Elsevier

Bioorganic & Medicinal Chemistry

Volume 19, Issue 21, 1 November 2011, Pages 6167-6173
Bioorganic & Medicinal Chemistry

‘Click’ synthesis of dextran macrostructures for combinatorial-designed self-assembled nanoparticles encapsulating diverse anticancer therapeutics

https://doi.org/10.1016/j.bmc.2011.09.024Get rights and content

Abstract

With the non-specific toxicity of anticancer drugs to healthy tissues upon systemic administration, formulations capable of enhanced selectivity in delivery to the tumor mass and cells are highly desirable. Based on the diversity of the drug payloads, we have investigated a combinatorial-designed strategy where the nano-sized formulations are tailored based on the physicochemical properties of the drug and the delivery needs. Individually functionalized C2 to C12 lipid-, thiol-, and poly(ethylene glycol) (PEG)-modified dextran derivatives were synthesized via ‘click’ chemistry from O-pentynyl dextran and relevant azides. These functionalized dextrans in combination with anticancer drugs form nanoparticles by self-assembling in aqueous medium having PEG surface functionalization and intermolecular disulfide bonds. Using anticancer drugs with log P values ranging from −0.5 to 3.0, the optimized nanoparticles formulations were evaluated for preliminary cellular delivery and cytotoxic effects in SKOV3 human ovarian adenocarcinoma cells. The results show that with the appropriate selection of lipid-modified dextran, one can effectively tailor the self-assembled nano-formulation for intended therapeutic payload.

Graphical abstract

Schematic illustration for combinatorial approach in designing nanoparticle assemblies using C2 to C12 lipid-modified, thiol-modified, and poly(ethylene glycol) (PEG)-modified dextrans.

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Introduction

Since the discovery of nitrogen mustard and folate antagonists in 1940’s, chemotherapy has become one of the main arsenals against the war on cancer.1 Although the discovery of novel chemotherapeutic agents has led to significant excitement, one of the major challenges of cancer chemotherapy is the lack of specificity of the drugs against tumor cells. Majority of chemotherapeutic agents inhibit cellular proliferation and, as such, do not discriminate between healthy and neoplastic cells. In addition to the toxicity, poor bioavailability and short residence of systemic chemotherapy is also associated with the development of multidrug resistance (MDR) in cancer. Systemic delivery of anticancer agents that can achieve tumor specificity is highly desirable.

In an attempt to circumvent these limitations and improve systemic anticancer therapy, tremendous research efforts have been concentrated on the development of drug delivery systems, such as nanoparticles.2 Polymeric materials, in particular, play a significant role as drug carriers and therapeutic agents can be either physically incorporated into a polymeric matrix or covalently bound to the polymer backbone.3 The drug carrier systems, such as encapsulated polymeric nanoparticles,4 emulsions,5 micelles,3 liposomes,6 have emerged as promising approaches in anticancer treatment with major advantages. The preferential drug localization at target sites through the ‘enhanced permeability and retention (EPR)’ effect and lower distribution in healthy tissues and capacity to deliver hydrophobic drugs, high drug loading, and control drug release rate7, 8 are among these advantages. With the United States Food and Drug Administration approval of albumin-taxol nanoparticles (Abraxane®),9 doxorubicin long-circulating liposomes (Doxil®),10 and a formulation of rapamycin encapsulated in microemulsion system (Rapamune®),11 the development of nanoscale delivery systems for other drugs with the aim of targeting drug more onto the cancer cells and less onto healthy tissues is needed.

