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You searched for +publisher:"Rutgers University" +contributor:("Michniak-Kohn, Bozena B"). Showing records 1 – 5 of 5 total matches.

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Rutgers University

1. Kaushik, Diksha, 1978-. Investigation of novel penetration modifiers as enhancers and retardants and human pharmacokinetics and pharmacodynamics of orally administered Quercetin.

Degree: PhD, Pharmaceutical Science, 2010, Rutgers University

The delivery of the actives through the outermost layer of the skin, the stratum corneum has posed a challenge for scientists for a very long… (more)

Subjects/Keywords: Pharmacokinetics; Skin – Effect of drugs on; Quercetin

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

APA (6th Edition):

Kaushik, Diksha, 1. (2010). Investigation of novel penetration modifiers as enhancers and retardants and human pharmacokinetics and pharmacodynamics of orally administered Quercetin. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056451

Chicago Manual of Style (16th Edition):

Kaushik, Diksha, 1978-. “Investigation of novel penetration modifiers as enhancers and retardants and human pharmacokinetics and pharmacodynamics of orally administered Quercetin.” 2010. Doctoral Dissertation, Rutgers University. Accessed October 14, 2019. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056451.

MLA Handbook (7th Edition):

Kaushik, Diksha, 1978-. “Investigation of novel penetration modifiers as enhancers and retardants and human pharmacokinetics and pharmacodynamics of orally administered Quercetin.” 2010. Web. 14 Oct 2019.

Vancouver:

Kaushik, Diksha 1. Investigation of novel penetration modifiers as enhancers and retardants and human pharmacokinetics and pharmacodynamics of orally administered Quercetin. [Internet] [Doctoral dissertation]. Rutgers University; 2010. [cited 2019 Oct 14]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056451.

Council of Science Editors:

Kaushik, Diksha 1. Investigation of novel penetration modifiers as enhancers and retardants and human pharmacokinetics and pharmacodynamics of orally administered Quercetin. [Doctoral Dissertation]. Rutgers University; 2010. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056451


Rutgers University

2. Meng, Wei, 1988-. Investigation of continuous wet granulation processes via implementation of pharmaceutical quality by design principles.

Degree: PhD, Pharmaceutical Science, 2018, Rutgers University

Wet granulation is a widely used downstream unit operation for size enlargement in the manufacturing of solid oral dosage forms. It has also been considered… (more)

Subjects/Keywords: Granulation; Pharmaceutical industry

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

APA (6th Edition):

Meng, Wei, 1. (2018). Investigation of continuous wet granulation processes via implementation of pharmaceutical quality by design principles. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/57658/

Chicago Manual of Style (16th Edition):

Meng, Wei, 1988-. “Investigation of continuous wet granulation processes via implementation of pharmaceutical quality by design principles.” 2018. Doctoral Dissertation, Rutgers University. Accessed October 14, 2019. https://rucore.libraries.rutgers.edu/rutgers-lib/57658/.

MLA Handbook (7th Edition):

Meng, Wei, 1988-. “Investigation of continuous wet granulation processes via implementation of pharmaceutical quality by design principles.” 2018. Web. 14 Oct 2019.

Vancouver:

Meng, Wei 1. Investigation of continuous wet granulation processes via implementation of pharmaceutical quality by design principles. [Internet] [Doctoral dissertation]. Rutgers University; 2018. [cited 2019 Oct 14]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/57658/.

Council of Science Editors:

Meng, Wei 1. Investigation of continuous wet granulation processes via implementation of pharmaceutical quality by design principles. [Doctoral Dissertation]. Rutgers University; 2018. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/57658/


Rutgers University

3. Tsai, Pei-Chin, 1984-. Development of three dimensional human skin equivalents based on decellularized extracellular matrices and tyrosine-derived polycarbonate polymers for in-vitro drug screening applications.

Degree: PhD, Pharmaceutical Science, 2016, Rutgers University

Three-dimensional (3D) human skin equivalents (HSEs) are in-vitro models that have morphology and function similar to native human skin. Traditionally, drug discovery for lead compounds… (more)

Subjects/Keywords: Drug development

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

APA (6th Edition):

Tsai, Pei-Chin, 1. (2016). Development of three dimensional human skin equivalents based on decellularized extracellular matrices and tyrosine-derived polycarbonate polymers for in-vitro drug screening applications. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/50236/

Chicago Manual of Style (16th Edition):

Tsai, Pei-Chin, 1984-. “Development of three dimensional human skin equivalents based on decellularized extracellular matrices and tyrosine-derived polycarbonate polymers for in-vitro drug screening applications.” 2016. Doctoral Dissertation, Rutgers University. Accessed October 14, 2019. https://rucore.libraries.rutgers.edu/rutgers-lib/50236/.

