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You searched for subject:(PBPK). Showing records 1 – 30 of 68 total matches.

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University of Georgia

1. Crowell, Susan Ritger. Integration of experimental and computational approaches to physiologically based pharmacokinetic modeling of triadimefon and triadimenol.

Degree: PhD, Toxicology, 2009, University of Georgia

 A physiologically based pharmacokinetic (PBPK) model was experimentally parameterized and constructed for the conazole fungicides triadimefon and triadimenol. In vitro metabolic parameters for reduction of… (more)

Subjects/Keywords: PBPK

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Crowell, S. R. (2009). Integration of experimental and computational approaches to physiologically based pharmacokinetic modeling of triadimefon and triadimenol. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/crowell_susan_r_200912_phd

Chicago Manual of Style (16th Edition):

Crowell, Susan Ritger. “Integration of experimental and computational approaches to physiologically based pharmacokinetic modeling of triadimefon and triadimenol.” 2009. Doctoral Dissertation, University of Georgia. Accessed October 21, 2019. http://purl.galileo.usg.edu/uga_etd/crowell_susan_r_200912_phd.

MLA Handbook (7th Edition):

Crowell, Susan Ritger. “Integration of experimental and computational approaches to physiologically based pharmacokinetic modeling of triadimefon and triadimenol.” 2009. Web. 21 Oct 2019.

Vancouver:

Crowell SR. Integration of experimental and computational approaches to physiologically based pharmacokinetic modeling of triadimefon and triadimenol. [Internet] [Doctoral dissertation]. University of Georgia; 2009. [cited 2019 Oct 21]. Available from: http://purl.galileo.usg.edu/uga_etd/crowell_susan_r_200912_phd.

Council of Science Editors:

Crowell SR. Integration of experimental and computational approaches to physiologically based pharmacokinetic modeling of triadimefon and triadimenol. [Doctoral Dissertation]. University of Georgia; 2009. Available from: http://purl.galileo.usg.edu/uga_etd/crowell_susan_r_200912_phd


University of Manchester

2. Salem, Farzaneh. APPLICATIONS OF PHYSIOLOGICALLY BASED PHARMACOKINETIC MODELLING TO PREDICTION OF THE LIKELIHOOD OF METABOLIC DRUG INTERACTIONS IN PAEDIATRIC POPULATION AND STUDYING DISPARITIES IN PHARMACOKINETICS BETWEEN CHILDREN AND ADULTS.

Degree: 2014, University of Manchester

 Anticipation of drug-drug interactions (DDIs) in the paediatric population are merely based on data generated in adults. Hence decision on avoiding certain combinations or attempts… (more)

Subjects/Keywords: Paediatric; PBPK

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APA (6th Edition):

Salem, F. (2014). APPLICATIONS OF PHYSIOLOGICALLY BASED PHARMACOKINETIC MODELLING TO PREDICTION OF THE LIKELIHOOD OF METABOLIC DRUG INTERACTIONS IN PAEDIATRIC POPULATION AND STUDYING DISPARITIES IN PHARMACOKINETICS BETWEEN CHILDREN AND ADULTS. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:225622

Chicago Manual of Style (16th Edition):

Salem, Farzaneh. “APPLICATIONS OF PHYSIOLOGICALLY BASED PHARMACOKINETIC MODELLING TO PREDICTION OF THE LIKELIHOOD OF METABOLIC DRUG INTERACTIONS IN PAEDIATRIC POPULATION AND STUDYING DISPARITIES IN PHARMACOKINETICS BETWEEN CHILDREN AND ADULTS.” 2014. Doctoral Dissertation, University of Manchester. Accessed October 21, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:225622.

MLA Handbook (7th Edition):

Salem, Farzaneh. “APPLICATIONS OF PHYSIOLOGICALLY BASED PHARMACOKINETIC MODELLING TO PREDICTION OF THE LIKELIHOOD OF METABOLIC DRUG INTERACTIONS IN PAEDIATRIC POPULATION AND STUDYING DISPARITIES IN PHARMACOKINETICS BETWEEN CHILDREN AND ADULTS.” 2014. Web. 21 Oct 2019.

Vancouver:

Salem F. APPLICATIONS OF PHYSIOLOGICALLY BASED PHARMACOKINETIC MODELLING TO PREDICTION OF THE LIKELIHOOD OF METABOLIC DRUG INTERACTIONS IN PAEDIATRIC POPULATION AND STUDYING DISPARITIES IN PHARMACOKINETICS BETWEEN CHILDREN AND ADULTS. [Internet] [Doctoral dissertation]. University of Manchester; 2014. [cited 2019 Oct 21]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:225622.

Council of Science Editors:

Salem F. APPLICATIONS OF PHYSIOLOGICALLY BASED PHARMACOKINETIC MODELLING TO PREDICTION OF THE LIKELIHOOD OF METABOLIC DRUG INTERACTIONS IN PAEDIATRIC POPULATION AND STUDYING DISPARITIES IN PHARMACOKINETICS BETWEEN CHILDREN AND ADULTS. [Doctoral Dissertation]. University of Manchester; 2014. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:225622

3. Salem, Farzaneh. Applications of physiologically based pharmacokinetic modelling to prediction of the likelihood of metabolic drug interactions in paediatric population and studying disparities in pharmacokinetics between children and adults.

Degree: PhD, 2014, University of Manchester

 Anticipation of drug-drug interactions (DDIs) in the paediatric population are merely based on data generated in adults. Hence decision on avoiding certain combinations or attempts… (more)

Subjects/Keywords: 615.7; Paediatric; PBPK

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APA (6th Edition):

Salem, F. (2014). Applications of physiologically based pharmacokinetic modelling to prediction of the likelihood of metabolic drug interactions in paediatric population and studying disparities in pharmacokinetics between children and adults. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/applications-of-physiologically-based-pharmacokinetic-modelling-to-prediction-of-the-likelihood-of-metabolic-drug-interactions-in-paediatric-population-and-studying-disparities-in-pharmacokinetics-between-children-and-adults(1fdefe9a-037a-4738-b92a-5904a60960db).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.617991

Chicago Manual of Style (16th Edition):

Salem, Farzaneh. “Applications of physiologically based pharmacokinetic modelling to prediction of the likelihood of metabolic drug interactions in paediatric population and studying disparities in pharmacokinetics between children and adults.” 2014. Doctoral Dissertation, University of Manchester. Accessed October 21, 2019. https://www.research.manchester.ac.uk/portal/en/theses/applications-of-physiologically-based-pharmacokinetic-modelling-to-prediction-of-the-likelihood-of-metabolic-drug-interactions-in-paediatric-population-and-studying-disparities-in-pharmacokinetics-between-children-and-adults(1fdefe9a-037a-4738-b92a-5904a60960db).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.617991.

MLA Handbook (7th Edition):

Salem, Farzaneh. “Applications of physiologically based pharmacokinetic modelling to prediction of the likelihood of metabolic drug interactions in paediatric population and studying disparities in pharmacokinetics between children and adults.” 2014. Web. 21 Oct 2019.

Vancouver:

Salem F. Applications of physiologically based pharmacokinetic modelling to prediction of the likelihood of metabolic drug interactions in paediatric population and studying disparities in pharmacokinetics between children and adults. [Internet] [Doctoral dissertation]. University of Manchester; 2014. [cited 2019 Oct 21]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/applications-of-physiologically-based-pharmacokinetic-modelling-to-prediction-of-the-likelihood-of-metabolic-drug-interactions-in-paediatric-population-and-studying-disparities-in-pharmacokinetics-between-children-and-adults(1fdefe9a-037a-4738-b92a-5904a60960db).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.617991.

Council of Science Editors:

Salem F. Applications of physiologically based pharmacokinetic modelling to prediction of the likelihood of metabolic drug interactions in paediatric population and studying disparities in pharmacokinetics between children and adults. [Doctoral Dissertation]. University of Manchester; 2014. Available from: https://www.research.manchester.ac.uk/portal/en/theses/applications-of-physiologically-based-pharmacokinetic-modelling-to-prediction-of-the-likelihood-of-metabolic-drug-interactions-in-paediatric-population-and-studying-disparities-in-pharmacokinetics-between-children-and-adults(1fdefe9a-037a-4738-b92a-5904a60960db).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.617991


University of Manchester

4. Tsamandouras, Nikolaos. Development and applications of physiologically-based pharmacokinetic models for population data analyses.

