Thermal investigation of PEG 4000 — oxazepam binary system

A thermal study using DSC and Hot Stage Microscopy (HSM) was carried out to investigate the interaction in solid state of the binary system PEG 4000 — oxazepam, and to establish their phase diagram. The eutectic composition, which melting occurs at lower temperature as compared with the pure components, has been determined. The results obtained by DSC and HSM have indicated that PEG 4000 — oxazepam mixtures displays no obvious incompatibilities, and that the system shows a typical eutectic behaviour. However because of the closeness of the melting of PEG 4000 to the eutectic temperature, it was difficult to determine precisely the eutectic composition and temperature on the basis of DSC measurements alone. The use of heats of fusion corresponding to physical mixtures allowed an estimation of the eutectic composition at 6% w/w oxazepam. Additional information of temperature (57.6C) and composition (5–10% w/w oxazepam) of the eutectic was obtained by HSM using the contact method. This low melting temperature in this range of compositions offers advantages in terms of drug stability and easy manufacture.     

浅谈存储区域网的管理

本文首先从存储管理的角度介绍了SAN的物理结构和逻辑结构，简要介绍了SAN存储管理的特点，详细分析了SAN存储管理的结构及其关键技术。     

全新可升级ATE保障未来三代器件需求

存储器制造商一直在寻找一种既能满足其生产和功能需求又能提供比一代器件寿命更长、投资价值更高的节约型ATE解决方案.     

Thermal Behavior of Paracetamol-Polymeric Excipients Mixtures

The thermal behavior of binary mixtures of paracetamol and a polymeric excipient (microcrystalline cellulose, hydroxypropylmethylcellulose and cross-linked poly(vinylpyrrolidone)) was investigated. The physical mixtures, ranging from 50 to 90% by mass of drug, were submitted to a heating-cooling-heating program in the 35–180°C temperature range. Solid-state analysis was performed by means of differential scanning calorimetry (DSC), hot stage microscopy (HSM), micro-Fourier transformed infrared spectroscopy (MFTIR), and scanning electron microscopy (SEM). The polymeric excipients were found to address in a reproducible manner the recrystallization of molten paracetamol within the binary mixture into Form II or Form III. The degree of crystallinity of paracetamol in the binary mixtures, evaluated from fusion enthalpies during the first and second heating scans, was influenced by the composition of the mixture, the nature of the excipient and the thermal history. In particular, DSC on mixtures with cross-linked poly(vinylpyrrolidone) and hydroxypropylmethylcellulose with drug contents below 65 and75%, respectively, evidenced the presence only of amorphous paracetamol after the cooling phase. Microcrystalline cellulose was very effective in directing the recrystallization of molten paracetamol as Form II. This revised version was published online in August 2006 with corrections to the Cover Date.     

Thermal and structural characterization of two polymorphs of the bronchodilator tulobuterol

Two polymorphs of the bronchodilator tulobuterol (2-chloro-α-[[(1,1-dimethylethyl)- amino]-methyl]benzenemethanol) with melting points differing by ~10 K were isolated and characterized by thermal analysis (HSM, TG, DSC), as well as powder and single crystal X-ray diffraction. Analysis of melting data for Forms 1 and 2 revealed a monotropic relationship, with ΔG ₀, the Gibbs free energy difference at the melting temperature of the lower melting form, less than 1 kJ mol^-1. This small difference is reconciled with known structural features in the crystals of the two forms. The hydrogen bonding capacity of the tulobuterol molecule is fully utilised in both polymorphs in forming a common trimeric unit via three strong O-H···N interactions. Consequently only weak intermolecular forces characterize the packing of the trimers in the monoclinic polymorph (Form 1, P2₁/n, Z =12) and the triclinic polymorph (Form 2, P(-1),Z =6). This revised version was published online in July 2006 with corrections to the Cover Date.     

Characterization of adsorption processes in analytical liquid–solid chromatography

This review discusses nonlinear chromatographic methods of importance for proper characterization of the adsorption processes in analytical chromatographic systems, with focus on reversed-phase liquid chromatography. Linear methods such as the linear solvation energy relationship (LSER) method and the Snyder–Dolan hydrophobic-subtraction model will also be reviewed briefly. The nonlinear methods for adsorption isotherm determination and the tools for further treatment of the nonlinear adsorption data will be extensively treated in a way suitable for the general chromatographer. Applications of the various methods will be given and the outcome and conclusions will be discussed. Special emphasis will be placed on discussing the possibilities of combining linear and nonlinear methods in order to obtain a deeper and more complete investigation of the interactions in the actual phase system.     

