甜菜颗粒干粕与甜菜渣提取果胶的比较研究

分别以甜菜颗粒干粕和甜菜渣为原料，采用酸法萃取，乙醇沉淀工艺提取果胶。在相同的条件下，甜菜颗粒干粕的果胶产量比甜菜渣的果胶产量高２８．７％～４２．８％，甜菜颗粒干粕提取果胶的最高产量比甜菜渣提取果胶的最高产量高２３％，产品的各项质量指标均与甜菜渣提取的果胶相近。甜菜颗粒干粕提取果胶的最佳萃取条件为：ｐＨ１．５、温度８０％℃、时间６ｈ，较甜菜渣提取果胶的最佳萃取条件（ｐＨ１．５、温度８５℃、时间６～８ｈ［１］）温和，而且产品色泽明显好于甜菜渣提取的果胶。

柑桔皮果胶的提取条件研究

以柑桔皮为原料，采用酸法萃取、乙醇沉淀工艺提取果酸。最佳条件为水料比１０：１，ｐＨ值１．５，萃取温度８５℃，萃取时间９０ｍｉｎ。果胶质量达到食用果胶的国家标准。

Preparation and in Vitro Evaluation of Polylactic Acid (PLA) or Polylactic-co-Glycolic Acid (PLGA) Microcapsules Loaded with Estradiol

Aim PLA/PLGA was used as biodegradable and biocompatible carriers to achieve sustained release of estradiol (E 2). Methods Microcapsules (MC) were prepared by an emulsification solvent extraction method, and then the properties and in vitro drug release behavior of MC were examined. An analysis of variance (ANOVA) was used to test the statistical significance. Then, multiple comparisons were made with a T method between levels to examine the significance of difference further. For all the results a P value 】0 05 was considered statistically insignificant . Results Under the same conditions, the water adding speed and the particle size had significant effects ( P 【0 01) on the entrapment efficiency of MC; the water adding speed and the concentration of PLA in the oil phase had significant effects ( P 【0 01) on the diameter MC in medium. Release of E 2 from MC was influenced significantly ( P 【0 01) by the water adding speed and the type and molecule weight of the polymers. But the differences between levels of the variates were not all significant. Conclusion E 2 PLA/PLGA MC with various properties can be formed when the formulation and the technology were changed accordingly.

Optimization of acidic extraction of astaxanthin from Phaffia rhodozyma

Optimization of a process for extracting astaxanthin from Phaffia rhodozyma by acidic method was investigated, regarding several extraction factors such as acids, organic solvents, temperature and time. Fractional factorial design, central composite design and response surface methodology were used to derive a statistically optimal model, which corresponded to the following optimal condition： concentration of lactic acid at 5.55 mol/L, ratio of ethanol to yeast dry weight at 20.25 ml/g, temperature for cell-disruption at 30 ℃, and extraction time for 3 min. Under this condition, astaxanthin and the total carotenoids could be extracted in amounts of 1294.7 μg/g and 1516.0 μg/g, respectively. This acidic method has advantages such as high extraction efficiency, low chemical toxicity and no special requirement of instruments. Therefore, it might be a more feasible and practical method for industrial practice.

Kinetics of Forward Extraction of Boric Acid from Salt Lake Brine by2-Ethyl-1,3-hexanediol in Toluene Using Single Drop Technique

The kinetics of forward extraction of boric acid from salt lake brine by 2-ethyl-1,3-hexanediol in toluene was investigated using the single drop technique. The factors affecting the extraction rate include interfacial area between aqueous phase and organic phase, initial concentration of boric acid in aqueous phase, initial concentration of 2-ethyl-1,3-hexanediol in organic phase, and extraction temperature. The experimental results show that the extraction rate increases with the increase of the initial concentration of boric acid and2-ethyl-1,3-hexanediol, interfacial area of two phases, and temperature. With the temperature-dependence study, it is showed that the extraction is a diffusion-controlled process. The kinetic equation is presented for pH 1.0 in the aqueous phase and temperature of 318 K.

