Evaluation of a Commercially Available Hyaluronic Acid Hydrogel (Restylane) as Injectable Scaffold for Dental Pulp Regeneration: An In Vitro Evaluation

被引:48
作者
Chrepa, Vanessa [1 ]
Austab, Obadab [2 ,3 ]
Diogenes, Anibal [2 ]
机构
[1] Univ Washington, Dept Endodont, 1959 NE Pacific St,Box 357448, Seattle, WA 98195 USA
[2] Univ Texas Hlth Sci Ctr San Antonio, Dept Endodont, San Antonio, TX 78229 USA
[3] King Abdulaziz Univ, Fac Dent, Dept Endodont, Jeddah, Saudi Arabia
关键词
Dental pulp regeneration; FDA approved; hyaluronic acid-based gel; regenerative endodontics; Restylane; scaffolds; PLATELET-RICH PLASMA; STEM-CELLS; APICAL PERIODONTITIS; TISSUE; TOOTH; DIFFERENTIATION; ENDODONTICS; TEETH; VIVO; PROLIFERATION;
D O I
10.1016/j.joen.2016.10.026
中图分类号
R78 [口腔科学];
学科分类号
100302 [口腔临床医学];
摘要
Introduction: Regenerative endodontic procedures (REPs) are viable alternatives for treating immature teeth, yet these procedures do not predictably lead to pulp-dentin regeneration. A true bioengineering approach for dental pulp regeneration requires the incorporation of a scaffold conducive with the regeneration of the pulp-dentin complex. Several materials have been proposed as scaffolds for REPs; nonetheless, the majority are not eligible for immediate clinical chairside use. Thus, the aim of this study was to evaluate Restylane, a Food and Drug Administration-approved hyaluronic acid based gel, as possible scaffold for REPs. Methods: Stem cells of the apical papilla (SCAP) were cultured either alone or in mixtures with either Restylane or Matrigel scaffolds. Groups were cultured in basal culture medium for 6, 24, and 72 hours, and cell viability was assessed. For the mineralizing differentiation experiments, groups were cultured in differentiation medium either for 7 days and processed for alkaline phosphatase activity or for 14 days and processed for gene expression by using quantitative reverse-transcription polymerase chain reaction. SCAP in basal medium served as control. Results: Cell encapsulation in either Restylane or Matrigel demonstrated reduced cell viability compared with control. Nonetheless, cell viability significantly increased in the Restylane group in the course of 3 days, whereas it decreased significantly" in the Matrigel group. Restylane promoted significantly greater alkaline phosphatase activity and upregulation of dentin sialophosphoprotein, dentin matrix acidic phosphoprotein-1, and matrix extracellular phosphoglycoprotein, compared with control. Conclusions: A Food and Drug Administration-approved hyaluronic acid based injectable gel promoted SCAP survival, mineralization, and differentiation into an odontoblastic phenotype and may be a promising scaffold material for REPs.
引用
收藏
页码:257 / 262
页数:6
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