Nadia Katir
Paul Sabatier University
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Publication
Featured researches published by Nadia Katir.
Molecular Pharmaceutics | 2012
Karol Ciepluch; Nadia Katir; El Kadib A; Aleksandra Felczak; Katarzyna Zawadzka; Monika Weber; Barbara Klajnert; Katarzyna Lisowska; Anne Marie Caminade; Bousmina M; Maria Bryszewska; Jean-Pierre Majoral
Some biological properties of eight dendrimers incorporating both phosphorus linkages and viologen units within their cascade structure or at the periphery were investigated for the first time. In particular cytotoxicity, hemotoxicity, and antimicrobial and antifungal activity of these new macromolecules were examined. Even if for example all these species exhibited good antimicrobial properties, it was demonstrated that their behavior strongly depends on several parameters as their size and molecular weight, the number of viologen units and the nature of the terminal groups.
New Journal of Chemistry | 2012
Abdelkrim El Kadib; Nadia Katir; Mosto Bousmina; Jean-Pierre Majoral
Dendrimers and silica inorganic materials are two effective building blocks that have attracted growing interest in both fundamental and applied material chemistry. The fruitful association of these soft and hard skeletons resulted in an unlimited library of materials and nanodevices with different tailored properties. The aim of this review is to shed light on different strategies of combination of dendrimer–silica materials. Special attention has been accorded to the porosity control and the accessibility of the functional groups of these organic–inorganic hybrid mesoporous materials.
Molecular Pharmaceutics | 2013
Katarzyna Milowska; Justyna Grochowina; Nadia Katir; Abdelkrim El Kadib; Jean-Pierre Majoral; Maria Bryszewska; Teresa Gabryelak
Inhibition of α-synuclein (ASN) fibril formation is a potential therapeutic strategy in Parkinsons disease and other synucleinopathies. The aim of this study was to examine the role of viologen-phosphorus dendrimers in the α-synuclein fibrillation process and to assess the structural changes in α-synuclein under the influence of dendrimers. ASN interactions with phosphonate and pegylated surface-reactive viologen-phosphorus dendrimers were examined by measuring the zeta potential, which allowed determining the number of dendrimer molecules that bind to the ASN molecule. The fibrillation kinetics and the structural changes were examined using ThT fluorescence and CD spectroscopy. Depending on the concentration of the used dendrimer and the nature of the reactive groups located on the surface, ASN fibrillation kinetics can be significantly reduced, and even, in the specific case of phosphonate dendrimers, the fibrillation can be totally inhibited at low concentrations. The presented results indicate that viologen-phosphorus dendrimers are able to inhibit ASN fibril formation and may be used as fibrillar regulating agents in neurodegenerative disorders.
Journal of Materials Chemistry | 2009
Abdelkrim El Kadib; Nadia Katir; Nathalie Marcotte; Karine Molvinger; Annie Castel; P. Riviere; Daniel Brunel
This work describes the synthesis of new, environmentally friendly, robust and biocompatible organic–inorganic hybrid materials based on fatty acid methyl ester-functionalised silica. The hydrosilylation reaction was used to covalently anchor 10-undecenoic methyl ester to a cyclic and acyclic backbone based on methylsiloxane repeating units. These as-synthesised amphiphilic precursors exhibit a self-assembling ability as shown by the formation of nanoobjects evidenced by fluorescence experiments, transmission electronic microscopy (TEM) and dynamic light scattering (DLS) analyses. Spherical nanocomposites featuring unprecedented flexibility, hydrophobicity and improved hydrolytic and thermal properties were built using sol–gel condensation of tetraethoxysilane (TEOS) controlled by these new self-assembling nanobuilding blocks. The textural characteristics and the morphology of these composite materials were dependent on the type of catalyst (acidic or basic) and the nature of the solvent (polar or apolar) used during the sol–gel polymerisation. This strategy opens new opportunities for advanced applications in various fields of nanochemistry and biomaterials.
Nanoscale | 2013
Younes Brahmi; Nadia Katir; Mykhailo Ianchuk; Vincent Collière; El Mokhtar Essassi; Armelle Ouali; Anne-Marie Caminade; Mosto Bousmina; Jean-Pierre Majoral; Abdelkrim El Kadib
The scarcity of low temperature syntheses of anatase nanocrystals prompted us to explore the use of surface-reactive fourth generation phosphorus-dendrimers as molds to control the nucleation and growth of titanium-oxo-species during the sol-gel mineralization process. Unexpectedly, the dendritic medium provides at low temperature, discrete anatase nanocrystals (4.8 to 5.2 nm in size), in marked contrast to the routinely obtained amorphous titanium dioxide phase under standard conditions. Upon thermal treatment, heteroatom migration from the branches to the nanoparticle surface and the ring opening polymerization of the cyclophosphazene core provide stable, interpenetrating mesoporous polyphosphazene-anatase hybrid materials (-P[double bond, length as m-dash]N-)n-TiO2. The steric hindrance of the dendritic skeleton, the passivation of the anatase surface by heteroatoms and the ring opening of the core limit the crystal growth of anatase to 7.4 nm and prevent, up to 800 °C, the commonly observed anatase-to-rutile phase transformation. Performing this mineralization in the presence of similar surface-reactive but non-dendritic skeletons (referred to as branch-mimicking dendrimers) failed to generate crystalline anatase and to efficiently limit the crystal growth, bringing thus clear evidence of the virtues of phosphorus dendrimers in the design of novel nanostructured materials.
