2018
DOI: 10.1007/s10126-018-9858-9
|View full text |Cite
|
Sign up to set email alerts
|

Characterization and Cytotoxicity Evaluation of a Marine Sponge Biosilica

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

2
24
0

Year Published

2019
2019
2024
2024

Publication Types

Select...
8
2

Relationship

1
9

Authors

Journals

citations
Cited by 21 publications
(26 citation statements)
references
References 56 publications
2
24
0
Order By: Relevance
“…BS treated tibial bone defect presented an accelerated material degradation, with an intense ingrowth of granulation tissue into the defect area [25][26][27][28]. It is well known that silica ion is an important element for bone formation stimulation [17,29] and interaction with bone tissue, allowing the formation of a silica gel layer. This layer constitutes a template for calcium and phosphate deposition, which attracts macrophages, mesenchimal stem cells and osteoprogenitor cells [30,31].…”
Section: Discussionmentioning
confidence: 99%
“…BS treated tibial bone defect presented an accelerated material degradation, with an intense ingrowth of granulation tissue into the defect area [25][26][27][28]. It is well known that silica ion is an important element for bone formation stimulation [17,29] and interaction with bone tissue, allowing the formation of a silica gel layer. This layer constitutes a template for calcium and phosphate deposition, which attracts macrophages, mesenchimal stem cells and osteoprogenitor cells [30,31].…”
Section: Discussionmentioning
confidence: 99%
“…In all the cases the cell metabolic activity was between 80 and 100% confirming their non-cytotoxic character. In addition, Gabbai-Armelin et al (2019) showed that extracts from biosilica obtained from Tedania ignis and Dragmacidon reticulatum marine sponges, at a concentration of 50 mg/mL, promoted the increment of cell viability. Our results showed that the presence of biosilica from the GB, SN, AI, and PV sponges is noncytotoxic.…”
Section: Evaluation Of Cytotoxicitymentioning
confidence: 99%
“…For characterization of the BCM, the samples were dried at room temperature in a laminar flow cabinet and covered with coverslip [25]. Finally, the dried BCM membranes were mounted on carbon tapes and aluminum stubs, sputtercoated and analyzed by SEM at 1000x and 1200x magnification for checking the surface on both sides of the BCM.…”
Section: Scanning Electron Microscopy (Sem)mentioning
confidence: 99%