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- rifapentine liposomes 利福喷丁脂质体
- Aim To prepare rifapentine(RIF) liposomes modified by surfactants for studying their the water-solubility,drug loading effeciency,release rate and pulmonary drug delivery. 目的制备表面活性剂修饰利福喷丁(RIF)脂质体,进行该脂质体水化性能、载药量、释药速度和肺部给药研究。
- Objective To optimize the prescription of tea tree oil liposomes. 目的优化制备茶树油纳米脂质体的处方。
- Objective To prepare and optimize formulation of ATRA liposomes. 目的通过制备不同配方全反式维甲酸脂质体,对处方进行优化。
- AIM To study the preparation and stability of sinomenine liposomes. 目的:优选青藤碱脂质体的制备方法,并研究其稳定性。
- Hydrostatic Pressure Effects on Transport in Liposomes and Red Cells. 静水压力对脂质体、红细胞运输的影响。
- OBJECTIVE To determine the trap efficiency of liposomes using Sephadex. 目的考察用葡聚糖凝胶法测定脂质体包封率的影响因素。
- OBJECTIVE To optimize the preparation formulation of the taspine liposomes. 目的优化塔斯品碱脂质体的制备处方。
- Two clinical trials are scheduled to study high-dose and daily combinations with rifapentine. 两项临床试验,预计研究高剂量和每日组合与利福喷丁。
- Although Rifapentine is already approved for use in humans, it has no current market, not even a prescription price. 虽然利福喷丁已批准用于人类,它并没有目前市场上,甚至没有医生处方的代价。
- Methods To observe the cases with positive PPD reaction by adopting the treatment scheme including rifapentine. 方法追踪观察结核菌素强阳性患者的利福喷丁预防性治疗过程,了解方案的可接受性及结核病发病情况。
- The measuring range of 3 to 6,000 nm covers the size of very small micelles as well as the larger liposomes. 测量范围在3至6000纳米之间,非常小的微胶粒和大微脂粒同样适用。
- He says that phase II clinical trials will begin as quickly as possible by mid-2008 to gauge the effectiveness of rifapentine as a key component to daily, anti-TB drug regimens. 他说,二期临床试验将开始尽快由2008年年中,以评估成效,利福喷丁作为一个重要组成部分,每天的抗结核药物方案。
- Observe the suscitation of podophyllotoxin liposomes chitosan film torabbits' vagina. 三、察鬼臼毒素脂质体壳聚糖涂膜剂对家兔阴道的刺激性。
- Objective:To study the relations between the polymorphic forms of rifamycin derivatives rifampicin(RFP), rifapentin(RFT) and rifamdeni(IPR) and the drug content in plasma(urine). 目的:探讨利福霉素类抗生素的衍生物(利福平,利福定,利福喷丁)的晶型与血(尿)药浓度的关系。
- The experimental study on in vivo pharmacokinetics of carboplatin liposomes via intralymphatic vessel perfusion. 经淋巴管灌注卡铂脂质体的药代动力学实验研究。
- METHODS the pharmacokinetics of EPC and HEPC sterically stabilized liposomes (EPC-SSL, and HEPC-SSL) were studied by HPLC. 方法用高效液相色谱法研究EPC和HEPC长循环阿霉素脂质体在大鼠体内的药物动力学。
- The results revealed that DPPC:Chol:DCP liposomes could markedly enhance the immunogenicity of the ESS. 结果表明,DPPC:Chol:DCP 脂质体能显著增强ESS的免疫原性。
- The entrapment efficiency in cationic liposomes was in the same range even if the drug loading was increased. 即使填充药量增加,带有阳离子的脂质体的包封率(仍处于相同范围)没有变化。
- OBJECTIVE To prepare Lomustine thermo-sensitive liposomes(CCNU-TSL) and investigate the anti-tumor activity in vitro. 目的制备洛莫司汀热敏脂质体并考察其体外抗肿瘤活性。