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Improved pH-Responsive Release of Phenformin from Low-Defect Graphene Compared to Graphene Oxide
被引:7
|作者:
Alhourani, Abdelnour
[1
]
Forde, Jan-Lukas
[2
,3
]
Eichacker, Lutz Andreas
[1
]
Herfindal, Lars
[2
]
Hagland, Hanne Roland
[1
]
机构:
[1] Univ Stavanger, Dept Chem Biosci & Environm Technol, N-4021 Stavanger, Norway
[2] Univ Bergen, Ctr Pharm, Dept Clin Sci, N-5007 Bergen, Norway
[3] Haukeland Hosp, Dept Internal Med, N-5021 Bergen, Norway
来源:
关键词:
DRUG-DELIVERY;
NANO-GRAPHENE;
IN-VITRO;
SIZE;
EFFICIENCY;
NANOPARTICLES;
BIGUANIDES;
STABILITY;
D O I:
10.1021/acsomega.1c03283
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Graphene-based drug carriers provide a promising addition to current cancer drug delivery options. Increased accessibility of high-quality graphene made by plasma-enhanced chemical vapor deposition (PE-CVD) makes it an attractive material to revisit in comparison to the widely studied graphene oxide (GO) in drug delivery. Here, we show the potential of repurposing the metabolic drug phenformin for cancer treatment in terms of stability, binding, and pH-responsive release. Using covalent attachment of poly(ethylene glycol) (PEG) onto pristine (PE-CVD) graphene, we show that PEG stabilized graphene nanosheets (PGNS) are stable in aqueous solutions and exhibit higher binding affinity toward phenformin than GO. Moreover, we experimentally demonstrate an improved drug release from PGNS than GO at pH levels lower than physiological conditions, yet comparable to that found in tumor microenvironments.
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页码:24619 / 24629
页数:11
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