2021
DOI: 10.1016/j.joen.2021.04.012
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Adipose Tissue–derived Microvascular Fragments as Vascularization Units for Dental Pulp Regeneration

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Cited by 27 publications
(20 citation statements)
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“…Figure 6 presents DDM with opened dentinal tubules after demineralization. Sterilization was performed by maintaining the matrices in sterile phosphate-buffered saline (PBS) with 100 units/ml of penicillin and 100 μg/ml of streptomycin at 37 °C, for 72 h and then washed in sterilized deionized water for 5 min [ 17 , 21 , 22 , 24 , 28 , 30 – 36 , 38 44 ], socking into penicillin and streptomycin [ 72 ] only, preservation in 5% peracetic acid and 75% ethanol for 10 min [ 53 , 80 , 81 ], immersion in 5 ml alcohol/2 ml of gentamicin [ 61 , 69 – 71 ], rinsing with sterile saline for 10 min [ 75 ], washing in sterilized deionized water for 10 min [ 82 ], rinsing twice in 0.1 M Tris-HCl (pH 7.4) for 10 min [ 55 , 62 ] and using gradient ethanol concentrations [ 47 ]. Other methods of sterilization were gamma irradiation processing using Cobalt 60 radiation with a dose of 5 kGy [ 66 ], ethylene oxide gas sterilization at low temperatures [ 19 , 45 , 49 , 52 , 57 , 58 , 60 , 67 , 68 , 76 ], steam sterilization at 121°C and a pressure of 1 bar for 15 min [ 23 ], lyophilization and freeze-drying [ 46 ], or mixing was accomplished in a sterile container [ 65 ].…”
Section: Resultsmentioning
confidence: 99%
“…Figure 6 presents DDM with opened dentinal tubules after demineralization. Sterilization was performed by maintaining the matrices in sterile phosphate-buffered saline (PBS) with 100 units/ml of penicillin and 100 μg/ml of streptomycin at 37 °C, for 72 h and then washed in sterilized deionized water for 5 min [ 17 , 21 , 22 , 24 , 28 , 30 – 36 , 38 44 ], socking into penicillin and streptomycin [ 72 ] only, preservation in 5% peracetic acid and 75% ethanol for 10 min [ 53 , 80 , 81 ], immersion in 5 ml alcohol/2 ml of gentamicin [ 61 , 69 – 71 ], rinsing with sterile saline for 10 min [ 75 ], washing in sterilized deionized water for 10 min [ 82 ], rinsing twice in 0.1 M Tris-HCl (pH 7.4) for 10 min [ 55 , 62 ] and using gradient ethanol concentrations [ 47 ]. Other methods of sterilization were gamma irradiation processing using Cobalt 60 radiation with a dose of 5 kGy [ 66 ], ethylene oxide gas sterilization at low temperatures [ 19 , 45 , 49 , 52 , 57 , 58 , 60 , 67 , 68 , 76 ], steam sterilization at 121°C and a pressure of 1 bar for 15 min [ 23 ], lyophilization and freeze-drying [ 46 ], or mixing was accomplished in a sterile container [ 65 ].…”
Section: Resultsmentioning
confidence: 99%
“…One of the main challenges in vascular tissue engineering involve the lack of cell-cell interactions and microvasculature network sprouting in the cell culture systems which can be addressed by generation of cell-laden spheroids or micro-sized aggregates. Due to the ability of spheroids to fuse, they can be used to form robust endogenous capillary-like networks which can offer new opportunities for creating highly organized vascularized microtissues [147]. In this regard, it has been shown that sprouting of capillary angiogenesis is capable of changing mechanobiological properties of a fibrin cell-laden matrix altering cell fate [148,149].…”
Section: Micro-sized Aggregates and Microspheres/ Microbeadsmentioning
confidence: 99%
“…DPSCs and adipose tissue-derived microvascular fragments mixed with matrigel promoted pulp-like tissue regeneration in tooth root segments (RSs). 36 Furthermore, gelatin methacryloyl (GelMA) hydrogel supports cell encapsulation and adjustable physical properties, contributing to the construction of biomimetic 3D tooth bud models and delivery of DPSCs and HUVECs for pulp regeneration. 37 , 38 However, there is no clear conclusion about which hydrogel is more suitable for endogenous pulp regeneration.…”
Section: Introductionmentioning
confidence: 99%