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91.
戴素杰 《辽宁化工》2006,35(4):236-237
对气流干燥的原理、装置、特点以及广泛应用进行了概括论述。通过对干燥器设计计算的论证,证明了具有广泛的现实意义及推广价值。  相似文献   
92.
导湿快干系列纤维和纱线的研制开发现状   总被引:1,自引:0,他引:1  
文章介绍了国内外导湿快干系列纤维和纱线的研制开发现状,以及导湿快干纤维种类、导湿快干机理-毛细管效应、以及纺丝方法、应用范围等。  相似文献   
93.
Drying of sewage sludge is an effective way for treatment and utilization of sewage sludge,where reduction of energy consumption is one of the major technical challenges.So we experimentally investigated the possibility of the hydrothermal treatment.We have found that treatment of sewage sludge by saturated steam with the temperature of 190°C and pressure of 20 bar can dramatically improve the dehydration performance of the slurry like product.And the water content can be reduced down to about 55% by a mech...  相似文献   
94.
Although curcumin is considered to have various therapeutic effects, its use as a functional food or supplement is restricted owing to its low water solubility and bioavailability. To increase the solubility of curcumin in water, the use of polyvinylpyrrolidone (PVP) and vinylpyrrolidone-vinyl acetate copolymers with a pyrrolidone skeleton was noted to be promising. In particular, the bi-component formulations of curcumin/PVP prepared through spray drying exhibited an amorphous state in powder X-ray diffraction observations and temporally increased the apparent solubility of curcumin to over 5000 times that of untreated curcumin; nevertheless, after 24 h, the solubility decreased owing to the unstable supersaturated state of curcumin. The addition of α-cyclodextrin (α-CyD) in the bi-component curcumin/PVP formulation helped maintain the supersaturated state of curcumin, whereas the addition of β- and γ-CyD led to the collapse of the supersaturated state. The addition of α-CyD can likely help inhibit the nucleation and crystal growth of curcumin, through the interaction among the solubilized units of curcumin/PVP and α-CyD.  相似文献   
95.
Context: The clinical applications of cilostazol (CLZ) are limited by its low aqueous solubility (<5?µg/ml) and high biovariability.

Objective: The aim of this study was to enhance the solubility of CLZ by forming inclusion complexes (ICs) with beta cyclodextrin (β-CD) and formulating them into oral disintegrating tablets.

Methods: Phase solubility study of CLZ with β-CD was performed in water. Job’s plot was constructed to determine the stoichiometry of ICs. ICs, prepared by spray-drying technique, were characterized using Fourier transform infrared spectroscopy, differential scanning calorimetry, hot stage microscopy, powder X-ray diffraction and nuclear magnetic resonance. Molecular modeling studies were performed to understand the mode of interaction of CLZ with β-CD. The formulation process was undertaken using a reproducible design of experiment generated model, attained by variation of diluents and disintegrants at three levels. Tablets were evaluated for drug content, hardness, friability, disintegration time (DT), wetting time (WT) and dissolution profiles.

Results and discussion: Phase solubility studies suggested an AL type curve with stability constant (Ks) of 922.52?M?1. Job’s plot revealed 1:2 stoichiometry. All analytical techniques confirmed inclusion complexation. Molecular modeling revealed dispersive van der Waals interaction energy as a major contributor for stabilization of complex. The spray-dried complexes showed higher solubility and faster dissolution compared to plain CLZ. The optimized formulation showed DT of 11.1?±?0.8?s, WT of 8.7?±?0.9?s and almost complete dissolution of CLZ in 15?min.

Conclusion: The prepared tablets with low DT and fast dissolution will prove to be a promising drug delivery system with improved bioavailability and better patient compliance.  相似文献   
96.
Bioavailability of a poorly soluble drug can be improved by preparing a drug nanosuspension and subsequently drying it into nanocomposite microparticles (NCMPs). Unfortunately, drug nanoparticles aggregate during milling and drying, causing incomplete recovery and slow dissolution. The aim of this study is to investigate the impact of various classes of dispersants on drug dissolution from drug NCMPs, with the ultimate goal of enhancing the bioavailability of poorly water-soluble drugs via high drug nanoparticle loaded, surfactant-free NCMPs. Precursor suspensions of griseofulvin (GF, model drug) nanoparticles in the presence of various dispersants were prepared via wet stirred media milling and spray dried to form the NCMPs. Hydroxypropyl cellulose (HPC, polymer) alone and with sodium dodecyl sulfate (SDS, surfactant) was used as a base-line stabilizer/dispersant during milling. Two swellable crosslinked polymers, croscarmellose sodium (CCS) and sodium starch glycolate (SSG), and a conventional soluble matrix former, Mannitol, were used in addition to HPC. Besides being used as-received, CCS was also wet co-milled with GF for two different durations to examine the impact of CCS particle size. Laser diffraction, scanning electron microscopy, powder X-ray diffraction (XRD), UV spectroscopy, NCMP redispersion and dissolution tests were used for characterization. The results show that incorporation of CCS/SSG, preferably wet-milled to a wide particle size distribution, into the spray-dried NCMPs resulted in fast release and dispersion of drug nanoparticle clusters. The swellable dispersants were superior to Mannitol in dissolution enhancement, and could achieve fast release comparable to SDS, demonstrating the feasibility of spray drying to prepare high drug-loaded, surfactant-free nanocomposites.  相似文献   
97.
加入HDPE-g-MAH、CG-8831和KH-550制备HDPE/木粉改性复合材料。研究其长效吸水性,发现吸水率随时间延长先快速增加,浸水35 d后缓慢增至平衡,HDPE-g-MAH改性效果最好,其饱和吸水率仅为1.503%。利用Fick第二扩散定律拟合吸水动力学曲线,得扩散系数D的顺序:HDPE-g-MAH增容HDPE/木粉复合材料HDPE/木粉复合材料KH-550改性HDPE/木粉复合材料CG-8831改性HDPE/木粉复合材料。并证明该吸水过程符合Fick第二扩散定律,相关系数R2值达0.99以上。HDPE/木粉改性复合材料尺寸变化系数CDCWCT。  相似文献   
98.
99.
根据修补区混凝土可开放交通的要求,优选出全再生快速修补混凝土最优配合比,并与常用的再生粗骨料快速修补混凝土进行比较.结果表明,全再生快速修补混凝土的抗压强度和粘结强度较易满足要求;其最优化配合比参数为:胶凝材料总量为500 kg/m3,再生细骨料在细骨料中掺量为30%,而其砂率为35%;其干燥收缩略大于常用的再生粗骨料快速修补混凝土,但显著提高了其抗氯离子渗透性能.  相似文献   
100.
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