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You searched for +publisher:"Rutgers University" +contributor:("Michniak-Kohn, Bozena"). Showing records 1 – 29 of 29 total matches.

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Rutgers University

1. Martos Gibaile, Nathaly Cristina, 1991-. Effect of insecticide diethyltoluamide (DEET) and co-applied sunscreens on percutaneous absorption.

Degree: MS, Pharmaceutical Science, 2016, Rutgers University

 The combination of sunscreens and insect repellents is widely used by the population, in all regions of the globe. Several published papers reported that the… (more)

Subjects/Keywords: Insect baits and repellents – Health aspects; Skin absorption; Sunscreens (Cosmetics)

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APA (6th Edition):

Martos Gibaile, Nathaly Cristina, 1. (2016). Effect of insecticide diethyltoluamide (DEET) and co-applied sunscreens on percutaneous absorption. (Masters Thesis). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/50047/

Chicago Manual of Style (16th Edition):

Martos Gibaile, Nathaly Cristina, 1991-. “Effect of insecticide diethyltoluamide (DEET) and co-applied sunscreens on percutaneous absorption.” 2016. Masters Thesis, Rutgers University. Accessed July 14, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/50047/.

MLA Handbook (7th Edition):

Martos Gibaile, Nathaly Cristina, 1991-. “Effect of insecticide diethyltoluamide (DEET) and co-applied sunscreens on percutaneous absorption.” 2016. Web. 14 Jul 2020.

Vancouver:

Martos Gibaile, Nathaly Cristina 1. Effect of insecticide diethyltoluamide (DEET) and co-applied sunscreens on percutaneous absorption. [Internet] [Masters thesis]. Rutgers University; 2016. [cited 2020 Jul 14]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/50047/.

Council of Science Editors:

Martos Gibaile, Nathaly Cristina 1. Effect of insecticide diethyltoluamide (DEET) and co-applied sunscreens on percutaneous absorption. [Masters Thesis]. Rutgers University; 2016. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/50047/


Rutgers University

2. Wu, Jinwei, 1986-. Structure, function and regulation of drug/xenobiotic transporter.

Degree: MS, Pharmaceutical Science, 2011, Rutgers University

 Organic anion transporters (OATs), as one group of the important Drug/xenobitic transporters, play vital roles in the body disposition of environmental toxins and clinically anionic… (more)

Subjects/Keywords: Xenobiotics; Toxins

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APA (6th Edition):

Wu, Jinwei, 1. (2011). Structure, function and regulation of drug/xenobiotic transporter. (Masters Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000061542

Chicago Manual of Style (16th Edition):

Wu, Jinwei, 1986-. “Structure, function and regulation of drug/xenobiotic transporter.” 2011. Masters Thesis, Rutgers University. Accessed July 14, 2020. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000061542.

MLA Handbook (7th Edition):

Wu, Jinwei, 1986-. “Structure, function and regulation of drug/xenobiotic transporter.” 2011. Web. 14 Jul 2020.

Vancouver:

Wu, Jinwei 1. Structure, function and regulation of drug/xenobiotic transporter. [Internet] [Masters thesis]. Rutgers University; 2011. [cited 2020 Jul 14]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000061542.

Council of Science Editors:

Wu, Jinwei 1. Structure, function and regulation of drug/xenobiotic transporter. [Masters Thesis]. Rutgers University; 2011. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000061542


Rutgers University

3. Al-Mahmood, Sumayah Abed Ahmed, 1982-. Nanotechnology approach for targeted treatment of triple negative breast cancer.

Degree: MS, Pharmaceutical Science, 2016, Rutgers University

 Breast cancer is one of the most devastating diseases worldwide. Triple negative breast cancer cells (TNBCs) are defined by the lack of progesterone receptor (PR),… (more)

Subjects/Keywords: Nanotechnology; Breast – Cancer – Treatment

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APA (6th Edition):

Al-Mahmood, Sumayah Abed Ahmed, 1. (2016). Nanotechnology approach for targeted treatment of triple negative breast cancer. (Masters Thesis). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/49904/

Chicago Manual of Style (16th Edition):

Al-Mahmood, Sumayah Abed Ahmed, 1982-. “Nanotechnology approach for targeted treatment of triple negative breast cancer.” 2016. Masters Thesis, Rutgers University. Accessed July 14, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/49904/.

MLA Handbook (7th Edition):

Al-Mahmood, Sumayah Abed Ahmed, 1982-. “Nanotechnology approach for targeted treatment of triple negative breast cancer.” 2016. Web. 14 Jul 2020.

Vancouver:

Al-Mahmood, Sumayah Abed Ahmed 1. Nanotechnology approach for targeted treatment of triple negative breast cancer. [Internet] [Masters thesis]. Rutgers University; 2016. [cited 2020 Jul 14]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/49904/.

