Choi Eun-Hye, Lee Sang Kwang, Ihm Chunhwa, Sohn Young-Hak
Eulji Medi-Bio Research Institute (EMBRI), Daejeon, Korea.
Eulji Medi-Bio Research Institute (EMBRI), Daejeon, Korea ; Department of Laboratory Medicine, Eulji University Hospital, Daejeon, Korea.
Osong Public Health Res Perspect. 2014 Dec;5(6):351-7. doi: 10.1016/j.phrp.2014.09.005. Epub 2014 Nov 1.
Dried blood spot (DBS) technology is a microsampling alternative to traditional plasma or serum sampling for pharmaco- or toxicokinetic evaluation. DBS technology has been applied to diagnostic screening in drug discovery, nonclinical, and clinical settings. We have developed an improved elution protocol involving boiling of blood spots dried on Whatman filter paper.
The purpose of this study was to compare the quality, purity, and quantity of DNA isolated from frozen blood samples and DBSs. We optimized a method for extraction and estimation of DNA from blood spots dried on filter paper (3-mm FTA card). A single DBS containing 40 μL blood was used.
DNA was efficiently extracted in phosphate-buffered saline (PBS) or Tris-EDTA (TE) buffer by incubation at 37°C overnight. DNA was stable in DBSs that were stored at room temperature or frozen. The housekeeping genes GAPDH and beta-actin were used as positive standards for polymerase chain reaction (PCR) validation of general diagnostic screening.
Our simple and convenient DBS storage and extraction methods are suitable for diagnostic screening by using very small volumes of blood collected on filter paper, and can be used in biobanks for blood sample storage.
干血斑(DBS)技术是一种用于药物或毒代动力学评估的微量采样方法,可替代传统的血浆或血清采样。DBS技术已应用于药物发现、非临床和临床环境中的诊断筛查。我们开发了一种改进的洗脱方案,包括对在Whatman滤纸上干燥的血斑进行煮沸。
本研究的目的是比较从冷冻血样和DBS中分离的DNA的质量、纯度和数量。我们优化了一种从滤纸上干燥的血斑(3毫米FTA卡)中提取和估计DNA的方法。使用了一个含有40μL血液的单一DBS。
通过在37°C孵育过夜,DNA在磷酸盐缓冲盐水(PBS)或Tris-EDTA(TE)缓冲液中被有效提取。DNA在室温或冷冻保存的DBS中是稳定的。管家基因GAPDH和β-肌动蛋白用作一般诊断筛查的聚合酶链反应(PCR)验证的阳性标准。
我们简单便捷的DBS储存和提取方法适用于使用在滤纸上采集的极少量血液进行诊断筛查,并且可用于生物样本库中血液样本的储存。