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Dept: Biomedical Engineering

You searched for subject:(Drug delivery). Showing records 1 – 30 of 122 total matches.

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1. Wu, Chia-Hsuan. Controlled drug delivery via Carbon Nanotube.

Degree: PhD, Biomedical Engineering, 2012, Brown University

 This dissertation focuses on the development of new drug delivery platforms using carbon nanotubes. Two nanotube systems, namely single walled carbon nanotubes (SWNTs) and multi-walled… (more)

Subjects/Keywords: drug delivery

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APA (6th Edition):

Wu, C. (2012). Controlled drug delivery via Carbon Nanotube. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:297575/

Chicago Manual of Style (16th Edition):

Wu, Chia-Hsuan. “Controlled drug delivery via Carbon Nanotube.” 2012. Doctoral Dissertation, Brown University. Accessed March 23, 2019. https://repository.library.brown.edu/studio/item/bdr:297575/.

MLA Handbook (7th Edition):

Wu, Chia-Hsuan. “Controlled drug delivery via Carbon Nanotube.” 2012. Web. 23 Mar 2019.

Vancouver:

Wu C. Controlled drug delivery via Carbon Nanotube. [Internet] [Doctoral dissertation]. Brown University; 2012. [cited 2019 Mar 23]. Available from: https://repository.library.brown.edu/studio/item/bdr:297575/.

Council of Science Editors:

Wu C. Controlled drug delivery via Carbon Nanotube. [Doctoral Dissertation]. Brown University; 2012. Available from: https://repository.library.brown.edu/studio/item/bdr:297575/

2. Goldenshtein, Victoria. Effect Of Mucin On Hydrodynamic Diameter And Zeta Potential Of Polymeric Nanospheres.

Degree: Biomedical Engineering, 2017, Brown University

 The degree of interaction between nanoencapsulated material and gastrointestinal mucin can be an important determinant in efficiency of absorption of orally delivered therapeutics. Mucus lining… (more)

Subjects/Keywords: Oral Drug Delivery

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APA (6th Edition):

Goldenshtein, V. (2017). Effect Of Mucin On Hydrodynamic Diameter And Zeta Potential Of Polymeric Nanospheres. (Thesis). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:733342/

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):

Goldenshtein, Victoria. “Effect Of Mucin On Hydrodynamic Diameter And Zeta Potential Of Polymeric Nanospheres.” 2017. Thesis, Brown University. Accessed March 23, 2019. https://repository.library.brown.edu/studio/item/bdr:733342/.

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

MLA Handbook (7th Edition):

Goldenshtein, Victoria. “Effect Of Mucin On Hydrodynamic Diameter And Zeta Potential Of Polymeric Nanospheres.” 2017. Web. 23 Mar 2019.

Vancouver:

Goldenshtein V. Effect Of Mucin On Hydrodynamic Diameter And Zeta Potential Of Polymeric Nanospheres. [Internet] [Thesis]. Brown University; 2017. [cited 2019 Mar 23]. Available from: https://repository.library.brown.edu/studio/item/bdr:733342/.

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

Council of Science Editors:

Goldenshtein V. Effect Of Mucin On Hydrodynamic Diameter And Zeta Potential Of Polymeric Nanospheres. [Thesis]. Brown University; 2017. Available from: https://repository.library.brown.edu/studio/item/bdr:733342/

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


Vanderbilt University

3. Evans, Brian Connor. Enhanced intracellular peptide delivery with pH-responsive, endosomolytic nano-polyplexes to modulate vascular smooth muscle cell behavior.

Degree: MS, Biomedical Engineering, 2013, Vanderbilt University

 Peptide-based therapeutics have significant potential for use in a variety of clinical applications ranging from cancer therapy to promotion of cardiovascular health. However, the efficacy… (more)

Subjects/Keywords: intracellular; polyplex; Drug delivery; peptide

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APA (6th Edition):

Evans, B. C. (2013). Enhanced intracellular peptide delivery with pH-responsive, endosomolytic nano-polyplexes to modulate vascular smooth muscle cell behavior. (Masters Thesis). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu//available/etd-03252013-145713/ ;

Chicago Manual of Style (16th Edition):

Evans, Brian Connor. “Enhanced intracellular peptide delivery with pH-responsive, endosomolytic nano-polyplexes to modulate vascular smooth muscle cell behavior.” 2013. Masters Thesis, Vanderbilt University. Accessed March 23, 2019. http://etd.library.vanderbilt.edu//available/etd-03252013-145713/ ;.

MLA Handbook (7th Edition):

Evans, Brian Connor. “Enhanced intracellular peptide delivery with pH-responsive, endosomolytic nano-polyplexes to modulate vascular smooth muscle cell behavior.” 2013. Web. 23 Mar 2019.

Vancouver:

Evans BC. Enhanced intracellular peptide delivery with pH-responsive, endosomolytic nano-polyplexes to modulate vascular smooth muscle cell behavior. [Internet] [Masters thesis]. Vanderbilt University; 2013. [cited 2019 Mar 23]. Available from: http://etd.library.vanderbilt.edu//available/etd-03252013-145713/ ;.

Council of Science Editors:

Evans BC. Enhanced intracellular peptide delivery with pH-responsive, endosomolytic nano-polyplexes to modulate vascular smooth muscle cell behavior. [Masters Thesis]. Vanderbilt University; 2013. Available from: http://etd.library.vanderbilt.edu//available/etd-03252013-145713/ ;


University of Texas – Austin

4. Dawson, Eileen Regina. Simultaneous, single-carrier delivery of antigens and immune-modulatory molecules to dendritic cells.

Degree: Biomedical Engineering, 2013, University of Texas – Austin

 Immunotherapy as a means for cancer treatment has been investigated for over a century. While studies have been completed using different immunological strategies, development of… (more)

Subjects/Keywords: Vaccine; Drug delivery; Protein; Adjuvant

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APA (6th Edition):

Dawson, E. R. (2013). Simultaneous, single-carrier delivery of antigens and immune-modulatory molecules to dendritic cells. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/30326

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):

Dawson, Eileen Regina. “Simultaneous, single-carrier delivery of antigens and immune-modulatory molecules to dendritic cells.” 2013. Thesis, University of Texas – Austin. Accessed March 23, 2019. http://hdl.handle.net/2152/30326.