状态机在离子注入机中的应用

报告了在离子注入机控制软件建模时使用状态机的原因,以及控制软件的结构、状态机的层次结构和由状态机自动生成代码的方法,并介绍了应用状态机设计开发的离子注入机控制软件的优点。     

Thermal studies of solvent exchange in isostructural solvates of a tetroxoprim-sulfametrole complex

Isostructural solvates of the 1:1 molecular complex between the antibacterial drugs tetroxoprim (TXP) and sulfametrole (SMTR) with formulae TXP·SMTR·CH₃OH (I), TXP·SMTR·C₂H₅OH (II) and TXP·SMTR·H₂O (III), were investigated to establish their propensity for guest exchange. Separate exposure of powdered (I), (II) and (III) to a saturated atmosphere of each solvent of the complementary solvate pair at ambient temperature resulted in reversible solvent exchange in all cases. DSC and TG were the methods of choice for monitoring the exchange processes since (I)-(III) have distinct onset temperatures of desolvation and characteristic mass losses. Interpretation of the results in terms of the known locations of the solvent molecules in crystals of (I)-(III) led to the conclusion that solvent exchange probably proceeds by a co-operative mechanism involving material transport through channels while the common host framework is maintained. This revised version was published online in July 2006 with corrections to the Cover Date.     

18-crown-6 ether complexes with aralkylammonium perchlorates

Thermochemical properties of crown ether complexes have been studied by simultaneous TG-DTA (thermogravimetric analysis-differential thermal analysis) coupled with a mass spectrometer, DSC (differential scanning calorimetry) and hot stage microscopy (HSM). The examined complexes contain benzylammonium- [BA], (R)-(+)-a-phenylethylammonium- [(R)-PEA], (R)-(+)- and (S)-(-)-a-(1-naphthyl)ethylammonium perchlorate [(R)-NEA and (S)-NEA] salts as guests. In the cases of BA and (R)-PEA an achiral pyridono-18-crown-6 ligand [P18C6], and in the case of (R)-NEA and (S)-NEA a chiral (R,R)-dimethylphenazino-18-crown-6 ligand [(R,R)-DMPh18C6] was used as host molecule to obtain four different crown ether complexes. In all cases, the melting points of the complexes were higher than those of both the host and the guest compounds. The decomposition of the complexes begins immediately after their melting is completed, while the BA and (R)-PEA salts and the crown ether ligands are thermally stable by 50 to 100 K above their melting points. During the decomposition of the salts and the four complexes strongly exothermic processes can be observed which are due to oxidative reactions of the perchlorate anion. Ammonium perchlorate crystals were identified among the decomposition residues of the salts. P18C6 was observed to crystallize with two molecules of water. The studied complexes of P18C6 did not contain any solvate. BA was observed to exhibit a reversible solid-solid phase transition upon heating. The heterochiral complex consisting of (S)-NEA and (R,R)-DMPh18C6 shows a solid-solid phase transition followed by two melting points. HSM observations identified three crystal modifications, two of them simultaneously co-existing. This revised version was published online in July 2006 with corrections to the Cover Date.     

The use of hot‐stage microscopy and thermal micro‐Raman spectroscopy in the study of phase transformation of metoclopramide HCl monohydrate

The aim of this work was to investigate the transformation behavior of metoclopramide HCl with monohydrate (MCP HCl H₂O) using differential scanning calorimetry (DSC), thermogravimetric analysis, hot‐stage microscopy (HSM), and thermal micro‐Raman spectroscopy. The results of the present study indicate that the three‐step phase transformation of MCP HCl H₂O was clearly determined via the thermal‐dependant Raman spectral changes. These three steps of phase transformation were dehydration, recrystallization, and new crystal formation, which were markedly correlated with the endothermic and exothermic results of DSC study and the observations of HSM. The results generally evidence that MCP HCl H₂O crystals were first dehydrated to form an anhydrous sample, then recrystallized and transformed to a new crystal form of MCP HCl. Copyright © 2011 John Wiley & Sons, Ltd.