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.
纳米级尺寸的颗粒使得包裹在其上的抗原不被降解，意味着他们可以在人体系统中存在更长时间，这样可以减少给药次数和剂量。
The nanoparticles shield the antigens from degradation, meaning they stay in the system much longer, so they can be delivered at fewer intervals and at lower doses.
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.
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.
按载体分类综述了近年来的脂质体、微球、纳米粒、乳剂等几类中药靶向给药系统的研究进展。
Recent advances of research on TODDSs of CMM classified according to carriers, such as liposomes, microspheres, nanocapsules, and emulsions are reviewed.
作为一种新型给药系统，纳米粒在口服给药方面具有广阔的开发及应用前景。
Recent studies of this technology is reviewed in the respects of preparation methods, surface modifications, drug release and pharmaceutical applications, implying a prosperous future of development.
本文针对经皮给药系统新型压敏胶及新型经皮给药技术需求，研制了三类亲水性压敏胶及两种药物纳米载体材料，并对其性能进行了研究。
In this study, three kinds of hydrophilic pressure sensitive adhesives and two kinds of nanocarrier materials were prepared for technology requirement of TDDS and their properties were investigated.
结论优化条件制备出的补骨脂素皮肤用纳米粒载药系统有可能成为临床上改进补骨素光化学疗法降低其毒副作用的一种新的经皮给药制剂。
CONCLUSION Psoralen loaded PLGA nanospartilcles might be a promising transdermal delivery system in order to improve the efficacy and reduce the side effects in the PUVA therapy.
结论优化条件制备出的补骨脂素皮肤用纳米粒载药系统有可能成为临床上改进补骨素光化学疗法降低其毒副作用的一种新的经皮给药制剂。
CONCLUSION Psoralen loaded PLGA nanospartilcles might be a promising transdermal delivery system in order to improve the efficacy and reduce the side effects in the PUVA therapy.
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