Quality assurance of Chinese herbal medicines: Procedure for multiple‐herb extraction

A quality assurance (QA) procedure for multiple‐herb extraction, which takes into account the existence of common chemical markers and multiple‐herb‐extraction effects, has been developed for producing Chinese herbal medicines (CHMs) of consistent quality. The experimental method for determining related correlation function of the multiple‐herb‐extraction effect was designed. A systematic solution strategy was also developed to appropriately decompose the multiple‐herb extraction system into several subsystems for obtaining solution(s) and determining the overall behavior of the system. An example of QA of Danshen–Gegen (DG) decoction was used to demonstrate the QA procedure. An H9c2 cell assay was used to test the efficacy of consistent quality DG decoctions prepared by different herb combinations with different material costs of herbs. It was observed that a multiple‐herb‐extraction effect was present in the aqueous extraction of Danshensu and this effect was depended on the extraction solvent. The possible mechanism of this multiple‐herb‐extraction effect in the aqueous DG extraction was speculated to be the change of initial pH value of the aqueous extraction solvent by an unknown component from Gegen. The experimental chemical marker concentrations fell within ±10% of the specified chemical marker compositions by using the amount of herb from each herb class as predicted by the QA model. Furthermore, an H9c2 cell assay was used to test the efficacy of three consistent quality DG extracts, which were produced by different herb combinations with different material costs of herbs. The results showed that the three DG extracts provided consistent biological efficacy against menadione‐induced toxicity. This study extended a recently developed QA procedure of single‐herb extraction to multiple‐herb extraction. It provides a solution of QA in extraction, which is one of the most important unresolved problems in the modernization of traditional Chinese medicines. With this modified model and the companion experiments, the amount of herbs needed from different quality classes to produce a multiple‐herb formula CHM product decoction with consistent quality can be exactly determined. © 2014 American Institute of Chemical Engineers AIChE J 60: 4014–4026, 2014     

可编程器件为多种应用提供强大驱动力

几年前,超过半数的半导体消费均归功于企业用户,而如今,普通消费者已成为推动这一消费增长的主要推动力.从手机到电视,从计算机到汽车,普通消费者在半导体领域的需求占主导地位,市场竞争也比以往任何时候都更为激烈,成功与否取决于能否推出独树一帜的产品,而价格则是最重要的决定性因素.对系统制造商而言,这意味着必须展开激烈的市场"拼杀",而产品的生命周期则日益缩短.与此同时,市场细分进一步明显,过去的大规模市场被细分为更为狭窄的市场领域,只有提供具有各种不同特性、功能和地域特征的产品才能充分满足客户的特定需求.     

65nm半导体工艺发展策略

本文研究Altera在65nm工艺上的工程策略,介绍公司如何为客户降低生产和计划风险,并同时从根本上提高密度、性能,及降低成本和功耗.     

Polycyclic aromatic hydrocarbons (PAHs) in urban surface dust of Guangzhou, China: Status, sources and human health risk assessment

Ninety-six urban surface dust samples collected from Guangzhou, a typical urban center in South China, were analyzed for 16 PAHs (2-6 rings). ∑ PAHs concentrations in the urban surface dust ranged from 0.84 to 12.3 μg/g with a mean of 4.80 μg/g. High molecular weight compounds (4-6 rings) contributed to 62 to 94% of ∑ PAHs mass in the surface dust samples. Four hotspots with highest ∑ PAHs were identified via kriging prediction mapping, representing the highly-urbanized regions: central downtown, highway and industrial area. Two major origins of PAHs inputs to urban surface dust were identified as vehicle emissions (51.9%) and coal combustion (26.8%). The 95% UCL of Incremental Lifetime Cancer Risk (ILCR) due to human exposure to urban surface dust PAHs in central South China was 3.03 × 10⁻⁶ for children and 2.92 × 10⁻⁶ for adults.     

A Modification of schwarz's sequential likelihood ratio tests in multivariate sequential analysis

By developing and applying certain results on boundary crossing probabilities of generalized likelihood ratio statistics in multiparameter exponential families, we show that Lai's (1988a) modification of Schwarz's (1962) sequential likelihood ratio tests of one-sided hypotheses in the one-parameter case can be extended to general hypotheses in the multiparameter case. Such tests are shown to be asymptotically optimal, from both frequentist and Bayesian points of view, and numerical results are also given to demonstrate their performance.     

