A magnetic nanoparticle functionalized reduced graphene oxide-based drug carrier system for a chemo-photodynamic cancer therapy

被引:39
|
作者
Vinothini, Kandasamy [1 ,2 ]
Rajendran, Naresh Kumar [3 ]
Mariappan, Rajan [2 ]
Andy, Ramu [1 ]
Marraiki, Nataj [4 ]
Elgorban, Abdallah M. [4 ,5 ]
机构
[1] Madurai Kamaraj Univ, Sch Chem, Dept Inorgan Chem, Madurai 625021, Tamil Nadu, India
[2] Madurai Kamaraj Univ, Sch Chem, Dept Nat Prod Chem, Biomat Med Chem Lab, Madurai 625021, Tamil Nadu, India
[3] Univ Johannesburg, Fac Hlth Sci, Laser Res Ctr, ZA-2028 Johannesburg, South Africa
[4] King Saud Univ, Coll Sci, Dept Bot & Microbiol, POB 2455, Riyadh 11451, Saudi Arabia
[5] King Saud Univ, Ctr Excellence Biotechnol Res, POB 2455, Riyadh 11451, Saudi Arabia
关键词
LACTATE-DEHYDROGENASE; DELIVERY; CELLS; CYCLODEXTRIN; NANOCARRIER; RELEASE;
D O I
10.1039/d0nj00049c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Combination therapy has gained increasing attention for the treatment of cancer. In this study, a versatile reduced graphene oxide (rGO)-based drug delivery system (DDS) was developed for chemophotodynamic cancer therapy. The reduced graphene oxide surface was decorated with magnetic nanoparticles (MNPs) and camptothecin (CPT) chemo drug. The photosensitizer 4-hydroxycoumarin (4-HC) was cross-linked with rGO via an allylamine (AA) linker. The CPT-loaded MrGO-AA-g-4-HC was characterized via FT-IR, SEM, HR-TEM, XRD, AFM, and DLS techniques. The CPT-loaded nanocarrier exhibits a pH-sensitive drug-release behavior and it was investigated using a UV-Visible spectrophotometer at the lambda(max) value of 263 nm for CPT and 353 nm for 4-HC. The cytotoxic effects of CPT and 4-HC loaded carriers show higher toxicity effect against the human breast cancer cell line (MCF-7) compared with the normal fibroblast cell line (WS-1). The 365 nm laser irradiation of 20 mW cm(-2) for 3 min on CPT-loaded MrGO-AA-g-4-HC could be efficacious in absorbing the UV-light for 4-HC excitation to produce a higher amount of reactive oxygen species (ROS) for higher inhibition towards MCF-7 cells; the combined treatment exhibits outstanding cell apoptosis that leads to cell death. In vivo anti-tumor effects established that CPT-loaded MrGO-AA-g-4-HC could exhibit excellent synergistic anti-tumor efficiency, which is better than monotherapy. Thus, this work presents a new nano-platform for the loading of both chemo drug and photosensitizers with high loading ability for the synergistic effect of chemophotodynamic cancer treatment.
引用
收藏
页码:5265 / 5277
页数:13
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