Optical properties of porcine dermis in the mid-infrared absorption band of glucose
Literature Information
Arthur Schönhals, Hans Tholl, Mathias Glasmacher, Niels Kröger-Lui, Annemarie Pucci, Wolfgang Petrich
The optical properties of skin in the mid-infrared range are not known, despite their importance for e.g. non-invasive glucose monitoring. In this paper, transmission, absorption, scattering, and reduced scattering coefficients are quantified using a custom-built goniometer based on a quantum cascade laser operated at the glucose absorption band at a wavelength of around 9.7 μm. The measurements show a strong dominance of absorption and moderate contributions from scattering. The scattered radiation is dominated by single scattering events in the forward direction (g = 0.967) within the range of the investigated dermis layer thicknesses of up to 50 μm, whereby the fraction of multiple scattering is expected to increase with the layer thickness.
Recommended Journals
Related Literature
Computing vibrational spectra from ab initio molecular dynamics
Martin Thomas, Martin Brehm, Reinhold Fligg, Peter Vöhringer, Barbara Kirchner
DOI: 10.1039/C3CP44302G
Reducing the spin–spin interaction of stable carbon radicals
Sharon Ruthstein
DOI: 10.1039/C3CP50533B
Stable and high-rate overcharge protection for rechargeable lithium batteries
Bin Wang, Thomas J. Richardson, Guoying Chen
DOI: 10.1039/C3CP50992C
An etched nanoporous Ge anode in a novel metal–air energy conversion cell
Sunghyun Uhm
DOI: 10.1039/C3CP50885D
Reliable contact fabrication on nanostructured Bi2Te3-based thermoelectric materials
Shien-Ping Feng, Ya-Huei Chang, Jian Yang, Bed Poudel, Bo Yu, Zhifeng Ren, Gang Chen
DOI: 10.1039/C3CP50993A
Ultrafast photoinduced dynamics of halogenated cyclopentadienes: observation of geminate charge-transfer complexes in solution
T. J. A. Wolf, R. Radloff, P. Lang, A. Stolow, A.-N. Unterreiner
DOI: 10.1039/C3CP44295K
Benchmarks for 0–0 transitions of aromatic organic molecules: DFT/B3LYP, ADC(2), CC2, SOS-CC2 and SCS-CC2 compared to high-resolution gas-phase data
Nina O. C. Winter, Nora K. Graf, Samuel Leutwyler, Christof Hättig
DOI: 10.1039/C2CP42694C
Rotational spectroscopy meets theory
Cristina Puzzarini
DOI: 10.1039/C3CP44301A
Enhancing the stability of polymer solar cells by improving the conductivity of the nanostructured MoO3 hole-transport layer
Amitaksha Saha, Chellappan Vijila, Rajan Jose, Zhang Jie, Seeram Ramakrishna
DOI: 10.1039/C3CP50994J
You might also like
What is the market or research trend for N-(4-Methoxybenzyl)-2-pyridinamine (CAS: 52818-63-0)?
N-(4-Methoxybenzyl)-2-pyridinamine (CAS: 52818-63-0) is increasingly being used ...
What precautions should be taken when handling Ethyl 4-(2-chlorophenyl)-1,3-thiazole-2-carboxylate (CAS: 1050507-06-6)?
When handling Ethyl 4-(2-chlorophenyl)-1,3-thiazole-2-carboxylate, appropriate p...
What regulatory guidelines apply to diethyldiselane (CAS: 628-39-7)?
Diethyldiselane (CAS: 628-39-7) is classified under the Globally Harmonized Syst...
What is the market or research trend for oxocopper (CAS: 12053-18-8)?
The market for oxocopper (CAS: 12053-18-8) is primarily driven by its use in cat...
What is the market or research trend for 5-{[(2-Methyl-2-propanyl)oxy]carbonyl}-5-azaspiro[2.4]heptane-7-carboxylic acid?
The market for 5-{[(2-Methyl-2-propanyl)oxy]carbonyl}-5-azaspiro[2.4]heptane-7-c...
What is 2-(1-Pyrrolidinyl)-4-pyridinamine (CAS: 35981-63-6)?
2-(1-Pyrrolidinyl)-4-pyridinamine is a chemical compound with the CAS number 359...
What are the physical and chemical properties of 2-(3-Pyridinyl)-1-azabicyclo[2.2.2]octane (CAS: 91556-75-1)?
2-(3-Pyridinyl)-1-azabicyclo[2.2.2]octane (CAS: 91556-75-1) is a crystalline sol...
How is (S)-Alpha-allyl-proline hydrochloride (CAS: 129704-91-2) typically synthesized?
(S)-Alpha-allyl-proline hydrochloride is usually synthesized via a Wittig reacti...
What is 3-Methyl-1,2-oxazole-5-carboxylic acid (CAS: 4857-42-5)?
3-Methyl-1,2-oxazole-5-carboxylic acid (CAS: 4857-42-5) is an organic compound w...
How is Lys-SMCC-DM1 (CAS: 1281816-04-3) typically synthesized?
Lys-SMCC-DM1 is synthesized via a multi-step process involving the coupling of S...
Source Journal
Analyst

Analyst publishes analytical and bioanalytical research that reports premier fundamental discoveries and inventions, and the applications of those discoveries, unconfined by traditional discipline barriers.














