4.3 Article

Silver nanoparticles-quercetin conjugation to siRNA against drug-resistant Bacillus subtilis for effective gene silencing: in vitro and in vivo

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ELSEVIER
DOI: 10.1016/j.msec.2016.03.024

关键词

AgNPs; Quercetin; Fluorescence; Antibacterial activity; siRNA; In vitro and in vivo

资金

  1. National Natural Science Foundation of China [21401002]
  2. Natural Science Foundation of Anhui Province, China [1508085QB37]
  3. Youth Science Fund Key Project of Anhui Agricultural University [2013ZR011]
  4. Science Foundation of Young Teachers of Anhui Agricultural University [ZHSJ2013057]
  5. New Specialty of Biopharmaceutical Construction of Anhui Agricultural University [SJJD201313]

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Quercetin (Qe) exhibited extremely low water solubility, and thus, it was modified using silver nanoparticles (AgNPs). We fabricated AgNPs combined with Qe (AgNPs-Qe). The modification suggested that the synergistic properties of Qe enhanced the antibacterial activity of AgNPs. However, AgNPs-Qe exerted no effect on many kinds of drug-resistant bacteria, including Pseudomonas aeruginosa and Bacillus subtilis. RNA interference has considerable therapeutic potential because of its high specificity and potential capability to evade drug resistance. Therefore, we stabilized AgNPs-Qe with a layer of molecules (siRNA). The newly fabricated nanoparticles exerted improved effect on many kinds of bacteria, including the most prominent drug-resistant species B. subtilis. Agarose gel electrophoresis showed that the highest critical nitrogen-to-phosphorus (N/P) ratio occurred at a vector/siRNA with a w/w ratio of 7:1. Characterization experiment indicated that the diameter of siRNA/AgNPs-Qe was approximately 40 nm (40 +/- 10 nm). Moreover, AgNPs-Qe were stabilized with a layer of siRNA that was approximately 10 nm thick. Results of the in vitro study suggested that siRNA/AgNPs-Qe could destroy the cell wall and inhibit bacterial propagation. Meanwhile, the in vivo experiment on the animal bacteremia model, as well as the optical imaging of nude mice and their isolated organs, demonstrated that bacteria accumulated in the blood, heart, liver, spleen, lungs, and kidneys after the intravenous injection of B. subtilis. The bacteria in the blood and organs, as well as the inflamed cells in the tissues, gradually decreased after the mice received intravenous tail injection of siRNA/AgNPs-Qe for treatment. Both the in vitro and the in vivo studies exhibit that siRNA/AgNPs-Qe can be a potential nanoscale drug delivery system for B. subtilis targeting bacterimia. (C) 2016 Elsevier B.V. All rights reserved.

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