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Research Articles

Multifunctional magnetic nanoparticles for MRI-guided co-delivery of erlotinib and L-asparaginase to ovarian cancer

, , ORCID Icon, , ORCID Icon & ORCID Icon
Pages 394-408 | Received 18 Mar 2022, Accepted 21 Jun 2022, Published online: 05 Jul 2022

References

  • Abdolahinia, E.D., et al., 2019. Enhanced penetration and cytotoxicity of metformin and collagenase conjugated gold nanoparticles in breast cancer spheroids. Life sciences. 231, 116545.
  • Aghanejad, A., et al., 2014. Radiosynthesis and biodistribution studies of [62Zn/62Cu]-plerixafor complex as a novel in vivo PET generator for chemokine receptor imaging. Journal of radioanalytical and nuclear chemistry, 299 (3), 1635–1644.
  • Aghanejad, A., et al., 2016. Optimized production and quality control of 68Ga-DOTATATE. Iranian journal of nuclear medicine, 24 (1), 29–36.
  • Aithal, A., et al., 2018. MUC16 as a novel target for cancer therapy. Expert opinion on therapeutic targets, 22 (8), 675–686.
  • Ajoolabady, A., et al., 2020. Enzyme-based autophagy in anti-neoplastic management: from molecular mechanisms to clinical therapeutics. Biochimica et biophysica acta - reviews on Cancer, 1874 (1), 188366.
  • Ali, A.A.A., et al., 2016. Erlotinib-conjugated iron oxide nanoparticles as a smart cancer-targeted theranostic probe for MRI. Scientific reports, 6, 36650.
  • Anisuzzaman, A.S.M., et al., 2017. In vitro and in vivo synergistic antitumor activity of the combination of BKM120 and erlotinib in head and neck cancer: mechanism of apoptosis and resistance. Molecular cancer therapeutics, 16 (4), 729–738.
  • Antonella, A., and Magnani, M., 2022. SPIO nanoparticles and magnetic erythrocytes as contrast agents for biomedical and diagnostic applications. Journal of magnetism and magnetic materials, 541, 168520.
  • Asgari, D., Aghanejad, A., and Mojarrad, J.S., 2011. An improved convergent approach for synthesis of erlotinib, a tyrosine kinase inhibitor, via a ring closure reaction of phenyl benzamidine intermediate. Bulletin of the Korean chemical society. 32 (3), 909–914.
  • Barghi, L., et al., 2012. Modified synthesis of erlotinib hydrochloride. Advanced pharmaceutical bulletin, 2 (1), 119–122.
  • Boss, A., et al., 2022. Assessment of iron nanoparticle distribution in mouse models using ultrashort echo-time magnetic resonance imaging. NMR in biomedicine, 35 (6), e4690.
  • Cano, M., et al., 2017. Partial PEGylation of superparamagnetic iron oxide nanoparticles thinly coated with amine-silane as a source of ultrastable tunable nanosystems for biomedical applications. Nanoscale, 9 (2), 812–822.
  • Chou, T.-C., 2006. Theoretical basis, experimental design, and computerized simulation of synergism and antagonism in drug combination studies. Pharmacological reviews, 58 (3), 621–681.
  • Chou, T.C., and Talalay, P., 1981. Generalized equations for the analysis of inhibitions of Michaelis‐Menten and higher‐order kinetic systems with two or more mutually exclusive and nonexclusive inhibitors. European journal of biochemistry, 115 (1), 207–216.
  • Cui, L., Xu, H., and Zhang, Y., 2022. Diagnostic accuracies of the ultrasound and magnetic resonance imaging ADNEX scoring systems for ovarian adnexal mass: systematic review and meta-analysis. Academic radiology, 29 (6), 897–908.
  • Effenberger, F.B., et al., 2017. Economically attractive route for the preparation of high quality magnetic nanoparticles by the thermal decomposition of iron (III) acetylacetonate. Nanotechnology, 28 (11), 115603.
  • Erol, A., Niemira, M., and Krętowski, A.J., 2019. Novel approaches in ovarian cancer research against heterogeneity, late diagnosis, drug resistance, and transcoelomic metastases. International journal of molecular sciences, 20 (11), 2649.
  • Evertsson, M., et al., 2017. Combined magnetomotive ultrasound, PET/CT, and MR imaging of 68 Ga-labelled superparamagnetic iron oxide nanoparticles in rat sentinel lymph nodes in vivo. Scientific reports, 7 (1), 1–9.
  • Foroughi-Nia, B., et al., 2021. Progresses in polymeric nanoparticles for delivery of tyrosine kinase inhibitors. Life sciences. 278, 119642.
  • Foroughi-Nia, B., et al., 2022. AS1411 conjugated magnetic-based poly N-isopropyl acrylamide nanoparticles for delivery of erlotinib to prostate cancer cells. Applied organometallic chemistry, 36 (7), e6691.
  • Garon, E.B., et al., 2018. Randomized phase II study of fulvestrant and erlotinib compared with erlotinib alone in patients with advanced or metastatic non-small cell lung cancer. Lung cancer, 123, 91–98.
  • Giannakouros, P., et al., 2015. MUC16 mucin (CA125) regulates the formation of multicellular aggregates by altering β-catenin signaling. American journal of cancer research, 5 (1), 219–230.
