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 20,729 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The acidic amino acid, such as aspartic acid (l-Asp), and glutamic acid are the primary active molecules of the glycoprotein on the organic/inorganic interface of biomineralized tissue. In this study, aspartic acid was used as the organic template in inducing the nucleation and growth of calcium carbonate. With the analysis of X-ray diffraction we investigated the relationship between the l-Asp concentration and the precipitation phase crystal structure of calcium carbonate. SEM and TEM were employed in the analysis of the morphological characteristic of the precipitation and the aggregation of the nanoscale porous phase. In order to get the direct evidence of the interaction between Ca2+ and l-Asp, the technique of QCM was used in the investigation of the coordinate interaction of Ca2+/l-Asp. As the results have shown, l-Asp alone is adequate to switch the transformation between calcite and vaterite, and neither soluble organic additions nor metal ions are needed. Meanwhile, the morphology, size and aggregative way of the deposition are also mediated with change of l-Asp concentration. To interpret the cause of the hierarchic structure range from nanoscale to micron-scale and the formation of the porous spheres of vaterite, an assumption of limited-fusion was proposed from the view of the small biomolecules polarity that can control over the growth of the crystals and the aggregation of the micro crystals. The conclusion also provide a new material synthesize strategy.
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PMID:Control over the crystal phase, shape, size and aggregation of calcium carbonate via a L-aspartic acid inducing process. 1502 Jan 69

In this study, a novel nanoparticle system for paracellular transport was prepared using a simple and mild ionic-gelation method upon addition of a poly-gamma-glutamic acid (gamma-PGA) solution into a low-molecular-weight chitosan (low-MW CS) solution. The particle size and the zeta potential value of the prepared nanoparticles can be controlled by their constituted compositions. The results obtained by the TEM and AFM examinations showed that the morphology of the prepared nanoparticles was spherical in shape. Evaluation of the prepared nanoparticles in enhancing intestinal paracellular transport was investigated in vitro in Caco-2 cell monolayers. It was found that the nanoparticles with CS dominated on the surfaces could effectively reduce the transepithelial electrical resistance (TEER) of Caco-2 cell monolayers. After removal of the incubated nanoparticles, a gradual increase in TEER was noticed. The confocal laser scanning microscopy observations confirmed that the nanoparticles with CS dominated on the surface were able to open the tight junctions between Caco-2 cells and allowed transport of the nanoparticles via the paracellular pathways.
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PMID:Preparation of nanoparticles composed of chitosan/poly-gamma-glutamic acid and evaluation of their permeability through Caco-2 cells. 1576 83

In the study, poly(gamma-glutamic acid) (gamma-PGA) and poly(lactide) (PLA) were used to synthesize block copolymers via a simple coupling reaction between gamma-PGA and PLA to prepare self-assembled nanoparticles. For the potential of targeting liver cancer cells, galactosamine was further conjugated on the prepared nanoparticles as a targeting moiety. gamma-PGA, a water-soluble, biodegradable, and non-toxic compound, was produced by microbial fermentation (Bacillus licheniformis, ATCC 9945a) and then was hydrolyzed. The hydrolyzed gamma-PGA with a molecular weight of 4 kDa and a polydispersity of 1.3 was used, together with PLA (10 kDa, polydispersity 1.1), to synthesize block copolymers. The prepared nanoparticles had a mean particle size of about 140 nm with a zeta potential of about -20 mV. The results obtained by the TEM and AFM examinations showed that the morphology of the prepared nanoparticles was spherical in shape with a smooth surface. In the stability study, no aggregation or precipitation of nanoparticles was observed during storage for up to 1 month, as a result of the electrostatic repulsion between the negatively charged nanoparticles. With increasing the galactosamine content conjugated on the rhodamine-123-containing nanoparticles, the intensity of fluorescence observed in HepG2 cells increased significantly. Additionally, the intensity of fluorescence observed in HepG2 cells incubated with the nanoparticles with or without galactosamine conjugated increased approximately linearly with increasing the duration of incubation. In contrast, there was no fluorescence observed in Hs68 cells (without ASGP receptors) incubated with the nanoparticles with galactosamine conjugated. The aforementioned results indicated that the galactosylated nanoparticles prepared in the study had a specific interaction with HepG2 cells via ligand-receptor recognition.
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PMID:Preparation of nanoparticles composed of poly(gamma-glutamic acid)-poly(lactide) block copolymers and evaluation of their uptake by HepG2 cells. 1591 30

