微透析-毛细管电泳联用研究盐酸雷尼替丁在家兔血液中的代谢过程

将毛细管区带电泳(CZE)与微透析采样技术联用,研究了盐酸雷尼替丁在家兔血液中的代谢过程.首先研究了毛细管电泳的pH值、缓冲液浓度、分离电压、进样时间等电泳条件对盐酸雷尼替丁与法莫替丁分离的影响.结果采用pH6.2磷酸缓冲液,分离电压为10kV,进样压力2758Pa,4s的条件,能够使盐酸雷尼替丁与法莫替丁达到基线分离,据此以法莫替丁为内标建立了一种测定盐酸雷尼替丁的方法,峰面积比与相应的盐酸雷尼替丁浓度在1.5×10-7g·mL-1～8.0×10-6g·mL-1范围内成线性关系(r=0.998),最低检测限9.0×10-8g·mL-1.药物代谢动力学参数由“NDST21”计算软件求得,代谢符合一室开放模型,其半衰期为89.8min.     

龟鳖类血细胞研究的进展

文章概述了龟鳖类血细胞——红细胞、有粒细胞(包括嗜酸性粒细胞、嗜喊性粒细胞、嗜天青粒细胞和嗜中性粒细胞)、淋巴细胞、单核细胞、血栓细胞的特性,显微和超微结构特点,血细胞发生及功能等方面的研究进展.     

铝电解槽焙烧用矩形高速燃烧器的研制

铝电解槽的焙烧对槽的正常生产和以后的槽寿命有着直接影响，燃料焙烧法具有加热均匀、升温速度容易控制、对扎缝和边部扎固糊的焙烧充分等优点，是一种非常有前途的新焙烧方法。而燃烧器的设计是燃料焙烧法的关键技术之一，在实验的基础上开发出一种矩形高速燃烧器，并对该燃烧器的结构进行了优化，研制的矩形顺具有点火容易、燃烧稳定、负荷调节比大燃烧完全度高、噪音低等特点，能完全满足铝电解槽燃料焙烧方法的要求，它的研制成功为铝电解槽焙烧新技术的应用提供了技术保证。     

Inhibitory effect of the adenovirus type 5 E1A protein expressed in the yeast system

The human adenovirus type 5 E1A, a tumor- suppressor gene[1], codes for two major related proteins of 243 amino acids (12S) and 289 amino acids (13S) by al-ternative splicing in two exons[2]. Studies have been shown that E1A can regulate expression of many genes and cell cycle[3]. Both in vitro and in vivo experiments indicated that E1A could induce tumor cells differentia-tion, convert tumor cells into an epithelial phenotype, in-hibit tumor cell growth and metastasis and strongly en-ha…     

Building of hFⅨ transgenic mice by spermatogenic cells

Human FⅨ expression vector pCMVⅨ was packaged by effectene^TM reagent and injected into mice seminiferous tubules with glass pipettes.The expressional frame of pCMVⅨ was examined by PCR and Southern blotting among 41 progenies.There were 2(4%) mice being integrated with hFⅨ gene into chromosomes.4.6ng/mL of hFⅨ protein was expressed in plasma of one mouse,which was tested by ELISA.We demonstrated that building of transgenic animals by spermatogonial stem cells is an efficient method.Meanwhile,it has also been proved to be an alternative choice for mammary gland bioreactor.     

Inhibitory effect of the adenovirus type 5 E1A protein expressed in the yeast system of the human tumor cell growth

Adenovirus 5 type E1A as a tumor suppressor gene can inhibit tumor growth and enhance the censitivity of chemotherapy and radiotherapy.E1A have the ability to integrate into the host genome,resulting in long-time expres-sion that induces Rb gene inactivation and animal cells im-mortalization.This prompted us to select the E1A protein for treatment of cancer in order to overcome the limitations of E1A gene therapy.Thus,we firstly comstructed E1A eu-caryotic expression vector (pPIC9/E1A),transformated the pichia pastoris yeast cells(GS115) and screened the high-expressing recombinant strains.The positive yeast strains were cultured in the shake flask,and induced for 3d.The crude E1A protein was purified using two steps of col-umu chromatography on HiTrap Q and HiTrap SP.The pu-rified E1A protein was identified by SDS-PAGE and Western blot.E1A protein was mostly located at cellular unclear when Cheriot delivered E1A protein into cells.The analysis in vitro indicated that the E1A protein arrested LN686 cell cycle at G2/M phase,and significantly inhibited the growth of LN686 tumor cells.The current studies firstly provided an experimental basis to further develop E1A protein for tumor treatment.     

废旧锌锰电池的回收利用

分析了我国废旧电池的回收利用现状。阐述了废旧电池对生态环境造成的危害和回收利用废旧电池的重大意义。介绍了回收利用废旧锌锰电池的工艺流程和实验原理。在现有的实验条件下,初步研究了利用废旧锌锰电池制备高锰酸钾、氯化锌、氯化铵等物质的实验方法;分析讨论了制备高锰酸钾的各种影响因素,如反应物的量、反应温度等。     

同源重组在染色体DNA基因克隆中的应用方法

同源重组是生物界普遍存在的现象，从噬菌体、细菌到真核生物都有能发生同源重组的种类。如何把同源重组应用到基因克隆中成为近年来生物学家研究的热点。本文从宿主细胞的改造、重组功能的诱导、感受态细胞的制备、线性同源载体的获得及重组体的鉴定等几个方面具体叙述这种基因克隆的新方法，从分子水平上较为详尽地介绍了同源重组在染色体基因克隆中的应用、前景展望及存在的局限性。     

超声喷雾热分解法制备电极材料LiCoO2薄膜

以硝酸锂和乙酸钴为原料,玻璃为基片,通过超声喷雾热分解法制备了锂钴氧化物薄膜,并讨论了制备条件对形成薄膜如Li与Co摩尔比对薄膜晶型、不同溶剂对雾化效果、热分解温度对产物晶型和薄膜外观、反应时间对膜厚等的影响,经X-射线衍射分析和电镜测试,给出了制备较好晶型结构LiCoO2薄膜的条件.     

人正常子宫内膜树突状细胞的周期性变化

目的：研究人正常子宫内膜上树突状细胞(dendritic cell，DC)的分布特点。方法：对10例人正常子宫内膜组织应用HLA-DR单克隆抗体和CD1a蛋白抗体进行免疫组化染色，其中增殖期内膜4例、分泌期内膜3例、绝经期内膜3例，观察其中的阳性细胞。结果：10例正常子宫内膜标本中，5例呈HLA-DR阳性表达(增殖期4例，分泌期1例，绝经期0例)；4例呈CD1a阳性表达(增殖期3例，分泌期1例，绝经期0例)。结论：人正常子宫内膜组织中存在表达主要组织相容性复合体-Ⅱ(MHC-Ⅱ)类分子的DC，各时期的子宫内膜DC检出率不同。