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

MLA Handbook (7th Edition):

Dawson, Eileen Regina. “Simultaneous, single-carrier delivery of antigens and immune-modulatory molecules to dendritic cells.” 2013. Web. 23 Mar 2019.

Vancouver:

Dawson ER. Simultaneous, single-carrier delivery of antigens and immune-modulatory molecules to dendritic cells. [Internet] [Thesis]. University of Texas – Austin; 2013. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/2152/30326.

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

Council of Science Editors:

Dawson ER. Simultaneous, single-carrier delivery of antigens and immune-modulatory molecules to dendritic cells. [Thesis]. University of Texas – Austin; 2013. Available from: http://hdl.handle.net/2152/30326

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


University of Akron

5. Vishwanathan, Anusha. In Vitro Characterization Of Simvastatin Loaded Microspheres In The PolyRing Device.

Degree: MSin Engineering, Biomedical Engineering, 2008, University of Akron

 Intimal hyperplasia is the most common mechanism of failure for interventional and revascularization procedures like coronary artery bypass grafts (CABG), peripheral artery bypass surgery and… (more)

Subjects/Keywords: Biomedical Research; Controlled Drug Delivery Sytems; Perivascular drug delivery; Simvastatin

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APA (6th Edition):

Vishwanathan, A. (2008). In Vitro Characterization Of Simvastatin Loaded Microspheres In The PolyRing Device. (Masters Thesis). University of Akron. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=akron1205934178

Chicago Manual of Style (16th Edition):

Vishwanathan, Anusha. “In Vitro Characterization Of Simvastatin Loaded Microspheres In The PolyRing Device.” 2008. Masters Thesis, University of Akron. Accessed March 23, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=akron1205934178.

MLA Handbook (7th Edition):

Vishwanathan, Anusha. “In Vitro Characterization Of Simvastatin Loaded Microspheres In The PolyRing Device.” 2008. Web. 23 Mar 2019.

Vancouver:

Vishwanathan A. In Vitro Characterization Of Simvastatin Loaded Microspheres In The PolyRing Device. [Internet] [Masters thesis]. University of Akron; 2008. [cited 2019 Mar 23]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=akron1205934178.

Council of Science Editors:

Vishwanathan A. In Vitro Characterization Of Simvastatin Loaded Microspheres In The PolyRing Device. [Masters Thesis]. University of Akron; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=akron1205934178


Case Western Reserve University

6. Vesole, Steven Michael. Affinity-Based Delivery of Retinoids.

Degree: MSs (Engineering), Biomedical Engineering, 2011, Case Western Reserve University

 Age-related Macular Degeneration (AMD) is a debilitating disease that deteriorates central vision. Retinoid analogues have shown promise in treating AMD and other ocular conditions by… (more)

Subjects/Keywords: Biomedical Engineering; AMD; drug delivery; cyclodextrin; hydrogel; retinoid; tunable delivery; extended delivery; ocular delivery

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APA (6th Edition):

Vesole, S. M. (2011). Affinity-Based Delivery of Retinoids. (Masters Thesis). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1310138396

Chicago Manual of Style (16th Edition):

Vesole, Steven Michael. “Affinity-Based Delivery of Retinoids.” 2011. Masters Thesis, Case Western Reserve University. Accessed March 23, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1310138396.

MLA Handbook (7th Edition):

Vesole, Steven Michael. “Affinity-Based Delivery of Retinoids.” 2011. Web. 23 Mar 2019.

Vancouver:

Vesole SM. Affinity-Based Delivery of Retinoids. [Internet] [Masters thesis]. Case Western Reserve University; 2011. [cited 2019 Mar 23]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1310138396.

Council of Science Editors:

Vesole SM. Affinity-Based Delivery of Retinoids. [Masters Thesis]. Case Western Reserve University; 2011. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1310138396


The Ohio State University

7. Li, Jie. Polymeric Nanoparticles for Ultrasonic Enhancement and Targeted Drug Delivery.

Degree: MS, Biomedical Engineering, 2010, The Ohio State University

 In this study, we aim to (1) test the feasibility of using polymeric nanoparticles for ultrasonic enhancement of tumor xenografts in mice through high frequency… (more)

Subjects/Keywords: Engineering; polymeric nanoparticle; ultrasonic enhancement; drug delivery

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APA (6th Edition):

Li, J. (2010). Polymeric Nanoparticles for Ultrasonic Enhancement and Targeted Drug Delivery. (Masters Thesis). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1280349038

Chicago Manual of Style (16th Edition):

Li, Jie. “Polymeric Nanoparticles for Ultrasonic Enhancement and Targeted Drug Delivery.” 2010. Masters Thesis, The Ohio State University. Accessed March 23, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1280349038.

MLA Handbook (7th Edition):

Li, Jie. “Polymeric Nanoparticles for Ultrasonic Enhancement and Targeted Drug Delivery.” 2010. Web. 23 Mar 2019.

Vancouver:

Li J. Polymeric Nanoparticles for Ultrasonic Enhancement and Targeted Drug Delivery. [Internet] [Masters thesis]. The Ohio State University; 2010. [cited 2019 Mar 23]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1280349038.

Council of Science Editors:

Li J. Polymeric Nanoparticles for Ultrasonic Enhancement and Targeted Drug Delivery. [Masters Thesis]. The Ohio State University; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1280349038


Georgia Tech

8. Andrews, Samantha Nacole. Microdermabrasion for transdermal drug delivery.

Degree: PhD, Biomedical Engineering, 2010, Georgia Tech

 The skin serves as a semi-permeable barrier that protects the body from pathogens and water loss. The stratum corneum, the upper 10-15 µm layer of… (more)

Subjects/Keywords: Microdermabrasion; Transdermal drug delivery; Skin; Transdermal medication

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APA (6th Edition):

Andrews, S. N. (2010). Microdermabrasion for transdermal drug delivery. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/37150

Chicago Manual of Style (16th Edition):

Andrews, Samantha Nacole. “Microdermabrasion for transdermal drug delivery.” 2010. Doctoral Dissertation, Georgia Tech. Accessed March 23, 2019. http://hdl.handle.net/1853/37150.

