国际检验医学杂志
國際檢驗醫學雜誌
국제검험의학잡지
INTERNATIONAL JOURNAL OF LABORATORY MEDICINE
2014年
5期
562-564
,共3页
纳米二氧化硅%固相吸附%聚合酶链反应
納米二氧化硅%固相吸附%聚閤酶鏈反應
납미이양화규%고상흡부%취합매련반응
silica nano-particles%solid-phase adsorption%polymerase chain reaction
目的:通过对固相吸附法的改良,探讨采用固相吸附法提取血清中丙型肝炎病毒RN A在实时荧光定量检测中的应用。方法首先对HCV RNA的提取方法进行改良,对固相载体纳米二氧化硅颗粒表面进行硅醇基化以提高其核酸吸附能力;同时对病毒裂解液进行优化,获得异硫氰酸胍(GuSCN )的最佳浓度用于 HCV RNA 的提取;最后使用改良方法提取的 HCV RNA进行实时荧光定量PCR实验,并绘制其标准曲线,计算出线性方程,同时检测该提取方法下实时荧光定量PCR对血清样本中HCV RNA的最低检测限并对其检测重复性进行验证。结果纳米二氧化硅颗粒硅醇基化后其吸附核酸的能力显著提高;病毒裂解液中GuSCN的最佳浓度为4.23 mol/L。使用改良方法提取血清样本中的HCV RNA用于实时荧光定量PCR ,获得标准曲线和线性方程,其线性相关系数(R2)达到0.999,检测的线性范围为2.52~5.52 IU/mL ,或者102.52~105.52病原体数/毫升。该方法的检测限达到(2.52±0.50)IU/mL ,且其检测重复性良好。结论改良后的固相吸附法可以大大降低实时荧光定量PCR的最低检测限,提高了HCV的阳性检测率。该方法操作简单,成本低,可以广泛应用于临床中HCV的检测和其他病毒的核酸检测。
目的:通過對固相吸附法的改良,探討採用固相吸附法提取血清中丙型肝炎病毒RN A在實時熒光定量檢測中的應用。方法首先對HCV RNA的提取方法進行改良,對固相載體納米二氧化硅顆粒錶麵進行硅醇基化以提高其覈痠吸附能力;同時對病毒裂解液進行優化,穫得異硫氰痠胍(GuSCN )的最佳濃度用于 HCV RNA 的提取;最後使用改良方法提取的 HCV RNA進行實時熒光定量PCR實驗,併繪製其標準麯線,計算齣線性方程,同時檢測該提取方法下實時熒光定量PCR對血清樣本中HCV RNA的最低檢測限併對其檢測重複性進行驗證。結果納米二氧化硅顆粒硅醇基化後其吸附覈痠的能力顯著提高;病毒裂解液中GuSCN的最佳濃度為4.23 mol/L。使用改良方法提取血清樣本中的HCV RNA用于實時熒光定量PCR ,穫得標準麯線和線性方程,其線性相關繫數(R2)達到0.999,檢測的線性範圍為2.52~5.52 IU/mL ,或者102.52~105.52病原體數/毫升。該方法的檢測限達到(2.52±0.50)IU/mL ,且其檢測重複性良好。結論改良後的固相吸附法可以大大降低實時熒光定量PCR的最低檢測限,提高瞭HCV的暘性檢測率。該方法操作簡單,成本低,可以廣汎應用于臨床中HCV的檢測和其他病毒的覈痠檢測。
목적:통과대고상흡부법적개량,탐토채용고상흡부법제취혈청중병형간염병독RN A재실시형광정량검측중적응용。방법수선대HCV RNA적제취방법진행개량,대고상재체납미이양화규과립표면진행규순기화이제고기핵산흡부능력;동시대병독렬해액진행우화,획득이류청산고(GuSCN )적최가농도용우 HCV RNA 적제취;최후사용개량방법제취적 HCV RNA진행실시형광정량PCR실험,병회제기표준곡선,계산출선성방정,동시검측해제취방법하실시형광정량PCR대혈청양본중HCV RNA적최저검측한병대기검측중복성진행험증。결과납미이양화규과립규순기화후기흡부핵산적능력현저제고;병독렬해액중GuSCN적최가농도위4.23 mol/L。사용개량방법제취혈청양본중적HCV RNA용우실시형광정량PCR ,획득표준곡선화선성방정,기선성상관계수(R2)체도0.999,검측적선성범위위2.52~5.52 IU/mL ,혹자102.52~105.52병원체수/호승。해방법적검측한체도(2.52±0.50)IU/mL ,차기검측중복성량호。결론개량후적고상흡부법가이대대강저실시형광정량PCR적최저검측한,제고료HCV적양성검측솔。해방법조작간단,성본저,가이엄범응용우림상중HCV적검측화기타병독적핵산검측。
Objective To explore the application of adopting the solid phase adsorption method to extract serum hepatitis C virus (HCV) RNA in the real-time fluorescence quantification PCR( RT-qPCR) by the improvement of solid phase adsorption method . Methods Firstly ,the surface of silica nano-particles was modified with Si-OH for increasing their adsorption ability with HCV RNA .Then the concentration of guanidinium thiocyanate (GuSCN) in the viral lysate was optimized .Thirdly ,the HCV RNA of standard serum samples was extracted using the modified solid-phase adsorption method and then performed in the RT-qPCR .Its standard curve was drawn and the linear equation was calculated .At the same time ,the lowest detection limit of RT-qPCR for de-tecting HCVRNA in serum sample was measured and the detection repeatability was verified .Results The adsorption ability of sil-ica nano-particles for HCV RNA in serum samples was remarkably improved after surface modification with Si-OH .The optimal GuSCN concentration in viral lysates was 4 .23 mol/L .Using the modified method to extract HCV RNA in serum samples was ap-plied in RT-qPCR ,the standard curve and the linear equation were obtained ,the linear correlation coefficient(R2) reached to 0 .999 and the detected linear range was (2 .52 -5 .52) IU/mL or 102 .52 -105 .52 pathogen number/mL .The detection limit of HCV RNA in serum samples was (2 .52 ± 0 .50)IU/mL with good detection repeatability .Conclusion The modified solid-phase adsorp-tion method can greatly decrease the lowest detection limit of RT-qPCR and increase the positive detection rate of HCV .This meth-od is simple to operate ,has low cost and can be widely applied in the HCV detection and the nucleic acid detection of other viruses in clinic .