藥物釋放度 的英文怎麼說

中文拼音 [yàowùshìfàngdù]
藥物釋放度 英文
drug release
  • 藥 : Ⅰ名詞1 （藥物） medicine; drug; remedy 2 （某些有化學作用的物質） certain chemicals Ⅱ動詞1 [書面...
  • 物 : 名詞1 （東西） thing; matter; object 2 （指自己以外的人或與己相對的環境） other people; the outsi...
  • 釋 : Ⅰ動詞1 （解釋） explain; elucidate 2 （消除） clear up; dispel 3 （放開; 放下） let go; be reliev...
  • 放 : releaseset freelet go
  • 度 : 度動詞[書面語] （推測; 估計） surmise; estimate
  • 藥物 : medicinal; medicine; medicant; medication; drug; pharmaceuticals; medicaments
  • 釋放 : 1 （恢復被拘押者的人身自由） release; deliver; clearing; set free 2 [物理學] relief; rid; detachm...
  1. Methods the solid dispersion of estradiol was prepared using pvp k30 as a carrier by the solvent method ; dissolution and dialysis were used to compare the release rate between estradiol capsules and estradiol tablets respectively

    方法以聚維酮k30為載體，溶劑法制備雌二醇固體分散微粒；採用溶出度測定儀和動態透析2種方法分別評價優化后的處方及對照片劑的體外藥物釋放情況。
  2. Clsm, afm and tem testified the deposition of these drugs and the experiments carried out in ( 1 ) different initial incubation concentration, ( 2 ) different temperature, ( 3 ) different nacl concentration and ( 4 ) different ph revealed that the drugs have a relative high deposition efficiency in the high initial incubation concentration, high temperature, high nacl concentration and high ph environment, and relatively stable release properties in the low initial incubation concentration, low temperature, high nacl concentration and low ph environment

    在（ 1 ）不同初始濃度、 （ 2 ）不同溫度、 （ 3 ）不同鹽濃度和（ 4 ）不同ph值下對模型藥物rdb和抗癌藥物dnr沉積和釋放的研究發現高初始濃度、高溫、高鹽和高ph值環境下有利於藥物的沉積；而低初始載藥量、低溫、高鹽和低ph值環境下，沉積后的藥物則具有相對平緩的釋放性能。
  3. 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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