9 research outputs found
Environmental Application, Fate, Effects, and Concerns of Ionic Liquids: A Review
Ionic liquids (ILs)
comprise mostly of organic salts with negligible
vapor pressure and low flammability that are proposed as replacements
for volatile solvents. ILs have been promoted as “green”
solvents and widely investigated for their various applications. Although
the utility of these chemicals is unquestionable, their toxic effects
have attracted great attention. In order to manage their potential
hazards and design environmentally benign ILs, understanding their
environmental behavior, fate and effects is important. In this review,
environmentally relevant issues of ILs, including their environmental
application, environmental behavior and toxicity are addressed. In
addition, also presented are the influence of ILs on the environmental
fate and toxicity of other coexisting contaminants, important routes
for designing nontoxic ILs and the techniques that might be adopted
for the removal of ILs
All hVISA and VISA isolates identified from different clinical specimens <sup>a</sup>.
a<p>All data are presented as number (%).</p>b<p>BHIA-3V is the brain heart infusion agar containing 3 ÎĽg/mL vancomycin; 757 isolates were screened for hVISA and VISA on BHIA-3V plates.</p>c<p>PAP-AUC is the population analysis profile-area under the curve; 209 screen-positive isolates were further confirmed by PAP-AUC.</p>d<p>Prevalence of hVISA and VISA isolated from sputum versus other specimens (p<0.001).</p
MIC<sub>50/90</sub> determined by CLSI broth microdilution and the prevalence of <i>agr</i>-dysfunction.
a<p>n = 209; <i><sup>b</sup></i> n = 129; <i><sup>c</sup></i> n = 76; <i><sup>d</sup></i> n = 4; <i><sup>e</sup></i> Prevalence of <i>agr</i> dysfunction in hVISA/VISA isolates versus VSSA isolates (p<0.001).</p
Quantification of biofilm formation was determined by crystal violet staining and read as an OD value.
<p>Each rhombus represents the mean OD value of one strain from five independent experiments. The ODs of most VSSA isolates (77/129, 59.7%) scattered above that of ATCC 29213 (the blue line; OD<sub>570</sub> = 2.180), and the ODs of the majority of hVISA isolates (48/76, 63.2%) scattered between those of ATCC29213 and Mu3 (the green line; OD<sub>570</sub> = 1.350). On the other hand, the ODs of the four VISA isolates scattered between those of Mu3 and Mu50 (the red line; OD<sub>570</sub> = 0.848).</p
Antimicrobial activity of 15 antimicrobial agents against 209 screen-positive isolates <i>in vitro</i>.
a<p>n = 57; <i><sup>b</sup></i> n = 72; <i><sup>c</sup></i> n = 129; <i><sup>d</sup></i> n = 63; <i><sup>e</sup></i> n = 17; <i><sup>f</sup></i> n = 80; <i><sup>g</sup></i> No. of total VSSA isolates versus no. of total hVISA/VISA isolates; <i><sup>h</sup></i> TMP-SMX, trimethoprim-sulfamethoxazole.</p
Biomimetic Choline-Like Graphene Oxide Composites for Neurite Sprouting and Outgrowth
Neurodegenerative diseases or acute
injuries of the nervous system
always lead to neuron loss and neurite damage. Thus, the development
of effective methods to repair these damaged neurons is necessary.
The construction of biomimetic materials with specific physicochemical
properties is a promising solution to induce neurite sprouting and
guide the regenerating nerve. Herein, we present a simple method for
constructing biomimetic graphene oxide (GO) composites by covalently
bonding an acetylcholine-like unit (dimethylaminoethyl methacrylate,
DMAEMA) or phosphorylcholine-like unit (2-methacryloyloxyethyl phosphorylcholine,
MPC) onto GO surfaces to enhance neurite sprouting and outgrowth.
