天津医药
天津醫藥
천진의약
Tianjin Medical Journal
2015年
10期
1187-1189,1190
,共4页
方谦%周雪%穆玉%陈乃玲%赵艳萍%刘庆辉%彭伟
方謙%週雪%穆玉%陳迺玲%趙豔萍%劉慶輝%彭偉
방겸%주설%목옥%진내령%조염평%류경휘%팽위
龋齿%牙釉质%牙再矿化%早期釉质龋%生物活性玻璃%显微硬度
齲齒%牙釉質%牙再礦化%早期釉質齲%生物活性玻璃%顯微硬度
우치%아유질%아재광화%조기유질우%생물활성파리%현미경도
dental caries%dental enamel%tooth remineralization%early enamel caries%bioactive glass%microhardness
目的:探讨生物活性玻璃促进早期釉质龋再矿化的最适浓度。方法收集新鲜拔除的牛切牙,制备釉质标本,随机分成显微硬度组和荧光组两大组,每组又分为3%、6%和9%小组,每小组5个标本。所有标本放在37℃人工脱矿液中脱矿72 h后,分别浸泡在质量分数为3%、6%和9%生物活性玻璃溶液内,5 min/次,2次/d,循环15 d。显微硬度仪测量脱矿前后及再矿化后牙釉质表面的显微硬度,并计算再矿化前后的显微硬度差值。荧光显微镜观察早期釉质龋表层下的荧光带厚度,从而评价再矿化效果。结果6%组的显微硬度差值最高,3%组的差值最低,差异均有统计学意义(均P<0.05)。6%组脱矿深度差值大于3%和9%组(均P<0.05),3%和9%组的脱矿深度差值差异无统计学意义。结论质量分数为6%的生物活性玻璃溶液是促进早期釉质龋再矿化的最适浓度,对早期釉质龋再矿化效果最理想。
目的:探討生物活性玻璃促進早期釉質齲再礦化的最適濃度。方法收集新鮮拔除的牛切牙,製備釉質標本,隨機分成顯微硬度組和熒光組兩大組,每組又分為3%、6%和9%小組,每小組5箇標本。所有標本放在37℃人工脫礦液中脫礦72 h後,分彆浸泡在質量分數為3%、6%和9%生物活性玻璃溶液內,5 min/次,2次/d,循環15 d。顯微硬度儀測量脫礦前後及再礦化後牙釉質錶麵的顯微硬度,併計算再礦化前後的顯微硬度差值。熒光顯微鏡觀察早期釉質齲錶層下的熒光帶厚度,從而評價再礦化效果。結果6%組的顯微硬度差值最高,3%組的差值最低,差異均有統計學意義(均P<0.05)。6%組脫礦深度差值大于3%和9%組(均P<0.05),3%和9%組的脫礦深度差值差異無統計學意義。結論質量分數為6%的生物活性玻璃溶液是促進早期釉質齲再礦化的最適濃度,對早期釉質齲再礦化效果最理想。
목적:탐토생물활성파리촉진조기유질우재광화적최괄농도。방법수집신선발제적우절아,제비유질표본,수궤분성현미경도조화형광조량대조,매조우분위3%、6%화9%소조,매소조5개표본。소유표본방재37℃인공탈광액중탈광72 h후,분별침포재질량분수위3%、6%화9%생물활성파리용액내,5 min/차,2차/d,순배15 d。현미경도의측량탈광전후급재광화후아유질표면적현미경도,병계산재광화전후적현미경도차치。형광현미경관찰조기유질우표층하적형광대후도,종이평개재광화효과。결과6%조적현미경도차치최고,3%조적차치최저,차이균유통계학의의(균P<0.05)。6%조탈광심도차치대우3%화9%조(균P<0.05),3%화9%조적탈광심도차치차이무통계학의의。결론질량분수위6%적생물활성파리용액시촉진조기유질우재광화적최괄농도,대조기유질우재광화효과최이상。
Objective To explore the optimum concentration of bioactive glass that promotes early enamel caries remineralization. Methods Fresh bovine incisors were selected and used for enamel specimen preparation. All specimens were randomly divided into two groups:micro hardness group and fluorescence group. Both groups were further divided into 3%, 6%and 9%groups. These specimens were placed in containers with demineralization liquid at 37℃for 72 hours. Then they were treat with 3%, 6%and 9%bioactive glass solution respectively twice a day for 5 minutes each. Samples in all three groups were dipped circularly into an artificial demineralization solution and an artificial saliva solution for 15 days. The mi?crohardness of enamel surface was measured before and after demineralization and remineralization. The different value of microhardness before and after remineralization was calculated. The thickness of fluorescence beneath the surface of early enamel caries was observed to evaluate the extend of remineralization effect. Results The difference in value of micro hard?ness in 6%group was the highest while that in 3%group was the lowest. The differences were significant. The difference in value of demineralization depth in 6%group was greater than those in 3%and 9%groups (P<0.05). There was no statistical?ly significance between those in 3%group and 9%group. Conclution The optimum concentration of bioactive glass solu?tion that promotes the remineralization of early enamel caries is 6%, which is ideal for remineralization of early enamel caries.