Council of Science Editors:

Al-Mahmood, Sumayah Abed Ahmed 1. Nanotechnology approach for targeted treatment of triple negative breast cancer. [Masters Thesis]. Rutgers University; 2016. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/49904/


Rutgers University

4. Ramezanli, Tannaz, 1985-. Tyrosine-derived polymeric nanocarriers: an innovative approach for topical drug delivery in acne therapy.

Degree: PhD, Pharmaceutical Science, 2016, Rutgers University

The importance of nanotechnology in the field of drug delivery has been dramatically increased and nanocarriers are finding potential applications in many areas of medicine.… (more)

Subjects/Keywords: Polymeric composites; Drug delivery systems; Acne – Treatment; Hair follicles

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APA (6th Edition):

Ramezanli, Tannaz, 1. (2016). Tyrosine-derived polymeric nanocarriers: an innovative approach for topical drug delivery in acne therapy. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/50137/

Chicago Manual of Style (16th Edition):

Ramezanli, Tannaz, 1985-. “Tyrosine-derived polymeric nanocarriers: an innovative approach for topical drug delivery in acne therapy.” 2016. Doctoral Dissertation, Rutgers University. Accessed July 14, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/50137/.

MLA Handbook (7th Edition):

Ramezanli, Tannaz, 1985-. “Tyrosine-derived polymeric nanocarriers: an innovative approach for topical drug delivery in acne therapy.” 2016. Web. 14 Jul 2020.

Vancouver:

Ramezanli, Tannaz 1. Tyrosine-derived polymeric nanocarriers: an innovative approach for topical drug delivery in acne therapy. [Internet] [Doctoral dissertation]. Rutgers University; 2016. [cited 2020 Jul 14]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/50137/.

Council of Science Editors:

Ramezanli, Tannaz 1. Tyrosine-derived polymeric nanocarriers: an innovative approach for topical drug delivery in acne therapy. [Doctoral Dissertation]. Rutgers University; 2016. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/50137/


Rutgers University

5. Shah, Milinkumar, 1981-. Strategies to overcome physicochemical and biological barriers in chemotherapy by formulation and drug delivery device combination.

Degree: PhD, Pharmaceutical Science, 2016, Rutgers University

The success of chemotherapy depends on efficacy of drug to enter the cancer cell to exert cytotoxicity. This feat is extremely challenging for drugs with… (more)

Subjects/Keywords: Cyclodextrins; Chemotherapy

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APA (6th Edition):

Shah, Milinkumar, 1. (2016). Strategies to overcome physicochemical and biological barriers in chemotherapy by formulation and drug delivery device combination. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/51461/

Chicago Manual of Style (16th Edition):

Shah, Milinkumar, 1981-. “Strategies to overcome physicochemical and biological barriers in chemotherapy by formulation and drug delivery device combination.” 2016. Doctoral Dissertation, Rutgers University. Accessed July 14, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/51461/.

MLA Handbook (7th Edition):

Shah, Milinkumar, 1981-. “Strategies to overcome physicochemical and biological barriers in chemotherapy by formulation and drug delivery device combination.” 2016. Web. 14 Jul 2020.

Vancouver:

Shah, Milinkumar 1. Strategies to overcome physicochemical and biological barriers in chemotherapy by formulation and drug delivery device combination. [Internet] [Doctoral dissertation]. Rutgers University; 2016. [cited 2020 Jul 14]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/51461/.

Council of Science Editors:

Shah, Milinkumar 1. Strategies to overcome physicochemical and biological barriers in chemotherapy by formulation and drug delivery device combination. [Doctoral Dissertation]. Rutgers University; 2016. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/51461/


Rutgers University

6. Karry-Rivera, Krizia Marie, 1986-. Flexible continuous manufacturing platforms for solid dispersion formulations.

Degree: PhD, Chemical and Biochemical Engineering, 2015, Rutgers University

In 2013 16,000 people died in the US due to overdose from prescription drugs and synthetic narcotics. As of that same year, 90% of new… (more)

Subjects/Keywords: Solid dosage forms; Pharmaceutical chemistry

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APA (6th Edition):

Karry-Rivera, Krizia Marie, 1. (2015). Flexible continuous manufacturing platforms for solid dispersion formulations. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/48538/

Chicago Manual of Style (16th Edition):

Karry-Rivera, Krizia Marie, 1986-. “Flexible continuous manufacturing platforms for solid dispersion formulations.” 2015. Doctoral Dissertation, Rutgers University. Accessed July 14, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/48538/.

MLA Handbook (7th Edition):

Karry-Rivera, Krizia Marie, 1986-. “Flexible continuous manufacturing platforms for solid dispersion formulations.” 2015. Web. 14 Jul 2020.

