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You searched for +publisher:"Rutgers University" +contributor:("Uhrich, Kathryn "). Showing records 1 – 28 of 28 total matches.

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Rutgers University

1. Demirdirek, Bahar. Synthesis and evaluation of amphiphilic scorpion-like and star macromolecules for biomedical applications.

Degree: MS, Chemistry and Chemical Biology, 2009, Rutgers University

 Self-assembled and unimolecular amphiphilic macromolecules with pseudo-double branched and single tails were synthesized. Degradation behavior, drug loading efficiency, drug release rate and stability of macromolecules… (more)

Subjects/Keywords: Drug delivery systems

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APA (6th Edition):

Demirdirek, B. (2009). Synthesis and evaluation of amphiphilic scorpion-like and star macromolecules for biomedical applications. (Masters Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000050505

Chicago Manual of Style (16th Edition):

Demirdirek, Bahar. “Synthesis and evaluation of amphiphilic scorpion-like and star macromolecules for biomedical applications.” 2009. Masters Thesis, Rutgers University. Accessed March 21, 2019. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000050505.

MLA Handbook (7th Edition):

Demirdirek, Bahar. “Synthesis and evaluation of amphiphilic scorpion-like and star macromolecules for biomedical applications.” 2009. Web. 21 Mar 2019.

Vancouver:

Demirdirek B. Synthesis and evaluation of amphiphilic scorpion-like and star macromolecules for biomedical applications. [Internet] [Masters thesis]. Rutgers University; 2009. [cited 2019 Mar 21]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000050505.

Council of Science Editors:

Demirdirek B. Synthesis and evaluation of amphiphilic scorpion-like and star macromolecules for biomedical applications. [Masters Thesis]. Rutgers University; 2009. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000050505


Rutgers University

2. del Rosario, Leilani Singson. Preparation and evaluation of amphiphilic macromolecules-based conjugates and micelles for anticancer drug delivery:.

Degree: PhD, Chemistry and Chemical Biology, 2009, Rutgers University

Micelles assembled from amphiphilic macromolecules (AM) or drug-conjugated AMs were evaluated as anticancer drug carriers in terms of drug content, sustained/controlled drug release and cytotoxicity… (more)

Subjects/Keywords: Drug delivery systems

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APA (6th Edition):

del Rosario, L. S. (2009). Preparation and evaluation of amphiphilic macromolecules-based conjugates and micelles for anticancer drug delivery:. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051195

Chicago Manual of Style (16th Edition):

del Rosario, Leilani Singson. “Preparation and evaluation of amphiphilic macromolecules-based conjugates and micelles for anticancer drug delivery:.” 2009. Doctoral Dissertation, Rutgers University. Accessed March 21, 2019. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051195.

MLA Handbook (7th Edition):

del Rosario, Leilani Singson. “Preparation and evaluation of amphiphilic macromolecules-based conjugates and micelles for anticancer drug delivery:.” 2009. Web. 21 Mar 2019.

Vancouver:

del Rosario LS. Preparation and evaluation of amphiphilic macromolecules-based conjugates and micelles for anticancer drug delivery:. [Internet] [Doctoral dissertation]. Rutgers University; 2009. [cited 2019 Mar 21]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051195.

Council of Science Editors:

del Rosario LS. Preparation and evaluation of amphiphilic macromolecules-based conjugates and micelles for anticancer drug delivery:. [Doctoral Dissertation]. Rutgers University; 2009. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051195


Rutgers University

3. Carbone, Ashley Lauren, 1984. Natural bioactive-based polyanhydrides for controlled release applications:.

Degree: PhD, Chemistry, 2009, Rutgers University

Hydrolytically degradable polyanhydrides are of interest for a variety of controlled release applications because of their surface-eroding behavior and tunable degradation rate based on polymer… (more)

Subjects/Keywords: Controlled release technology; Anhydrides

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APA (6th Edition):

Carbone, Ashley Lauren, 1. (2009). Natural bioactive-based polyanhydrides for controlled release applications:. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051788

Chicago Manual of Style (16th Edition):

Carbone, Ashley Lauren, 1984. “Natural bioactive-based polyanhydrides for controlled release applications:.” 2009. Doctoral Dissertation, Rutgers University. Accessed March 21, 2019. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051788.

MLA Handbook (7th Edition):

Carbone, Ashley Lauren, 1984. “Natural bioactive-based polyanhydrides for controlled release applications:.” 2009. Web. 21 Mar 2019.

Vancouver:

Carbone, Ashley Lauren 1. Natural bioactive-based polyanhydrides for controlled release applications:. [Internet] [Doctoral dissertation]. Rutgers University; 2009. [cited 2019 Mar 21]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051788.

Council of Science Editors:

Carbone, Ashley Lauren 1. Natural bioactive-based polyanhydrides for controlled release applications:. [Doctoral Dissertation]. Rutgers University; 2009. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051788


Rutgers University

4. Rojas Escontrillas, Ramiro, 1980-. Exploration of biomaterials design space through combinatorial and high-throughput approaches: tyrosine-derived polycarbonates as a case study.

Degree: PhD, Chemistry and Chemical Biology, 2009, Rutgers University

The use of combinatorial and high-throughput approaches in the design and exploration of materials space has been gaining increasing acceptance in recent years. While these… (more)

Subjects/Keywords: Biopolymers; Biomedical materials; Tyrosine

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APA (6th Edition):

Rojas Escontrillas, Ramiro, 1. (2009). Exploration of biomaterials design space through combinatorial and high-throughput approaches: tyrosine-derived polycarbonates as a case study. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000052262

Chicago Manual of Style (16th Edition):

Rojas Escontrillas, Ramiro, 1980-. “Exploration of biomaterials design space through combinatorial and high-throughput approaches: tyrosine-derived polycarbonates as a case study.” 2009. Doctoral Dissertation, Rutgers University. Accessed March 21, 2019. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000052262.

