pH-controlled doxorubicin delivery from PDEAEMA-based nanogels
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作者:
Pikabea, Aintzane
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Univ Basque Country, UPV EHU, Fac Chem, Dept Appl Chem,Bionanoparticles Grp, Apdo 1072, Donostia San Sebastian 20080, SpainUniv Basque Country, UPV EHU, Fac Chem, Dept Appl Chem,Bionanoparticles Grp, Apdo 1072, Donostia San Sebastian 20080, Spain
Pikabea, Aintzane
[1
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Villar-Alvarez, Eva
[2
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Forcada, Jacqueline
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Univ Basque Country, UPV EHU, Fac Chem, Dept Appl Chem,Bionanoparticles Grp, Apdo 1072, Donostia San Sebastian 20080, SpainUniv Basque Country, UPV EHU, Fac Chem, Dept Appl Chem,Bionanoparticles Grp, Apdo 1072, Donostia San Sebastian 20080, Spain
Forcada, Jacqueline
[1
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Taboada, Pablo
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Univ Santiago de Compostela, Fac Phys, Particle Phys Dept, Colloids & Polymers Phys Grp, Campus Sur, Santiago De Compostela 15782, SpainUniv Basque Country, UPV EHU, Fac Chem, Dept Appl Chem,Bionanoparticles Grp, Apdo 1072, Donostia San Sebastian 20080, Spain
Taboada, Pablo
[2
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[1] Univ Basque Country, UPV EHU, Fac Chem, Dept Appl Chem,Bionanoparticles Grp, Apdo 1072, Donostia San Sebastian 20080, Spain
[2] Univ Santiago de Compostela, Fac Phys, Particle Phys Dept, Colloids & Polymers Phys Grp, Campus Sur, Santiago De Compostela 15782, Spain
In this work, the feasibility of some poly(2-(diethylamino)ethyl methacrylate) (PDEAEMA)-based pH-sensitive nanogels as drug nanocarriers is evaluated. The anticancer drug doxorubicin (DOXO) is successfully encapsulated into the nanogels, achieving high drug loading and encapsulation efficiency. It has been found that the in vitro delivery of DOXO from the nanogels was pH-dependent: DOXO release rate is accelerated by decreasing pH from 7.4 (healthy cells) to 5.2 (pH condition for endo/lysosomial compartments and unhealthy cells) due to the swelling of the nanogel particles. The uptake of DOXO-loaded nanogels into MDA-MB-231 tumoral cells and the progressive release of the drug from the nanogels to the cell nuclei are demonstrated by fluorescence microscopy measurements. These results suggest a great potential of these DOXO-loaded nanogels for antitumor drug delivery. (C) 2018 Elsevier B.V. All rights reserved.
机构:
Univ Bordeaux 1, UMR CBMN CNRS5248, IECB, F-33607 Pessac, France
Univ Bordeaux, LCPO, UMR 5629, F-33600 Pessac, France
CNRS, LCPO, UMR 5629, F-33600 Pessac, FranceUniv Bordeaux 1, UMR CBMN CNRS5248, IECB, F-33607 Pessac, France
Pichavant, Loic
Amador, Gilles
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Univ Nantes, Fac Med, EA3826, F-44035 Nantes, FranceUniv Bordeaux 1, UMR CBMN CNRS5248, IECB, F-33607 Pessac, France
Amador, Gilles
Jacqueline, Cedric
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Univ Nantes, Fac Med, EA3826, F-44035 Nantes, FranceUniv Bordeaux 1, UMR CBMN CNRS5248, IECB, F-33607 Pessac, France
Jacqueline, Cedric
Brouillaud, Brigitte
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Univ Bordeaux Segalen, U1026, F-33000 Bordeaux, FranceUniv Bordeaux 1, UMR CBMN CNRS5248, IECB, F-33607 Pessac, France
Brouillaud, Brigitte
Heroguez, Valerie
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Univ Bordeaux, LCPO, UMR 5629, F-33600 Pessac, France
CNRS, LCPO, UMR 5629, F-33600 Pessac, FranceUniv Bordeaux 1, UMR CBMN CNRS5248, IECB, F-33607 Pessac, France