Degree: 2015, University of Manchester

 Physiologically-based pharmacokinetic (PBPK) modelling is traditionally employed to predict drug concentration-time profiles in plasma and tissues using information from physiology / biology, in vitro experiments… (more)

Subjects/Keywords: PBPK modelling; population pharmacokinetics; simvastatin

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APA (6th Edition):

Tsamandouras, N. (2015). Development and applications of physiologically-based pharmacokinetic models for population data analyses. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:260385

Chicago Manual of Style (16th Edition):

Tsamandouras, Nikolaos. “Development and applications of physiologically-based pharmacokinetic models for population data analyses.” 2015. Doctoral Dissertation, University of Manchester. Accessed October 21, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:260385.

MLA Handbook (7th Edition):

Tsamandouras, Nikolaos. “Development and applications of physiologically-based pharmacokinetic models for population data analyses.” 2015. Web. 21 Oct 2019.

Vancouver:

Tsamandouras N. Development and applications of physiologically-based pharmacokinetic models for population data analyses. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2019 Oct 21]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:260385.

Council of Science Editors:

Tsamandouras N. Development and applications of physiologically-based pharmacokinetic models for population data analyses. [Doctoral Dissertation]. University of Manchester; 2015. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:260385

5. Ball, Kathryn. Physiologically based pharmacokinetic modelling of the central nervous system : strategies for drug development : Des modèles pharmacocinétiques basés sur la physiologie du système nerveux central : stratégies lors du développement du médicament.

Degree: Docteur es, Pharmacocinétique, 2014, Université Paris Descartes – Paris V

 Une étape critique au cours du développement de médicaments est la mesure ou la prédiction des concentrations du médicament dans un tissu cible, qui peuvent… (more)

Subjects/Keywords: PBPK; SNC; BHE; Modélisation; Pharmacocinétique; PBPK; CNS; BBB; Modeling; Pharmacokinetics; 615.7

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APA (6th Edition):

Ball, K. (2014). Physiologically based pharmacokinetic modelling of the central nervous system : strategies for drug development : Des modèles pharmacocinétiques basés sur la physiologie du système nerveux central : stratégies lors du développement du médicament. (Doctoral Dissertation). Université Paris Descartes – Paris V. Retrieved from http://www.theses.fr/2014PA05P630

Chicago Manual of Style (16th Edition):

Ball, Kathryn. “Physiologically based pharmacokinetic modelling of the central nervous system : strategies for drug development : Des modèles pharmacocinétiques basés sur la physiologie du système nerveux central : stratégies lors du développement du médicament.” 2014. Doctoral Dissertation, Université Paris Descartes – Paris V. Accessed October 21, 2019. http://www.theses.fr/2014PA05P630.

MLA Handbook (7th Edition):

Ball, Kathryn. “Physiologically based pharmacokinetic modelling of the central nervous system : strategies for drug development : Des modèles pharmacocinétiques basés sur la physiologie du système nerveux central : stratégies lors du développement du médicament.” 2014. Web. 21 Oct 2019.

Vancouver:

Ball K. Physiologically based pharmacokinetic modelling of the central nervous system : strategies for drug development : Des modèles pharmacocinétiques basés sur la physiologie du système nerveux central : stratégies lors du développement du médicament. [Internet] [Doctoral dissertation]. Université Paris Descartes – Paris V; 2014. [cited 2019 Oct 21]. Available from: http://www.theses.fr/2014PA05P630.

Council of Science Editors:

Ball K. Physiologically based pharmacokinetic modelling of the central nervous system : strategies for drug development : Des modèles pharmacocinétiques basés sur la physiologie du système nerveux central : stratégies lors du développement du médicament. [Doctoral Dissertation]. Université Paris Descartes – Paris V; 2014. Available from: http://www.theses.fr/2014PA05P630

6. Tsamandouras, Nikolaos. Development and applications of physiologically-based pharmacokinetic models for population data analyses.

Degree: PhD, 2015, University of Manchester

 Physiologically-based pharmacokinetic (PBPK) modelling is traditionally employed to predict drug concentration-time profiles in plasma and tissues using information from physiology/biology, in vitro experiments and in… (more)

Subjects/Keywords: 615.7; PBPK modelling; population pharmacokinetics; simvastatin

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Tsamandouras, N. (2015). Development and applications of physiologically-based pharmacokinetic models for population data analyses. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/development-and-applications-of-physiologicallybased-pharmacokinetic-models-for-population-data-analyses(5793d86f-75e4-4ed9-89ec-b93e9bc6b2e6).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.686748

Chicago Manual of Style (16th Edition):

Tsamandouras, Nikolaos. “Development and applications of physiologically-based pharmacokinetic models for population data analyses.” 2015. Doctoral Dissertation, University of Manchester. Accessed October 21, 2019. https://www.research.manchester.ac.uk/portal/en/theses/development-and-applications-of-physiologicallybased-pharmacokinetic-models-for-population-data-analyses(5793d86f-75e4-4ed9-89ec-b93e9bc6b2e6).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.686748.

MLA Handbook (7th Edition):

Tsamandouras, Nikolaos. “Development and applications of physiologically-based pharmacokinetic models for population data analyses.” 2015. Web. 21 Oct 2019.

Vancouver:

Tsamandouras N. Development and applications of physiologically-based pharmacokinetic models for population data analyses. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2019 Oct 21]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/development-and-applications-of-physiologicallybased-pharmacokinetic-models-for-population-data-analyses(5793d86f-75e4-4ed9-89ec-b93e9bc6b2e6).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.686748.

Council of Science Editors:

Tsamandouras N. Development and applications of physiologically-based pharmacokinetic models for population data analyses. [Doctoral Dissertation]. University of Manchester; 2015. Available from: https://www.research.manchester.ac.uk/portal/en/theses/development-and-applications-of-physiologicallybased-pharmacokinetic-models-for-population-data-analyses(5793d86f-75e4-4ed9-89ec-b93e9bc6b2e6).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.686748


University of Washington

7. Zhang, Zufei. Predicting Maternal-Fetal Disposition of Drugs Using In Vitro and In Silico Tools.

Degree: PhD, 2017, University of Washington

 During pregnancy, physiological and ADMET changes in the maternal-fetal dyad can significantly alter drug pharmacokinetics (PK) in the mother and may necessitate dosing regimen adjustments.… (more)

Subjects/Keywords: CYP3A; fetal; PBPK; Pharmacokinetics; Pharmaceutical sciences; Pharmaceutics

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APA (6th Edition):

Zhang, Z. (2017). Predicting Maternal-Fetal Disposition of Drugs Using In Vitro and In Silico Tools. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/38672

Chicago Manual of Style (16th Edition):

Zhang, Zufei. “Predicting Maternal-Fetal Disposition of Drugs Using In Vitro and In Silico Tools.” 2017. Doctoral Dissertation, University of Washington. Accessed October 21, 2019. http://hdl.handle.net/1773/38672.

MLA Handbook (7th Edition):

Zhang, Zufei. “Predicting Maternal-Fetal Disposition of Drugs Using In Vitro and In Silico Tools.” 2017. Web. 21 Oct 2019.

Vancouver:

Zhang Z. Predicting Maternal-Fetal Disposition of Drugs Using In Vitro and In Silico Tools. [Internet] [Doctoral dissertation]. University of Washington; 2017. [cited 2019 Oct 21]. Available from: http://hdl.handle.net/1773/38672.

Council of Science Editors:

Zhang Z. Predicting Maternal-Fetal Disposition of Drugs Using In Vitro and In Silico Tools. [Doctoral Dissertation]. University of Washington; 2017. Available from: http://hdl.handle.net/1773/38672


University of Manchester

8. Harwood, Matthew Dillston. Towards a fully mechanistic prediction of oral drug absorption: Investigating intestinal transporter abundance and function relationships.

Degree: 2015, University of Manchester

 Background: Elucidating the role of intestinal drug transporter function in drug development is crucial, as transporter proteins can impact on drug absorption, efficacy and adverse… (more)

Subjects/Keywords: Transporter proteins; PBPK-IVIVE; Intestine; Absolute Abundance

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APA (6th Edition):

Harwood, M. D. (2015). Towards a fully mechanistic prediction of oral drug absorption: Investigating intestinal transporter abundance and function relationships. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:265614

Chicago Manual of Style (16th Edition):

Harwood, Matthew Dillston. “Towards a fully mechanistic prediction of oral drug absorption: Investigating intestinal transporter abundance and function relationships.” 2015. Doctoral Dissertation, University of Manchester. Accessed October 21, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:265614.