International Journal of Biological Macromolecules | 2013
Karol Ciepluch; Monika Weber; Nadia Katir; Anne-Marie Caminade; Abdelkrim El Kadib; Barbara Klajnert; Jean-Pierre Majoral; Maria Bryszewska
The inhibition of acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) is the first step in checking whether new compounds can be considered as drugs for treating neurodegenerative diseases. The effect of viologen-phosphorus dendrimers on AChE and BChE activities was studied. The results show that the effects on the cholinesterase activities depend on dendrimer type and size. Viologen dendrimers can interact with the enzymes in two ways: they can bind either to a peripheral site of the enzyme or to amino acids located near the active site, inhibiting catalysis by both cholinesterases. All tested non-toxic viologen-phosphorus dendrimers inhibited the activities of both cholinesterases, showing their potential as new drugs for treating neurodegenerative diseases.
Molecules | 2013
Joanna Lazniewska; Anna Janaszewska; Katarzyna Milowska; Anne-Marie Caminade; Serge Mignani; Nadia Katir; Abdelkrim El Kadib; Maria Bryszewska; Jean-Pierre Majoral; Teresa Gabryelak; Barbara Klajnert-Maculewicz
A new class of viologen-phosphorus dendrimers (VPDs) has been recently shown to possess the ability to inhibit neurodegenerative processes in vitro. Nevertheless, in the Central Nervous Systems domain, there is little information on their impact on cell functions, especially on neuronal cells. In this work, we examined the influence of two VPD (VPD1 and VPD3) of zero generation (G0) on murine hippocampal cell line (named mHippoE-18). Extended analyses of cell responses to these nanomolecules comprised cytotoxicity test, reactive oxygen species (ROS) generation studies, mitochondrial membrane potential (ΔΨm) assay, cell death detection, cell morphology assessment, cell cycle studies, as well as measurements of catalase (CAT) activity and glutathione (GSH) level. The results indicate that VPD1 is more toxic than VPD3. However, these two tested dendrimers did not cause a strong cellular response, and induced a low level of apoptosis. Interestingly, VPD1 and VPD3 treatment led to a small decline in ROS level compared to untreated cells, which correlated with slightly increased catalase activity. This result indicates that the VPDs can indirectly lower the level of ROS in cells. Summarising, low-cytotoxicity on mHippoE-18 cells together with their ability to quench ROS, make the VPDs very promising nanodevices for future applications in the biomedical field as nanocarriers and/or drugs per se.
Cellular & Molecular Biology Letters | 2013
Joanna Lazniewska; Katarzyna Milowska; Nadia Katir; Abdelkim El Kadib; Maria Bryszewska; Jean-Pierre Majoral; Teresa Gabryelak
Dendrimers containing viologen (derivatives of 4,4′-bipyridyl) units in their structure have been demonstrated to exhibit antiviral activity against human immunodeficiency virus (HIV-1). It has also recently been revealed that novel dendrimers with both viologen units and phosphorus groups in their structure show different antimicrobial, cytotoxic and hemotoxic properties, and have the ability to influence the activity of cholinesterases and to inhibit α-synuclein fibrillation. Since the influence of viologen-phosphorus structures on basic cellular processes had not been investigated, we examined the impact of such macromolecules on the murine neuroblastoma cell line (N2a). We selected three water-soluble viologen-phosphorus (VPD) dendrimers, which differ in their core structure, number of viologen units and number and type of surface groups, and analyzed several aspects of the cellular response. These included cell viability, generation of reactive oxygen species (ROS), alterations in mitochondrial activity, morphological modifications, and the induction of apoptosis and necrosis. The MTT assay results suggest that all of the tested dendrimers are only slightly cytotoxic. Although some changes in ROS formation and mitochondrial function were detected, the three compounds did not induce apoptosis or necrosis. In light of these results, we can assume that the tested VPD are relatively safe for mouse neuroblastoma cells. Although more research on their safety is needed, VPD seem to be promising nanoparticles for further biomedical investigation.
Biomacromolecules | 2009
Nadia Katir; Abdelkrim El Kadib; Mohamed Dahrouch; Annie Castel; Nicolás Gatica; Zahra Benmaarouf; P. Riviere
New classes of amphiphilic polyesters were prepared from metallated (Si, Ge) fatty methyl ester (FAME) precursors and poly(tetramethylene oxide) glycol. Hydrosilylation of 10-undecenoic methyl ester by tetramethyldisiloxane occurred at 80 degrees C in the presence of Karstedts catalyst, and hydrogermylation of the same FAME derivative was obtained at the same temperature under radical AIBN initiation. These diester precursors, obtained in high yields (approximately 90%), reacted with poly(tetramethylene oxide) glycol under free solvent to give silicon polymers or germanium oligomers. These condensed materials display both the characteristic of organic-inorganic hybrid materials and those of amphiphilic polymers. The nature of organometallic fragment (hydrophobicity of tetramethyldisiloxy and sterical hindrance of diphenylgermyl) was shown to influence the chemical reactivity of the polymerizable monomers and the physical properties of the resulting copolymers. The amphiphilicity of these materials provides a driving force for the formation of small objects (approximately 1 nm), making them very attractive as hybrid nanocontainers.
Chemistry and Physics of Lipids | 2013
Nadia Katir; Abdelkrim El Kadib; Annie Castel
With the aim of designing novel transformable fatty acid diesters, various strategies for introducing phosphorus arms to the fatty backbone have been examined. While lithiated phosphine reacts classically to brominated fatty esters to afford the mono-addition product, the synthesis of phosphorylated diesters was found to be difficult, a fact related to the bulkiness of fatty acids and phosphine reagents. A base-induced dehydrochlorination reaction using ArPCl2 and hydroxy-terminated fatty esters resulted in metastable diester for which hydrolytic cleavage undergo phosphine oxidation and expulsion of one fatty chain. Alternatively, ArPOCl2 alleviates this drawback and provides stable, phosphorylated fatty acid diesters.