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University: University of Utah

You searched for subject:(Drug delivery). Showing records 1 – 22 of 22 total matches.

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University of Utah

1. Preston, J. Processing of MRI data for simulation and monitoring of drug delivery.

Degree: MS;, Computing (School of);, 2009, University of Utah

 The work in this thesis centers around monitoring and simulation of a novel drug delivery system. The major features are the development of a pipeline… (more)

Subjects/Keywords: Drug delivery systems

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APA (6th Edition):

Preston, J. (2009). Processing of MRI data for simulation and monitoring of drug delivery. (Masters Thesis). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1224/rec/934

Chicago Manual of Style (16th Edition):

Preston, J. “Processing of MRI data for simulation and monitoring of drug delivery.” 2009. Masters Thesis, University of Utah. Accessed March 19, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1224/rec/934.

MLA Handbook (7th Edition):

Preston, J. “Processing of MRI data for simulation and monitoring of drug delivery.” 2009. Web. 19 Mar 2019.

Vancouver:

Preston J. Processing of MRI data for simulation and monitoring of drug delivery. [Internet] [Masters thesis]. University of Utah; 2009. [cited 2019 Mar 19]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1224/rec/934.

Council of Science Editors:

Preston J. Processing of MRI data for simulation and monitoring of drug delivery. [Masters Thesis]. University of Utah; 2009. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1224/rec/934


University of Utah

2. Hubbard, Dallin Andrew. Transepithelial transport of pamam dendrimers across isolated intestinal tissue.

Degree: PhD, Bioengineering, 2016, University of Utah

 Poly(amido amine) (PAMAM) dendrimers have shown potential to carry poorly absorbed drugs across the intestinal barrier and into systemic circulation, reducing the need for intravenous… (more)

Subjects/Keywords: dendrimer; drug delivery; oral delivery; Ussing

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APA (6th Edition):

Hubbard, D. A. (2016). Transepithelial transport of pamam dendrimers across isolated intestinal tissue. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/4102/rec/2779

Chicago Manual of Style (16th Edition):

Hubbard, Dallin Andrew. “Transepithelial transport of pamam dendrimers across isolated intestinal tissue.” 2016. Doctoral Dissertation, University of Utah. Accessed March 19, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/4102/rec/2779.

MLA Handbook (7th Edition):

Hubbard, Dallin Andrew. “Transepithelial transport of pamam dendrimers across isolated intestinal tissue.” 2016. Web. 19 Mar 2019.

Vancouver:

Hubbard DA. Transepithelial transport of pamam dendrimers across isolated intestinal tissue. [Internet] [Doctoral dissertation]. University of Utah; 2016. [cited 2019 Mar 19]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/4102/rec/2779.

Council of Science Editors:

Hubbard DA. Transepithelial transport of pamam dendrimers across isolated intestinal tissue. [Doctoral Dissertation]. University of Utah; 2016. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/4102/rec/2779


University of Utah

3. Gupta, Kavita Madanlal. Novel Technologies for Vaginal Delivery of Microbicides.

Degree: PhD, Bioengineering;, 2009, University of Utah

 There is a pressing need for microbicides—vaginally applied drug delivery systems that create a pharmacological barrier to HIV—to prevent the male-tofemale sexual transmission of HIV.… (more)

Subjects/Keywords: Drug Delivery Systems; AIDS (Disease)

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APA (6th Edition):

Gupta, K. M. (2009). Novel Technologies for Vaginal Delivery of Microbicides. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1239/rec/823

Chicago Manual of Style (16th Edition):

Gupta, Kavita Madanlal. “Novel Technologies for Vaginal Delivery of Microbicides.” 2009. Doctoral Dissertation, University of Utah. Accessed March 19, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1239/rec/823.

MLA Handbook (7th Edition):

Gupta, Kavita Madanlal. “Novel Technologies for Vaginal Delivery of Microbicides.” 2009. Web. 19 Mar 2019.

Vancouver:

Gupta KM. Novel Technologies for Vaginal Delivery of Microbicides. [Internet] [Doctoral dissertation]. University of Utah; 2009. [cited 2019 Mar 19]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1239/rec/823.

