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Morphological diversity of block copolymer/lipid chimeric nanostructures

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Abstract

Different in nature biomaterials, which are used for the development of drug delivery nanosystems, could be mixed, in order to produce chimeric/mixed nanostructures. Their morphological characteristics and biophysical properties depend on the degree of association and interactions between the self-assembling biomaterials. For the purpose of this study, chimeric nanosystems composed of phospholipid and amphiphilic diblock copolymers were developed, at different molar ratios. Light scattering and imaging techniques were employed, in order to extract information on the nanostructure physicochemical characteristics and their morphology. Certain morphological characteristics were assessed for vesicle membranes, which are considered to be of paramount importance for their fate inside the physiological environment and their biophysical behavior. Besides vesicles, a variety of structures appeared in the phospholipid/copolymer chimeric systems, depending on both the composition and the concentration of the utilized polymer, declaring the lyotropic effect on the self-assembly of the biomaterials. The size range of most objects, including vesicles, was around 100 nm. Membrane irregularities, such as domains and rafts, are considered as functional biophysical factors, rendering liposomes appropriate artificial models for approaching various diseases on the level of living cell membranes. Such information is of paramount importance for the utilization of chimeric nanostructures in drug delivery and in therapy.

Combining of different in nature biomaterials, e.g. phospholipid and amphiphilic polymer, leads to divergent morphogenesis, concerning both structural conformation and membrane morphology.

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References

  • Andersson M, Hammarstroem L, Edwards K (1995) Effect of bilayer phase transitions on vesicle structure, and its influence on the kinetics of viologen reduction. The J Phys Chem 99:14531–14538

    Article  Google Scholar 

  • Bermudez H, Brannan AK, Hammer DA, Bates FS, Discher DE (2002) Molecular weight dependence of polymersome membrane structure, elasticity, and stability. Macromolecules 35:8203–8208

    Article  Google Scholar 

  • Binder WH, Barragan V, Menger FM (2003) Domains and rafts in lipid membranes. Angew Chem Int Ed 42:5802–5827

    Article  Google Scholar 

  • Bowick MJ, Sknepnek R (2013) Pathways to faceting of vesicles. Soft Matter 9:8088–8095

    Article  Google Scholar 

  • Colombo S, Cun D, Remaut K, Bunker M, Zhang J, Martin-Bertelsen B, Yaghmur A, Braeckmans K, Nielsen HM, Foged C (2015) Mechanistic profiling of the siRNA delivery dynamics of lipid–polymer hybrid nanoparticles. J Control Release 201:22–31

    Article  Google Scholar 

  • Dao TPT, Fernandes F, Er-Rafik M, Salva R, Schmutz M, Brûlet A, Prieto M, Sandre O, Le Meins JF (2015) Phase separation and nanodomain formation in hybrid polymer/lipid vesicles. ACS Macro Lett 4:182–186

    Article  Google Scholar 

  • Dao TPT, Brûlet A, Fernandes F, Er-Rafik M, Ferji K, Schweins R, Chapel JP, Fedorov A, Schmutz M, Prieto M, Sandre O, Le Meins JF (2017) Mixing block copolymers with phospholipids at the nanoscale: from hybrid polymer/lipid wormlike micelles to vesicles presenting lipid nanodomains. Langmuir 33:1705–1715

    Article  Google Scholar 

  • Ickenstein LM, Sandström MC, Mayer LD, Edwards K (2006) Effects of phospholipid hydrolysis on the aggregate structure in DPPC/DSPE-PEG2000 liposome preparations after gel to liquid crystalline phase transition. Biochim Biophys Acta 1758:171–180

    Article  Google Scholar 

  • Itel F, Chami M, Najer A, Lörcher S, Wu D, Dinu IA, Meier W (2014) Molecular organization and dynamics in polymersome membranes: a lateral diffusion study. Macromolecules 47:7588–7596

    Article  Google Scholar 

  • Johnsson M, Edwards K (2003) Liposomes, disks, and spherical micelles: aggregate structure in mixtures of gel phase phosphatidylcholines and poly(ethylene glycol)-phospholipids. Biophys J 85:3839–3847

    Article  Google Scholar 

  • Kaiser N, Kimpfler A, Massing U, Burger AM, Fiebig HH, Brandl M, Schubert R (2003) 5-Fluorouracil in vesicular phospholipid gels for anticancer treatment: entrapment and release properties. Int J Pharm 256:123–131

    Article  Google Scholar 

  • Khan S, Li M, Muench SP, Jeuken LJ, Beales PA (2016) Durable proteo-hybrid vesicles for the extended functional lifetime of membrane proteins in bionanotechnology. Chem Commun (Camb) 52:11020–11023

    Article  Google Scholar 

  • Khougaz K, Astafieva I, Eisenberg A (1995) Micellization in block polyelectrolyte solutions. 3. Static light scattering characterization. Macromolecules 28:7135–7147

    Article  Google Scholar 

  • Kolman I, Pippa N, Meristoudi A, Pispas S, Demetzos C (2016) A dual-stimuli-responsive polymer into phospholipid membranes. J Therm Anal Calorim 123:2257–2271

