Výsledky vyhledávání - "Jantratid, E."

Akademický článek

Biowaiver Monographs for Immediate Release Solid Oral Dosage Forms: Mefloquine Hydrochloride

Autor: Strauch, S., Jantratid, E. ^*, Dressman, J.B., Junginger, H.E., Kopp, S., Midha, K.K., Shah, V.P., Stavchansky, S., Barends, D.M.

Publikováno v: In Journal of Pharmaceutical Sciences January 2011 100(1):11-21

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Akademický článek

Biowaiver monographs for immediate release solid oral dosage forms: Doxycycline hyclate

Autor: Jantratid, E., Strauch, S., Becker, C., Dressman, J.B., Amidon, G.L., Junginger, H.E., Kopp, S., Midha, K.K., Shah, V.P., Stavchansky, S., Barends, D.M. ^*

Publikováno v: In Journal of Pharmaceutical Sciences April 2010 99(4):1639-1653

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The quantitation of atorvastatin in human plasma by solid phase micro-extraction followed by LC-MS/MS and its application to pharmacokinetics study

Autor: Rukthong, P., Polkit Sangvanich, Kitchaiya, S., Jantratid, E., Sathirakul, K.

Publikováno v: Songklanakarin Journal of Science and Technology (SJST), Vol 35, Iss 1, Pp 41-50 (2013)
Scopus-Elsevier

Determination of atorvastatin in human plasma using LC-MS/MS has been widely accepted as an effective methodowing to its practical applicability in routine drug analysis in pharmacokinetic and pharmacogenetic study. Nevertheless, themethod sensitivit

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::c09e65569ae17b8d45a1b2b2af9ca78e
http://rdo.psu.ac.th/sjstweb/journal/35-1/35-1-41-50.pdf

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Predicting the oral absorption of a poorly soluble, poorly permeable weak base using biorelevant dissolution and transfer model tests coupled with a physiologically based pharmacokinetic model

Autor: Wagner, C. Jantratid, E. Kesisoglou, F. Vertzoni, M. Reppas, C. B. Dressman, J.

For predicting food effects and simulating plasma profiles of poorly soluble drugs, physiologically based pharmacokinetic models have become a widely accepted tool in academia and the pharmaceutical industry. Up till now, however, simulations appeari

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2127::1f7f4a94dc93ac913cefe3405ac8458c
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3061412

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Biorelevant in vitro dissolution testing of products containing micronized or nanosized fenofibrate with a view to predicting plasma profiles

Autor: Juenemann, D. Jantratid, E. Wagner, C. Reppas, C. Vertzoni, M. Dressman, J.B.

The ability of in vitro biorelevant dissolution tests to predict the in vivo performance of nanosized fenofibrate (Lipidil 145 ONE®) and microsized fenofibrate (Lipidil - Ter®) was evaluated in this study. In vitro dissolution was carried out using

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2127::1b515dccb918fafd1bd335dc7a8fac3d
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3061769

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Forecasting in vivo oral absorption and food effect of micronized and nanosized aprepitant formulations in humans

Autor: Shono, Y. Jantratid, E. Kesisoglou, F. Reppas, C. Dressman, J.B.

This study coupled results from biorelevant dissolution tests with in silico simulation technology to forecast in vivo oral absorption of micronized and nanosized aprepitant formulations in the pre- and post-prandial states. In vitro dissolution test

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2127::290c607ab2b0657eb1139bfbbba3bd20
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3061858

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Application of biorelevant dissolution tests to the prediction of in vivo performance of diclofenac sodium from an oral modified-release pellet dosage form

Autor: Jantratid, E. De Maio, V. Ronda, E. Mattavelli, V. Vertzoni, M. Dressman, J.B.

In vitro biorelevant dissolution tests enabling the prediction of in vivo performance of an oral modified-release (MR) dosage form were developed in this study. In vitro dissolution of MR diclofenac sodium pellets containing 100 mg active ingredient

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2127::e8e041e0525ba27a7d0a2ee1938f512e
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3062107

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Prediction of food effects on the absorption of celecoxib based on biorelevant dissolution testing coupled with physiologically based pharmacokinetic modeling

Autor: Shono, Y. Jantratid, E. Janssen, N. Kesisoglou, F. Mao, Y. Vertzoni, M. Reppas, C. Dressman, J.B.

Since the rate-determining step to the intestinal absorption of poorly soluble drugs is the dissolution in the gastrointestinal (GI) tract, postprandial changes in GI physiology, in addition to any specific interactions between drug and food, are exp

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2127::adb14c9cdbe35302afbe19b12a524eb9
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3062060

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Akademický článek

COMMENTARY: Biowaiver Monographs for Immediate Release Solid Oral Dosage Forms: Lamivudine

Autor: Strauch, S., Jantratid, E., Dressman, J.B., Junginger, H.E., Kopp, S., Midha, K.K., Shah, V.P., Stavchansky, S., Barends, D.M. ^*

Publikováno v: In Journal of Pharmaceutical Sciences June 2011 100(6):2054-2063

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Dissolution media simulating conditions in the proximal human gastrointestinal tract: An update

Autor: Jantratid, E. Janssen, N. Reppas, C. Dressman, J.B.

Purpose. The aim of this study was to update the compositions of biorelevant media to represent the composition and physical chemical characteristics of the gastrointestinal fluids as closely as possible while providing physical stability during diss

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2127::6f03acc9aae73568f8ca92cc1199d1d7
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3062360

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