分析科学学报
分析科學學報
분석과학학보
JOURNAL OF ANALYTICAL SCIENCE
2010年
1期
35-38
,共4页
小牛胸腺DNA%盐酸小檗碱%荧光光谱法
小牛胸腺DNA%鹽痠小檗堿%熒光光譜法
소우흉선DNA%염산소벽감%형광광보법
Berberine%Calf Thymus DNA%Fluorescence spectroscopy
采用荧光和紫外(UV)光谱等手段,研究了中药有效成分小檗碱(Ber)与脱氧核糖核酸(DNA)的键合作用.结果发现,小檗碱能插入到DNA双螺旋碱基对之间的空腔中,使小檗碱在λ_(em)=530 nm处较弱的荧光强度显著提高;酸度显著影响其相互之间的作用;随着DNA浓度的增大,Ber的荧光强度增大,显示了很好的光敏性能.偏振、荧光猝灭实验等也进一步表明:Ber与DNA的作用方式主要是嵌插结合;离子强度的大小会影响Ber与DNA之间的作用.在pH=3.0适宜酸度条件下,建立了以Ber为探针定量测定DNA的分析方法.方法线性范围为0~5.2×10~(-5) mol/L,精密度(RSD)为2.7%(n=7),检出限为1.43×10~(-7) mol/L.
採用熒光和紫外(UV)光譜等手段,研究瞭中藥有效成分小檗堿(Ber)與脫氧覈糖覈痠(DNA)的鍵閤作用.結果髮現,小檗堿能插入到DNA雙螺鏇堿基對之間的空腔中,使小檗堿在λ_(em)=530 nm處較弱的熒光彊度顯著提高;痠度顯著影響其相互之間的作用;隨著DNA濃度的增大,Ber的熒光彊度增大,顯示瞭很好的光敏性能.偏振、熒光猝滅實驗等也進一步錶明:Ber與DNA的作用方式主要是嵌插結閤;離子彊度的大小會影響Ber與DNA之間的作用.在pH=3.0適宜痠度條件下,建立瞭以Ber為探針定量測定DNA的分析方法.方法線性範圍為0~5.2×10~(-5) mol/L,精密度(RSD)為2.7%(n=7),檢齣限為1.43×10~(-7) mol/L.
채용형광화자외(UV)광보등수단,연구료중약유효성분소벽감(Ber)여탈양핵당핵산(DNA)적건합작용.결과발현,소벽감능삽입도DNA쌍라선감기대지간적공강중,사소벽감재λ_(em)=530 nm처교약적형광강도현저제고;산도현저영향기상호지간적작용;수착DNA농도적증대,Ber적형광강도증대,현시료흔호적광민성능.편진、형광졸멸실험등야진일보표명:Ber여DNA적작용방식주요시감삽결합;리자강도적대소회영향Ber여DNA지간적작용.재pH=3.0괄의산도조건하,건립료이Ber위탐침정량측정DNA적분석방법.방법선성범위위0~5.2×10~(-5) mol/L,정밀도(RSD)위2.7%(n=7),검출한위1.43×10~(-7) mol/L.
The binding of berberine to calf thymus DNA was investigated by fluorescence and ultraviolet-visible absorption spectroscopy. The experimental results revealed that the intercalation of berberine into calf thymus DNA leaded to a dramatic enhancement of the photoluminescence of the drug at 530 nm. The absorption and fluorescence spectra, salt concentration effect, KI quenching, fluorescence polarization and DNA denaturation experiments were given. These results provided the evidence that Ber was inserted into the base-stacking domain of DNA double helix. The intrinsic binding constant and the binding site number were estimated.The analytical characteristics were also reported. Linear range was 0~5.2×10~(-5) mol/L, precision RSD=2.7%(n=7), and detection limit was 1.43×10~(-7) mol/L.