Galactosylated ternary DNA/polyphosphoramidate nanoparticles mediate high gene transfection efficiency in hepatocytes
Introduction
Gene therapy promises new approaches for treating many inherited and acquired diseases. However, its full potential can not be realized until successful delivery systems become available [1]. An ideal gene delivery vector should be safe, stable, and cost-effective to produce in clinically relevant quantities, and capable of efficient and tissue-specific gene delivery. Viral vectors [2], [3] such as retroviruses and adenoviruses have been extensively investigated and demonstrate transfection efficiency relevant to clinical applications. However, their applications in clinical settings are limited because of safety concerns [4] and limitation on packaging sizes of genes. Cationic polymeric gene carriers, as non-viral carriers, offer promising alternatives. Cationic polymeric carriers mediate gene transfer by condensing DNA into nanoparticles, protecting DNA from enzymatic degradation, and facilitating cellular uptake and/or endolysosomal escape and/or nuclear translocation. A number of polycations have been reported to effect gene transfection, including poly-l-lysine (PLL) [5], [6], chitosan [7], [8], polyamidoamine dendrimers [9], polyethylenimine [10], [11], [12], poly[α-(4-aminobutyl)-l-glycolic acid] [13], [14], poly-l-glutamic acid derivatives [15], poly (β-amino esters) [16], [17]. Despite the extensive effort in synthesizing new polymeric carriers, an efficient polycation with low toxicity and good stability has not yet emerged.
Incorporating cell- or tissue-specific ligands to a polycationic carrier has been widely investigated as an effective approach to improve gene transfer efficiency in target tissue or cells. A number of ligands have been examined including galactose, transferrin, folate, RGD peptides and antibodies [18], [19], [20], [21], [22]. Among them, galactose is the most extensively studied to target genes to liver parenchymal cells since galactose moiety can be specifically recognized by asialoglycoprotein receptors (ASGPR) on hepatocytes. Gene transfer efficiency can be improved as a result of the enhanced cell uptake via ASGPR-mediated endocytosis. For instance, galactosylated polylysine (Gal-PLL) showed a more than 10-fold increase in transfection efficiency in HepG2 cells compared with unmodified PLL [23]. Gal-PLL/DNA complexes were preferentially taken up by liver parenchymal cells after intravenous injection [24]. In a study by Sagara et al. [25], galactosylated poly(ethylene glycol)-PEI showed 2-fold higher transfection efficiency than unmodified PEI.
Recently, we developed a series of phosphorus containing polymeric gene carriers with phosphoester linkage in the backbone [26], [27]. The unique characteristic of the pentavalency of the phosphorus atom makes it possible to conjugate functional groups in its side chains, including charged groups through a phosphate or phosphoramide bond, categorized into polyphosphoester and polyphosphoramidate, respectively. Both polyphosphoesters and polyphosphoramidates have demonstrated marked capabilities for DNA compaction and protection. Previous results have shown that polyphosphoester [28], [29] and polyphosphoramidate [30] with primary amino group side chains exhibit higher transfection efficiencies than those that carry secondary, tertiary or quaternary amino group side chains [30]. Polyphosphoramidate gene carriers bearing primary amino side chains with branching spacers are 7- to 10-fold more efficient than that with linear spacers (Fig. 1). Among all polyphosphoramidates with primary amino groups, those with N,N-bis (aminopropyl) amino side chains, for example, PPA-DPA (Fig. 1), showed similar transfection efficiency as PEI at a charge ratio of 10, but much lowered cytotoxicity in cell line. The LD50 of PPA-DPA is four times higher than PEI [31]. These results have motivated us to explore further improvement on transfection and biocompatibility of PPA-DPA (hereafter called PPA for short) based on the ligand conjugation approach.
In this study, we have synthesized three galactose-bearing carriers, Gal-PPAs, with different degrees of substitutions (6.5%, 12.5% and 21.8%) as hepatocyte-targeted gene carriers, aiming to improve gene transfer efficiency to the liver. We also explored two different schemes in preparing galactosylated PPA/DNA nanoparticles, taking advantage of the high DNA compaction capacity of PPA-DPA carrier. These two types of nanoparticles, namely, Gal-PPA/DNA binary nanoparticles and Gal-PPA/DNA/PPA ternary nanoparticles, were characterized for their physicochemical properties, cytotoxicity and transfection efficiency in cell lines and primary rat hepatocytes. The effects of formulation scheme, N/P ratio and the galactosylation degree on transfection efficiency of the particles were investigated.
Section snippets
Materials
Chloroform, benzene (Merck, Germany) and N,N-dimethylformamide (DMF) (Aldrich Chemical, Milwaukee, WI) were purified according to the typical procedures [32]. 4-Methyl-2-oxo-2-hydro-1,3,2-dioxaphospholane was prepared according to the method reported by Lucas et al. [33]. N1,N9-Bis(trifluoroacetyl) dipropyltriamine trifluoroacetate was synthesized following the procedure reported by O'Sullivan et al. [34]. Triisobutylaluminum (TCI, Tokyo, Japan) and triethylamine (99.5%, Aldrich) were used as
Synthesis of Gal-PPAs with different ligand substitution degrees and Man-PPA
We have synthesized a series of polyphosphoramidate (PPA) carriers with different side chains on the same polyphosphoester backbone. These polymers (structures are shown in Fig. 1) were derived from the same precursor polymer, namely poly(4-methyl-2-oxo-2-hydro-1,3,2-dioxaphospholane), which was obtained by ring opening polymerization of a cyclic monomer, 4-methyl-2-oxo-2-hydro-1,3,2-dioaphospholane [36]. PPA-DPA was chosen as a model for galactosylation because it is among the most efficient
Conclusions
Galactosylation of polyphosphoramidates significantly affects physiochemical properties of PPA/DNA nanoparticles. Galactosylated PPAs showed lower DNA compaction capacity than unmodified PPA-DPA and resulted in reduced stability and larger particle size for the binary Gal-PPA/DNA nanoparticles. DNA compaction capacity of Gal-PPA reduced as the galactosylation degree increased. Although Gal-PPAs exhibited lower cytotoxicity compared to PPA-DPA, and Gal-PPA/DNA binary particles efficiently
Acknowledgements
This work is supported by Agency for Science, Technology and Research (A*STAR) of Singapore and Division of Johns Hopkins in Singapore.
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