Council of Science Editors:

Gupta KM. Novel Technologies for Vaginal Delivery of Microbicides. [Doctoral Dissertation]. University of Utah; 2009. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1239/rec/823


University of Utah

4. Brozek, Eric. Synthesis and postmodification of functionally relevant organically modified silica particles.

Degree: PhD, Chemistry, 2013, University of Utah

 This thesis describes the synthesis and properties of organically modifiedsilica (ORMOSIL) particles with possible applications in the field of drug delivery.Nanoparticle drug delivery methods take… (more)

Subjects/Keywords: Drug delivery; ORMOSIL; Silica

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APA (6th Edition):

Brozek, E. (2013). Synthesis and postmodification of functionally relevant organically modified silica particles. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2279/rec/2334

Chicago Manual of Style (16th Edition):

Brozek, Eric. “Synthesis and postmodification of functionally relevant organically modified silica particles.” 2013. Doctoral Dissertation, University of Utah. Accessed March 19, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2279/rec/2334.

MLA Handbook (7th Edition):

Brozek, Eric. “Synthesis and postmodification of functionally relevant organically modified silica particles.” 2013. Web. 19 Mar 2019.

Vancouver:

Brozek E. Synthesis and postmodification of functionally relevant organically modified silica particles. [Internet] [Doctoral dissertation]. University of Utah; 2013. [cited 2019 Mar 19]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2279/rec/2334.

Council of Science Editors:

Brozek E. Synthesis and postmodification of functionally relevant organically modified silica particles. [Doctoral Dissertation]. University of Utah; 2013. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2279/rec/2334


University of Utah

5. Jay, Julie I. Modification of the Phenylboronate-diol Crosslink: Applications in pH-Responsive Vehicles and Synthetic Lectin for Women Controlled HIV Prevention.

Degree: PhD, Pharmacology & Toxicology;, 2010, University of Utah

 The HIV-1 pandemic continues to devastate women in resource-poor regions. Without a vaccine, the development of microbicides, vaginal drug delivery systems containing anti-HIV-1 active agents… (more)

Subjects/Keywords: Drug Delivery Systems; HIV Infections; AIDS (Disease)

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APA (6th Edition):

Jay, J. I. (2010). Modification of the Phenylboronate-diol Crosslink: Applications in pH-Responsive Vehicles and Synthetic Lectin for Women Controlled HIV Prevention. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/467/rec/783

Chicago Manual of Style (16th Edition):

Jay, Julie I. “Modification of the Phenylboronate-diol Crosslink: Applications in pH-Responsive Vehicles and Synthetic Lectin for Women Controlled HIV Prevention.” 2010. Doctoral Dissertation, University of Utah. Accessed March 19, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/467/rec/783.

MLA Handbook (7th Edition):

Jay, Julie I. “Modification of the Phenylboronate-diol Crosslink: Applications in pH-Responsive Vehicles and Synthetic Lectin for Women Controlled HIV Prevention.” 2010. Web. 19 Mar 2019.

Vancouver:

Jay JI. Modification of the Phenylboronate-diol Crosslink: Applications in pH-Responsive Vehicles and Synthetic Lectin for Women Controlled HIV Prevention. [Internet] [Doctoral dissertation]. University of Utah; 2010. [cited 2019 Mar 19]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/467/rec/783.

Council of Science Editors:

Jay JI. Modification of the Phenylboronate-diol Crosslink: Applications in pH-Responsive Vehicles and Synthetic Lectin for Women Controlled HIV Prevention. [Doctoral Dissertation]. University of Utah; 2010. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/467/rec/783


University of Utah

6. Christensen, Lane. Reducible poly(amido ethylenimine)s for gene delivery;.

Degree: PhD, Pharmaceutics & Pharmaceutical Chemistry;, 2007, University of Utah

 Much has been learned from the success and, more so, from the early failures of gene therapy, thereby providing a realistic therapeutic alternative for a… (more)

Subjects/Keywords: Polymetric Drug Delivery System; Gene Therapy

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APA (6th Edition):

Christensen, L. (2007). Reducible poly(amido ethylenimine)s for gene delivery;. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1611/rec/1085

Chicago Manual of Style (16th Edition):

Christensen, Lane. “Reducible poly(amido ethylenimine)s for gene delivery;.” 2007. Doctoral Dissertation, University of Utah. Accessed March 19, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1611/rec/1085.

MLA Handbook (7th Edition):

Christensen, Lane. “Reducible poly(amido ethylenimine)s for gene delivery;.” 2007. Web. 19 Mar 2019.

