对中国药典诺氟沙星对照品在不同溶媒中的稳定性研究

目的：考察不同溶媒配制的诺氟沙星对照品溶液能否保存。方法：用紫外分光光度法分别对5℃放置的使用不同溶媒的对照品溶液在0d、10d、20d、30d、40d测定最大吸收波长、吸收值。结果；以0．4％NaOH溶液为溶媒的诺氟沙星对照液于5℃放置40d，最大吸收波长、吸收值均未发生变化（无显著性差异P＞0．05）。而以pH4.0醛酸缓冲液、pH7．4磷酸盐缓冲液为溶媒的两种对照液5℃放置40d，最大吸收波长未发生变化，但吸收值明显降低（有显著性差异P＜0．05）。结论：用0．4％NaOH溶液配制的诺氟沙星对照品溶液在适宜的条件下（5℃，避光密闭）保存，40d内是稳定的，可继续使用。而用pH4．0醋酸缓冲注和pH7．4磷酸盐缓冲液配制的诺氟沙星对照品溶液则不能保存使用，必须临用新配。     

血小板衍生性生长因子对低氧培养内皮细胞增殖的影响

目的　观察低氧条件下血小板衍生性生长因子 (PDGF)对于培养人脐静脉内皮细胞 (HUVEC)增殖的影响。方法　流式细胞仪分析细胞周期各时相分布 ,氚 -亮氨酸 (3 H -Leu)掺入实验评价蛋白质合成 ,免疫组织化学方法检测增殖细胞核抗原 (PCNA)水平。结果　低氧可显著减少S期及G2 /M期细胞数 ,使停留于G0 /G1 期HUVEC细胞数增加 ,降低HUVEC3 H -Leu的掺入量及PCHA水平。低浓度的PDGF(5ng/ml)对低氧条件培养的HUVEC细胞周期时相分布、3 H -Leu的掺入量及PCNA水平影响不明显 ;高浓度PDGF(1 0ng、2 0ng)加速HUVEC由G1 期S期的转换 ,显著增加低氧培养HUVEC3 H -Leu掺入量 ,PCNA水平 ,此作用呈剂量依赖性。结论　PDGF能够拮抗低氧所致的培养HUVEC增生能力的下降 ,但低浓度PDGF(5ng/ml)作用不显著 ,剂量越大 ,拮抗作用愈显著。     

小学生吸烟行为健康教育干预实验

本文报告了自１９９１年以来在四川省什邡县所进行的小学生吸烟行为健康教育干预实验。结果显示，实验达到了预期目的。根据基线调查资料对对象儿童吸烟行为影响因素所作的分析以及在此基础上所采取的干预策略是正确的，干预方法是有效的。从而证明了在一个成人吸烟占主流的社会环境中通过健康教育劝阻儿童吸烟尽管是很困难的，但却是完全有成功把握的。     

An Analysis of Chromosome on Sterility Caused by Azoospermia or Oligospermia

ＡｎＡｎａｌｙｓｉｓｏｆＣｈｒｏｍｏｓｏｍｅｏｎＳｔｅｒｉｌｉｔｙＣａｕｓｅｄｂｙＡｚｏｏｓｐｅｒｍｉａｏｒＯｌｉｇｏｓｐｅｒｍｉａ￥ＷｕＭｅｉｈｅｎｇ；ＴａｎｇＷｉｎｇｎｕｏ．（ＡＣＴＡＡＣＡＤＥＭＩＡＥＭＥＤＩＣＩＮＡＥＮＡＮＪＩＮＧ，１９９５（...     

~（99m）Tc－新半乳糖白蛋白体外受体介导结合特性的研究

本文报道￣９９ｍＴｃ－新半乳糖白蛋白（￣９９ｍＴｃ－ＮＧＡ）与大鼠肝细胞膜进行体外结合试验。结果表明：￣９９ｍＴｃ－ＮＧＡ系与肝细胞膜上的高亲和力低容量（Ｋ＿１：８．４０８９×１０￣９Ｌ／ｍｏｌ；Ｒ＿１：１．７３５０×１０￣（－１２）ｍｏｌ／ｍｇ）和低亲和力高容量（Ｋ＿２：２．０８２７×１０￣８Ｌ／ｍｏｌ；Ｒ＿２：６．９５３０×１０￣（－１２）ｍｏｌ／ｍｇ）２个结合位点相结合，其结合表现出高特异性、可饱和性及对细胞膜蛋白浓度的线性依赖性，具备受体介导结合的基本特征。￣（９９ｍ）Ｔｃ－ＮＧＡ是一个很有希望的肝受体显像剂。     

硫酸镍对红细胞毒性研究

健康小鼠腹腔注射硫酸镍10.0,5.0,2.5mg/kg,导致外周血中红细胞增高,血红蛋白不变或降低,红细胞中点彩红细胞和碱粒红细胞占有比值明显增高,网织红细胞含量升高、提示镍对外周血红细胞有毒性损害。     

Human autoantibodies to poly(adenosine diphosphate-ribose) polymerase.

The chromatin-bound enzyme poly(ADP-ribose) polymerase (ADPRP) is strongly stimulated by DNA with single- or double-stranded breaks, and transfers the ADP-ribose moiety of NAD to nuclear proteins. The activation of ADPRP is important for DNA repair and replication, and also has been postulated to play a role in the pathogenesis of lymphocyte dysfunction associated with chronic inflammatory diseases, and inborn errors of nucleoside metabolism. We have detected high titers of IgG autoantibodies to the ADPRP protein in six patients with rheumatic complaints. No other autoantibodies were detected in any of the six sera. The specificity of the anti-enzyme antibodies was established by (a) immunoprecipitation of ADPRP activity, (b) immunoprecipitation and immunoblotting of both the native 116-kD enzyme and its proteolytic digestion products. ADPRP was purified from human thymus and calf thymus. The autoantibodies reacted equivalently with both enzymes. The anti-ADPRP antibodies had a distinctive immunofluorescent pattern with HEp-2 cells, reacting intensely with nucleoli and metaphase chromosomes, and diffusely with the nucleus. Autoantibodies to ADPRP have not been described previously. The presence of a specific immune response against an enzyme that has been associated with various immunodeficiency syndromes raises intriguing possibilities concerning the relationship between DNA damage, immunodeficiency, and autoimmunity.     

Punch technique--an alternative approach to the repair of pierced earlobe deformities

The punch technique of repairing pierced earlobe deformities is a practical and simplified alternative to the usual method of repair. The procedure can easily be performed in any dermatology office since the instruments required are very basic. The technique is presented in a series of illustrations, and the results are cosmetically acceptable.     

Production and characterization of genetically engineered antibody molecules

Expression of antibody heavy- and light-chain genes by transfection permits the production of monoclonal antibodies with improved biological and antigen-binding properties. The immunoglobulin genes are placed in vectors containing a gene for encoding a protein that provides a biochemically selectable function in eukaryotic cells; these vectors are transfected into myeloma and hybridoma cells. Selection of drug-resistant cells permits the efficient isolation of the rare cells that express the transfected DNA. By placing heavy and light chains on plasmids with different selectable markers, one can deliver heavy- and light-chain genes simultaneously to the same cell. The transfected immunoglobulin genes are efficiently expressed and the proteins produced are a faithful mirror of the genes that were introduced. Using the standard techniques of genetic engineering and gene transfection, we can now produce antibodies of widely varying structures, including chimeric antibodies with segments derived from different species. These antibodies provide useful reagents to study structure-function relationships within the antibody molecule. Ultimately it will be possible to produce a new generation of antibody molecules with improved antigen-binding properties and effector functions.