MLA Handbook (7th Edition):

Rojas Escontrillas, Ramiro, 1980-. “Exploration of biomaterials design space through combinatorial and high-throughput approaches: tyrosine-derived polycarbonates as a case study.” 2009. Web. 21 Mar 2019.

Vancouver:

Rojas Escontrillas, Ramiro 1. Exploration of biomaterials design space through combinatorial and high-throughput approaches: tyrosine-derived polycarbonates as a case study. [Internet] [Doctoral dissertation]. Rutgers University; 2009. [cited 2019 Mar 21]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000052262.

Council of Science Editors:

Rojas Escontrillas, Ramiro 1. Exploration of biomaterials design space through combinatorial and high-throughput approaches: tyrosine-derived polycarbonates as a case study. [Doctoral Dissertation]. Rutgers University; 2009. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000052262


Rutgers University

5. Cui, Han, 1971-. An investigation of Poly (caprolactone-co-glycolide) interaction with bioactive proteins and cellular responses.

Degree: PhD, Pharmaceutical Science, 2010, Rutgers University

The objective of the present investigation is to systematically evaluate the role of polymer crystallinity on osteoblast adhesion, proliferation, osteogenic gene expression and bioactive protein… (more)

Subjects/Keywords: Polymers – Testing; Crystalline polymers

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APA (6th Edition):

Cui, Han, 1. (2010). An investigation of Poly (caprolactone-co-glycolide) interaction with bioactive proteins and cellular responses. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000053021

Chicago Manual of Style (16th Edition):

Cui, Han, 1971-. “An investigation of Poly (caprolactone-co-glycolide) interaction with bioactive proteins and cellular responses.” 2010. Doctoral Dissertation, Rutgers University. Accessed March 21, 2019. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000053021.

MLA Handbook (7th Edition):

Cui, Han, 1971-. “An investigation of Poly (caprolactone-co-glycolide) interaction with bioactive proteins and cellular responses.” 2010. Web. 21 Mar 2019.

Vancouver:

Cui, Han 1. An investigation of Poly (caprolactone-co-glycolide) interaction with bioactive proteins and cellular responses. [Internet] [Doctoral dissertation]. Rutgers University; 2010. [cited 2019 Mar 21]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000053021.

Council of Science Editors:

Cui, Han 1. An investigation of Poly (caprolactone-co-glycolide) interaction with bioactive proteins and cellular responses. [Doctoral Dissertation]. Rutgers University; 2010. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000053021


Rutgers University

6. Iverson, Nicole M, 1981-. Multifunctional polymers for inhibition of oxidized lipoprotein accumulation and inflammation in macrophage cells.

Degree: PhD, Biomedical Engineering, 2010, Rutgers University

A major cause of cardiovascular disease is atherosclerosis, the progressive accumulation and modification of low density lipoproteins (LDL) within the vascular wall associated with a… (more)

Subjects/Keywords: Macrophages; Low density lipoproteins; Atherosclerosis – Treatment; Polymers in medicine

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APA (6th Edition):

Iverson, Nicole M, 1. (2010). Multifunctional polymers for inhibition of oxidized lipoprotein accumulation and inflammation in macrophage cells. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000053095

Chicago Manual of Style (16th Edition):

Iverson, Nicole M, 1981-. “Multifunctional polymers for inhibition of oxidized lipoprotein accumulation and inflammation in macrophage cells.” 2010. Doctoral Dissertation, Rutgers University. Accessed March 21, 2019. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000053095.

MLA Handbook (7th Edition):

Iverson, Nicole M, 1981-. “Multifunctional polymers for inhibition of oxidized lipoprotein accumulation and inflammation in macrophage cells.” 2010. Web. 21 Mar 2019.

Vancouver:

Iverson, Nicole M 1. Multifunctional polymers for inhibition of oxidized lipoprotein accumulation and inflammation in macrophage cells. [Internet] [Doctoral dissertation]. Rutgers University; 2010. [cited 2019 Mar 21]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000053095.

Council of Science Editors:

Iverson, Nicole M 1. Multifunctional polymers for inhibition of oxidized lipoprotein accumulation and inflammation in macrophage cells. [Doctoral Dissertation]. Rutgers University; 2010. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000053095

7. Schachter, David, 1987-. The source of toxicity in CTAB and CTAB-stabilized gold nanorods.

Degree: MS, Biomedical Engineering, 2013, Rutgers University

 The use of nanoparticles for sensing, cell imaging, and therapy has seen an extraordinary increase, in recent years. But, one of the issues commonly encountered… (more)

Subjects/Keywords: Nanoparticles – Toxicology; Nanostructured materials – Therapeutic use – Side effects

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APA (6th Edition):

Schachter, David, 1. (2013). The source of toxicity in CTAB and CTAB-stabilized gold nanorods. (Masters Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000067830

Chicago Manual of Style (16th Edition):

Schachter, David, 1987-. “The source of toxicity in CTAB and CTAB-stabilized gold nanorods.” 2013. Masters Thesis, Rutgers University. Accessed March 21, 2019. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000067830.

MLA Handbook (7th Edition):

Schachter, David, 1987-. “The source of toxicity in CTAB and CTAB-stabilized gold nanorods.” 2013. Web. 21 Mar 2019.

