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Assessment of Dosage Forms In Vitro
1988This chapter presents descriptions of some in vitro tests which can be applied to pharmaceutical products, using some of the background physical chemistry discussed in other chapters. In particular, we will examine the influence of some of the key parameters of pharmaceutical systems, such as particle size, viscosity, adhesion or formulation in general
A. T. Florence, D. Attwood
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Evaluation of Dosage Forms. IV. Studies on Commercial Phenylbutazone Tablet Dosage Forms
Drug Development and Industrial Pharmacy, 1998In order to determine the feasibility of dissolution-dialysis as a suitable technique for in vitro evaluation, studies on commercial phenylbutazone tablets were carried out. Although disintegration time and dissolution parameters did not give a true indication of bioavailability, an excellent correlation was obtained between the dialysis rate constant (
B, Razdan, A R, Paradkar
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Dosage forms are the means by which drug molecules are delivered to sites of action within the body. They are essential for ensuring the safe, effective, and controlled delivery of medication to achieve the desired therapeutic effect. The introduction to dosage forms encompasses a wide range of formulations designed to meet various medical needs and ...
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International Journal of Clinical Pharmacy, 2020
Aida Sefidani Forough +6 more
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Aida Sefidani Forough +6 more
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The prominence of the dosage form design to treat ocular diseases.
International journal of pharmaceutics, 2020P. M. Campos, R. Petrilli, R. Lopez
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American Cancer Society nutrition and physical activity guideline for cancer survivors
Ca-A Cancer Journal for Clinicians, 2022Cheryl L Rock +2 more
exaly
European Journal of Pharmaceutical Sciences, 2018
C. Gioumouxouzis +6 more
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C. Gioumouxouzis +6 more
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