Light-sensitive liposomes |
UV, near infrared or visible light irradiation, |
Modification of fatty acyl chains of the phospholipids with light-sensitive functional groups and the resulting phospholipids have yielded photoactivable liposomes |
Controlling time, exposure, wavelength, and intensity |
[131, 132] |
Thermosensitive (temperature-sensitive) liposomes |
Radiofrequency or microwave ablation |
Lipids with a transition temperature of 40–45 °C, such as DPPC, have been employed to make these liposomes |
Drug release at high-temperature sites |
[133, 134, 135, 136] |
Redox-sensitive liposomes |
Reactive oxygen species (ROS) peroxides, hydroxyl radicals, singlet oxygen |
Depends on the redox potential difference between the intracellular reducing space and oxidizing extracellular space that occur during biological activities. |
ROS leads to high concentration levels of glutathione (GSH) in tumor cells cleaving the liposomal formulations |
[137, 138] |
Enzyme-responsive liposomes |
Protease, amidase, and esterase enzymes |
Based on amides or esters hydrolysis by protease or esterase enzymes release loaded drugs. |
Decreases the adverse side effects of toxic drugs and enable encapsulation of prodrugs |
[139, 140, 141] |
pH-sensitive liposomes |
pH change |
Cholesteryl hemisuccinate (CHEMS) and 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine (DOPE), were used to prepare pH-sensitive liposomes |
Liposomes with pH-dependent release features |
[142, 143, 144] |