2017
DOI: 10.1016/j.jconrel.2017.06.029
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Near-infrared light-triggered drug release from a multiple lipid carrier complex using an all-in-one strategy

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Cited by 62 publications
(38 citation statements)
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“…The behavior of light‐induced liposome membrane permeability could occur through several possible pathways, including photoinduced oxidation/isomerization/decomposition/crosslinking of membrane components, local heating induced increase of lipid motions and thus membrane permeabilities, etc . It was demonstrated that NIR light (808 nm, 1 W cm −2 , 4 min) irradiation of a hydrophobic IR780 dye and hydrophilic anti‐metastatic drug AMD3100 coloaded liposome results in release of AMD3100, which then binds the chemokine receptor 4 (CXCR4) receptor of cancer cell membrane, leading to effective inhibition of cancer cell migration and metastasis . CXCR4 is known to be able to inhibit migration and metastasis of breast cancer cells.…”
Section: Photodynamic Therapymentioning
confidence: 99%
“…The behavior of light‐induced liposome membrane permeability could occur through several possible pathways, including photoinduced oxidation/isomerization/decomposition/crosslinking of membrane components, local heating induced increase of lipid motions and thus membrane permeabilities, etc . It was demonstrated that NIR light (808 nm, 1 W cm −2 , 4 min) irradiation of a hydrophobic IR780 dye and hydrophilic anti‐metastatic drug AMD3100 coloaded liposome results in release of AMD3100, which then binds the chemokine receptor 4 (CXCR4) receptor of cancer cell membrane, leading to effective inhibition of cancer cell migration and metastasis . CXCR4 is known to be able to inhibit migration and metastasis of breast cancer cells.…”
Section: Photodynamic Therapymentioning
confidence: 99%
“…These nanoparticles were typically formed by the physical addition of small molecular CXCR4 inhibitor like AMD3100 to the formulation. AMD3100 can act as both cancer targeting ligand for improved nanoparticles delivery and CXCR4 antagonism for cancer therapy (Li, Yang, et al, ; Liu et al, ; Zhang et al, ). Chen's group reported a series of CXCR4‐targeted nanoparticles with the ability to deliver both functional siRNA and small drugs for the treatment of liver cancer and liver fibrosis (Gao et al, ; Liu et al, ; Sung et al, ).…”
Section: Cxcr4‐targeted Nanoparticlesmentioning
confidence: 99%
“…IR780 iodide, which converts NIR (750-1000 nm) laser energy into heat aer irradiation, is a lipophilic heptamethine NIR absorber with a characteristic absorption peak at 780 nm. [24][25][26][27] It was found to have extraordinary intrinsic tumor targeting properties without further modication. 28 However, IR780 iodide has several limitations, including poor aqueous stability and photostability, which may severely impede its further clinical applications.…”
Section: Introductionmentioning
confidence: 99%
“…28 However, IR780 iodide has several limitations, including poor aqueous stability and photostability, which may severely impede its further clinical applications. 24,29,30 Additionally, the toxicity of IR780 cannot be ignored because of its maximum tolerable dose of 1.5 mg kg À1 in mice. 26,31 To overcome these limitations, some investigators have encapsulated IR780 iodide in various nanoparticles (NPs).…”
Section: Introductionmentioning
confidence: 99%