12C离子束的剂量学研究

研究了L-α-丙氨酸剂量计测量^12C离子辐射的剂量学特性，实验证明丙氨酸剂量计适用于^12C离子辐射的剂量学测量。另外，还研究了^12C离子照射人外周血诱发的染色体畸变（双着丝粒＋着丝粒环）的剂量效应，在0-8．0Gy范围内拟合的最佳回归方程为Y=0．858503D＋0．3615×10^-2D^2。Dosimetric characteristics of L-α-alanine dosemeter used for dosimetry of ^12C ion radiation have been studied. The experimental results indicate that the alanine dosemeter can be used to measure the ^12C ion radiation. In addition, dose effects of chromosome aberration dicentrics and cenric rings were studied after human peripheral blood being irradiated by ^12C ions; the best regression equation, Y = 0. 858 503D ＋ 0. 361 5 ×10^-2D^2, was obtained within 8.0 Gy.     

重离子束治癌中深度剂量分布优化

针对兰州重离子研究装置所加速的120MeV/u ¹²C离子束,利用模拟退火优化算法进行了Bragg峰展宽的剂量优化.取相同的展宽区域(30mm),4种不同的步长(2,1,0.5,0.25mm)进行Bragg峰展宽模拟.对所得到的剂量平均值,均方差,入射口剂量,峰坪比等优化结果的参数做了比较.讨论了重离子束治癌临床上最优的Bragg峰展宽模型的选取.     

肿瘤治疗的重离子束物理性质研究

重离子在肿瘤治疗方面的优势主要是由于其优越的物理性质，因此，研究其与生物体相互作用也就成为肿瘤治疗中的基本课题，介绍一些研究结果来解决人们关心的问题.The advance of tumor therapy with heavy ions beam is due to the physics quality of heavy ions.So,the investigation of heavy ions action with biological materials will be a basic task. In the paper, the investigated results show a picture to resolve some problems which attract people＇s attention.     

12C6+离子辐照小鼠Lewis肿瘤的研究

研究了HIRFL提供的12C6+离子辐照C57BL/6J小鼠右后腿移植的Lewis肿瘤的生长延迟和碳离子辐照对Lewis肿瘤小鼠寿命的延长.结果表明,碳离子照射的小鼠肿瘤生长体积明显地小于对照的体积.在剂量相同、分次数辐照越多时,肿瘤生长就越缓慢,肿瘤抑制就越高.在辐照分次数相同时,不同剂量对受照肿瘤生长体积未产生差异.在4Gy×3,8Gy×3和12Gy×2组3种辐照剂量下,小鼠寿命的P值小于0.05;可知小鼠的寿命延长具有统计学意义. Growth delay of the transplantable Lewis tumors growing in right hind legs of C(57) BL/6J mice and life prolongation of the mice with Lewis tumors were investigated after()~(12)C~(6+) ion radiation at HIRFL. The results show that growth volumes of the mouse tumors following carbon radiation are distinctly less than control during 21 days; the more fractions of radiation with same doses, the slower growth of tumors and the higher inhibition of tumors; different doses with the same fractions of radiation ...     

HIRFL辐照终端照射野均匀度与离子通量的关系

采用固体核径迹探测器聚碳酸脂膜,测定了兰州重离子研究装置提供的55MeV/u40Ar和80MeV/u20Ne离子束经辐照终端束流均匀化扫描装置后照射野均匀度与离子通量之间的关系.结果表明:对于40Ar和20Ne离子束,离子通量小于1×106和2×107ions/cm2时,横向照射野均匀度缓Ne离子束照射慢增加;当离子通量分别介于1×106—1×107和2×107—1×108ions/cm2时,40Ar和20野均匀度逐渐增加;离子通量达到1×107和1×108ions/cm2时,40Ar和20Ne离子束照射野均匀度分别约为58%和61%.从而说明,辐照终端束流扫描装置对束流的均匀化程度目前并不能满足辐照生物效应、辐射育种和重离子治癌等研究工作的需要,须对其性能做进一步的提高. Using 55 MeV/u 40Ar and 80 MeV/u20Ne ion beams delivered by the Heavy Ion Research Facility at Lanzhou (HIRFL), the relationships between the irradiation homogeneities in irradiation fields generated by the beam scanning device located at the irradiation terminal of the HIRFL and ion fluence were measured respectively with 100 μm polycarbonate films by means of nuclear track detection. The results show that the homogeneity increases when the ion fluence are lower than ........     

重离子诱导的质粒DNA双链断裂分布研究

利用能量为7．2MeV／u氖离子束辐照体外质粒DNA:pUC18，采用恒场凝胶电泳结合多功能荧光成像系统研究了pUC18双链断裂片段的分布。证实了双链断裂片段分布的非随机性，结果还发现DNA断裂后片段的交联现象，而且交联片段的分布也是非随机的。DNA is considered to be the most important and sensitive target in biological systems. In addition to the base damage, DNA strand breaks are the major lesion in the genome due to exposure to ionizing radiation. Mutation can be introduced to DNA as a result of enzymatic processing of DNA lesions or post irradiation replication. However, the mechanisms of radiation induced mutations are not well clarified at the molecular level. To study the effect on the simple plasmid DNA of heavy ion is even predominant or more feasible. Plasmid pUC18 DNA was prepared and irradiated by neon beam (7.199 MeV/u). The fragment distributions were determined by quantifying the ethidium bromide fluorescence. It can be seen that the shape of the intensity distributions is vastly different for the used radiation Dose. The distribution produced shows an excess of fragments particularly in 3 000 and 10 000 Gy the size range between 20—40 kbp and 20—50 bp. This clustering of double stranded fragments might be influenced by the higher order chromatin structure of genomic DNA. If so, DNA loop structures could correspond to the size range for which we observed DSB clustering. Further studies aim at elucidating the heterogeneity of DSB induction within the genome and investigate the influence of chromatin structure on the non random fragment distribution.