Synthetic and natural polymeric materials used for preparing drug delivery systems should be biocompatible such as poly(epsilon-caprolactone), poly(d,l-lactide-co-glycolide), polysaccharides, and proteins. Because of their biocompatibility, biodegradability, and cell surface recognition sites, polysaccharides are a popular class of material among them.12 Also polysaccharides, such as dextran, chitosan, and cellulose, have a large number of reactive hydroxyl groups and variable molecular weight, contributing to their structural diversity and property for intended applications. Dextran is composed of α-(1→6) and partly α-(1→3) linked d-glucose units with varying branches depending on the dextran-producing bacterial strain and it has been used clinically for more than five decades as plasma volume expansion, peripheral flow promotion, and antithrombolytic agents.13 Dextran has no surface charge, providing additional advantage for a drug delivery system as the systems without surface charge could reduce plasma protein adsorption and increase the rate of non-specific cellular uptake.14 Due to the presence of high amount of hydroxyl groups facilitating the introduction of drugs into the polymer backbone, Dextran has been functionalized with various pharmaceutical agents, like naproxen,15 daunorubicin,16 mitomycin C,17 and cisplatin18 as efficient prodrugs. Dextran is fully water-soluble and hydrophobically modified dextran forms micelles which can be used to entrap drug. Recently, Susa et al.19 reported the use of a lipid-modified dextran-based polymeric nanosystem for doxorubicin loading and small interfering RNA delivery in tumor cells.20 This nanosystem showed pronounced antiproliferative effects against osteosarcoma cell lines and had potential for reversing MDR in osteosarcoma.

However, due to the fact that many newer generations of anticancer agents have varying degrees of physicochemical properties, such as molecular weight, charge, hydrophobicity, and intracellular target, there is a need to develop a versatile platform of nanoparticles that can encapsulate variety of different types of payloads. In this study, we report the development of a comprehensive and flexible dextran-based polymeric nanoparticle platform that can be customized to encapsulate therapeutic drugs with varying physicochemical properties. Individual functional blocks having (1) lipid chains (C2 to C12) for self-assembly in aqueous solution, (2) thiol groups for intermolecular disulfide crosslinking, and (3) poly(ethylene glycol) (PEG, Mw. 2 kDa) for surface functionalization were synthesized from dextran (40 kDa) with controlled functionalization by ‘click’ chemical conjugation method. With the use of combinatorial-design principles, representative anticancer drugs from the class of anthracyclines, topoisomerase inhibitors, and taxanes having different physicochemical properties were encapsulated using different combination of functional blocks utilizing different encapsulation techniques to develop a library of nanoparticle formulations. The optimized nanoparticle formulations were characterized and evaluated for preliminary cellular delivery and cytotoxic effects in SKOV3 human ovarian adenocarcinoma cells.

Section snippets

Materials

All reagents were purchased from Sigma–Aldrich and used as received without further purification. Dextran from Leuconostoc mesenteroides strain with Mw 40 kDa was purchased from Sigma Chemicals (St. Louis, MO) and used as received. Rhodamine-conjugated PTX was purchased from Natural Pharmaceuticals (Beverley, MA). Cell Titre 96 Aqueous One Solution Proliferation Assay kit was purchased from Promega Corporation (Madison, WI). SKOV3 human ovarian adenocarcinoma cells were purchased from American

‘Click’ synthesis of dextran derivatives (68)

In order for ‘click chemistry’ to be applied to the synthesis of lipid, thiol, and PEG-modified dextrans, dextran needs to contain an alkyne or azide moiety. O-pentynyl dextran (2) was synthesized by etherification of dextran (1) in DMSO with 5-chloro-1-pentyne using MeLi as base. The transformation of O-pentynyl dextran dissolved in H2O with relevant azides forming a 1,4-disubstituted 1,2,3-triazole linker for the covalent attachment of fatty acid chains, PEG chains, and thiol groups to the

Conclusions

Dextran was individually functionalized with lipid, thiol and PEG via a click chemistry methodology. The combined molecules self-assemble into nanoparticles in water, with PEG surface modification and intramolecular disulfide bond formation, making them an interesting novel potential drug delivery system. It has been shown that different therapeutic drugs with different physicochemical properties can be loaded into the nanosystem from a combinatorial approach where encapsulation efficiency and

Acknowledgments

This study was supported by the National Cancer Institute’s Alliance in Nanotechnology for Cancer Platform Partnership grant U01-CA151452. Transmission electron microscopy analysis was performed by Ms. Jing Xu at the Electron Microscopy Center of Northeastern University.

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