نتایج جستجو برای: immediate release

تعداد نتایج: 287164  

Journal: :Journal of pharmaceutical sciences 2006
E Jantratid S Prakongpan J B Dressman G L Amidon H E Junginger K K Midha D M Barends

Literature data relevant to the decision to allow a waiver of in vivo bioequivalence (BE) testing for the approval of immediate release (IR) solid oral dosage forms containing cimetidine are reviewed. According to the current Biopharmaceutics Classification System (BCS), cimetidine would be assigned to Class III. Cimetidine's therapeutic use and therapeutic index, its pharmacokinetic properties...

Journal: :Journal of pharmaceutical sciences 2010
G E Granero M R Longhi M J Mora H E Junginger K K Midha V P Shah S Stavchansky J B Dressman D M Barends

Literature and new experimental data relevant to the decision to allow a waiver of in vivo bioequivalence (BE) testing for the approval of immediate release (IR) solid oral dosage forms containing furosemide are reviewed. The available data on solubility, oral absorption, and permeability are sufficiently conclusive to classify furosemide into Class IV of the Biopharmaceutics Classification Sys...

2013
JR Valdizán-Usón A Cánovas-Martínez MT De Lucas-Taracena F Díaz-Atienza LS Eddy-Ives A Fernández-Jaén M Fernández-Pérez M García-Giral P García-Magán M Garraus-Oneca MA Idiazábal-Alecha M López-Benito G Lorenzo-Sanz J Martínez-Antón MA Martínez-Granero F Montañés-Rada F Mulas-Delgado G Ochando-Perales E Ortega-García A Pelaz-Antolín JA Ramos-Quiroga FC Ruiz-Sanz J Vaquerizo-Madrid A Yusta-Izquierdo

BACKGROUND The purpose of this multicenter Spanish study was to evaluate the response to immediate-release methylphenidate by children and adults diagnosed with attention-deficit/hyperactivity disorder (ADHD), as well as to obtain information on current therapy patterns and safety characteristics. METHODS This multicenter, observational, retrospective, noninterventional study included 730 pat...

2015
Krishna Devarakonda Kenneth Kostenbader Michael J Giuliani Jim L Young

OBJECTIVE To characterize the single-dose and steady-state pharmacokinetics (PK) of biphasic immediate-release/extended-release hydrocodone bitartrate/acetaminophen (IR/ER HB/APAP), IR HB/ibuprofen, and IR tramadol HCl/APAP. METHODS In this single-center, open-label, randomized, four-period crossover study, healthy participants received four treatments under fasted conditions: 1) a single dos...

2015
Martin Čulen Paweł K. Tuszyński Sebastian Polak Renata Jachowicz Aleksander Mendyk Jiří Dohnal

Different batches of atorvastatin, represented by two immediate release formulation designs, were studied using a novel dynamic dissolution apparatus, simulating stomach and small intestine. A universal dissolution method was employed which simulated the physiology of human gastrointestinal tract, including the precise chyme transit behavior and biorelevant conditions. The multicompartmental di...

Journal: :Journal of pharmaceutical sciences 2011
M E Olivera R H Manzo H E Junginger K K Midha V P Shah S Stavchansky J B Dressman D M Barends

Literature data relevant to the decision to allow a waiver of in vivo bioequivalence (BE) testing for the approval of new multisource and reformulated immediate release (IR) solid oral dosage forms containing ciprofloxacin hydrochloride as the only active pharmaceutical ingredient (API) are reviewed. Ciprofloxacin hydrochloride's solubility and permeability, its therapeutic use and index, pharm...

2014
Iruthayapandi Selestin Raja Nishter Nishad Fathima

Conventional studies on hydrogel properties such as viscosity, pH and swelling provide information without treating the components of hydrogel, viz., water and polymer individually. Water and hydrophilic polymers need to be studied individually to understand their relationship with each other to relate their influence on drug release. In this context, we have assigned the combination of porosit...

2012
Rajesh A. Keraliya Chirag Patel Pranav Patel Vipul Keraliya Tejal G. Soni Rajnikant C. Patel M. M. Patel

Conventional drug delivery systems are known to provide an immediate release of drug, in which one can not control the release of the drug and can not maintain effective concentration at the target site for longer time. Controlled drug delivery systems offer spatial control over the drug release. Osmotic pumps are most promising systems for controlled drug delivery. These systems are used for b...

1996
IAIN J. MCGILVERAY Iain J. McGilveray

Scientists from industry, academia, and the regulatory agencies met to discuss the role of dissolution tests with immediate release dosage forms. Dissolution is clearly important in formulation development and can provide evidence for later use in quality control. Regulatory agencies also need such information in assessing “change” in manufacture to decide when in vivo information would be requ...

2010
Scheubel Emmanuel Lindenberg Marc Beyssac Eric Cardot Jean-Michel

Standard compendia dissolution apparatus are the first choice for development of new dissolution methods. Nevertheless, limitations coming from the amount of material available, analytical sensitivity, lack of discrimination or biorelevance may warrant the use of non compendial methods. In this regard, the use of small volume dissolution methods offers strong advantages. The present study aims ...

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