  • He, Y., et al., 2016. Co-delivery of erlotinib and doxorubicin by pH-sensitive charge conversion nanocarrier for synergistic therapy. Journal of controlled release, 229, 80–92.
  • Hejazi, M., et al., 2020. MicroRNA-193a and taxol combination: a new strategy for treatment of colorectal cancer. Journal of cellular biochemistry, 121 (2), 1388–1399.
  • Jabir, M.S., Nayef, U.M., and Kadhim, W.K.A., 2019. Polyethylene glycol-functionalized magnetic (Fe3O4) nanoparticles: a novel DNA-mediated antibacterial agent. Nano biomedicine & engineering, 11 (1), 18–27.
  • Kadkhoda, J., et al., 2021. Advances in antibody nanoconjugates for diagnosis and therapy: a review of recent studies and trends. International journal of biological macromolecules, 185, 664–678.
  • Karimzadeh, I., et al., 2017. Saccharide-coated superparamagnetic Fe3O4 nanoparticles (SPIONs) for biomedical applications: an efficient and scalable route for preparation and in situ surface coating through cathodic electrochemical deposition (CED). Materials letters, 189, 290–294.
  • Khajeh, S., et al., 2018. Phage display selection of fully human antibody fragments to inhibit growth-promoting effects of glycine-extended gastrin 17 on human colorectal cancer cells. Artificial cells, nanomedicine, and biotechnology, 46 (sup2), 1082–1090.
  • Li, H., et al., 2022. Sub-100 nm and ultra-thin hollow Gd2O3 nanospheres for effective magnetic resonance imaging T1 contrast agent. Journal of alloys and compounds, 897, 163190.
  • Loret, N., et al., 2019. The role of epithelial-to-mesenchymal plasticity in ovarian cancer progression and therapy resistance. Cancers, 11 (6), 838.
  • 5 - Mathematical models of drug release. In: M.L. Bruschi, ed. Strategies to modify the drug release from pharmaceutical systems. Amsterdam: Woodhead Publishing, 2015, 63–86.
  • Madariaga, A., Lheureux, S., and Oza, A.M., 2019. Tailoring ovarian cancer treatment: implications of BRCA1/2 mutations. Cancers, 11 (3), 416.
  • Marinca, T., et al., 2016. Mechanosynthesis, structural, thermal and magnetic characteristics of oleic acid coated Fe3O4 nanoparticles. Materials chemistry and physics, 171, 336–345.
  • Mirzaei, A., et al., 2015. Preparation and evaluation of 68Ga-ECC as a PET renal imaging agent. Nuclear medicine and molecular imaging, 49 (3), 208–216.
  • Moffitt, L., et al., 2019. Therapeutic targeting of collective invasion in ovarian cancer. International journal of molecular sciences, 20 (6), 1466.
  • Nabi, P.N., et al., 2021. Mucin-1 conjugated polyamidoamine-based nanoparticles for image-guided delivery of gefitinib to breast cancer. International journal of biological macromolecules, 174, 185–197.
  • Napoletano, C., et al., 2019. Bevacizumab-based chemotherapy triggers immunological effects in responding multi-treated recurrent ovarian cancer patients by favoring the recruitment of effector t cell subsets. Journal of clinical medicine, 8 (3), 380.
  • Panwar, V., et al., 2015. PEGylated magnetic nanoparticles (PEG@ Fe3O4) as cost effective alternative for oxidative cyanation of tertiary amines via CH activation. Applied catalysis A: general, 498, 25–31.
  • Prabha, G., and Raj, V., 2016. Preparation and characterization of polymer nanocomposites coated magnetic nanoparticles for drug delivery applications. Journal of magnetism and magnetic materials, 408, 26–34.
  • Raizer, J., et al., 2016. A phase II study of bevacizumab and erlotinib after radiation and temozolomide in MGMT unmethylated GBM patients. Journal of neuro-oncology, 126 (1), 185–192.
  • Santala, E.E.E., et al., 2021. Antihypertensive drug use and the risk of ovarian cancer death among finnish ovarian cancer patients—a nationwide cohort study. Cancers, 13 (9), 2087.
  • Tarighatnia, A., et al., 2021. Engineering and quantification of bismuth nanoparticles as targeted contrast agent for computed tomography imaging in cellular and animal models. Journal of drug delivery science and technology, 66, 102895.
  • Tarighatnia, A., et al., 2021. Mucin-16 targeted mesoporous nano-system for evaluation of cervical cancerviadual-modal computed tomography and ultrasonography. New journal of chemistry, 45 (40), 18871–18880.
  • Tarighatnia, A., et al., 2022. Recent trends of contrast agents in ultrasound imaging: a review of the classifications and applications. Materials advances, 3 (9), 3726–3741.
  • Verma, A., and Stellacci, F., 2010. Effect of surface properties on nanoparticle–cell interactions. Small, 6 (1), 12–21.
  • Xie, X., et al., 2016. EpCAM aptamer-functionalized mesoporous silica nanoparticles for efficient colon cancer cell-targeted drug delivery. European journal of pharmaceutical sciences, 83, 28–35.
  • Yi, Y., et al., 2017. A smart, photocontrollable drug release nanosystem for multifunctional synergistic cancer therapy. ACS applied materials & interfaces, 9 (7), 5847–5854.

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