MLA Handbook (7th Edition):

Harwood, Matthew Dillston. “Towards a fully mechanistic prediction of oral drug absorption: Investigating intestinal transporter abundance and function relationships.” 2015. Web. 21 Oct 2019.

Vancouver:

Harwood MD. Towards a fully mechanistic prediction of oral drug absorption: Investigating intestinal transporter abundance and function relationships. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2019 Oct 21]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:265614.

Council of Science Editors:

Harwood MD. Towards a fully mechanistic prediction of oral drug absorption: Investigating intestinal transporter abundance and function relationships. [Doctoral Dissertation]. University of Manchester; 2015. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:265614

9. Real, Ivan Manuel Reis Sousa. A importância dos parâmetros farmacocinéticos na terapêutica individualizada.

Degree: 2016, RCAAP

Dissertação para obtenção do grau de Mestre no Instituto Superior de Ciências da Saúde Egas Moniz

A terapêutica individualizada é um procedimento que separa os… (more)

Subjects/Keywords: Terapêutica individualizada; Farmacocinética; PBPK; Doenças órfãs

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APA (6th Edition):

Real, I. M. R. S. (2016). A importância dos parâmetros farmacocinéticos na terapêutica individualizada. (Thesis). RCAAP. Retrieved from https://www.rcaap.pt/detail.jsp?id=oai:comum.rcaap.pt:10400.26/17606

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Real, Ivan Manuel Reis Sousa. “A importância dos parâmetros farmacocinéticos na terapêutica individualizada.” 2016. Thesis, RCAAP. Accessed October 21, 2019. https://www.rcaap.pt/detail.jsp?id=oai:comum.rcaap.pt:10400.26/17606.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Real, Ivan Manuel Reis Sousa. “A importância dos parâmetros farmacocinéticos na terapêutica individualizada.” 2016. Web. 21 Oct 2019.

Vancouver:

Real IMRS. A importância dos parâmetros farmacocinéticos na terapêutica individualizada. [Internet] [Thesis]. RCAAP; 2016. [cited 2019 Oct 21]. Available from: https://www.rcaap.pt/detail.jsp?id=oai:comum.rcaap.pt:10400.26/17606.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Real IMRS. A importância dos parâmetros farmacocinéticos na terapêutica individualizada. [Thesis]. RCAAP; 2016. Available from: https://www.rcaap.pt/detail.jsp?id=oai:comum.rcaap.pt:10400.26/17606

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

10. Cartiser, Nathalie. Intérêts et limites de l'analyse de la moelle osseuse en toxicologie médicolégale : contribution à l'interprétation quantitative des concentrations médullaires : Interests and limits of bone marrow analysis in forensic toxicology : contribution to quantitative interpretation of bone marrow concentrations.

Degree: Docteur es, Chimie analytique. Toxicologie médicolégale, 2011, Université Claude Bernard – Lyon I

L'objectif de cette thèse était de faire le point sur la place de l'analyse de la moelle osseuse (MO) en tant que matrice alternative au… (more)

Subjects/Keywords: Toxicologie médicolégale; Moelle Osseuse; Interprétation; Modèle PBPK; Distribution tissulaire; Forensic toxicology; Bone Marrow; Interpretation; PBPK; Tissue distribution; 615.9

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APA (6th Edition):

Cartiser, N. (2011). Intérêts et limites de l'analyse de la moelle osseuse en toxicologie médicolégale : contribution à l'interprétation quantitative des concentrations médullaires : Interests and limits of bone marrow analysis in forensic toxicology : contribution to quantitative interpretation of bone marrow concentrations. (Doctoral Dissertation). Université Claude Bernard – Lyon I. Retrieved from http://www.theses.fr/2011LYO10149

Chicago Manual of Style (16th Edition):

Cartiser, Nathalie. “Intérêts et limites de l'analyse de la moelle osseuse en toxicologie médicolégale : contribution à l'interprétation quantitative des concentrations médullaires : Interests and limits of bone marrow analysis in forensic toxicology : contribution to quantitative interpretation of bone marrow concentrations.” 2011. Doctoral Dissertation, Université Claude Bernard – Lyon I. Accessed October 21, 2019. http://www.theses.fr/2011LYO10149.

MLA Handbook (7th Edition):

Cartiser, Nathalie. “Intérêts et limites de l'analyse de la moelle osseuse en toxicologie médicolégale : contribution à l'interprétation quantitative des concentrations médullaires : Interests and limits of bone marrow analysis in forensic toxicology : contribution to quantitative interpretation of bone marrow concentrations.” 2011. Web. 21 Oct 2019.

Vancouver:

Cartiser N. Intérêts et limites de l'analyse de la moelle osseuse en toxicologie médicolégale : contribution à l'interprétation quantitative des concentrations médullaires : Interests and limits of bone marrow analysis in forensic toxicology : contribution to quantitative interpretation of bone marrow concentrations. [Internet] [Doctoral dissertation]. Université Claude Bernard – Lyon I; 2011. [cited 2019 Oct 21]. Available from: http://www.theses.fr/2011LYO10149.

Council of Science Editors:

Cartiser N. Intérêts et limites de l'analyse de la moelle osseuse en toxicologie médicolégale : contribution à l'interprétation quantitative des concentrations médullaires : Interests and limits of bone marrow analysis in forensic toxicology : contribution to quantitative interpretation of bone marrow concentrations. [Doctoral Dissertation]. Université Claude Bernard – Lyon I; 2011. Available from: http://www.theses.fr/2011LYO10149

11. Sousa Mendes, Maïlys de. Prédiction du passage transplacentaire in-vivo des médicaments à partir de modèles ex-vivo : In-vivo prediction of transplacental transfer using ex-vivo experiment.

Degree: Docteur es, Pharmacologie, 2016, Sorbonne Paris Cité

Les femmes enceintes sont exposées à de nombreux médicaments et les essais cliniques sont difficilement réalisables dans cette population, c'est pourquoi avoir une méthode qui… (more)

Subjects/Keywords: Pharmacocinétique; PBPK; Grossesse; Foetus; Cotyledon; Placenta; Névirapine; Ténofovir; Emtricitabine; Lamivudine; Pharmacockinetics; PBPK; Pregnancy; Foetus; Cotyledon; Placenta; Nevirapine; Tenofovir; Emtricitabine; Lamivudine; 615.7

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APA (6th Edition):

Sousa Mendes, M. d. (2016). Prédiction du passage transplacentaire in-vivo des médicaments à partir de modèles ex-vivo : In-vivo prediction of transplacental transfer using ex-vivo experiment. (Doctoral Dissertation). Sorbonne Paris Cité. Retrieved from http://www.theses.fr/2016USPCB144

Chicago Manual of Style (16th Edition):

Sousa Mendes, Maïlys de. “Prédiction du passage transplacentaire in-vivo des médicaments à partir de modèles ex-vivo : In-vivo prediction of transplacental transfer using ex-vivo experiment.” 2016. Doctoral Dissertation, Sorbonne Paris Cité. Accessed October 21, 2019. http://www.theses.fr/2016USPCB144.

MLA Handbook (7th Edition):

Sousa Mendes, Maïlys de. “Prédiction du passage transplacentaire in-vivo des médicaments à partir de modèles ex-vivo : In-vivo prediction of transplacental transfer using ex-vivo experiment.” 2016. Web. 21 Oct 2019.

Vancouver:

Sousa Mendes Md. Prédiction du passage transplacentaire in-vivo des médicaments à partir de modèles ex-vivo : In-vivo prediction of transplacental transfer using ex-vivo experiment. [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; 2016. [cited 2019 Oct 21]. Available from: http://www.theses.fr/2016USPCB144.

Council of Science Editors:

Sousa Mendes Md. Prédiction du passage transplacentaire in-vivo des médicaments à partir de modèles ex-vivo : In-vivo prediction of transplacental transfer using ex-vivo experiment. [Doctoral Dissertation]. Sorbonne Paris Cité; 2016. Available from: http://www.theses.fr/2016USPCB144

12. Harwood, Matthew Dillston. Towards a fully mechanistic prediction of oral drug absorption : investigating intestinal transporter abundance & function relationships.

