Light-induced functionalization of amphiphilic block copolymers: Application to nanoparticles for drug targeting

Photografting of bifunctional photolinker on biocompatible amphiphilic copolymers, such as PCL-b-PEGs and PLGA-b-PEGs, has been developed as a practical and versatile strategy for the materials functionalisation. Depending on the copolymer nature (block length, % of crystallinity) and the experimental conditions we could selectively direct the grafting on the hydrophilic PEG segments. The resulting copolymers were further derivatized with molecules of interest (RGD-peptides, LDV-peptides, “home-made”peptidomimetics, mannose derivatives,…) by substitution of the O-succinimidyl ester of the photolinker. The derivatization rates were controlled by radiolabelling, colorimetric assay and XPS spectroscopy. The functionalized copolymers were used in the formulation of nanoparticles displaying the ligands on their outer-shell. This nanoparticulate system was successfully employed for the oral vectorisation of antigen and for the targeted delivery of an anticancer drug

Clickable PEG conjugate obtained by ‘‘clip’’ photochemistry: Synthesis and

In this paper, we describe a grafting methodology associated to a quantitative 19F NMR method (qNMR) for the conjugation of small molecules on a PEG building block aimed at click chemistry applications in the domain of drug delivery systems. Acetylenic PEG (PEG-yne) was first derivatized with a fluorinated benzyl amine (TagF6) by means of photografting of a trifluoromethylphenyl diazirine bifunctional linker (TPD-clip). The amount of TagF6 grafted on PEG-yne was calculated by NMR using an internal standard (trifluoroethanol) and adjusting of the acquisition and processing parameters. NMR is used as a valuable alternative to the complex procedures often employed for the quantification of functionalities on biomaterials. The accuracy of the qNMR methodology was attested by controlling its linearity, the determination of limits of quantification and the percentage of recovery. A good assessment of the TagF6 grafting rates was obtained after taking into account the inherent unspecific adsorption that occurs on materials. This versatile methodology that combines simple chemistry and a common analytical tool was, in a second time, applied to the preparation of a PEG conjugated with a RGD (Arg-Gly-Asp) peptidomimetic in a controlled manner

Surface Grafting on Poly(ethylene terephthalate) Track-Etched Microporous Membrane by Activation with Trifluorotriazine: Application to the Biofunctionalization with GRGDS Peptide

A two-step wet chemistry protocol has been developed for the surface derivatization of poly(ethylene terephthalate) (PET) track-etched membrane used as cell culturing support, that is, (a) activation by trifluorotriazine (1 M in acetonitrile (ACN), 30 degrees C, 3 h); (b) coupling to amine-terminated molecules, namely 3,5-bis(trifluoromethyl)benzylamine ((F)Tag), (L)-4,5-[H-3]-lysine, and Gly-Arg-Gly-Asp-Ser (GRGDS) pentapeptide (10(-3) M in PB-ACN, 1:1 (v/v), 20 degrees C, 17 h). The grafting rates determined by X-ray photoelectron spectroscopy, from the F/C and N/C atomic ratios, are in the range of 100-140 pmol/cm(2) (apparent surface), whereas the liquid scintillation counting assays give higher values (180-d230 pmol/cm(2)) corresponding to the open surface reactivity. PET-g-(F)Tag is reasonably stable under two usual sterilization conditions of biomaterials, that is, steam heating at 121 degrees C and gamma-irradiation at 25 kGy. On the other hand, PET-g-GRGDS is found to be stable only under ionization radiation (84% of remaining peptide molecules), but damaged in a large extent by the autoclave treatment (23% of remaining peptide molecules). The surfaces of the sterilized PET and PET-g-GRGDS samples have been characterized by water contact angle measurement and by atomic force microscopy analysis in air and under water. Comparatively to the corresponding nonsterilized surfaces, gamma-irradiated surfaces are slightly more hydrophilic and also slightly more rough and jagged. (C) 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 195-208, 201

Synthesis and application of new photocrosslinkers for poly(ethylene glycol)

Photocrosslinking of polyethylene glycol (PEG) using exogenous agents is a convenient way to produce branched PEG from commercial sources thus avoiding the tricky synthesis of new reactive and functional polymers. In this study, we synthesized two series of new photocrosslinkers, i.e. bis-fluorophenyl azide and bis-trifluoromethyl diazirine, which under soft UV-irradiation produce reactive species (i.e. nitrene and carbene respectively) that insert into the CH bond of the polymer backbone, building new bridges between macromolecular chains. These photocrosslinkers are different in terms of behaviour under irradiation and affinity for the target substrate (i.e. PEG). Thus, practical conditions for photocrosslinking of a 10-kDa PEG were studied and followed by NMR and size-exclusion chromatography. In particular, we investigated irradiation in bulk or in solvent, at different irradiation times, with several concentrations of PEG and photolinkers. Finally, we were able to design a procedure to obtain soluble crosslinked PEGs of 300kDa. © 2012 CSIRO

A graftable LDV peptidomimetic: design, synthesis and application to a blood filtration membrane.

