Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Mazen L. Hamad"'
Autor:
Harsh S. Shah, Mazen L. Hamad, Kaushalendra Chaturvedi, Kenneth R. Morris, Simon Bates, Ajaz S. Hussain
Publikováno v:
AAPS PharmSciTech. 20
Levothyroxine sodium pentahydrate (LEVO) tablets have been on the US market since the mid-twentieth century and remain the most highly prescribed product. Unfortunately, levothyroxine sodium tablets have also been one of the most highly recalled prod
Publikováno v:
Journal of Pharmaceutical and Biomedical Analysis. 56:944-949
Fusing complex data from two disparate sources has been demonstrated to improve the accuracy in quantifying active ingredients in mixtures of pharmaceutical powders. A four-component simplex-centroid design was used to prepare blended powder mixtures
Publikováno v:
Chemical Engineering Science. 65:5625-5638
Understanding the properties and behavior of pharmaceutical materials is critical to the design of a safe and effective dosage form. The desired performance of pharmaceutical products differs from other areas of engineered material products. With pha
Publikováno v:
The Journal of Nutrition. 139:1783S-1787S
As described in this Supplement and elsewhere, consumption of grapes or grape products has been associated with various health benefits. Resveratrol is a unique component of grapes. Following our report on potential cancer chemopreventive activity, t
Publikováno v:
AAPS PharmSciTech. 10:500-504
The purpose of this work was to evaluate and compare the functionality of bovine fatty acids-derived (MgSt-B) and vegetable fatty acids-derived (MgSt-V) magnesium stearate powders when used for the lubrication of granules prepared by high-shear (HSG)
Autor:
Mazen L. Hamad, Alan S. Carlin, Ruyi He, Mansoor A. Khan, Mónica I. Pagán Motta, Y. Watanuki, E.E. Pinnow, Patrick J. Faustino, Yongsheng Yang
Publikováno v:
Journal of Women's Health. 18:303-310
This study aimed to track the inclusion of women in clinical trials for new drugs approved by the Food and Drug Administration (FDA) between 2000 and 2002 and to evaluate the extent of analyses by sex.Data were extracted from FDA reviewers' reports,
Autor:
Robbe C. Lyon, Mansoor A. Khan, Vilayat A. Sayeed, Abhay Gupta, Mazen L. Hamad, Rakhi B. Shah
Publikováno v:
Journal of Pharmaceutical Sciences. 97:5328-5340
Magnesium stearate is a functional excipient used to ensure efficient ejection of tablets. This study compares the functionality of a vegetable and bovine grade of magnesium stearate. Tablets were prepared by direct compression and dry granulation of
Publikováno v:
Journal of Pharmaceutical Sciences. 96:3390-3401
Traditional monitoring of pharmaceutical manufacturing combines physical sampling and analytical methodologies (e.g. HPLC). Process analytical technology (PAT) can be implemented to collect real-time measurements, although successful monitoring requi
Autor:
Jaroon Jakmunee, Yuthapong Udnan, Sumalee Tanikkul, Bryan J. Prazen, Robert E. Synovec, Kate Grudpan, Narong Lenghor, Bethany A. Staggemeier, Mazen L. Hamad
Publikováno v:
Talanta. 65:722-729
Design and development of a dynamic interfacial pressure detector (DIPD) is reported. The DIPD measures the differential pressure as a function of time across the liquid-liquid interface of organic liquid drops (i.e., n-hexane) that repeatedly grow i
Autor:
Mazen L. Hamad
Publikováno v:
Journal of Chemical Education. 90:1662-1664
Dissolution testing is a quantitative analytical technique used to measure the release rate of ingredients from tablets and capsules. This instrumental analysis lab experiment teaches students how to compress tablets from a mixture of powders and cha