| Literature DB >> 27943679 |
Vedran Milosavljevic1, Pavlina Jelinkova1, Ana Maria Jimenez Jimenez1,2, Amitava Moulick1,2, Yazan Haddad1,2, Hana Buchtelova1, Sona Krizkova1,2, Zbynek Heger1,2, Lukas Kalina3, Lukas Richtera1,2, Pavel Kopel1,2, Vojtech Adam1,2.
Abstract
Herein we describe a novel alternative synthesis route of polyvinylpyrrolidone nanoparticles using salting-out method at a temperature close to polyvinylpyrrolidone decomposition. At elevated temperatures, the stability of polyvinylpyrrolidone decreases and the opening of pyrrolidone ring fractions occurs. This leads to cross-linking process, where separate units of polyvinylpyrrolidone interact among themselves and rearrange to form nanoparticles. The formation/stability of these nanoparticles was confirmed by transmission electron microscopy, X-ray photoelectron spectroscopy, mass spectrometry, infrared spectroscopy, and spectrophotometry. The obtained nanoparticles possess exceptional biocompatibility. No toxicity and genotoxicity was found in normal human prostate epithelium cells (PNT1A) together with their high hemocompatibility. The antimicrobial effects of polyvinylpyrrolidone nanoparticles were tested on bacterial strains isolated from the wounds of patients suffering from hard-to-heal infections. Molecular analysis (qPCR) confirmed that the treatment can induce the regulation of stress-related survival genes. Our results strongly suggest that the polyvinylpyrrolidone nanoparticles have great potential to be developed into a novel antibacterial compound.Entities:
Keywords: antibacterial; cross-linking; polyvinylpyrrolidone nanoparticles; salting-out; toxicity
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Year: 2016 PMID: 27943679 DOI: 10.1021/acs.molpharmaceut.6b00807
Source DB: PubMed Journal: Mol Pharm ISSN: 1543-8384 Impact factor: 4.939