4.8 Review

Mechanisms and biomaterials in pH-responsive tumour targeted drug delivery: A review

Journal

BIOMATERIALS
Volume 85, Issue -, Pages 152-167

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2016.01.061

Keywords

pH-sensitive nanocarriers; Tumour targeted drug delivery; pH-sensitive bond; Protonation; Intracellular delivery; PEG detachment

Funding

  1. Marsden Fund by the Royal Society of New Zealand [UOA1201]

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As the mainstay in the treatment of various cancers, chemotherapy plays a vital role, but still faces many challenges, such as poor tumour selectivity and multidrug resistance (MDR). Targeted drug delivery using nanotechnology has provided a new strategy for addressing the limitations of the conventional chemotherapy. In the last decade, the volume of research published in this area has increased tremendously, especially with functional nano drug delivery systems (nanocarriers). Coupling a specific stimuli triggered drug release mechanism with these delivery systems is one of the most prevalent approaches for improving therapeutic outcomes. Among the various stimuli, pH triggered delivery is regarded as the most general strategy, targeting the acidic extracellular microenvironment and intracellular organelles of solid tumours. In this review, we discuss recent advances in the development of pH-sensitive nanocarriers for tumour-targeted drug delivery. The review focuses on the chemical design of pH-sensitive biomaterials, which are used to fabricate nanocarriers for extracellular and/or intracellular tumour site-specific drug release. The pH-responsive biomaterials bring forth conformational changes in these nanocarriers through various mechanisms such as protonation, charge reversal or cleavage of a chemical bond, facilitating tumour specific cell uptake or drug release. A greater understanding of these mechanisms will help to design more efficient drug delivery systems to address the challenges encountered in conventional chemotherapy. (C) 2016 Elsevier Ltd. All rights reserved.

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