鼻咽癌常规放疗靶体积合理性的初步探讨

目的分析鼻咽癌常规放疗的局部控制情况和局部复发的剂量学模式,初步探讨照射靶体积确定的合理性.方法共476例初治鼻咽癌患者接受规范化单纯常规根治性放疗.全部病例均采用常规模拟定位,鼻咽靶体积为CT检查所见的原发病灶范围以及可能侵犯的亚临床病灶区域.利用Kaplan-Meier方法计算局部累积复发率;将鼻咽局部复发患者疗前和复发时局部病灶范围（Vnx和Vrecur）勾画于三维治疗计划系统,复制首程放疗的射野并按原处方剂量进行计算,根据剂量体积直方图进行剂量学评价：recurV95（95%处方剂量曲线包括的Vrecur）≥95%定义为野内复发,95%＞recurV95≥20%定义为野边缘复发,20%＞recurV95定义为野外复发.结果局部复发共52例,全组1、2、3、4年局部累积复发率分别为0.6%、3.9%、8.7%、11.5%.对42例局部复发的剂量学分析显示野内复发占多数（52%）,而大部分野边缘复发和全部野外复发均与射野设置不当、影像学阅片能力欠缺使首程放疗剂量不足有关.结论较好的局部控制率、复发的剂量学模式的分析结果提示该靶体积的设置比较合理.提高影像阅片能力,准确的射野设计,充分利用生物影像学工具,有针对性地提高照射剂量,有望进一步提高局部控制率.     

Influence of Preparation Factors on the Sustained Release of Nifedipine from Eudragit RL/RS Microspheres

用乳剂—溶剂挥发法制备硝苯地平的丙烯酸树脂缓释微球。微球中药物的释放速度随丙烯酸树脂ＥｕｄｒａｇｉｔＲＬ／ＲＳ比率的增加以及制备时搅拌速率的增加而增大，随内相聚合物浓度的增加及微球粒径的增加而减小，释药５０％所需时间与微球粒径呈良好线性。微球的释药速率也随药物含量的增加（从４．２％到１６．７％）而增大，并快于药物结晶的溶解速率，但药物含量达２６．６％时，微球释药速率明显下降并低于药物结晶的溶解速率。用差热分析和Ｘ射线衍射分析证明，药物含量为４．２，９．４和１６．７％的微球中药物完全是以非晶态分散的，而含药２６．６％的微球中有药物结晶存在。不同微球释药低于７０％时，释放方式均符合Ｈｉｇｕｃｈｉ时间平方根方程。     

Imaging findings of the developing temporal bone in fetal specimens.

PURPOSETo trace the development of the normal fetal temporal bone by means of plain radiography, MR, and CT.METHODSEighteen formalin-fixed fetal specimens, 13.5 to 24.4 weeks'' gestational age, were examined with a mammographic plain film technique, CT, and MR imaging at 1.5 T. Temporal bone development and ossification were assessed.RESULTSThe membranous labyrinth grows with amazing rapidity and attains adult size by the middle of the gestation period. The cochlea, vestibule, and semicircular canals are very prominent and easily recognized on MR images. The otic capsule develops from a cartilage model. Ossification of the otic capsule proceeds rapidly between 18 and 24 weeks from multiple ossification centers that replace the cartilaginous framework. The mastoid, internal auditory canal, vestibular aqueduct, and external auditory canal continue to grow after birth.CONCLUSIONThe study of fetal developmental anatomy may lead to a better understanding of congenital disorders of the ear. Faster MR scanning techniques may provide a method for in utero evaluation of the fetal temporal bone.     