MLA Handbook (7th Edition):

Tsai, Pei-Chin, 1984-. “Development of three dimensional human skin equivalents based on decellularized extracellular matrices and tyrosine-derived polycarbonate polymers for in-vitro drug screening applications.” 2016. Web. 14 Oct 2019.

Vancouver:

Tsai, Pei-Chin 1. Development of three dimensional human skin equivalents based on decellularized extracellular matrices and tyrosine-derived polycarbonate polymers for in-vitro drug screening applications. [Internet] [Doctoral dissertation]. Rutgers University; 2016. [cited 2019 Oct 14]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/50236/.

Council of Science Editors:

Tsai, Pei-Chin 1. Development of three dimensional human skin equivalents based on decellularized extracellular matrices and tyrosine-derived polycarbonate polymers for in-vitro drug screening applications. [Doctoral Dissertation]. Rutgers University; 2016. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/50236/


Rutgers University

4. Wang, Hu, 1966-. Studies on Nrf2-targeted phytochemicals: signal transduction, bioanalysis, pharmacokinetics, and pharmacodynamics for their druggability.

Degree: Pharmaceutical Science, 2012, Rutgers University

Subjects/Keywords: Phytochemicals – Therapeutic use – Testing; Cancer – Treatment

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

APA (6th Edition):

Wang, Hu, 1. (2012). Studies on Nrf2-targeted phytochemicals: signal transduction, bioanalysis, pharmacokinetics, and pharmacodynamics for their druggability. (Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000064189

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):

Wang, Hu, 1966-. “Studies on Nrf2-targeted phytochemicals: signal transduction, bioanalysis, pharmacokinetics, and pharmacodynamics for their druggability.” 2012. Thesis, Rutgers University. Accessed October 14, 2019. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000064189.

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

MLA Handbook (7th Edition):

Wang, Hu, 1966-. “Studies on Nrf2-targeted phytochemicals: signal transduction, bioanalysis, pharmacokinetics, and pharmacodynamics for their druggability.” 2012. Web. 14 Oct 2019.

Vancouver:

Wang, Hu 1. Studies on Nrf2-targeted phytochemicals: signal transduction, bioanalysis, pharmacokinetics, and pharmacodynamics for their druggability. [Internet] [Thesis]. Rutgers University; 2012. [cited 2019 Oct 14]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000064189.

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

Council of Science Editors:

Wang, Hu 1. Studies on Nrf2-targeted phytochemicals: signal transduction, bioanalysis, pharmacokinetics, and pharmacodynamics for their druggability. [Thesis]. Rutgers University; 2012. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000064189

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


Rutgers University

5. Ghosh, Anasuya A., 1976-. Salt solid dispersions: a formulation strategy to enhance dissolution rate of poorly water-soluble ionic drugs.

Degree: Pharmaceutical Science, 2012, Rutgers University

Subjects/Keywords: Drugs – Solubility; Drugs – Solubility – Testing

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

APA (6th Edition):

Ghosh, Anasuya A., 1. (2012). Salt solid dispersions: a formulation strategy to enhance dissolution rate of poorly water-soluble ionic drugs. (Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000066746

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):

Ghosh, Anasuya A., 1976-. “Salt solid dispersions: a formulation strategy to enhance dissolution rate of poorly water-soluble ionic drugs.” 2012. Thesis, Rutgers University. Accessed October 14, 2019. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000066746.

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

MLA Handbook (7th Edition):

Ghosh, Anasuya A., 1976-. “Salt solid dispersions: a formulation strategy to enhance dissolution rate of poorly water-soluble ionic drugs.” 2012. Web. 14 Oct 2019.

Vancouver:

Ghosh, Anasuya A. 1. Salt solid dispersions: a formulation strategy to enhance dissolution rate of poorly water-soluble ionic drugs. [Internet] [Thesis]. Rutgers University; 2012. [cited 2019 Oct 14]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000066746.

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

Council of Science Editors:

Ghosh, Anasuya A. 1. Salt solid dispersions: a formulation strategy to enhance dissolution rate of poorly water-soluble ionic drugs. [Thesis]. Rutgers University; 2012. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000066746

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

.