Degree: PhD, 2015, University of Manchester

 Background: Elucidating the role of intestinal drug transporter function in drug development is crucial, as transporter proteins can impact on drug absorption, efficacy and adverse… (more)

Subjects/Keywords: 615.1; Transporter proteins; PBPK-IVIVE; Intestine; Absolute Abundance

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Harwood, M. D. (2015). Towards a fully mechanistic prediction of oral drug absorption : investigating intestinal transporter abundance & function relationships. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/towards-a-fully-mechanistic-prediction-of-oral-drug-absorption-investigating-intestinal-transporter-abundance-and-function-relationships(a211b130-b8ac-4ce3-bf8f-728cf08df216).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.654832

Chicago Manual of Style (16th Edition):

Harwood, Matthew Dillston. “Towards a fully mechanistic prediction of oral drug absorption : investigating intestinal transporter abundance & function relationships.” 2015. Doctoral Dissertation, University of Manchester. Accessed October 21, 2019. https://www.research.manchester.ac.uk/portal/en/theses/towards-a-fully-mechanistic-prediction-of-oral-drug-absorption-investigating-intestinal-transporter-abundance-and-function-relationships(a211b130-b8ac-4ce3-bf8f-728cf08df216).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.654832.

MLA Handbook (7th Edition):

Harwood, Matthew Dillston. “Towards a fully mechanistic prediction of oral drug absorption : investigating intestinal transporter abundance & function relationships.” 2015. Web. 21 Oct 2019.

Vancouver:

Harwood MD. Towards a fully mechanistic prediction of oral drug absorption : investigating intestinal transporter abundance & function relationships. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2019 Oct 21]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/towards-a-fully-mechanistic-prediction-of-oral-drug-absorption-investigating-intestinal-transporter-abundance-and-function-relationships(a211b130-b8ac-4ce3-bf8f-728cf08df216).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.654832.

Council of Science Editors:

Harwood MD. Towards a fully mechanistic prediction of oral drug absorption : investigating intestinal transporter abundance & function relationships. [Doctoral Dissertation]. University of Manchester; 2015. Available from: https://www.research.manchester.ac.uk/portal/en/theses/towards-a-fully-mechanistic-prediction-of-oral-drug-absorption-investigating-intestinal-transporter-abundance-and-function-relationships(a211b130-b8ac-4ce3-bf8f-728cf08df216).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.654832


University of Manchester

13. Graham, Helen Sarah. Prediction of drug distribution in rat and human.

Degree: PhD, 2012, University of Manchester

 Many methods exist in the literature for the prediction of pharmacokinetic parameters which describe drug distribution in rat and human, such as tissue-to-plasma partition coefficients… (more)

Subjects/Keywords: 615; Pharmacokinetics; PBPK modelling; Partition coefficients; Volume of distribution

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APA (6th Edition):

Graham, H. S. (2012). Prediction of drug distribution in rat and human. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/prediction-of-drug-distribution-in-rat-and-human(231d1935-4fde-4b2d-8338-4e74091224f3).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.555572

Chicago Manual of Style (16th Edition):

Graham, Helen Sarah. “Prediction of drug distribution in rat and human.” 2012. Doctoral Dissertation, University of Manchester. Accessed October 21, 2019. https://www.research.manchester.ac.uk/portal/en/theses/prediction-of-drug-distribution-in-rat-and-human(231d1935-4fde-4b2d-8338-4e74091224f3).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.555572.

MLA Handbook (7th Edition):

Graham, Helen Sarah. “Prediction of drug distribution in rat and human.” 2012. Web. 21 Oct 2019.

Vancouver:

Graham HS. Prediction of drug distribution in rat and human. [Internet] [Doctoral dissertation]. University of Manchester; 2012. [cited 2019 Oct 21]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/prediction-of-drug-distribution-in-rat-and-human(231d1935-4fde-4b2d-8338-4e74091224f3).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.555572.

Council of Science Editors:

Graham HS. Prediction of drug distribution in rat and human. [Doctoral Dissertation]. University of Manchester; 2012. Available from: https://www.research.manchester.ac.uk/portal/en/theses/prediction-of-drug-distribution-in-rat-and-human(231d1935-4fde-4b2d-8338-4e74091224f3).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.555572


East Tennessee State University

14. Forbes, Whitney. Physiologically-Based Pharmacokinetic Model for Ertapenem.

Degree: MS, Mathematical Sciences, 2014, East Tennessee State University

  Ertapenem is a carbapenem used to treat a wide range of bacterial infections. What sets ertapenem apart from other carbapenems is its longer half-life… (more)

Subjects/Keywords: PBPK; Pharmacokinetic; MIC; Ertapenem; ADME; Applied Mathematics; Chemicals and Drugs; Mathematics

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APA (6th Edition):

Forbes, W. (2014). Physiologically-Based Pharmacokinetic Model for Ertapenem. (Masters Thesis). East Tennessee State University. Retrieved from https://dc.etsu.edu/etd/2342

Chicago Manual of Style (16th Edition):

Forbes, Whitney. “Physiologically-Based Pharmacokinetic Model for Ertapenem.” 2014. Masters Thesis, East Tennessee State University. Accessed October 21, 2019. https://dc.etsu.edu/etd/2342.

MLA Handbook (7th Edition):

Forbes, Whitney. “Physiologically-Based Pharmacokinetic Model for Ertapenem.” 2014. Web. 21 Oct 2019.

Vancouver:

Forbes W. Physiologically-Based Pharmacokinetic Model for Ertapenem. [Internet] [Masters thesis]. East Tennessee State University; 2014. [cited 2019 Oct 21]. Available from: https://dc.etsu.edu/etd/2342.

Council of Science Editors:

Forbes W. Physiologically-Based Pharmacokinetic Model for Ertapenem. [Masters Thesis]. East Tennessee State University; 2014. Available from: https://dc.etsu.edu/etd/2342


University of Cincinnati

15. Moorthy, Ganesh. Clinical Pharmacokinetics of the Novel Combination of BEZ235, PI3K/mTOR Inhibitor, and Everolimus, mTOR Inhibitor: Phase I Clinical Studies and Non-clinical Mechanistic Assessment.

Degree: PhD, Pharmacy: Pharmaceutical Sciences/Biopharmaceutics, 2015, University of Cincinnati

 Dysregulation of PI3K/Akt/mTOR pathway has been implicated in tumorigenesis and malignancy in numerous solid tumors. Everolimus is a potent allosteric inhibitor of mTORC1, and has… (more)

Subjects/Keywords: Pharmaceuticals; pharmacokinetics; Phase I; PBPK; DDI; BEZ235; Everolimus

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APA (6th Edition):

Moorthy, G. (2015). Clinical Pharmacokinetics of the Novel Combination of BEZ235, PI3K/mTOR Inhibitor, and Everolimus, mTOR Inhibitor: Phase I Clinical Studies and Non-clinical Mechanistic Assessment. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1439296033

Chicago Manual of Style (16th Edition):

Moorthy, Ganesh. “Clinical Pharmacokinetics of the Novel Combination of BEZ235, PI3K/mTOR Inhibitor, and Everolimus, mTOR Inhibitor: Phase I Clinical Studies and Non-clinical Mechanistic Assessment.” 2015. Doctoral Dissertation, University of Cincinnati. Accessed October 21, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1439296033.

MLA Handbook (7th Edition):

Moorthy, Ganesh. “Clinical Pharmacokinetics of the Novel Combination of BEZ235, PI3K/mTOR Inhibitor, and Everolimus, mTOR Inhibitor: Phase I Clinical Studies and Non-clinical Mechanistic Assessment.” 2015. Web. 21 Oct 2019.

Vancouver:

Moorthy G. Clinical Pharmacokinetics of the Novel Combination of BEZ235, PI3K/mTOR Inhibitor, and Everolimus, mTOR Inhibitor: Phase I Clinical Studies and Non-clinical Mechanistic Assessment. [Internet] [Doctoral dissertation]. University of Cincinnati; 2015. [cited 2019 Oct 21]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1439296033.

