Evaluation of a combined emulsion process to encapsulate methylene blue into PLGA nanoparticles

被引:15
作者
Alejandra Gutierrez-Valenzuela, Cindy [1 ]
Esquivel, Reynaldo [2 ]
Guerrero-German, Patricia [3 ]
Zavala-Rivera, Paul [3 ]
Carlos Rodriguez-Figueroa, Jose [3 ]
Guzman-Z, Roberto [4 ]
Lucero-Acuna, Armando [3 ]
机构
[1] Univ Sonora, Dept Phys, Nanotechnol Grad Program, Hermosillo, Sonora, Mexico
[2] Natl Council Sci & Technol Mexico, Mexico City, DF, Mexico
[3] Univ Sonora, Dept Chem & Met Engn, Col Ctr, Blvd Luis Encinas & Rosales S-N, Hermosillo 83000, Sonora, Mexico
[4] Univ Arizona, Dept Chem & Environm Engn, Tucson, AZ USA
关键词
DRUG-DELIVERY SYSTEMS; PHOTODYNAMIC THERAPY; IN-VITRO; POLYMERIC NANOPARTICLES; CANCER-CELLS; CONTROLLED-RELEASE; SOLVENT; NANOPRECIPITATION; PHTHALOCYANINE; CHEMOTHERAPY;
D O I
10.1039/c7ra12296a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The delivery of photosensitizer compounds using biodegradable nanoparticles could improve dosage, controlled release and its bioavailability. In this study, methylene blue (MB) loaded PLGA nanoparticles (MB-PNP) are prepared by a new approach combining single and double emulsification techniques. Comparisons of MB-PNP obtained with the combined and the individual techniques are presented. Nanoparticles are characterized by dynamic light scattering, laser Doppler electrophoresis and scanning electron microscopy. Particles prepared by the combined technique presented hydrodynamic diameters of 186 nm. The sizes of MB-PNP obtained from the single emulsion technique are similar to the combined technique, while the diameter of particles prepared by double emulsion increased from 201 nm to 287 nm as the TDL increased. MB-PNP displayed an average zeta potential between -21 mV and -28 mV for all formulations. MB loading ranges between 0.3-1.4%, while the encapsulation efficiency ranges from 8-14%, both depending on the TDL and the preparation technique. In vitro release studies show a monophasic release profile that was analyzed by considering the mechanisms of initial burst, drug diffusion and a combination of them. Experimental results could be better described using a mathematical model of release that simultaneously combines the mechanisms of initial burst and drug diffusion. The approach presented to encapsulate MB and also to analyze the drug release could be extended to other drugs with partial solubility.
引用
收藏
页码:414 / 422
页数:9
相关论文
共 47 条
  • [1] A theoretical model of erosion and macromolecular drug release from biodegrading microspheres
    Batycky, RP
    Hanes, J
    Langer, R
    Edwards, DA
    [J]. JOURNAL OF PHARMACEUTICAL SCIENCES, 1997, 86 (12) : 1464 - 1477
  • [2] Nanoparticles as vehicles for delivery of photodynamic therapy agents
    Bechet, Denise
    Couleaud, Pierre
    Frochot, Celine
    Viriot, Marie-Laure
    Guillemin, Francois
    Barberi-Heyob, Muriel
    [J]. TRENDS IN BIOTECHNOLOGY, 2008, 26 (11) : 612 - 621
  • [3] Nanospheres based on PLGA/amphiphilic cyclodextrin assemblies as potential enhancers of Methylene Blue neuroprotective effect
    Cannava, C.
    Stancanelli, R.
    Marabeti, M. R.
    Venuti, V.
    Cascio, C.
    Guarneri, P.
    Bongiorno, C.
    Sortino, G.
    Majolino, D.
    Mazzaglia, A.
    Tommasini, S.
    Ventura, C. A.
    [J]. RSC ADVANCES, 2016, 6 (20) : 16720 - 16729
  • [4] Polymer-surfactant nanoparticles for sustained release of water-soluble drugs
    Chavanpatil, Mahesh D.
    Khdair, Ayman
    Patil, Yogesh
    Handa, Hitesh
    Mao, Guangzhao
    Panyam, Jayanth
    [J]. JOURNAL OF PHARMACEUTICAL SCIENCES, 2007, 96 (12) : 3379 - 3389
  • [5] Lipophilic drug loaded nanospheres prepared by nanoprecipitation: effect of formulation variables on size, drug recovery and release kinetics
    Chorny, M
    Fishbein, I
    Danenberg, HD
    Golomb, G
    [J]. JOURNAL OF CONTROLLED RELEASE, 2002, 83 (03) : 389 - 400
  • [6] A new double emulsion solvent diffusion technique for encapsulating hydrophilic molecules in PLGA nanoparticles
    Cohen-Sela, Einat
    Chorny, Michael
    Koroukhov, Nickolay
    Danenberg, Haim D.
    Golomb, Gershon
    [J]. JOURNAL OF CONTROLLED RELEASE, 2009, 133 (02) : 90 - 95
  • [7] Quantifying drug release from PLGA nanoparticulates
    Corrigan, Owen I.
    Li, Xue
    [J]. EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2009, 37 (3-4) : 477 - 485
  • [8] Modeling and comparison of dissolution profiles
    Costa, P
    Manuel, J
    Lobo, S
    [J]. EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2001, 13 (02) : 123 - 133
  • [9] PLGA-based nanoparticles: An overview of biomedical applications
    Danhier, Fabienne
    Ansorena, Eduardo
    Silva, Joana M.
    Coco, Regis
    Le Breton, Aude
    Preat, Veronique
    [J]. JOURNAL OF CONTROLLED RELEASE, 2012, 161 (02) : 505 - 522
  • [10] Chitosan nanoparticles enhance the efficiency of methylene blue-mediated antimicrobial photodynamic inactivation of bacterial biofilms: An in vitro study
    Darabpour, Esmaeil
    Kashef, Nasim
    Mashayekhan, Shohreh
    [J]. PHOTODIAGNOSIS AND PHOTODYNAMIC THERAPY, 2016, 14 : 211 - 217