Graphene Oxide-PEG-Protocatechuic Acid Nanocomposite Formulation with Improved Anticancer Properties

被引:30
作者
Saifullah, Bullo [1 ,2 ]
Buskaran, Kalaivani [1 ,3 ]
Shaikh, Rabia Baby [4 ]
Barahuie, Farahnaz [5 ]
Fakurazi, Sharida [1 ,3 ]
Moklas, Mohd Aris Mohd [3 ]
Hussein, Mohd Zobir [2 ]
机构
[1] Univ Putra Malaysia, Inst Biosci, Lab Vaccine & Immunotherapeut, Serdang 43400, Selangor, Malaysia
[2] Univ Putra Malaysia, Inst Adv Technol ITMA, Mat Synth & Characterizat Lab, Serdang 43400, Selangor, Malaysia
[3] Univ Putra Malaysia, Fac Med & Hlth Sci, Dept Human Anat, Serdang 43400, Selangor, Malaysia
[4] Sukkur IBA Univ, Educ Dept, Sukkur 65200, Sindh, Pakistan
[5] Univ Sistan & Baluchestan, Fac Ind & Min, Zahedan 98167, Iran
来源
NANOMATERIALS | 2018年 / 8卷 / 10期
关键词
graphene oxide; PEG; cancer; drug delivery; protocatechuic acid; liver cancer; colon cancer; POLYETHYLENE-GLYCOL; FOLATE-RECEPTOR; TARGETED DELIVERY; DRUG-DELIVERY; FOLIC-ACID; CONTROLLED-RELEASE; TUMOR PROMOTION; CANCER-CELLS; NANOMEDICINE; NANOCARRIER;
D O I
10.3390/nano8100820
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The treatment of cancer through chemotherapy is limited by its toxicity to healthy tissues and organs, and its inability to target the cancer site. In this study, we have designed an anticancer nanocomposite delivery system for protocatechuic acid (PCA) using graphene oxide-polyethylene glycol as the nanocarrier, and coated with folic acid (GO-PEG-PCA-FA) for targeting the cancer cells. The designed anticancer delivery system was found to show much better anticancer activity than the free drug PCA against liver cancer HEP-G2 cells and human colon cancer HT-29 cells; at same time, it was found to be less toxic to normal fibroblast 3T3 cells. The folate-coated anticancer delivery system was found to show better activity then the free drug and the uncoated anticancer delivery system. The in vitro release of the PCA was found to be sustained in human physiological pHs, i.e., blood pH 7.4 and intracellular lysosomal pH 4.8. These in vitro findings are highly encouraging for further in vivo evaluation studies.
引用
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页数:15
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