Vancouver:

Schachter, David 1. The source of toxicity in CTAB and CTAB-stabilized gold nanorods. [Internet] [Masters thesis]. Rutgers University; 2013. [cited 2019 Mar 21]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000067830.

Council of Science Editors:

Schachter, David 1. The source of toxicity in CTAB and CTAB-stabilized gold nanorods. [Masters Thesis]. Rutgers University; 2013. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000067830

8. Memoli, Kevin A., 1959-. Polymers for the sustained and localized release of anti-inflammatory and anti-cancer drugs.

Degree: MS, Chemistry and Chemical Biology, 2012, Rutgers University

 The practical utility of chemically incorporating drugs into polymers for the localized and sustained delivery of such drugs has been well established. Sustained release provides… (more)

Subjects/Keywords: Polymeric drug delivery systems; Drugs – Controlled release; Anti-inflammatory agents – Controlled release; Cancer – Treatment

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APA (6th Edition):

Memoli, Kevin A., 1. (2012). Polymers for the sustained and localized release of anti-inflammatory and anti-cancer drugs. (Masters Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000066913

Chicago Manual of Style (16th Edition):

Memoli, Kevin A., 1959-. “Polymers for the sustained and localized release of anti-inflammatory and anti-cancer drugs.” 2012. Masters Thesis, Rutgers University. Accessed March 21, 2019. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000066913.

MLA Handbook (7th Edition):

Memoli, Kevin A., 1959-. “Polymers for the sustained and localized release of anti-inflammatory and anti-cancer drugs.” 2012. Web. 21 Mar 2019.

Vancouver:

Memoli, Kevin A. 1. Polymers for the sustained and localized release of anti-inflammatory and anti-cancer drugs. [Internet] [Masters thesis]. Rutgers University; 2012. [cited 2019 Mar 21]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000066913.

Council of Science Editors:

Memoli, Kevin A. 1. Polymers for the sustained and localized release of anti-inflammatory and anti-cancer drugs. [Masters Thesis]. Rutgers University; 2012. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000066913

9. Lee, Yong Soo, 1983-. In vivo evaluation of nerve guidance conduits comprised of a salicylic acid-based poly(anhydride-ester) blend.

Degree: MS, Biomedical Engineering, 2012, Rutgers University

 Unlike the central nervous system, peripheral nervous system can regenerate from injury. However, without surgical intervention, the results are often poor. Autologous nerve grafting is… (more)

Subjects/Keywords: Neural circuitry; Nerves, Peripheral

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APA (6th Edition):

Lee, Yong Soo, 1. (2012). In vivo evaluation of nerve guidance conduits comprised of a salicylic acid-based poly(anhydride-ester) blend. (Masters Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000066890

Chicago Manual of Style (16th Edition):

Lee, Yong Soo, 1983-. “In vivo evaluation of nerve guidance conduits comprised of a salicylic acid-based poly(anhydride-ester) blend.” 2012. Masters Thesis, Rutgers University. Accessed March 21, 2019. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000066890.

MLA Handbook (7th Edition):

Lee, Yong Soo, 1983-. “In vivo evaluation of nerve guidance conduits comprised of a salicylic acid-based poly(anhydride-ester) blend.” 2012. Web. 21 Mar 2019.

Vancouver:

Lee, Yong Soo 1. In vivo evaluation of nerve guidance conduits comprised of a salicylic acid-based poly(anhydride-ester) blend. [Internet] [Masters thesis]. Rutgers University; 2012. [cited 2019 Mar 21]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000066890.

Council of Science Editors:

Lee, Yong Soo 1. In vivo evaluation of nerve guidance conduits comprised of a salicylic acid-based poly(anhydride-ester) blend. [Masters Thesis]. Rutgers University; 2012. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000066890

10. Solanki, Aniruddh P. Nanotechnology-based approaches for regenerative medicine and biosensing.

Degree: Chemistry and Chemical Biology, 2013, Rutgers University

Subjects/Keywords: Nanomedicine; Regenerative medicine; Biosensors

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APA (6th Edition):

Solanki, A. P. (2013). Nanotechnology-based approaches for regenerative medicine and biosensing. (Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000068971

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):

Solanki, Aniruddh P. “Nanotechnology-based approaches for regenerative medicine and biosensing.” 2013. Thesis, Rutgers University. Accessed March 21, 2019. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000068971.

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

MLA Handbook (7th Edition):

Solanki, Aniruddh P. “Nanotechnology-based approaches for regenerative medicine and biosensing.” 2013. Web. 21 Mar 2019.

Vancouver:

Solanki AP. Nanotechnology-based approaches for regenerative medicine and biosensing. [Internet] [Thesis]. Rutgers University; 2013. [cited 2019 Mar 21]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000068971.

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

Council of Science Editors:

Solanki AP. Nanotechnology-based approaches for regenerative medicine and biosensing. [Thesis]. Rutgers University; 2013. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000068971

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

11. Palombo, Matthew S., 1982-. CXCR4 targeted peptide carriers for the inhibition of HIV and delivery of anti-viral drugs.

Degree: Pharmaceutical Science, 2013, Rutgers University

Subjects/Keywords: Chemokines; HIV infections – Treatment; HIV (Viruses); Peptide drugs – Dosage forms

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APA (6th Edition):

Palombo, Matthew S., 1. (2013). CXCR4 targeted peptide carriers for the inhibition of HIV and delivery of anti-viral drugs. (Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000068930

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):

Palombo, Matthew S., 1982-. “CXCR4 targeted peptide carriers for the inhibition of HIV and delivery of anti-viral drugs.” 2013. Thesis, Rutgers University. Accessed March 21, 2019. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000068930.