Council of Science Editors:

Moorthy G. Clinical Pharmacokinetics of the Novel Combination of BEZ235, PI3K/mTOR Inhibitor, and Everolimus, mTOR Inhibitor: Phase I Clinical Studies and Non-clinical Mechanistic Assessment. [Doctoral Dissertation]. University of Cincinnati; 2015. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1439296033


University of South Florida

16. Thompson, Zachary John. Statistical Estimation of Physiologically-based Pharmacokinetic Models: Identifiability, Variation, and Uncertainty with an Illustration of Chronic Exposure to Dioxin and Dioxin-like-compounds.

Degree: 2012, University of South Florida

 Assessment of human exposure to environmental chemicals is inherently subject to uncertainty and variability. There are data gaps concerning the inventory, source, duration, and intensity… (more)

Subjects/Keywords: MCMC; PBPK; Risk assesment; TCDD; American Studies; Arts and Humanities; Biostatistics

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APA (6th Edition):

Thompson, Z. J. (2012). Statistical Estimation of Physiologically-based Pharmacokinetic Models: Identifiability, Variation, and Uncertainty with an Illustration of Chronic Exposure to Dioxin and Dioxin-like-compounds. (Thesis). University of South Florida. Retrieved from https://scholarcommons.usf.edu/etd/4241

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Thompson, Zachary John. “Statistical Estimation of Physiologically-based Pharmacokinetic Models: Identifiability, Variation, and Uncertainty with an Illustration of Chronic Exposure to Dioxin and Dioxin-like-compounds.” 2012. Thesis, University of South Florida. Accessed October 21, 2019. https://scholarcommons.usf.edu/etd/4241.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Thompson, Zachary John. “Statistical Estimation of Physiologically-based Pharmacokinetic Models: Identifiability, Variation, and Uncertainty with an Illustration of Chronic Exposure to Dioxin and Dioxin-like-compounds.” 2012. Web. 21 Oct 2019.

Vancouver:

Thompson ZJ. Statistical Estimation of Physiologically-based Pharmacokinetic Models: Identifiability, Variation, and Uncertainty with an Illustration of Chronic Exposure to Dioxin and Dioxin-like-compounds. [Internet] [Thesis]. University of South Florida; 2012. [cited 2019 Oct 21]. Available from: https://scholarcommons.usf.edu/etd/4241.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Thompson ZJ. Statistical Estimation of Physiologically-based Pharmacokinetic Models: Identifiability, Variation, and Uncertainty with an Illustration of Chronic Exposure to Dioxin and Dioxin-like-compounds. [Thesis]. University of South Florida; 2012. Available from: https://scholarcommons.usf.edu/etd/4241

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Waterloo

17. Offman, Elliot. In-Silico Methods for De-Risking the Clinical Development of Subcutaneously Administered Therapeutic Macromolecules.

Degree: 2016, University of Waterloo

 Prediction of human pharmacokinetics (PK) following subcutaneous (SC) administration to animals is challenged by potential interspecies differences in skin anatomy and physiology. With respect to… (more)

Subjects/Keywords: biologic; subcutaneous; pharmacokinetic; model; simulation; prediction; monkey; lymph; PBPK; mixed-effect

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APA (6th Edition):

Offman, E. (2016). In-Silico Methods for De-Risking the Clinical Development of Subcutaneously Administered Therapeutic Macromolecules. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/10595

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Offman, Elliot. “In-Silico Methods for De-Risking the Clinical Development of Subcutaneously Administered Therapeutic Macromolecules.” 2016. Thesis, University of Waterloo. Accessed October 21, 2019. http://hdl.handle.net/10012/10595.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Offman, Elliot. “In-Silico Methods for De-Risking the Clinical Development of Subcutaneously Administered Therapeutic Macromolecules.” 2016. Web. 21 Oct 2019.

Vancouver:

Offman E. In-Silico Methods for De-Risking the Clinical Development of Subcutaneously Administered Therapeutic Macromolecules. [Internet] [Thesis]. University of Waterloo; 2016. [cited 2019 Oct 21]. Available from: http://hdl.handle.net/10012/10595.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Offman E. In-Silico Methods for De-Risking the Clinical Development of Subcutaneously Administered Therapeutic Macromolecules. [Thesis]. University of Waterloo; 2016. Available from: http://hdl.handle.net/10012/10595

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Cincinnati

18. Ananthula, Hari Krishna. Pharmacokinetic Evaluation and Modeling of Tyrosine Kinase Inhibitors Nilotinib and Imatinib in Preclinical Species to Aid their Repurposing As Anti-Viral Agents.

Degree: PhD, Pharmacy: Pharmaceutical Sciences/Biopharmaceutics, 2017, University of Cincinnati

 Tyrosine kinase inhibitors (TKIs) imatinib and nilotinib developed as anti-cancer drugs, also appear to have anti-viral activity due to their ability to disrupt productive replication… (more)

Subjects/Keywords: Pharmaceuticals; Tyrosine kinase inhibitor; Pharmacokinetics; Animal rule; Allometry; PBPK

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APA (6th Edition):

Ananthula, H. K. (2017). Pharmacokinetic Evaluation and Modeling of Tyrosine Kinase Inhibitors Nilotinib and Imatinib in Preclinical Species to Aid their Repurposing As Anti-Viral Agents. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1504802233495176

Chicago Manual of Style (16th Edition):

Ananthula, Hari Krishna. “Pharmacokinetic Evaluation and Modeling of Tyrosine Kinase Inhibitors Nilotinib and Imatinib in Preclinical Species to Aid their Repurposing As Anti-Viral Agents.” 2017. Doctoral Dissertation, University of Cincinnati. Accessed October 21, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1504802233495176.

MLA Handbook (7th Edition):

Ananthula, Hari Krishna. “Pharmacokinetic Evaluation and Modeling of Tyrosine Kinase Inhibitors Nilotinib and Imatinib in Preclinical Species to Aid their Repurposing As Anti-Viral Agents.” 2017. Web. 21 Oct 2019.

Vancouver:

Ananthula HK. Pharmacokinetic Evaluation and Modeling of Tyrosine Kinase Inhibitors Nilotinib and Imatinib in Preclinical Species to Aid their Repurposing As Anti-Viral Agents. [Internet] [Doctoral dissertation]. University of Cincinnati; 2017. [cited 2019 Oct 21]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1504802233495176.

Council of Science Editors:

Ananthula HK. Pharmacokinetic Evaluation and Modeling of Tyrosine Kinase Inhibitors Nilotinib and Imatinib in Preclinical Species to Aid their Repurposing As Anti-Viral Agents. [Doctoral Dissertation]. University of Cincinnati; 2017. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1504802233495176

19. Viel, Alexis. Usages de la colistine en médecine humaine et vétérinaire : exploration pharmacocinétique et problématique d'antibiorésistance : Use of colistin in veterinary and human medicine : pharmacokinetic exploration and antimicrobial resistance issue.

Degree: Docteur es, Pharmacie, 2017, Poitiers

La colistine est un vieil antibiotique, utilisé à la fois en médecine humaine et vétérinaire. Cependant, l'arsenal antibiotique étant de plus en plus limité, la… (more)

Subjects/Keywords: Colistine; Antibiorésistance; Pharmacocinétique; Modèle animal; Gène mcr-1; Modèle PBPK; Médecine humaine; Médecine vétérinaire; Colistin; Antibioresistance; Pharmacokinetics; Animal model; Mcr-1; PBPK model; Human medecine; Veterinary medecine; 615.17

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Viel, A. (2017). Usages de la colistine en médecine humaine et vétérinaire : exploration pharmacocinétique et problématique d'antibiorésistance : Use of colistin in veterinary and human medicine : pharmacokinetic exploration and antimicrobial resistance issue. (Doctoral Dissertation). Poitiers. Retrieved from http://www.theses.fr/2017POIT1801

Chicago Manual of Style (16th Edition):

Viel, Alexis. “Usages de la colistine en médecine humaine et vétérinaire : exploration pharmacocinétique et problématique d'antibiorésistance : Use of colistin in veterinary and human medicine : pharmacokinetic exploration and antimicrobial resistance issue.” 2017. Doctoral Dissertation, Poitiers. Accessed October 21, 2019. http://www.theses.fr/2017POIT1801.

MLA Handbook (7th Edition):

Viel, Alexis. “Usages de la colistine en médecine humaine et vétérinaire : exploration pharmacocinétique et problématique d'antibiorésistance : Use of colistin in veterinary and human medicine : pharmacokinetic exploration and antimicrobial resistance issue.” 2017. Web. 21 Oct 2019.

