Increasing the penetration depth for ultrafast laser tissue ablation using glycerol based optical clearing

Author(s):  
Ilan Gabay ◽  
Kaushik G. Subramanian ◽  
Chris Martin ◽  
Murat Yildirim ◽  
Valery V. Tuchin ◽  
...  
2010 ◽  
Vol 03 (03) ◽  
pp. 177-181 ◽  
Author(s):  
RAN LIAO ◽  
NAN ZENG ◽  
DONGZHI LI ◽  
TIANLIANG YUN ◽  
YONGHONG HE ◽  
...  

Optical clearing improves the penetration depth of optical measurements in turbid tissues. Polarization imaging has been demonstrated as a potentially promising tool for detecting cancers in superficial tissues, but its limited depth of detection is a major obstacle to the effective application in clinical diagnosis. In the present paper, detection depths of two polarization imaging methods, i.e., rotating linear polarization imaging (RLPI) and degree of polarization imaging (DOPI), are examined quantitatively using both experiments and Monte Carlo simulations. The results show that the contrast curves of RLPI and DOPI are different. The characteristic depth of DOPI scales with transport mean free path length, and that of RLPI increases slightly with g. Both characteristic depths of RLPI and DOPI are on the order of transport mean free path length and the former is almost twice as large as the latter. It is expected that they should have different response to optical clearing process in tissues.


eLife ◽  
2017 ◽  
Vol 6 ◽  
Author(s):  
Tobias Boothe ◽  
Lennart Hilbert ◽  
Michael Heide ◽  
Lea Berninger ◽  
Wieland B Huttner ◽  
...  

In light microscopy, refractive index mismatches between media and sample cause spherical aberrations that often limit penetration depth and resolution. Optical clearing techniques can alleviate these mismatches, but they are so far limited to fixed samples. We present Iodixanol as a non-toxic medium supplement that allows refractive index matching in live specimens and thus substantially improves image quality in live-imaged primary cell cultures, planarians, zebrafish and human cerebral organoids.


2019 ◽  
Vol 13 (02) ◽  
pp. 2050004
Author(s):  
D. Li ◽  
Y. Zhang ◽  
B. Chen

The effect of optical cleaning method combined with laser speckle imaging (LSI) was discussed to improve the detection depth of LSI due to high scattering characteristics of skin, which limit its clinical application. A double-layer skin tissue model embedded with a single blood vessel was established, and the Monte Carlo method was used to simulate photon propagation under the action of light-permeating agent. 808[Formula: see text]nm semiconductor and 632.8[Formula: see text]nm He–Ne lasers were selected to study the effect of optical clearing agents (OCAs) on photon deposition in tissues. Results show that the photon energy deposition density in the epidermis increases with the amount of tissue fluid replaced by OCA. Compared with glucose solution, polyethylene glycol 400 (PEG 400) and glycerol can considerably increase the average penetration depth of photons in the skin tissue, thereby raising the sampling depth of the LSI. After the action of glycerol, PEG 400, and glucose, the average photon penetration depth is increased by 51.78%, 51.06%, and 21.51% for 808nm, 68.93%, 67.94%, and 26.67% for 632.8 nm lasers, respectively. In vivo experiment by dorsal skin chamber proves that glycerol can cause a substantial decrease in blood flow rate, whereas PEG 400 can significantly improve the capability of light penetration without affecting blood velocity, which exhibits considerable potential in the monitoring of blood flow in skin tissues.


Author(s):  
Chris W. Drew ◽  
Christopher G. Rylander

The highly disordered refractive index distribution in biological tissue causes multiple-scattering of incident light and inhibits optical penetration depth. “Tissue optical clearing” increases penetration depth of near-collimated light in biological tissue, potentially resulting in improved optical analysis and treatment techniques. Numerous methods of tissue optical clearing have been hypothesized using hyperosmostic agents [1]. These methods propose reduction in light scattering by means of dehydration of tissue constituents, replacement of interstitial or intracellular water with higher refractive agents, or structural modification or dissociation of collagen fibers [2,3]. It has been suggested that dehydration of tissue constituents alone can reduce light scattering by expulsing water between collagen fibrils, increasing protein and sugar concentrations, and decreasing refractive index mismatch [4].


1998 ◽  
Vol 23 (3) ◽  
pp. 286-286
Author(s):  
Jones ◽  
Viridov ◽  
Sobol
Keyword(s):  

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