中华生物医学工程杂志
中華生物醫學工程雜誌
중화생물의학공정잡지
CHINESE JOURNAL OF BIOMEDICAL ENGINEERING
2012年
5期
366-371
,共6页
雷秀霞%梁广铁%王维%刘紫娟%刘大渔%周小棉
雷秀霞%樑廣鐵%王維%劉紫娟%劉大漁%週小棉
뢰수하%량엄철%왕유%류자연%류대어%주소면
实验室技术和方法%聚合酶链反应%正交试验%毛细管%DNA提取
實驗室技術和方法%聚閤酶鏈反應%正交試驗%毛細管%DNA提取
실험실기술화방법%취합매련반응%정교시험%모세관%DNA제취
Laboratory techniques and procedures%Polymerase chain reaction%Orthogonal test%Capillary%DNA extraction
目的 利用正交试验优化毛细管DNA提取的实验条件,并对优化后的毛细管DNA提取法进行考察.方法 结合液滴与磁珠控制方法,在聚四氟乙烯毛细管中依次完成进样、DNA结合、洗涤以及洗脱等过程,建立毛细管DNA提取法.对照方法采用传统煮沸裂解法.采用正交试验考察血液乙型肝炎病毒(HBV DNA)提取的实验条件,包括结合时间、洗脱时间与洗脱温度等对DNA提取效果的影响.考察毛细管DNA提取法的DNA提取效果与重现性,分析提取的DNA定量(Ct值)与原始样品浓度的相关性.比较毛细管DNA提取法与对照方法提取DNA定量结果及耗时.结果 正交试验提示毛细管DNA提取法的最佳实验条件为磁珠DNA结合时间5 min,洗脱温度60℃,洗脱时间1 min.荧光定量PCR显示,毛细管DNA提取法DNA提取效果较好,回收DNA定量具有良好的重现性,提取的DNA定量与原始样品浓度呈正相关(r=0.9999,P<0.01).配对t检验显示,毛细管DNA提取法的回收DNA定量显著高于对照方法(t=-4.263,P<0.001).采用优化的实验条件,整个毛细管DNA提取操作在23min内完成,而对照方法耗时45 min以上.结论 利用正交试验实现了毛细管DNA提取实验参数的优化,建立了一种快速、高效的DNA提取方法.
目的 利用正交試驗優化毛細管DNA提取的實驗條件,併對優化後的毛細管DNA提取法進行攷察.方法 結閤液滴與磁珠控製方法,在聚四氟乙烯毛細管中依次完成進樣、DNA結閤、洗滌以及洗脫等過程,建立毛細管DNA提取法.對照方法採用傳統煮沸裂解法.採用正交試驗攷察血液乙型肝炎病毒(HBV DNA)提取的實驗條件,包括結閤時間、洗脫時間與洗脫溫度等對DNA提取效果的影響.攷察毛細管DNA提取法的DNA提取效果與重現性,分析提取的DNA定量(Ct值)與原始樣品濃度的相關性.比較毛細管DNA提取法與對照方法提取DNA定量結果及耗時.結果 正交試驗提示毛細管DNA提取法的最佳實驗條件為磁珠DNA結閤時間5 min,洗脫溫度60℃,洗脫時間1 min.熒光定量PCR顯示,毛細管DNA提取法DNA提取效果較好,迴收DNA定量具有良好的重現性,提取的DNA定量與原始樣品濃度呈正相關(r=0.9999,P<0.01).配對t檢驗顯示,毛細管DNA提取法的迴收DNA定量顯著高于對照方法(t=-4.263,P<0.001).採用優化的實驗條件,整箇毛細管DNA提取操作在23min內完成,而對照方法耗時45 min以上.結論 利用正交試驗實現瞭毛細管DNA提取實驗參數的優化,建立瞭一種快速、高效的DNA提取方法.
목적 이용정교시험우화모세관DNA제취적실험조건,병대우화후적모세관DNA제취법진행고찰.방법 결합액적여자주공제방법,재취사불을희모세관중의차완성진양、DNA결합、세조이급세탈등과정,건립모세관DNA제취법.대조방법채용전통자비렬해법.채용정교시험고찰혈액을형간염병독(HBV DNA)제취적실험조건,포괄결합시간、세탈시간여세탈온도등대DNA제취효과적영향.고찰모세관DNA제취법적DNA제취효과여중현성,분석제취적DNA정량(Ct치)여원시양품농도적상관성.비교모세관DNA제취법여대조방법제취DNA정량결과급모시.결과 정교시험제시모세관DNA제취법적최가실험조건위자주DNA결합시간5 min,세탈온도60℃,세탈시간1 min.형광정량PCR현시,모세관DNA제취법DNA제취효과교호,회수DNA정량구유량호적중현성,제취적DNA정량여원시양품농도정정상관(r=0.9999,P<0.01).배대t검험현시,모세관DNA제취법적회수DNA정량현저고우대조방법(t=-4.263,P<0.001).채용우화적실험조건,정개모세관DNA제취조작재23min내완성,이대조방법모시45 min이상.결론 이용정교시험실현료모세관DNA제취실험삼수적우화,건립료일충쾌속、고효적DNA제취방법.
Objective To optimize the experimental conditions for in-capillary DNA extraction through orthogonal test and to evaluate the optimized DNA extraction.Methods By using a protocol that controls droplet with magnetic beads,the in-capillary DNA extraction method was developed which involved sample introduction,DNA binding,magnetic beads rinsing and elution of DNA sequentially processed in a polytetrafluoroethylene (PTFE) capillary.Conventional cleavage by boiling was used as control approach.The orthogonal test was used to study the experimental conditions for DNA extraction of blood hepatitis B virus (HBV),which included the effects of DNA binding time,elution time and elution temperature on the performance of the in-capillary DNA extraction.Efficiency and reproducibility of the in-capillary DNA extraction assay,as well as the dependence of Ct value of extracted DNA on input DNA concentration were also appraised.The quantitative DNA recovery and time needed for DNA extraction were compared between the capillary-based and conventional methods.Results DNA binding for 5 min and elution at 60 ℃ for 1 min was the optimal experimental condition for in-capillary method showed by the orthogonal test.Fluorescent quantitative PCR showed good repeatability of DNA recovery and positive correlation of the DNA production with the amount of HBV DNA input (r=0.9999,P<0.01).Paired t-test analysis showed significantly higher DNA recovery using the capillary method compared to the conventional one (t=-4.263,P<0.001).Under optimized condition,the entire process of DNA extraction could be completed in 23 min vs 45 min or longer with conventional approach.Conclusion The experimental condition of in-capillary DNA extraction is optimized successfully using orthogonal test,and a rapid and highly efficient DNA extraction mothod is established.