藥物釋出 的英文怎麼說

中文拼音 [yàowùshìchū]
藥物釋出 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...
  • 藥物 : medicinal; medicine; medicant; medication; drug; pharmaceuticals; medicaments
  • 釋出 : disengagement釋出劑 releasing agent
  1. Because, this is of chinese herbal medicine outer the organization is stimulated suddenly by high fever, instantly constrictive, caky even, its protein is formed on cellular wall cannot go against the metamorphic layer that turn, prevent moisture development, organize interior to composition dissolves hard and be released, such, the decoct of medicaments active ingredient goes out rate reduce greatly, affect curative effect badly

    這是因為中草藥的外層組織忽然受到高熱刺激，立即緊縮，甚至凝固，其蛋白質便在細胞壁上形成不可逆轉的變性層，防止水分深入，組織內部成分難以溶解並釋放出來，這樣，藥物有效成分的煎出率大大降低，嚴重影響療效。
  2. Nanodroplets of the microemulsion bind with nanoparticles of the nutraceutical or cosmetoceutical. the nanodroplets carry the nutraceutical nanoparticals through membranes and release them upon reaching their destination

    該微小乳狀液中的納米液滴與營養食品或藥用美容品的納米顆粒結合，納米液滴攜帶著營養物質的納米顆粒穿過細胞膜，在到達目的地后把它釋放出來。
  3. Methods 101 gonococcal isolates obtained from 2003 to 2004 in hengyang city, hunan province, were tested for their susceptibilities to macrolides using agar dilution method

    方法採用瓊脂稀釋法對分離出的101株淋球菌流行株進行了藥物敏感性測定。
  4. It is orig inated from precious medical materical materials and extracted from its marrows. high - tech wall - broken extraction technology releases the drug marrow to activate your life and full improve sleeping

    源自神秘藥材，萃取藥性精華。高科技破壁萃取技術，使名貴藥材中蘊含的藥物精華成份，釋放出新生、活化功效，全面深刻改善睡眠狀態。
  5. Interpretation : drug combinations involving antiplatelets and anticoagulants are associated with a high risk of gastrointestinal bleeding beyond that associated with each drug used alone

    解釋：抗血小板制劑和抗凝藥物的聯用可以增加胃腸出血的風險，高於單用每種藥物的出血風險。
  6. Results nanoparticle carrier system can protect the genes, have a high carrying efficiency and a well targeting property, it also can improve the bioavailability, sustained and controlled release

    結果納米顆粒轉運系統能夠保護被轉運的基因，有較高的轉染效率，具有良好的靶向性，並且提高了藥物的生物利用度，顯示出一定的緩控釋作用。
  7. 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。
  8. In this paper, based on analysis the distributing rule of permanent magnetic field, a novel method for dynamic tracing micro drug delivering device in alimentary canal has been proposed

    本文在分析永磁體空間磁場分佈規律的基礎上，提出了利用磁定位原理實現動態跟蹤微型藥物釋放裝置在消化道運動狀態的方法。
  9. The basic principle of the method is that, when the micro drug delivering device mounted with a permanent magnet pass through the alimentary canal, the variety of magnetic field was detected by hall sensors, so the location of micro drug delivering device could be deduced and dynamic tracing can be achieved

    其基本過程是在微型藥物釋放裝置上固定永磁體，當其通過消化道時在體外檢測磁場變化，進而實時計算出微型藥物釋放裝置的空間位置，並描記出運動軌跡，實現動態跟蹤。
  10. Hence it is important to understand the factors which influence the stability of phenolic compounds and identify methods to control the oxidative degradation of phenolics. scientific workers attached importance to amphiphilic structures ( liposomes and micelles ) since its " discovery, especially in extensive use in slow - release and target drug carriers. since the eighties last century, some advanced countries such as germany, sweden and usa have done much basic researches on application of amphiphilic structures at the expense of much manpower and financial resources, resulting in appearance of liposome target anticancer drugs

    脂質體（ liposomes ）和膠束體（ micelles ）類雙親和結構自發現以來，引起了科技界的高度重視，特別是脂質體結構的緩釋性和靶向性在醫藥上的用途更為廣泛，國外八十年代開始投入大量人力和財力進行研究，於九十年代開發出了脂質體靶向抗癌藥物面市；我國九十年代引起重視並投入一定的經費開始研究，但到目前國內尚無一例成功開發上市的脂質體靶向藥物。
  11. The drug release can be sustained for years and the treatment is specific and focused

    植入劑自動在眼球內不停地釋放出類固醇藥物，並可維持達三年之久。
  12. They are able to protect a protein drug such as insulin from the acidic ph of the stomach and then release it in the more alkaline ph of the intestine

    它們可以保護胰島素之類的蛋白質類藥物免受酸性胃液的攻擊，然後在到達比較鹼性的腸道后將蛋白質釋出。
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