نتایج جستجو برای: excipient

تعداد نتایج: 14233  

2012
Kevin Menard

mixtures strives to develop a product with good shelf life and that allows efficient dissolution by the end user with minimal change to the properties of the drug. One of the key properties used in the design of the formulations is the glass transition temperature, Tg, which must be sufficiently above the storage temperature to limit any degradation properties from occurring at significant rate...

Journal: :Biopolymers 2006
L A E Batista de Carvalho M Paula M Marques John Tomkinson

Ketoprofen (3-benzoyl-alpha-methylbenzeneacetic acid) is a widely used nonsteroidal anti-inflammatory drug (NSAID), always administered in the form of drug-excipient physical mixtures (PMs). The occurrence of possible interactions between ketoprofen and two commonly used excipients-lactose (LAC) and polyvinylpyrrolidone (PVP)-was evaluated, through vibrational spectroscopy techniques [both Rama...

2017
Qingguo Li Deen Huang Tiejun Lu Lei Xing Gary A. Leeke

a r t i c l e i n f o

2015
Harshal A. Pawar K. G. Lalitha

The objective of the present work was extraction of polysaccharide from Senna tora L. seed and its characterization as a pharmaceutical excipient. Polysaccharide extraction was based on mechanical separation of the endosperm of seeds of Senna tora, water dissolution, centrifugation, and precipitation with acetone. Standard procedures were used to study the viscosity, micromeritic properties, an...

2010
Rajendra Awasthi Garima Garg Vivek Pawar Gaurav Sharma Giriraj T Kulkarni

The tablets manufactured by direct compression method using co-processed excipient showed relatively better disintegration time and in vitro drug release, with omission of number of laborious steps as compared to tablets manufactured by conventional wet granulation method. Melt granulation technique is a potential alternative for the development of directly compressible adjuvants. Lactose and m...

Journal: :The journal of physical chemistry. B 2016
Esther Amstad Frans Spaepen David A Weitz

The bioavailability of hydrophobic drugs strongly increases if they are formulated as amorphous materials because the solubility of the amorphous phase is much higher than that of the crystal. Moreover, the stability of these particles against crystallization during storage increases with decreasing particle size. Hence, it is advantageous to formulate poorly water soluble drugs as amorphous na...

Journal: :Journal of pharmaceutical and biomedical analysis 2018
Gregory W Sluggett Todd Zelesky Evan M Hetrick Yelizaveta Babayan Steven W Baertschi

Accelerated stability studies of pharmaceutical products are commonly conducted at various combinations of temperature and relative humidity (RH). The RH of the sample environment can be controlled to set points using humidity-controlled stability chambers or via storage of the sample in a closed container in the presence of a saturated aqueous salt solution. Herein we report an unexpected N-ni...

Journal: :Journal of animal science 1989
R G Campbell N C Steele T J Caperna J P McMurtry M B Solomon A D Mitchell

Twenty-eight barrows were used to investigate the effects of exogenous porcine growth hormone (pGH) administration (0 and 100 micrograms.kg-1.d-1) between 30 and 60 kg on the subsequent and overall performance and carcass composition of pigs grown to 90 kg. The pGH was administered by daily i.m. injection and all pigs were fed one diet. Control animals were pair-fed to the intake noted for pGH-...

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