尿氚的分析测量和氚人体半排期的实验研究

用液体闪烁计数法测定了本所老点核退役过程中直接和间接接触氚工作人员的尿样几十个 ,氚浓度在 1 0 2 ～ 1 0 5 Bq/L ,最大氚浓度为 2 7× 1 0 5 Bq/L ,折合剂量当量约为 0 1 9mSv。短期观测 2 3名人体氚半排期 ,其范围为 5 5～ 1 4 8d ,中期观测 5名人体氚半排期 ,其范围为 7 6～ 9 4d。 2 8名人员半排期不仅与理论值 1 0d接近 ,而且与国内外的观测值十分符合。     

钢渣湿法脱硫试验研究

以某厂钢渣为吸收剂,以旋流板塔为吸收器,对湿法脱硫进行了试验研究。通过分析钢渣脱硫前后的化学成分变化,以及试验脱硫率随反应过程的变化,提出了钢渣湿法脱硫的反应机理。同时,试验研究了液气比、进气SO_2浓度、浆液浓度等主要参数对脱硫率的影响,以及加添加剂的效果。试验结果表明,通过合理的设计和适当的操作,可使钢渣湿法应用于中低脱硫率(50％～70％)的场合,以取得综合治理、以废治废的效果。     

Normal development in two six-year-old boys born after prenatal diagnosis of trisomy 20 mosaicism

Prenatal diagnosis of trisomy 20 mosaicism was made in two pregnancies by chromosome analysis of cultured amniotic fluid cells. In both cases, the pregnancy continued to term and a healthy male infant was delivered. Regular assessments up to the age of 6-5 years revealed normal physical and intellectual development in both children.     

Chorionic villus culture for prenatal diagnosis of chromosome defects: Reduction of the long-term cultivation time

We report in detail two series of chorionic villus cultivation for prenatal chromosomal diagnosis. Chorionic villi were sampled from both first- and second-trimester pregnancies. One hundred cultures were treated with trypsin–EDTA for 2 h and collagenase overnight, (method A) and 100 were treated with trypsin–EDTA for 1 h and collagenase for 2 h (method B). Using short-term enzymatic digestion, the cultivation time was reduced from 14 days to 6 days. Sufficient amounts of metaphases of good quality were present in 93 per cent of primary cultures harvested in situ, whereas enough metaphases of sufficiently good quality were in most cases present only after subcultivation of the cultures using method A. The decrease in cultivation time obtained is probably due to a higher yield of viable cells in monocellular suspension, an increased attachment efficiency, and a more rapid attachment of single cells (within 24 h).     

Amniotic fluid alpha-fetoprotein levels and prenatal diagnosis of autosomal trisomies

Pregnancies with fetal trisomy 21 have been associated with low amniotic fluid alpha-fetoprotein levels (AFAFP). This observation led to the suggestion that low AFAFP levels be used as a criterion for completion of a chromosomal analysis in patients who are not otherwise at increased risk for a fetal chromosome abnormality and in whom karyotyping might not have been completed for economic reasons. In order to assess the usefulness of such criteria, we reviewed the AFAFP levels of 90 cases of fetal trisomy 21, 23 cases of trisomy 18, and 10 cases of trisomy 13. These were compared with 2400 control samples with normal chromosome constitution. AFAFP levels were generally lower in pregnancies with trisomy 21, showing a median value of 0·72 MoM. However, 40 per cent of the trisomy 21 samples had AFAFP values greater than 0·8 MoM and 20 per cent were over 1·0 MoM. These data imply that over 50 per cent of Down syndrome cases might have been missed using a cut-off level of 0·70 MoM for completion of chromosome analysis. Using a higher cut-off level will leave only a small percentage of samples unkaryotyped. The distribution of AFP levels in trisomy 13 and 18 is no different from controls; we therefore believe that fetal karyotyping should be completed in every amniotic fluid sample obtained.