中华口腔医学杂志
中華口腔醫學雜誌
중화구강의학잡지
Chinese Journal of Stomatology
2011年
z1期
94-98
,共5页
卟啉单胞菌,牙髓%纯钛%白色念珠菌%聚酰胺-胺树枝形分子
卟啉單胞菌,牙髓%純鈦%白色唸珠菌%聚酰胺-胺樹枝形分子
계람단포균,아수%순태%백색념주균%취선알-알수지형분자
Porphyromonas,endodontalis%Titanium%Candida Albicans%Polyamidoamine Dendrimer
目的 评价聚酰胺-胺对纯钛表面白色念珠菌和牙龈卟啉单胞菌黏附的影响.方法 将64个纯钛试件采用抽签法随机分为8组.A、A1为对照组,B、B1聚酰胺-胺处理,C、C1唾液处理,D、D1聚酰胺-胺+唾液处理,A、B、C、D4组试件加入2 ml白色念珠菌菌液;A1、B1、C1、D1组试件加入牙龈卟啉单胞菌液.试件于白色念珠菌和牙龈卟啉单胞菌液中培养,染色,荧光观察.结果A、B、C、D4组白色念珠菌黏附量值为227.1±17.6、175.4±17.0、340.7±26.0和283.5±27.8,析因设计方差分析结果显示聚酰胺-胺处理组的菌黏附量减少(F=46.405,P<0.001);A1、B1、C1、D1组黏附的牙龈卟啉单胞菌活菌率为(59.42±2.76)%、(40.97±1.93)%、(63.03±1.99)%和(43.92±2.27)%,聚酰胺-胺处理组的活菌率低于未处理组(F =552.037,P<0.001).结论聚酰胺-胺对纯钛表面黏附的白色念珠菌和牙龈卟啉单胞菌均有抑制作用.
目的 評價聚酰胺-胺對純鈦錶麵白色唸珠菌和牙齦卟啉單胞菌黏附的影響.方法 將64箇純鈦試件採用抽籤法隨機分為8組.A、A1為對照組,B、B1聚酰胺-胺處理,C、C1唾液處理,D、D1聚酰胺-胺+唾液處理,A、B、C、D4組試件加入2 ml白色唸珠菌菌液;A1、B1、C1、D1組試件加入牙齦卟啉單胞菌液.試件于白色唸珠菌和牙齦卟啉單胞菌液中培養,染色,熒光觀察.結果A、B、C、D4組白色唸珠菌黏附量值為227.1±17.6、175.4±17.0、340.7±26.0和283.5±27.8,析因設計方差分析結果顯示聚酰胺-胺處理組的菌黏附量減少(F=46.405,P<0.001);A1、B1、C1、D1組黏附的牙齦卟啉單胞菌活菌率為(59.42±2.76)%、(40.97±1.93)%、(63.03±1.99)%和(43.92±2.27)%,聚酰胺-胺處理組的活菌率低于未處理組(F =552.037,P<0.001).結論聚酰胺-胺對純鈦錶麵黏附的白色唸珠菌和牙齦卟啉單胞菌均有抑製作用.
목적 평개취선알-알대순태표면백색념주균화아간계람단포균점부적영향.방법 장64개순태시건채용추첨법수궤분위8조.A、A1위대조조,B、B1취선알-알처리,C、C1타액처리,D、D1취선알-알+타액처리,A、B、C、D4조시건가입2 ml백색념주균균액;A1、B1、C1、D1조시건가입아간계람단포균액.시건우백색념주균화아간계람단포균액중배양,염색,형광관찰.결과A、B、C、D4조백색념주균점부량치위227.1±17.6、175.4±17.0、340.7±26.0화283.5±27.8,석인설계방차분석결과현시취선알-알처리조적균점부량감소(F=46.405,P<0.001);A1、B1、C1、D1조점부적아간계람단포균활균솔위(59.42±2.76)%、(40.97±1.93)%、(63.03±1.99)%화(43.92±2.27)%,취선알-알처리조적활균솔저우미처리조(F =552.037,P<0.001).결론취선알-알대순태표면점부적백색념주균화아간계람단포균균유억제작용.
Objective To evaluate the influence of polyamidoamine dendrimer on the adhesion of Candida albicans ( Ca ) and Porphyromonas gingialis ( Pg ) to titanium specimens.Methods Sixty-four titanium specimens ( 10 mm × 10 mm × 1 mm) were prepared and divided into eight groups of A,B,C,D,A1,B1,C1 and D1.Group A and A1 were the control groups.B and B1 were treated with polyamidoamine dendrimer,C and C1 were coated with saliva,D and D1 were treated with polyamidoamine dendrimer and saliva.The specimens were incubated in Ca and Pg cell suspension,and then fluorescence stained,photographed by fluorescence microscopy.Results Number of adherent Ca on A,B,C and D is 227.1 ±17.6,175.4 ± 17.0,340.7 ± 26.0 and 283.5 ± 27.8 respectively.The main effect of pellicle was statistically significant ( F =191.973,P < 0.001 ).Adherent Ca on the surfaces of specimens coated with saliva were more than those on the specimens coated without saliva.The main effect of polyamidoamine dendrimer was statistically significant ( F =46.405,P < 0.001 ).The number of adherent Ca on specimens treated with polyamidoamine dendrimer was less than that in control group ( P < 0.05 ).The percentages of vital adherent C.a were (57.07 ± 1.83 ) %,(44.18 ± 2.72) %,(59.04 ± 2.44) % and (45.89 ± 3.19 ) %respectively.The main effect of pellicle was not statistically significant ( F =4.043,P > 0.05 ).The main effect of polyamidoamine dendrimer was statistically significant ( F =202.066,P < 0.001 ).The percentage of vital adherent Ca on specimens treated with polyamidoamine dendrimer was lower than that in control group.The number of adherent Pg on surfaces of Group A1,B1,C1 and D1 was 536.78 ±30.27,336.15 ± 26.13,1219.20 ± 172.04,and 859.85 ± 47.04 respectively.There was statistically significant interaction between the pellicle and polyamidoamine dendrime (F =4.350,P < 0.05 ).The pellicle enhanced the effect of polyamidoamine dendrime inhibiting pg adhesion,while the polyamidoamine dendrime weakened the effect of pellicle.The percentages of vital adherent bacterias of group A1,B1,C1 and D1 were (59.40 ± 2.77 ) %,(40.97 ± 2.50) %,( 63.04 ± 1.99) % and (43.93 ± 3.11 ) % respectively.The values of groups coated with saliva were higher than the non-coated ( F =16.903,P < 0.001 ).The values of groups treated with polyamidoamine dendrimer were lower than non-treated ( F =552.037,P < 0.001 ).Conclusions Polyamidoamine dendrimer can inhibit the adhension of Ca and Pg on titanium materials.