On-Demand Sequential Release of Dual Drug from pH-Responsive Electrospun Janus Nanofiber Membranes toward Wound Healing and Infection Control.
Altangerel AmarjargalOlga CegielskaDorota KolbukBartlomiej KalaskaPaweł Ł SajkiewiczPublished in: ACS applied materials & interfaces (2023)
Drugs against bacteria and abnormal cells, such as antibiotics and anticancer drugs, may save human lives. However, drug resistance is becoming more common in the clinical world. Nowadays, a synergistic action of multiple bioactive compounds and their combination with smart nanoplatforms has been considered an alternative therapeutic strategy to fight drug resistance in multidrug-resistant cancers and microorganisms. The present study reports a one-step fabrication of innovative pH-responsive Janus nanofibers loaded with two active compounds, each in separate polymer compartments for synergistic combination therapy. By dissolving one of the compartments from the nanofibers, we could clearly demonstrate a highly yielded anisotropic Janus structure with two faces by scanning electron microscopy (SEM) analysis. To better understand the distinctive attributes of Janus nanofibers, several analytical methods, such as X-ray diffraction (XRD), FTIR spectroscopy, and contact angle goniometry, were utilized to examine and compare them to those of monolithic nanofibers. Furthermore, a drug release test was conducted in pH 7.4 and 6.0 media since the properties of Janus nanofibers correlate significantly with different environmental pH levels. This resulted in the on-demand sequential codelivery of octenidine (OCT) and curcumin (CUR) to the corresponding pH stimulus. Accordingly, the antibacterial properties of Janus fibers against Escherichia coli and Staphylococcus aureus , tested in a suspension test, were pH-dependent, i.e., greater in pH 6 due to the synergistic action of two active compounds, and Eudragit E100 (EE), and highly satisfactory. The biocompatibility of the Janus fibers was confirmed in selected tests.
Keyphrases
- electron microscopy
- wound healing
- combination therapy
- high resolution
- escherichia coli
- drug release
- multidrug resistant
- staphylococcus aureus
- cancer therapy
- endothelial cells
- induced apoptosis
- single molecule
- magnetic resonance imaging
- climate change
- magnetic resonance
- diabetic retinopathy
- adverse drug
- acinetobacter baumannii
- optical coherence tomography
- cystic fibrosis
- risk assessment
- signaling pathway
- gram negative
- pseudomonas aeruginosa
- endoplasmic reticulum stress
- young adults
- crystal structure
- induced pluripotent stem cells
- molecularly imprinted