本发明还提供了该缓释微球制剂的制备方法。
The invention also provides the preparation method of the slow release microsphere agents.
从微球制剂、复合性乳剂以及脂质体三方面对中药靶向制剂的研究进展作了介绍和展望。
The advance of TDDS including microsphere, multi-emulsion and liposome for TCM was introduced and evaluated.
探讨微球制剂的载药、释药机制，为处方设计和水溶性小分子药物微球制剂的开发提供指导。
The aim of the paper is to provide helpful Suggestions for the formula design and development of microspheres loaded with small molecular and water soluble drugs.
结论：将抗结核药利福平制备成微球制剂，肺部分可提高药物在肺部的分布，静注后无明显不良反应。
CONCLUSION: the lung tissue pulmonary distribution rate of rifampin may be promoted by making rifampin into microsphere dosage form and there were no significant side effects.
结果：LHRH类似物的药理作用较为广泛，其剂型主要为埋植剂和微球，二者相比，微球制剂具有更大的优势。
Results: LHRH analogues had extensive clinical applications and the main formulations were implants and microspheres. Microspheres had much broader advantages over implants.
探索茶多酚磁性白蛋白微球的制备工艺，用作治疗肿瘤的新型动脉栓塞制剂。
To explore the method of preparing tea polyphenols magnetic albumin microspheres, which are used to a new arterial embolization formulation.
方法：测定破伤风类毒素聚乳酸微球免疫动物后1年中动物血清抗体反应及疫苗制剂的生物利用度。
Methods: The antibody levels elicited by microsphere formulations in mice for 1 year were examined, and the bioavailability of microsphere formulations was calculated.
本发明涉及一种兽用氟苯尼考肺靶向明胶微球的制备方法，属于兽用制剂的技术领域。
The invention relates to a method for preparing a veterinary florfenicol lung targeting gelatin microsphere, which belongs to the technical field of veterinary preparation.
将具有免疫原性的抗原蛋白吸附到上述多孔微球中制成冻干制剂可得到多孔微球疫苗。
A freeze-dried preparation can be prepared by absorbing antigen protein of immunogenicity onto the porous microspheres to further obtain the vaccines of the porous microspheres.
近年来国内外研制成缓释、控释制剂的主要有片剂、胶囊剂、微球剂、滴眼剂、注射植入剂等。
In recent years, many sustained-released and controlled-release agents have been prepared successfully internal and abroad, such as tablets, capsule, micro spheres, eye drops, injection implant etc.
近年来国内外研制成缓释、控释制剂的主要有片剂、胶囊剂、微球剂、滴眼剂、注射植入剂等。
In recent years, many sustained-released and controlled-release agents have been prepared successfully internal and abroad, such as tablets, capsule, micro spheres, eye drops, injection implant etc.
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