MLA Handbook (7th Edition):

Andrews, Samantha Nacole. “Microdermabrasion for transdermal drug delivery.” 2010. Web. 23 Mar 2019.

Vancouver:

Andrews SN. Microdermabrasion for transdermal drug delivery. [Internet] [Doctoral dissertation]. Georgia Tech; 2010. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/1853/37150.

Council of Science Editors:

Andrews SN. Microdermabrasion for transdermal drug delivery. [Doctoral Dissertation]. Georgia Tech; 2010. Available from: http://hdl.handle.net/1853/37150


University of Southern California

9. Lo, Ronalee. Modular bio microelectromechanical systems (bioMEMS): intraocular drug delivery device and microfluidic interconnects.

Degree: PhD, Biomedical Engineering, 2009, University of Southern California

 Presented in this work are two devices, an ocular drug delivery device with a dual-regulation check valve, and an arrayed, horizontal microfluidic interconnect. Both devices… (more)

Subjects/Keywords: bioMEMS; drug delivery; intraocular; microfluidic; interconnects

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APA (6th Edition):

Lo, R. (2009). Modular bio microelectromechanical systems (bioMEMS): intraocular drug delivery device and microfluidic interconnects. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/601081/rec/4159

Chicago Manual of Style (16th Edition):

Lo, Ronalee. “Modular bio microelectromechanical systems (bioMEMS): intraocular drug delivery device and microfluidic interconnects.” 2009. Doctoral Dissertation, University of Southern California. Accessed March 23, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/601081/rec/4159.

MLA Handbook (7th Edition):

Lo, Ronalee. “Modular bio microelectromechanical systems (bioMEMS): intraocular drug delivery device and microfluidic interconnects.” 2009. Web. 23 Mar 2019.

Vancouver:

Lo R. Modular bio microelectromechanical systems (bioMEMS): intraocular drug delivery device and microfluidic interconnects. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2019 Mar 23]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/601081/rec/4159.

Council of Science Editors:

Lo R. Modular bio microelectromechanical systems (bioMEMS): intraocular drug delivery device and microfluidic interconnects. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/601081/rec/4159


Rutgers University

10. Khan, Isaac John, 1965-. The utility of L-tyrosine based polycarbonate copolymers containing poly(ethylene glycol) as a degradable carrier for the release of a hydrophobic peptide molecule:.

Degree: PhD, Biomedical Engineering, 2009, Rutgers University

The utility of biodegradable polymers as localized drug delivery carriers is an ongoing area of research where investigators attempt to deliver a wide range of… (more)

Subjects/Keywords: Eye – Diseases – Treatment; Drug delivery systems

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APA (6th Edition):

Khan, Isaac John, 1. (2009). The utility of L-tyrosine based polycarbonate copolymers containing poly(ethylene glycol) as a degradable carrier for the release of a hydrophobic peptide molecule:. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051844

Chicago Manual of Style (16th Edition):

Khan, Isaac John, 1965-. “The utility of L-tyrosine based polycarbonate copolymers containing poly(ethylene glycol) as a degradable carrier for the release of a hydrophobic peptide molecule:.” 2009. Doctoral Dissertation, Rutgers University. Accessed March 23, 2019. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051844.

MLA Handbook (7th Edition):

Khan, Isaac John, 1965-. “The utility of L-tyrosine based polycarbonate copolymers containing poly(ethylene glycol) as a degradable carrier for the release of a hydrophobic peptide molecule:.” 2009. Web. 23 Mar 2019.

Vancouver:

Khan, Isaac John 1. The utility of L-tyrosine based polycarbonate copolymers containing poly(ethylene glycol) as a degradable carrier for the release of a hydrophobic peptide molecule:. [Internet] [Doctoral dissertation]. Rutgers University; 2009. [cited 2019 Mar 23]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051844.

Council of Science Editors:

Khan, Isaac John 1. The utility of L-tyrosine based polycarbonate copolymers containing poly(ethylene glycol) as a degradable carrier for the release of a hydrophobic peptide molecule:. [Doctoral Dissertation]. Rutgers University; 2009. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051844


Virginia Commonwealth University

11. Yuan, Quan. ENGINEERING OF POLYAMIDOAMINE (PAMAM) DENDRIMERS FOR GENE AND DRUG DELIVERY.

Degree: PhD, Biomedical Engineering, 2012, Virginia Commonwealth University

 Dendrimers are a class of polymers with a highly branched, three-dimensional architecture composed of an initiator core, several interior layers of repeating units and multiple… (more)

Subjects/Keywords: Dendrimers; PAMAM; Gene Delivery; Drug Delivery; EGFR; Tumor; Biomaterials; Biomedical Engineering and Bioengineering; Engineering

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APA (6th Edition):

Yuan, Q. (2012). ENGINEERING OF POLYAMIDOAMINE (PAMAM) DENDRIMERS FOR GENE AND DRUG DELIVERY. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/2766

Chicago Manual of Style (16th Edition):

Yuan, Quan. “ENGINEERING OF POLYAMIDOAMINE (PAMAM) DENDRIMERS FOR GENE AND DRUG DELIVERY.” 2012. Doctoral Dissertation, Virginia Commonwealth University. Accessed March 23, 2019. https://scholarscompass.vcu.edu/etd/2766.

MLA Handbook (7th Edition):

Yuan, Quan. “ENGINEERING OF POLYAMIDOAMINE (PAMAM) DENDRIMERS FOR GENE AND DRUG DELIVERY.” 2012. Web. 23 Mar 2019.

Vancouver:

Yuan Q. ENGINEERING OF POLYAMIDOAMINE (PAMAM) DENDRIMERS FOR GENE AND DRUG DELIVERY. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2012. [cited 2019 Mar 23]. Available from: https://scholarscompass.vcu.edu/etd/2766.

