drug concentration 中文意思是什麼

drug concentration 解釋
藥物濃度
  • drug : n 1 藥，藥品，藥物，藥劑。2 〈俚語〉麻醉藥品，麻醉劑，使人上癮的毒品 （＝narcotic drugs）。3 〈pl...
  • concentration : n. 1. 集中。2. 【化學】提濃，蒸濃，濃縮；濃度；稠密度；【礦物】汰選，選礦，富化。3. 集中注意，專心。
  1. 2 - e4 and s2 is induced respectively by 8 - ag and 5 - brdu with different drug concentration to make them deficient in hypoxanthine - guanine phosphoribosyl transferase ( hgprt ) and in thymidine kinase ( tk ) respectively and renamed 2 - e4 - a and 82 - 6. their antibodies " isotypes are tested by goad anti - mouse isotype regent

    取馴化好並處于對數生長期的2 - e _ 4 - a和s _ 2 - b細胞，再常規融合和篩選，三次克隆化后得穩定分泌雙特異性抗體的雜交-雜交瘤細胞株6株。
  2. Analysis 198 cases of clozapine clood - drug concentration monitory schizophrenies

    精神分裂癥患者氯氮平血藥濃度監測198例分析
  3. Determination of metronidazole drug blood concentration in rabbit ' s plasm

    家兔血漿中甲硝唑的血藥濃度測定
  4. Children rhinitis, sinusitis in children, children with allergic rhinitis, children rhinitis, sinusitis children, children allergic rhinitis : clinical treatment : children rhinitis occurs when adults take to avoid readily rhinitis medication, children ' s nose points rhinitis nasal drug concentration required to reduce infant banned vasoconstrictor, intranasal net, ephedrine, rhinitis in children should be treated conservatively, with the age growth and development, many cases will disappear naturally

    臨床治療：小兒鼻炎發生時，切忌隨手拿成人鼻炎藥物治療，小兒的鼻炎鼻部點鼻藥物需要減濃度，嬰兒禁用血管收縮劑，如滴鼻凈、麻黃素等，小兒鼻炎應採用保守治療方法，隨著年齡增長發育，許多病癥會自然消失。
  5. This is supported further by pharmacokinetic / pharmacodynamic ( pk / pd ) analyses which suggest, at most, a modest association of drug concentration with viral response in this concentration range

    藥動學/藥效學的分析結果進一步證明了以上觀點，其分析結果表明，在這個濃度范圍內，藥物濃度與病毒反應略有相關性。
  6. Conclusion : only by integrating blood drug concentration monitoring with clinical pharmaceutical care by pharmacists can rational administration of digoxin to patients be realized

    結論：只有將地高辛血藥濃度監測與臨床藥學服務緊密結合，使地高辛給藥方案由常規化、經驗化轉向個體化，才能真正做到合理用藥。
  7. Most drug molecules are transported across a membrane by simple diffusion from a region of high concentration ( eg, gi fluids ) to one of low concentration ( eg, blood )

    大多數藥物分子以簡單擴散方式從高濃度區（如胃腸液）透膜進入低濃度區（如血液） 。
  8. Results : its kinetic curve had an analogy with zero - order kinetics, which indicated that ruyanqing could maintain a steady drug concentration and a longer effect time in plasma

    結果：動力學曲線類似零級動力學，說明乳炎清塗膜劑具有維持恆定的血藥濃度或藥理效應、延長作用時間等優點。
  9. Objective : to introduce the work pattern of clinical pharmaceutical care associated with monitoring drug concentration of digoxin

    摘要目的：介紹開展地高辛血藥濃度監測與臨床藥學服務的工作模式。
  10. When the weak acid is given orally, the concentration gradient for un - ionized drug between stomach and plasma tends to be large, favoring diffusion through the gastric mucosa

    當這種弱酸性藥物經口服給藥時，胃與血漿之間的非解離型藥物濃度梯度很大，從而有利於透過胃粘膜擴散。
  11. At equilibrium, the concentrations of un - ionized drug in the stomach and in the plasma are equal because only un - ionized drug can penetrate the membranes ; the concentration of ionized drug in the plasma would then be about 1000 times greater than that in the stomach

    在平衡狀態下，只有非解離型藥物能透過細胞膜，因此，非解離型藥物在胃中和血漿中的濃度相等，而血漿中的解離型藥物濃度則要比胃中高約1000倍。
  12. Liposomes can increase the drug concentration in the target, reduce the toxicity and improve the therapeutic efficacy of drugs

    脂質體給藥系統可降低藥物的毒性，增加藥物在靶點的聚集並提高藥物的療效。
  13. He were enrolled in a trial of concentration - controlled therapeutic drug monitoring in clinical practice

    他進入了一項治療藥物濃度對照監測的臨床試驗。
  14. An appropriate response to a drug requires the appropriate concentration of drug at the site of action

    藥物要獲得適宜的效應，就需要在作用部位達到適當的藥物濃度。
  15. 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。
  16. The extra volume makes up for the lower concentration of the drug

    額外的氣流量可以彌補尼古丁濃度的不足。
  17. Influence of low power diode laser irradiation on the minimal inhibitory concentration of drug resistant staphylococus aureus and pseudomonas aeruginosa

    低功率半導體激光照射后耐藥金黃色葡萄球菌與銅綠假單胞菌的耐藥性變化
  18. Because drug molecules are rapidly removed by the systemic circulation and distributed into a large volume of body fluids and tissues, drug concentration in blood is initially low compared with that at the administration site, producing a large gradient

    由於藥物分子是經體循環快速轉運並分佈到大容積體液和組織中去的，所以開始時，血液中的藥物濃度低於給藥部位的藥物濃度，形成大的濃度梯度。
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