    Article  Google Scholar 

  • Kowal J, Wu D, Mikhalevich V, Palivan CG, Meier W (2015) Hybrid polymer−lipid films as platforms for directed membrane protein insertion. Langmuir 31:4868–4877

    Article  Google Scholar 

  • Kuntsche J, Freisleben I, Steiniger F, Fahr A (2010) Temoporfin-loaded liposomes: physicochemical characterization. Eur J Pharm Sci 40:305–315

    Article  Google Scholar 

  • Kuntsche J, Horst JC, Bunjes H (2011) Cryogenic transmission electron microscopy (cryo-TEM) for studying the morphology of colloidal drug delivery systems. Int J Pharm 417:120–137

    Article  Google Scholar 

  • Lim SK, Wong ASW, de Hoog HPM, Rangamani P, Parikh AN, Nallani M, Sandin S, Liedberg B (2017) Spontaneous formation of nanometer scale tubular vesicles in aqueous mixtures of lipid and block copolymer amphiphiles. Soft Matter 13:1107–1115

    Article  Google Scholar 

  • Naziris N, Pippa N, Pispas S, Demetzos C (2016) Stimuli-responsive drug delivery Nanosystems: from bench to clinic. Curr Nanomed 6:166–185

    Article  Google Scholar 

  • Pippa N, Kaditi E, Pispas S, Demetzos C (2013) PEO-b-PCL-DPPC chimeric nanocarriers: self-assembly aspects in aqueous and biological media and drug incorporation. Soft Matter 9:4073–4082

    Article  Google Scholar 

  • Pippa N, Deli E, Mentzali E, Pispas S, Demetzos C (2014) PEO-b-PCL grafted DPPC liposomes: physicochemical characterization and stability studies of novel bio-inspired advanced drug delivery nano systems (aDDnSs). J Nanosci Nanotechnol 14:5676

    Article  Google Scholar 

  • Pippa N, Stellas D, Skandalis A, Pispas S, Demetzos C, Libera M, Marcinkowski A, Trzebicka B (2016) Chimeric lipid/block copolymer nanovesicles: Physico-chemical and bio-compatibility evaluation. Eur J Pharm Biopharm 107:295–309

    Article  Google Scholar 

  • Pirc K, Ulrih NP (2015) α-Synuclein interactions with phospholipid model membranes: key roles for electrostatic interactions and lipid-bilayer structure. Biochim Biophys Acta 1848:2002–2012

    Article  Google Scholar 

  • Pispas S, Hadjichristidis N (2003) Micellization behavior of poly(butadiene-b-sodium methacrylate) copolymers in dilute aqueous media. Macromolecules 36:8732–8737

    Article  Google Scholar 

  • Samsonova O, Pfeiffer C, Hellmund M, Merkel OM, Kissel T (2011) Low molecular weight pDMAEMA-block-pHEMA block-copolymers synthesized via RAFT-polymerization: potential non-viral gene delivery agents? Polymers 3:693–718

    Article  Google Scholar 

  • Sandström MC, Johansson E, Edwards K (2007) Structure of mixed micelles formed in PEG-lipid/lipid dispersions. Langmuir 23:4192–4198

    Article  Google Scholar 

  • Schulz M, Binder WH (2015) Mixed hybrid lipid/polymer vesicles as a novel membrane platform. Macromol Rapid Commun 36:2031–2014

    Article  Google Scholar 

  • Tribet C, Vial F (2008) Flexible macromolecules attached to lipid bilayers: impact on fluidity, curvature, permeability and stability of the membranes. Soft Matter 4:68–81

    Article  Google Scholar 

  • Vaccaro M, von Corswant C, Söderman O (2007) Investigation of the adsorption of PEG1500-12-acyloxystearate surfactants onto phospholipid bilayers: an ellipsometry and Cryo-TEM study. Biophys J 93:4300–4306

    Article  Google Scholar 

  • Ward MA, Georgiou TK (2011) Thermoresponsive polymers for biomedical applications. Polymers 3:1215–1242

    Article  Google Scholar 

  • Wei X, Cohen R, Barenholz Y (2016) Insights into composition/structure/function relationships of Doxil® gained from “high-sensitivity” differential scanning calorimetry. Eur J Pharm Biopharm 104:260–270

    Article  Google Scholar 

  • Winzen S, Bernhardt M, Schaeffel D, Koch A, Kappl M, Koynov K, Landfester K, Kroeger A (2013) Submicron hybrid vesicles consisting of polymer-lipid and polymer-cholesterol blends. Soft Matter 9:5883–5890

    Article  Google Scholar 

  • Zhong S, Pochan DJ (2010) Cryogenic transmission electron microscopy for direct observation of polymer and small-molecule materials and structures in solution. Polym Rev 50:287–320

    Article  Google Scholar 

Download references

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Correspondence to Stergios Pispas, Costas Demetzos or Barbara Trzebicka.

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Naziris, N., Pippa, N., Chrysostomou, V. et al. Morphological diversity of block copolymer/lipid chimeric nanostructures. J Nanopart Res 19, 347 (2017). https://doi.org/10.1007/s11051-017-4021-5

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  • DOI: https://doi.org/10.1007/s11051-017-4021-5

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