Vancouver:

Christensen L. Reducible poly(amido ethylenimine)s for gene delivery;. [Internet] [Doctoral dissertation]. University of Utah; 2007. [cited 2019 Mar 19]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1611/rec/1085.

Council of Science Editors:

Christensen L. Reducible poly(amido ethylenimine)s for gene delivery;. [Doctoral Dissertation]. University of Utah; 2007. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1611/rec/1085


University of Utah

7. Welborn, Austin Ray. Simulation of diffusion in three unique situations for the novel capsule drug ring.

Degree: MS;, Mechanical Engineering;, 2010, University of Utah

 This work reports the results of simulations of drug release from a capsule drug ring (CDR) and the diffusion of that drug throughout the eye.… (more)

Subjects/Keywords: Capsule drug ring; Bevacizumab; Avastin; Retinal degeneration; Macular degeneration; Drug release; Drug delivery systems

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APA (6th Edition):

Welborn, A. R. (2010). Simulation of diffusion in three unique situations for the novel capsule drug ring. (Masters Thesis). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/2083/rec/1032

Chicago Manual of Style (16th Edition):

Welborn, Austin Ray. “Simulation of diffusion in three unique situations for the novel capsule drug ring.” 2010. Masters Thesis, University of Utah. Accessed March 19, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/2083/rec/1032.

MLA Handbook (7th Edition):

Welborn, Austin Ray. “Simulation of diffusion in three unique situations for the novel capsule drug ring.” 2010. Web. 19 Mar 2019.

Vancouver:

Welborn AR. Simulation of diffusion in three unique situations for the novel capsule drug ring. [Internet] [Masters thesis]. University of Utah; 2010. [cited 2019 Mar 19]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/2083/rec/1032.

Council of Science Editors:

Welborn AR. Simulation of diffusion in three unique situations for the novel capsule drug ring. [Masters Thesis]. University of Utah; 2010. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/2083/rec/1032


University of Utah

8. Jensen, Keith Dale. Internalization and fate of HPMA copolymers and antisense-HPMA copolymer conjugates in Hep G2 cells;.

Degree: PhD, Pharmaceutics & Pharmaceutical Chemistry;, 2002, University of Utah

 To better understand the fate of macromolecules in cells and begin to alter that fate, we studied a antisense oligonucleotide designed to inhibit the hepatitis… (more)

Subjects/Keywords: Drug Targeting; Polymeric Drug Delivery Systems

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APA (6th Edition):

Jensen, K. D. (2002). Internalization and fate of HPMA copolymers and antisense-HPMA copolymer conjugates in Hep G2 cells;. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/292/rec/709

Chicago Manual of Style (16th Edition):

Jensen, Keith Dale. “Internalization and fate of HPMA copolymers and antisense-HPMA copolymer conjugates in Hep G2 cells;.” 2002. Doctoral Dissertation, University of Utah. Accessed March 19, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/292/rec/709.

MLA Handbook (7th Edition):

Jensen, Keith Dale. “Internalization and fate of HPMA copolymers and antisense-HPMA copolymer conjugates in Hep G2 cells;.” 2002. Web. 19 Mar 2019.

Vancouver:

Jensen KD. Internalization and fate of HPMA copolymers and antisense-HPMA copolymer conjugates in Hep G2 cells;. [Internet] [Doctoral dissertation]. University of Utah; 2002. [cited 2019 Mar 19]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/292/rec/709.

Council of Science Editors:

Jensen KD. Internalization and fate of HPMA copolymers and antisense-HPMA copolymer conjugates in Hep G2 cells;. [Doctoral Dissertation]. University of Utah; 2002. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/292/rec/709


University of Utah

9. Gilbert, Donna Lynn. Collagen macromolecular drug delivery systems;.

Degree: PhD, Pharmaceutics & Pharmaceutical Chemistry;, 1988, University of Utah

 Controlled release systems have been successfully applied for the delivery of low molecular weight compounds. The application of these systems to high molecular weight compounds… (more)

Subjects/Keywords: Drug Delivery Systems; Polymers; Pharmacy

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APA (6th Edition):

Gilbert, D. L. (1988). Collagen macromolecular drug delivery systems;. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1145/rec/173

Chicago Manual of Style (16th Edition):

Gilbert, Donna Lynn. “Collagen macromolecular drug delivery systems;.” 1988. Doctoral Dissertation, University of Utah. Accessed March 19, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1145/rec/173.

