• 目的:制备微泡型口腔

    AIM: To develop the micro-effervescing fast-release oral tablet.

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  • 试验研究释片机理

    The release mechanism was investigated through the dissolution tests.

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  • 目的制备别嘌醇释片探讨机理

    Objective To prepare the allopurinol sustained-release tablets and study the release mechanism.

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  • 目的制备药特征皮酚缓释片

    Objective: To prepare Paeonol Sustained-release Tablets of zero order release.

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  • 目的:研制马尼地平释片考察机制

    Objective: To prepare manidipine sustained-release tablets and to investigate the release mechanism.

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  • 结果制备杨宁渗透释片体外速度平稳

    Results:Preparation of Huangyangning osmotic pump controlled release tablets in vitro release rate of more stable.

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  • 结论黄杨宁缓释片好的作用药以扩散为主

    Conclusion HSRT have a better release effect in the test condition and its release is in a way of diffusion mainly.

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  • 结果:该处方、制备工艺简单体外符合释片的规律。

    RESULTS Prescription and process are simple and the in vitro drug released complied with relevant requirement.

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  • 目的建立罗通定释片体外测定方法评价体外行为

    Objective to establish a UV method to determine the release degree of rotundine sustained-release tablets and to evaluate its in-vitro release behavior.

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  • 结论单层渗透释片工艺稳定明显零级特征

    Conclusion The drug release of sodium ferulate single-layer osmotic pump controlled release tablets is stable and had obvious characteristic of zero release.

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  • 目的以羟丙甲基纤维素骨架材料制得灯盏素缓释片机制进行探讨

    OBJECTIVE Breviscapine sustained-release tablets(BST)were formulated with hydroxypropyl-methylcellulose as the matrix material and the release mechanism of the tablets was studied.

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  • 结论盐酸氨溴索渗透释片稳定药明显,具备优良制剂的特征。

    Conclusions: The ambroxol HCl osmotic pump controlled release tablets have a stable release curve and conform to zero release order.

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  • 目的建立复方丹参释片多指标成分体外测定方法评价体外行为

    Objective: to develop the methods to determine the in vitro release of multi-target ingredients in Compound Danshen Sustained-release Tablets and to evaluate its release behavior in vitro.

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  • 亲水凝胶骨架释片过程转变过程、凝胶屏障及区域前沿移动行为密切相关

    The phase transition, barrier function and front movement of the gel layer are closely related to drug release process of hydrophlic gel matrix sustained-release tablets.

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  • 结论联合应用不同黏度用量HPMC制备具有理想行为布洛芬骨架释片

    Conclusions Ibuprofen sustained release tablets with ideal release behavior could be prepared by selecting HPMC with different viscosity and adjusting the content of HPMC.

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  • 结果表明,制的酒石酸美托洛尔释片具有明显的缓作用,体外符合一级动力学规律

    The results indicated that the sustained-release tablets had an expected sustained-release quality, and drug release pattern was in accorded with the first order kinetics.

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  • 结论两种制剂生物等效性,且释片有峰浓度差异、血药浓度波动幅度小特点。

    CONCLUSION: The two formulations were bioequivalent and the sustained release tablet showed smaller difference between C max and C min and smaller DF compared with the ordinary tablet.

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  • 弹簧中间部分撕裂成若干个指针大小般的充当回力力)杠杆

    The center portion of the diaphragm spring is slit into numerous fingers that act as release levers .

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  • 目的制备度米渗透,以控制体外药维持零级达80%以上。

    Objective To prepare Domiphen osmotic tablets of zero release above 80% in vitro.

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  • 结论通过选择中的崩解剂、调整包衣层组成厚度可以用包衣方法得到不同时间脉冲药的阿司匹林剂。

    Conclusion: the pulsatile release of aspirin can be controlled by selection of disintegrants of the core and changing composition and thickness of the coating film.

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  • 结论黏附生物黏附性体外行为具有一定相关性通过调整处方可筛选出生物黏附性和体外药均较理想的处方。

    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.

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  • 目的以对乙酰氨基酚(扑热息痛)模型药物制备新型口服剂型口腔崩解

    OBJECTIVE To develop a novel rapidly release oral solid dosage form orally disintegrating tablet using acetaminophen as the model drug.

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  • 目的研制三七总皂苷生物黏附考察体外动力学离体肠黏膜的黏附

    OBJECTIVE To prepare the Panax Notoginseng Saponines (PNS) bioadhesive tablets, and to study their release kinetics and bioadhesive tablets force to rabbit small intestine in vitro.

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  • 目的制备酒石酸托特罗定渗透考察体外药特性。

    OBJECTIVE to prepare the tolterodine osmotic pump tablet and study its release profiles in vitro.

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  • 目的优化银杏叶分散处方,制备中药口服固体速制剂。

    Objective: To optimize the formulation of the Ginkgobiloba immediate release tablet.

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  • 介绍TLD-3500热光读出器GR-100M型热剂量构成探测器脉冲X射线辐射参数测量中的应用

    This paper introduces the application of thermoluminescence dosimeter(TLD) which composed by TLD3500 reader and GR100M chips on the measurement of hard Xray pulse energy spectrum.

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  • 优选那格列奈盐酸二甲双组成的双层处方

    To optimize the formula of the double-layer tablet of nateglinide rapid-release layer and metformin hydrochloride sustained-release layer.

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  • 综述了胃漂浮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。

    The release mechanism, applicability, formulation ingredients of floating drug delivery system were summarized. And some new forms of this system were exemplified.

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  • 目的:解决硫酸沙丁胺醇延迟定时药问题。

    Objective:To Study the preparation and dissolution in vitro of salbutamol sulfate delayed -release tablets.

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  • 目的考察芦丁骨架机制影响因素

    Objective: to study the factors influencing the release mechanism of rutin from sustained release matrix tablets.

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