Abstract

Paclitaxel (PTX) is used as a major antitumor agent for the treatment of recurrent and metastatic breast cancer. For the clinical application of PTX, it needs to be dissolved in an oil/detergent-based solvent due to its poor solubility in an aqueous medium. However, the formulation often causes undesirable complications including hypersensitivity reactions and limited tumor distribution, resulting in a lower dose-dependent antitumor effect. Herein, we introduce a facile and oil-free method to prepare albumin-based PTX nanoparticles for efficient systemic cancer therapy using a conjugate of human serum albumin (HSA) and poly(ethyleneglycol) (PEG). PTX were efficiently incorporated in the self-assembled HSA-PEG nanoparticles (HSA-PEG/PTX) using a simple film casting and re-hydration procedure without additional processes such as application of high pressure/shear or chemical crosslinking. The spherical HSA-PEG nanoparticle with a hydrodynamic diameter of ca. 280 nm mediates efficient cellular delivery, leading to comparable or even higher cytotoxicity in various breast cancer cells than that of the commercially available Abraxane®. When systemically administered in a mouse xenograft model for human breast cancer, the HSA-PEG-based nanoparticle formulation exhibited an extended systemic circulation for more than 96 h and enhanced intratumoral accumulation, resulting in a remarkable anticancer effect and prolonged survival of the animals.

Highlights

  • Self-assembled nanostructures have attracted much attention in the field of drug delivery due to their ability to be targeted to the site of disease, improving drug pharmacokinetics and enhancing the cellular uptake (Grzelczak et al, 2010)

  • human serum albumin (HSA)-based nanoparticles can accumulate in solid tumors via the enhanced permeation and retention (EPR) effect and the interaction with 60-kDa glycoprotein receptors that are preferentially expressed on tumors (Desai et al, 2006)

  • The results suggest that the HSA-PEG-based nanoparticles can be used as a simple, cost-effective, and green theranostic platform with reduced formulation-mediated toxicity for various poorly water-soluble drugs and hydrophobic imaging probes

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Summary

Introduction

Self-assembled nanostructures have attracted much attention in the field of drug delivery due to their ability to be targeted to the site of disease, improving drug pharmacokinetics and enhancing the cellular uptake (Grzelczak et al, 2010). The binding of HSA to therapeutic agents, such as taxanes, sulfonamides, penicillin, and benzodiazepines, can greatly affect the biodistribution, bioactivity and metabolism of the drugs (Carter & Ho, 1994; Curry et al, 1998; Neumann et al, 2010). Owing to these features, HSA has been widely employed as a biomaterial with clinically proven safety for designing drug delivery systems (Geny et al, 1993; Sparreboom et al, 2005; Yang et al, 2007; Kratz, 2008). HSA-based nanoparticles can accumulate in solid tumors via the enhanced permeation and retention (EPR) effect and the interaction with 60-kDa glycoprotein (gp60) receptors that are preferentially expressed on tumors (Desai et al, 2006)

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