The resulting GO composites were characterized by Fourier-transform
infrared spectroscopy, X-ray photoelectron spectroscopy, Raman spectroscopy,
UV–vis spectrometry, scanning electron microscopy, and contact
angle analyses. Primary rat hippocampal neurons were used to investigate
nerve cell adhesion, spreading, and proliferation on these biomimetic
GO composites. GO–DMAEMA and GO–MPC composites provide
the desired biomimetic properties for superior biocompatibility without
affecting cell viability. At 2 to 7 days after cell seeding was performed,
the number of neurites and average neurite length on GO–DMAEMA
and GO–MPC composites were significantly enhanced compared
with the control GO. In addition, analysis of growth-associate protein-43
(GAP-43) by Western blot showed that GAP-43 expression was greatly
improved in biomimetic GO composite groups compared to GO groups,
which might promote neurite sprouting and outgrowth. All the results
demonstrate the potential of DMAEMA- and MPC-modified GO composites
as biomimetic materials for neural interfacing and provide basic information
for future biomedical applications of graphene oxide
sj-pdf-1-ajs-10.1177_03635465221130448 – Supplemental material for Double-Limb Graft Versus Single-Limb Graft Medial Patellofemoral Ligament Reconstruction for Recurrent Patellar Dislocation: A Meta-analysis of Randomized Controlled Trials and Cohort Studies
Supplemental material, sj-pdf-1-ajs-10.1177_03635465221130448 for Double-Limb Graft Versus Single-Limb Graft Medial Patellofemoral Ligament Reconstruction for Recurrent Patellar Dislocation: A Meta-analysis of Randomized Controlled Trials and Cohort Studies by Long Pang, Kefan Mou, Yinghao Li, Tao Li, Jian Li, Jing Zhu and Xin Tang in The American Journal of Sports Medicine</p
Small Molecule-Initiated Light-Activated Semiconducting Polymer Dots: An Integrated Nanoplatform for Targeted Photodynamic Therapy and Imaging of Cancer Cells
Photodynamic therapy (PDT) is a noninvasive
and light-activated
method for cancer treatment. Two of the vital parameters that govern
the efficiency of PDT are the light irradiation to the photosensitizer
and visual detection of the selective accumulation of the photosensitizer
in malignant cells. Herein, we prepared an integrated nanoplatform
for targeted PDT and imaging of cancer cells using folic acid and
horseradish peroxidase (HRP)-bifunctionalized semiconducting polymer
dots (FH-Pdots). In the FH-Pdots, meta-tetraÂ(hydroxyphenyl)-chlorin
(m-THPC) was used as photosensitizer to produce cytotoxic reactive
oxygen species (ROS); fluorescent semiconducting polymer polyÂ[2-methoxy-5-((2-ethylhexyl)Âoxy)-<i>p</i>-phenylenevinylene] was used as light antenna and hydrophobic
matrix for incorporating m-THPC, and amphiphilic Janus dendrimer was
used as a surface functionalization agent to conjugate HRP and aminated
folic acid onto the surface of FH-Pdots. Results indicated that the
doped m-THPC can be simultaneously excited by the on-site luminol–H<sub>2</sub>O<sub>2</sub>–HRP chemiluminescence system through
two paths. One is directly through chemiluminescence resonance energy
transfer (CRET), and the other is through CRET and subsequent fluorescence
resonance energy transfer. In vitro PDT and specificity studies of
FH-Pdots using a standard transcriptional and translational assay
against MCF-7 breast cancer cells, C6 glioma cells, and NIH 3T3 fibroblast
cells demonstrated that cell viability decreased with increasing concentration
of FH-Pdots. At the same concentration of FH-Pdots, the decrease in
cell viability was positively relevant with increasing folate receptor
expression. Results from in vitro fluorescence imaging exhibited that
more FH-Pdots were internalized by cancerous MCF-7 and C6 cells than
by noncancerous NIH 3T3 cells. All the results demonstrate that the
designed semiconducting FH-Pdots can be used as an integrated nanoplatform
for targeted PDT and on-site imaging of cancer cells