Council of Science Editors:

Yuan Q. ENGINEERING OF POLYAMIDOAMINE (PAMAM) DENDRIMERS FOR GENE AND DRUG DELIVERY. [Doctoral Dissertation]. Virginia Commonwealth University; 2012. Available from: https://scholarscompass.vcu.edu/etd/2766


Georgia Tech

12. Zern, Blaine Joseph. A biocompatible, heparin-binding polycation for the controlled delivery of growth factors.

Degree: PhD, Biomedical Engineering, 2009, Georgia Tech

 The delivery of growth factors has been attempted for a number of different therapies. The approach of delivering therapeutic growth factors in a safe and… (more)

Subjects/Keywords: Polycation; Growth factor delivery; Heaprin; Growth factors; Drug delivery systems; Heparin; Biocompatibility

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APA (6th Edition):

Zern, B. J. (2009). A biocompatible, heparin-binding polycation for the controlled delivery of growth factors. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/28145

Chicago Manual of Style (16th Edition):

Zern, Blaine Joseph. “A biocompatible, heparin-binding polycation for the controlled delivery of growth factors.” 2009. Doctoral Dissertation, Georgia Tech. Accessed March 23, 2019. http://hdl.handle.net/1853/28145.

MLA Handbook (7th Edition):

Zern, Blaine Joseph. “A biocompatible, heparin-binding polycation for the controlled delivery of growth factors.” 2009. Web. 23 Mar 2019.

Vancouver:

Zern BJ. A biocompatible, heparin-binding polycation for the controlled delivery of growth factors. [Internet] [Doctoral dissertation]. Georgia Tech; 2009. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/1853/28145.

Council of Science Editors:

Zern BJ. A biocompatible, heparin-binding polycation for the controlled delivery of growth factors. [Doctoral Dissertation]. Georgia Tech; 2009. Available from: http://hdl.handle.net/1853/28145


Georgia Tech

13. Chu, Leonard Yi. Dissolving microneedles for cutaneous drug and vaccine delivery.

Degree: PhD, Biomedical Engineering, 2009, Georgia Tech

 Currently, biopharmaceuticals including vaccines, proteins, and DNA are delivered almost exclusively through the parenteral route using hypodermic needles. However, injection by hypodermic needles generates pain… (more)

Subjects/Keywords: Microneedles; Biotechnology; Pharmaceutical; Drug delivery; Transdermal; Medical devices; Formulation; Drug delivery devices; Transdermal medication; Drugs Administration

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APA (6th Edition):

Chu, L. Y. (2009). Dissolving microneedles for cutaneous drug and vaccine delivery. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/37177

Chicago Manual of Style (16th Edition):

Chu, Leonard Yi. “Dissolving microneedles for cutaneous drug and vaccine delivery.” 2009. Doctoral Dissertation, Georgia Tech. Accessed March 23, 2019. http://hdl.handle.net/1853/37177.

MLA Handbook (7th Edition):

Chu, Leonard Yi. “Dissolving microneedles for cutaneous drug and vaccine delivery.” 2009. Web. 23 Mar 2019.

Vancouver:

Chu LY. Dissolving microneedles for cutaneous drug and vaccine delivery. [Internet] [Doctoral dissertation]. Georgia Tech; 2009. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/1853/37177.

Council of Science Editors:

Chu LY. Dissolving microneedles for cutaneous drug and vaccine delivery. [Doctoral Dissertation]. Georgia Tech; 2009. Available from: http://hdl.handle.net/1853/37177


Virginia Commonwealth University

14. Xu, Leyuan. Semi-Interpenetrating Network Gelatin Fiber Sca old for Oral Mucosal Delivery of Insulin.

Degree: MS, Biomedical Engineering, 2013, Virginia Commonwealth University

 Common therapy for diabetes mellitus is subcutaneous administration of insulin that is subject to serious disadvantages, such as patient noncompliance and occasional hypoglycemia. Hence, oral… (more)

Subjects/Keywords: Drug delivery; insulin; photoinitiator; scaffold; Biomedical Engineering and Bioengineering; Engineering

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APA (6th Edition):

Xu, L. (2013). Semi-Interpenetrating Network Gelatin Fiber Sca old for Oral Mucosal Delivery of Insulin. (Thesis). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/3191

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):

Xu, Leyuan. “Semi-Interpenetrating Network Gelatin Fiber Sca old for Oral Mucosal Delivery of Insulin.” 2013. Thesis, Virginia Commonwealth University. Accessed March 23, 2019. https://scholarscompass.vcu.edu/etd/3191.

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

MLA Handbook (7th Edition):

Xu, Leyuan. “Semi-Interpenetrating Network Gelatin Fiber Sca old for Oral Mucosal Delivery of Insulin.” 2013. Web. 23 Mar 2019.

Vancouver:

Xu L. Semi-Interpenetrating Network Gelatin Fiber Sca old for Oral Mucosal Delivery of Insulin. [Internet] [Thesis]. Virginia Commonwealth University; 2013. [cited 2019 Mar 23]. Available from: https://scholarscompass.vcu.edu/etd/3191.

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

Council of Science Editors:

Xu L. Semi-Interpenetrating Network Gelatin Fiber Sca old for Oral Mucosal Delivery of Insulin. [Thesis]. Virginia Commonwealth University; 2013. Available from: https://scholarscompass.vcu.edu/etd/3191

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


The Ohio State University

15. Chakrapani, Aravind. Processing and characterization of polymer microparticles for controlled drug delivery systems.

Degree: PhD, Biomedical Engineering, 2006, The Ohio State University

 We report a novel soft lithography based technique to fabricate non-spherical biodegradable polymeric microparticles of different sizes and shapes as drug delivery systems. Geometrical control… (more)

Subjects/Keywords: Polymer microparticles; drug delivery

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APA (6th Edition):

Chakrapani, A. (2006). Processing and characterization of polymer microparticles for controlled drug delivery systems. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1164827297

Chicago Manual of Style (16th Edition):

Chakrapani, Aravind. “Processing and characterization of polymer microparticles for controlled drug delivery systems.” 2006. Doctoral Dissertation, The Ohio State University. Accessed March 23, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1164827297.

MLA Handbook (7th Edition):

Chakrapani, Aravind. “Processing and characterization of polymer microparticles for controlled drug delivery systems.” 2006. Web. 23 Mar 2019.

