Development of innovative paclitaxel-loaded small PLGA nanoparticles: Study of their antiproliferative activity and their molecular interactions on prostatic cancer cells |
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Authors: | D. Le Broc-Ryckewaert R. Carpentier E. Lipka S. Daher C. Vaccher D. Betbeder C. Furman |
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Affiliation: | 1. Université Lille Nord de France, F-59000 Lille, France;2. UDSL, EA 4483, UFR Pharmacie, F-59000 Lille, France;3. CHU Lille, EA 4483, IMPRT, IFR 114, Faculté de Médecine pôle recherche, Université de Lille 2, F-59000 Lille, France;4. UDSL, EA GRIIOT, UFR Pharmacie, F-59000 Lille, France;5. Université d’Artois, 9 rue du temple, F-59000 Lille, France;6. UDSL, ICPAL, Plateforme de Binding, F-59000 Lille, France |
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Abstract: | Taxanes, including paclitaxel, are anti-cancer drugs approved for the treatment of prostate cancer but which have limited clinical application due to their hydrophobicity, their low therapeutic index and the emergence of chemoresistance. These side effects may be avoided through the use of new drug delivery systems such as nanoparticles, and paclitaxel-loaded PLGA nanoparticles up to 200 nm in size have shown encouraging results. As it is known that size affects the tissular penetration and distribution of tumors via the enhanced permeability and retention effect, so nanoparticles smaller than 100 nm are potentially interesting vehicles for improving paclitaxel delivery and efficacy. |
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Keywords: | BCA, bicinchoninic acid BSA, bovine serum albumin CTAB, hexadecyltrimethylammonium bromide DiI, 1,1&prime -dioctadecyl-3,3,3&prime ,3&prime -tetramethylindocarbocyanine perchlorate EP, R effectenhanced and permeability retention effect FBS, foetal bovine serum HPLC, high performance liquid chromatography MTT, 3-[4,5-dimethylthiazol-2-yl]-2,5 diphenyltetrazolium bromide NP, nanoparticles PBS, phosphate buffer saline PDI, polydispersity index P-gp, p-glycoprotein PMSF, phenylmethanesulfonylfluoride PLGA, poly(lactic-co-glycolic) acid Ptx, paclitaxel SDS, sodium dodecyl sulfate |
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