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

MLA Handbook (7th Edition):

Palombo, Matthew S., 1982-. “CXCR4 targeted peptide carriers for the inhibition of HIV and delivery of anti-viral drugs.” 2013. Web. 21 Mar 2019.

Vancouver:

Palombo, Matthew S. 1. CXCR4 targeted peptide carriers for the inhibition of HIV and delivery of anti-viral drugs. [Internet] [Thesis]. Rutgers University; 2013. [cited 2019 Mar 21]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000068930.

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

Council of Science Editors:

Palombo, Matthew S. 1. CXCR4 targeted peptide carriers for the inhibition of HIV and delivery of anti-viral drugs. [Thesis]. Rutgers University; 2013. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000068930

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

12. Plourde, Nicole M., 1982-. Structure-binding activity relations of amphiphilic polymers and macrophage scavenger receptors: implications for therapeutic inhibition of atherosclerosis.

Degree: PhD, Chemical and Biochemical Engineering, 2010, Rutgers University

Scavenger receptors mediate the uptake of oxidized low density lipoprotein (oxLDL), leading to cholesterol accumulation and the development of atherosclerosis. A promising avenue of interest… (more)

Subjects/Keywords: Atherosclerosis – Treatment; Low density lipoproteins; Cardiovascular receptors; Molecules – Models

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APA (6th Edition):

Plourde, Nicole M., 1. (2010). Structure-binding activity relations of amphiphilic polymers and macrophage scavenger receptors: implications for therapeutic inhibition of atherosclerosis. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056724

Chicago Manual of Style (16th Edition):

Plourde, Nicole M., 1982-. “Structure-binding activity relations of amphiphilic polymers and macrophage scavenger receptors: implications for therapeutic inhibition of atherosclerosis.” 2010. Doctoral Dissertation, Rutgers University. Accessed March 21, 2019. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056724.

MLA Handbook (7th Edition):

Plourde, Nicole M., 1982-. “Structure-binding activity relations of amphiphilic polymers and macrophage scavenger receptors: implications for therapeutic inhibition of atherosclerosis.” 2010. Web. 21 Mar 2019.

Vancouver:

Plourde, Nicole M. 1. Structure-binding activity relations of amphiphilic polymers and macrophage scavenger receptors: implications for therapeutic inhibition of atherosclerosis. [Internet] [Doctoral dissertation]. Rutgers University; 2010. [cited 2019 Mar 21]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056724.

Council of Science Editors:

Plourde, Nicole M. 1. Structure-binding activity relations of amphiphilic polymers and macrophage scavenger receptors: implications for therapeutic inhibition of atherosclerosis. [Doctoral Dissertation]. Rutgers University; 2010. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056724

13. Rosario-Melendez, Roselin, 1986-. Polymeric drugs for controlled release of analgesics.

Degree: Chemistry and Chemical Biology, 2013, Rutgers University

Subjects/Keywords: Analgesics; Polymeric drugs; Polymeric drug delivery systems; Morphine

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APA (6th Edition):

Rosario-Melendez, Roselin, 1. (2013). Polymeric drugs for controlled release of analgesics. (Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000067825

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):

Rosario-Melendez, Roselin, 1986-. “Polymeric drugs for controlled release of analgesics.” 2013. Thesis, Rutgers University. Accessed March 21, 2019. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000067825.

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

MLA Handbook (7th Edition):

Rosario-Melendez, Roselin, 1986-. “Polymeric drugs for controlled release of analgesics.” 2013. Web. 21 Mar 2019.

Vancouver:

Rosario-Melendez, Roselin 1. Polymeric drugs for controlled release of analgesics. [Internet] [Thesis]. Rutgers University; 2013. [cited 2019 Mar 21]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000067825.

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

Council of Science Editors:

Rosario-Melendez, Roselin 1. Polymeric drugs for controlled release of analgesics. [Thesis]. Rutgers University; 2013. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000067825

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

14. Griffin, Jeremy. The design and fabrication of novel polyanhydride blend scaffolds for peripheral nerve repair.

Degree: PhD, Biomedical Engineering, 2011, Rutgers University

Implantable biodegradable nerve guidance conduits (NGCs) are promising alternatives to autograft nerve for tissue regeneration. The conduit scaffolds have the potential to align and support… (more)

Subjects/Keywords: Nerves, Peripheral; Nervous system – Degeneration; Neural circuitry; Salicylic acid

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APA (6th Edition):

Griffin, J. (2011). The design and fabrication of novel polyanhydride blend scaffolds for peripheral nerve repair. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000057587

Chicago Manual of Style (16th Edition):

Griffin, Jeremy. “The design and fabrication of novel polyanhydride blend scaffolds for peripheral nerve repair.” 2011. Doctoral Dissertation, Rutgers University. Accessed March 21, 2019. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000057587.

MLA Handbook (7th Edition):

Griffin, Jeremy. “The design and fabrication of novel polyanhydride blend scaffolds for peripheral nerve repair.” 2011. Web. 21 Mar 2019.

Vancouver:

Griffin J. The design and fabrication of novel polyanhydride blend scaffolds for peripheral nerve repair. [Internet] [Doctoral dissertation]. Rutgers University; 2011. [cited 2019 Mar 21]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000057587.

Council of Science Editors:

Griffin J. The design and fabrication of novel polyanhydride blend scaffolds for peripheral nerve repair. [Doctoral Dissertation]. Rutgers University; 2011. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000057587

15. Harmon, Alexander M., 1971-. Amphiphilic macromolecule-lipid complexes as drug delivery systems: physical and biological characterization.

