Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0276640 (TEM)
 20,729 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

In this paper, we innovatively immobilized few-walled carbon nanotubes (FWCNTs) perpendicularly on Au surface through conductive thionine instead of aminoalkanethiols so as to improve electrochemical properties. Because FWCNTs own smaller aggregates, stronger chemical corrosion resistant, and higher conductivity than single-walled carbon nanotubes (SWCNTs), and thionine is a good electron transfer mediator can provide amino and sulfhydryl groups playing the same function as insulating aminoalkanethiols. The strategy for obtaining perpendicularly aligned FWCNTs (p-FWCNTs) is electrostatically assembled thionine and 11-amino-n-undecanethiol (AUT) on Au surface via Au-S bond to provide amino groups for covalently combining terminus-carboxylated FWCNTs, we confirmed and compared the results by AFM, Raman spectroscopy and electrochemical methods. In order to prove the constructed basement has excellent electrochemical properties can provide a good platform for sensors fabrication, we developed a novel non-enzymatic hydrogen peroxide (H2O2) sensor by electrodepositing Pt nanoparticles (PtNPs) on p-FWCNTs/Thionine/Au electrode surface, and verified the result by TEM, EDX and electrochemical techniques. Furthermore, polyallylamine (PAA) and poly(vinyl sulfate) (PVS) permselective layer, poly(diallyldimethylammonium) (PDDA) and glucose oxidase (GOx) multilayer films were layer-by-layer self-assembled on p-FWCNTs/Thionine/Au surface to fabricate a glucose biosensor. Either the non-enzymatic H2O2 sensor or the enzyme-based glucose biosensor showed good sensitivity, selectivity, reproducibility and stability, both them had been applied for biological sample analysis with satisfactory results. The results show that the p-FWCNTs/Thionine/Au electrode can work as an ideal platform for the development of highly sensitive sensors, coupled with p-FWCNTs are rich in functional groups could be used for fabricating diverse sensors.
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PMID:Highly-ordered perpendicularly immobilized FWCNTs on the thionine monolayer-modified electrode for hydrogen peroxide and glucose sensors. 2528 55

An ordered bicontinuous double-diamond (OBDD) morphology was found in polystyrene-block-(poly-4-vinylphenyldimethylvinylsilane-graft-polyisoprene), PS-b-(PVS-g-PI), block-graft copolymer. We obtained a 3D image of the microdomain structure formed in PS-b-(PVS-g-PI) using 3D-TEM. The 3D image shows that the polystyrene (PS) phase consists of two independent and interwoven networks. The structures of the two networks are identical and include tetrapod units that form planar six-membered rings. The features of the networks agree with those in the OBDD morphology, indicating that PS-b-(PVS-g-PI) exhibits ordered three-dimensional OBDD networks with the PS phase in the polyisoprene (PI) matrix phase. The grafted PI chains induce the frustration of the PS chains; thus, the effects of the specific interface are more dominant than those of packing frustration in the formation of the morphology, and the OBDD phase is stabilized.
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PMID:3D-TEM study on the novel bicontinuous microdomain structure. 2913 88

Extracellular vesicles (EVs) are highly specific and multi-purpose vesicular structures that are released by various cell and tissue types in the body. However, the secretion of EVs from mammalian embryos, especially human, has not been well characterized. Thus, the aim of this study was to 1) identify EVs in human preimplantation embryos at different stages of their development using scanning and electron microscopy, and 2) investigate whether EVs can cross the zona pellucida (ZP) and be released from human embryos cultured in vitro. Human oocytes, zygotes, cleavage embryos and blastocysts donated for research were labeled with the tetraspanin EV marker CD9 and analyzed by scanning and transmission electron microscopy. Embryo culture conditioned media collected 3- and 5-days post fertilization were examined for the presence of EVs using electron microscopy. We detected numerous CD9 positive vesicles released from all embryos examined. They were observed on the surface of the plasma membrane, within the perivitelline space as well as throughout the zona pellucida. Interestingly, EVs were not seen in the ZP of all mature metaphase II oocytes, however, were detected just after fertilization in the ZP of zygotes and embryos. Electron microscopy using negative staining, and nanoparticle tracking analysis (NTA) of embryo conditioned culture media also showed the presence of vesicles of various sizes, which were round shaped, and had a lipid bilayer. Their size ranged from 30 to 500 nm, consistent with the sizes of exosomes and microvesicles. In conclusion, the results of the study provide evidence that human preimplantation embryos at all developmental stages secrete EVs into the perivitelline space, which then traverse through the ZP, and are then released into the surrounding culture medium. Abbreviations: EVs: extracellular vesicles; ZP: zona pellucida; CD9, CD63, and CD81: tetraspanin EV markers; NTA: nanoparticle tracking analysis; ESCRT: endosomal sorting complexes required for transport; SEM: scanning electron microscopy; TEM: transmission electron microscopy; TE: trophectoderm; ICM: inner cell mass; PVS: perivitelline space; MI: metaphase I; MII: metaphase II; GV: germinal vesicle; MVs/EXs: microvesicles/exosomes; hCG: human chorionic gonadotrophin; GnRH: gonadogrophin releasing hormone; ICSI: intracytoplasmic sperm injection; SPS: serum protein substitute; 1PN: one pronuclear zygote; 3PN: tri-pronuclear zygote; IgG: immunoglobulin G; PBS: phosphate buffer saline; ETHO: ethanol; ESED: Environmental Secondary Electron Detector; BSA: bovine serum albumin.
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PMID:Ultrastructural identification of CD9 positive extracellular vesicles released from human embryos and transported through the zona pellucida. 3113 9

Poly(hydroxyethyl acrylate-co-phenyl vinyl sulfide) (P(HEA-co-PVS)), as an oxidizable amphiphilic polymer, was prepared for the fabrication of an oxidation- and temperature-responsive micelle for the delivery of doxorubicin (DOX). The interfacial activity of H2O2-treated P(HEA-co-PVS) was significantly lower than that of the untreated variety, possibly because of the oxidization of PVS. P(HEA-co-PVS) exhibited a lower critical solution temperature (LCST) behavior and the LCST increased upon H2O2 treatment. The copolymer micelles, prepared by the dialysis method, were found to be round particles (less than 100 nm) on TEM micrograph. The release degree of Nile red loaded in the micelles was higher when the H2O2 concentration was higher, possibly because the micelles could be solubilized more readily at a higher H2O2 concentration. The release degree was more strongly dependent on the oxidizing agent concentration when the temperature was higher. DOX loaded in the micelles suppressed the in vitro growth of KB cells (a human cancer cell type originating from the cervix) much more effectively than DOX loaded in an unoxidizable control micelle and free DOX, possibly because the copolymer would undergo an increase in its LCST, lose its amphiphilic property, and the micelles would be disassembled. The DOX-loaded micelles were readily internalized into KB cells, as evidenced by flow cytometry (FACS) and confocal laser scanning microscopy (CLSM).
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PMID:Oxidation- and Temperature-Responsive Poly(hydroxyethyl acrylate-co-phenyl vinyl sulfide) Micelle as a Potential Anticancer Drug Carrier. 3150 Jan 54