Lipid-based nanosystems for CD44 targeting in cancer treatment: recent significant advances, ongoing challenges and unmet needs

被引:34
|
作者
Nascimento, Thais Leite [1 ,2 ,3 ]
Hillaireau, Herve [1 ,2 ]
Vergnaud, Juliette [1 ,2 ]
Fattal, Elias [1 ,2 ]
机构
[1] Univ Paris 11, Fac Pharm, Inst Galien Paris Sud, 5 Rue JB Clement, F-92296 Chatenay Malabry, France
[2] CNRS, UMR 8612, 5 Rue JB Clement, F-92296 Chatenay Malabry, France
[3] Minist Educ Brazil, CAPES Fdn, BR-70040020 Brasilia, DF, Brazil
关键词
CD44; grafting density; hyaluronic acid; lipid-based nanoparticles; pharmacokinetics; toxicity; trafficking pathways; LIPOSOME-ENCAPSULATED DOXORUBICIN; INVASIVE FUNGAL-INFECTIONS; CELL-PENETRATING PEPTIDES; OF-THE-ART; HYALURONIC-ACID; AMPHOTERICIN-B; DRUG-DELIVERY; MOLECULAR-WEIGHT; STEM-CELLS; HYALURONAN-CD44; INTERACTIONS;
D O I
10.2217/nnm-2016-5000
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Extensive experimental evidence demonstrates the important role of hyaluronic acid (HA)-CD44 interaction in cell proliferation and migration, inflammation and tumor growth. Taking advantage of this interaction, the design of HA-modified nanocarriers has been investigated for targeting CD44-overexpressing cells with the purpose of delivering drugs to cancer or inflammatory cells. The effect of such modification on targeting efficacy is influenced by several factors. In this review, we focus on the impact of HA-modification on the characteristics of lipid-based nanoparticles. We try to understand how these modifications influence particle physicochemical properties, interaction with CD44 receptors, intracellular trafficking pathways, toxicity, complement/macrophage activation and pharmacokinetics. Our aim is to provide insight in tailoring particle modification by HA in order to design more efficient CD44-targeting lipid nanocarriers.
引用
收藏
页码:1865 / 1887
页数:23
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