这些剂型都是一种高度复杂的递药系统。
These dosage forms are highly sophisticated delivery systems.
固体脂质纳米粒是一种新型的纳米给药系统。
Solid lipid nanoparticle is a new drug delivery system of nano-range.
本文研究了生物降解聚合物纳米粒载药系统。
Biodegradable polymeric nanoparticles as drug delivery systems have been investigated in this dissertation.
植入型给药系统适用于长期给药和靶向给药。
Implantable drug delivery systems (IDDS) are long term acting controlled release systems.
本文给出了一个用于血压控制的自动给药系统。
An automated drug administration system used for control of blood pressure is presented.
目的：考察甲硝唑微囊口服结肠定位给药系统的制备工艺。
OBJECTIVE To investigate preparation method for the oral colon specific drug delivery system.
这种新型给药系统已成为近年来非胃肠给药研究的热点之一。
The novel drug delivery system has become a spotlight of the research on parenteral drug delivery in recent years.
目的对近年来微粒给药系统在肝靶向治疗的研究进展做一综述。
OBJECTIVE To introduce liver targeting particles drug delivery systems and its research progress in recent years.
本文仅就纳米给药系统在肿瘤靶向治疗中的研究进展作一综述。
The current paper reviews the recent proceedings of targeted cancer therapy by nano drug delivery systems.
结论：聚烯烃非pvc软包装输液是一种很有前途的新型给药系统。
Conclusion: Non - PVC polyolefin soft - packing transfusion is a very promising novel type of administration system.
还可以修正遗传病症，这项技术可以为治疗蛋白提供生物递药系统。
In addition to correction of inherited disorders, this technology can serve as a biologic delivery system for therapeutic proteins.
方法介绍我院住院药房摆药系统的流程，并将其与传统模式进行比较。
METHODS: the flow of the dispensing system in our hospital is introduced, then compared with the traditional mode.
本课题为进一步研制LMWH口服给药系统奠定了理论基础和实验依据。
The study provided the theoretical foundation and experiment evidence for preparing oral drug delivery system of LMWH.
结论采用均匀设计法优选的配方组成符合骨架控释型透皮给药系统的要求。
Conclusion the prescription composition optimized by uniform design meets the requirement of skeleton-controlled transdermal delivery system.
固体脂质纳米粒作为一种新型给药系统，可以提高难溶性药物生物利用度。
Solid lipid nanoparticles is a new drug delivery system, which can enhance the bioavailability of poorly soluble drugs.
选择恰当的给药系统能明显增强药物疗效、延长作用时间及减少不良反应。
Choosing appropriate drug delivery system can apparently improve drug efficacy, prolong action time and decrease adverse reaction.
本文介绍了一种不需要微流体通道、泵或瓣膜的纳克量分子运输和递药系统。
A transport and delivery system for nanogram quantities of molecular species that does not use microfluidic channels, pumps, or valves is described.
现对其结构式、已上市品种及最新给药系统的研究情况及其进展进行了综述。
The current paper reviews the structure, recent marketed products and the research status on the delivery systems of calcitonin.
结果表明，作为一种新型给药系统，纳米分散系具有广阔的开发与应用前景。
The result indicates that, as a new type of drug-delivery system, nano-disperse systems have a wide prospect in its development and application.
目的筛选合适的释放介质，用于魔芋胶为载体结肠定位给药系统的体外评价。
OBJECTIVE To select the in vitro release medium for elevating the colon-specific effect of preparations prepared with konjac glucomannan.
本文叙述了浮选自动加药系统的技术要求、方案设计、设备选型等方面的问题。
This paper introduced on the request of technology, blue print design, unit select and so on, of the automatic drug adding system of floatation.
目的：研究长春西汀自乳化释药系统（VIN-SEDDS）的体外释药特性。
Objective:To study the release characters in vitro of Vinpocetine self- microemulsifying drug delivery system (VIN-SEDDS).
选择壳聚糖作为透皮给药系统的控释材料，并对壳聚糖的成膜条件进行了研究。
Chitosan was chosen as the controlling materials for the transdermal drug delivery system, and the conditions of preparing chitosan membranes were researched.
研究结果将为温度感应型控制释放系统或给药系统的设计与开发提供理论基础。
The results in this study provided valuable guidance for the design and application of thermo-sensitive controlled-release systems or drug delivery systems.
结果提示，这种聚乙烯醇凝胶可望作为药物透皮给药系统的一种新的良好载体。
The results show that the PVA gel may be a fine carrier for transdermal therapeutic system.
结果表明，该聚氨酯压敏胶贴剂具有良好的药物控释能力，适用于经皮给药系统。
The results indicated that the hydrophilic polyurethane PSA prepared show good transdermal drug release properties, which suit for the TDDs application.
结果表明，该聚氨酯压敏胶贴剂具有良好的药物控释能力，适用于经皮给药系统。
The results indicated that the hydrophilic polyurethane PSA prepared show good transdermal drug release properties, which suit for the TDDs application.
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