Preparation of dual drug-loaded polymer nanoconjugate to enhance treatment efficacy for ovarian cancer cells

被引:0
|
作者
Ozel, Buket [1 ]
Sanlier, Senay [2 ]
Gunduz, Cumhur [1 ]
Gunel, Nur Selvi [1 ]
机构
[1] Ege Univ, Fac Med, Dept Med Biol, TR-35100 Izmir, Turkiye
[2] Ege Univ, Fac Sci, Dept Biochem, Izmir, Turkiye
关键词
Ovarian cancer; Polymer drug nanoconjugate; pH-sensetive bonds; Cabozantinib; Ki16425; VEGF; LPA; ENDOTHELIAL GROWTH-FACTOR; NANOPARTICLES; DELIVERY; DOXORUBICIN; MIGRATION; INVASION; CHITOSAN; PATHWAY;
D O I
10.1016/j.ejpb.2024.114526
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Ovarian cancer is the deadliest gynecological malignancy, representing 2.5 % of all female cancers and accounting for 5 % of female cancer-related fatalities. Despite numerous strategies in its treatment, the disease shows a high recurrence rate and a low survival rate. Consequently, there is a growing focus on targeted therapies in ovarian cancer treatment. It is well-known that VEGFR and LPA pathways undergo alterations in ovarian cancer and stimulate survival, adhesion, migration, invasion, tumor growth and angiogenesis. Cabozantinib (CBZ) is a multi-receptor tyrosine kinase inhibitor that effectively targets MET, VEGFR-1, 2, 3, FLT3, c-KIT, and RET. Ki16425 is a selective inhibitor of LPA receptors 1, 2, and 3. Therefore, targeting LPA receptors and combining with VEGFR inhibitor is a strategic approach for ovarian cancer treatment. In this study, it was aimed to prepare polymer-drug nanoconjugate for both VEGFR and LPAR inhibition. For this, O-(2-Carboxyethyl) polyethylene glycol (PEG5000) 5000 ) which advantages are known in cancer studies, was chosen as the carrier system, and a nanoconjugate containing Ki16425 and CBZ (Ki-PEG-CBZ) was synthesized and its potential was evaluated. Initially, CBZ and Ki16425 were conjugated to the PEG 5000 through pH-sensitive hydrazone and ester bonds. After nanoconjugate characterization, in vitro release and its ovarian cancer treatment potential were evaluated on A2780, OVCAR3 and SKOV3 ovarian cancer cell lines. A nanoconjugate was obtained with a particle size of 169 f 15.23 nm, a zeta potential of-13.5 f 1.21 mV, and a release profile lasting 48 h, containing CBZ and Ki16425 with drug loading efficiencies of 73.71 f 0.53% and 77.72 f 2.51 %, respectively. In vitro studies have demonstrated that Ki-PEG-CBZ is highly effective against ovarian cancer. We suggest that the developed polymer-drug nanoconjugate is an effective and safe nanoconjugate for the treatment of ovarian cancer.
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页数:15
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