Diselenide-Bearing Liposomes for Intracellular Delivery of a Vitamin C Derivative in Cancer Cells
Diselenide-Bearing Liposomes for Intracellular Delivery of a Vitamin C Derivative in Cancer Cells
Van Quy Nguyen(Sungkyunkwan University); 유동길(성균관대학교); 오병훈(성균관대학교); Van Dat Bui(Sungkyunkwan University); 안재윤(성균관대학교); 엄우람(성균관대학교); 박재형(성균관대학교)
29권 5호, 327~330쪽
초록
Vitamin C, which promotes oxidative stress, has emerged as an alternative to conventional chemotherapy for treating cancers. However, owing to its cytotoxicity, vitamin C should be delivered to cells in its oxidized form, dehydroascorbate (DHA). Glutathione (GSH)-responsive nanoparticles (G-NPs) have been prepared as potential carriers of DHA by incorporating diselenide-based amphiphilic lipids into the liposomal membrane. Bare liposomes without diselenide-based lipids were prepared as control NPs; these exhibited particle sizes and surface charges comparable to those of G-NPs. DHA was physically encapsulated in NPs using the dehydrationrehydration method. DHA-loaded G-NPs induced much higher GSH depletion in HT29 colon cancer cells than DHA-loaded controls. Interestingly, DHA-loaded G-NPs significantly increased the intracellular levels of reactive oxygen species, implying enhanced oxidative stress by stimuli-responsive DHA release. Consequently, DHA-loaded G-NPs exhibited significant cytotoxicity against HT29 colon cancer cells. Overall, G-NPs might serve as potential carriers for intracellular delivery of DHA during cancer treatment.
Abstract
Vitamin C, which promotes oxidative stress, has emerged as an alternative to conventional chemotherapy for treating cancers. However, owing to its cytotoxicity, vitamin C should be delivered to cells in its oxidized form, dehydroascorbate (DHA). Glutathione (GSH)-responsive nanoparticles (G-NPs) have been prepared as potential carriers of DHA by incorporating diselenide-based amphiphilic lipids into the liposomal membrane. Bare liposomes without diselenide-based lipids were prepared as control NPs; these exhibited particle sizes and surface charges comparable to those of G-NPs. DHA was physically encapsulated in NPs using the dehydrationrehydration method. DHA-loaded G-NPs induced much higher GSH depletion in HT29 colon cancer cells than DHA-loaded controls. Interestingly, DHA-loaded G-NPs significantly increased the intracellular levels of reactive oxygen species, implying enhanced oxidative stress by stimuli-responsive DHA release. Consequently, DHA-loaded G-NPs exhibited significant cytotoxicity against HT29 colon cancer cells. Overall, G-NPs might serve as potential carriers for intracellular delivery of DHA during cancer treatment.
- 발행기관:
- 한국고분자학회
- 분류:
- 고분자공학