Vancouver:

Viel A. Usages de la colistine en médecine humaine et vétérinaire : exploration pharmacocinétique et problématique d'antibiorésistance : Use of colistin in veterinary and human medicine : pharmacokinetic exploration and antimicrobial resistance issue. [Internet] [Doctoral dissertation]. Poitiers; 2017. [cited 2019 Oct 21]. Available from: http://www.theses.fr/2017POIT1801.

Council of Science Editors:

Viel A. Usages de la colistine en médecine humaine et vétérinaire : exploration pharmacocinétique et problématique d'antibiorésistance : Use of colistin in veterinary and human medicine : pharmacokinetic exploration and antimicrobial resistance issue. [Doctoral Dissertation]. Poitiers; 2017. Available from: http://www.theses.fr/2017POIT1801

20. Ferreira, Carolina Martins André Oliveira. Utilização de modelos farmacocinéticos de base fisiológica em estudos toxicológicos.

Degree: 2015, Universidade Fernando Pessoa

Projeto de Pós-Graduação/Dissertação apresentado à Universidade Fernando Pessoa como parte dos requisitos para obtenção do grau de Mestre em Ciências Farmacêuticas

Os efeitos adversos decorrentes… (more)

Subjects/Keywords: Estudos toxicológicos; Modelos farmacocinéticos de base fisiológica (PBPK); Farmacocinética; Toxicocinética; Métodos in silico; Toxicological studies; Physiologically-based pharmacokinetic modeling (PBPK); Pharmacokinetics; Toxicokinetics; In silico methods

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Ferreira, C. M. A. O. (2015). Utilização de modelos farmacocinéticos de base fisiológica em estudos toxicológicos. (Thesis). Universidade Fernando Pessoa. Retrieved from http://www.rcaap.pt/detail.jsp?id=oai:bdigital.ufp.pt:10284/5154

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Ferreira, Carolina Martins André Oliveira. “Utilização de modelos farmacocinéticos de base fisiológica em estudos toxicológicos.” 2015. Thesis, Universidade Fernando Pessoa. Accessed October 21, 2019. http://www.rcaap.pt/detail.jsp?id=oai:bdigital.ufp.pt:10284/5154.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Ferreira, Carolina Martins André Oliveira. “Utilização de modelos farmacocinéticos de base fisiológica em estudos toxicológicos.” 2015. Web. 21 Oct 2019.

Vancouver:

Ferreira CMAO. Utilização de modelos farmacocinéticos de base fisiológica em estudos toxicológicos. [Internet] [Thesis]. Universidade Fernando Pessoa; 2015. [cited 2019 Oct 21]. Available from: http://www.rcaap.pt/detail.jsp?id=oai:bdigital.ufp.pt:10284/5154.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Ferreira CMAO. Utilização de modelos farmacocinéticos de base fisiológica em estudos toxicológicos. [Thesis]. Universidade Fernando Pessoa; 2015. Available from: http://www.rcaap.pt/detail.jsp?id=oai:bdigital.ufp.pt:10284/5154

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Université de Lorraine

21. Domínguez-Romero, Elena. Modélisation du devenir de l’hexabromocyclododécane (HBCD) chez la poule pondeuse : influence des caractéristiques physiologiques : Modelling the hexabromocyclododecane (HBCD) transfer kinetics in the laying hen : impact of the physiological features.

Degree: Docteur es, Sciences agronomiques, 2016, Université de Lorraine

L’hexabromocyclododécane (HBCD) a été utilisé comme additif dans des polystyrènes (PS). En 2013, l’HBCD a été inclus à la Convention de Stockholm comme Polluant Organique… (more)

Subjects/Keywords: Sécurité Sanitaire des Aliments; HBCD; Modèle PBPK; Poule pondeuse; Caractéristiques physiologiques; Food Safety; HBCD; PBPK model; Laying hen; Physiological features; 636.5; 363.192; 664.07

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APA (6th Edition):

Domínguez-Romero, E. (2016). Modélisation du devenir de l’hexabromocyclododécane (HBCD) chez la poule pondeuse : influence des caractéristiques physiologiques : Modelling the hexabromocyclododecane (HBCD) transfer kinetics in the laying hen : impact of the physiological features. (Doctoral Dissertation). Université de Lorraine. Retrieved from http://www.theses.fr/2016LORR0167

Chicago Manual of Style (16th Edition):

Domínguez-Romero, Elena. “Modélisation du devenir de l’hexabromocyclododécane (HBCD) chez la poule pondeuse : influence des caractéristiques physiologiques : Modelling the hexabromocyclododecane (HBCD) transfer kinetics in the laying hen : impact of the physiological features.” 2016. Doctoral Dissertation, Université de Lorraine. Accessed October 21, 2019. http://www.theses.fr/2016LORR0167.

MLA Handbook (7th Edition):

Domínguez-Romero, Elena. “Modélisation du devenir de l’hexabromocyclododécane (HBCD) chez la poule pondeuse : influence des caractéristiques physiologiques : Modelling the hexabromocyclododecane (HBCD) transfer kinetics in the laying hen : impact of the physiological features.” 2016. Web. 21 Oct 2019.

Vancouver:

Domínguez-Romero E. Modélisation du devenir de l’hexabromocyclododécane (HBCD) chez la poule pondeuse : influence des caractéristiques physiologiques : Modelling the hexabromocyclododecane (HBCD) transfer kinetics in the laying hen : impact of the physiological features. [Internet] [Doctoral dissertation]. Université de Lorraine; 2016. [cited 2019 Oct 21]. Available from: http://www.theses.fr/2016LORR0167.

Council of Science Editors:

Domínguez-Romero E. Modélisation du devenir de l’hexabromocyclododécane (HBCD) chez la poule pondeuse : influence des caractéristiques physiologiques : Modelling the hexabromocyclododecane (HBCD) transfer kinetics in the laying hen : impact of the physiological features. [Doctoral Dissertation]. Université de Lorraine; 2016. Available from: http://www.theses.fr/2016LORR0167


Université de Montréal

22. Kaveh, Nazanin. Modélisation toxicocinétique d’un mélange de composés organiques volatils dans l’eau potable .

Degree: 2013, Université de Montréal

 L'évaluation des risques de l'exposition aux mélanges de produits chimiques par voies multiples peut être améliorée par une compréhension de la variation de la dose… (more)

Subjects/Keywords: Analyse de risque; Mélange; Voies multiples; PBPK; Risk assessment; Mixture; Multiple routes

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Kaveh, N. (2013). Modélisation toxicocinétique d’un mélange de composés organiques volatils dans l’eau potable . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/9104

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Kaveh, Nazanin. “Modélisation toxicocinétique d’un mélange de composés organiques volatils dans l’eau potable .” 2013. Thesis, Université de Montréal. Accessed October 21, 2019. http://hdl.handle.net/1866/9104.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Kaveh, Nazanin. “Modélisation toxicocinétique d’un mélange de composés organiques volatils dans l’eau potable .” 2013. Web. 21 Oct 2019.

Vancouver:

Kaveh N. Modélisation toxicocinétique d’un mélange de composés organiques volatils dans l’eau potable . [Internet] [Thesis]. Université de Montréal; 2013. [cited 2019 Oct 21]. Available from: http://hdl.handle.net/1866/9104.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Kaveh N. Modélisation toxicocinétique d’un mélange de composés organiques volatils dans l’eau potable . [Thesis]. Université de Montréal; 2013. Available from: http://hdl.handle.net/1866/9104

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Helsinki

23. Järvinen, Hanna. Sytokromi P450 2C19- tai sytokromi P450 2D6 -genotyypatut ihmisen maksan mikrosomit lääkeaineiden farmakokinetiikassa esiintyvän yksilöllisen vaihtelun ennustamisessa.

