Title of article :
Injectable scaffold as minimally invasive technique for cartilage tissue engineering: in vitro and in vivo preliminary study
Author/Authors :
Solouk, Atefeh Biomedical Engineering Faculty - Amirkabir University of Technology , Mirzadeh, Hamid Polymer Engineering Faculty - Amirkabir University of Technology (Tehran Polytechnic) , Amanpour, Saeed Cancer Research Center - Cancer Institute of Iran - Tehran University of Medical Sciences
Abstract :
Cartilage is a tissue with limited repair capacity
and also sparse population of cells entrapped within a
dense extracellular matrix, therefore, delivery of the cells
to site of damaged cartilage can improve its healing
potential. Synthetic biomaterials such as poly (D,L-lactideco-
glycolide) (PLGA) have been used as both preformed or
injectable scaffolds in tissue engineering in order to carry
and keep cells in the site of injury with minimal side
effects. The injectable biocompatible polymeric scaffolds
can reach to effected area via minimally invasive injection
without need to open the joint, less painful approach and
also having possibility to fill complicated shape defects. In
this study, it was hypothesized that PLGA solved in nmethyl
pyrrolidine (NMP) may act as a proper carrier for
cell delivery to the site of the damage and also supports
their growth. The results of in vitro assays including both
live/dead (AO/PI) and MTT showed the majority of the
cells were remained alive between 3 up to 21 days,
respectively. The amount of resealed GAG from the mesenchymal
stem cells (MSCs) which were in contact with
both PLGA and alginate constructs (used as control) indicated
that for day 7 MSCs in contact with alginate secreted
more GAG (3.45 ± 0.453 lg/mL for alginate and
2.36 ± 0.422 lg/mL for PLGA matrices), but at longer
times (21 days) cells in contact with PLGA elicited more
GAG (6.26 ± 0.968 lg/mL for alginate and 8.47 ±
0.871 lg/mL for the PLGA matrices). Sol–gel systems
comprising PLGA, NMP, and cells as well as alginate/cells
were subcutaneously injected into four nude mice (each
mouse had three injection sites). PLGA/NMP was solidify
immediately and formed an interconnecting 3-D porous
structure that allowed body fluid to penetrate through them.
In vivo evaluation showed that PLGA/NMP scaffolds
could support injected cells as a fibrocartilage tissue was
formed after 6 months of injection. We found that PLGA/
NMP system might be a proper minimally invasive therapeutics
option for cartilage repair.
Keywords :
Cartilage tissue engineering , Injectable scaffolds , poly (D,L-lactide-co-glycolide) , Mesenchymal stem cells (MSCs)
Journal title :
Progress in Biomaterials
Journal title :
Progress in Biomaterials