4.8 Article

Development of Novel Amphotericin B-Immobilized Nitric Oxide-Releasing Platform for the Prevention of Broad-Spectrum Infections and Thrombosis

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 13, Issue 17, Pages 19613-19624

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c01330

Keywords

multifunctional surfaces; nitric oxide-releasing surfaces; antimicrobial surfaces; hemocompatible; medical device

Funding

  1. National Institutes of Health, USA grant [R01HL134899]

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This study developed a novel surface combining nitric oxide (NO) with antifungal medication for a broad-spectrum antimicrobial and antithrombotic effect, successfully reducing the viability of bacteria and yeast, as well as decreasing platelet adhesion. This innovative approach offers a promising solution to reduce infection and thrombosis associated with indwelling medical devices.
Indwelling medical devices currently used to diagnose, monitor, and treat patients invariably suffer from two common clinical complications: broad-spectrum infections and device-induced thrombosis. Currently, infections are managed through antibiotic or antifungal treatment, but the emergence of antibiotic resistance, the formation of recalcitrant biofilms, and difficulty identifying culprit pathogens have made treatment increasingly challenging. Additionally, systemic anticoagulation has been used to manage device-induced thrombosis, but subsequent life-threatening bleeding events associated with all available therapies necessitates alternative solutions. In this study, a broad-spectrum antimicrobial, antithrombotic surface combining the incorporation of the nitric oxide (NO) donor S-nitroso-N-acetylpenicillamine (SNAP) with the immobilization of the antifungal Amphotericin B (AmB) on polydimethylsiloxane (PDMS) was developed in a two-step process. This novel strategy combines the key advantages of NO, a bactericidal agent and platelet inhibitor, with AmB, a potent antifungal agent. We demonstrated that SNAP-AmB surfaces significantly reduced the viability of adhered Staphylococcus aureus (99.0 +/- 0.2%), Escherichia coli (89.7 +/- 1.0%), and Candida albicans (93.5 +/- 4.2%) compared to controls after 24 h of in vitro exposure. Moreover, SNAP-AmB surfaces reduced the number of platelets adhered by 74.6 +/- 3.9% compared to controls after 2 h of in vitro porcine plasma exposure. Finally, a cytotoxicity assay validated that the materials did not present any cytotoxic side effects toward human fibroblast cells. This novel approach is the first to combine antifungal surface functionalization with NO-releasing technology, providing a promising step toward reducing the rate of broad-spectrum infection and thrombosis associated with indwelling medical devices.

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