Mesoporous self-assembled nanoparticles of biotransesterified cyclodextrins and nonlamellar lipids as carriers of water-insoluble substances. Issue 36 (30th August 2016)
- Record Type:
- Journal Article
- Title:
- Mesoporous self-assembled nanoparticles of biotransesterified cyclodextrins and nonlamellar lipids as carriers of water-insoluble substances. Issue 36 (30th August 2016)
- Main Title:
- Mesoporous self-assembled nanoparticles of biotransesterified cyclodextrins and nonlamellar lipids as carriers of water-insoluble substances
- Authors:
- Zerkoune, Leïla
Lesieur, Sylviane
Putaux, Jean-Luc
Choisnard, Luc
Gèze, Annabelle
Wouessidjewe, Denis
Angelov, Borislav
Vebert-Nardin, Corinne
Doutch, James
Angelova, Angelina - Abstract:
- Abstract : Biotransesterified cyclodextrin βCD- n C10 induces Im 3 m cubic lattice nanostructures in host Pn 3 m monoglyceride lipid assemblies as evidenced by SAXS and cryo-TEM (FFT) analyses. Abstract : Soft mesoporous hierarchically structured particles were created by the self-assembly of an amphiphilic deep cavitand cyclodextrin βCD- n C10 (degree of substitution n = 7.3), with a nanocavity grafted by multiple alkyl (C10 ) chains on the secondary face of the βCD macrocycle through enzymatic biotransesterification, and the nonlamellar lipid monoolein (MO). The effect of the non-ionic dispersing agent polysorbate 80 (P80) on the liquid crystalline organization of the nanocarriers and their stability was studied in the context of vesicle-to-cubosome transition. The coexistence of small vesicular and nanosponge membrane objects with bigger nanoparticles with inner multicompartment cubic lattice structures was established as a typical feature of the employed dispersion process. The cryogenic transmission electron microscopy (cryo-TEM) images and small-angle X-ray scattering (SAXS) structural analyses revealed the dependence of the internal organization of the self-assembled nanoparticles on the presence of embedded βCD- n C10 deep cavitands in the lipid bilayers. The obtained results indicated that the incorporated amphiphilic βCD- n C10 building blocks stabilize the cubic lattice packing in the lipid membrane particles, which displayed structural features beyond theAbstract : Biotransesterified cyclodextrin βCD- n C10 induces Im 3 m cubic lattice nanostructures in host Pn 3 m monoglyceride lipid assemblies as evidenced by SAXS and cryo-TEM (FFT) analyses. Abstract : Soft mesoporous hierarchically structured particles were created by the self-assembly of an amphiphilic deep cavitand cyclodextrin βCD- n C10 (degree of substitution n = 7.3), with a nanocavity grafted by multiple alkyl (C10 ) chains on the secondary face of the βCD macrocycle through enzymatic biotransesterification, and the nonlamellar lipid monoolein (MO). The effect of the non-ionic dispersing agent polysorbate 80 (P80) on the liquid crystalline organization of the nanocarriers and their stability was studied in the context of vesicle-to-cubosome transition. The coexistence of small vesicular and nanosponge membrane objects with bigger nanoparticles with inner multicompartment cubic lattice structures was established as a typical feature of the employed dispersion process. The cryogenic transmission electron microscopy (cryo-TEM) images and small-angle X-ray scattering (SAXS) structural analyses revealed the dependence of the internal organization of the self-assembled nanoparticles on the presence of embedded βCD- n C10 deep cavitands in the lipid bilayers. The obtained results indicated that the incorporated amphiphilic βCD- n C10 building blocks stabilize the cubic lattice packing in the lipid membrane particles, which displayed structural features beyond the traditional CD nanosponges. UV-Vis spectroscopy was employed to characterize the nanoencapsulation of a model hydrophobic dimethylphenylazo-naphthol guest compound (Oil red) in the created nanocarriers. In perspective, these dual porosity carriers should be suitable for co-encapsulation and sustained delivery of peptide, protein or siRNA biopharmaceuticals together with small molecular weight drug compounds or imaging agents. … (more)
- Is Part Of:
- Soft matter. Volume 12:Issue 36(2016)
- Journal:
- Soft matter
- Issue:
- Volume 12:Issue 36(2016)
- Issue Display:
- Volume 12, Issue 36 (2016)
- Year:
- 2016
- Volume:
- 12
- Issue:
- 36
- Issue Sort Value:
- 2016-0012-0036-0000
- Page Start:
- 7539
- Page End:
- 7550
- Publication Date:
- 2016-08-30
- Subjects:
- Soft condensed matter -- Periodicals
530.413 - Journal URLs:
- http://www.rsc.org/Publishing/Journals/sm/index.asp ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c6sm00661b ↗
- Languages:
- English
- ISSNs:
- 1744-683X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8321.419000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 1651.xml