Setting up multivariate specifications on critical raw material attributes to ensure consistent drug dissolution from high drug-load sustained-release matrix tablet-Reference-Cited by-同舟云学术

Setting up multivariate specifications on critical raw material attributes to ensure consistent drug dissolution from high drug-load sustained-release matrix tablet

Published:2018-09-03 Issue:11 Volume:44 Page:1733-1743
ISSN:0363-9045
Container-title:Drug Development and Industrial Pharmacy
language:en
Short-container-title:Drug Development and Industrial Pharmacy

Author:

Zhang Yi¹,Xu Bing¹²,Wang Xin¹,Dai Shengyun¹,Sun Fei¹,Ma Qun¹,Shi Xinyuan¹²,Qiao Yanjiang¹²

Affiliation:

1. Research Center of Chinese Medicine Information Engineering, Beijing University of Chinese Medicine, Beijing, PR China;

2. Beijing Key Laboratory of Chinese Medicine Manufacturing Process Control and Quality Evaluation, Beijing, PR China

Funder

National Natural Science Foundation of China

Publisher

Informa UK Limited

Subject

Organic Chemistry,Drug Discovery,Pharmaceutical Science,Pharmacology

Link

https://www.tandfonline.com/doi/pdf/10.1080/03639045.2018.1492608

Reference40 articles.

1. Attitude and perception of patients and health care practitioners toward oral sustained release dosage forms in Palestine

2. Hydrophilic thermoplastic polyurethanes for the manufacturing of highly dosed oral sustained release matrices via hot melt extrusion and injection molding

3. Pharmacokinetic profile of extended-release versus immediate-release oral naproxen sodium after single and multiple dosing under fed and fasting conditions: two randomized, open-label trials

4. Effect of crospovidone and hydroxypropyl cellulose on carbamazepine in high-dose tablet formulation

5. Controlling the hydration rate of a hydrophilic matrix in the core of an intravaginal ring determines antiretroviral release

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