ABSTRACT
Two new kelsoane-type sesquiterpenes, namely kelsoenethiol (1) and dikelsoenyl ether (2), were obtained from the Formosan soft coral Nephthea erecta. Their structures were elucidated through extensive spectroscopic analyses, ESI orbitrap mass and quantum chemical calculations (QCC). The cytotoxicity against A-459 (human lung carcinoma), P-388 (mouse lymphocytic leukemia), and HT-29 (human colon adenocarcinoma) cancer cell lines of 1 and 2 was evaluated in vitro. Compound 1 showed cytotoxicity against P-388 and HT-29 cells with ED50s of 1.3 and 1.8 µg/mL, respectively.
Subject(s)
Anthozoa , Sesquiterpenes/chemistry , Animals , Drug Screening Assays, Antitumor/methods , HT29 Cells , Humans , Leukemia P388 , Mice , Sesquiterpenes/isolation & purificationABSTRACT
In this report, the effects of conductive polymer oxidation states and structures on the design and development of ionic liquid (IL)/conductive polymer (CP) composite films for gas sensing are systematically characterized. Four different polyvinyl ferrocene (PVF) films synthesized by varying the conditioning potential (0.7 vs 0.0 V) and the electrolyte are tested for their gas-sensing properties (e.g., sensitivity, selectivity, response time, linearity, and dynamic range against various gas analytes such as dichloromethane, ethanol, natural gas, methane, formaldehyde (37%), and benzene) utilizing the quartz crystal microbalance (QCM) and ATR-FT-IR. The best available film is further studied as a substrate for the immobilization of various ILs that enhanced both the sensitivity and selectivity. Finally, two arrays, each comprising four sensors with the following scheme are developed and characterized for their ability to classify the four target analytes by using linear discriminant analysis: (1) the highest sensitivity PVF film immobilized with four different ILs and (2) the highest sensitivity IL immobilized in four different PVF films. Array 2 is proven to be much better than array 1 in discriminating the analytes, which is very significant in establishing the fact that a diverse set of PVF redox states allow the rational development of a PVF/IL composite-based sensor array in order to analyze complex mixtures utilizing structural differences and the extent of intermolecular interactions.
Subject(s)
Ferrous Compounds/chemistry , Gases , Ionic Liquids , Polyvinyls/chemistry , Electrochemical Techniques , Metallocenes , Oxidation-ReductionABSTRACT
A Huisgen 1,3-dipolar cycloaddition "click chemistry" was employed to immobilize azido sugars (mannose, lactose, alpha-Gal) to fabricate carbohydrate self-assembled monolayers (SAMs) on gold. This fabrication was based on preformed SAM templates incorporated with alkyne terminal groups, which could further anchor the azido sugars to form well-packed, stable, and rigid sugar SAMs. The clicked mannose, lactose, and alpha-Gal trisaccharide SAMs were used in the analysis of specific carbohydrate-protein interactions (i.e., mannose-Con A; ECL-lactose, alpha-Gal-anti-Gal). The apparent affinity constant of Con A binding to mannose was (8.7 +/- 2.8) x 10(5) and (3.9 +/- 0.2) x 10(6) M(-1) measured by QCM and SPR, respectively. The apparent affinity constants of lactose binding with ECL and alpha-Gal binding with polyclonal anti-Gal antibody were determined to be (4.6 +/- 2.4) x 10(6) and (6.7 +/- 3.3) x 10(6) M(-1), respectively by QCM. SPR, QCM, AFM, and electrochemistry studies confirmed that the carbohydrate SAM sensors maintained the specificity to their corresponding lectins and nonspecific adsorption on the clicked carbohydrate surface was negligible. This study showed that the clicked carbohydrate SAMs in concert with nonlabel QCM or SPR offered a potent platform for high-throughput characterization of carbohydrate-protein interactions. Such a combination should complement other methods such as ITC and ELISA in a favorable manner and provide insightful knowledge for the corresponding complex glycobiological processes.
Subject(s)
Carbohydrates/chemistry , Membranes, Artificial , Proteins/chemistry , Combinatorial Chemistry Techniques , Electrochemistry , Electrodes , Microscopy, Atomic Force , Molecular Structure , Sensitivity and Specificity , Surface Plasmon Resonance , Time FactorsABSTRACT
A simple method was used to prepare a "switchable" electrode surface by using self-assembled monolayers of dodecanethiol on a gold electrode. The dodecane-modified electrode was electrochemically inactive until the monolayer was soaked in solutions of 1,10-phenanthroline or 2,2'-bipyridine. The electroactive form of the electrode could be reverted back to the nonelectroactive form by rinsing the electrode. Surface IR results showed that both dodecanethiol and 1,10-phenanthroline exist in the mixed monolayer.
