Advances in Experimental Medicine and Biology
DOI: 10.1007/978-0-387-34133-0_24
|View full text |Cite
|
Sign up to set email alerts
|

Fibrin in Tissue Engineering

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1

Citation Types

2
34
0

Publication Types

Select...
6
3

Relationship

0
9

Authors

Journals

citations
Cited by 36 publications
(36 citation statements)
references
References 91 publications
2
34
0
Order By: Relevance
“…46,47 As a result, many regenerative design strategies have focused on isolating and concentrating portions of human blood such as platelets and plasma (e.g., platelet-rich plasma [PRP]) or pro-coagulation molecules (e.g., fibrin sealants) to enhance endogenous healing responses. [48][49][50][51][52][53][54] It remains to be seen whether a scaffold with only inflammation-related chemical and mechanical cues can elicit enough of an EC ossification response to heal critical-sized bone defects. Pure fibrin scaffolds and PRP alone do not appear to exhibit sufficient cartilage [48][49][50]52 and bone 51,53,54 regeneration in critical-sized defects, which suggests that additional regenerative stimuli such as bioactive molecules and progenitor stem cells may be required.…”
Section: Coupling In Vivo Developmental Engineering With Native Ecm Bmentioning
confidence: 99%
“…46,47 As a result, many regenerative design strategies have focused on isolating and concentrating portions of human blood such as platelets and plasma (e.g., platelet-rich plasma [PRP]) or pro-coagulation molecules (e.g., fibrin sealants) to enhance endogenous healing responses. [48][49][50][51][52][53][54] It remains to be seen whether a scaffold with only inflammation-related chemical and mechanical cues can elicit enough of an EC ossification response to heal critical-sized bone defects. Pure fibrin scaffolds and PRP alone do not appear to exhibit sufficient cartilage [48][49][50]52 and bone 51,53,54 regeneration in critical-sized defects, which suggests that additional regenerative stimuli such as bioactive molecules and progenitor stem cells may be required.…”
Section: Coupling In Vivo Developmental Engineering With Native Ecm Bmentioning
confidence: 99%
“…[17,24,26] Following isolation, periosteum cells were seeded into fibrin hydrogels, which critically permit selfassembly and imaging of a de novo collagen matrix, and because as materials, fibrin scaffolds have structural and biochemical similarities to the microenvironment of the callus formed early in fracture healing. [27][28][29] Both cortical and trabecular bone show a similar matrix alignment at the microscale, which is essential for development and mechanical resistance. To mimic this important feature, the environment of the fracture callus was further emulated by introducing two calcium phosphate (CaP) anchors at the extremities of the culture dish.…”
Section: Introductionmentioning
confidence: 99%
“…Fibrin, as a nature biomaterial, has been widely used in tissue engineering applications. [12][13][14] When applied as a cardiac patch to treat MI, fibrin has been shown to provide temporary physical support of the infarct tissue and prevent negative left ventricular remodeling. 15,16 The investigation on…”
Section: Introductionmentioning
confidence: 99%