Vancouver:

Karry-Rivera, Krizia Marie 1. Flexible continuous manufacturing platforms for solid dispersion formulations. [Internet] [Doctoral dissertation]. Rutgers University; 2015. [cited 2020 Jul 14]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/48538/.

Council of Science Editors:

Karry-Rivera, Krizia Marie 1. Flexible continuous manufacturing platforms for solid dispersion formulations. [Doctoral Dissertation]. Rutgers University; 2015. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/48538/


Rutgers University

7. Hu, Longsheng. Transdermal and transbuccal drug delivery: enhancement using iontophoresis and chemical enhancers.

Degree: PhD, Pharmaceutical Science, 2010, Rutgers University

Transdermal and transbuccal routes offer attractive alternatives for systemic delivery of drugs due to their distinct advantages: non-invasive, avoidance of first-pass effect, improved bioavailability and… (more)

Subjects/Keywords: Drug delivery systems; Transdermal medication; Iontophoresis

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APA (6th Edition):

Hu, L. (2010). Transdermal and transbuccal drug delivery: enhancement using iontophoresis and chemical enhancers. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056369

Chicago Manual of Style (16th Edition):

Hu, Longsheng. “Transdermal and transbuccal drug delivery: enhancement using iontophoresis and chemical enhancers.” 2010. Doctoral Dissertation, Rutgers University. Accessed July 14, 2020. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056369.

MLA Handbook (7th Edition):

Hu, Longsheng. “Transdermal and transbuccal drug delivery: enhancement using iontophoresis and chemical enhancers.” 2010. Web. 14 Jul 2020.

Vancouver:

Hu L. Transdermal and transbuccal drug delivery: enhancement using iontophoresis and chemical enhancers. [Internet] [Doctoral dissertation]. Rutgers University; 2010. [cited 2020 Jul 14]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056369.

Council of Science Editors:

Hu L. Transdermal and transbuccal drug delivery: enhancement using iontophoresis and chemical enhancers. [Doctoral Dissertation]. Rutgers University; 2010. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056369


Rutgers University

8. 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 (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 July 14, 2020. 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 Jul 2020.

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 2020 Jul 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

9. Lee, Serom, 1985-. Classification models for identifying skin sensitizers using in vitro alternatives to animal testing.

Degree: PhD, Biomedical Engineering, 2014, Rutgers University

Allergic contact dermatitis (ACD) is an inflammatory disease that occurs when chemicals known as sensitizers come in contact with the skin. Recent European legislation prohibits… (more)

Subjects/Keywords: Contact dermatitis; Alternative toxicity testing

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APA (6th Edition):

Lee, Serom, 1. (2014). Classification models for identifying skin sensitizers using in vitro alternatives to animal testing. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/45328/

Chicago Manual of Style (16th Edition):

Lee, Serom, 1985-. “Classification models for identifying skin sensitizers using in vitro alternatives to animal testing.” 2014. Doctoral Dissertation, Rutgers University. Accessed July 14, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/45328/.

MLA Handbook (7th Edition):

Lee, Serom, 1985-. “Classification models for identifying skin sensitizers using in vitro alternatives to animal testing.” 2014. Web. 14 Jul 2020.

Vancouver:

Lee, Serom 1. Classification models for identifying skin sensitizers using in vitro alternatives to animal testing. [Internet] [Doctoral dissertation]. Rutgers University; 2014. [cited 2020 Jul 14]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/45328/.

Council of Science Editors:

Lee, Serom 1. Classification models for identifying skin sensitizers using in vitro alternatives to animal testing. [Doctoral Dissertation]. Rutgers University; 2014. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/45328/


Rutgers University

10. 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 (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 July 14, 2020. 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 Jul 2020.

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 2020 Jul 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

11. Wang, Haoxun, 1989-. Regulation of renal organic anion transporters.

Degree: PhD, Pharmaceutical Science, 2019, Rutgers University

Organic anion transporters (OATs) are a group of membrane proteins that are mainly involved in the body disposition of organic anionic molecules or zwitterions, including… (more)

Subjects/Keywords: Kidneys  – Molecular aspects; Anions

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APA (6th Edition):

Wang, Haoxun, 1. (2019). Regulation of renal organic anion transporters. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/60932/

Chicago Manual of Style (16th Edition):

Wang, Haoxun, 1989-. “Regulation of renal organic anion transporters.” 2019. Doctoral Dissertation, Rutgers University. Accessed July 14, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/60932/.

MLA Handbook (7th Edition):

Wang, Haoxun, 1989-. “Regulation of renal organic anion transporters.” 2019. Web. 14 Jul 2020.

