MicroRNAs (miRNAs) have had a revolutionary impact on cancer research over the recent years. They emerge as important players in tumourigenesis, leading to a paradigm shift in oncology. Ovarian cancer is the leading cause of death among gynaecologic malignancies. Therefore, there is a strong need for prognostic and predictive markers for early diagnosis which helps optimize and personalize treatment. Asymptomatically, ovarian cancer is often diagnosed at advanced and incurable stages. Efficient targeting and sustained release of miRNAs/anti-miRNAs using nanoparticles conjugated with antibodies and/or peptides could reduce the required therapeutic dosage while minimizing systemic and cellular toxicity. Given miRNAs importance in clinical oncology, here we focus on the development of miRNA nanoformulations to achieve enhanced cellular uptake, bioavailability and accumulation at the tumour site. Although many obstacles need to be overcome, miRNA therapy could be a powerful tool for ovarian cancer prevention and treatment. In this review, we discuss about the emerging roles of miRNAs in various aspects of ovarian cancer.
Magnetic nanoparticles have properties that cause to apply them in cancer therapy and vehicles for the delivery of drugs such as 5FU, especially when they are modified with biocompatible copolymers. The aim of this study is to modify superparamagnetic iron oxide nanoparticles (SPIONPs) with PCL-PEG-PCL copolymers and then utilization of these nanoparticles for encapsulation of anticancer drug 5FU. The ring-opening polymerization (ROP) was used for the synthesis of PCL-PEG-PCL copolymer by ε-caprolactone (PCL) and polyethylene glycol (PEG2000). We used the double emulsion method (water/oil/water) to prepare 5FU-encapsulated FeO magnetic nanoparticles modified with PCL-PEG-PCL copolymer. Chemical structure and magnetic properties of 5FU-loaded magnetic-polymer nanoparticles were investigated systematically by employing FT-IR, XRD, VSM and SEM techniques. In vitro release profile of 5FU-loaded NPs was also determined. The results showed that the encapsulation efficiency value for nanoparticles were 90%. Moreover, the release of 5FU is significantly higher at pH 5.8 compared to pH 7.4. Therefore, these nanoparticles have sustained release and can apply for cancer therapy.
The wettability preference of carbonate reservoirs is neutral-wet or oil-wet as the prevailing of hydrocarbon reserves that affects approximately half of the total production of hydrocarbons of the world. Therefore, due to surface wettability of carbonate rocks the notable fraction of oil is held inside their pores in comparison with sandstones. Since shifting the wettability preference toward water-wet system is of great interest, numerous components were used for this purpose. In this experimental research, the wettability alteration of dolomite surface by interacting with a novel nano-surfactant–alkaline fluid has been investigated in order to diminish its adhesion to crude oil droplets. The solutions were prepared by homogenous mixing of nanosilica particles with cetyl trimethyl ammonium bromide and sodium carbonate, respectively, as a cationic surfactant and alkaline agent. The maximum wettability alteration from oil-wet to water system was obtained by employing a mixture of nanoparticles in association with surfactant–alkaline. Then, the fluids were employed in core-surface from detached and attached forms to compare their interfacial effects on saturated thin sections by crude oil and to measure the wettability. In addition, the interfacial tension (IFT) between solutions and crude oil was investigated and the maximum IFT reduction was obtained from nano-surfactant. Finally, all chemical solutions were flooded to the dolomite plugs separately after water flooding in order to evaluate the maximum oil recovery factor acquired by nano-surfactant.
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