Degree: PhD, Chemistry and Chemical Biology, 2011, Rutgers University

Cancer is the second most common death in the US accounting for 25% of all deaths. Many of the potent anti-cancer drugs are insoluble in… (more)

Subjects/Keywords: Drug delivery systems; Cancer – Treatment; Micelles; Paclitaxel; Liposomes

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APA (6th Edition):

Harmon, Alexander M., 1. (2011). Amphiphilic macromolecule-lipid complexes as drug delivery systems: physical and biological characterization. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000057591

Chicago Manual of Style (16th Edition):

Harmon, Alexander M., 1971-. “Amphiphilic macromolecule-lipid complexes as drug delivery systems: physical and biological characterization.” 2011. Doctoral Dissertation, Rutgers University. Accessed March 21, 2019. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000057591.

MLA Handbook (7th Edition):

Harmon, Alexander M., 1971-. “Amphiphilic macromolecule-lipid complexes as drug delivery systems: physical and biological characterization.” 2011. Web. 21 Mar 2019.

Vancouver:

Harmon, Alexander M. 1. Amphiphilic macromolecule-lipid complexes as drug delivery systems: physical and biological characterization. [Internet] [Doctoral dissertation]. Rutgers University; 2011. [cited 2019 Mar 21]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000057591.

Council of Science Editors:

Harmon, Alexander M. 1. Amphiphilic macromolecule-lipid complexes as drug delivery systems: physical and biological characterization. [Doctoral Dissertation]. Rutgers University; 2011. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000057591

16. Sparks, Sarah Marie, 1984-. Design, synthesis, and utility of fuctionalized nanoscale amphiphilic macromolecules for biomedical applications.

Degree: PhD, Chemistry and Chemical Biology, 2011, Rutgers University

Polymeric micelles are spherical assemblies of amphiphilic polymers widely studied for many biomedical applications. Nanoscale amphiphilic macromolecules (AMs) are novel amphiphilic polymers composed of an… (more)

Subjects/Keywords: Micelles; Macromolecules; Biomedical materials; Polymers in medicine; Nanotechnology

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APA (6th Edition):

Sparks, Sarah Marie, 1. (2011). Design, synthesis, and utility of fuctionalized nanoscale amphiphilic macromolecules for biomedical applications. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000057691

Chicago Manual of Style (16th Edition):

Sparks, Sarah Marie, 1984-. “Design, synthesis, and utility of fuctionalized nanoscale amphiphilic macromolecules for biomedical applications.” 2011. Doctoral Dissertation, Rutgers University. Accessed March 21, 2019. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000057691.

MLA Handbook (7th Edition):

Sparks, Sarah Marie, 1984-. “Design, synthesis, and utility of fuctionalized nanoscale amphiphilic macromolecules for biomedical applications.” 2011. Web. 21 Mar 2019.

Vancouver:

Sparks, Sarah Marie 1. Design, synthesis, and utility of fuctionalized nanoscale amphiphilic macromolecules for biomedical applications. [Internet] [Doctoral dissertation]. Rutgers University; 2011. [cited 2019 Mar 21]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000057691.

Council of Science Editors:

Sparks, Sarah Marie 1. Design, synthesis, and utility of fuctionalized nanoscale amphiphilic macromolecules for biomedical applications. [Doctoral Dissertation]. Rutgers University; 2011. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000057691

17. Sundara Rajan, Sujata, 1982-. Poly(ethylene glycol) (PEG) nanocarrier-based hydrogels for the prevention of vaginal HIV transmission.

Degree: Biomedical Engineering, 2013, Rutgers University

Subjects/Keywords: HIV infections – Prevention; Women – Diseases – Prevention; Colloids in medicine

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APA (6th Edition):

Sundara Rajan, Sujata, 1. (2013). Poly(ethylene glycol) (PEG) nanocarrier-based hydrogels for the prevention of vaginal HIV transmission. (Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000068979

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):

Sundara Rajan, Sujata, 1982-. “Poly(ethylene glycol) (PEG) nanocarrier-based hydrogels for the prevention of vaginal HIV transmission.” 2013. Thesis, Rutgers University. Accessed March 21, 2019. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000068979.

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

MLA Handbook (7th Edition):

Sundara Rajan, Sujata, 1982-. “Poly(ethylene glycol) (PEG) nanocarrier-based hydrogels for the prevention of vaginal HIV transmission.” 2013. Web. 21 Mar 2019.

Vancouver:

Sundara Rajan, Sujata 1. Poly(ethylene glycol) (PEG) nanocarrier-based hydrogels for the prevention of vaginal HIV transmission. [Internet] [Thesis]. Rutgers University; 2013. [cited 2019 Mar 21]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000068979.

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

Council of Science Editors:

Sundara Rajan, Sujata 1. Poly(ethylene glycol) (PEG) nanocarrier-based hydrogels for the prevention of vaginal HIV transmission. [Thesis]. Rutgers University; 2013. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000068979

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

18. Snyder, Sabrina Sachiko, 1986-. Design and fabrication of salicylic acid-based polyanhydride devices for wound healing and tissue regeneration.

Degree: Biomedical Engineering, 2013, Rutgers University

Subjects/Keywords: Wounds and injuries – Treatment; Salicylic acid; Drug delivery systems; Guided tissue regeneration – Equipment and supplies

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APA (6th Edition):

Snyder, Sabrina Sachiko, 1. (2013). Design and fabrication of salicylic acid-based polyanhydride devices for wound healing and tissue regeneration. (Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000068970

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):

Snyder, Sabrina Sachiko, 1986-. “Design and fabrication of salicylic acid-based polyanhydride devices for wound healing and tissue regeneration.” 2013. Thesis, Rutgers University. Accessed March 21, 2019. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000068970.

