PLGA-Based Nanoparticles: a Safe and Suitable Delivery Platform for Osteoarticular Pathologies

Abstract : Despite the promising applications of PLGA based particles, studies examining the fate and consequences of these particles after intra-articular administration in the joint are scanty. This study was carried out to evaluate the neutrality of the unloaded delivery system on different articular cell types. To facilitate tracking, we have thus developed a fluorescent core of particles, combined to a hyaluronate shell for cell recognition. Fluorescence pictures were taken at time intervals to assess the internalization and the corresponding inflammatory response was monitored by RT-qPCR and biochemical measurements. After NPs pre-treatment, mesenchymal stem cells (MSCs) were cultured into chondrogenic, adipogenic or osteogenic differentiation media, to investigate if NPs exposure interferes with differentiation ability. Finally, intra-articular injections were performed in healthy rat knees and joint's structure analysed by histological studies. Particles were detected in cytoplasm 8 h after exposure. Internalization led to a slight and reversible increase of inflammatory markers, but lower than in inflammatory conditions. We have confirmed particles exposure minimal neutrality on MSCs pluripotency. Histological exams of joint after intra-articular injections do not demonstrate any side effects of NPs. Our findings suggest that such a delivery platform is well tolerated locally and could be used to deliver active molecules to the joint.
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Pharmaceutical Research, American Association of Pharmaceutical Scientists, 2015, 32 (12), pp.3886-3898. 〈10.1007/s11095-015-1748-5〉
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https://hal.univ-lorraine.fr/hal-01451916
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Soumis le : mercredi 1 février 2017 - 15:10:23
Dernière modification le : jeudi 11 janvier 2018 - 06:27:33

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Mathieu Riffault, Jean-Luc Six, Patrick Netter, Pierre Gillet, Laurent Grossin. PLGA-Based Nanoparticles: a Safe and Suitable Delivery Platform for Osteoarticular Pathologies. Pharmaceutical Research, American Association of Pharmaceutical Scientists, 2015, 32 (12), pp.3886-3898. 〈10.1007/s11095-015-1748-5〉. 〈hal-01451916〉

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