4.2 Article

Antibody-Functionalized Halloysite Nanotubes for Targeting Bacterial Cells

期刊

ACS APPLIED BIO MATERIALS
卷 4, 期 5, 页码 4094-4104

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsabm.0c01332

关键词

Halloysite nanotubes; bacteria; hybrid; targeting; E. coli; antibody; flow cytometry

资金

  1. European Union's Horizon 2020 research and innovation programme [720815]
  2. H2020 Societal Challenges Programme [720815] Funding Source: H2020 Societal Challenges Programme

向作者/读者索取更多资源

Halloysite nanotubes (HNTs) have emerged as a promising nanomaterial for various applications due to their large pore volume, high specific surface area, and biocompatibility. This research focuses on designing and synthesizing functionalized HNTs to selectively bind to target bacterial cells, providing a method for treating challenging heterogeneous cell populations. The functionalized HNTs show selective binding to target bacteria and demonstrate biocompatibility, serving as a generic platform for targeted delivery against any microorganism through facile antibody adjustment.
Halloysite nanotubes (HNTs) are naturally occurring tubular clay particles which have emerged in recent years as a promising nanomaterial for numerous applications. Specifically, HNTs' large pore volume and high specific surface area in combination with their biocompatibility make them ideal nano-carriers for bioactive compounds. This research aims to design and synthesize functionalized HNTs, which could selectively bind to target bacterial cells in suspension. Such a system can allow us to treat target cells within a challenging heterogeneous population, such as contaminated ecosystems or gut flora. HNTs functionalization is achieved by immobilizing specific antibodies onto the nanotube surface. The synthetic route is realized by the following subsequent steps: acidic etching of the HNTs, silanization of reactive surface hydroxyls, conjugation of protein A, and oriented immobilization of the antibody. HNT functionalization is studied by a set of analytical techniques including attenuated total reflectance Fourier-transform infrared spectroscopy, zeta potential measurements, thermal gravimetric analysis, scanning and transmission electron microscopy, as well as fluorescence microscopy. The selective binding of the functionalized HNTs to their target bacteria is observed upon incubation with live homogenous and heterogeneous cultures using fluorescence microscopy and high-throughput flow cytometry. Plate count and live/dead staining experiments demonstrate the biocompatibility of the antibody-HNT hybrid with its target bacteria. The suggested HNT-based smart carrier constitutes a generic platform for targeted delivery that could be selectively tailored against any microorganism by facile antibody adjustment.

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