Vancouver:

Chakrapani A. Processing and characterization of polymer microparticles for controlled drug delivery systems. [Internet] [Doctoral dissertation]. The Ohio State University; 2006. [cited 2019 Mar 23]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1164827297.

Council of Science Editors:

Chakrapani A. Processing and characterization of polymer microparticles for controlled drug delivery systems. [Doctoral Dissertation]. The Ohio State University; 2006. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1164827297


Case Western Reserve University

16. Fu, Andrew Song. Affinity-based Delivery and Reloading of Doxorubicin For Treatment of Glioblastoma Multiforme.

Degree: PhD, Biomedical Engineering, 2013, Case Western Reserve University

 A reloadable drug delivery implant would allow for customizable chemotherapy tailored to the tumor progression of the individual patient. We report, for the first time,… (more)

Subjects/Keywords: Biomedical Engineering; affinity-based drug delivery; glioblastoma multiforme

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APA (6th Edition):

Fu, A. S. (2013). Affinity-based Delivery and Reloading of Doxorubicin For Treatment of Glioblastoma Multiforme. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1372345676

Chicago Manual of Style (16th Edition):

Fu, Andrew Song. “Affinity-based Delivery and Reloading of Doxorubicin For Treatment of Glioblastoma Multiforme.” 2013. Doctoral Dissertation, Case Western Reserve University. Accessed March 23, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1372345676.

MLA Handbook (7th Edition):

Fu, Andrew Song. “Affinity-based Delivery and Reloading of Doxorubicin For Treatment of Glioblastoma Multiforme.” 2013. Web. 23 Mar 2019.

Vancouver:

Fu AS. Affinity-based Delivery and Reloading of Doxorubicin For Treatment of Glioblastoma Multiforme. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2013. [cited 2019 Mar 23]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1372345676.

Council of Science Editors:

Fu AS. Affinity-based Delivery and Reloading of Doxorubicin For Treatment of Glioblastoma Multiforme. [Doctoral Dissertation]. Case Western Reserve University; 2013. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1372345676


UCLA

17. Linsley, Chase Schilling. Development of a Light Actuated Drug Delivery-on-Demand System.

Degree: Biomedical Engineering, 2015, UCLA

 The need for temporal-spatial control over the release of biologically active molecules has motivated efforts to engineer novel drug delivery-on-demand strategies actuated via light irradiation.… (more)

Subjects/Keywords: Biomedical engineering; Chromophore; Drug Delivery; Light Actuated; Photothermal; Poly (N-isopropylacrylamide)

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APA (6th Edition):

Linsley, C. S. (2015). Development of a Light Actuated Drug Delivery-on-Demand System. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/1wg4c9nq

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):

Linsley, Chase Schilling. “Development of a Light Actuated Drug Delivery-on-Demand System.” 2015. Thesis, UCLA. Accessed March 23, 2019. http://www.escholarship.org/uc/item/1wg4c9nq.

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

MLA Handbook (7th Edition):

Linsley, Chase Schilling. “Development of a Light Actuated Drug Delivery-on-Demand System.” 2015. Web. 23 Mar 2019.

Vancouver:

Linsley CS. Development of a Light Actuated Drug Delivery-on-Demand System. [Internet] [Thesis]. UCLA; 2015. [cited 2019 Mar 23]. Available from: http://www.escholarship.org/uc/item/1wg4c9nq.

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

Council of Science Editors:

Linsley CS. Development of a Light Actuated Drug Delivery-on-Demand System. [Thesis]. UCLA; 2015. Available from: http://www.escholarship.org/uc/item/1wg4c9nq

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


University of California – Irvine

18. Shih, Roger. High-Rate Production, Size Control, and Destruction of Microfluidic Bubbles for Ultrasound and Drug Delivery.

Degree: Biomedical Engineering, 2014, University of California – Irvine

 Ultrasound imaging often calls for the injection of contrast agents, micron-sized bubbles which echo strongly in blood and help distinguish vascularized tissue. Such microbubbles are… (more)

Subjects/Keywords: Biomedical engineering; bubble; drug delivery; flow focusing; microbubble; microfluidics; ultrasound

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APA (6th Edition):

Shih, R. (2014). High-Rate Production, Size Control, and Destruction of Microfluidic Bubbles for Ultrasound and Drug Delivery. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/5h7046fg

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):

Shih, Roger. “High-Rate Production, Size Control, and Destruction of Microfluidic Bubbles for Ultrasound and Drug Delivery.” 2014. Thesis, University of California – Irvine. Accessed March 23, 2019. http://www.escholarship.org/uc/item/5h7046fg.

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

MLA Handbook (7th Edition):

Shih, Roger. “High-Rate Production, Size Control, and Destruction of Microfluidic Bubbles for Ultrasound and Drug Delivery.” 2014. Web. 23 Mar 2019.

Vancouver:

Shih R. High-Rate Production, Size Control, and Destruction of Microfluidic Bubbles for Ultrasound and Drug Delivery. [Internet] [Thesis]. University of California – Irvine; 2014. [cited 2019 Mar 23]. Available from: http://www.escholarship.org/uc/item/5h7046fg.

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

Council of Science Editors:

Shih R. High-Rate Production, Size Control, and Destruction of Microfluidic Bubbles for Ultrasound and Drug Delivery. [Thesis]. University of California – Irvine; 2014. Available from: http://www.escholarship.org/uc/item/5h7046fg

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


University of Southern California

19. Gensler, Heidi Marie. A wireless implantable MEMS micropump system for site-specific anti-cancer drug delivery.

Degree: PhD, Biomedical Engineering, 2014, University of Southern California

 The manner in which a drug is delivered to the body plays a major role in its efficacy. There are several implantable pump technologies for… (more)

Subjects/Keywords: bellows electrochemical actuator; drug delivery; implants; MEMS; micropump; Parylene C

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APA (6th Edition):

Gensler, H. M. (2014). A wireless implantable MEMS micropump system for site-specific anti-cancer drug delivery. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/349546/rec/452

Chicago Manual of Style (16th Edition):

Gensler, Heidi Marie. “A wireless implantable MEMS micropump system for site-specific anti-cancer drug delivery.” 2014. Doctoral Dissertation, University of Southern California. Accessed March 23, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/349546/rec/452.

