Anne-Marie Caminade

Dr. Anne-Marie Caminade

Laboratoire de Chimie de Coordination (LCC, CNRS UPR8241), 205 route de Narbonne, 31077 Toulouse Cedex 4, France
orcid

Research Focus & Metrics

Academic Career Length

44Years (1983-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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12 February 1999 in Chemical Reviews
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JMJean-Pierre Majoral
Jean-Pierre Majoral
Anne-Marie CaminadeAnne-Marie Caminade
Anne-Marie Caminade

2 September 1994 in Angewandte Chemie International Edition
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NLNathalie Launay
Nathalie Launay
Anne-Marie CaminadeAnne-Marie Caminade
Anne-Marie Caminade
RLRoger Lahana
Roger Lahana
JMJean‐Pierre Majoral
Jean‐Pierre Majoral

28 April 2014 in Journal of Materials Chemistry B
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Anne-Marie CaminadeAnne-Marie Caminade
Anne-Marie Caminade
CTCedric-Olivier Turrin
Cedric-Olivier Turrin
Due to their nanometric size, dendrimers have been considered as potentially suitable as new vehicles for drug delivery since their infancy. The association of a dendrimer and a drug may occur in different ways, either through covalent or non-covalent interactions. A non-covalent interaction can be the simple encapsulation inside dendrimers that enhances the solubility of lipophilic drugs in water, or electrostatic interactions between the surface and charged drugs (or DNA, RNA, or siRNA). The covalent association may occur through stable bonds, in particular for dendrimers that are considered as active per se, or through cleavable bonds that should be cleaved only when reaching the target (often cancerous cells). In addition, the full structure of the dendrimer can be disassembled under the influence of a trigger such as pH variations. This review will present these strategies and their consequences for drug delivery.

4 May 2011 in Science Translational Medicine
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MHMyriam Hayder
Myriam Hayder
Mary PoupotMary Poupot
Mary Poupot
MBMichel Baron
Michel Baron
DNDelphine Nigon
Delphine Nigon
CTCedric-Olivier Turrin
Cedric-Olivier Turrin
Jean-Luc DAVIGNONJean-Luc DAVIGNON
Jean-Luc DAVIGNON
Dendrimers are highly branched “tree-like” polymers that have demonstrated therapeutic potential in drug delivery, medical imaging, and tissue engineering in recent years. In addition, we have shown that an azabisphosphonate (ABP)–capped dendrimer selectively targets monocytes and directs them toward anti-inflammatory activation. We explored this property to assess the therapeutic potential of dendrimer ABP in the treatment of an inflammatory disease, rheumatoid arthritis. Intravenous injections of dendrimer ABP inhibited the development of inflammatory arthritis in two animal models: IL-1ra−/− mice and mice undergoing K/BxN serum transfer. Suppression of disease was characterized by normal synovial membranes, reduced levels of inflammatory cytokines, and the absence of cartilage destruction and bone erosion. Dendrimer ABP also exhibited anti-osteoclastic activity on mouse and human cells, mediated by c-FMS (cellular-feline McDonough strain sarcoma virus oncogene homolog) inhibition. These preclinical demonstrations suggest the potential use of dendrimer ABP as a nanotherapeutic for rheumatoid arthritis.

20 November 2017 in Chemical Society Reviews
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SMSerge Mignani
Serge Mignani
João RodriguesJoão Rodrigues
João Rodrigues
Helena TomásHelena Tomás
Helena Tomás
MZMaria Zablocka
Maria Zablocka
Xiangyang ShiXiangyang Shi
Xiangyang Shi
JMJean-Pierre Majoral
Jean-Pierre Majoral
Overview of the use of dendrimers in combination with encapsulated and conjugated natural products and analogues as anti-cancer agents.

29 May 2015 in Chemical Society Reviews
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Anne-Marie CaminadeAnne-Marie Caminade
Anne-Marie Caminade
SXShuting Xu
Shuting Xu
DSDavid Smith
David Smith
Guest editors Anne-Marie Caminade, Deyue Yan and David K. Smith introduce the Dendrimers and Hyperbranched Polymers issue of Chemical Society Reviews