Review Article

Drug Delivery Innovations for Enhancing the Anticancer Potential of Vitamin E Isoforms and Their Derivatives

Table 1

Novel formulations to improve the delivery and anticancer effect of tocopherols alone and in combination with other drugs.

FormulationCancer modelEffectIC50Reference

α-TOS-HDLA549 lung cancer cells in vitro, LL2 mouse lung cancer in vivo High capacity of α-TOS uptake via the SR-BI receptor, inhibition of growth7 μg α-TOS/25 μg HDL-protein/mL medium[59]

α-TOS-TPP+ (MitoVES)T-cell lymphoma, mesothelioma, breast, colorectal, lung, and cervical cancer, neuroblastoma, FVB/N c-neu mice carrying the rat HER-2/neu proto-oncogene, and Balb c mice injected with colorectal HCT116 cellsRobust apoptosis due to mitochondrial targeting of α-TOS and production of ROS, suppression of tumorsMitoVES IC50 ranging from 0.48 to 21 μM depending on the cell line[61]

α-TOS-TPP+ (MitoVES)Mesothelioma cells in vitro and in vivo Mitochondrial destabilization, loss of mitochondrial membrane potential, generation of ROS, destabilization of respiratory supercomplexes, and suppression of mesothelioma growth in nude miceMitoVES IC50 ranging from 0.25 to 2 μM depending on the cell line[63]

TS-EPC-NVsB16-F1 mouse melanoma cells in vitro and in vivo Homogenous cellular uptake, enhanced cytosolic delivery and effective intratumoral distribution, induction of apoptosis in vitro, and suppression of tumor growthN/A[65]

Liposomal formulation of α-TAMMCF-7 or B16F10 cells implanted in the peritoneum of Balb/c mice, transgenic FVB/N c-neu mice bearing spontaneous breast carcinomasInhibition of proliferation of cancer cells in vivo and suppression of breast carcinomas13.3 and 5.2 μM for MCF-4 and B16F10 cells, respectively[69]

Liposomal formulation of α-TEA and 9-NCMouse mammary gland cell line 66 cl-4-GFP in Balb/c miceInhibition of tumor growth and metastasisN/A[70]

Micelle system of α-TOS-CS-PTXMCF-7 cells in vitro, U14 cervical cancer cells in Kunming miceCytotoxicity in vitro, inhibition of tumor growthN/A[74]

Micelle system of α-TOS-CS-PTXHuman ovarian cancer cells in vitro Improved micelle stability and PTX release, increased cytotoxicity110 and 188 ng/mL PTX-loaded micelles modified and unmodified with α-TOS, respectively[75]

Nanoparticle ssPalmE loaded with VEGFRRenal cell carcinoma (OS-RC-2-bearing mice)Successful delivery of VEGFR and significant suppression of tumor growthN/A[77]

High-density lipoprotein (HDL), triphenylphosphonium group (TPP+), TS (α-TOS), egg phosphatidylcholine (EPC), nanovesicle (NV), chitosan (CS), paclitaxel (PTX), and SS-cleavable Proton-Activated Lipid-like Material Vitamin E (ssPalmE).