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

MLA Handbook (7th Edition):

Snyder, Sabrina Sachiko, 1986-. “Design and fabrication of salicylic acid-based polyanhydride devices for wound healing and tissue regeneration.” 2013. Web. 21 Mar 2019.

Vancouver:

Snyder, Sabrina Sachiko 1. Design and fabrication of salicylic acid-based polyanhydride devices for wound healing and tissue regeneration. [Internet] [Thesis]. Rutgers University; 2013. [cited 2019 Mar 21]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000068970.

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

Council of Science Editors:

Snyder, Sabrina Sachiko 1. Design and fabrication of salicylic acid-based polyanhydride devices for wound healing and tissue regeneration. [Thesis]. Rutgers University; 2013. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000068970

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

19. Waite, Carolyn Leigh, 1983-. Engineering tumor-targeted poly(amidoamine) (PAMAM) dendrimers for improved penetration and cellular delivery of short-interfering RNA (siRNA) through solid tumors.

Degree: Chemical and Biochemical Engineering, 2011, Rutgers University

Subjects/Keywords: Drug delivery systems; Dendrimers in medicine; Gliomas – Treatment; RNA

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APA (6th Edition):

Waite, Carolyn Leigh, 1. (2011). Engineering tumor-targeted poly(amidoamine) (PAMAM) dendrimers for improved penetration and cellular delivery of short-interfering RNA (siRNA) through solid tumors. (Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063690

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):

Waite, Carolyn Leigh, 1983-. “Engineering tumor-targeted poly(amidoamine) (PAMAM) dendrimers for improved penetration and cellular delivery of short-interfering RNA (siRNA) through solid tumors.” 2011. Thesis, Rutgers University. Accessed March 21, 2019. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063690.

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

MLA Handbook (7th Edition):

Waite, Carolyn Leigh, 1983-. “Engineering tumor-targeted poly(amidoamine) (PAMAM) dendrimers for improved penetration and cellular delivery of short-interfering RNA (siRNA) through solid tumors.” 2011. Web. 21 Mar 2019.

Vancouver:

Waite, Carolyn Leigh 1. Engineering tumor-targeted poly(amidoamine) (PAMAM) dendrimers for improved penetration and cellular delivery of short-interfering RNA (siRNA) through solid tumors. [Internet] [Thesis]. Rutgers University; 2011. [cited 2019 Mar 21]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063690.

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

Council of Science Editors:

Waite, Carolyn Leigh 1. Engineering tumor-targeted poly(amidoamine) (PAMAM) dendrimers for improved penetration and cellular delivery of short-interfering RNA (siRNA) through solid tumors. [Thesis]. Rutgers University; 2011. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063690

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


Rutgers University

20. Langowski, Bryan Alfred. Preparation and surface characterization of plasma-treated and biomolecular-micropatterened polymer substrates:.

Degree: PhD, Chemistry and Chemical Biology, 2007, Rutgers University

 A micropatterning process creates distinct microscale domains on substrate surfaces that differ from the surfaces' original chemical/physical properties. Numerous micropatterning methods exist, each having relative… (more)

Subjects/Keywords: Tissue engineering; Biomedical engineering

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APA (6th Edition):

Langowski, B. A. (2007). Preparation and surface characterization of plasma-treated and biomolecular-micropatterened polymer substrates:. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.13476

Chicago Manual of Style (16th Edition):

Langowski, Bryan Alfred. “Preparation and surface characterization of plasma-treated and biomolecular-micropatterened polymer substrates:.” 2007. Doctoral Dissertation, Rutgers University. Accessed March 21, 2019. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.13476.

MLA Handbook (7th Edition):

Langowski, Bryan Alfred. “Preparation and surface characterization of plasma-treated and biomolecular-micropatterened polymer substrates:.” 2007. Web. 21 Mar 2019.

Vancouver:

Langowski BA. Preparation and surface characterization of plasma-treated and biomolecular-micropatterened polymer substrates:. [Internet] [Doctoral dissertation]. Rutgers University; 2007. [cited 2019 Mar 21]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.13476.

Council of Science Editors:

Langowski BA. Preparation and surface characterization of plasma-treated and biomolecular-micropatterened polymer substrates:. [Doctoral Dissertation]. Rutgers University; 2007. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.13476


Rutgers University

21. Han, Qianwei. Synthesis of dinucleoside tetraphosphates and their analogs.

Degree: PhD, Chemistry and Chemical Biology, 2007, Rutgers University

Dinucleoside polyphosphates, NpnN' (n = 2 - 7), are observed in many biological processes and are recognized as playing important regulatory functions. Ap4A is a… (more)

Subjects/Keywords: Dinucleoside polyphosphates

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APA (6th Edition):

Han, Q. (2007). Synthesis of dinucleoside tetraphosphates and their analogs. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.16087

Chicago Manual of Style (16th Edition):

Han, Qianwei. “Synthesis of dinucleoside tetraphosphates and their analogs.” 2007. Doctoral Dissertation, Rutgers University. Accessed March 21, 2019. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.16087.

MLA Handbook (7th Edition):

Han, Qianwei. “Synthesis of dinucleoside tetraphosphates and their analogs.” 2007. Web. 21 Mar 2019.

