Highly Sensitive Bacteria-Responsive Membranes Consisting of Core-Shell Polyurethane Polyvinylpyrrolidone Electrospun Nanofibers for In Situ Detection of Bacterial Infections.
Sarah CurrieFarinaz Jonidi ShariatzadehHardev SinghSarvesh LogsettySong LiuPublished in: ACS applied materials & interfaces (2020)
Bacteria responsive color-changing wound dressings offer a valuable platform for continuous monitoring of the wound bed facilitating early detection of bacterial infections. In this study, we present a highly sensitive electrospun nanofibrous polyurethane wound dressing incorporating a hemicyanine-based chromogenic probe with a labile ester linkage that can be enzymatically cleaved by bacterial lipase released from clinically relevant strains, such as Pseudomonas aeruginosa and methicillin-resistant Staphylococcus aureus (MRSA). A rapid chromogenic response was achieved by localizing the dye at the surface of core-shell fibers, resulting in a 5x faster response relative to conventional nanofibers. By incorporating polyvinylpyrrolidone (PVP) dopant in the shell, the sensitivity was boosted to enable detection of bacteria at clinically relevant concentrations after 2 h exposure: 2.5 × 105 CFU/cm2 P. aeruginosa and 1.0 × 106 CFU/cm2 MRSA. Introduction of PVP in the shell also boosted the degree of hydrolysis of the chromogenic probe by a factor of 1.2× after a 3 h exposure to a low concentration of P. aeruginosa (105 CFU/cm2). PVP was also found to improve the discernibility of the color change at high bacterial concentrations. The co-operativity between the chromogenic probe, fiber structure, and polymer composition is well-suited for timely in situ detection of wound infection.
Keyphrases
- methicillin resistant staphylococcus aureus
- loop mediated isothermal amplification
- wound healing
- living cells
- staphylococcus aureus
- tissue engineering
- label free
- pseudomonas aeruginosa
- real time pcr
- quantum dots
- fluorescent probe
- surgical site infection
- cystic fibrosis
- cancer therapy
- escherichia coli
- molecularly imprinted
- human immunodeficiency virus
- acinetobacter baumannii
- genome wide
- single molecule
- gene expression
- hiv testing
- anaerobic digestion