郑州大学学报(医学版)
鄭州大學學報(醫學版)
정주대학학보(의학판)
JOURNAL OF ZHENGZHOU UNIVERSITY(MEDICAL SCIENCES)
2014年
5期
648-650
,共3页
王丹%彭伟%李明珠%陈乃玲%穆玉
王丹%彭偉%李明珠%陳迺玲%穆玉
왕단%팽위%리명주%진내령%목옥
羧甲基壳聚糖%温敏凝胶%NIH3T3细胞%增殖%牙周组织再生
羧甲基殼聚糖%溫敏凝膠%NIH3T3細胞%增殖%牙週組織再生
최갑기각취당%온민응효%NIH3T3세포%증식%아주조직재생
carboxymethyl chitosan%thermosensitive hydrogel%NIH3T3 cell%proliferation%periodontal tissue regeneration
目的:观察羧甲基壳聚糖(CMCS)温敏凝胶对病变牙根面NIH3T3细胞附着和增殖的影响。方法:60颗患牙制成60个牙根片,分为5组。 A组:超声刮治+EDTA处理3 min+CMCS浸提液涂擦牙根表面5 min;B组:超声刮治+EDTA处理3 min+无菌生理盐水涂擦牙根表面5 min;C组:手动刮治+EDTA处理3 min+CMCS浸提液涂擦牙根表面5 min;D组:手动刮治+EDTA处理3 min+无菌生理盐水涂擦牙根表面5 min;E组(对照组):EDTA处理3 min+无菌生理盐水涂擦牙根表面5 min。将NIH3T3细胞与5组牙根片分别共培养16、24、72 h,采用细胞计数法和MTT法观察结果。结果:培养16 h时,A、B、C、D组细胞计数均高于对照组。培养24、72 h时,A、B、C、D组细胞增殖能力均高于对照组,且使用CMCS浸提液的A组及C组的细胞增殖能力高于使用无菌生理盐水的B组及D组(F=31.813和41.579,P<0.05)。结论:采用手动或超声进行牙周刮治及根面平整均有助于NIH3T3细胞的附着;联合使用CMCS温敏凝胶处理牙根表面可以促进NIH3T3细胞在牙根面的附着与增殖。
目的:觀察羧甲基殼聚糖(CMCS)溫敏凝膠對病變牙根麵NIH3T3細胞附著和增殖的影響。方法:60顆患牙製成60箇牙根片,分為5組。 A組:超聲颳治+EDTA處理3 min+CMCS浸提液塗抆牙根錶麵5 min;B組:超聲颳治+EDTA處理3 min+無菌生理鹽水塗抆牙根錶麵5 min;C組:手動颳治+EDTA處理3 min+CMCS浸提液塗抆牙根錶麵5 min;D組:手動颳治+EDTA處理3 min+無菌生理鹽水塗抆牙根錶麵5 min;E組(對照組):EDTA處理3 min+無菌生理鹽水塗抆牙根錶麵5 min。將NIH3T3細胞與5組牙根片分彆共培養16、24、72 h,採用細胞計數法和MTT法觀察結果。結果:培養16 h時,A、B、C、D組細胞計數均高于對照組。培養24、72 h時,A、B、C、D組細胞增殖能力均高于對照組,且使用CMCS浸提液的A組及C組的細胞增殖能力高于使用無菌生理鹽水的B組及D組(F=31.813和41.579,P<0.05)。結論:採用手動或超聲進行牙週颳治及根麵平整均有助于NIH3T3細胞的附著;聯閤使用CMCS溫敏凝膠處理牙根錶麵可以促進NIH3T3細胞在牙根麵的附著與增殖。
목적:관찰최갑기각취당(CMCS)온민응효대병변아근면NIH3T3세포부착화증식적영향。방법:60과환아제성60개아근편,분위5조。 A조:초성괄치+EDTA처리3 min+CMCS침제액도찰아근표면5 min;B조:초성괄치+EDTA처리3 min+무균생리염수도찰아근표면5 min;C조:수동괄치+EDTA처리3 min+CMCS침제액도찰아근표면5 min;D조:수동괄치+EDTA처리3 min+무균생리염수도찰아근표면5 min;E조(대조조):EDTA처리3 min+무균생리염수도찰아근표면5 min。장NIH3T3세포여5조아근편분별공배양16、24、72 h,채용세포계수법화MTT법관찰결과。결과:배양16 h시,A、B、C、D조세포계수균고우대조조。배양24、72 h시,A、B、C、D조세포증식능력균고우대조조,차사용CMCS침제액적A조급C조적세포증식능력고우사용무균생리염수적B조급D조(F=31.813화41.579,P<0.05)。결론:채용수동혹초성진행아주괄치급근면평정균유조우NIH3T3세포적부착;연합사용CMCS온민응효처리아근표면가이촉진NIH3T3세포재아근면적부착여증식。
Aim:To observe the effect of carboxymethyl chitosan ( CMCS) thermosensitive hydrogel on the attachment and proliferation of NIH3T3 cells on the root slices with periodontitis after scaling and root planning (SRP).Methods:Sixty teeth with periodontitis were used to prepare root slices and allocated into 5 groups randomly .Group A and group B were trea-ted by SRP using ultrasonator ,and group C and group D through manual treatment .After sterilizing the slices ,all of them were treated by EDTA for 3 min,then group A and group C were smeared with CMCS thermosensitive hydrogel ,and the other 3 groups were smeared by normal saline for 5 min.Then the NIH3T3 cells and the root slices were cocultured for 16,24,and 72 h,and the results were observed by cell counting method or MTT assay .Results:At 16 h,there were more cells in groups A,B, C,and D than those in control.At 24 and 72 h,the OD values of groups A,B,C,and D were higher than those in control;the OD values of groups A and C using CMCS thermosensitive hydrogel were higher than those in groups B and D using normal saline (F=31.813 and 41.579,P<0.05).Conclusion:Treating the teeth with SRP using ultrasonator or by hand both help the attach-ment of NIH3T3 cells.CMCS thermosensitive hydrogel could promote the adhesion and proliferation of NIH3T3 cells.