Vancouver:

Wang, Haoxun 1. Regulation of renal organic anion transporters. [Internet] [Doctoral dissertation]. Rutgers University; 2019. [cited 2020 Jul 14]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/60932/.

Council of Science Editors:

Wang, Haoxun 1. Regulation of renal organic anion transporters. [Doctoral Dissertation]. Rutgers University; 2019. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/60932/


Rutgers University

12. 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 (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 July 14, 2020. 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 Jul 2020.

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 2020 Jul 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

13. Omar, Thamer A., 1978-. Impregnation of active pharmaceutical ingredients into porous carriers.

Degree: PhD, Pharmaceutical Science, 2019, Rutgers University

 Launching of a new drug into the market consumes significant resources and research effort and it involves a number of complex steps in drug substance… (more)

Subjects/Keywords: Impregnation; Drug delivery systems

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APA (6th Edition):

Omar, Thamer A., 1. (2019). Impregnation of active pharmaceutical ingredients into porous carriers. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/61900/

Chicago Manual of Style (16th Edition):

Omar, Thamer A., 1978-. “Impregnation of active pharmaceutical ingredients into porous carriers.” 2019. Doctoral Dissertation, Rutgers University. Accessed July 14, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/61900/.

MLA Handbook (7th Edition):

Omar, Thamer A., 1978-. “Impregnation of active pharmaceutical ingredients into porous carriers.” 2019. Web. 14 Jul 2020.

Vancouver:

Omar, Thamer A. 1. Impregnation of active pharmaceutical ingredients into porous carriers. [Internet] [Doctoral dissertation]. Rutgers University; 2019. [cited 2020 Jul 14]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/61900/.

Council of Science Editors:

Omar, Thamer A. 1. Impregnation of active pharmaceutical ingredients into porous carriers. [Doctoral Dissertation]. Rutgers University; 2019. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/61900/

14. Dorrani, Mania, 1983-. Overcoming challenges for skin deposition of drugs: SiRNA and antimicrobial agents.

Degree: PhD, Pharmaceutical Science, 2017, Rutgers University

Delivery of macromolecules such as siRNA into cells that reside in the basal epidermis of the skin is a major challenge due to the transport… (more)

Subjects/Keywords: Liposomes; Anti-infective agents

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APA (6th Edition):

Dorrani, Mania, 1. (2017). Overcoming challenges for skin deposition of drugs: SiRNA and antimicrobial agents. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/53476/

Chicago Manual of Style (16th Edition):

Dorrani, Mania, 1983-. “Overcoming challenges for skin deposition of drugs: SiRNA and antimicrobial agents.” 2017. Doctoral Dissertation, Rutgers University. Accessed July 14, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/53476/.

MLA Handbook (7th Edition):

Dorrani, Mania, 1983-. “Overcoming challenges for skin deposition of drugs: SiRNA and antimicrobial agents.” 2017. Web. 14 Jul 2020.

Vancouver:

Dorrani, Mania 1. Overcoming challenges for skin deposition of drugs: SiRNA and antimicrobial agents. [Internet] [Doctoral dissertation]. Rutgers University; 2017. [cited 2020 Jul 14]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/53476/.

Council of Science Editors:

Dorrani, Mania 1. Overcoming challenges for skin deposition of drugs: SiRNA and antimicrobial agents. [Doctoral Dissertation]. Rutgers University; 2017. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/53476/

15. Zhang, Qiang, 1978-. Regulation of drug transporters.

Degree: Pharmaceutical Science, 2012, Rutgers University

Subjects/Keywords: Anions; Drug delivery systems

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APA (6th Edition):

Zhang, Qiang, 1. (2012). Regulation of drug transporters. (Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000065308

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):

Zhang, Qiang, 1978-. “Regulation of drug transporters.” 2012. Thesis, Rutgers University. Accessed July 14, 2020. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000065308.

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

MLA Handbook (7th Edition):

Zhang, Qiang, 1978-. “Regulation of drug transporters.” 2012. Web. 14 Jul 2020.

Vancouver:

Zhang, Qiang 1. Regulation of drug transporters. [Internet] [Thesis]. Rutgers University; 2012. [cited 2020 Jul 14]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000065308.

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

Council of Science Editors:

Zhang, Qiang 1. Regulation of drug transporters. [Thesis]. Rutgers University; 2012. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000065308

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

16. Zhang, Ji. Investigation of microemulsions and their microstructures for transdermal and dermal drug delivery.

Degree: PhD, Pharmaceutical Science, 2017, Rutgers University

 Drug delivery through the skin, transdermally and topically, offers many advantages including reduced systemic toxicity and side-effects, avoidance of the hepatic first pass metabolism, improved… (more)

Subjects/Keywords: Emulsions; Drug delivery systems

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APA (6th Edition):

Zhang, J. (2017). Investigation of microemulsions and their microstructures for transdermal and dermal drug delivery. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/55809/

Chicago Manual of Style (16th Edition):

Zhang, Ji. “Investigation of microemulsions and their microstructures for transdermal and dermal drug delivery.” 2017. Doctoral Dissertation, Rutgers University. Accessed July 14, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/55809/.

