Biocompatibility Profile and In Vitro Cellular Uptake of Self-assembled Alginate Nanoparticles

被引:17
作者
Zhang, Pei [1 ,2 ]
Zhao, Shirui [1 ]
Yu, Yaoyao [2 ]
Wang, Huan [2 ]
Yang, Yan [1 ]
Liu, Chenguang [1 ]
机构
[1] Ocean Univ China, Coll Marine Life Sci, Qingdao 266003, Peoples R China
[2] Luoyang Normal Univ, Dept Life Sci, Luoyang 471934, Peoples R China
关键词
alginate; degree of substitution; nanoparticles; cytotoxicity; cellular uptake; NEUTRAL AMINO-ACID; CHITOSAN NANOPARTICLES; L-PHENYLALANINE; TRANSPORT; DELIVERY; SIZE; CACO-2; PERMEABILITY; CELLS; CYTOTOXICITY;
D O I
10.3390/molecules24030555
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Polymeric nanoparticles could offer promising controlled drug delivery. The biocompatibility is of extreme importance for future applications in humans. Self-assembled polymeric nanoparticles based on phenylalanine ethyl ester (PAE)-modified alginate (Alg) had been successfully prepared and characterized in our lab. However, little is known about their interaction with cells and other biological systems. In this study, nanoparticles (NPs) based on PAE-Alg conjugates (PEA-NPs) with different degree of substitution (DS) were prepared and investigated. Our results showed that PEA-NPs had no effects on the proliferation of the human intestinal epithelial Caco-2 cells at concentrations up to 1000 mu g/mL. Furthermore, the in vitro cellular uptake profile of PEA-NPs, concerning several parameters involved in the application of therapeutic or diagnostic NPs, such as NPs concentration, time and temperature, was described. Different NPs have been adopted for cellular uptake studies and the NPs internalized into Caco-2 cells were quantified. Cellular uptake efficiency could reach 60% within 4 h. PEA-NPs also showed greater cell permeability than oleoyl alginate ester nanoparticles (OAE-NPs) previously prepared in our lab. Our studies reveal that NPs based on PEA conjugate are promising nanosystems for cellular delivery.
引用
收藏
页数:12
相关论文
共 52 条
  • [1] Nanoparticle vaccines against respiratory viruses
    Adair, Brian M.
    [J]. WILEY INTERDISCIPLINARY REVIEWS-NANOMEDICINE AND NANOBIOTECHNOLOGY, 2009, 1 (04) : 405 - 414
  • [2] Preparation and characterization of biodegradable nanoparticles based on poly(γ-glutamic acid) with L-phenylalanine as a protein carrier
    Akagi, T
    Kaneko, T
    Kida, T
    Akashi, M
    [J]. JOURNAL OF CONTROLLED RELEASE, 2005, 108 (2-3) : 226 - 236
  • [3] Akiyoshi K., 1996, SUPRAMOL SCI, V3, P157, DOI [10.1016/0968-5677(96)00031-4, DOI 10.1016/0968-5677(96)00031-4]
  • [4] Drug delivery systems: Entering the mainstream
    Allen, TM
    Cullis, PR
    [J]. SCIENCE, 2004, 303 (5665) : 1818 - 1822
  • [5] ARTURSSON P, 1991, CRIT REV THER DRUG, V8, P305
  • [6] Transport mechanisms of the large neutral amino acid L-phenylalanine in the human intestinal epithelial Caco-2 cell line
    Berger, V
    Larondelle, Y
    Trouet, A
    Schneider, YJ
    [J]. JOURNAL OF NUTRITION, 2000, 130 (11) : 2780 - 2788
  • [7] Biomedical nanoparticles modulate specific CD4+ T cell stimulation by inhibition of antigen processing in dendritic cells
    Blank, Fabian
    Gerber, Peter
    Rothen-Rutishauser, Barbara
    Sakulkhu, Usawadee
    Salaklang, Jatuporn
    De Peyer, Karin
    Gehr, Peter
    Nicod, Laurent P.
    Hofmann, Heinrich
    Geiser, Thomas
    Petri-Fink, Alke
    Von Garnier, Christophe
    [J]. NANOTOXICOLOGY, 2011, 5 (04) : 606 - 621
  • [8] Self-assembled chitosan-alginate polyplex nanoparticles containing temoporfin
    Brezaniova, Ingrid
    Trousil, Jiri
    Cernochova, Zulfiya
    Kral, Vladimir
    Hruby, Martin
    Stepanek, Petr
    Slouf, Miroslav
    [J]. COLLOID AND POLYMER SCIENCE, 2017, 295 (08) : 1259 - 1270
  • [9] Biocompatibility and internalization of molecularly imprinted nanoparticles
    Canfarotta, Francesco
    Waters, Alicia
    Sadler, Robyn
    McGill, Paul
    Guerreiro, Antonio
    Papkovsky, Dmitri
    Haupt, Karsten
    Piletsky, Sergey
    [J]. NANO RESEARCH, 2016, 9 (11) : 3463 - 3477
  • [10] Components Simulation of Viral Envelope via Amino Acid Modified Chitosans for Efficient Nucleic Acid Delivery: In Vitro and In Vivo Study
    Chang, Jing
    Xu, Xianghui
    Li, Haiping
    Jian, Yeting
    Wang, Gang
    He, Bin
    Gu, Zhongwei
    [J]. ADVANCED FUNCTIONAL MATERIALS, 2013, 23 (21) : 2691 - 2699