Transport properties of ibuprofen encapsulated in cyclodextrin nanosponge hydrogels: A proton HR-MAS NMR spectroscopy study

The chemical cross-linking of β-cyclodextrin (β-CD) with ethylenediaminetetraacetic dianhydride (EDTA) led to branched polymers referred to as cyclodextrin nanosponges (CDNSEDTA). Two different preparations are described with 1:4 and 1:8 CD-EDTA molar ratios. The corresponding cross-linked polymers were contacted with 0.27 M aqueous solution of ibuprofen sodium salt (IP) leading to homogeneous, colorless, drug loaded hydrogels. The systems were characterized by high resolution magic angle spinning (HR-MAS) NMR spectroscopy. Pulsed field gradient spin echo (PGSE) NMR spectroscopy was used to determine the mean square displacement (MSD) of IP inside the polymeric gel at different observation times td. The data were further processed in order to study the time dependence of MSD: MSD = f(td). The proposed methodology is useful to characterize the different diffusion regimes that, in principle, the solute may experience inside the hydrogel, namely normal or anomalous diffusion. The full protocols including the polymer preparation and purification, the obtainment of drug-loaded hydrogels, the NMR sample preparation, the measurement of MSD by HR-MAS NMR spectroscopy and the final data processing to achieve the time dependence of MSD are here reported and discussed. The presented experiments represent a paradigmatic case and the data are discussed in terms of innovative approach to the characterization of the transport properties of an encapsulated guest within a polymeric host of potential application for drug delivery

Combining Raman and infrared spectroscopy as a powerful tool for the structural elucidation of cyclodextrin-based polymeric hydrogels

A detailed experimental and theoretical vibrational analysis of hydrogels of b-cyclodextrin nanosponges (b-CDNS), obtained by polymerization of b-cyclodextrin (b-CD) with the cross-linking agent ethylenediaminetetraacetic acid (EDTA), is reported here. Thorough structural characterization is achieved by exploiting the complementary selection rules of FTIR-ATR and Raman spectroscopies and by supporting the spectral assignments by DFT calculations of the spectral profiles. The combined analysis of the FTIR-ATR spectra of the polymers hydrated with H2O and D2O allowed us to isolate the HOH bending of water molecules not involved in symmetrical, tetrahedral environments. The analysis of the HOH bending mode was carried out as a function of temperature, showing the existence of a supercooled state of the water molecules. The highest level of cooperativity of the hydrogen bond scheme was reached at a value of the b-CD/EDTA molar ratio n = 6. Finally, the connectivity pattern of ‘‘uncoupled’’ water molecules bound to the nanosponge backbone was found to be weakened by increasing T. The temperature above which the population of non-tetracoordinated water molecules becomes predominant turned out to be independent of the parameter n

Anomalous diffusion of Ibuprofen in cyclodextrin nanosponge hydrogels: an HRMAS NMR study

Ibuprofen sodium salt (IP) was encapsulated in cyclodextrin nanosponges (CDNS) obtained by cross-linking of β-cyclodextrin with ethylenediaminetetraacetic acid dianhydride (EDTAn) in two different preparations: CDNSEDTA 1:4 and 1:8, where the 1:n notation indicates the CD to EDTAn molar ratio. The entrapment of IP was achieved by swelling the two polymers with a 0.27 M solution of IP in D2O, leading to colourless, homogeneous hydrogels loaded with IP. The molecular environment and the transport properties of IP in the hydrogels were studied by high resolution magic angle spinning (HRMAS) NMR spectroscopy. The mean square displacement (MSD) of IP in the gels was obtained by a pulsed field gradient spin echo (PGSE) NMR pulse sequence at different observation times td. The MSD is proportional to the observation time elevated to a scaling factor α. The α values define the normal Gaussian random motion (α = 1), or the anomalous diffusion (α 1 superdiffusion). The experimental data here reported point out that IP undergoes subdiffusive regime in CDNSEDTA 1:4, while a slightly superdiffusive behaviour is observed in CDNSEDTA 1:8. The transition between the two dynamic regimes is triggered by the polymer structure. CDNSEDTA 1:4 is characterized by a nanoporous structure able to induce confinement effects on IP, thus causing subdiffusive random motion. CDNSEDTA 1:8 is characterized not only by nanopores, but also by dangling EDTA groups ending with ionized COO− groups. The negative potential provided by such groups to the polymer backbone is responsible for the acceleration effects on the IP anion thus leading to the superdiffusive behaviour observed. These results point out that HRMAS NMR spectroscopy is a powerful direct method for the assessment of the transport properties of a drug encapsulated in polymeric scaffolds. The diffusion properties of IP in CDNS can be modulated by suitable polymer synthesis; this finding opens the possibility to design suitable systems for drug delivery with predictable and desired drug release properties

Synthesis and characterization of a hyper-branched water-soluble β-cyclodextrin polymer

A new hyper-branched water-soluble polymer was synthesized by reacting β-cyclodextrin with pyromellitic dianhydride beyond the critical conditions that allow the phenomenon of gelation to occur. The molar ratio between the monomers is a crucial parameter that rules the gelation process. Nevertheless, the concentration of monomers in the solvent phase plays a key role as well. Hyperbranched β-cyclodextrin-based polymers were obtained performing the syntheses with excess of solvent and cross-linking agent, and the conditions for critical dilution were determined experimentally. A hyper-branched polymer with very high water solubility was obtained and fully characterized both as for its chemical structure and for its capability to encapsulate substances. Fluorescein was used as probe molecule to test the complexation properties of the new material

Magnetic behavior of cyclodextrin-based nanosponges bearing nitroxyl persistent radicals

Paramagnetic organic materials are attracting an increasing interest due to their potential use in nanomedicine. In particular, it has been reported that polymeric matrices containing TEMPO radical moieties are capable to combine drug delivery properties with intracellular scavenging action of reactive oxygen species. Paramagnetic cyclodextrin nanosponges (pmCDNS) are a new class of nanodevices with potential application in nanomedicine, due to the following properties: a) adsorption and release capability of bioactive molecules; b) detectability by EPR and MRI spectroscopies during in vitro and in vivo experiments thanks to the presence of spin labels. Moreover, they may open the way to the synthesis of metal-free organic magnets. pmCDNS were prepared by reaction in anhydrous DMSO of a mono-functionalized β-cyclodextrin (βCD), bearing a TEMPO radical moiety, with suitable cross-linkers (CL) like EDTA or pyromellitic dianhydride (PMA), with variable βCD/CL molar ratio. An alternative approach consisted into the one-pot reaction between pristine βCD, CL and a phthalic anhydride derivative bearing a TEMPO radical unit. The paramagnetic behavior of the obtained materials was investigated by EPR spectroscopy and SQUID magnetometry. Magnetic measurements, corrected for the diamagnetic contribution of the nanosponge matrix, displayed a Curie-Weiss behaviour with a negative paramagnetic Curie temperature (p = -4.3 K), suggesting that antiferromagnetic interactions were predominant in this system. The isothermal magnetisation at 2K was well fitted by the Brillouin function with a single spin moment (J=½), as expected by the TEMPO radical. A quantitative evaluation of the magnetic data suggested that around 50 mg of TEMPO radicals were present per gram of material