Development of Chitosan-Coated Graphene Oxide and Iron Oxide Nanocomposites for Targeted Delivery of Camptothecin to Liver Cancer Cells

被引:4
作者
Sukumar, Kalpana [1 ]
Bharathi, Muruganantham [2 ]
Hirad, Abdurahman Hajinur [3 ]
Alarfaj, Abdullah A. [3 ]
Hussein-Al-Ali, Samer Hasan [4 ]
Surya, Parthasarathy [5 ]
机构
[1] Saveetha Engn Coll, Dept Phys, Chennai 602105, India
[2] Karpagam Acad Higher Educ, Ctr Drug Discovery, Dept Biochem, Coimbatore 641021, Tamil Nadu, India
[3] King Saud Univ, Coll Sci, Dept Bot & Microbiol, POB 2455, Riyadh 11451, Saudi Arabia
[4] Isra Univ, Fac Sci, Dept Chem, Amman 11622, Jordan
[5] Saveetha Univ, Saveetha Dent Coll & Hosp, Saveetha Inst Med & Tech Sci, Dept Res Analyt, Chennai 600077, Tamil Nadu, India
关键词
Chitosan; Nanocomposite; Drug delivery; Camptothecin; Liver cancer; Apoptosis; DRUG-DELIVERY; HEPATOCELLULAR-CARCINOMA; NANOPARTICLES; MICELLES; ENHANCE; DOXORUBICIN; THERAPY; RELEASE; SYSTEM; BREAST;
D O I
10.1002/cbdv.202401817
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Innovative drug delivery platforms for selective, regulated, and sustained release of anticancer drugs are crucial in cancer treatment. This study presents nanoparticles developed from chitosan (CS), graphene oxide (GO), and magnetite (Fe3O4), and their nanocomposites to enhance the loading and release efficiency of camptothecin (CPT). Nanostructures were characterized using imaging microscopy, FT-IR, and X-ray diffraction, with an average crystallite size of 5.5 nm. Camptothecin binding proportions were 70 % for CS, 81 % for CS@Fe3O4, 58 % for CS@GO, and 74 % for CS@GO/Fe3O4. At pH 5.0, CPT release ratios were 87 %, 80 %, 88 %, and 90 %, respectively, and at pH 7.4, 84 %, 72 %, 89 %, and 87 %. Cytotoxicity was assessed using the MTT assay against HepG2 and SMMC-7721 cancer cells. CPT-CS@GO/Fe3O4 exhibited the highest survival at 5 mu M and 12.5 mu M concentrations, indicating it as the most effective nanocarrier for camptothecin delivery. The study demonstrates CS@GO/Fe3O4 ' s potential as a superior drug delivery system.
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页数:13
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