MLA Handbook (7th Edition):

Gilbert, Donna Lynn. “Collagen macromolecular drug delivery systems;.” 1988. Web. 19 Mar 2019.

Vancouver:

Gilbert DL. Collagen macromolecular drug delivery systems;. [Internet] [Doctoral dissertation]. University of Utah; 1988. [cited 2019 Mar 19]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1145/rec/173.

Council of Science Editors:

Gilbert DL. Collagen macromolecular drug delivery systems;. [Doctoral Dissertation]. University of Utah; 1988. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1145/rec/173


University of Utah

10. Tang, Aijun. A lymphocyte-targeting polymeric drug delivery system mediated by receptor-binding epitopes: design, synthesis, and characterization.

Degree: PhD, Pharmaceutics & Pharmaceutical Chemistry;, 2002, University of Utah

 Extensive studies have demonstrated that the use of targetable polymeric drug delivery systems is an efficient approach for improving cancer chemotherapy. In this dissertation, a… (more)

Subjects/Keywords: Pharmaceutical Preparations; Drug Delivery Systems

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APA (6th Edition):

Tang, A. (2002). A lymphocyte-targeting polymeric drug delivery system mediated by receptor-binding epitopes: design, synthesis, and characterization. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1096/rec/26

Chicago Manual of Style (16th Edition):

Tang, Aijun. “A lymphocyte-targeting polymeric drug delivery system mediated by receptor-binding epitopes: design, synthesis, and characterization.” 2002. Doctoral Dissertation, University of Utah. Accessed March 19, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1096/rec/26.

MLA Handbook (7th Edition):

Tang, Aijun. “A lymphocyte-targeting polymeric drug delivery system mediated by receptor-binding epitopes: design, synthesis, and characterization.” 2002. Web. 19 Mar 2019.

Vancouver:

Tang A. A lymphocyte-targeting polymeric drug delivery system mediated by receptor-binding epitopes: design, synthesis, and characterization. [Internet] [Doctoral dissertation]. University of Utah; 2002. [cited 2019 Mar 19]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1096/rec/26.

Council of Science Editors:

Tang A. A lymphocyte-targeting polymeric drug delivery system mediated by receptor-binding epitopes: design, synthesis, and characterization. [Doctoral Dissertation]. University of Utah; 2002. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1096/rec/26


University of Utah

11. Lin, Keng-Min. Refilling mechanism to stabilize a free-floating intraocular capsule drug ring.

Degree: MS, Mechanical Engineering, 2011, University of Utah

 This work discusses several ways to grab and refill an intraocular drug device targeting age-related macular degeneration (AMD). The capsule drug ring (CDR) is an… (more)

Subjects/Keywords: AMD; CDR; Implant; Intraocular drug delivery; Macular degeneration; Refill

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APA (6th Edition):

Lin, K. (2011). Refilling mechanism to stabilize a free-floating intraocular capsule drug ring. (Masters Thesis). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/576/rec/2050

Chicago Manual of Style (16th Edition):

Lin, Keng-Min. “Refilling mechanism to stabilize a free-floating intraocular capsule drug ring.” 2011. Masters Thesis, University of Utah. Accessed March 19, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/576/rec/2050.

MLA Handbook (7th Edition):

Lin, Keng-Min. “Refilling mechanism to stabilize a free-floating intraocular capsule drug ring.” 2011. Web. 19 Mar 2019.

Vancouver:

Lin K. Refilling mechanism to stabilize a free-floating intraocular capsule drug ring. [Internet] [Masters thesis]. University of Utah; 2011. [cited 2019 Mar 19]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/576/rec/2050.

Council of Science Editors:

Lin K. Refilling mechanism to stabilize a free-floating intraocular capsule drug ring. [Masters Thesis]. University of Utah; 2011. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/576/rec/2050


University of Utah

12. Suh, Won-Hee. Cell-specific targeting polymeric gene delivery carriers;.

Degree: PhD, Pharmaceutics & Pharmaceutical Chemistry;, 2001, University of Utah

 Cell-specific polymeric gene delivery carriers targeted to leukemia T cells and angiogenic endothelial cells, were designed and developed using anti-JL1 antibody and alpha-v-beta3/alpha-v-beta5 integrin-binding RCD-4C… (more)

Subjects/Keywords: Drug Delivery Systems; Polymeric Drugs

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APA (6th Edition):

Suh, W. (2001). Cell-specific targeting polymeric gene delivery carriers;. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/467/rec/121

Chicago Manual of Style (16th Edition):

Suh, Won-Hee. “Cell-specific targeting polymeric gene delivery carriers;.” 2001. Doctoral Dissertation, University of Utah. Accessed March 19, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/467/rec/121.

