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Original Articles

Designing siRNA-conjugated plant oil-based nanoparticles for gene silencing and cancer therapy

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Pages 635-648 | Received 11 May 2019, Accepted 04 Sep 2019, Published online: 19 Sep 2019

References

  • Allı, A., et al., 2014. One-pot synthesis of poly(linoleic acid)-g-poly(styrene)-g-poly(ecaprolactone) graft copolymers. Journal of the American oil chemists' society, 91(5), 849–858.
  • Allı, A., and Hazer, B., 2008. Poly(N-isopropylacrylamide) thermoresponsive cross-linked conjugates containing polymeric soybean oil and/or polypropylene glycol. European polymer journal, 44(6), 1701–1713.
  • Allı, A., and Hazer, B., 2011. Synthesis and characterization of poly(N-isopropyl acryl amide)-g poly(linoleic acid)/poly(linolenic acid) graft copolymers. Journal of the American oil chemists' society, 88, 255–263.
  • Alli, S., et al., 2012. Hyperbranched homo and thermoresponsive graft copolymers by using ATRP-macromonomer initiators. Applied polymer science, 124, 536–548.
  • Anitha, A., et al., 2014. Combinatorial anticancer effects of curcumin and 5-fluorouracil loaded thiolated chitosan nanoparticles towards colon cancer treatment. Biochimica et biophysica acta (BBA), 1840(9), 2730–2743.
  • Benoit, S., and Boutin, M.E., 2012. Controlling mesenchymal stem cell gene expression using polymer-mediated delivery of siRNA. Biomacromolecules, 13(11), 3841–3849.
  • Bertrand, J.R., et al., 2002. Comparison of antisense oligonucleotides and siRNAs in cell culture and in vivo. Biochemical and biophysical research communications, 296(4), 1000–1004.
  • Cakmakli, B., et al., 2004. Synthesis and characterization of polymeric linseed oil grafted methyl methacrylate or styrene. Macromolecular bioscience, 4(7), 649–655.
  • Cakmakli, B., et al., 2005. Synthesis and characterization of polymeric soybean oil-g-methyl methacrylate (and n-butyl methacrylate) graft copolymers: biocompatibility and bacterial adhesion. Biomacromolecules, 6(3), 1750–1758.
  • Cakmakli, B., et al., 2007. PMMA-multigraft copolymers derived from linseed oil, soybean oil, and linoleic acid: protein adsorption and bacterial adherence. Journal of the American oil chemists' society, 84, 73–81.
  • Cakmakli, B., et al., 2007. Polymeric linoleic acid‐polyolefin conjugates: cell adhesion and biocompatibility. Journal of the American oil chemists' society, 84, 73–81.
  • Cakmakli, B., et al., 2013. DNA adsorption and dynamic mechanical analysis of polymeric oil/oil acid copolymers. Journal of polymer research, 20, 93.
  • Chevalier, M.T., et al., 2017. Non-covalently coated biopolymeric nanoparticles for improved tamoxifen delivery. European polymer journal, 95, 348–357.
  • Clifford, A., et al., 2019. Biomimetic modification of poly-l-lysine and electrodeposition of nanocomposite coatings for orthopaedic applications. Colloids and surfaces B: biointerfaces, 176, 115–121.
  • Cohen-Sela, E., et al., 2009. A new double emulsion solvent diffusion technique for encapsulating hydrophilic molecules in PLGA nanoparticles. Journal of controlled release, 133(2), 90–95.
  • Convertine, A.J., et al., 2009. Development of a novel endosomolytic diblock copolymer for siRNA delivery. Journal of controlled release, 133(3), 221–229.
  • Desai, M.P., et al., 1997. The mechanism of uptake of biodegradable microparticles in Caco-2 cells is size dependent. Pharmaceutical research, 14(11), 1568–1573.
  • Farhood, H., et al., 1992. Effect of cationic cholesterol derivatives on gene transfer and protein kinase C activity. Biochimica et biophysica acta, 1111(2), 239–246.
  • Felgner, J.H., et al., 1994. Enhanced gene delivery and mechanism studies with a novel series of cationic lipid formulations. Journal of biological chemistry, 269(4), 2550–2561.
  • Guo, P., et al., 2010. Engineering RNA for targeted siRNA delivery and medical application. Advanced drug delivery reviews, 62(6), 650–666.
  • Heyes, J., Palmer, L., et al., 2005. Cationic lipid saturation influences intracellular delivery of encapsulated nucleic acids. Journal of controlled release, 107(2), 276–287.
  • İnce, O., et al., 2016. Synthesis and characterization of novel rod-coil (tadpole) poly(linoleic acid) based graft copolymers. Journal of polymer research, 23, 5.
  • Jere, D., et al., 2009. Chitosan-graft-polyethylenimine for Akt1 siRNA delivery to lung cancer cells. International journal of pharmaceutics, 378(1-2), 194–200.
  • Kachalaki, S., et al., 2015. Reversal of chemoresistance with small interference RNA (siRNA) in etoposide resistant acute myeloid leukemia cells (HL-60). Biomedicine & pharmacotherapy, 75, 100–104.
  • Kano, A., et al., 2011. Grafting of poly(ethylene glycol) to poly-lysine augments its lifetime in blood circulation and accumulation in tumors without loss of the ability to associate with siRNA. Journal of controlled release: official journal of the controlled release society, 149(1), 2–7.
  • Khoee, S., and Hossainzadeh, M.T., 2010. Effect of O/S/W process parameters on 17β-EV loaded nanoparticles properties. Colloids and surfaces B: biointerfaces, 75(1), 133–140.