MLA Handbook (7th Edition):

Zhang, Ji. “Investigation of microemulsions and their microstructures for transdermal and dermal drug delivery.” 2017. Web. 14 Jul 2020.

Vancouver:

Zhang J. Investigation of microemulsions and their microstructures for transdermal and dermal drug delivery. [Internet] [Doctoral dissertation]. Rutgers University; 2017. [cited 2020 Jul 14]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/55809/.

Council of Science Editors:

Zhang J. Investigation of microemulsions and their microstructures for transdermal and dermal drug delivery. [Doctoral Dissertation]. Rutgers University; 2017. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/55809/

17. Yu, Guo, 1983-. Vibrational microspectroscopic imaging of normal, wounded, and artificial skin. I.Wound characterization in skin punch biopsies and diabetic foot ulcers. II. Molecular organization of human skin equivalents.

Degree: Chemistry, 2013, Rutgers University

Subjects/Keywords: Spectrum analysis; Foot – Wounds and injuries – Complications; Skin – Wounds and injuries – Complications; Diabetes – Complications

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APA (6th Edition):

Yu, Guo, 1. (2013). Vibrational microspectroscopic imaging of normal, wounded, and artificial skin. I.Wound characterization in skin punch biopsies and diabetic foot ulcers. II. Molecular organization of human skin equivalents. (Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10002600001.ETD.000068791

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):

Yu, Guo, 1983-. “Vibrational microspectroscopic imaging of normal, wounded, and artificial skin. I.Wound characterization in skin punch biopsies and diabetic foot ulcers. II. Molecular organization of human skin equivalents.” 2013. Thesis, Rutgers University. Accessed July 14, 2020. http://hdl.rutgers.edu/1782.1/rucore10002600001.ETD.000068791.

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

MLA Handbook (7th Edition):

Yu, Guo, 1983-. “Vibrational microspectroscopic imaging of normal, wounded, and artificial skin. I.Wound characterization in skin punch biopsies and diabetic foot ulcers. II. Molecular organization of human skin equivalents.” 2013. Web. 14 Jul 2020.

Vancouver:

Yu, Guo 1. Vibrational microspectroscopic imaging of normal, wounded, and artificial skin. I.Wound characterization in skin punch biopsies and diabetic foot ulcers. II. Molecular organization of human skin equivalents. [Internet] [Thesis]. Rutgers University; 2013. [cited 2020 Jul 14]. Available from: http://hdl.rutgers.edu/1782.1/rucore10002600001.ETD.000068791.

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

Council of Science Editors:

Yu, Guo 1. Vibrational microspectroscopic imaging of normal, wounded, and artificial skin. I.Wound characterization in skin punch biopsies and diabetic foot ulcers. II. Molecular organization of human skin equivalents. [Thesis]. Rutgers University; 2013. Available from: http://hdl.rutgers.edu/1782.1/rucore10002600001.ETD.000068791

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

18. Bose, Sonali, 1973-. Development and characterization of lipid based nanosystems of quercetin for topical delivery.

Degree: Pharmaceutical Science, 2012, Rutgers University

Subjects/Keywords: Quercetin; Nanoparticles; Lipids – Research

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

APA (6th Edition):

Bose, Sonali, 1. (2012). Development and characterization of lipid based nanosystems of quercetin for topical delivery. (Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000066641

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):

Bose, Sonali, 1973-. “Development and characterization of lipid based nanosystems of quercetin for topical delivery.” 2012. Thesis, Rutgers University. Accessed July 14, 2020. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000066641.

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

MLA Handbook (7th Edition):

Bose, Sonali, 1973-. “Development and characterization of lipid based nanosystems of quercetin for topical delivery.” 2012. Web. 14 Jul 2020.

Vancouver:

Bose, Sonali 1. Development and characterization of lipid based nanosystems of quercetin for topical delivery. [Internet] [Thesis]. Rutgers University; 2012. [cited 2020 Jul 14]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000066641.

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

Council of Science Editors:

Bose, Sonali 1. Development and characterization of lipid based nanosystems of quercetin for topical delivery. [Thesis]. Rutgers University; 2012. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000066641

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

19. Batheja, Priya B., 1975-. Polymeric nanospheres for skin penetration enhancement: in vitro and in vivo assessment in skin models.

