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Objective To investigate in vivo drug release behaviors of cefixime sustained-release tablets. 目的建立头孢克肟缓释片释放度测定方法,评价其体外释药行为。
CONCLUSION: Kuaijing pessary has satisfactory pharmacokinetic characteristics with a steady in vivo drug release rate and long time action.It is worth popularizing. 结论:快净栓具优异的药动学特性，体内释药平稳，作用时间长，值得推广应用。
CONCLUSION： Kuaijing pessary has satisfactory pharmacokinetic characteristics with a steady in vivo drug release rate and long time action.It is worth popularizing. 结论：快净栓具优异的药动学特性，体内释药平稳，作用时间长，值得推广应用。
in vivo drug release 体内药物释放
This article gives a review of preparation, drug release and in vivo study of the floating ability of different multiple-unit FDDS. 本文介绍了目前国内外多单元胃漂浮给药系统的类型、制备方法、释药情况及其体内漂浮性能的研究方法。
Advances of in vivo drug interaction studies 体内药物相互作用研究进展
STUDY ON ADRIAMYCIN-POROUS TRICALCIUM PHOSPHATE CERAMIC DRUG DELIVERY SYSTEM AND ITS DRUG RELEASE TEST IN VIVO 阿霉素-多孔磷酸三钙陶瓷缓释体的研制及体内释药试验
Adl2 ElB 55kDa binds hDaxx in vivo or in vitro. 共免疫沉淀反应和Western blot结果证实Ad12 E1B 55KD能在细胞内外与hDaxx直接结合。
Influence of PEG chain length on in vitro drug release and in vivo pharmacokinetics of hydroxycamptothecin(HCPT) loaded PEG-PHDCA niosomes 不同聚乙二醇相对分子质量对包载羟基喜树碱的PEG-PHDCA纳米囊泡体外释放和体内药动学行为的影响
The expression product shows activity of antitumor in vivo. 表达产物在体内具有一定的抗肿瘤活性。
Result Nicardipine can induce rat mesangial cell apoptosis in vivo. 结论尼卡地平在体内有诱导大鼠系膜细胞凋亡的作用。
Methods Using the in vivo micropuncture technique in SD r ats. 方法利用活体微穿刺技术。
CONCLUSION Survivin T34A might inhibit A549 tumors growing in vivo. 结论 Survivin T34A在体内可明显抑制A549肺癌生长。
At last, tumorigenesis assay was undertaken in nude mice in vivo. 进行黑素瘤细胞体外克隆形成实验观察,计算各组细胞的克隆形成率;
The embryos from the in vivo fertilization develop best. 体内受精胚胎的体外发育最佳。
SR on the drug release was great, variations of Kollidon? SR用量对药物释放影响较大；
And, these monkeys were injected in vivo dose must SIV virus. 然后，这些猴子体内均被注入一定剂量的SIV病毒。
The mechanism of drug release from swellable polymer was studied . 对药物从亲水聚合物凝胶系统中释放的机理进行了研究。
Conclusion The VH containing extra-sequence may exist in vivo. 结论提示这段异常序列在体内可能存在于该VH之中。
Methods Gelatin microspheres containing diclofenac sodium were prepared by simple coacervation technique and the drug release in vitro and vivo were tested. 方法采用单凝聚法制备双氯芬酸钠明胶微球,并对微球的体内外释药进行考察。