Tag Archives: vitreous fluid

Passive nanorheology measurements

What do marshmallows, jelly (or Jell-O), cream cheese and Chinese soup dumplings have in common?  They are often made with gelatin.  Gelatin is derived from the skin and bones of cattle and pigs through the partial hydrolysis of collagen.  Gelatin is a physical hydrogel meaning that it consists of a three-dimensional network of polymer molecules in which a large amount of water is absorbed, as much as 90% in gelatin.  These polymer molecules are cross-linked by hydrogen bonds, hydrophobic interactions and chain entanglements.  External stimuli, such as temperature, can change the level of cross-linking causing the material to transition between its solid, liquid and gel states.  This is why jelly sets in the fridge and melts when it’s heated up – the cross-links holding the molecules together break down.  This type of responsive behaviour allows the properties of hydrogels to be controlled at the micro and sub-micron scale for a host of applications including tissue engineering, drug delivery, water treatment, wearable technologies, and supercapacitors.  However, the design and manufacture of soft hydrogels can be challenging due to the lack of technology for measuring the local properties.  Current quantitative techniques for measuring the properties of hydrogels usually focus on bulk properties and provide little data about local variations or real-time responses to external stimuli.  My colleagues and I have used gold nanoparticles as probes in hydrogels to map the properties at the microscale of thermosensitive hydrogels undergoing real-time transition from the solid to gel phases [see ‘Passive nanorheological tool to characterise hydrogels’].  This is an extension, or perhaps more accurately an application, of our earlier work on tracking nanoparticles through the vitreous humour of the eye [see ‘Nanoparticle motion-through heterogeneous hydrogels’ on November 6th, 2024].  The novel technique, which yields passive nanorheological measurements, allows us to evaluate local viscosity, identify time-varying heterogeniety and monitor dynamic phase transitions at the micro through to nano scale.  The significant challenges of other techniques, such as weak signals due to high water content and the dynamism of hydrogels, are overcome with a fast, inexpensive and user-friendly technology.  Although, even with these advantages, you are unlikely to use it when you are making jelly or roasting marshmallows over the campfire; however, it is really useful for understanding the transport of drugs through biological hydrogels or designing manufacturing processes for artificial tissue.

Reference

Moira Lorenzo Lopez, Victoria R. Kearns, Eann A. Patterson & Judith M. Curran, Passive nanorheological tool to characterise hydrogels, Nanoscale, 2025,17, 15338-15347.

Image: Figure 5 from the above reference showing a hydrogel transitioning to a gel phase as result of an increase in temperature with 100 nm diameter gold nanoparticles with some particles (yellow arrows) at the interface between phases.  The image was taken in an inverted optical microscope set up for tracking the nanoparticles.

Seeing things with nanoparticles

Photograph showing optical microscope and ancilliary equipment set up on an optical benchLast week brought excitement and disappointment in approximately equal measures for my research on tracking nanoparticles [see ‘Slow moving nanoparticles‘ on December 13th, 2017 and ‘Going against the flow‘ on February 3rd, 2021]. The disappointment was that our grant proposal on ‘Optical tracking of virus-cell interaction’ was not ranked highly enough to receive funding from Engineering and Physical Sciences Research Council. Rejection is an occupational hazard for academics seeking to win grants and you learn to accept it, learn from the constructive criticism and look for ways of reworking the ideas into a new proposal. If you don’t compete then you can’t win. The excitement was that we have moved our apparatus for tracking nanoparticles into a new laboratory, which has been set up for it, so that we can start work on a pilot study looking at the ‘Interaction of bacteria and viruses with cellular and hard surfaces’.  We are also advertising for a PhD student to start in September 2021 to work on ‘Developing pre-clinical models to optimise nanoparticle based drug delivery for the treatment of diabetic retinopathy‘.  This is an exciting development because it represents our first step from fundamental research on tracking nanoparticles in biological media towards clinical applications of the technology. Diabetic retinopathy is an age-related condition that threatens your sight and currently is managed by delivery of drugs to the inside of the eye which requires frequent visits to a clinic for injections into the vitreous fluid of the eye.  There is potential to use nanoparticles to deliver drugs more efficiently and to support these developments we plan that the PhD student will use our real-time, non-invasive, label-free tracking technology to quantify nanoparticle motion through the vitreous fluid and the interaction of nanoparticles with the cells of the retina.