prodrug
- 网络前药;前体药物;药物前体;前体药
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Prodrug is a new drug delivery system ( DDS ) based on polymer compounds .
大分子前药是以大分子化合物为载体的一种新的药物传输体系。
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Therefore , the porphyrin anticancer prodrug system has a widely applicable prospect .
因此,光控释放卟啉抗癌前药系统在医学上有广阔的应用前景。
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These data demonstrate the use of an enzyme prodrug strategy in experimental pancreatic cancer .
证实了酶解药物前体在实验性胰腺癌的治疗作用。
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The killing effects of two prodrug sensitivity genes on human pancreatic carcinoma cells PC 2
不同药物敏感基因对人胰腺癌细胞PC-2的杀伤作用
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Chiral Separation of Propranolol Vinyl Ester Prodrug by High Performance Liquid Chromatography
普萘洛尔乙烯酯前药的高效液相色谱对映体分离
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Synthesis and delivery characteristics of colon specific dexamethasone prodrug
地塞米松·葡聚糖的合成及其肠内容物中的转释特性
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Every proton pump inhibitor so far developed is administered in a prodrug form .
迄今为止每个质子泵抑制剂都被研究开发为一个前药的管理形式。
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Killing effect of combined application of double suicide gene / prodrug systems and radiotherapy on osteosarcoma cells
联合应用自杀基因/前药系统和放疗对人骨肉瘤细胞的杀伤作用
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Synthesis and in vitro evaluation of the hemolytic property of the puerarin prodrug
葛根素前药合成及其体外溶血特性研究
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Experimental study on the efficacy of β G gene and β G prodrug system in the human bladder cancer cell
βG基因及βG前体药自杀基因系统对人膀胱癌细胞作用的实验研究
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Cholesterol-curcumin prodrug synthesis and preliminary research of its anti-tumor effects
胆固醇-姜黄素前药合成及其抗肿瘤作用的实验研究
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Ester prodrug of scutellarin : synthesis , physicochemical property and degradation
灯盏乙素酯类前药的合成、理化性质及降解研究
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Expression , Purification and Bioactivity of Prodrug of Recombinant Human GLPs
重组人胰高血糖素样肽前药的表达、纯化及生物活性分析
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Astragaloside Extraction and Synthesis of Water-soluble Prodrug Research
黄芪甲苷的提取及其磷酸酯水溶性前药的合成研究
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CONCLUSION The prodrug of4-Aminotetrahydroacridine can be synthesized by this method .
结论该法有助于他克林前体药物的研究。
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Prodrug structural modifications of cyclovirobuxine D and their biological activity
环维黄杨星D的前药改造及生物活性研究
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Effects of NO prodrug JS-K on HL-60 cell proliferation and differentiation
NO前药JS-K对HL-60细胞增殖、分化的影响
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Study of Horseradish Peroxidase / Indole-3-acetic Acid System in Gene-directed Enzyme Prodrug Therapy
辣根过氧化物酶/吲哚乙酸系统作为基因导向性酶前体药物疗法的研究
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The main degradation product of the lipidic prodrug was acyclovir .
前药在弱酸和中性环境中保持稳定,主要降解成阿昔洛韦。
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Colon - specific delivery release mechanism of prednisolone-dextran prodrug
泼尼松龙葡聚糖前体药物的结肠定位转释机制研究
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Study on the Synthesis , Colon Targeting Characteristics and Pharmacodynamics of Pectin-ketoprofen Prodrug
果胶&酮洛芬前药的合成、结肠靶向性和药效学研究
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Double prodrugs group showed more apoptosis cells than the single prodrug group according to Hoechst-PI colorant analysis .
利用Hoechst-PI双染色法检测经前体药物作用后转染细胞,各组均可见凋亡细胞,但联合用药组凋亡细胞较单一用药组多。
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Combining FCU / 5-FU suicide gene / prodrug system and radiation in treating nasopharyngeal carcinoma : an experimental study
FCU/5-氟胞嘧啶自杀基因前体药物系统联合放射治疗鼻咽癌的实验研究
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Pharmacokinetics of colon specific delivery of dexamethasone prodrug
地塞米松前体药结肠定位释放的药代动力学
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The Investigation of a Prednisolone Prodrug for Colon-Specific Drug Delivery
泼尼松龙前体药物的结肠定位研究
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5-fluorouridine prodrug liposome inhibits proliferation and improves apoptosis of laryngeal cancer cell line HEP-2
5-氟尿嘧啶核苷前药脂质体对人喉癌HEP-2细胞株增殖与凋亡作用的影响
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The Synthesis of a Novel Biodegradable Amphiphilic Dendritic Polyester and Preparation of Its Anti-tumor Prodrug
一种新型两亲性树枝状聚酯的合成以及抗肿瘤前药的制备
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Objective To investigate the killing effect of UPRT / 5-FU Enzyme / Prodrug System on murine gastric cancer .
目的探讨UPRT/5FU前药转换酶系统对小鼠胃癌细胞MFC的杀伤效应。
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Pharmacokinetics of site-specific delivery of dexamethasone-dextran prodrug in rat gastrointestinal tract
糖皮质激素前体药在大鼠胃肠道中定位转释的药代动力学
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Synthesis and in vitro evaluation of pectin-ketoprofen prodrug
果胶酮洛芬前药的合成及体外评价