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

被引:735
|
作者
Kanamala, Manju [1 ]
Wilson, William R. [2 ]
Yang, Mimi [1 ]
Palmer, Brian D. [2 ]
Wu, Zimei [1 ]
机构
[1] Univ Auckland, Sch Pharm, Fac Med & Hlth Sci, Auckland 1142, New Zealand
[2] Univ Auckland, Auckland Canc Soc, Fac Med & Hlth Sci, Res Ctr, Auckland 1142, New Zealand
关键词
pH-sensitive nanocarriers; Tumour targeted drug delivery; pH-sensitive bond; Protonation; Intracellular delivery; PEG detachment; CELL-PENETRATING PEPTIDE; INCORPORATING MICELLAR NANOPARTICLE; MEDIATED COMPLEMENT ACTIVATION; FLUORESCENT HPMA COPOLYMERS; SUBSTITUTED VINYL ETHERS; POLYMER NETWORK HYDROGEL; ACID-TRIGGERED RELEASE; PLGA-PEG-PLGA; IN-VIVO; INTRACELLULAR DELIVERY;
D O I
10.1016/j.biomaterials.2016.01.061
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
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.
引用
收藏
页码:152 / 167
页数:16
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