Degree: Farmaceutiska fakulteten, 2017, University of Helsinki

 Interindividual variability in drug responses can complicate the determination of drug doses and increase drug-related risks. The variability can be caused by pharmacokinetics or pharmacodynamics… (more)

Subjects/Keywords: CYP2C19; CYP2D6; interindividual variability; genetic polymorphism; PBPK simulation models; genotyped microsomes; genotype-phenotype correlation; yksilöllinen vaihtelu; geneettinen polymorfia; PBPK-simulaatiomallit; genotyypatut mikrosomit; genotyyppi-fenotyyppi-korrelaatio; Biofarmaci; Biopharmacy; Biofarmasia; CYP2C19; CYP2D6; interindividual variability; genetic polymorphism; PBPK simulation models; genotyped microsomes; genotype-phenotype correlation; yksilöllinen vaihtelu; geneettinen polymorfia; PBPK-simulaatiomallit; genotyypatut mikrosomit; genotyyppi-fenotyyppi-korrelaatio

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APA (6th Edition):

Järvinen, H. (2017). Sytokromi P450 2C19- tai sytokromi P450 2D6 -genotyypatut ihmisen maksan mikrosomit lääkeaineiden farmakokinetiikassa esiintyvän yksilöllisen vaihtelun ennustamisessa. (Masters Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/199518

Chicago Manual of Style (16th Edition):

Järvinen, Hanna. “Sytokromi P450 2C19- tai sytokromi P450 2D6 -genotyypatut ihmisen maksan mikrosomit lääkeaineiden farmakokinetiikassa esiintyvän yksilöllisen vaihtelun ennustamisessa.” 2017. Masters Thesis, University of Helsinki. Accessed October 21, 2019. http://hdl.handle.net/10138/199518.

MLA Handbook (7th Edition):

Järvinen, Hanna. “Sytokromi P450 2C19- tai sytokromi P450 2D6 -genotyypatut ihmisen maksan mikrosomit lääkeaineiden farmakokinetiikassa esiintyvän yksilöllisen vaihtelun ennustamisessa.” 2017. Web. 21 Oct 2019.

Vancouver:

Järvinen H. Sytokromi P450 2C19- tai sytokromi P450 2D6 -genotyypatut ihmisen maksan mikrosomit lääkeaineiden farmakokinetiikassa esiintyvän yksilöllisen vaihtelun ennustamisessa. [Internet] [Masters thesis]. University of Helsinki; 2017. [cited 2019 Oct 21]. Available from: http://hdl.handle.net/10138/199518.

Council of Science Editors:

Järvinen H. Sytokromi P450 2C19- tai sytokromi P450 2D6 -genotyypatut ihmisen maksan mikrosomit lääkeaineiden farmakokinetiikassa esiintyvän yksilöllisen vaihtelun ennustamisessa. [Masters Thesis]. University of Helsinki; 2017. Available from: http://hdl.handle.net/10138/199518


University of Florida

24. Bei, Di. Pharmacokinetics and Tissue Distribution of 5,7-Dimethoxyflavone in Mice.

Degree: PhD, Pharmaceutical Sciences - Pharmaceutics, 2015, University of Florida

Subjects/Keywords: adme; lc-msms; pbpk; pharmacokinetics; phytochemical

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APA (6th Edition):

Bei, D. (2015). Pharmacokinetics and Tissue Distribution of 5,7-Dimethoxyflavone in Mice. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0049455

Chicago Manual of Style (16th Edition):

Bei, Di. “Pharmacokinetics and Tissue Distribution of 5,7-Dimethoxyflavone in Mice.” 2015. Doctoral Dissertation, University of Florida. Accessed October 21, 2019. http://ufdc.ufl.edu/UFE0049455.

MLA Handbook (7th Edition):

Bei, Di. “Pharmacokinetics and Tissue Distribution of 5,7-Dimethoxyflavone in Mice.” 2015. Web. 21 Oct 2019.

Vancouver:

Bei D. Pharmacokinetics and Tissue Distribution of 5,7-Dimethoxyflavone in Mice. [Internet] [Doctoral dissertation]. University of Florida; 2015. [cited 2019 Oct 21]. Available from: http://ufdc.ufl.edu/UFE0049455.

Council of Science Editors:

Bei D. Pharmacokinetics and Tissue Distribution of 5,7-Dimethoxyflavone in Mice. [Doctoral Dissertation]. University of Florida; 2015. Available from: http://ufdc.ufl.edu/UFE0049455


University of Illinois – Chicago

25. Kuo, Ilin. Exploring the ‘Lipid Sink’ as a mechanism for Reversal of Local Anesthetic Toxicity:A PBPK Modeling Study.

Degree: 2012, University of Illinois – Chicago

 Intravenous lipid emulsions (ILE) have been demonstrated to be effective mitigators of systemic toxicity caused by drug overdose, with dramatic resuscitations observed in small animals… (more)

Subjects/Keywords: Lipid rescue; lipid emulsion; lipid sink; bupivacaine; PBPK; drug overdose; intravenous lipid emulsion; intralipid

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APA (6th Edition):

Kuo, I. (2012). Exploring the ‘Lipid Sink’ as a mechanism for Reversal of Local Anesthetic Toxicity:A PBPK Modeling Study. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/9151

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Kuo, Ilin. “Exploring the ‘Lipid Sink’ as a mechanism for Reversal of Local Anesthetic Toxicity:A PBPK Modeling Study.” 2012. Thesis, University of Illinois – Chicago. Accessed October 21, 2019. http://hdl.handle.net/10027/9151.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Kuo, Ilin. “Exploring the ‘Lipid Sink’ as a mechanism for Reversal of Local Anesthetic Toxicity:A PBPK Modeling Study.” 2012. Web. 21 Oct 2019.

Vancouver:

Kuo I. Exploring the ‘Lipid Sink’ as a mechanism for Reversal of Local Anesthetic Toxicity:A PBPK Modeling Study. [Internet] [Thesis]. University of Illinois – Chicago; 2012. [cited 2019 Oct 21]. Available from: http://hdl.handle.net/10027/9151.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Kuo I. Exploring the ‘Lipid Sink’ as a mechanism for Reversal of Local Anesthetic Toxicity:A PBPK Modeling Study. [Thesis]. University of Illinois – Chicago; 2012. Available from: http://hdl.handle.net/10027/9151

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

26. M.M. Ulaszewska. THE INTERPRETATION OF ITALIAN BREAST MILK MONITORING OF DIOXIN-LIKE AND NON-DIOXIN LIKE POLLUTANTS WITH A PBPK MODEL INTEGRATING A NOVEL APPROACH TO DESCRIBE PRE- AND POSTNATAL MOTHER/CHILD TRANSFER.

Degree: 2010, Università degli Studi di Milano

 Polychlorinated dibenzo-p-dioxins, dibenzofurans (PCDD/Fs) and polychlorinated biphenyls (PCBs) are widespread environmental contaminants. They enter the human body mainly with food and because of lipophilic character… (more)

Subjects/Keywords: dioxin; PCB; PBPK model; human biomonitoring; dietary exposure; Settore AGR/13 - Chimica Agraria

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APA (6th Edition):

Ulaszewska, M. (2010). THE INTERPRETATION OF ITALIAN BREAST MILK MONITORING OF DIOXIN-LIKE AND NON-DIOXIN LIKE POLLUTANTS WITH A PBPK MODEL INTEGRATING A NOVEL APPROACH TO DESCRIBE PRE- AND POSTNATAL MOTHER/CHILD TRANSFER. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/150138

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Ulaszewska, M.M.. “THE INTERPRETATION OF ITALIAN BREAST MILK MONITORING OF DIOXIN-LIKE AND NON-DIOXIN LIKE POLLUTANTS WITH A PBPK MODEL INTEGRATING A NOVEL APPROACH TO DESCRIBE PRE- AND POSTNATAL MOTHER/CHILD TRANSFER.” 2010. Thesis, Università degli Studi di Milano. Accessed October 21, 2019. http://hdl.handle.net/2434/150138.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Ulaszewska, M.M.. “THE INTERPRETATION OF ITALIAN BREAST MILK MONITORING OF DIOXIN-LIKE AND NON-DIOXIN LIKE POLLUTANTS WITH A PBPK MODEL INTEGRATING A NOVEL APPROACH TO DESCRIBE PRE- AND POSTNATAL MOTHER/CHILD TRANSFER.” 2010. Web. 21 Oct 2019.