MLA Handbook (7th Edition):

Suh, Won-Hee. “Cell-specific targeting polymeric gene delivery carriers;.” 2001. Web. 19 Mar 2019.

Vancouver:

Suh W. Cell-specific targeting polymeric gene delivery carriers;. [Internet] [Doctoral dissertation]. University of Utah; 2001. [cited 2019 Mar 19]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/467/rec/121.

Council of Science Editors:

Suh W. Cell-specific targeting polymeric gene delivery carriers;. [Doctoral Dissertation]. University of Utah; 2001. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/467/rec/121


University of Utah

13. Mohan, Praveena. Stimuli-sensitive perfluorocarbon emulsions as drug carriers and embolizing agents for tumor therapy.

Degree: PhD, Bioengineering;, 2010, University of Utah

 Perfluorocarbon (PFC) microbubbles have been used for several decades as contrast agents in ultrasound imaging; over the last decade, microbubbles have attracted attention as potential… (more)

Subjects/Keywords: Doxorubicin; Drug delivery; Microbubbles; Nanodroplets; Tumor therapy; Ultrasound

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APA (6th Edition):

Mohan, P. (2010). Stimuli-sensitive perfluorocarbon emulsions as drug carriers and embolizing agents for tumor therapy. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/867/rec/1077

Chicago Manual of Style (16th Edition):

Mohan, Praveena. “Stimuli-sensitive perfluorocarbon emulsions as drug carriers and embolizing agents for tumor therapy.” 2010. Doctoral Dissertation, University of Utah. Accessed March 19, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/867/rec/1077.

MLA Handbook (7th Edition):

Mohan, Praveena. “Stimuli-sensitive perfluorocarbon emulsions as drug carriers and embolizing agents for tumor therapy.” 2010. Web. 19 Mar 2019.

Vancouver:

Mohan P. Stimuli-sensitive perfluorocarbon emulsions as drug carriers and embolizing agents for tumor therapy. [Internet] [Doctoral dissertation]. University of Utah; 2010. [cited 2019 Mar 19]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/867/rec/1077.

Council of Science Editors:

Mohan P. Stimuli-sensitive perfluorocarbon emulsions as drug carriers and embolizing agents for tumor therapy. [Doctoral Dissertation]. University of Utah; 2010. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/867/rec/1077


University of Utah

14. Gormley, Adam Joseph. Improved delivery of polymer therapeutics to prostate tumors using plasmonic photothermal therapy.

Degree: PhD, Bioengineering, 2012, University of Utah

 When a patient is presented with locally advanced prostate cancer, it is possible toprovide treatment with curative intent. However, once the disease has formed distantmetastases,… (more)

Subjects/Keywords: Drug Delivery; EPR; Gold Nanorods; HPMA Copolymers; Hyperthermia; Photothermal Therapy

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APA (6th Edition):

Gormley, A. J. (2012). Improved delivery of polymer therapeutics to prostate tumors using plasmonic photothermal therapy. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2054/rec/1311

Chicago Manual of Style (16th Edition):

Gormley, Adam Joseph. “Improved delivery of polymer therapeutics to prostate tumors using plasmonic photothermal therapy.” 2012. Doctoral Dissertation, University of Utah. Accessed March 19, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2054/rec/1311.

MLA Handbook (7th Edition):

Gormley, Adam Joseph. “Improved delivery of polymer therapeutics to prostate tumors using plasmonic photothermal therapy.” 2012. Web. 19 Mar 2019.

Vancouver:

Gormley AJ. Improved delivery of polymer therapeutics to prostate tumors using plasmonic photothermal therapy. [Internet] [Doctoral dissertation]. University of Utah; 2012. [cited 2019 Mar 19]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2054/rec/1311.

