formulation of agent 中文意思是什麼
formulation of agent
解釋
制劑形態- formulation : 編制
- of : OF ＝Old French 古法語。
- agent : n 1 行為者，動作者；【語法】主動者。2 原因；動因；作用物，（作用）藥劑。3 代理人，代辦人；代理商...
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Several formulation of mental states of intelligent agent are discussed
研究了智能體的精神（心智）狀態的幾種形式化表示。 -
The study on the formulation and the influence factors to the property of copper - base ir interfering smoke agent as well as measurement results of the property are described
摘要對銅基紅外干擾發煙劑的配方及影響配方性能的主要因素進行了實驗研究，並對其性能進行了測試。 -
Interactions among oxidation - corrosion inhibitor, and among oxidation - corrosion inhibitor and the peace and quiet dispersing agent are stress researched. on this foundation the optimum formulation of compound oxidation - corrosion inhibitor is presented
重點考察了抗氧劑間、抗氧劑與清凈分散劑間的協同作用，在此基礎上，提出了復合抗氧劑的優化配方。 -
Third, the mechanical properties were conducted by tensile test, and analyzed the relationship between the length, content, coupling agent levels and the tensile strength, tensile modulus of composites films. the result showed that the optimum formulation was the contents of long milled glass fiber 20. 0wt % and coupling agent kh - 550 1. 0wt %
最後，利用動態力學分析（ dma ）和差示掃描量熱儀（ dsc ）對所制備的應變片基底材料進行了熱學性能測試，得到了材料的玻璃化轉變溫度tg 、蠕變和應變回復率。 -
Liposome is an effective nuclide delivery agent for neutron capture therapy. in this paper liposomes containing encapsulated gadolinium complex were prepared and characterized. the influence of formulation factors such as ph, ionic strength, buffer, and storage time upon the stability of liposomes was investigated. the uptake rate constant and its concentration dependence of lgd in tumor cells were compared in vitro with that of gd complex itself. the results indicate that the uptake rate of lgd in tumor cells increases to eight times as much as that of gd - edta, but the release rate of gd from tumor cells containing lgd is remarkably lower than that from the tumor cells containing gd - edta. the results reveal that lgd would be a potential drug for neutron capture therapy of cancer
制備和表徵了包埋gd - edta的脂質體，測定了ph ，離子強度，緩沖液組成及溫度對gd - edta脂質體的影響，比較了gd - edta脂質體和gd - edta被腫瘤細胞攝入的動力學曲線。結果表明， gd - edta脂質體在37和生理條件下最穩定，腫瘤細胞攝入gd - edta脂質體速率是gd - edta的8倍，而釋放gd的速率， gd - edta脂質體遠遠低於gd - edta ，這些結果提供了脂質體包埋gd - edta作為釓中子俘獲治療藥物的可能性。
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