Pharmaceutical Machinery, Pharmaceutical formulations, Pharma Machinery, Tablet Filler Binders, Excipients and Drug formulation Pharmaceutical Machinery.
采购产品制药机械，制药配方，制药机械，片填料的粘合剂。
Patients should be strongly advised to visually inspect their tablets to verify that they are the correct drug and formulation each time they fill their prescription.
患者应该被强烈建议，每一次服用处方药，确实地检查他们的药片，确保这就是他们真正所需的药以及规格正确。
The formulation and drug-related biopharmaceutical aspects of these systems that govern oral absorption have been widely studied.
这些给药系统的口服制剂的组成和与药物相关的生物药剂学方面已经进行了广泛的研究。
The submitted drug product samples should be from a batch made with the proposed market formulation.
所递交的制剂样品必须是根据拟定的上市配方生产的。
The oral pharmaceutical formulation contains a core and a drug coating layer.
所述口服药物制剂含有核和药物涂层。
The invention employs the side effects of the opioid formulation to permit patients to self-limit drug intake, thereby avoiding toxicity while achieving analgesia.
本发明利用了该阿片样物质制剂的副作用使得患者可以自我限制药物摄入，从而在达到止痛效果的同时避免了中毒。
An opioid formulation for pulmonary administration in the treatment or management of pain, a pulmonary drug delivery device containing, method of administering, kit containing, and USES of same.
本发明涉及通过肺部施用治疗或控制疼痛的一种阿片样物质制剂、含该制剂的肺部药物递送装置、该制剂的施用方法、含该制剂的药盒及其用途。
The impact of polymorphism on characterization, bioavailability and formulation of drug were discussed.
讨论了药物多晶型对理化性质、生物利用度、相关制剂的影响。
The effects of PVP in formulation and freeze thawing steps on drug leakage and aggregation of tanshinone liposomes were investigated.
考察了聚乙烯吡咯烷酮(pvp)以及冻融处理对丹参酮脂质体的药物渗漏和微粒聚结特性的影响。
However, aerosol droplets were larger, total drug and mass outputs were lower and aerosolization performance was dependent on formulation.
然而，雾滴比较大，总的药品及质量产量比较低，并且雾化过程依赖于处方。
Objective To screen the formulation for tanshinone self-emulsifying drug delivery system (SEDDS) and evaluate its stability.
目的筛选丹参酮自乳化药物传递系统的处方，考察其稳定性。
CONCLUSION the adhesive property of the tablets and the release behavior of drug are relevant. Also, the formulation of buccal adhesive tablets is optimized by adjusting the composition.
结论口颊黏附片的生物黏附性与体外释药行为具有一定的相关性，通过调整处方可筛选出生物黏附性和体外释药均较理想的处方。
The formulation, technological characteristics, the superiority in drug dissolution and bioavailability of dispersible tablets are summarized.
分析了分散片的处方和工艺特点，及其在药物溶出度和生物利用度方面的优越性。
The preclinical study of it as lnd category new drug of China have been finished basically and the formulation has been patented.
本研究基本完成了国家一类新药制剂学部分的临床前资料，处方已申请专利。
Thermosensible gel formulation can prolong the nasal residence time of drug greatly except for the merits of traditional nasal preparation.
这种温敏凝胶剂除了具有一般鼻用制剂的优点以外，还可以明显延长药物在鼻腔的滞留时间。
Objective: To design the formulation of self emulsifying drug delivery system for silymarin and evaluate its dissolution.
目的：设计水飞蓟素自乳化系统处方并评价其溶出度。
Conclusion Coating floating beads made by Alginate-Na and liquid paraffin can be considered as a gastro-floating formulation releasing drug consistently and locally.
结论含液体石蜡的海藻酸钙小丸经包衣处理可以达到胃内漂浮和局部缓释药物的目的。
The factors that control the drug release character of the tablets were investigated. The drug release mechanism of the formulation was also studied.
分别考察了上述因素对于控释片体外释放度的影响以及药物释放机制。
The release mechanism, applicability, formulation ingredients of floating drug delivery system were summarized. And some new forms of this system were exemplified.
综述了胃漂浮片的释药机理、适用性、处方组成及制备中的关键影响因素等方面的内容，并列举一些新型剂型实例；综述。
Optimization of preparation and formulation was accomplished by evaluating the drug-loading amounts and the entrapment efficiency of luteolin liposomes.
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。
The characters, mechanism and formulation design of self emulsifying drug delivery system were reviewed. Its quality and affecting factors, and pharmaceutical applications were discussed.
对自我乳化药物传递系统的特点，形成机制，目前采用的处方组成等进行了综述，并对该系统的质量，影响因素及制剂学应用作了一般性介绍。
The new formulation provides more predictable and reliable drug absorption.
新的提法提供了更多的可预测和可靠的药物吸收。
Methods Orthogonal experiment was carried out to optimize the formulation. Several mathematic models were used to imitated the drug release.
方法采用正交试验法进行处方优化，用数学模型拟合释放曲线。
The USP tablet dissolution test is an analytical tool used for the verification of drug release processes and formulation selection within the pharmaceutical industry.
USP规定的片剂溶出试验被广泛用于医药工业中药物释放过程的验证和处方筛选。
The externally applied drug can be prepared into any externally applied formulation on the pharmacy.
它可以制备成任何一种药剂学上所说的外用剂型。
Effects of formulation of drug layer, push layer and membrane on the release behavior of controlled release tablets were investigated and the optimal formulation was obtained.
考察含药层促渗聚合物、乳糖用量、助推层聚氧乙烯用量、助推层氯化钠用量及包衣液中含水量、醋酸纤维素浓度对释放度的影响，并对处方进行优化。
Methods Orthogonal design was used to optimize the formulation of the tablets, and in vitro drug release was investigated with an UV method.
方法采用正交试验设计法对片剂处方进行筛选与优化，确定最佳处方并制备马来酸罗格列酮胃漂浮缓释片剂；
Conclusions The glipizide film-controlled sustained-release pellets were successfully prepared and the in-vitro drug release conformed to the requirements of the sustained-release formulation.
结论成功制备了膜控型格列吡嗪缓释微丸，体外释放符合缓释制剂要求。
Conclusions The glipizide film-controlled sustained-release pellets were successfully prepared and the in-vitro drug release conformed to the requirements of the sustained-release formulation.
结论成功制备了膜控型格列吡嗪缓释微丸，体外释放符合缓释制剂要求。
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