MLA Handbook (7th Edition):

Gensler, Heidi Marie. “A wireless implantable MEMS micropump system for site-specific anti-cancer drug delivery.” 2014. Web. 23 Mar 2019.

Vancouver:

Gensler HM. A wireless implantable MEMS micropump system for site-specific anti-cancer drug delivery. [Internet] [Doctoral dissertation]. University of Southern California; 2014. [cited 2019 Mar 23]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/349546/rec/452.

Council of Science Editors:

Gensler HM. A wireless implantable MEMS micropump system for site-specific anti-cancer drug delivery. [Doctoral Dissertation]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/349546/rec/452


University of Southern California

20. Sheybani, Roya. Wireless electrochemical drug delivery micropump with fully integrated electrochemical dose tracking feedback system.

Degree: PhD, Biomedical Engineering, 2015, University of Southern California

Drug delivery is essential for the treatment of chronic diseases. Implantable site‐specific drug delivery devices can deliver a potent and effective dose of drug directly… (more)

Subjects/Keywords: drug delivery; electrolysis; micropump; dose sensing; electrochemical sensors; wireless system

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APA (6th Edition):

Sheybani, R. (2015). Wireless electrochemical drug delivery micropump with fully integrated electrochemical dose tracking feedback system. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/574468/rec/7943

Chicago Manual of Style (16th Edition):

Sheybani, Roya. “Wireless electrochemical drug delivery micropump with fully integrated electrochemical dose tracking feedback system.” 2015. Doctoral Dissertation, University of Southern California. Accessed March 23, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/574468/rec/7943.

MLA Handbook (7th Edition):

Sheybani, Roya. “Wireless electrochemical drug delivery micropump with fully integrated electrochemical dose tracking feedback system.” 2015. Web. 23 Mar 2019.

Vancouver:

Sheybani R. Wireless electrochemical drug delivery micropump with fully integrated electrochemical dose tracking feedback system. [Internet] [Doctoral dissertation]. University of Southern California; 2015. [cited 2019 Mar 23]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/574468/rec/7943.

Council of Science Editors:

Sheybani R. Wireless electrochemical drug delivery micropump with fully integrated electrochemical dose tracking feedback system. [Doctoral Dissertation]. University of Southern California; 2015. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/574468/rec/7943


University of Iowa

21. Wadkins, David Allen. Nanoparticles: nanoscale systems for medical applications.

Degree: MS, Biomedical Engineering, 2017, University of Iowa

  The goal of this project was to develop a series of nano platforms for single cell analysis and drug delivery. Nanoparticles are a promising… (more)

Subjects/Keywords: Drug Delivery; Nanoparticle; Single cell tracking; Biomedical Engineering and Bioengineering

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APA (6th Edition):

Wadkins, D. A. (2017). Nanoparticles: nanoscale systems for medical applications. (Masters Thesis). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/6008

Chicago Manual of Style (16th Edition):

Wadkins, David Allen. “Nanoparticles: nanoscale systems for medical applications.” 2017. Masters Thesis, University of Iowa. Accessed March 23, 2019. https://ir.uiowa.edu/etd/6008.

MLA Handbook (7th Edition):

Wadkins, David Allen. “Nanoparticles: nanoscale systems for medical applications.” 2017. Web. 23 Mar 2019.

Vancouver:

Wadkins DA. Nanoparticles: nanoscale systems for medical applications. [Internet] [Masters thesis]. University of Iowa; 2017. [cited 2019 Mar 23]. Available from: https://ir.uiowa.edu/etd/6008.

Council of Science Editors:

Wadkins DA. Nanoparticles: nanoscale systems for medical applications. [Masters Thesis]. University of Iowa; 2017. Available from: https://ir.uiowa.edu/etd/6008

22. Jayagopal, Ashwath. Nanoscale surface engineering for bioimaging and drug delivery.

Degree: PhD, Biomedical Engineering, 2008, Vanderbilt University

 BIOMEDICAL ENGINEERING NANOSCALE SURFACE ENGINEERING FOR BIOIMAGING AND DRUG DELIVERY ASHWATH JAYAGOPAL Dissertation under the direction of Professor Frederick R. Haselton Nanoengineering of device interfaces… (more)

Subjects/Keywords: drug delivery; nanotechnology; imaging

…and drug delivery applications. Additionally, paracellular and subcellular translocation… …drug delivery applications. SLN consist of a biocompatible solid lipid matrix which during… …x29; formulations for targeted drug delivery and sustained drug release strategies (1-4… …modality, while also potentially functioning as a biocompatible drug delivery device. Three… …nanoparticles used for vascular imaging, or for passive tumor accumulation in drug delivery… 

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APA (6th Edition):

Jayagopal, A. (2008). Nanoscale surface engineering for bioimaging and drug delivery. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu//available/etd-04182008-172450/ ;

Chicago Manual of Style (16th Edition):

Jayagopal, Ashwath. “Nanoscale surface engineering for bioimaging and drug delivery.” 2008. Doctoral Dissertation, Vanderbilt University. Accessed March 23, 2019. http://etd.library.vanderbilt.edu//available/etd-04182008-172450/ ;.

MLA Handbook (7th Edition):

Jayagopal, Ashwath. “Nanoscale surface engineering for bioimaging and drug delivery.” 2008. Web. 23 Mar 2019.

Vancouver:

Jayagopal A. Nanoscale surface engineering for bioimaging and drug delivery. [Internet] [Doctoral dissertation]. Vanderbilt University; 2008. [cited 2019 Mar 23]. Available from: http://etd.library.vanderbilt.edu//available/etd-04182008-172450/ ;.

Council of Science Editors:

Jayagopal A. Nanoscale surface engineering for bioimaging and drug delivery. [Doctoral Dissertation]. Vanderbilt University; 2008. Available from: http://etd.library.vanderbilt.edu//available/etd-04182008-172450/ ;


Vanderbilt University

23. Evans, Brian Connor. Development of pH-responsive nano-polyplexes for intracellular delivery of therapeutic biomacromolecules.