Vancouver:

Han Q. Synthesis of dinucleoside tetraphosphates and their analogs. [Internet] [Doctoral dissertation]. Rutgers University; 2007. [cited 2019 Mar 21]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.16087.

Council of Science Editors:

Han Q. Synthesis of dinucleoside tetraphosphates and their analogs. [Doctoral Dissertation]. Rutgers University; 2007. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.16087


Rutgers University

22. Ray, Amlan. Iridium catalyzed alkane dehydrogenation, olefin isomerization and related chemistry.

Degree: PhD, Chemistry and Chemical Biology, 2007, Rutgers University

Excellent alkane dehydrogenation activity exhibited by the pincer-ligated iridium complexes of the type  – (X-RPCP)IrH2 (X-RPCP = 4-X-C6H2-2,6-(CH2PR2)2 with X = H, MeO; R =… (more)

Subjects/Keywords: Alkanes; Iridium catalysts; Dehydrogenation; Alkenes; Isomerization

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APA (6th Edition):

Ray, A. (2007). Iridium catalyzed alkane dehydrogenation, olefin isomerization and related chemistry. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.16759

Chicago Manual of Style (16th Edition):

Ray, Amlan. “Iridium catalyzed alkane dehydrogenation, olefin isomerization and related chemistry.” 2007. Doctoral Dissertation, Rutgers University. Accessed March 21, 2019. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.16759.

MLA Handbook (7th Edition):

Ray, Amlan. “Iridium catalyzed alkane dehydrogenation, olefin isomerization and related chemistry.” 2007. Web. 21 Mar 2019.

Vancouver:

Ray A. Iridium catalyzed alkane dehydrogenation, olefin isomerization and related chemistry. [Internet] [Doctoral dissertation]. Rutgers University; 2007. [cited 2019 Mar 21]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.16759.

Council of Science Editors:

Ray A. Iridium catalyzed alkane dehydrogenation, olefin isomerization and related chemistry. [Doctoral Dissertation]. Rutgers University; 2007. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.16759


Rutgers University

23. Wang, Jinzhong, 1979-. Synthesis and evaluation of novel amphiphilic macromolecules as drug carriers and therapeutics.

Degree: PhD, Chemistry and Chemical Biology, 2007, Rutgers University

Novel amphiphilic star-like macromolecules (ASM) and amphiphilic scorpion-like macromolecules (AScM) with double-chained and single-chained tails were synthesized and characterized. All macromolecules are composed of mucic… (more)

Subjects/Keywords: Drug delivery systems; Drug carriers (Pharmacy); Pharmaceutical technology

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APA (6th Edition):

Wang, Jinzhong, 1. (2007). Synthesis and evaluation of novel amphiphilic macromolecules as drug carriers and therapeutics. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.16792

Chicago Manual of Style (16th Edition):

Wang, Jinzhong, 1979-. “Synthesis and evaluation of novel amphiphilic macromolecules as drug carriers and therapeutics.” 2007. Doctoral Dissertation, Rutgers University. Accessed March 21, 2019. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.16792.

MLA Handbook (7th Edition):

Wang, Jinzhong, 1979-. “Synthesis and evaluation of novel amphiphilic macromolecules as drug carriers and therapeutics.” 2007. Web. 21 Mar 2019.

Vancouver:

Wang, Jinzhong 1. Synthesis and evaluation of novel amphiphilic macromolecules as drug carriers and therapeutics. [Internet] [Doctoral dissertation]. Rutgers University; 2007. [cited 2019 Mar 21]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.16792.

Council of Science Editors:

Wang, Jinzhong 1. Synthesis and evaluation of novel amphiphilic macromolecules as drug carriers and therapeutics. [Doctoral Dissertation]. Rutgers University; 2007. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.16792


Rutgers University

24. Johnson, Michelle Linette. Polyanhydride blends as drug delivery matrices to control biofilms, bone and nerve regeneration.

Degree: PhD, Chemistry and Chemical Biology, 2008, Rutgers University

Biodegradable polyanhydrides were fabricated into disks, coatings, microspheres, and tubes for controlled drug delivery as well as enhanced thermal and mechanical properties. The polymer systems… (more)

Subjects/Keywords: Drug delivery systems

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APA (6th Edition):

Johnson, M. L. (2008). Polyanhydride blends as drug delivery matrices to control biofilms, bone and nerve regeneration. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.17333

Chicago Manual of Style (16th Edition):

Johnson, Michelle Linette. “Polyanhydride blends as drug delivery matrices to control biofilms, bone and nerve regeneration.” 2008. Doctoral Dissertation, Rutgers University. Accessed March 21, 2019. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.17333.

MLA Handbook (7th Edition):

Johnson, Michelle Linette. “Polyanhydride blends as drug delivery matrices to control biofilms, bone and nerve regeneration.” 2008. Web. 21 Mar 2019.

Vancouver:

Johnson ML. Polyanhydride blends as drug delivery matrices to control biofilms, bone and nerve regeneration. [Internet] [Doctoral dissertation]. Rutgers University; 2008. [cited 2019 Mar 21]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.17333.

Council of Science Editors:

Johnson ML. Polyanhydride blends as drug delivery matrices to control biofilms, bone and nerve regeneration. [Doctoral Dissertation]. Rutgers University; 2008. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.17333


Rutgers University

25. Steege, Karen Elizabeth. Fluorescence probing of complex solvent environments: polymeric nanocarrier aggregates and rilpivirine.

