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MicroRNA (miRNA) has emerged as a promising alternative therapeutic treatment for cancer, but its delivery has been hindered by low cellular uptake and degradation during circulation. In this review, we discuss the various methods of delivering miRNA, including viral and non-viral delivery systems such as liposomes and nanoparticles. We also examine the use of nanoparticles for miRNA-based diagnostics. We focus specifically on non-viral delivery systems utilizing coinage metals in the form of nanoparticles and the use of self-assembled monolayers (SAMs) as a method of surface modification. We review the use of SAMs for the conjugation and delivery of small noncoding ribonucleic acid (ncRNA), particularly SAMs derived from positively charged adsorbates to generate charged surfaces that can interact electrostatically with negatively charged miRNA. We also discuss the effects of the cellular uptake of gold and other plasmonic nanoparticles, as well as the challenges associated with the degradation of oligonucleotides. Our review highlights the potential of SAM-based systems as versatile and robust tools for delivering miRNA and other RNAs in vitro and in vivo and the need for further research to address the challenges associated with miRNA delivery and diagnostics.
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Crosslinked organosulfur-based self-assembled monolayers: formation and applications
Self-assembled monolayers (SAMs) have found use in diverse applications that range from corrosion prevention to biosensing. However, for all of these applications, stability remains a key challenge for the utilization of SAMs. Over the last decade, intermolecular crosslinking as a method to enhance the thermal and chemical stability of SAMs has attracted increased attention from scientists and engineers. As such, this review introduces a variety of crosslinked SAMs: (1) aromatic thiol-based SAMs; (2) olefinic- and acetylenic-based alkanethiols; (3) other aliphatic alkanethiols; (4) silane-based alkanethiols; (5) boronic acid-based alkanethiols; and (6) crosslinked SAMs realized by hydrogen bonding. By offering insight into the structure-application relationships of the aforementioned SAMs, this review seeks to inspire researchers toward the development of new classes of SAMs with enhanced stabilities and working lifetimes.
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- Award ID(s):
- 2109174
- PAR ID:
- 10377938
- Publisher / Repository:
- Soft Science
- Date Published:
- Journal Name:
- Soft Science
- Volume:
- 2
- Issue:
- 2
- ISSN:
- 2769-5441
- Page Range / eLocation ID:
- 5
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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The molecular electronic devices based on self-assembled monolayer (SAM) on metal surfaces demonstrate novel electronic functions for device minimization yet are unable to realize in practical applications, due to their instability against oxidation of the sulfur-metal bond. This paper describes an alternative to the thiolate anchoring group to form stable SAMs on gold by selenides anchoring group. Because of the formation of strong selenium-gold bonds, these stable SAMs allow us to incorporate them in molecular tunnel junctions to yield extremely stable junctions for over 200 days. A detailed structural characterization supported by spectroscopy and first-principles modeling shows that the oxidation process is much slower with the selenium-gold bond than the sulfur-gold bond, and the selenium-gold bond is strong enough to avoid bond breaking even when it is eventually oxidized. This proof of concept demonstrates that the extraordinarily stable SAMs derived from selenides are useful for long-lived molecular electronic devices and can possibly become important in many air-stable applications involving SAMs.more » « less
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