An Amphiphilic BODIPY‐Porphyrin Conjugate: Intense Two‐Photon Absorption and Rapid Cellular Uptake for Two‐Photon‐Induced Imaging and Photodynamic Therapy

The new amphiphilic BODPY‐porphyrin conjugate BZnPP and its precursor BZnPH were synthesised, and their linear and two‐photon photophysical properties, together with their cellular uptake and photo‐cytotoxicity, were studied. This amphiphilic conjugate consists of a hydrophobic BODIPY moiety and a hydrophilic tetra(ethylene glycol) chain bridging a cationic triphenylphosphonium group to an amphiphilic porphyrin ZnP through acetylide linkers at its meso positions. A large two‐photon absorption cross‐section (σ=1725 GM) and a high singlet oxygen quantum yield (0.52) were recorded. Intense linear‐ and two‐photon‐induced red emissions were also observed for both BZnPP and BZnPH. Further in vitro studies showed that BZnPP exhibited very efficient cellular uptake and strong photocytotoxic but weak dark cytotoxic properties towards human breast carcinoma MCF‐7 cells. In summary, the two‐photon‐induced emission and the potent photo‐cytotoxicity of BZnPP make it an efficacious dual‐purpose tumour‐imaging and photodynamic therapeutic agent in the tissue‐transparent spectral windows.     

Varying the wetting properties of polycarbonate substrate by varying the nanomolding temperature

Polycarbonate (PC) nanofibers were produced using anodized aluminum oxide (AAO) template assisted nanomolding. The effects of temperature on the nanoflow were investigated. It was found that higher temperature apparently enhanced the polycarbonate nanoflow and resulted in longer nanofibers in the same duration. The surface wettabilities of the polycarbonate nanofiber coated substrates showed apparent dependency on the morphology of the surface. It was found that larger honeycomb patterns would result in higher hydrophobicity than smaller honeycomb patterns. POLYM. ENG. SCI., 2012. © 2012 Society of Plastics Engineers     

Biofilm in the sediment phase of a sanitary gravity sewer

Microbial activity of the sediment phase in a 1.5-km-long concrete sewer section with a cement pipe in a 540-mm diameter was investigated in this paper. SEM examinations and elementary composition analyses of the sediment samples have identified the presence of a biofilm layer at the sediment surface. Bacterial counting results with a DNA-staining technique have revealed that the amount of bacteria in this layer was 2.1 x 10(11)cellg(-1) dry wt, which is close to that of activated sludge. ATP content in the sewer biofilm was found relatively high, demonstrating that the sewer biofilm is active. Throughout the entire 1.5-km sewer section, the biofilm activity was maintained at almost the same level. Lab-scale sediment oxygen uptake flux (SOUF) tests showed that the shear flow velocity above the sediment phase linearly increases the SOUF, which of the potential value was determined to be 32gO(2)m(-2) day(-1) at an estimated shear flow velocity of 0.055ms(-1) at 25 degrees C in the sewer line, provided that the mean flow velocity was 1.5ms(-1), and the mean water depth was 220mm. Such a high SOUF value further endorsed the existence of the active sewer biofilm.     

Kinetics of the multi-step catalytic degradation of a polymer to its constituent subunits

The stepwise catalytic degradation of a polymer to its constituent subunits results in many molecules of polymers of shorter chain length. Using the Law of Mass Action, ordinary differential equations for each species can be obtained from the set of elementary reactions and these can be integrated to obtain species concentrations as a function of time. A special case of catalytic degradation of polymers, in which one subunit is released at each step, is examined. A mathematical dissertation on the kinetics of the series of reactions involved is presented. The solution of the set of differential equations involve tedious computations and cannot be easily adapted to the analysis of experimental data. Two additional methods of analysis are described. The first one makes use of the property that for any intermediary polymer whose initial and final concentrations are zero, the integral of its concentration with respect to time is inversely proportional to the degradation rate constant. Stepwise calculation of the rate constants can thus be obtained by determining the area under the concentration-time trajectories while the degradation rate constant of the first polymer is known. The second method makes use of the property that the maximum concentration attained by any individual intermediary polymer is inversely proportional to its degradation constant. These methods have the advantage of being simple since the degradation constants can be obtained stepwise from experimental data.     

Mathematical modeling of ammonia-fed solid oxide fuel cells with different electrolytes

An electrochemical model was developed to study the ammonia (NH₃)-fed solid oxide fuel cells with proton-conducting electrolyte (SOFC-H) and oxygen ion-conducting electrolyte (SOFC-O). Different from previous thermodynamic analysis, the present study reveals that the actual performance of the NH₃-fed SOFC-H is considerably lower than the SOFC-O, mainly due to higher ohmic overpotential of the SOFC-H electrolyte. More analyses have been performed to study the separate overpotentials of the NH₃-fed SOFC-H and SOFC-O. Compared with the NH₃-fed SOFC-H, the SOFC-O has higher anode concentration overpotential and lower cathode concentration overpotential. The effects of temperature and electrode porosity on concentration overpotentials have also been studied in order to identify possible methods for improvement of SOFC performance. This study reveals that the use of different electrolytes not only causes different ion conduction characteristics at the electrolyte, but also significantly influences the concentration overpotentials at the electrodes. The model developed in this article can be extended to 2D and 3D models for further design optimization.