4.8 Article

A pH-Responsive Persistent Luminescence Nanozyme for Selective Imaging and Killing of Helicobacter pylori and Common Resistant Bacteria

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 13, Issue 51, Pages 60955-60965

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c21318

Keywords

Helicobacter pylori; pH-responsive; persistent luminescence; nanozyme; antibacterial effect

Funding

  1. National Natural Science Foundation of China [21934002, 21804056, 21804057]
  2. Postgraduate Research & Practice Innovation Program of Jiangsu Province [KYCX20_1858]
  3. Natural Science Foundation of Jiangsu Province, China [BK20180581, BK20180584]
  4. National First-Class Discipline Program of Food Science and Technology [JUFSTR20180301]
  5. Program of the Collaborative Innovation Center of Food Safety and Quality Control in Jiangsu Province

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A novel pH-responsive nanozyme was reported for in vivo imaging and inactivation of H. pylori, showing multifunctional properties for targeted imaging and activated deactivation of the bacteria under extreme gastric acid conditions. This promising nanozyme platform has the potential to combat other bacterial infections as well.
Helicobacter pylori (H. pylori) infection is implicated in the etiology of many diseases. H. pylori eradication by antibiotic therapy is limited by the extreme acidic environment in the stomach, the undesired side effect of intestinal commensal bacteria, and the development of drug resistance. Here, we report a pH-responsive persistent luminescence (PL) nanozyme (MSPLNP-Au-CB) for in vivo imaging and inactivation of H. pylori. This PL nanozyme is composed of mesoporous silica (MS)-coated persistent luminescence nanoparticles (MSPLNP), Au nanoparticles (AuNP), and chitosan-benzeneboronic acid (CB), taking advantage of the long PL of PLNP to realize autofluorescence-free imaging, the pH-activated oxidase- and peroxidase-like nanozyme activity of AuNP, and the bacterial binding capacity of CB. The MSPLNP-Au-CB nanozyme can resist the corrosion of gastric acid and exhibit pH-activated dual nanozyme activity to catalyze bactericidal reactive oxygen species generation. This multifunctional nanozyme enables targeted imaging and activated deactivation of H. pylori under extreme gastric acid conditions as well as methicillin-resistant Staphylococcus aureus in common slightly acidic environments, while it has no side effects on the commensal bacteria and normal cells in normal physiological environments. This work provides a promising PL nanozyme platform for bioimaging and therapy of bacterial infection under harsh conditions.

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