Abstract

A first accurate measurement of the complex refractive index in an intralipid emulsion is demonstrated, and thereby the average scatterer particle size using standard Mie scattering calculations is extracted. Our method is based on measurement and modeling of the reflectance of a divergent laser beam from the sample surface. In the absence of any definitive reference data for the complex refractive index or particle size in highly turbid intralipid emulsions, we base our claim of accuracy on the fact that our work offers several critically important advantages over previously reported attempts. First, our measurements are in situ in the sense that they do not require any sample dilution, thus eliminating dilution errors. Second, our theoretical model does not employ any fitting parameters other than the two quantities we seek to determine, i.e., the real and imaginary parts of the refractive index, thus eliminating ambiguities arising from multiple extraneous fitting parameters. Third, we fit the entire reflectance-versus-incident-angle data curve instead of focusing on only the critical angle region, which is just a small subset of the data. Finally, despite our use of highly scattering opaque samples, our experiment uniquely satisfies a key assumption behind the Mie scattering formalism, namely, no multiple scattering occurs. Further proof of our method's validity is given by the fact that our measured particle size finds good agreement with the value obtained by dynamic light scattering.

Highlights

  • We have demonstrated a first accurate in situ measurement of the real refractive index, attenuation coefficient, and average scatterer-size in an intralipid emulsion

  • Because no sample dilution is required, our method has the potential to offer in situ longterm stability monitoring of lipid emulsions against the formation of potentially embolic fat globules larger than 5 μm owing to coalescence during on-shelf storage

  • We initially tested our theoretical model for total internal reflection (TIR) in a highly turbid medium [i.e., Eq (2)] in milk-cream mixtures,[16,17,18] and have performed a more rigorous test in intralipid emulsions

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Summary

Introduction

The measurement of optical properties of biological tissue, or tissue-like turbid media, has received considerable attention, with various novel methodologies being proposed and demonstrated.[1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17,18,19,20,21] Here, “turbid” refers to a colloidal suspension of light-scattering oil droplets of size comparable to the optical wavelength. From the point of view of particle sizing, Journal of Biomedical Optics

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