Photochemical mechanisms of light-triggered release from nanocarriers

被引:402
作者
Fomina, Nadezda [1 ]
Sankaranarayanan, Jagadis [1 ]
Almutairi, Adah [1 ]
机构
[1] Univ Calif San Diego, Skaggs Sch Pharm & Pharmaceut Sci, Dept Mat Sci & Engn, Dept NanoEngn, La Jolla, CA 92093 USA
关键词
Photochemical; Triggered release; Light; Near infrared; Nanocarriers; Nanoparticles; NEAR-INFRARED LIGHT; PHOTO-CROSS-LINKING; PHOTOSENSITIVE LIPOSOMES; GOLD NANOPARTICLES; SOLUTE RELEASE; DRUG-RELEASE; SIZE-CHANGE; DELIVERY; ABSORPTION; ASSEMBLIES;
D O I
10.1016/j.addr.2012.02.006
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Over the last three decades, a handful of photochemical mechanisms have been applied to a large number of nanoscale assemblies that encapsulate a payload to afford spatio-temporal and remote control over activity of the encapsulated payload. Many of these systems are designed with an eye towards biomedical applications, as spatio-temporal and remote control of bioactivity would advance research and clinical practice. This review covers five underlying photochemical mechanisms that, govern the activity of the majority of photoresponsive nanocarriers: 1. photo driven isomerization and oxidation, 2. surface plasmon absorption and photothermal effects, 3. photo driven hydrophobicity changes, 4. photo driven polymer backbone fragmentation and 5. photo driven de-crosslinking. The ways in which these mechanisms have been incorporated into nanocarriers and how they affect release are detailed, as well as the advantages and disadvantages of each system. (c) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:1005 / 1020
页数:16
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