Council of Science Editors:

Gormley AJ. Improved delivery of polymer therapeutics to prostate tumors using plasmonic photothermal therapy. [Doctoral Dissertation]. University of Utah; 2012. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2054/rec/1311


University of Utah

15. Li, Xiaoling. Biodegradable polymeric prodrugs of antihypertensive agents;.

Degree: PhD, Pharmaceutics & Pharmaceutical Chemistry;, 1991, University of Utah

 Biodegradable polymeric prodrugs of antihypertensive agents were developed by covalently binding minoxidil, clonidine, prazosin, and CGS 16617 to poly(alpha-amino acids) via labile linkages. The amide… (more)

Subjects/Keywords: Drug Carrierse; Drug Delivery Systems; Prodrugs; Polymers

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APA (6th Edition):

Li, X. (1991). Biodegradable polymeric prodrugs of antihypertensive agents;. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/26/rec/101

Chicago Manual of Style (16th Edition):

Li, Xiaoling. “Biodegradable polymeric prodrugs of antihypertensive agents;.” 1991. Doctoral Dissertation, University of Utah. Accessed March 19, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/26/rec/101.

MLA Handbook (7th Edition):

Li, Xiaoling. “Biodegradable polymeric prodrugs of antihypertensive agents;.” 1991. Web. 19 Mar 2019.

Vancouver:

Li X. Biodegradable polymeric prodrugs of antihypertensive agents;. [Internet] [Doctoral dissertation]. University of Utah; 1991. [cited 2019 Mar 19]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/26/rec/101.

Council of Science Editors:

Li X. Biodegradable polymeric prodrugs of antihypertensive agents;. [Doctoral Dissertation]. University of Utah; 1991. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/26/rec/101


University of Utah

16. Liu, Xin. Quantitative in vivo drug delivery research using magnetic resonance.

Degree: PhD, Physics, 2011, University of Utah

 Over the past decade, molecular imaging has emerged as a powerful tool to visualize biological processes of living subjects on the cellular or molecular level.… (more)

Subjects/Keywords: Drug delivery; In vivo; Magnetic resonance imaging; Quantitative; Gadolinium based contrast agent; GBCA

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APA (6th Edition):

Liu, X. (2011). Quantitative in vivo drug delivery research using magnetic resonance. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/164/rec/2006

Chicago Manual of Style (16th Edition):

Liu, Xin. “Quantitative in vivo drug delivery research using magnetic resonance.” 2011. Doctoral Dissertation, University of Utah. Accessed March 19, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/164/rec/2006.

MLA Handbook (7th Edition):

Liu, Xin. “Quantitative in vivo drug delivery research using magnetic resonance.” 2011. Web. 19 Mar 2019.

Vancouver:

Liu X. Quantitative in vivo drug delivery research using magnetic resonance. [Internet] [Doctoral dissertation]. University of Utah; 2011. [cited 2019 Mar 19]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/164/rec/2006.

Council of Science Editors:

Liu X. Quantitative in vivo drug delivery research using magnetic resonance. [Doctoral Dissertation]. University of Utah; 2011. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/164/rec/2006


University of Utah

17. Brown, Daniel. Drug release mechanisms from heterogeneous interpenetrating networks;.

Degree: PhD, Pharmaceutics & Pharmaceutical Chemistry;, 1994, University of Utah

 The objective of this research was to determine drug release mechanisms from HIPNs composed of a PTMO network and a copolymer of DMAAm and St.… (more)

Subjects/Keywords: Polymetic Drug Delivery Systems; Copolymer Networks

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APA (6th Edition):

Brown, D. (1994). Drug release mechanisms from heterogeneous interpenetrating networks;. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/525/rec/355

Chicago Manual of Style (16th Edition):

Brown, Daniel. “Drug release mechanisms from heterogeneous interpenetrating networks;.” 1994. Doctoral Dissertation, University of Utah. Accessed March 19, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/525/rec/355.

MLA Handbook (7th Edition):

Brown, Daniel. “Drug release mechanisms from heterogeneous interpenetrating networks;.” 1994. Web. 19 Mar 2019.

Vancouver:

Brown D. Drug release mechanisms from heterogeneous interpenetrating networks;. [Internet] [Doctoral dissertation]. University of Utah; 1994. [cited 2019 Mar 19]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/525/rec/355.

Council of Science Editors:

Brown D. Drug release mechanisms from heterogeneous interpenetrating networks;. [Doctoral Dissertation]. University of Utah; 1994. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/525/rec/355


University of Utah

18. Singhal, Dharmendra. Enzymatic barrier to oral and central nervous system delivery of anti-HIV nucleoside reverse transcriptase inhibitors;.

