本发明涉及制备药物和固体粘合剂的附聚物的方法。
The invention relates to a method of producing an agglomerate of drug and solid binder.
本发明还公开了所述偶合物的制备方法及在制备药物方面的应用。
The invention also discloses a preparation method and applications of the conjugates in preparing medicaments.
苯并环庚烯，其制备方法，包含该化合物的药物制剂以及在制备药物中的应用。
Benzocycloheptenes, method for production thereof, pharmaceutical preparations contg. these compounds, and their use for producing medicaments.
方法采用浸渍法制备药物并拟订质量控制方法，观察治疗带状疱疹60例的疗效。
Methods This tincture was prepared by alcohol extract from Gamboge and its quality control was designed. To observe the curative effects using compound Gamboge tincture for zoster in 60 cases.
介绍了溶剂蒸发法制备微胶囊的原理，分析了溶剂蒸发法制备药物微胶囊的工艺的研究现状。
The preparation of drug microcapsules by the solvent evaporation method is reviewed, and the technical principles of solvent evaporation are introduced.
无核细胞是通过药物、细胞松驰素b把细胞核去掉制备的。
Enucleated cells are prepared by removing cell nuclei in the presence of the drug, cytochalasin b.
方法乙醇注入法制备盐酸丁卡因脂质体，研和法制备脂质体凝胶，透析法测定盐酸丁卡因脂质体以及脂质体凝胶中药物的释放。
METHOD Prepare the hydrochloride tetracaine liposome by ethanol injection method, prepare hydrochloride tetracaine liposome gel by mixing method, and determine the liberation of drug by dialysis.
目的制备5氨基水杨酸(5ASA)肠溶包衣片，使药物在结肠释放。
OBJECTIVE To prepare the 5 aminosalicylic acid (5 ASA) enteric time controlled released tablets with site specific drug delivery in colon.
详细介绍了药物微胶囊的组成、制备技术，并讨论了其应用现状与发展趋势。
The components, preparation of the drug microcapsule is described in detail. and its applied present condition and development trend is also discussed.
新的2，3-二氢化茚醇化合物，其制备方法和包含它们的药物组合物。
New 2,3-dioxide, indanol compounds, process for their preparation and pharmaceutical compositions containing them.
新的含酰胺键的硫衍生物，它们的制备方法，它们作为药物的用途以及含有它们的药物组合物。
Sulphur derivatives comprising amide bond, method for preparing same, use thereof as drugs, and pharmaceutical compositions containing such derivatives.
三肽类似物，其制备方法，含它们的药物组合物及其用途。
Tripeptide analog, preparing method, medicine composition containing the same and USES.
结论利用红细胞在高渗液中脱水在低渗药液中膨胀的原理，制备红细胞药物载体。
CONCLUSION Preparation of carrier erythrocyte carrier encapsulating drugs was based on a principle that erythrocytes were dehydrated in hyperosmotic solutions and expanded in hypotonic solutions.
目的制备以法莫替丁为模型药物的脉冲控释胶囊；探索制备脉冲微丸的方法。
Objective To prepare pulsed-release capsule(PRC) using famotidine(FM) as a model drug and to explore the way of preparing pulsed-release pellets(PRP).
结论：采用控释薄膜包衣技术和骨架控释技术可用于制备强水溶性药物控释制剂。
CONCLUSION: the controlled release film-coated technique and the matrix technique can be used to prepare controlled release tablets for highly hydrophilic drugs.
用于微生物或其亚单位的载体颗粒，含有该颗粒的药物组合物，该组合物的制备方法及其在动物治疗中的用途。
Carrier particle for a microorganism or subunit thereof, pharmaceutical composition comprising such particles, method for preparation of this composition and its use in the treatment of animals.
故认为是一制备简便、实用的利胆药物新剂型。
目的以对乙酰氨基酚(扑热息痛)为模型药物制备新型口服速释剂型口腔崩解片。
OBJECTIVE To develop a novel rapidly release oral solid dosage form orally disintegrating tablet using acetaminophen as the model drug.
不同制备条件对微球药物包封率的影响程度较小。
The drug incorporation efficiency was affected in a narrow range by the conditions.
此外，本发明还公开了这种药物的制备方法。
The invention also discloses the process for preparing the medicament.
对药物树脂的制备、体外释放及缓释包衣都进行了研究。
The research work was composed of preparation and releasing and coating.
碱性基取代的苯甲酰胍，其制备方法，其作为药物或诊断试剂的用途，以及含有它们的药物。
Basic group substituted benzoyl guanidine, its preparing process, its use as medicine or diagnostic reagent, and medicine containing the same.
杂环化合物，制备方法，药物组合物和用途。
New heterocyclic compounds, preparing method, pharmaceutical composition and use.
可以通过调节这些因素来制备释放时间不同的药物缓释剂。
We can adjust these factors to produce different drug controlled release agent.
苯乙酮衍生物的不对称还原合成手性醇，制备手性药物是现在研究的热点。
Asymmetric reduction of acetophenone derivatives preparing chiral aromatic alcohol has become a new focus of study.
天麻素衍生物，其制备方法，药物组合物及其用途。
Gastrodine derivative, its preparation method, pharmaceutical composition and USES.
抗结核药物异烟肼制备成药质体能靶向巨噬细胞，提高药物渗透性。
The anti-tuberculosis drug isoniazid pharmacosomes was prepared, can improve drug permeability and target macrophage.
本发明涉及一种乙醇化噻托溴铵结晶及其制备方法和药物组合物。
The present invention relates to alcoholated tiotropium bromide crystal and its preparation process and medicine composition.
本发明涉及一种乙醇化噻托溴铵结晶及其制备方法和药物组合物。
The present invention relates to alcoholated tiotropium bromide crystal and its preparation process and medicine composition.
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