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碱性液

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Materials and methods: The composite was respectively prepared by blending Lysine, Histidine, Arginine with PLGA, while the composite respectively prepared by blending Algin, chitosan, NaHCO3 with PLGA as the comparison and the pure PLGA as the control. All composites were degradated in tri-distilled-water at 37℃ for 7 weeks. The degradation property of PLGA with the addition of basic additives was investigated by using gross observation, the pH change of degradation solution and the mass loss ration of the composite.

材料方法:将赖氨酸、组氨酸、精氨酸分别各按5%和10%的比例与PLGA制成复合物,于体外在37℃下在三蒸水中进行降解2个月;通过总体观察、降解液PH的变化、复合物的失重率等指标来考察碱性氨基酸对PLGA体外降解特性的调节作用,同时将碱性氨基酸的调节效果与海藻酸钠、壳聚糖、碳酸氢钠的进行对比。

Results We found GM1 antibody in 36% and cephalin antibody in 43% of MS patients in serum,GM1 antibody in 11% and cephalin antibody 18% in cerebrospinal fluid.The levels of antibody in serum of treated_MS patients were significantly lower than those in active MS patients.The levels of myelin basic protein in serum and cerebrospinal fluid in MS were significantly higher than those in control group.

结果 多发性硬化患者血清GM1抗体阳性率 36%,脑磷脂抗体为43%;脑脊液GM1抗体为11%,脑磷脂抗体为18%,与对照组比较差异均有显著性;血清和脑脊液的髓鞘碱性蛋白增高亦有意义。

Results We found GM1 antibody in 36%and cephalin antibody in 43%of MS patients in serum,GM1 antibody in 11%and cephalin antibody 18%in cerebrospinal fluid.The levels of antibody in serum of treated_MS patients were significantly lower than those in active MS patients.

结果 多发性硬化患者血清GM1抗体阳性率为36%,脑磷脂抗体为43%;脑脊液GM1抗体为11%,脑磷脂抗体为18%,与对照组比较差异均有显著性;血清和脑脊液的髓鞘碱性蛋白增高亦有意义。

By n-butanol extraction, ammonium sulfate fractionation and sodium chloride dialyzation, the partially purified enzyme was gained by means of gel filtration on sephadex G-150 column, and some properties of the enzyme were determined.

方法]以DFRKN-1为提酶材料,经正丁醇提取,硫酸按分级沉淀分离,透析获得酶的粗提取液,用SephadexG-150凝胶过滤柱层析纯化,获得纯化碱性磷酸酶,并测定纯化碱性磷酸酶的理化性质。

In general, the chrome-included solution with the rain shows alkalescent, so it shows significant practical value to electrolyze and reduct Cr6+ in alkalescent media directly to dispose the extraction of chromium residues to disposal the chromium waste pollutant.

一般情况下,雨水淋淅出的含铬液体呈弱碱性,因此,直接在弱碱性介质中采用电解还原Cr~(6+)来处理铬渣浸出液,以治理铬渣污染具有实际意义。

Photopolymerization-CTP plate is used in developering, and alkalescence of the photoptic layer of resin and monosomic or oligmer, with a certain amount of acid in alkaline solution can be dissolved in the treatment of development by 4(18) and alkalescence developering, which is beneficial to the environment.

平撮合型CTP版材拔取的显影液是碱性的,而感平层洋的不败膜树脂及单体或齐聚物具有必定的硷性,可以凝固于碱液洋不纬显影裁撤,且碱性显影液浑浊小,有利于环保。

Basic drugs, lidocaine, benghexolum, chlorpromazine, diazepam, clozapine, internal standard of SKF525A(all of 5μg), estazdam and alprazolam (all of 10μg), are extracted from superfatted necrogenic tissues with mixture reagents of ethyl acetate and diethyl ether under basic condition, and determined by gas chromatography with nitrogenphosphorus detector.

在高度腐败及脂肪较多的脏器中加入碱性药物利多卡因、安坦、氯丙嗪、安定、氯氮平及内标物SKF_525A各5.0μg,舒乐安定、佳静安定各10.0μg,在碱性条件下用乙酸乙酯与乙醚混合液提取,经GC/NPD分析。

The samples of decalcified bone matrix, composite material and recombinant human bone morphogenetic protein 2 were respectively co-incubated with C2C12 cells for 72 hours.

细胞裂解后用比色法分别检测裂解液中成骨细胞特异性标记物碱性磷酸酶及总蛋白的吸光度值,以两者的比值表示单位数量的C2C12细胞所含有的碱性磷酸酶含量,以此衡量待测生物材料成骨活性的高低。

NOVELTY - Alkali chemicals are added to the cyanogen group gold-containing liquid, to obtain an alkaline liquid. Zinc is added to the alkaline liquid, and the formed deposit is dissolved in aqua regia. A reducing agent is added to the deposit solution and a deposit is produced. Gold is then separated by heat-processing the deposit.

本发明的新颖性在于:将碱性化学物质添加到氰化含金液中,以获取碱液;将锌加入到碱液中,并将形成的沉积物溶解到王水中;然后在沉积溶液中加入一种还原剂,形成新的沉积物;最后通过加热处理沉积物来分离金。

Following successful modeling, rats of bFGF group were intratracheally injected with 400 U bFGF and rats of VEGF group with 2 μg VEGF, once a week for three times. MSCs group was injected 1 mL suspension of 4×109/L MSCs into tail vein. MSCs+VEGF group was injected MSCs into tail vein and intratracheally injected VEGF (2 ug, three times) at the same time. Model control and normal control groups were intratracheally injected with equal volume of sodium chloride.

成功造模后,碱性成纤维细胞生长因子组气管内注入400 U碱性成纤维细胞生长因子,血管内皮生长因子组气管内注入2 μg血管内皮生长因子,1次/周,共3次;单纯细胞移植组于尾静脉注入4×109 L-1骨髓间充质干细胞悬液1 mL;血管内皮生长因子+细胞移植组气管内注入血管内皮生长因子的同时,尾静脉注入骨髓间充质干细胞;模型对照组、正常对照组给予相同体积的生理盐水。

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