Abstract |
Integrating advantages of mitomycin C (MMC)- phospholipid complex for increased drug encapsulation efficiency and reduced premature drug release, DSPE- PEG-folate ( DSPE-PEG-FA) for specific tumor targeting, we reported a simple one-pot self-assembly route to prepare the MMC- phospholipid complex-loaded DSPE-PEG-based nanoparticles (MP-PEG-FA NPs). Both confocal imaging and flow cytometry demonstrated that MMC was distributed into nuclei after cellular uptake and intracellular drug delivery. More importantly, the systemically administered MP-PEG-FA NPs led to increased blood persistence and enhanced tumor accumulation in HeLa tumor-bearing nude mice. This study introduces a simple and effective strategy to design the anticancer drug- phospholipid complex-based targeted drug delivery system for sustained/controlled drug release.
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Authors | Yang Li, Jinyan Lin, Xiangrui Yang, Yanxiu Li, Shichao Wu, Yu Huang, Shefang Ye, Liya Xie, Lizong Dai, Zhenqing Hou |
Journal | ACS applied materials & interfaces
(ACS Appl Mater Interfaces)
Vol. 7
Issue 32
Pg. 17573-81
(Aug 19 2015)
ISSN: 1944-8252 [Electronic] United States |
PMID | 26234408
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antineoplastic Agents
- Drug Carriers
- Phospholipids
- poly(ethylene glycol)-folate
- Polyethylene Glycols
- Mitomycin
- Folic Acid
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Topics |
- Animals
- Antineoplastic Agents
(administration & dosage, chemistry, pharmacokinetics)
- Cell Survival
(drug effects)
- Drug Carriers
(chemistry, metabolism, toxicity)
- Drug Liberation
- Female
- Folic Acid
(analogs & derivatives, chemistry)
- Half-Life
- HeLa Cells
- Humans
- Mice
- Mice, Nude
- Microscopy, Confocal
- Mitomycin
(administration & dosage, chemistry, pharmacokinetics)
- Nanoparticles
(chemistry)
- Phospholipids
(chemistry)
- Polyethylene Glycols
(chemistry)
- Rats
- Tissue Distribution
- Transplantation, Heterologous
- Uterine Cervical Neoplasms
(drug therapy)
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