Degree: PhD, Pharmaceutical Science, 2010, Rutgers University

Research and development in the field of topical and transdermal delivery has been particularly challenging due to the tough penetration barrier provided by the stratum… (more)

Subjects/Keywords: Polymeric drug delivery systems; Transdermal medication

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APA (6th Edition):

Batheja, Priya B., 1. (2010). Polymeric nanospheres for skin penetration enhancement: in vitro and in vivo assessment in skin models. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000052097

Chicago Manual of Style (16th Edition):

Batheja, Priya B., 1975-. “Polymeric nanospheres for skin penetration enhancement: in vitro and in vivo assessment in skin models.” 2010. Doctoral Dissertation, Rutgers University. Accessed July 14, 2020. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000052097.

MLA Handbook (7th Edition):

Batheja, Priya B., 1975-. “Polymeric nanospheres for skin penetration enhancement: in vitro and in vivo assessment in skin models.” 2010. Web. 14 Jul 2020.

Vancouver:

Batheja, Priya B. 1. Polymeric nanospheres for skin penetration enhancement: in vitro and in vivo assessment in skin models. [Internet] [Doctoral dissertation]. Rutgers University; 2010. [cited 2020 Jul 14]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000052097.

Council of Science Editors:

Batheja, Priya B. 1. Polymeric nanospheres for skin penetration enhancement: in vitro and in vivo assessment in skin models. [Doctoral Dissertation]. Rutgers University; 2010. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000052097


Rutgers University

20. Cook, Rebecca Ann. In-vitro testing of the influence of ethanol on the release rate of oral extended-release solid dosage forms.

Degree: MS
[bibliography], Pharmaceutical Science, 2006, Rutgers University

 There are many factors that can affect the rate of drug release from an extended-release formulation, such pH of the gastrointestinal tract and dietary intake… (more)

Subjects/Keywords: Drugs; Enteric-coated tablets; Tablets (Medicine)

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

APA (6th Edition):

Cook, R. A. (2006). In-vitro testing of the influence of ethanol on the release rate of oral extended-release solid dosage forms. (Masters Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.13454

Chicago Manual of Style (16th Edition):

Cook, Rebecca Ann. “In-vitro testing of the influence of ethanol on the release rate of oral extended-release solid dosage forms.” 2006. Masters Thesis, Rutgers University. Accessed July 14, 2020. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.13454.

MLA Handbook (7th Edition):

Cook, Rebecca Ann. “In-vitro testing of the influence of ethanol on the release rate of oral extended-release solid dosage forms.” 2006. Web. 14 Jul 2020.

Vancouver:

Cook RA. In-vitro testing of the influence of ethanol on the release rate of oral extended-release solid dosage forms. [Internet] [Masters thesis]. Rutgers University; 2006. [cited 2020 Jul 14]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.13454.

Council of Science Editors:

Cook RA. In-vitro testing of the influence of ethanol on the release rate of oral extended-release solid dosage forms. [Masters Thesis]. Rutgers University; 2006. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.13454


Rutgers University

21. Terebetski, Jenna Leschek, 1981-. Influence of polymers on supersaturation of ibuprofen sodium in vitro and in vivo: a mechanistic evaluation.

Degree: Pharmaceutical Science, 2014, Rutgers University

Subjects/Keywords: Ibuprofen; Absorption (Physiology); Polymers in medicine; Polymeric drug delivery systems

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

APA (6th Edition):

Terebetski, Jenna Leschek, 1. (2014). Influence of polymers on supersaturation of ibuprofen sodium in vitro and in vivo: a mechanistic evaluation. (Thesis). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/44246/

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):

Terebetski, Jenna Leschek, 1981-. “Influence of polymers on supersaturation of ibuprofen sodium in vitro and in vivo: a mechanistic evaluation.” 2014. Thesis, Rutgers University. Accessed July 14, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/44246/.

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

MLA Handbook (7th Edition):

Terebetski, Jenna Leschek, 1981-. “Influence of polymers on supersaturation of ibuprofen sodium in vitro and in vivo: a mechanistic evaluation.” 2014. Web. 14 Jul 2020.

Vancouver:

Terebetski, Jenna Leschek 1. Influence of polymers on supersaturation of ibuprofen sodium in vitro and in vivo: a mechanistic evaluation. [Internet] [Thesis]. Rutgers University; 2014. [cited 2020 Jul 14]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/44246/.

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

Council of Science Editors:

Terebetski, Jenna Leschek 1. Influence of polymers on supersaturation of ibuprofen sodium in vitro and in vivo: a mechanistic evaluation. [Thesis]. Rutgers University; 2014. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/44246/

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


Rutgers University

22. Brown, Marlena. The feasibility of the utilization of drop-on-demand technology in the fabrication of flexible dosing, poly-pharmacy, and novel multi-drug design dosage forms.