A graftable LDV (Leu-Asp-Val) peptidomimetic molecule (B-c) has been prepared from 3-(5-amino-2-hydroxy)phenyl-propionic acid, as alpha(4)beta(1) (VLA-4) integrin ligand. For that purpose, the mechanism of 3-(4-azidophenyl)propionic acid rearrangement has been revisited. Activation of Durapore DVPP-hydrophilic membrane, by surface wet chemistry using triazine trifluoride, followed by covalent coupling of B-c produced a modified filter (0.8% of derivatisation from XPS analysis) with improved capacity of leukocyte retention

Surface functionalization of a poly(butylene terephthalate) (PBT) melt-blown filtration membrane by wet chemistry and photo-grafting.

The surface functionalization of PBT melt-blown membrane, making up a whole filter of blood components, was achieved via two methods. Hydroxyl chain-end activation by tosylation (method A), followed by coupling of F- and (3)H-tagged molecules (probes), led to 1% of surface derivatization (XPS) and 290 pmol/cm(2) of lysine fixation (LSC). Deposition of O-succinimidyl 4-(p-azido-phenyl)butanoate ("molecular clip") and 2 h irradiation at 254 nm led to the implanting of activated ester functions, randomly on the polymer surface (method B). Further coupling of F- and (3)H-probes by wet chemistry gave highly functionalized surface (4% by XPS and 1000 pmol/cm(2) by LSC). However, control experiments showed that about 80% of the surface derivatization resulted from the UV treatment alone. Thus, the effect of UV irradiation on PBT membrane was systematically studied and analyzed by XPS, contact angle measurements, GPC and surface reactivity assays. The optimized conditions of "molecular clip" photo-grafting (negligible polymer photo-oxidation/photo-degradation) led to the covalent fixation of 45 pmol/cm(2) of (3)H-probe. Throughout our study, the behaviour of PBT melt-blown membrane was compared to PBT film and PET track-etched membrane similarly treated. Lastly, the method B was applied to couple GRGDS peptide on the PBT membrane; this material showed improved properties of leukocyte depletion in buffy coat filtration experiments

Targeting of tumor endothelium by RGD-grafted PLGA-nanoparticles

The destruction of the neovessels in solid tumors can cause the death of tumor cells resulting from the lack of oxygen and nutrients. Peculiarities of the tumor vasculature, however, also position angiogenic endothelial cells as obvious targets to address cytotoxic drugs into the tumor. In particular, the identification of a three-amino acids sequence, arginine-glycine-aspartate (RGD), as a fundamental recognition site for proliferating endothelial attachment to the extracellular matrix leads to the development of tumor-targeting ligands for nanoparticles. The RGD peptide can target the α(v)β(3) integrin overexpressed by the tumor endothelium, and thereby increases the accumulation of drug-loaded RGD-grafted nanoparticles. RGD-nanoparticles may thus extravasate more efficiently and enter the tumor via the enhanced permeability and retention (EPR) effect. This combination of active and passive processes leads to the penetration of nanoparticles into the tumor tissue, followed by cellular uptake and intracellular delivery of the cytotoxic payload. Since cancer cells may also express α(v)β(3) integrin, the entrapping of RGD-nanoparticles into the tumor interstitial fluid may yet be facilitated through direct binding to cancer cells. Here, we describe methods used for the preparation of RGD-nanoparticles and for the validation of their potential of tumor endothelium targeting both in vitro and in vivo. We also illustrate how RGD-nanoparticles may be more suited than nontargeted modalities for the tumor delivery of poorly soluble and/or highly cytotoxic drugs, using different mouse tumor xenograft models

Ultrasmall particle of iron oxide-RGD peptidomimetic conjugate: synthesis and characterisation.

Ultrasmall particles of iron oxide (USPIOs) coated with 3,3'-bis(phosphonate)propionic acid were covalently coupled to a home-made Arg-Gly-Asp (RGD) peptidomimetic molecule via a short oligoethyleneglycol (OEG) spacer. The conjugation rate was measured by X-ray photoelectron spectroscopy (XPS). The particle size and magnetic characteristics were kept. Our novel conjugate targeted efficiently Jurkat cells (increase of 229% vs the control)