高效液相色谱-荧光检测法测定血浆总同型半胱氨酸浓度

目的 :建立测定血浆总同型半胱氨酸的高效液相色谱 (HPLC) 荧光检测分析方法。方法 :用TCEP将血浆中各种形式的同型半胱氨酸 (Hcy)还原成总同型半胱氨酸 (tHcy) ,以光胺作内标 ,巯基特异性荧光衍生剂SBD F对Hcy ,胱胺等含巯基化合物进行柱前衍生 ,然后行HPLC 荧光检测。结果 :本方法所检测的Hcy浓度在 2 .5～ 16 0 μmol·L- 1 范围具有良好的线性关系 (r =0 .9975 ) ,Hcy最低检测限 0 .6 2 5 μmol·L- 1 ,批内变异小于 5 .5 % ,批间变异小于 9.0 % ,平均回收率 98.87%。结论 :本法简便、灵敏、精确、稳定     

柴胡及甘草酸对小鼠肝细胞凋亡的影响

目的：研究柴胡（ＲＢ）及甘草酸（ＧＬ）对小鼠肝细胞凋亡的影响。方法：以肝／体重比，肝组织ＤＮＡ含量，组织学改变及原位凋亡细胞ＴＵＮＥＬ反应为指标，观察ＲＢ（１２．０ｇ／ｋｇ）及ＧＬ（５０ｍｇ／ｋｇ）ｉｐ，１次／８ｈ，对撇除苯巴比胺钠（ＰＢ）后引起的小鼠肝细胞凋亡的影响。结果：与对照组Ｃ相比，ＲＢ组小鼠肝／体重比及肝ＤＮＡ含量无明显回落，组织学检查未见明显凋亡改变，ＴＵＮＥＬ反应阴性，ＧＬ组小鼠肝／     

肝移植手术中的配合

自从 1 96 3年Starzl成功实施世界上第一例活体肝移植后 ,肝移植手术已经成为现代肝脏外科学领域里的一个比较实用、也比较时髦的手术及研究项目。结合我院已完成的 2例肝移植手术 ,简要介绍肝移植手术术前、术中及术后的相关问题 ,并介绍肝移植手术的主要步骤 ,叙述手术中的相关配合问题     

Glycine transporter I inhibitor, N-methylglycine (sarcosine), added to antipsychotics for the treatment of schizophrenia.

BACKGROUND: Hypofunction of N-methyl-D-aspartate glutamate receptor had been implicated in the pathophysiology of schizophrenia. Treatment with D-serine or glycine, endogenous full agonists of the glycine site of N-methyl-D-aspartate receptor, or D-cycloserine, a partial agonist, improve the symptoms of schizophrenia. N-methylglycine (sarcosine) is an endogenous antagonist of glycine transporter-1, which potentiates glycine's action on N-methyl-D-aspartate glycine site and can have beneficial effects on schizophrenia. METHODS: Thirty-eight schizophrenic patients were enrolled in a 6-week double-blind, placebo-controlled trial of sarcosine (2 g/d), which was added to their stable antipsychotic regimens. Twenty of them received risperidone. Measures of clinical efficacy and side effects were determined every other week. RESULTS: Patient who received sarcosine treatment revealed significant improvements in their positive, negative, cognitive, and general psychiatric symptoms. Similar therapeutic effects were observed when only risperidone-treated patients were analyzed. Sarcosine was well-tolerated, and no significant side effect was noted. CONCLUSIONS: Sarcosine treatment can benefit schizophrenic patients treated by antipsychotics including risperidone. The significant improvement with the sarcosine further supports the hypothesis of N-methyl-D-aspartate receptor hypofunction in schizophrenia. Glycine transporter-1 is a novel target for the pharmacotherapy to enhance N-methyl-D-aspartate function.     

三七总甙对人增生性瘢痕成纤维细胞TGF-β1和细胞周期的作用

目的 观察三七总甙对人增生性瘢痕成纤维细胞TGF-β1和细胞周期的作用。方法体外培养人增生性瘢痕成纤维细胞，并应用三七总甙进行干预，用免疫细胞化学染色法结合图像分析观察TGF-β1的表达变化，用流式细胞仪测定细胞周期的变化。结果与对照组相比，三七总甙能够显著抑制细胞TGF-β1的表达，并使细胞停滞于S期，而G0-G1期、G2-M期细胞明显减少（P〈0．01）。结论三七总甙改变细胞周期和抑制增生性瘢痕成纤维细胞TGF-β1的表达，可能成为防治增生性瘢痕的药物。