ISF

ISF
  • 文章类型: Journal Article
    微针(MN)是生物医学工程领域的一项新技术,因为它能够通过最小的侵入来评估生物信息。突破性医疗保健监测的迫切需要之一是持续监测。空心微针对提取皮肤间质液(ISF)进行分析非常有吸引力,这使得它们非常适合感知生物标志物和促进诊断。然而,其复杂的制造过程阻碍了其广泛应用。本研究在光聚合过程中聚乙二醇二丙烯酸酯(PEGDA)折射率变化的基础上,证明了一种简单的一步制备空心MNs的方法。制造的中空微针表现出穿透皮肤的理想机械特性。流体动力学模拟表明,液体在毛细管力作用下在空心微针中上升。此外,纸基葡萄糖传感器与空心微针集成。我们还观察到MN阵列通过毛细管作用在体外和体内顺利地提取了ISF。结果显示了MN贴片对持续性血糖(GLU)监测的适用性,患者和糖尿病前期个体的诊断相关测试。
    Microneedle (MN) is a novel technique of the biomedical engineering field because of its ability to evaluate bioinformation via minimal invasion. One of the urgent requirements for ground-breaking health care monitoring is persistent monitoring. Hollow microneedles are extremely attractive to extract skin interstitial fluid (ISF) for analysis, which makes them perfect for sensing biomarkers and facilitating diagnosis. Nevertheless, its intricate fabrication process has hampered its extensive application. The present research demonstrates an easy one-step preparation approach for hollow MNs on the foundation of the refraction index variations of polyethylene glycol diacrylate (PEGDA) in the process of photopolymerization. The fabricated hollow microneedle exhibited ideal mechanical characteristics to penetrate the skin. Hydrodynamic simulations showed that the liquid was risen in a hollow microneedle by capillary force. Furthermore, a paper-based glucose sensor was integrated with the hollow microneedle. We also observed that the MN array smoothly extracted ISF in vitro and in vivo by capillary action. The outcomes displayed the applicability of the MN patch to persistent blood glucose (GLU) monitoring, diagnosis-related tests for patients and pre-diabetic individuals.
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  • 文章类型: Journal Article
    Chlorophyll content, one of the most important physiological parameters related to plant photosynthesis, is usually used to predict yield potential. To map the quantitative trait loci (QTLs) underlying the chlorophyll content of rice leaves, a double haploid (DH) population was developed from an indica/japonica (Zhenshan 97/Wuyujing 2) crossing and two backcross populations were established subsequently by backcrossing DH lines with each of their parents. The contents of chlorophyll a and chlorophyll b were determined by using a spectrophotometer to directly measure the leaf chlorophyll extracts. To determine the leaf chlorophyll retention along with maturation, all measurements were performed on the day of heading and were repeated 30 days later. A total of 60 QTLs were resolved for all the traits using these three populations. These QTLs were distributed on 10 rice chromosomes, except chromosomes 5 and 10; the closer the traits, the more clustering of the QTLs residing on common rice chromosomal regions. In general, the majority of QTLs that specify chlorophyll a content also play a role in determining chlorophyll b content. Strangely, chlorophyll content in this study was found mostly to be lacking or to have a negative correlation with yield. In both backcross F1 populations, overdominant (or underdominant) loci were more important than complete or partially dominant loci for main-effect QTLs and epistatic QTLs, thereby supporting previous findings that overdominant effects are the primary genetic basis for depression in inbreeding and heterosis in rice.
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  • 文章类型: Journal Article
    黄病毒表现出广泛的遗传多样性并表现出不同的宿主关系。蚊媒黄病毒最近在世界范围内被分离和表征。中国云南省是物种多样性最丰富的地区之一,也是亚洲大陆多物种进化的中心,它支持许多节肢动物传播的病毒(虫媒病毒)的传播。在虫媒病毒的筛查程序中,2007年至2010年云南省蚊子活动季节采集蚊子。11株黄病毒,命名为云南库蚊黄病毒(YNCxFVs),是从三带囊状库蚊和中华按蚊标本中获得的。基于部分非结构蛋白(NS)5基因的序列分析表明,YNCxFV彼此之间具有92.8-99.6%的核苷酸同一性,并且与库蚊相关的黄病毒相似。一个代表性分离株的完整基因组,对LSFlaviV-A20-09进行测序。基因组长10,865个核苷酸,包含一个单一的,10,080个核苷酸的长开放阅读框(ORF),编码3360-aa多蛋白。该基因组与广平病毒(QBV)VN180株最密切相关,从越南库蚊中分离出的一种昆虫特异性黄病毒,但ORF序列只有83.0%的核苷酸和93.8%的氨基酸同一性。基因组与其他库蚊黄病毒具有约66.3%-68.5%的核苷酸序列和69.3-73.3%的氨基酸序列同一性,只有47.9-57.9%的核苷酸序列和38.7-55.1%的氨基酸序列同一性与Coquillettidia相关,曼索尼亚相关和伊蚊相关的黄病毒。系统发育分析表明,LSFlaviV-A20-09落入了与库蚊相关的黄病毒进化枝。我们的发现提供了有关感染蚊子的病毒异质性的更多信息。
    Flaviviruses present a wide range of genetic diversity and exhibit diverse host relationships. Mosquito-borne flaviviruses have recently been isolated and characterized worldwide. Yunnan Province of China is one of the richest areas of species diversity and is the center of multi-species evolution in mainland Asia, which supports the circulation of numerous arthropod-borne viruses (arboviruses). In a screening program of arboviruses, mosquitoes were collected during the mosquito activity season in the Yunnan Province from 2007 to 2010. Eleven flavivirus strains, named Yunnan Culex flaviviruses (YNCxFVs), were obtained from Culex tritaeniorhynchus and Anopheles sinensis specimens. Sequence analyses based on partial nonstructural protein (NS) 5 gene indicated that the YNCxFVs shared 92.8-99.6% nucleotide identity with each other and were similar to the Culex-related flaviviruses. The complete genome of one representative isolate, LSFlaviV-A20-09, was sequenced. The genome was 10,865 nucleotides long and contained a single, long open reading frame (ORF) of 10,080 nucleotides that encoded a 3360-aa polyprotein. This genome was most closely related to the Quang Binh virus (QBV) VN180 strain, an insect-specific flavivirus isolated from Culex mosquitoes in Vietnam, but only had 83.0% nucleotide and 93.8% amino acid identities for the ORF sequence. The genome has approximately 66.3%-68.5% nucleotide sequence and 69.3-73.3% amino acid sequence identities to other Culex flaviviruses, and only has 47.9-57.9% nucleotide sequence and 38.7-55.1% amino acid sequence identities to Coquillettidia-related, Mansonia-related and Aedes-related flaviviruses. Phylogenetic analyses revealed that the LSFlaviV-A20-09 fell into the Culex-related flavivirus clade. Our discoveries provide more information regarding the heterogeneity of viruses that infect mosquitoes.
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