From: Nanocarrier cancer therapeutics with functional stimuli-responsive mechanisms
Material | Description of carrier | Material advantage | Specificity | Refs. |
---|---|---|---|---|
CNT | Anti-P-glycoprotein antibody functionalized CNT-doxorubicin | Defeats multidrug resistance | Leukemia cells | [31] |
CNT | Multi-walled CNT decorated with guanidinylated dendritic molecular transporters | Efficient DOX delivery | Prostate cancer cells | [32] |
CNT | PEG-CNT complex | Mitochondrial targeting | Lung cancer cells | [33] |
Layered double hydroxide NPs | Co-delivery of 5-fluorouracil and siRNAs | Prevents drug resistance and enhances cancer treatment | Various cancer cells | [34] |
Layered double hydroxide NPs | Raloxifene intercalated into the interlayer gallery of LDH host | Improves therapeutic efficacy, reduction of adverse side effects | Solid tumors | [35] |
Iron oxide NPs | Phospholipid-PEG-coated superparamagnetic iron oxide NPs | Chemotherapy and hyperthermia treatment | Solid cancers | [36] |
Magnetic NPs | Pluronic F127-anchored iron oxide NPs | Active and passive delivery of hydrophobic drugs | Folate-positive cancer cells | [37] |
Magnetic NPs | Chitosan-coated superparamagnetic iron oxide NPs | Doxorubicin delivery | Ovarian cancer cells | [38] |
Mesoporous silica NPs | Azobenzene-modified mesoporous silica for NIR-triggered anticancer drug delivery | Drug release rate can be controlled by varying the intensity and/or time | Solid tumor | [39] |
Mesoporous silica NPs | Hyaluronic acid-capped mesoporous Silica NPs | Site-selective, controlled-release delivery | MDA-MB-231 and NIH3T3 cells | [40] |
QDs | Riboflavin-tageting graphene quantum dots-PEG-benzofuran | High potency, improved dispersibility | Laryngeal, lung and colorectal cancer cells | [2] |
QDs | Hyaluronic acid/ferrocene (Fc)-anchored nitrogen-doped graphene QDs (Fc-GQD-HA) | Selective binding to CD44 receptors, redox-based drug delivery | Diverse range of cancer cells | [41] |
QDs | Hederagenin anchored black phosphorus QDs encapsulated with platelet membrane | Mono-dispersive capacity, elevated drug-loading | In vivo application | [42] |