Efficacy of ferulic acid encapsulated chitosan nanoparticles against Candida albicans biofilm

被引:71
作者
Panwar, Richa [1 ]
Pemmaraju, Suma C. [1 ]
Sharma, Asvene K. [1 ]
Pruthi, Vikas [1 ]
机构
[1] Indian Inst Technol Roorkee, Dept Biotechnol, Roorkee 247667, Uttar Pradesh, India
关键词
Chitosan nanoparticles; Ferulic acid; Cytocompatibility; Antibiofilm activity; FESEM; ANTIOXIDANT; PHENYLPROPANOIDS;
D O I
10.1016/j.micpath.2016.02.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Candida albicans, an opportunistic fungal pathogen is a major causative agent of superficial to systemic life-threating biofilm infections on indwelling medical devices. These biofilms acts as double edge swords owing to their resistance towards antibiotics and immunological barriers. To overcome this threat ferulic acid encapsulated chitosan nanoparticles (FA-CSNPs) were formulated to assess its efficacy as an antibiofilm agent against C albicans. These FA-CSNPs were synthesized using ionotropic gelation method and observed through field emission scanning electron microscopy (FESEM) and fluorescent microscopy. Assessment of successful encapsulation and stability of ferulic acid into chitosan nanoparticles was made using Fourier transform infrared spectrum (FTIR), H-1 NMR and thermal analyses. Synthesized FA-CSNPs, were found to be cytocompatible, when tested using Human Embryonic Kidney (HEK-293) cell lines. XTT assay revealed that FA-CSNPs reduced the cell metabolic activity of C albicans upto 22.5% as compared to native ferulic acid (63%) and unloaded CSNPs (88%) after 24 h incubation. Disruption of C albicans biofilm architecture was visualized by FESEM. Results highlighted the potential of FA-CSNPs to be used as an effective alternative to the conventional antifungal therapeutics. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:21 / 31
页数:11
相关论文
共 41 条
  • [21] Candida species bloodstream infection: epidemiology and outcome in a single institution from 1991 to 2008
    Ortega, M.
    Marco, F.
    Soriano, A.
    Almela, M.
    Martinez, J. A.
    Lopez, J.
    Pitart, C.
    Mensa, J.
    [J]. JOURNAL OF HOSPITAL INFECTION, 2011, 77 (02) : 157 - 161
  • [22] Panwar R., 2015, APPL NANOSCI
  • [23] Targeted delivery of low molecular drugs using chitosan and its derivatives
    Park, Jae Hyung
    Saravanakumar, Gurusamy
    Kim, Kwangmeyung
    Kwon, Ick Chan
    [J]. ADVANCED DRUG DELIVERY REVIEWS, 2010, 62 (01) : 28 - 41
  • [24] Chitosan as a starting material for wound healing applications
    Patrulea, V.
    Ostafe, V.
    Borchard, G.
    Jordan, O.
    [J]. EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2015, 97 : 417 - 426
  • [25] Anticandidal low molecular compounds from higher plants with special reference to compounds from essential oils
    Pauli, A
    [J]. MEDICINAL RESEARCH REVIEWS, 2006, 26 (02) : 223 - 268
  • [26] Pemmaraju SC, 2013, INDIAN J EXP BIOL, V51, P1032
  • [27] Preparation and antibacterial activity of chitosan nanoparticles
    Qi, LF
    Xu, ZR
    Jiang, X
    Hu, CH
    Zou, XF
    [J]. CARBOHYDRATE RESEARCH, 2004, 339 (16) : 2693 - 2700
  • [28] Candida biofilms:: an update
    Ramage, G
    Saville, SP
    Thomas, DP
    López-Ribot, JL
    [J]. EUKARYOTIC CELL, 2005, 4 (04) : 633 - 638
  • [29] Ramage G, 2001, Am Clin Lab, V20, P42
  • [30] Phenylpropanoids of Plant Origin as Inhibitors of Biofilm Formation by Candida albicans
    Raut, Jayant Shankar
    Shinde, Ravikumar Bapurao
    Chauhan, Nitin Mahendra
    Karuppayil, Sankunny Mohan
    [J]. JOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY, 2014, 24 (09) : 1216 - 1225