2016
DOI: 10.1088/1742-6596/733/1/012044
|View full text |Cite
|
Sign up to set email alerts
|

Standard operating procedure to prepare agar phantoms

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
8
0

Year Published

2019
2019
2023
2023

Publication Types

Select...
4
3
1

Relationship

0
8

Authors

Journals

citations
Cited by 24 publications
(10 citation statements)
references
References 2 publications
0
8
0
Order By: Relevance
“…There was no notable change in refrigerated samples following two to three weeks of production in contrast to the slight desiccation observed in the unrefrigerated samples after a week. However, with the addition of antifungal agents, agar phantom can maintain stable optical properties for periods over two years [29]. Moreover, to assess the repeatability of the fabrication process, the measurement of the optical properties was performed for phantoms reproduced using our proposed method.…”
Section: Resultsmentioning
confidence: 99%
“…There was no notable change in refrigerated samples following two to three weeks of production in contrast to the slight desiccation observed in the unrefrigerated samples after a week. However, with the addition of antifungal agents, agar phantom can maintain stable optical properties for periods over two years [29]. Moreover, to assess the repeatability of the fabrication process, the measurement of the optical properties was performed for phantoms reproduced using our proposed method.…”
Section: Resultsmentioning
confidence: 99%
“…The hair thickness varies between 56 and 99 μm. Imaging of the suspended samples was done in three variations: in air (with OCT only), in deionized water and in agar phantom, which is often used as tissue‐mimicking phantoms for ultrasound and photoacoustic imaging [35–37].…”
Section: Methodsmentioning
confidence: 99%
“…Agarose phantoms mimic soft tissues and some preparation techniques are described in refs. [54][55][56]. Briefly, 100 mL DI water was heated at 300 °C and then 1.50 g of agarose was slowly added and gently mixed forming a homogeneous solution.…”
Section: Methodsmentioning
confidence: 99%