| PCL/PLGA6535/PLGA 8515 multilayered fibrous scaffold32
|
Directly blending |
NT-3 |
— |
Release of PLGA 6535 and PLGA 8515 reached a plateau after six weeks and eight weeks, respectively |
— |
Rat |
Neural tissue regeneration |
| BDNF |
| PDGF |
| PLGA nanofiber scaffolds34
|
Directly blending |
bFGF |
54% |
7 days (Group I), 14 days (Group II) |
BMSCs |
— |
Bone regeneration |
| PLLA nanofiber scaffolds35
|
Directly blending |
BMP-2 |
174 ng/implant |
— |
— |
Rat |
Bone regeneration |
| Bilayer scaffolds consisting of different PLGA nanofibers36
|
Directly blending |
VEGF |
57.27% of VEGF |
Release of VEGF from the PLGA 50/50 layer was faster than that of PDGF from the PLGA 75/25 layer |
HUVEC |
— |
Complex tissue engineering |
| PDGF |
51.76 %of PDGF |
| Multi-layered PLLA nanosheets37
|
Directly dropping onto the middle of the PLLA nanosheet |
rhFGF-2 |
— |
— |
— |
Mouse |
Bone regeneration |
| PLGA porous scaffold89
|
Directly soaking |
bFGF |
22.6% |
A high initial burst and reached a standstill about 10 days |
3T3 fibroblasts |
Mouse |
— |
| PLLA nanofibrous scaffold33
|
Directly blending (NGF) and soaking (VEGF) |
NGF |
— |
Release rate of VEGF is higher (35.72 ± 0.29%) within 1 day than that of NGF (4.86 ± 1.00%). Release of VEGF reach a standstill (58.56 ± 1.31%) at the fourth day, but that of NGF reach a standstill (29.52 ± 0.91%) at the eleventh day |
iPSCs-NCSCs |
Rat |
Peripheral nerve regeneration |
| VEGF |
| PLLA nanofibrous scaffold42
|
Surface collagen coating combined with covalent binding |
TGF-β3 |
— |
— |
hBMSCs |
— |
Cartilage repair |
| PLGA/HA porous scaffolds51
|
PDA-mediated method |
BMP-2 |
80% of IGF-1, 75% of BMP-2 |
After a burst release, the release subsequently slowed down with approximately 27% (IGF-1) and 39% (BMP-2) of the total growth factors released after 21 d |
MC3T3-E1 |
Rabbit |
Bone tissue engineering |
| IGF-1 |
| 3D-printed PLA scaffolds with interconnected microporous architectures52
|
PDA-mediated method |
BMP-2 |
375.4 ng/scaffold |
Sustained released of BMP-2 for up to 35 days |
hMSCs |
— |
Bone tissue engineering |
| Tubular PCL scaffolds53
|
PDA-mediated method |
VEGF |
56.6 ng/scaffold |
— |
SMC EC |
Rat |
Vascular tissue engineering |
| PLLA nanofibrous scaffold58
|
Nanoparticle embedding |
bFGF |
48.71% |
No burst release and a control release of nearly 30 days |
C3H10T½ (C3) cells |
Rat |
Promotion of tendon healing |
| PLGA nanofibrous scaffold62
|
Microspheres embedding |
VEGF |
44.39% |
Release last 20 days |
HUVEC |
Rat |
Abdominal wall repair |
| PLLA nano-fibrous scaffolds56,57
|
PLGA microspheres with PDGF-BB or rhBMP-7 post-seeding |
PDGF-BB rhBMP-7 |
77–93% |
Temporally controlled fashion with prolonged duration and varying temporal patterns because of different PLGA nanosphere |
Human gingival fibroblast |
Rat |
Complex tissue regeneration |
| PLGA films and porous scaffolds40
|
Plasma treatment combined with growth factor anchorage |
bFGF |
66.3% |
Continuous release about 7 days after a moderate burst release |
3T3 fibroblasts |
— |
Extensive tissue engineering |
| 3D microtubule-orientated PLGA scaffold78
|
Plasma treatment combined with growth factor anchorage |
bFGF |
75.0% |
Continuous release for 10 days after a moderate burst release |
vSMC |
— |
Vascular tissue engineering |
| PLGA/PLLA microfiber scaffolds88
|
Heparin-mediated method |
TGF-β1 |
26.8 ng/scaffold |
Continuous release for 4 weeks after a moderate initial burst release |
UCB-MSCs |
Rabbit |
Cartilage tissue engineering |
| H-PLGA/PLGA(70/30) porous scaffolds89
|
Heparin-mediated method |
bFGF |
71.3% |
Slowly release and last over two weeks |
3T3 fibroblasts |
— |
Extensive tissue engineering |
| PLLA nanofiber microspheres91
|
Heparin binding combined with nanospheres encapsulating |
VEGF |
— |
Average burst release of VEGF on the first day was 20.5%, 54.7% was released within 1 week |
HUVEC |
Nude mouse |
Pulp regeneration |
| Release of VEGF consistently at a rate of approximately 1–2% per day for the last 3 weeks |
| PLGA porous scaffold92
|
Heparin binding combined with nanospheres encapsulating |
BMP-7 |
79% of TGF-β3 |
No burst and sustained release in a near zero-order kinetics for least 27 days |
hMSCs |
— |
Cartilage regeneration |
| TGF-β3 |
50% of BMP-7 |
| PLGA scaffold with parallel arranged microgrooves and nanofiber structures93
|
Nanoparticle binding (TGF-β1) |
TGF-β1 |
— |
Continuous release for about 10 days of TGF-β1 |
vSMC |
— |
Vascular tissue engineering |
| Plasma treatment combined with anchorage (bFGF) |
bFGF |
Moderate burst release for bFGF and then about 7 days continuous release |