Degree: PhD, Biomedical Engineering, 2015, Vanderbilt University

 Peptide-based therapeutics hold significant therapeutic potential for use in a variety of clinical applications ranging from cancer to cardiovascular disease. However, the potential of peptide-based… (more)

Subjects/Keywords: intimal hyperplasia; peptide; drug delivery; endosomal escape; polyplex; nanoparticle

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APA (6th Edition):

Evans, B. C. (2015). Development of pH-responsive nano-polyplexes for intracellular delivery of therapeutic biomacromolecules. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu//available/etd-03182015-162324/ ;

Chicago Manual of Style (16th Edition):

Evans, Brian Connor. “Development of pH-responsive nano-polyplexes for intracellular delivery of therapeutic biomacromolecules.” 2015. Doctoral Dissertation, Vanderbilt University. Accessed March 23, 2019. http://etd.library.vanderbilt.edu//available/etd-03182015-162324/ ;.

MLA Handbook (7th Edition):

Evans, Brian Connor. “Development of pH-responsive nano-polyplexes for intracellular delivery of therapeutic biomacromolecules.” 2015. Web. 23 Mar 2019.

Vancouver:

Evans BC. Development of pH-responsive nano-polyplexes for intracellular delivery of therapeutic biomacromolecules. [Internet] [Doctoral dissertation]. Vanderbilt University; 2015. [cited 2019 Mar 23]. Available from: http://etd.library.vanderbilt.edu//available/etd-03182015-162324/ ;.

Council of Science Editors:

Evans BC. Development of pH-responsive nano-polyplexes for intracellular delivery of therapeutic biomacromolecules. [Doctoral Dissertation]. Vanderbilt University; 2015. Available from: http://etd.library.vanderbilt.edu//available/etd-03182015-162324/ ;


Virginia Commonwealth University

24. Holden, Christopher A. MODIFIED PAMAM DENDRIMERS IN TUNABLE DRUG-DELIVERY SYSTEMS: A SUSTAINED-RELEASE DENDRIMER HYDROGEL FOR ANTI-GLAUCOMA DRUGS AND SURFACE-ENGINEERED MACROPHAGES AS NANOPARTICLE CARRIERS FOR TARGETED ANTI-CANCER THERAPY.

Degree: MS, Biomedical Engineering, 2017, Virginia Commonwealth University

  Two specific drug-delivery applications were sought in this work using polyamidoamine (PAMAM) dendrimers. One drug-delivery system used a novel dendrimer hydrogel (DH) for sustained… (more)

Subjects/Keywords: PAMAM; hydrogel; nanoparticles; dendrimer; drug-delivery; ophthalmic; Biomedical Engineering and Bioengineering

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APA (6th Edition):

Holden, C. A. (2017). MODIFIED PAMAM DENDRIMERS IN TUNABLE DRUG-DELIVERY SYSTEMS: A SUSTAINED-RELEASE DENDRIMER HYDROGEL FOR ANTI-GLAUCOMA DRUGS AND SURFACE-ENGINEERED MACROPHAGES AS NANOPARTICLE CARRIERS FOR TARGETED ANTI-CANCER THERAPY. (Thesis). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/5038

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):

Holden, Christopher A. “MODIFIED PAMAM DENDRIMERS IN TUNABLE DRUG-DELIVERY SYSTEMS: A SUSTAINED-RELEASE DENDRIMER HYDROGEL FOR ANTI-GLAUCOMA DRUGS AND SURFACE-ENGINEERED MACROPHAGES AS NANOPARTICLE CARRIERS FOR TARGETED ANTI-CANCER THERAPY.” 2017. Thesis, Virginia Commonwealth University. Accessed March 23, 2019. https://scholarscompass.vcu.edu/etd/5038.

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

MLA Handbook (7th Edition):

Holden, Christopher A. “MODIFIED PAMAM DENDRIMERS IN TUNABLE DRUG-DELIVERY SYSTEMS: A SUSTAINED-RELEASE DENDRIMER HYDROGEL FOR ANTI-GLAUCOMA DRUGS AND SURFACE-ENGINEERED MACROPHAGES AS NANOPARTICLE CARRIERS FOR TARGETED ANTI-CANCER THERAPY.” 2017. Web. 23 Mar 2019.

Vancouver:

Holden CA. MODIFIED PAMAM DENDRIMERS IN TUNABLE DRUG-DELIVERY SYSTEMS: A SUSTAINED-RELEASE DENDRIMER HYDROGEL FOR ANTI-GLAUCOMA DRUGS AND SURFACE-ENGINEERED MACROPHAGES AS NANOPARTICLE CARRIERS FOR TARGETED ANTI-CANCER THERAPY. [Internet] [Thesis]. Virginia Commonwealth University; 2017. [cited 2019 Mar 23]. Available from: https://scholarscompass.vcu.edu/etd/5038.

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

Council of Science Editors:

Holden CA. MODIFIED PAMAM DENDRIMERS IN TUNABLE DRUG-DELIVERY SYSTEMS: A SUSTAINED-RELEASE DENDRIMER HYDROGEL FOR ANTI-GLAUCOMA DRUGS AND SURFACE-ENGINEERED MACROPHAGES AS NANOPARTICLE CARRIERS FOR TARGETED ANTI-CANCER THERAPY. [Thesis]. Virginia Commonwealth University; 2017. Available from: https://scholarscompass.vcu.edu/etd/5038

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

25. Peddada, Lavanya Y., 1983-. Design of poly (alkylene oxide) graft copolymer chemistries for improved antisense drug delivery.

Degree: Biomedical Engineering, 2012, Rutgers University

Subjects/Keywords: Drug delivery systems

…hydrophilic particles [19]. This has introduced the field of stealth drug delivery, which… …1 1.2 Challenges to nucleic acid delivery: Systemic and Cellular… …6 1.3 Carrier for antisense/nucleic acid delivery… …DELIVERY & IN VITRO GENE SILENCING IN SERUM… …26 2.3.7 Antisense ODN delivery and gene silencing… 

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APA (6th Edition):

Peddada, Lavanya Y., 1. (2012). Design of poly (alkylene oxide) graft copolymer chemistries for improved antisense drug delivery. (Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000064160

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):

Peddada, Lavanya Y., 1983-. “Design of poly (alkylene oxide) graft copolymer chemistries for improved antisense drug delivery.” 2012. Thesis, Rutgers University. Accessed March 23, 2019. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000064160.

