结论脂质体制备工艺可行，药剂学性质稳定。
CONCLUSION This preparation of BLCL is practicable and the pharmaceutical characterization showed stable.
脂质体制备的难点在于改善物理稳定性和提高包封率。
Physical stability and envelope rate remains the main problems in preparation of liposomes.
以包封率为评价指标，筛选脂质体制备的最佳工艺条件。
The optimal technological conditions were acquired by the evaluation of the encapsulation efficiencies.
结论氢醌脂质体制备工艺可行，质量控制方法简单、准确。
ConclusionThe technology of preparing Hydroquinone liposome was feasible and the method of quality control was simple and accurate.
结论干扰素脂质体制备的关键是提高包封率和稳定性，探索工业化生产的可行性。
Conclusion the key point of preparation of interferon liposome is to elevate the envelopment rate and stability, and to explore the feasibility of industrialization production.
结论干扰素脂质体制备的关键是提高包封率和稳定性，探索工业化生产的可行性。
Conclusion the key point of preparation of interferon liposome is to elevate the envelopment rate and stability, and to explore...
方法检索国内外文献资料，对已开展的几种干扰素脂质体制备方法特点进行归纳分析。
Methods To search literatures in recent years at home and abroad. The trait of preparative methods of interferon liposome was analyzed.
目的 进行新型抗癌药物盐酸拓扑替康的脂质体制备研究，以期得到具有较高包封率的制备方法。
OBJECTIVE To study the best preparation method of liposomal topotecan(TPT) hydrochloride by comparing the entrapment efficiencies of different methods.
方法采用薄膜分散法和冻干工艺进行木犀草素脂质体制备，并以载药量、包封率为评价指标，优化制备处方和工艺。
Optimization of preparation and formulation was accomplished by evaluating the drug-loading amounts and the entrapment efficiency of luteolin liposomes.
目的研究双氯芬酸钾(DP)脂质体制剂的制备及体外的经皮吸收特点。
Objective to study the preparation of topical liposomal diclofenac potassium (DP) formulation and the percutaneous absorption in vitro.
目的研究双氯芬酸钾(DP)脂质体制剂的制备及体外的经皮吸收特点。
Objective to study the preparation of topical liposomal diclofenac potassium (DP) formulation and the percutaneous absorption in vitro.
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