Degree: PhD, Pharmaceutics & Pharmaceutical Chemistry;, 1996, University of Utah

 Most of the dideoxynucleoside reverse transcriptase inhibitors used for treating HIV infection in humans exhibit very low central nervous system (CNS) uptake due to unknown… (more)

Subjects/Keywords: Oral Drug Delivery; HIV: Immune Deficiency; AIDS; Pharmacology: Pharmaceuticals

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APA (6th Edition):

Singhal, D. (1996). Enzymatic barrier to oral and central nervous system delivery of anti-HIV nucleoside reverse transcriptase inhibitors;. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/32/rec/454

Chicago Manual of Style (16th Edition):

Singhal, Dharmendra. “Enzymatic barrier to oral and central nervous system delivery of anti-HIV nucleoside reverse transcriptase inhibitors;.” 1996. Doctoral Dissertation, University of Utah. Accessed March 19, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/32/rec/454.

MLA Handbook (7th Edition):

Singhal, Dharmendra. “Enzymatic barrier to oral and central nervous system delivery of anti-HIV nucleoside reverse transcriptase inhibitors;.” 1996. Web. 19 Mar 2019.

Vancouver:

Singhal D. Enzymatic barrier to oral and central nervous system delivery of anti-HIV nucleoside reverse transcriptase inhibitors;. [Internet] [Doctoral dissertation]. University of Utah; 1996. [cited 2019 Mar 19]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/32/rec/454.

Council of Science Editors:

Singhal D. Enzymatic barrier to oral and central nervous system delivery of anti-HIV nucleoside reverse transcriptase inhibitors;. [Doctoral Dissertation]. University of Utah; 1996. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/32/rec/454


University of Utah

19. Kanwal, Charu. Progesterone receptor nucleocytoplasmic trafficking and applications in drug delivery.

Degree: PhD, Pharmaceutics & Pharmaceutical Chemistry;, 2004, University of Utah

 Nucleocytoplasmic trafficking of steroid hormone receptors is a conundrum that remains to be solved. The mechanism of nuclear import has been established, whereas the mode… (more)

Subjects/Keywords: Pharmacology; Molecular Biology; Progesterone Receptor; Nucleocytoplasmic Trafficking: drug Delivery; Nuclear Export; Protein Switch

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APA (6th Edition):

Kanwal, C. (2004). Progesterone receptor nucleocytoplasmic trafficking and applications in drug delivery. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1217/rec/935

Chicago Manual of Style (16th Edition):

Kanwal, Charu. “Progesterone receptor nucleocytoplasmic trafficking and applications in drug delivery.” 2004. Doctoral Dissertation, University of Utah. Accessed March 19, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1217/rec/935.

MLA Handbook (7th Edition):

Kanwal, Charu. “Progesterone receptor nucleocytoplasmic trafficking and applications in drug delivery.” 2004. Web. 19 Mar 2019.

Vancouver:

Kanwal C. Progesterone receptor nucleocytoplasmic trafficking and applications in drug delivery. [Internet] [Doctoral dissertation]. University of Utah; 2004. [cited 2019 Mar 19]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1217/rec/935.

Council of Science Editors:

Kanwal C. Progesterone receptor nucleocytoplasmic trafficking and applications in drug delivery. [Doctoral Dissertation]. University of Utah; 2004. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1217/rec/935


University of Utah

20. Sims, Sandra Marie. Iontophoretic transport mechanisms across skin;.

Degree: PhD, Pharmaceutics & Pharmaceutical Chemistry;, 1990, University of Utah

 Iontophoresis is the process of increasing the penetration rate of ions into or through a membrane by the application of an external electric field across… (more)

Subjects/Keywords: Drug Delivery Systems; Ion Transport; Iontophoresis; Models, Biological; Salicylates; Skin Absorption; Skin Absorption; Tetraethylammonium Compounds

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APA (6th Edition):

Sims, S. M. (1990). Iontophoretic transport mechanisms across skin;. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1503/rec/728

Chicago Manual of Style (16th Edition):

Sims, Sandra Marie. “Iontophoretic transport mechanisms across skin;.” 1990. Doctoral Dissertation, University of Utah. Accessed March 19, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1503/rec/728.

