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Chemoenzymatic synthesis of oligohyaluronan-lipid conjugates.

ABSTRACT: Herein, we describe an efficient and high-yielding method to synthesize hyaluronan oligosaccharide-lipid conjugates. This strategy is based on first covalently attaching diphytanoyl glycerophosphatidylethanolamine (DiPhPE) to commercially available high molecular weight hyaluronic acid (HA), via the carboxylate group of the glucuronic acid using carbodiimide chemistry. The HA-lipid conjugate mixture is then digested with bovine testicular hyaluronidase to yield HA-DiPhPE conjugates that have a narrow distribution of moderately sized HA oligosaccharides. These HA-lipid conjugates can be incorporated into liposomes or micelles to selectively target CD44 that is overexpressed on many cancer or cancer initiating cells.

SUBMITTER: Ruhela D

PROVIDER: S-EPMC3993934 | biostudies-literature | 2014 Apr

REPOSITORIES: biostudies-literature

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Chemoenzymatic synthesis of oligohyaluronan-lipid conjugates.

Ruhela Dipali D Kivimäe Saul S Szoka Francis C FC

Bioconjugate chemistry 20140328 4

Herein, we describe an efficient and high-yielding method to synthesize hyaluronan oligosaccharide-lipid conjugates. This strategy is based on first covalently attaching diphytanoyl glycerophosphatidylethanolamine (DiPhPE) to commercially available high molecular weight hyaluronic acid (HA), via the carboxylate group of the glucuronic acid using carbodiimide chemistry. The HA-lipid conjugate mixture is then digested with bovine testicular hyaluronidase to yield HA-DiPhPE conjugates that have a n ...[more]

PMID: 24646444

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