Separation and purification of tantalum from plumbomicrolite of amazonite deposit in Kola Peninsula by acid leaching and solvent extraction

A plumbomicrolite concentrate(PMC)was leached with the mixture of HF and H2SO4,HF and HNO3 acids,respectively.Optimal conditions ensuring high recovery of tantalum and niobium(up to 99%)into solution,and radionuclides into insoluble residue were determined.Fluoride-sulfuric acid and fluoride-nitric acid schemes were proposed for PMC leaching by an extractive separation of tantalum form niobium,lead and impurities,and production of high-purity tantalum compounds.Octanol-1 was used as an extractant.Optimal conditions for production of high-purity tantalum strip solutions were defined for all stages(extraction-scrubbing-stripping).Produced tantalum compounds,such as tantalum pentoxide and potassium heptafluotanthalate,comply with the norms for high-purity substances in terms of impurities content.Final choice of the PMC processing scheme is determined by its profitability.

Solvent extraction of zinc from zinc sulfate solution

The extraction of zinc from zinc sulfate solution was investigated, using 20% saponified D2EHPA as an extractam and 260^# sulfonate kerosene as a diluent. The solution was stirred for 8 min at phase ratio （Vσ/Va） of 1.0：1.0, initial pH of 2.0 and stirring speed of 200 r/min. The results show that 75% zinc can be extracted from the zinc sulfate solution when the concentration of zinc is 18.7 g/L after being settled for 10 min. 88.60% zinc can be stripped by 196 g/L sulfuric acid, and zinc ion can be separated from ferric ion.

Preparation of PLA or PLGA Microspheres with Estradiol the Effects of THF—adding on the Properties of MS

Aim Polylactic acid (PLA) or polylactide-co-glycolide (PLGA) was used asbiodegradable and biocom-patible carriers to achieve sustained release ofestradial-PLGA/PLA-Microspheres (E_2-PLGA/PLA-MS). THF was added in the organic phase to study itseffects on the properties of MS. Methods MS were formed by an emulsification-solvent extractionmethod with mixture of ethyl acetate (EtoAc) and tetrahydrofuran (THF) as the organic solvents, andthen the properties and in vitro drug release behavior were examined. Results The results indicatedthat the drug loading efficiency decreased when THF added, but when the ratio of EtoAc was more than50% , there was no obvious effect of THF ratio, but the particle size increased accordingly. Thecarriers' properties and the drug contents were the main factors influencing the in vitro drugrelease. Conclusions By controlling the technology and formulation, we can get sustained-release E_2biodegradable microsperes with proper particle size, drug content and low burst-release, althoughTHF with readily solubility in water was used in the organic phase.

Determination of chlorogenic acid in traditional Chinese prescription Shuanghuanglian capsule using quantitative nuclear magnetic resonance spectroscopy in combination with solid phase extraction

The determination method of chlorogenic acid in traditional Chinese prescription Shuanghuanglian capsule was established by using quantitative nuclear magnetic resonance spectroscopy(q NMR) in combination with solid phase extraction(SPE). As the capsule’s main active component, chlorogenic acid comes from the extraction of Chinese herb medicine Flos Lonicerae. The chlorogenic acid in capsule was ultrasonically extracted at room temperature using pure water as solvent. The extracting solution was enriched and cleaned using HC-C18 SPE cartridge. The effect of ultrasonic extraction, sample pretreatment conditions via SPE and q NMR experimental conditions were investigated. The q NMR experiment conditions were selected using deuterated DMSO as solvent, calibrated 1,4-phthalaldehyde as internal standard, and P1(pulse width) = 14.4 μs, d1(pulse delay time) = 1 s, NS(number of scan) = 512. The 1 H NMR peaks of δ 6.138–6.182(H-8’, d, 1 H) of chlorogenic acid was chosen as the quantitative peaks. Method validation was performed, including precision(the intra-day RSD = 1.2% and the inter-day RSD = 1.5%), linearity(correlation coefficient r>0.9999), LOD(0.0017 mg/g) and LOQ(0.079 mg/g). The recovery of the SPE-q NMR was within the range of 100.2%–103.2%. The result showed that the method was stable, accurate and reliabile. Determined by the method, the chlorogenic acid in a real Shuanghuanglian capsule was within the range of 9.68–10.35 mg/g.