• Forging molecular bonds with green light

    From ScienceDaily@1337:3/111 to All on Mon Aug 24 21:30:32 2020
    Forging molecular bonds with green light

    Date:
    August 24, 2020
    Source:
    Queensland University of Technology
    Summary:
    Scientists have created a new molecular coupling tool employing
    both green light and pH triggers that has potential for use in
    applications such as drug delivery and 3D cell culture platforms.



    FULL STORY ========================================================================== Queensland University of Technology (QUT) researchers have created a new molecular coupling tool employing both green light and pH triggers that
    has potential for use in applications such as drug delivery and 3D cell
    culture platforms.


    ========================================================================== Their research has been published in the journal Nature Communications.

    * The researchers designed photoreactive molecules that enabled
    them to
    couple together, using green light as the fuel, polymers commonly
    used in medical and industrial applications. They then controlled
    the molecules' photoreactivity by changing pH (the measure of how
    acid or alkaline a substance is).

    * It is the first time pH has been used as an on/off switch for
    a green
    light-activated, catalyst-free chemical process.

    * The green light used was also the longest wavelength of light
    (up to 500
    nanometres) employed to date to control a catalyst-free
    photochemical bond-forming reaction.

    * To demonstrate the application potential of this photochemical
    innovation, the team produced a range of hydrogels with varying
    mechanical properties. Hydrogels are commonly used in contact
    lenses, tissue engineering scaffolds, as drug delivery carriers,
    and for cell biology studies.

    The research was conducted by lead author and QUT PhD chemistry researcher Kubra Kalayci, Australian Research Council (ARC) DECRA Fellow Dr Hendrik Frisch, Research Fellow Dr Vinh Truong, and ARC Laureate Fellow Professor Christopher Barner-Kowollik from QUT's Soft Matter Materials Laboratory
    in the Science and Engineering Faculty Centre for Materials Science.

    Professor Barner-Kowollik said scientists were constantly seeking to move further away from using harsh UV light to activate chemical reactions.

    "Our photochemical innovation is another example of what is called
    red-shifting -- moving through the colours of light in the spectrum, from
    blue to green towards red, to light that has longer wavelengths," he said.

    "In the past, most of these types of photochemical reactions were
    triggered by harsh UV (ultra-violet) light. But that prevents applications
    in a biological context because UV light has so much energy it kills
    cells.



    ========================================================================== "Dentistry is an example of one of the areas that has shifted. Initially dentists were using UV lamps. Now anyone who has had a filling probably
    knows that the dentist uses a little lamp with longer wavelength blue
    light for curing.

    "The longer the wavelength of light the better, in principle. The
    radiation is less harmful, so it can be used for biological applications,
    and it allows for deeper light penetration. For dentistry, that means
    better and more uniform curing.

    "But it is also more difficult to do, because the longer the wavelength
    of light the less energy you have to drive the chemical reaction.

    "Adding an additional stimulus with the green light, such as we have with varying the pH as a reversible on-off switch for the reaction, provides
    the opportunity for better regulation. This is especially important
    for drug delivery systems, where the drug needs to be released under a
    specific pH, as pH varies throughout the human body.

    "This is also a catalyst-free reaction. It means there's no helper
    molecule to make it happen. That's important for biological application
    as well because in many cases helper molecules contain metal, and you
    don't want something that could leach out, or something that is found to
    be cytotoxic or carcinogenic." To investigate the new green light-pH
    coupling tool's suitability for biomaterials engineering, Ms Kalayci
    said the research team created hydrogels with different properties.



    ========================================================================== "These showed that green light allowed higher penetration depths,
    resulting in fabrication of thicker hydrogels," she said.

    Dr Truong said cells cultured inside the hydrogels "showed the process
    for creating the gels was non-toxic, and the cells also remained viable
    for several days." The team believes the new coupling tool has a range
    of other potential applications.

    "For example, in the context of personalised medicine," Dr Truong and
    Dr Frisch said. "You might want to use our reaction to attach a cancer
    drug to a specific part of a molecule to deliver the drug in a way
    that is suited to a particular patient." Professor Barner-Kowollik
    said it was also another step towards achieving "molecular surgery."
    "What chemists hope to do is be able to 'operate' on one part of a
    molecule without affecting anything else," he said.

    "So, for example, if you had a protein, a large complex molecule, we'd
    like to be able to use light like a chemical scalpel and very delicately
    go in and change part of that molecule without affecting any other
    part. That provides many potential applications." Applications could
    include, Dr Truong said, "looking at the selective crosslinking of DNA
    to study the underlying mechanism of a cancer, looking for avenues for
    targeted treatment, or creating dynamic hydrogel scaffolds to study cell interactions for tissue regeneration therapy.

    "Using light, we are providing chemical tools to be able to achieve
    these aims."

    ========================================================================== Story Source: Materials provided by
    Queensland_University_of_Technology. Note: Content may be edited for
    style and length.


    ========================================================================== Journal Reference:
    1. Kubra Kalayci, Hendrik Frisch, Vinh X. Truong, Christopher Barner-
    Kowollik. Green light triggered [2 2] cycloaddition of halochromic
    styrylquinoxaline--controlling photoreactivity by pH. Nature
    Communications, 2020; 11 (1) DOI: 10.1038/s41467-020-18057-9 ==========================================================================

    Link to news story: https://www.sciencedaily.com/releases/2020/08/200824092025.htm

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