Layered double hydroxide nanoparticles in gene and drug delivery

被引:243
作者
Ladewig, Katharina [1 ]
Xu, Zhi Ping [1 ]
Lu, Gao Qing [1 ]
机构
[1] Univ Queensland, ARC Ctr Excellence Funct Nanomat, Australian Inst Bioengn & Nanotechnol, St Lucia, Qld 4072, Australia
基金
澳大利亚研究理事会;
关键词
cellular uptake mechanism; gene and drug delivery; layered double hydroxides; nanoparticles; IN-VITRO RELEASE; HYDROTALCITE-LIKE COMPOUND; ANIONIC CLAYS; AMINO-ACIDS; CATALYTIC DECOMPOSITION; CELLULAR UPTAKE; NUCLEOSIDE MONOPHOSPHATES; INTERCALATION CHEMISTRY; SILICA-NANOPARTICLES; POLYTYPE DIVERSITY;
D O I
10.1517/17425240903130585
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Layered double hydroxides (LDHs) have been known for many decades as catalyst and ceramic precursors, traps for anionic pollutants, catalysts and additives for polymers, but their successful synthesis on the nanometer scale a few years ago opened up a whole new field for their application in nanomedicine. The delivery of drugs and other therapeutic/bioactive molecules (e.g., peptides, proteins, nucleic acids) to mammalian cells is an area of research that is of tremendous importance to medicine and provides manifold applications for any new developments in the area of nanotechnology. Among the many different nanoparticles that have been shown to facilitate gene and/or drug delivery, LDH nanoparticles have attracted particular attention owing to their many desirable properties. This review aims to report recent progress in gene and drug delivery using LDH nanoparticles. It summarizes the advantages and disadvantages of using LDH nanoparticles as carriers for nucleic acids and drugs against the general background of bottlenecks that are encountered by cellular delivery systems. It describes further the models that have been proposed for the internalization of LDH nanoparticles into cells so far and discusses the intracellular fate of the particles and their cargo. The authors offer some remarks on how this field of research will progress in the near future and which challenges need to be overcome before LDH nanoparticles can be used in a clinical setting.
引用
收藏
页码:907 / 922
页数:16
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