Klebsiella pneumoniae CH0905 strain exhibiting high-level cefotaxime resistance was isolated from a stool culture in the intensive care unit. The resistance gene responsible was shown to be located on a conjugative 60-kb plasmid designated pCH0905. The minimum inhibitory concentration (MIC) values for cefotaxime and ceftazidime of the original isolate and the transconjugates were 256 mug/ml. Isoelectric focusing of a protein preparation from the K. pneumoniae strain showed beta-lactamases with the pI values of 7.6 and 6.3. A 1,080-bp fragment amplified with PCR was cloned into the pGEM-T Easy vector. The nucleotide sequence of the complete 1,080 bp was determined. Sequence analysis revealed that the bla(TEM) gene of pCH0905 differed from bla(TEM-1) by two mutations, leading to the following amino acid substitutions: the glutamic acid residue at position 104 by lysine and the glycine residue at position 238 by serine (Ambler numbering). The association of these two mutations was described previously in TEM-15 beta-lactamase, but this is the first detection of this enzyme in Tunisia.
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PMID:First characterization in Tunisia of a TEM-15, extended-spectrum beta-lactamase-producing Klebsiella pneumoniae isolate. 1765 Sep 63

Gold nanoparticles of variable sizes have been prepared by reducing HAuCl4 with trisodium citrate by Frens' method. The synthesized gold particles show intense surface plasmon band in the visible region. The optical resonances in the visible are due to the surface plasmon oscillation, which is a function of geometry of the particles. The work reported here describes the interaction between nanoscale gold particles and a biomolecule, glutathione at low pH. Glutathione, which is a major cellular antioxidant and consists of amino acids glutamic acid, cysteine, and glycine, has been used as a molecular linker between the gold nanoparticles. In glutathione, the reactivity of the a-amines (adjacent to -COOH) is found to be pH-dependent. Linking via the a-amines are activated at low pH but suppressed at high pH due to electrostatic repulsive forces between the gold surfaces and the charged carboxylate groups. In colloidal solutions, the colour of gold nanoparticles may range from red to purple to blue, depending on the degree of aggregation as well as orientation of the individual particles within the aggregates. The citrate-functionalized gold nanoparticles with glutathione in variable acidic pH condition produce different but well-ordered aggregates. It is observed that a new peak appearing at a longer wavelength intensifies and shifts further to the red from the original peak position depending on the particle size, concentration of glutathione, and pH of the solution. The aggregates have been characterized by UV/Vis, FTIR, XRD, and TEM. On the basis of the first appearance of a clearly defined new peak at longer wavelength, a higher sensitivity of glutathione detection has been achieved with gold nanoparticles of larger dimension.
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PMID:Glutathione-induced aggregation of gold nanoparticles: electromagnetic interactions in a closely packed assembly. 1765 63

Photoluminescent nanoparticles of gold with size 3, 4, 6, and 9 nm are prepared by borohydride/citrate reduction in presence of polyethylene glycol (PEG)/tannic acid. The prepared nanomaterials are characterized by UV-vis spectroscopy and dynamic light scattering (DLS) technique. Intense photoluminescence (PL) is observed in nanoparticles prepared by fast reduction with borohydride in presence of PEG. A red shift of PL emission from 408 to 456 nm is observed for the change of size from 4 to 6 nm. Increase in PL intensity is observed for all the nanoparticles on the addition of KCl. Citrate reduced gold colloid which consists of large particles of size approximately 35 nm with anisotropic shapes showing two plasmon peaks is also prepared. The anisotropy is confirmed by TEM measurement. SERS activity of this colloid is tested using glutamic acid as an adsorbate probe. Assignment of the observed bands is given.
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PMID:Synthesis and spectroscopic characterization of gold nanoparticles. 1815 56

