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Multifunctional PLA/Gelatin Bionanocomposites for Tailored Drug Delivery Systems
被引:11
作者:
Moya-Lopez, Carmen
[1
]
Juan, Alberto
[2
]
Donizeti, Murillo
[1
]
Valcarcel, Jesus
[3
]
Vazquez, Jose A.
[3
]
Solano, Eduardo
[4
]
Chapron, David
[1
]
Bourson, Patrice
[1
]
Bravo, Ivan
[2
]
Alonso-Moreno, Carlos
[2
,5
]
Clemente-Casares, Pilar
[5
,6
]
Gracia-Fernandez, Carlos
[7
]
Longo, Alessandro
[8
,9
]
Salloum-Abou-Jaoude, Georges
[10
]
Ocana, Alberto
[11
,12
,13
]
Pineiro, Manuel M.
[14
]
Hermida-Merino, Carolina
[14
]
Hermida-Merino, Daniel
[1
,14
,15
]
机构:
[1] Univ Lorraine, Cent Supelec, Lab Mat Opt Photon & Syst LMOPS, F-57000 Metz, France
[2] Ctr Reg Invest Biomed, Unidad NanoCRIB, Albacete 02008, Spain
[3] CSIC, Marine Res Inst IIM, Grp Recycling & Valorizat Waste Mat REVAL, Vigo 36208, Spain
[4] ALBA Synchrotron Light Source, NCD SWEET Beamline, Cerdanyola Del Valles 08290, Spain
[5] Univ Castilla La Mancha, Fac Farm Albacete, Albacete 02008, Spain
[6] Ctr Reg Invest Biomed, Unidad Med Mol, Albacete 02008, Spain
[7] TA Instruments Waters Chromatog, Madrid 28760, Spain
[8] ESRF, ID20, 71 Ave Martyrs, F-38000 Grenoble, France
[9] UOS Palermo, CNR, Ist Studio Mat Nanostrutturati ISMN, Via Ugo Malfa 153, I-90146 Palermo, Italy
[10] Constellium C TEC Technol Ctr, Parc Econ Centralp,725 Rue Aristide Berges, F-38341 Voreppe, France
[11] Hosp Clin San Carlos, IdISSC, Expt Therapeut Unit, Madrid 28040, Spain
[12] CIBERONC, Madrid 28040, Spain
[13] Complejo Hosp Univ Albacete, Oncol Traslac, Unidad Invest, Albacete 02008, Spain
[14] Univ Vigo, CINBIO, Dept Fis Aplicada, Campus Lagoas Marcosende, Vigo 36310, Spain
[15] DUBBLE ESRF, Netherlands Org Sci Res NWO, BP CS40220, F-38043 Grenoble, France
关键词:
bionanocomposite;
gelatin;
polylactide;
stereocomplex;
hydrogel;
nanoparticles;
drug delivery;
GLASS-TRANSITION TEMPERATURE;
PEG-PLA NANOPARTICLES;
RELEASE;
BEHAVIOR;
ACID);
MICROPARTICLES;
STEREOCOMPLEX;
D O I:
10.3390/pharmaceutics14061138
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
A series of bionanocomposites composed of shark gelatin hydrogels and PLA nanoparticles featuring different nanostructures were designed to generate multifunctional drug delivery systems with tailored release rates required for personalized treatment approaches. The global conception of the systems was considered from the desired customization of the drug release while featuring the viscoelastic properties needed for their ease of storage and posterior local administration as well as their biocompatibility and cell growth capability for the successful administration at the biomolecular level. The hydrogel matrix offers the support to develop a direct thermal method to convert the typical kinetic trapped nanostructures afforded by the formulation method whilst avoiding the detrimental nanoparticle agglomeration that diminishes their therapeutic effect. The nanoparticles generated were successfully formulated with two different antitumoral compounds (doxorubicin and dasatinib) possessing different structures to prove the loading versatility of the drug delivery system. The bionanocomposites were characterized by several techniques (SEM, DLS, RAMAN, DSC, SAXS/WAXS and rheology) as well as their reversible sol-gel transition upon thermal treatment that occurs during the drug delivery system preparation and the thermal annealing step. In addition, the local applicability of the drug delivery system was assessed by the so-called "syringe test" to validate both the storage capability and its flow properties at simulated physiological conditions. Finally, the drug release profiles of the doxorubicin from both the PLA nanoparticles or the bionanocomposites were analyzed and correlated to the nanostructure of the drug delivery system.
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页数:21
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