Degree: Biomedical Engineering, 2014, Rutgers University

Subjects/Keywords: Drug delivery systems; Pharmaceutical technology; Drugs – Dosage forms

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APA (6th Edition):

Brown, M. (2014). The feasibility of the utilization of drop-on-demand technology in the fabrication of flexible dosing, poly-pharmacy, and novel multi-drug design dosage forms. (Thesis). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/44024/

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):

Brown, Marlena. “The feasibility of the utilization of drop-on-demand technology in the fabrication of flexible dosing, poly-pharmacy, and novel multi-drug design dosage forms.” 2014. Thesis, Rutgers University. Accessed July 14, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/44024/.

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

MLA Handbook (7th Edition):

Brown, Marlena. “The feasibility of the utilization of drop-on-demand technology in the fabrication of flexible dosing, poly-pharmacy, and novel multi-drug design dosage forms.” 2014. Web. 14 Jul 2020.

Vancouver:

Brown M. The feasibility of the utilization of drop-on-demand technology in the fabrication of flexible dosing, poly-pharmacy, and novel multi-drug design dosage forms. [Internet] [Thesis]. Rutgers University; 2014. [cited 2020 Jul 14]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/44024/.

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

Council of Science Editors:

Brown M. The feasibility of the utilization of drop-on-demand technology in the fabrication of flexible dosing, poly-pharmacy, and novel multi-drug design dosage forms. [Thesis]. Rutgers University; 2014. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/44024/

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


Rutgers University

23. LaMarche, Keirnan R. Electrostatic instabilities, charging and agglomeration in flowing granular materials.

Degree: PhD, Chemical and Biochemical Engineering, 2008, Rutgers University

The unpredictable behavior of granular materials is one of the largest stumbling blocks on the way to satisfactory design and control of many manufacturing processes.… (more)

Subjects/Keywords: Electrostatics; Granular materials

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APA (6th Edition):

LaMarche, K. R. (2008). Electrostatic instabilities, charging and agglomeration in flowing granular materials. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.17342

Chicago Manual of Style (16th Edition):

LaMarche, Keirnan R. “Electrostatic instabilities, charging and agglomeration in flowing granular materials.” 2008. Doctoral Dissertation, Rutgers University. Accessed July 14, 2020. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.17342.

MLA Handbook (7th Edition):

LaMarche, Keirnan R. “Electrostatic instabilities, charging and agglomeration in flowing granular materials.” 2008. Web. 14 Jul 2020.

Vancouver:

LaMarche KR. Electrostatic instabilities, charging and agglomeration in flowing granular materials. [Internet] [Doctoral dissertation]. Rutgers University; 2008. [cited 2020 Jul 14]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.17342.

Council of Science Editors:

LaMarche KR. Electrostatic instabilities, charging and agglomeration in flowing granular materials. [Doctoral Dissertation]. Rutgers University; 2008. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.17342


Rutgers University

24. Lee, Sung-Hack. Characterizing the mechanism of differential pharmacokinetic disposition of two structurally similar nucleoside reverse transcriptase inhibitors, zidovudine and didanosine.

Degree: PhD, Pharmaceutical Science, 2008, Rutgers University

The differential contributions of efflux transporters and metabolizing enzymes to the disposition of zidovudine (azidothymidine, AZT) and didanosine (dideoxyinosine, ddI) were investigated using murine and… (more)

Subjects/Keywords: Pharmacokinetics; Reverse transcriptase; Nucleosides – Derivatives; AZT (Drug); Antiviral agents

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APA (6th Edition):

Lee, S. (2008). Characterizing the mechanism of differential pharmacokinetic disposition of two structurally similar nucleoside reverse transcriptase inhibitors, zidovudine and didanosine. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.17344

Chicago Manual of Style (16th Edition):

Lee, Sung-Hack. “Characterizing the mechanism of differential pharmacokinetic disposition of two structurally similar nucleoside reverse transcriptase inhibitors, zidovudine and didanosine.” 2008. Doctoral Dissertation, Rutgers University. Accessed July 14, 2020. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.17344.

MLA Handbook (7th Edition):

Lee, Sung-Hack. “Characterizing the mechanism of differential pharmacokinetic disposition of two structurally similar nucleoside reverse transcriptase inhibitors, zidovudine and didanosine.” 2008. Web. 14 Jul 2020.

Vancouver:

Lee S. Characterizing the mechanism of differential pharmacokinetic disposition of two structurally similar nucleoside reverse transcriptase inhibitors, zidovudine and didanosine. [Internet] [Doctoral dissertation]. Rutgers University; 2008. [cited 2020 Jul 14]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.17344.

