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. 2024 Jan 13;27(1):2–10. doi: 10.4103/jcd.jcd_241_23

Table 1.

Summary of the benefits and drawbacks of several pulp-capping agents

Pulp-capping agents Benefits Drawbacks
CH: Hermann, 1930[7] Gold standard of DPC agent
Excellent antimicrobial properties (bacteriostatic after being initially bactericidal)
Low acid pH neutralization
Minimal cytotoxicity
Mineralization stimulation
Low price and not difficult to use[8,68,69]
Nonadhesive nature
High solubility
Disintegration over time
Deterioration following acid etching Tunnels found in reparative dentin
Excessive dentin growth entirely obliterates the pulp chamber
Leakage at margin upon amalgam condensation[8,68,69]
MTA: Torabinejad, 1993[24] Antibacterial property
Good cytocompatibility
Cells adhere and growth regulation
Bioactive dentin matrix protein solubilization
Limited inflammatory pulpal response and higher dentinal bridge formation compared to CH
No mutagenicity and toxicity
Radiopacity[29,68,69]
Difficult to manipulate clinically
Setting time is too long
Grey MTA results in postprocedural tooth discoloration
Two-step process
More expensive than CH[29,68,69]
BD: Septodont, Saint-Maur-des-fossés Cedex, France Excellent cytocompatibility
Good antimicrobial activity
Compared to MTA, limited inflammatory pulpal response and higher dentinal bridge formation
Stronger mechanically compared to CH
Less setting time and better handling capabilities compared to MTA[37,68,69]
Need long-term clinical studies for a definitive evaluation
Higher cost than CH[37,68,69]
NMP: Avalon Biomed Inc., Bradenton, Florida, USA Fine powder provides faster setting time than MTA
Gel enhances the handling qualities and washout resistance
Greater Ca2+and OHions release and lesser porosity than traditional MTA
Higher dentinal bridge formation compared to traditional MTA
No postprocedural tooth discoloration[49,68,69]
Early set material’s high solubility creates gaps[49,68,69]
Quick-Set2 (Primus Consulting, Bradenton, Florida, USA) Quick setting time Ultimate pH Tubule penetration
Acid and washout resistance
No postprocedural tooth discoloration
High ability for mineralogenic stimulation[54,55,68,69]
Low bridge quality compared to NMP[48,54,55,68,69]
iRoot SP (Innovative BioCeramix, Inc., Vancouver, Canada) Premixed putty Good antibacterial property Less cytotoxic compared to MTA[60,61,68,69] Small particle size for better hydration, and Ca2+and OHions release Crystalline structure production resembles tooth hydroxyapatite by moisture absorption in the dentinal tubules Higher dentinal bridge formation compared to NMP[60,61,68,69]
Glass ionomer (1995) Excellent sealing ability
Similar to dentin in terms of coefficient of thermal expansion, and modulus of elasticity
Inherent adhesive nature to enamel and dentin
Good pulp tissue cytocompatibility[67,68,69]
Chronic inflammation over time Lack of development of dentin bridges Poor pulp tissue cytocompatibility Unfavorable physical characteristics, an elevated solubility, and a sluggish setting time RMGIC is greater cytotoxic than traditional GIC[67,68,69]

CH: Calcium hydroxide, MTA: Mineral trioxide aggregate, BD: Biodentine, NMP: NeoMTA Plus, GIC: Glass ionomer cement, RMGIC: Resin-modified GIC, DPC: Direct pulp capping