MLA Handbook (7th Edition):

Sims, Sandra Marie. “Iontophoretic transport mechanisms across skin;.” 1990. Web. 19 Mar 2019.

Vancouver:

Sims SM. Iontophoretic transport mechanisms across skin;. [Internet] [Doctoral dissertation]. University of Utah; 1990. [cited 2019 Mar 19]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1503/rec/728.

Council of Science Editors:

Sims SM. Iontophoretic transport mechanisms across skin;. [Doctoral Dissertation]. University of Utah; 1990. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1503/rec/728

21. Clark, Justin Thomas. Engineering intravaginal rings for HIV prevention and contraception.

Degree: PhD, Bioengineering, 2014, University of Utah

 Three decades have passed since the discovery of HIV and still no viable vaccine technologies exist to prevent the spread of the virus. The concept… (more)

Subjects/Keywords: Contraception; HIV prevention; Intravaginal rings; Mathematical modeling; Pharmacokinetics; Vaginal drug delivery

…effectiveness. Several highlyeffective alternative drug delivery systems exist which can provide… …When designing an IVR for drug delivery, one must first estimate the desired daily drug dose… …116 APPENDIX: PROPOSED SPATIAL PK MODEL FOR PREDICTION OF DRUG AND VIRUS TRANSPORT IN THE… …constant decay of drug release rates from reservoirs ACN acetonitrile AIDS acquired… …immunodeficiency syndrome α fractional equilibrium polymer swelling ARV antiretroviral drug AUC… 

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APA (6th Edition):

Clark, J. T. (2014). Engineering intravaginal rings for HIV prevention and contraception. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2839/rec/875

Chicago Manual of Style (16th Edition):

Clark, Justin Thomas. “Engineering intravaginal rings for HIV prevention and contraception.” 2014. Doctoral Dissertation, University of Utah. Accessed March 19, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2839/rec/875.

MLA Handbook (7th Edition):

Clark, Justin Thomas. “Engineering intravaginal rings for HIV prevention and contraception.” 2014. Web. 19 Mar 2019.

Vancouver:

Clark JT. Engineering intravaginal rings for HIV prevention and contraception. [Internet] [Doctoral dissertation]. University of Utah; 2014. [cited 2019 Mar 19]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2839/rec/875.

Council of Science Editors:

Clark JT. Engineering intravaginal rings for HIV prevention and contraception. [Doctoral Dissertation]. University of Utah; 2014. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2839/rec/875

22. Avula, Mahender nath. Local drug delivery targeting mast cells to improve the functional lifetime of continuous glucose sensors.

Degree: PhD, Bioengineering, 2013, University of Utah

 Diabetes mellitus affects 5% of the world’s population and requires constant monitoring to avoid fatality. Tight control of blood glucose levels has shown to reduce… (more)

Subjects/Keywords: Biomaterials; Biosensors; Continuous glucose sensors; Foreign body response; Local drug delivery; Mast cells

delivery of an anti-inflammatory drug for implantable medical devices. Biomaterials. 2002;23:1649… …Grainger, medical device, drug delivery, blood coagulation, foreign body response, infection… …based on-board drug delivery mechanisms are among strategies employed to improve clinical IMD… …each other in structure and function, i.e., controlled drug delivery often is an add-on… …and merging new technologies, changes and refinements of both existing drug delivery… 

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APA (6th Edition):

Avula, M. n. (2013). Local drug delivery targeting mast cells to improve the functional lifetime of continuous glucose sensors. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2652/rec/1492

Chicago Manual of Style (16th Edition):

Avula, Mahender nath. “Local drug delivery targeting mast cells to improve the functional lifetime of continuous glucose sensors.” 2013. Doctoral Dissertation, University of Utah. Accessed March 19, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2652/rec/1492.

MLA Handbook (7th Edition):

Avula, Mahender nath. “Local drug delivery targeting mast cells to improve the functional lifetime of continuous glucose sensors.” 2013. Web. 19 Mar 2019.

Vancouver:

Avula Mn. Local drug delivery targeting mast cells to improve the functional lifetime of continuous glucose sensors. [Internet] [Doctoral dissertation]. University of Utah; 2013. [cited 2019 Mar 19]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2652/rec/1492.

Council of Science Editors:

Avula Mn. Local drug delivery targeting mast cells to improve the functional lifetime of continuous glucose sensors. [Doctoral Dissertation]. University of Utah; 2013. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2652/rec/1492

.