  • Kilicay, E., et al., 2011. Acetylsalicylic acid loading and release studies of the PMMA-g-polymeric oils/oily acids micro and nanospheres. Journal of applied polymer science, 119, 1610–1618.
  • Kim, S.H., et al., 2008. Local and systemic delivery of VEGF siRNA using polyelectrolyte complex micelles for effective treatment of cancer. Journal of controlled release, 129(2), 107–116.
  • Lee, S.J., et al., 2016. Delivery strategies and potential targets for siRNA in major cancer types. Advanced drug delivery reviews, 104, 2–15.
  • Legendre, J.Y., and Szoka, F.C., 1992. Delivery of plasmid DNA into mammalian-cell lines using ph-sensitive liposomes – comparison with cationic liposomes. Pharmaceutical research, 09(10), 1235–1242.
  • Leng, Q., et al., 2007. Histidine-lysine peptides as carriers of nucleic acids. Drug news & perspectives, 20(2), 77–86.
  • Liu, P., et al., 2012. A mPEG-PLGA-b-PLL copolymer carrier for adriamycin and siRNA delivery. Biomaterials, 33(17), 4403–4412.
  • Malcolm, D.W., et al., 2017. Diblock copolymer hydrophobicity facilitates efficient gene silencing and cytocompatible nanoparticle-mediated siRNA delivery to musculoskeletal cell types. Biomacromolecules, 18(11), 3753–3765.
  • Malcolm, D.W., et al., 2018. The effects of biological fluids on colloidal stability and siRNA delivery of a pH-responsive micellar nanoparticle delivery system. ACS nano, 12(1), 187–197.
  • Meyer, M., et al., 2009. Synthesis and biological evaluation of a bioresponsive and endosomolytic siRNA polymer conjugate. Molecular pharmaceutics, 6(3), 752–762.
  • Nag, O.K., and Awasthi, V., 2013. Surface engineering of liposomes for stealth behavior. Pharmaceutics, 5(4), 542–569.
  • Oh, Y.K., and Park, T.G., 2009. siRNA delivery systems for cancer treatment. Advanced drug delivery reviews, 61(10), 850–862.
  • Patil, Y., and Panyam, J., 2009. Polymeric nanoparticles for siRNA delivery and gene silencing. International journal of pharmaceutics, 367(1-2), 195–203.
  • Perez, C., et al., 2001. Poly(lactic acid)-poly(ethylene glycol) nanoparticles as new carriers for the delivery of plasmid DNA. Journal of controlled release, 75(1-2), 211–224.
  • Pittella, F., et al., 2011. Enhanced endosomal escape of siRNA-incorporation hybrid nanoparticles from calcium phosphate and PEG-block charge-conversional polymer for efficienct gene knockdown with negligible cytotoxicity. Biomaterials, 32(11), 3106–3114.
  • Raja, M.A.G., et al., 2015. Stability, intracellular delivery, and release of siRNA from chitosan nanoparticles using different cross-linkers. PloS one, 10(6), e0128963.
  • Reischl, D., and Zimmer, M., 2009. Drug delivery of siRNA therapeutics: potentials and limits of nanosystems. Nanomedicine: nanotechnology, biology, and medicine, 5(1), 8–20.
  • Rizvi, S.A., and Saleh, A.M., 2018. Applications of nanoparticle systems in drug delivery technology. Saudi pharmaceutical journal, 26(1), 64–70.
  • Sato, A., et al., 2007. Polymer brush-stabilized polyplex for a siRNA carrier with long circulatory half-life. Journal of controlled release , 122(3), 209–216.
  • Sato, Y., Hashiba, K., et al., 2019. Understanding structure-activity relationships of pH-sensitive cationic lipids facilitates the rational identification of promising lipid nanoparticles for delivering siRNAs in vivo. Journal of controlled release, 295, 140–152.
  • Singh, R., and Lillard, J.W., Jr., 2009. Nanoparticle-based targeted drug delivery. Experimental and molecular pathology, 86(3), 215–223.
  • Song, K.C., et al., 2006. The effect of type of organic phase solvents on the particle size of poly(d,l-lactideco-glycolide) nanoparticles. Colloids and surfaces A: physicochemical and engineering aspects, 276(1-3), 162–167.
  • Tan, S.J., et al., 2016. Engineering nanocarriers for siRNA delivery. Small, 7(7), 841–856.
  • Wang, Y., et al., 2017. Controlled and sustained delivery of siRNA/NPs from hydrogels expedites bone fracture healing. Biomaterials, 139, 127–138.
  • Whitehead, K.A., et al., 2009. Knocking down barriers: advances in siRNA delivery. Nature reviews drug discovery, 8(2), 129.
  • Wu, D., et al., 2016. Ideal and reality: barricade in the delivery of small interfering RNA for cancer therapy. Current pharmaceutical biotechnology, 17(3), 237–247.
  • Xia, C.F., et al., 2007. Intravenous siRNA of brain cancer with receptor targeting and avidin-biotin technology. Pharmaceutical research, 24(12), 2309–2316.
  • Xu, C.-F., et al., 2016. Tumor acidity-sensitive linkage-bridged block copolymer for therapeutic siRNA delivery. Biomaterials, 88, 48–59.
  • Yuan, Y., et al., 2018. Modification of porous PLGA microspheres by poly-l-lysine for use as tissue engineering scaffolds. Colloids and surfaces B: biointerfaces, 161, 162–168.
  • Zhou, X.H., and Huang, L., 1994. DNA transfection mediated by cationic liposomes containing lipopolylysine- characterization and mechanism of action. Biochimica et biophysica acta biomembranes, 1189(2), 195–203.

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