Two dioctadecyl L-glutamic acid derivatives with amide and ester type bondings have been synthesized and immobilized from 3-aminopropyltrimethoxysilane (APS) grafted silica (Sil-APS) to be used in reversed-phase high-performance liquid chromatography (RP-HPLC). Subsequent studies showed that dioctadecyl-L-glutamide derivative (GLN) can self-assemble into highly ordered structures by forming three-dimensional fibrillar aggregates as observed in scanning and transmission electron microscopes (SEM and TEM). Variable temperature (1)H NMR and FT-IR spectra of organogel revealed that the special aggregation morphology shown by GLN was stabilized by inter and or intra molecular hydrogen bonding among amide moieties. However, such ordered aggregated or self-assembled structures were not observed for the dioctadecyl-L-glutamate (GLU) derivative. The stationary phases Sil-GLN and Sil-GLU were characterized by DRIFT, elemental analysis, TGA, and (13)C and (29)Si CP-MAS NMR spectroscopic measurements. The chromatographic selectivity for both stationary phases was evaluated from the retention studies of different size and shape polycyclic aromatic hydrocarbons (PAHs). The chromatographic experiment for PAHs and geometrical isomers in RP-HPLC showed that Sil-GLN demonstrated extremely enhanced selectivity than Sil-GLU. The higher selectivity attributed by Sil-GLN has been brought by multiple pi-pi interactions among the pi-electrons of the grafted organic phase and pi-electrons of the guest PAHs molecules. Thermodynamic studies for linear and nonlinear PAHs revealed that the retention behavior does not change over a temperature range from 10 to 60 degrees C for both stationary phases.
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PMID:Evaluation of selectivity for L-glutamide-derived highly ordered assemblies in reversed-phase high-performance liquid chromatography. 1906 17

Self-assembling amphiphiles with unique chiroptical properties were derived from L-glutamic acid through omega-aminoalkylation and double long-chain alkylation. These amphiphiles can disperse in various solvents ranging from water to n-hexane. TEM and SEM observations indicate that the improvement in dispersity is induced by the formation of tubular and/or fibrillar aggregates with nanosized diameters, which makes these amphiphiles similar to aqueous lipid membrane systems. Spectroscopic observations, such as UV-visible and CD spectroscopies indicate that the aggregates are constructed on the basis of S- and R-chirally ordered structures through interamide interactions in water and organic media, respectively, and that these chiroptical properties can be controlled thermotropically and lyotropically. It is also reported that the chiral assemblies provide specific binding sites for achiral molecules and then induce chirality for the bonded molecules. Further, the applicability of the amphiphiles to template polymerization is discussed.
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PMID:Amphiphilic molecular gels from omega-aminoalkylated L-glutamic acid derivatives with unique chiroptical properties. 2010 7

The functionalization of pH-sensitiveness and cellular targeting is a promising strategy to fabricate drug delivery systems with high efficiency, high selectivity and low toxicity. In this paper, a poly(l-glutamic acid) dendrimer based drug delivery system with both pH-sensitive and targeting functions is reported. Poly(l-glutamic acid) dendrimers with a polyhedral oligomeric silsesquioxane (POSS) nanocubic core were synthesized. Its globular morphology and compact structure with multiple peripheral functional groups made it suitable for drug delivery. The OAS-G(3)-Glu dendrimer was conjugated with doxorubicin via pH-sensitive hydrazine bonds and targeting moiety (biotin). The cellular internalization and antitumor effects of the conjugates was evaluated in vitro. Both DLS and TEM results indicated that the conjugates aggregated into nanoparticles with diameters around 50 nm. The release rates of doxorubicin at pH 5.0 were much faster than those at pH 7.0 due to the acid cleavage of the hydrazine bonds. The internalization study revealed that the cellular uptake of the biotin modified conjugates was mainly through receptor-mediated endocytosis. These results indicate that our poly(l-glutamic acid) dendrimers with OAS core are promising vectors for fabricating smart and targeting drug delivery systems.
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PMID:A novel poly(l-glutamic acid) dendrimer based drug delivery system with both pH-sensitive and targeting functions. 2048 67

We report a facile method for the fabrication of spongelike gold/amino acid nanocomposites by the addition of NaBr to glutamic acid-stabilized gold nanoparticles (GNPs) at room temperature. The gold/glutamic acid (Glu) nanocomposite is characterized by TEM, SEM, UV-vis spectroscopy, and XRD measurements. The results suggest that the three-dimensional spongelike gold/Glu nanocomposites with mean diameter of 50 nm are formed via the nanospheres fusing into one another. The driving force for the fabrication of spongelike gold/amino acid nanocomposites is the van der Waals attractive forces of Br(-) partially coated GNPs. Furthermore, the obtained spongelike gold nanocomposites can be used as surface-enhanced Raman scattering (SERS) substrates with high SERS activity and stability for detecting Rhodamine 6G (R6G) molecules. Hence, NaBr-mediated preparation of SERS substrates described in this work has potential applications in chemical and biological analysis as well as medical detection.
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PMID:Br(-)-induced facile fabrication of spongelike gold/amino acid nanocomposites and their applications in surface-enhanced Raman scattering. 2069 94


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