Clinical Translation of SFDI Instrumentation

Clinical Translation of SFDI Instrumentation

In our group, we have developed comprehensive spectral imaging approaches like Spatial Frequency Domain Spectroscopy (SFDS) that can provide fine spectral detail of both absorption and scattering from in vivo tissue. Data from these systems are critical for the characterization of medical application specific tissue constituents as well as other sources of normal biological variance that may confound or corrupt the interpretation of optical data.  These approaches have also led towards the development of practical models and methods for extracting depth specific information in tissue non-invasively.  However, SFDS is often better suited in controlled environments and dedicated clinical studies rather than general clinical practice due to its size, cost and bulkiness. 

SFDS can characterize tissue spectral properties to within 1nm precision, but do we need all that detail? Under this project, we have developed analysis methods for data reduction and virtual instrument design to translate the critical spectral information content extracted from SFDS investigations down to the minimal necessary measurement details.  From this data-driven perspective, we can then search for optimized imaging solutions and instrument designs that would maintain the data integrity and robustness of SFDS, but deliver this tool in a smaller, easy to use, and cost effective formfactor.  

Objective: low-cost, handheld devices present a pragmatic approach toward seamless integration in to clinical practice, reducing translational barriers novel technologies and methods.

SFDI Resources/Prototypes available for LiU collaborations:

  • 5-wv, low-cost imager (460-620nm)

Graphics and a photo showing the results from the research.

  • 9-wv, compound eye system (450-1000nm)

Graphics and a photo showing the results from the research.

  • SFDS system (450-100nm), point spectroscopy at ~1nm spectral resolution

Graphics and a photo showing the results from the research.

Projects in quantifying skin reactivity in clinical settings:

#1 – Efficacy of Micro-needle Vaccination

The goal of this investigation is to assess whether microneedle arrays can reliably and robustly provoke the necessary skin response that would allow for low-dose, dry coated vaccinations to be effective. Here the reactivity of skin is characterized by depth resolved hemodynamics, illustrating that the magnitude and duration of this response can vary significantly between individual subjects, particularly among older, more vulnerable populations.

Photos and graphics showing the results of the research.

#2 – Differentiated Responses to Noxious Heating/Pain Stimulation of Skin

In this study, skin reactivity is monitored in response to localized heating of skin. The goal here is to ultimately correlate pain response to physiologic dynamics such as vascular reactivity and inflammation. To differentiate multiple mechanisms in skin non-invasively, a model has been developed to characterize vascular and microcirculatory dilation from that of extra vascular changes (e.g. oedema). This model decomposes water dynamics in to vascular dynamics (correlated with increases in hemoglobin) and extra-vascular changes in the tissue volumes.

Preliminary examples of strong and weak responders to noxious heating of skin:

Graphics showing the results from the research.

Project members