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- 저자 : Jiule Ding (검색결과 2 건)
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Jiule Ding,Wei Xing,Dongmei Wu,Jie Chen,Liang Pan,Jun Sun,Shijun Xing,Yongming Dai 대한영상의학회 2015 Korean Journal of Radiology Vol.16 No.4
To assess the feasibility of susceptibility-weighted imaging (SWI) while monitoring changes in renal oxygenation level after water loading. Thirty-two volunteers (age, 28.0 ± 2.2 years) were enrolled in this study. SWI and multi-echo gradient echo sequence-based T2* mapping were used to cover the kidney before and after water loading. Cortical and medullary parameters were measured using small regions of interest, and their relative changes due to water loading were calculated based on baseline and post-water loading data. An intraclass correlation coefficient analysis was used to assess inter-observer reliability of each parameter. A receiver operating characteristic curve analysis was conducted to compare the performance of the two methods for detecting renal oxygenation changes due to water loading. Both medullary phase and medullary T2* values increased after water loading (p < 0.001), although poor correlations were found between the phase changes and the T2* changes (p > 0.05). Interobserver reliability was excellent for the T2* values, good for SWI cortical phase values, and moderate for the SWI medullary phase values. The area under receiver operating characteristic curve of the SWI medullary phase values was 0.85 and was not different from the medullary T2* value (0.84). Susceptibility-weighted imaging enabled monitoring changes in the oxygenation level in the medulla after water loading, and may allow comparable feasibility to detect renal oxygenation level changes due to water loading compared with that of T2* mapping.
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Zhang, Lu,Feng, Qiang,Wang, Jiuling,Zhang, Shuai,Ding, Baoquan,Wei, Yujie,Dong, Mingdong,Ryu, Ji-Young,Yoon, Tae-Young,Shi, Xinghua,Sun, Jiashu,Jiang, Xingyu American Chemical Society 2015 ACS NANO Vol.9 No.10
<P>The functionalized lipid shell of hybrid nanoparticles plays an important role for improving their biocompatibility and <I>in vivo</I> stability. Yet few efforts have been made to critically examine the shell structure of nanoparticles and its effect on cell–particle interaction. Here we develop a microfluidic chip allowing for the synthesis of structurally well-defined lipid-polymer nanoparticles of the same sizes, but covered with either lipid-monolayer-shell (MPs, monolayer nanoparticles) or lipid-bilayer-shell (BPs, bilayer nanoparticles). Atomic force microscope and atomistic simulations reveal that MPs have a lower flexibility than BPs, resulting in a more efficient cellular uptake and thus anticancer effect than BPs do. This flexibility-regulated cell–particle interaction may have important implications for designing drug nanocarriers.</P><P><B>Graphic Abstract</B> <IMG SRC='http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/ancac3/2015/ancac3.2015.9.issue-10/acsnano.5b05792/production/images/medium/nn-2015-05792e_0007.gif'></P><P><A href='http://pubs.acs.org/doi/suppl/10.1021/nn5b05792'>ACS Electronic Supporting Info</A></P>
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