Vancouver:

Ulaszewska M. THE INTERPRETATION OF ITALIAN BREAST MILK MONITORING OF DIOXIN-LIKE AND NON-DIOXIN LIKE POLLUTANTS WITH A PBPK MODEL INTEGRATING A NOVEL APPROACH TO DESCRIBE PRE- AND POSTNATAL MOTHER/CHILD TRANSFER. [Internet] [Thesis]. Università degli Studi di Milano; 2010. [cited 2019 Oct 21]. Available from: http://hdl.handle.net/2434/150138.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Ulaszewska M. THE INTERPRETATION OF ITALIAN BREAST MILK MONITORING OF DIOXIN-LIKE AND NON-DIOXIN LIKE POLLUTANTS WITH A PBPK MODEL INTEGRATING A NOVEL APPROACH TO DESCRIBE PRE- AND POSTNATAL MOTHER/CHILD TRANSFER. [Thesis]. Università degli Studi di Milano; 2010. Available from: http://hdl.handle.net/2434/150138

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

27. Gerard, Cécile. Apport des modèles PBPK dans l'optimisation thérapeutique des inhibiteurs des calcineurines en transplantation : PBPK models in optimization of the immunosuppressive therapy by calcineurin inhibitors inn transplantation.

Degree: Docteur es, Recherche clinique, 2012, Université Claude Bernard – Lyon I

En transplantation d'organes solides ou en greffe de moelle osseuse, la ciclosporine et letacrolimus ont prouvé leur efficacité. Ils sont cependant de maniement délicat du… (more)

Subjects/Keywords: Médicaments immunosuppresseurs; Modélisation PBPK; Suivi thérapeutique; Immunosuppressant drugs; PBBK modeling; Therapeutic drug monitoring; 615.1

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APA (6th Edition):

Gerard, C. (2012). Apport des modèles PBPK dans l'optimisation thérapeutique des inhibiteurs des calcineurines en transplantation : PBPK models in optimization of the immunosuppressive therapy by calcineurin inhibitors inn transplantation. (Doctoral Dissertation). Université Claude Bernard – Lyon I. Retrieved from http://www.theses.fr/2012LYO10265

Chicago Manual of Style (16th Edition):

Gerard, Cécile. “Apport des modèles PBPK dans l'optimisation thérapeutique des inhibiteurs des calcineurines en transplantation : PBPK models in optimization of the immunosuppressive therapy by calcineurin inhibitors inn transplantation.” 2012. Doctoral Dissertation, Université Claude Bernard – Lyon I. Accessed October 21, 2019. http://www.theses.fr/2012LYO10265.

MLA Handbook (7th Edition):

Gerard, Cécile. “Apport des modèles PBPK dans l'optimisation thérapeutique des inhibiteurs des calcineurines en transplantation : PBPK models in optimization of the immunosuppressive therapy by calcineurin inhibitors inn transplantation.” 2012. Web. 21 Oct 2019.

Vancouver:

Gerard C. Apport des modèles PBPK dans l'optimisation thérapeutique des inhibiteurs des calcineurines en transplantation : PBPK models in optimization of the immunosuppressive therapy by calcineurin inhibitors inn transplantation. [Internet] [Doctoral dissertation]. Université Claude Bernard – Lyon I; 2012. [cited 2019 Oct 21]. Available from: http://www.theses.fr/2012LYO10265.

Council of Science Editors:

Gerard C. Apport des modèles PBPK dans l'optimisation thérapeutique des inhibiteurs des calcineurines en transplantation : PBPK models in optimization of the immunosuppressive therapy by calcineurin inhibitors inn transplantation. [Doctoral Dissertation]. Université Claude Bernard – Lyon I; 2012. Available from: http://www.theses.fr/2012LYO10265


University of Iowa

28. Ngeacharernkul, Pratak. Particle size distribution (PSD) equivalency using novel statistical comparators and PBPK input models.

Degree: PhD, Pharmacy, 2017, University of Iowa

  For disperse system drug formulations, meaningful particle size distribution (PSD) comparators are essential in determining pharmaceutical equivalency and predicting biopharmaceutical equivalence in terms of… (more)

Subjects/Keywords: Bioequivalence; Overlap metrics; Particle size distributions; PBPK; Similarity factor; Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Ngeacharernkul, P. (2017). Particle size distribution (PSD) equivalency using novel statistical comparators and PBPK input models. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/5973

Chicago Manual of Style (16th Edition):

Ngeacharernkul, Pratak. “Particle size distribution (PSD) equivalency using novel statistical comparators and PBPK input models.” 2017. Doctoral Dissertation, University of Iowa. Accessed October 21, 2019. https://ir.uiowa.edu/etd/5973.

MLA Handbook (7th Edition):

Ngeacharernkul, Pratak. “Particle size distribution (PSD) equivalency using novel statistical comparators and PBPK input models.” 2017. Web. 21 Oct 2019.

Vancouver:

Ngeacharernkul P. Particle size distribution (PSD) equivalency using novel statistical comparators and PBPK input models. [Internet] [Doctoral dissertation]. University of Iowa; 2017. [cited 2019 Oct 21]. Available from: https://ir.uiowa.edu/etd/5973.

Council of Science Editors:

Ngeacharernkul P. Particle size distribution (PSD) equivalency using novel statistical comparators and PBPK input models. [Doctoral Dissertation]. University of Iowa; 2017. Available from: https://ir.uiowa.edu/etd/5973


University of Kansas

29. Varkhede, Ninad. Understanding the metabolic processes and degradation of therapeutic proteins after subcutaneous administration.

Degree: PhD, Pharmaceutical Chemistry, 2018, University of Kansas

 Subcutaneous (SC) route is important for administration of various therapeutic proteins (TPs) like monoclonal antibodies (mAbs), human growth hormone (hGH), insulin, and recombinant subunit vaccines.… (more)

Subjects/Keywords: Pharmaceutical sciences; Inflammation; Lymphatics; Monoclonal antibody; PBPK modelling; Pharmacokinetics; Rat growth hormone

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APA (6th Edition):

Varkhede, N. (2018). Understanding the metabolic processes and degradation of therapeutic proteins after subcutaneous administration. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/27855

Chicago Manual of Style (16th Edition):

Varkhede, Ninad. “Understanding the metabolic processes and degradation of therapeutic proteins after subcutaneous administration.” 2018. Doctoral Dissertation, University of Kansas. Accessed October 21, 2019. http://hdl.handle.net/1808/27855.

MLA Handbook (7th Edition):

Varkhede, Ninad. “Understanding the metabolic processes and degradation of therapeutic proteins after subcutaneous administration.” 2018. Web. 21 Oct 2019.

Vancouver:

Varkhede N. Understanding the metabolic processes and degradation of therapeutic proteins after subcutaneous administration. [Internet] [Doctoral dissertation]. University of Kansas; 2018. [cited 2019 Oct 21]. Available from: http://hdl.handle.net/1808/27855.

Council of Science Editors:

Varkhede N. Understanding the metabolic processes and degradation of therapeutic proteins after subcutaneous administration. [Doctoral Dissertation]. University of Kansas; 2018. Available from: http://hdl.handle.net/1808/27855


Freie Universität Berlin

30. Pilari, Sabine. Lumping von PBPK-Modellen und Systembiologie.

Degree: 2011, Freie Universität Berlin

 In der Wirkstofffindung und -entwicklung wird pharmakokinetische und pharmakodynamische Modellierung erfolgreich zur Analyse und Vorhersage des zeitlichen Verlaufes von Wirkstoffkonzentrationen und Wirkstoffeffekten im Patienten genutzt.… (more)

Subjects/Keywords: Pharmacokinetics; Pharmacodynamics; PBPK; Systems Biology; Lumping; Mechanistic Modeling; 500 Naturwissenschaften und Mathematik

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APA (6th Edition):

Pilari, S. (2011). Lumping von PBPK-Modellen und Systembiologie. (Thesis). Freie Universität Berlin. Retrieved from https://refubium.fu-berlin.de/handle/fub188/13030

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Pilari, Sabine. “Lumping von PBPK-Modellen und Systembiologie.” 2011. Thesis, Freie Universität Berlin. Accessed October 21, 2019. https://refubium.fu-berlin.de/handle/fub188/13030.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Pilari, Sabine. “Lumping von PBPK-Modellen und Systembiologie.” 2011. Web. 21 Oct 2019.

Vancouver:

Pilari S. Lumping von PBPK-Modellen und Systembiologie. [Internet] [Thesis]. Freie Universität Berlin; 2011. [cited 2019 Oct 21]. Available from: https://refubium.fu-berlin.de/handle/fub188/13030.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Pilari S. Lumping von PBPK-Modellen und Systembiologie. [Thesis]. Freie Universität Berlin; 2011. Available from: https://refubium.fu-berlin.de/handle/fub188/13030

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

[1] [2] [3]

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