
• CPC Class Codes: C08G 65/329 with organic compounds
• CPC Class Codes: C08L 2203/02 for biomedical use

Abstract

Syntheses of polyethyleneglycol (PEG)-lipid conjugates are disclosed. Such syntheses involve stepwise addition of small PEG oligomers to a glycerol backbone until the desired chain size is attained. Polymers resulting from the syntheses are highly monodisperse. The present invention provides several advantages such as simplified synthesis, high product yield and low cost for starting materials. The present synthesis method is suitable for preparing a wide range of conjugates.

In another aspect, the invention comprises PEG lipid conjugates having a glycerol backbone covalently attached to one or two monodisperse PEG chains and one or two lipids. These conjugates are especially useful for pharmaceutical formulations.

Claims

1. A method of making a PEG chain of a defined length, the method comprising:

(a) selecting a glycerol derivative with a glycerol protecting group that is stable under a first set of conditions and convertible to free hydroxyl groups under a second set of conditions;

(b) selecting a initial PEG oligomer having between 1 and 12 subunits, where the initial PEG oligomer has an oligomer protecting group on its first terminus and the said oligomer protecting group converts to a hydroxyl group under the first set of conditions, and where the initial PEG oligomer has a reactive group on its second terminus, said reactive group forming a bond with a compound having a free hydroxyl group;

(c) reacting the glycerol derivative with the initial PEG oligomer to form a glycerol-PEG conjugate;

(d) removing the oligomer protective group by exposing the conjugate to the first set of conditions;

(e) repeating steps (f), (g) and (h) between 0 and 6 additional times, where steps are as described below;

(f) selecting an extending PEG oligomer having between 2 and 11 subunits, where the extending PEG oligomer has an oligomer protecting group on its first terminus and the said oligomer protecting group converts to a hydroxyl group under the first set of conditions, and where the extending PEG oligomer has a reactive group on its second terminus, said reactive group forming a bond with a compound having a free hydroxyl group;

(g) reacting the glycerol-PEG conjugate with the extending PEG oligomer to form an extended glycerol-PEG conjugate;

(h) removing the oligomer protective group by exposing the conjugate to the first set of conditions;

(i) terminating the PEG chain by either step (j) or steps (k) and (l), where the steps are as described below;

(j) adding a terminal group to the free hydroxyl group of the extended glycerol-PEG conjugate;

or

(k) selecting a terminal PEG oligomer having between 2 and 11 subunits, where the terminal PEG oligomer has terminal group on its first terminus, and where the terminal PEG oligomer has a reactive group on its second terminus, said reactive group forming a bond with a compound having a free hydroxyl group; and

(l) reacting the glycerol-PEG conjugate or extended glycerol-PEG conjugate with the terminal PEG oligomer; and

(m) exposing the terminated glycerol-PEG conjugate to the second set of conditions.

2. The method of claim 1, where the terminal group is methyl.

3. The method of claim 1, where the first set of conditions is catalytic reduction.

4. The method of claim 1, where the second set of conditions is exposure to acid.

5. The method of claim 1, where the glycerol derivative is a compound represented by the formula shown at Reaction Scheme 1(a).

6. The method of claim 1, where the glycerol derivative is a compound represented by the formula:

Chemical Structure 2.

7. The method of claim 1, where the glycerol derivative is a compound represented by the formula:

Chemical Structure 3.

8. The method of claim 1, where the glycerol derivative is a compound represented by the formula:

Chemical Structure 4.

9. The method of claim 1, where the glycerol protecting group is an alkyl group.

10. The method of claim 1, further comprising the steps of:

(n) removing the glycerol protecting group; and

(o) bonding a lipid group to the glycerol backbone.

11-76. -76. (canceled)