Council of Science Editors:

Lee S. Characterizing the mechanism of differential pharmacokinetic disposition of two structurally similar nucleoside reverse transcriptase inhibitors, zidovudine and didanosine. [Doctoral Dissertation]. Rutgers University; 2008. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.17344


Rutgers University

25. Rai, Vishwas. Drug permeability in tissue engineered models and cytotoxicity evaluations.

Degree: Pharmaceutical Science, 2011, Rutgers University

Subjects/Keywords: Toxicity testing—In vitro; Tissue engineering

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APA (6th Edition):

Rai, V. (2011). Drug permeability in tissue engineered models and cytotoxicity evaluations. (Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063578

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):

Rai, Vishwas. “Drug permeability in tissue engineered models and cytotoxicity evaluations.” 2011. Thesis, Rutgers University. Accessed July 14, 2020. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063578.

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

MLA Handbook (7th Edition):

Rai, Vishwas. “Drug permeability in tissue engineered models and cytotoxicity evaluations.” 2011. Web. 14 Jul 2020.

Vancouver:

Rai V. Drug permeability in tissue engineered models and cytotoxicity evaluations. [Internet] [Thesis]. Rutgers University; 2011. [cited 2020 Jul 14]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063578.

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

Council of Science Editors:

Rai V. Drug permeability in tissue engineered models and cytotoxicity evaluations. [Thesis]. Rutgers University; 2011. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063578

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


Rutgers University

26. Zhang, Min, 1979-. Two-in-one: combined targeted nanoscale-based chemo and gene therapy for tumor suppression and prevention of metastases.

Degree: Pharmaceutical Science, 2011, Rutgers University

Subjects/Keywords: Ovaries—Tumors; Ovaries – Cancer—Treatment; Ovaries – Cancer—Gene therapy

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APA (6th Edition):

Zhang, Min, 1. (2011). Two-in-one: combined targeted nanoscale-based chemo and gene therapy for tumor suppression and prevention of metastases. (Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063704

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):

Zhang, Min, 1979-. “Two-in-one: combined targeted nanoscale-based chemo and gene therapy for tumor suppression and prevention of metastases.” 2011. Thesis, Rutgers University. Accessed July 14, 2020. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063704.

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

MLA Handbook (7th Edition):

Zhang, Min, 1979-. “Two-in-one: combined targeted nanoscale-based chemo and gene therapy for tumor suppression and prevention of metastases.” 2011. Web. 14 Jul 2020.

Vancouver:

Zhang, Min 1. Two-in-one: combined targeted nanoscale-based chemo and gene therapy for tumor suppression and prevention of metastases. [Internet] [Thesis]. Rutgers University; 2011. [cited 2020 Jul 14]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063704.

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

Council of Science Editors:

Zhang, Min 1. Two-in-one: combined targeted nanoscale-based chemo and gene therapy for tumor suppression and prevention of metastases. [Thesis]. Rutgers University; 2011. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063704

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


Rutgers University

27. Kilfoyle, Brian E., 1978-. Tyrosine-derived nanoparticles for the topical treatment of psoriasis.

Degree: Pharmaceutical Science, 2011, Rutgers University

Subjects/Keywords: Psoriasis – Treatment; Nanoparticles; Tyrosine

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APA (6th Edition):

Kilfoyle, Brian E., 1. (2011). Tyrosine-derived nanoparticles for the topical treatment of psoriasis. (Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063491

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):

Kilfoyle, Brian E., 1978-. “Tyrosine-derived nanoparticles for the topical treatment of psoriasis.” 2011. Thesis, Rutgers University. Accessed July 14, 2020. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063491.

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

MLA Handbook (7th Edition):

Kilfoyle, Brian E., 1978-. “Tyrosine-derived nanoparticles for the topical treatment of psoriasis.” 2011. Web. 14 Jul 2020.

Vancouver:

Kilfoyle, Brian E. 1. Tyrosine-derived nanoparticles for the topical treatment of psoriasis. [Internet] [Thesis]. Rutgers University; 2011. [cited 2020 Jul 14]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063491.

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

Council of Science Editors:

Kilfoyle, Brian E. 1. Tyrosine-derived nanoparticles for the topical treatment of psoriasis. [Thesis]. Rutgers University; 2011. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063491

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


Rutgers University

28. 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 (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 July 14, 2020. 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 Jul 2020.

Vancouver:

Wang, Hu 1. Studies on Nrf2-targeted phytochemicals: signal transduction, bioanalysis, pharmacokinetics, and pharmacodynamics for their druggability. [Internet] [Thesis]. Rutgers University; 2012. [cited 2020 Jul 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

29. 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 (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 July 14, 2020. 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 Jul 2020.

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 2020 Jul 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

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