The Effect of PAMAM Dendrimer on the Dentin Remineralization and Matrix Metalloproteinases Activity

CHEN Wang, YANG De-qin, XIANG Ke-zhen, CHEN Liang

Abstract

The purpose of this study was to investigate the effect of G4.5 carboxyl-terminated poly dendrimer (PAMAM-COOH) on the dentin remineralization and the matrix metalloproteinases (MMPs) activity.  Methods  The dentine samples were averagely divided into four groups: 100 mg/mL PAMAM-COOH group (A group), 10 mg/mL PAMAM-COOH group (B group), 2% (wt) chlorhexidine (CHX) group (C group) and deionized water group (Control group). MMP Activity Assay Kit was used to detect the activity of dentin endogenous MMPs in the four groups. The loss of dry mass of dentin after 30 d were measured. In situ zymography analysis was performed to detect the effects of PAMAM dendrimer in each group (except A group) on gelatinase activity in dentin. After incubation in artificial saliva for 7 and 14 d incubated, the remineralization of each group (except A group) in dentin surfaces were examined using a field emission-scanning electron microscope (FESEM).  Results  Compared with the control group, the dentin endogenous MMPs activity in A, B and C groups were all decreased (P<0.05). The activity of endogenous MMPs in C group was lower than that of A and B groups (P<0.001), but the difference between A and B groups was not statistically significant. The loss of dry mass in A, B and C groups were lower than that in control group (P<0.05), but there were no significant difference in A, B and C groups. The in situ zymography analysis showed that 48 h later, the dentin gelatinase activity in B group was inhibited compared with the control group, but the inhibitory effect was weaker than that of CHX. After 7 d and 14 d, there were no obvious mineralization in the control group, while distinct mineralization were observed in B group. The mineralization effect in group B was better than group C.  Conclusion  G4.5 PAMAM-COOH could introduce remineralizationin and demineralizeddentin by effectively inhibiting endogenous MMPs and gelatinase, thus contributes as novel material to enhancing durability of adhesion.

 

Keywords: PAMAM dendrimer, Biomimetic mineralization, Matrix metalloproteinases, Gelatinase, Dentin

 

Full Text:

PDF


References


BRESCHI L, MARAVIC T, CUNHA S R, et al. Dentin bonding systems: from dentin collagen structure to bond preservation and clinical applications. Dent Mater,2018,34(1): 78–96.

PALOSAARI H, WAHLGREN J, LARMAS M, et al. The expression of MMP-8 in human odontoblasts and dental pulp cells is down-regulated by TGF-beta1. J Dent Res,2000,79(1): 77–84.

TJADERHANE L, LARJAVA H, SORSA T, et al. The activation and function of host matrix metalloproteinases in dentin matrix breakdown in caries lesions. J Dent Res,1998,77(8): 1622–1629.

EPASINGHE D J, YIU C K, BURROW M F, et al. The inhibitory effect of proanthocyanidin on soluble and collagen-bound proteases. J Dent, 2013,41(9): 832–839.

TAO S, HE L, XU H H K, et al. Dentin remineralization via adhesive containing amorphous calcium phosphate nanoparticles in a biofilm-challenged environment. J Dent, 2019, 89[2019-07-24]. https://doi. org/10.1016/j.jdent.2019.103193.

KLAJNERT B, BRYSZEWSKA M. Dendrimers: properties and applications. Acta Biochimica Polonica,2001,48(1): 199–208.

CHEN L, YUAN H, TANG B, et al. Biomimetic remineralization of human enamel in the presence of polyamidoamine dendrimers in vitro. Caries Res,2015,49(3): 282–290.

CIOLKOWSKI M, ROZANEK M, BRYSZEWSKA M, et al. The influence of PAMAM dendrimers surface groups on their interaction with porcine pepsin. Biochim Biophys Acta,2013,1834(10): 1982–1987.

CEROFOLINI L, BALDONESCHI V, DRAGONI E, et al. Synthesis and binding monitoring of a new nanomolar PAMAM-based matrix metalloproteinases inhibitor (MMPIs). Bioorgan Med Chem,2017,25(2): 523–527.

RICHICHI B, BALDONESCHI V, BURGALASSI S, et al. A divalent PAMAM-based matrix metalloproteinase/carbonic anhydrase inhibitor for the treatment of dry eye syndrome. Chemistry,2016,22(5): 1714–1721.

SESEOGULLARI-DIRIHAN R, APOLLONIO F, MAZZONI A, et al. Use of crosslinkers to inactivate dentin MMPs. Dent Mater,2016,32(3): 423–432.

ALTINCI P, MUTLUAY M, SESEOGULLARI-DIRIHAN R, et al. NaF inhibits matrix-bound cathepsin-mediated dentin matrix degradation. Caries Res,2016,50(2): 124–132.

THOMPSON J M, AGEE K, SIDOW S J, et al. Inhibition of endogenous dentin matrix metalloproteinases by ethylenediaminetetraacetic acid. J Endod,2012,38(1): 62–65.

TEZVERGIL-MUTLUAY A, AGEE K A, HOSHIKA T, et al. The inhibitory effect of polyvinylphosphonic acid on functional matrix metalloproteinase activities in human demineralized dentin. Acta Biomater,2010,6(10): 4136–4142.

MAZZONI A, APOLONIO F M, SABOIA V P, et al. Carbodiimide inactivation of MMPs and effect on dentin bonding. J Dent Res,2014, 93(3): 263–268.

MONTAGNER A F, SARKIS-ONOFRE R, PEREIRA-CENCI T, et al. MMP inhibitors on dentin stability: a systematic review and meta-analysis. J Dent Res,2014,93(8): 733–743.

CADENARO M, PASHLEY D H, MARCHESI G, et al. Influence of chlorhexidine on the degree of conversion and E-modulus of experimental adhesive blends. Dent Mater,2009,25(10): 1269–1274.

LIANG K, WEIR M D, XIE X, et al. Dentin remineralization in acid challenge environment via PAMAM and calcium phosphate composite. Dent Mater,2016,32(11): 1429–1440.

LI J, YANG J, LI J, et al. Bioinspired intrafibrillar mineralization of human dentine by PAMAM dendrimer. Biomaterials,2013,34(28): 6738–6747.


Refbacks

  • There are currently no refbacks.