Degree: PhD, Chemistry and Chemical Biology, 2008, Rutgers University

The local environment of a drug molecule in polymeric drug nanocarrier solutions impacts the bioavailability of the drug and its ability to reach its target… (more)

Subjects/Keywords: Drug delivery systems

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APA (6th Edition):

Steege, K. E. (2008). Fluorescence probing of complex solvent environments: polymeric nanocarrier aggregates and rilpivirine. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.17396

Chicago Manual of Style (16th Edition):

Steege, Karen Elizabeth. “Fluorescence probing of complex solvent environments: polymeric nanocarrier aggregates and rilpivirine.” 2008. Doctoral Dissertation, Rutgers University. Accessed March 21, 2019. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.17396.

MLA Handbook (7th Edition):

Steege, Karen Elizabeth. “Fluorescence probing of complex solvent environments: polymeric nanocarrier aggregates and rilpivirine.” 2008. Web. 21 Mar 2019.

Vancouver:

Steege KE. Fluorescence probing of complex solvent environments: polymeric nanocarrier aggregates and rilpivirine. [Internet] [Doctoral dissertation]. Rutgers University; 2008. [cited 2019 Mar 21]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.17396.

Council of Science Editors:

Steege KE. Fluorescence probing of complex solvent environments: polymeric nanocarrier aggregates and rilpivirine. [Doctoral Dissertation]. Rutgers University; 2008. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.17396


Rutgers University

26. Song, Minjung. Biomaterials and microfabrication techniques for improved peripheral nerve regeneration.

Degree: PhD, Biomedical Engineering, 2007, Rutgers University

 Following severe nerve injuries, surgery is required to physically reconnect the injured nerve for regeneration. Auto-grafting is typically considered to be the most effective method,… (more)

Subjects/Keywords: Nervous system; Regeneration (Biology); Nerve grafting

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APA (6th Edition):

Song, M. (2007). Biomaterials and microfabrication techniques for improved peripheral nerve regeneration. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.13833

Chicago Manual of Style (16th Edition):

Song, Minjung. “Biomaterials and microfabrication techniques for improved peripheral nerve regeneration.” 2007. Doctoral Dissertation, Rutgers University. Accessed March 21, 2019. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.13833.

MLA Handbook (7th Edition):

Song, Minjung. “Biomaterials and microfabrication techniques for improved peripheral nerve regeneration.” 2007. Web. 21 Mar 2019.

Vancouver:

Song M. Biomaterials and microfabrication techniques for improved peripheral nerve regeneration. [Internet] [Doctoral dissertation]. Rutgers University; 2007. [cited 2019 Mar 21]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.13833.

Council of Science Editors:

Song M. Biomaterials and microfabrication techniques for improved peripheral nerve regeneration. [Doctoral Dissertation]. Rutgers University; 2007. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.13833


Rutgers University

27. Kanwal, Alokik Paul. All organic memory devices utilizing C60 molecules and insulating polymers.

Degree: PhD, Ceramic and Materials Science and Engineering, 2008, Rutgers University

The convergence of mobile technologies combined with stricter power requirements and increasing demands have strained the current memory technology. Newer technologies such as phase changing,… (more)

Subjects/Keywords: Organic electronics

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APA (6th Edition):

Kanwal, A. P. (2008). All organic memory devices utilizing C60 molecules and insulating polymers. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.17337

Chicago Manual of Style (16th Edition):

Kanwal, Alokik Paul. “All organic memory devices utilizing C60 molecules and insulating polymers.” 2008. Doctoral Dissertation, Rutgers University. Accessed March 21, 2019. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.17337.

MLA Handbook (7th Edition):

Kanwal, Alokik Paul. “All organic memory devices utilizing C60 molecules and insulating polymers.” 2008. Web. 21 Mar 2019.

Vancouver:

Kanwal AP. All organic memory devices utilizing C60 molecules and insulating polymers. [Internet] [Doctoral dissertation]. Rutgers University; 2008. [cited 2019 Mar 21]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.17337.

Council of Science Editors:

Kanwal AP. All organic memory devices utilizing C60 molecules and insulating polymers. [Doctoral Dissertation]. Rutgers University; 2008. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.17337


Rutgers University

28. Delgado-Rivera, Roberto L., 1984-. Polymeric biomaterials for nerve regeneration applications: from promoting cellular organization to the delivery of bioactive molecules.

Degree: Chemistry and Chemical Biology, 2011, Rutgers University

Subjects/Keywords: Nervous system—Regeneration

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APA (6th Edition):

Delgado-Rivera, Roberto L., 1. (2011). Polymeric biomaterials for nerve regeneration applications: from promoting cellular organization to the delivery of bioactive molecules. (Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063393

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):

Delgado-Rivera, Roberto L., 1984-. “Polymeric biomaterials for nerve regeneration applications: from promoting cellular organization to the delivery of bioactive molecules.” 2011. Thesis, Rutgers University. Accessed March 21, 2019. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063393.

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

MLA Handbook (7th Edition):

Delgado-Rivera, Roberto L., 1984-. “Polymeric biomaterials for nerve regeneration applications: from promoting cellular organization to the delivery of bioactive molecules.” 2011. Web. 21 Mar 2019.

Vancouver:

Delgado-Rivera, Roberto L. 1. Polymeric biomaterials for nerve regeneration applications: from promoting cellular organization to the delivery of bioactive molecules. [Internet] [Thesis]. Rutgers University; 2011. [cited 2019 Mar 21]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063393.

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

Council of Science Editors:

Delgado-Rivera, Roberto L. 1. Polymeric biomaterials for nerve regeneration applications: from promoting cellular organization to the delivery of bioactive molecules. [Thesis]. Rutgers University; 2011. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063393

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

.