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131.
Botella P Ortega I Quesada M Madrigal RF Muniesa C Fimia A Fernández E Corma A 《Dalton transactions (Cambridge, England : 2003)》2012,41(31):9286-9296
Combined chemo and photothermal therapy in in vitro testing has been achieved by means of multifunctional nanoparticles formed by plasmonic gold nanoclusters with a protecting shell of porous silica that contains an antitumor drug. We propose a therapeutic nanoplatform that associates the optical activity of small gold nanoparticles aggregates with the cytotoxic activity of 20(S)-camptothecin simultaneously released for the efficient destruction of cancer cells. For this purpose, a method was used for the controlled assembly of gold nanoparticles into stable clusters with a tailored absorption cross-section in the vis/NIR spectrum, which involves aggregation in alkaline medium of 15 nm diameter gold colloids protected with a thin silica layer. Clusters were further encapsulated in an ordered homogeneous mesoporous silica coating that provides biocompatibility and stability in physiological fluids. After internalization in 42-MG-BA human glioma cells, these protected gold nanoclusters were able to produce effective photothermolysis under femtosecond pulse laser irradiation of 790 nm. Cell death occurred by combination of a thermal mechanism and mechanical disruption of the membrane cell due to induced generation of micrometer-scale bubbles by vaporizing the water inside the channels of the mesoporous silica coating. Moreover, the incorporation of 20(S)-camptothecin within the pores of the external shell, which was released during the process, provoked significant cell death increase. This therapeutic model could be of interest for application in the treatment and suppression of non-solid tumors. 相似文献
132.
Santiago?CalEmail author Juan?R?Peinado María?Llamazares Víctor?Quesada Angela?Moncada-Pazos Cecilia?Garabaya Carlos?López-Otín 《BMC biochemistry》2006,7(1):9
Background
We have previously described the identification and characterization of polyserase-1 and polyserase-2, two human serine proteases containing three different catalytic domains within the same polypeptide chain. Polyserase-1 shows a complex organization and it is synthesized as a membrane-bound protein which can generate three independent serine protease domains as a consequence of post-translational processing events. The two first domains are enzymatically active. By contrast, polyserase-2 is an extracellular glycosylated protein whose three protease domains remain embedded in the same chain, and only the first domain possesses catalytic activity. 相似文献133.
Ruiz J García-Granda S Díaz MR Quesada R 《Dalton transactions (Cambridge, England : 2003)》2006,(36):4371-4376
Treatment of fac-[Mn(CNR)(CO)3{(PMe2)2CH2}]ClO4 (1a R = Ph, R = tBu) with KOH produced the cleavage of one of the P-C bonds of the coordinated dmpm ligand, resulting in the formation of phosphine-phosphinite complexes fac-[Mn(PMe2O)(CNR)(CO)3(PMe3)] (2a,b). Alkoxides such as NaOMe and NaOEt promoted similar processes in 1a,b, yielding fac-[Mn(CNR)(CO)3(PMe3)(PMe2OR')]ClO4 (3a R = tBu, R' = Me; 3b R = Ph, R' = Me; 4a R = tBu, R' = Et; 4b R = Ph, R' = Et) derivatives. The phosphinite ligand in 2a, b can be sequentially protonated by addition of 0.5 and 1 equivalent of HBF4 leading to fac-[{Mn(CNR)(CO)3(PMe3)(PMe2O)}2H]BF4 (6a,b) and fac-[Mn(CNR)(CO)3(PMe3)(PMe2OH)]BF4 (5a,b), respectively. 相似文献
134.
Corn (Zea mays) stalk and poplar (Populus deltoides) wood lignin was converted into monomeric aromatic compounds and short chain aliphatic carboxylic acids. The main reaction products were separated and identified using capillary gas chromatography-mass spectrometry on an HP-5 column. The compounds were considered as positively identified when their mass spectra and GC retention times agreed with those of authentic standard samples. The quantitative estimation of the identified reaction products was accomplished on an OV-101 capillary column by gas chromatography-FID using the internal standard method. Among the aromatic compounds, aldehydes (p-hydroxybenzaldehyde, vanillin, and syringaldehyde), acids (p-hydroxybenzoic, vanillic, 3,4-dihydroxybenzoic, and syringic), and one phenol (hydroquinone) were determined. In addition, the aliphatic carboxylic acids: glycolic, oxalic, malonic, glyoxylic, butanedioic, glyceric, and malic acid were identified. All the calibration curves of the quantified compounds approximated to a straight line. For both corn stalk and poplar wood lignins, the major components were the aromatic aldehydes (71 and 64% of the characterized fraction, respectively), followed by the aliphatic carboxylic acids (20 and 21% of the characterized fraction, respectively). 相似文献
135.
L. Bengoechea T. Hernández C. Quesada B. Bartolomé I. Estrella C. Gómez-Cordovés 《Chromatographia》1995,41(5-6):94-98
Summary The present paper describes the development of a method for the differentiation of hydroxycinnamic acid derivatives by HPLC
with photodiode-array detection. Furthermore spectral data of the compounds under investigation are given. Whereas p-coumaric
acid derivatives are distinguishable from caffeic and ferulic acid derivatives by the positions of their spectrum maxima and
their convexity interval value, it is not possible to distinguish between caffeic and ferulic acid derivatives because of
overlapping spectrum maxima and convexity interval values. 相似文献
136.
A new method for the determination of the hydroxymetabolites of vitamin D(3) (24,25-(OH)(2)-D(3), 1,25-(OH)(2)-D(3) and 25-OH-D(3)) in plasma is reported. The method is based on the integration of three subsystems: continuous cleanup/preconcentration, HPL separation and post-column fluorimetric derivatisation. The derivatising subsystem is based on the dehydration reaction undergone by the secosteriod molecules in a strong-acid medium. The calibration graphs were run between 0.1 pg ml(-1) and 100 ng ml(-1) for each analyte with excellent regression coefficients (>/=0.9933) in all cases. The precision at two concentration levels was established with acceptable RSDs (%) in all instances (values between 2.1 and 5.2%). The method was also checked by applying it to human plasma samples spiked with the target analytes and the recoveries ranged between 86 and 106%. 相似文献
137.
Antonio Quesada John N. Low Manuel Melguizo Manuel Nogueras Christopher Glidewell 《Acta Crystallographica. Section C, Structural Chemistry》2002,58(6):o355-o358
The molecules of the title compound, C18H16N4O3, exhibit a very polarized molecular–electronic structure. The molecules are linked into chains by a combination of an asymmetric three‐centre N—H?(N,O) hydrogen bond [H?N 2.19, H?O 2.54, N?N 3.041 (4) and N?O 2.977 (4) Å, and N—H?N 168, N—H?O 112 and N?H?O 67°] and an N—H?π(arene) interaction [H?Cg 2.67 Å, N?Cg 3.496 (4) Å and N—H?Cg 163°; Cg is a benzyl ring centroid]. 相似文献
138.
Elizabeth J. MacLean John N. Low Antonio Quesada Manuel Melguizo Manuel Nogueras Christopher Glidewell 《Acta Crystallographica. Section C, Structural Chemistry》2002,58(7):o442-o444
In the title compound, C14H15N5O2, the intramolecular dimensions are consistent with a highly polarized electronic structure. The molecules are linked into chains by a combination of N—H?N, N—H?O and N—H?π(arene) hydrogen bonds, and the chains are linked in pairs by aromatic π–π‐stacking interactions 相似文献
139.
140.