PLGA cationic nanoparticles, obtained from nano-emulsion templating, as potential DNA vaccines

被引:16
作者
Soler Besumbes, Eduard [1 ,2 ]
Fornaguera, Cristina [1 ,2 ,3 ]
Monge, Marta [1 ,2 ,4 ]
Jose Garcia-Celma, Maria [2 ,4 ]
Carrion, Javier [5 ]
Solans, Conxita [1 ,2 ]
Dols-Perez, Aurora [1 ,2 ,6 ]
机构
[1] CSIC, Inst Adv Chem Catalonia, IQAC, C Jordi Girona 18-26, ES-08034 Barcelona, Spain
[2] CIBER Bioengn Biomat & Nanomed CIBER BBN, Barcelona 08034, Spain
[3] URL, IQS, Grp Engn Mat GEMAT, Barcelona 08017, Spain
[4] Univ Barcelona, Dept Pharm & Pharmaceut Technol & Phys Chem, Barcelona, Spain
[5] Univ Complutense Madrid, Dept Anim Hlth, INMIVET, Madrid, Spain
[6] Delft Univ Technol, Kavli Inst Nanosci, Dept Bionanosci, Maasweg 9, NL-2629HZ Delft, Netherlands
关键词
Nano-emulsion templating; Polymeric nanoparticles; Gene-delivery vector; Polyplexes; Non-viral gene therapy; DRUG-DELIVERY SYSTEMS; DENDRITIC CELLS; GENE DELIVERY; POLY(BETA-AMINO ESTER)S; SIRNA DELIVERY; NANOMEDICINE; EFFICIENT; POLYMERS; FUNCTIONALIZATION; PLATFORMS;
D O I
10.1016/j.eurpolymj.2019.109229
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Polymeric nanoparticles offer advantageous characteristics as gene-delivery vectors such as biocompatibility and biodegradability. With this aim, a smart and innovative strategy was followed here: Cationic PLGA nanoemulsions, prepared by a low energy method, were used as templates to obtain cationic nanoparticles (NPs) able to easily complex with nucleic acids (i.e. plasmid DNA) by electrostatic interactions. The strategy employed to produce stable positively-charged nanoparticles was the use of non-ionic/cationic surfactant mixtures to stabilize template nano-emulsions. This methodology allowed obtaining nanoparticles with reproducible nanometric sizes and positive zeta potential values, appropriate to successfully complex with nucleic acids, resulting in nanometric spherical polyplexes. Nanoparticles, plasmids and polyplexes proved to be biocompatible at the optimal concentration. Therefore, we can conclude that we have designed a novel strategy to efficiently obtain cationic polymeric nanoparticles that can be a promising approach to act as novel non-viral gene-delivery vectors, useful for many applications in gene therapy, such as gene vaccines.
引用
收藏
页数:8
相关论文
共 67 条
  • [1] Protein direct delivery to dendritic cells using nanoparticles based on amphiphilic poly(amino acid) derivatives
    Akagi, Takami
    Wang, Xin
    Uto, Tomofumi
    Baba, Masanori
    Akashi, Mitsuru
    [J]. BIOMATERIALS, 2007, 28 (23) : 3427 - 3436
  • [2] Reprint of: Nanoparticles for ex vivo siRNA delivery to dendritic cells for cancer vaccines: Programmed endosomal escape and dissociation
    Akita, Hidetaka
    Kogure, Kentaro
    Moriguchi, Rumiko
    Nakamura, Yoshio
    Higashi, Tomoko
    Nakamura, Takashi
    Serada, Satoshi
    Fujimoto, Minoru
    Naka, Tetsuji
    Futaki, Shiroh
    Harashima, Hideyoshi
    [J]. JOURNAL OF CONTROLLED RELEASE, 2011, 149 (01) : 58 - 64
  • [3] Alarcon J.B., 1999, ADV PARASIT, V42, P452
  • [4] The growing role of nanotechnology in combating infectious disease
    Blecher, Karin
    Nasir, Adnan
    Friedman, Adam
    [J]. VIRULENCE, 2011, 2 (05) : 395 - 401
  • [5] Nanoparticle-Based Medicines: A Review of FDA-Approved Materials and Clinical Trials to Date
    Bobo, Daniel
    Robinson, Kye J.
    Islam, Jiaul
    Thurecht, Kristofer J.
    Corrie, Simon R.
    [J]. PHARMACEUTICAL RESEARCH, 2016, 33 (10) : 2373 - 2387
  • [6] Nanomedicine applied to translational oncology: A future perspective on cancer treatment
    Bregoli, Lisa
    Movia, Dania
    Gavigan-Imedio, James D.
    Lysaght, Joanne
    Reynolds, John
    Prina-Mello, Adriele
    [J]. NANOMEDICINE-NANOTECHNOLOGY BIOLOGY AND MEDICINE, 2016, 12 (01) : 81 - 103
  • [7] Polymers and nanoparticles: Intelligent tools for intracellular targeting?
    Breunig, M.
    Bauer, S.
    Goefferich, A.
    [J]. EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2008, 68 (01) : 112 - 128
  • [8] Design of parenteral MNP-loaded PLGA nanoparticles by a low-energy emulsification approach as theragnostic platforms for intravenous or intratumoral administration
    Caldero, G.
    Fornaguera, C.
    Zadoina, L.
    Dols-Perez, A.
    Solans, C.
    [J]. COLLOIDS AND SURFACES B-BIOINTERFACES, 2017, 160 : 535 - 542
  • [9] Formation of polymeric nano-emulsions by a low-energy method and their use for nanoparticle preparation
    Caldero, Gabriela
    Garcia-Celma, Maria Jose
    Solans, Conxita
    [J]. JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2011, 353 (02) : 406 - 411
  • [10] 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