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

MLA Handbook (7th Edition):

Peddada, Lavanya Y., 1983-. “Design of poly (alkylene oxide) graft copolymer chemistries for improved antisense drug delivery.” 2012. Web. 23 Mar 2019.

Vancouver:

Peddada, Lavanya Y. 1. Design of poly (alkylene oxide) graft copolymer chemistries for improved antisense drug delivery. [Internet] [Thesis]. Rutgers University; 2012. [cited 2019 Mar 23]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000064160.

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

Council of Science Editors:

Peddada, Lavanya Y. 1. Design of poly (alkylene oxide) graft copolymer chemistries for improved antisense drug delivery. [Thesis]. Rutgers University; 2012. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000064160

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


University of Texas – Austin

26. Kasturi, Sudhir Pai. Design, synthesis, and evaluation of synthetic particulate delivery systems in DNA and protein vaccine delivery.

Degree: Biomedical Engineering, 2006, University of Texas – Austin

 Vaccination is not only a medical marvel in terms of unparalleled importance in safeguarding health but also considered to be one of the most economical… (more)

Subjects/Keywords: DNA vaccines; Drug delivery systems

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APA (6th Edition):

Kasturi, S. P. (2006). Design, synthesis, and evaluation of synthetic particulate delivery systems in DNA and protein vaccine delivery. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/2550

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):

Kasturi, Sudhir Pai. “Design, synthesis, and evaluation of synthetic particulate delivery systems in DNA and protein vaccine delivery.” 2006. Thesis, University of Texas – Austin. Accessed March 23, 2019. http://hdl.handle.net/2152/2550.

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

MLA Handbook (7th Edition):

Kasturi, Sudhir Pai. “Design, synthesis, and evaluation of synthetic particulate delivery systems in DNA and protein vaccine delivery.” 2006. Web. 23 Mar 2019.

Vancouver:

Kasturi SP. Design, synthesis, and evaluation of synthetic particulate delivery systems in DNA and protein vaccine delivery. [Internet] [Thesis]. University of Texas – Austin; 2006. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/2152/2550.

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

Council of Science Editors:

Kasturi SP. Design, synthesis, and evaluation of synthetic particulate delivery systems in DNA and protein vaccine delivery. [Thesis]. University of Texas – Austin; 2006. Available from: http://hdl.handle.net/2152/2550

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


University of Texas – Austin

27. Agarwal, Rachit, Ph. D. Effect of shape on cell internalization of polymeric hydrogel nanoparticles.

Degree: Biomedical Engineering, 2013, University of Texas – Austin

 Recent progress in drug discovery has enabled us to target specific intracellular molecules to achieve therapeutic effects. These next generation therapeutics are often biologics which… (more)

Subjects/Keywords: Nanoparticles; Hydrogel; Cell uptake; Shape; Nanoimprinting; Uptake Mechanisms; Drug Delivery

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APA (6th Edition):

Agarwal, Rachit, P. D. (2013). Effect of shape on cell internalization of polymeric hydrogel nanoparticles. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/30325

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):

Agarwal, Rachit, Ph D. “Effect of shape on cell internalization of polymeric hydrogel nanoparticles.” 2013. Thesis, University of Texas – Austin. Accessed March 23, 2019. http://hdl.handle.net/2152/30325.

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

MLA Handbook (7th Edition):

Agarwal, Rachit, Ph D. “Effect of shape on cell internalization of polymeric hydrogel nanoparticles.” 2013. Web. 23 Mar 2019.

Vancouver:

Agarwal, Rachit PD. Effect of shape on cell internalization of polymeric hydrogel nanoparticles. [Internet] [Thesis]. University of Texas – Austin; 2013. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/2152/30325.

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

Council of Science Editors:

Agarwal, Rachit PD. Effect of shape on cell internalization of polymeric hydrogel nanoparticles. [Thesis]. University of Texas – Austin; 2013. Available from: http://hdl.handle.net/2152/30325

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


University of Texas – Austin

28. Fakhoury, Jean Raymond Garcia. Porous silicon microparticles as an embolic agent for the treatment of hepatocellular carcinoma.

Degree: Biomedical Engineering, 2011, University of Texas – Austin

 Hepatocellular carcinoma (HCC) is the third most common cause of cancer-related deaths worldwide, accounting for over 600,000 deaths per year. The most common treatment strategy… (more)

Subjects/Keywords: Hepatocellular carcinoma; Porous silicon; Multistage drug delivery system; Transarterial chemoembolization

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APA (6th Edition):

Fakhoury, J. R. G. (2011). Porous silicon microparticles as an embolic agent for the treatment of hepatocellular carcinoma. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/14781

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):

Fakhoury, Jean Raymond Garcia. “Porous silicon microparticles as an embolic agent for the treatment of hepatocellular carcinoma.” 2011. Thesis, University of Texas – Austin. Accessed March 23, 2019. http://hdl.handle.net/2152/14781.

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

MLA Handbook (7th Edition):

Fakhoury, Jean Raymond Garcia. “Porous silicon microparticles as an embolic agent for the treatment of hepatocellular carcinoma.” 2011. Web. 23 Mar 2019.

Vancouver:

Fakhoury JRG. Porous silicon microparticles as an embolic agent for the treatment of hepatocellular carcinoma. [Internet] [Thesis]. University of Texas – Austin; 2011. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/2152/14781.

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

Council of Science Editors:

Fakhoury JRG. Porous silicon microparticles as an embolic agent for the treatment of hepatocellular carcinoma. [Thesis]. University of Texas – Austin; 2011. Available from: http://hdl.handle.net/2152/14781

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


University of Texas – Austin

29. Homan, Kimberly Ann. Nanosystems for combined therapy and imaging of pancreatic cancer.

Degree: Biomedical Engineering, 2010, University of Texas – Austin

 Pancreatic cancer remains a major unsolved health problem, with conventional cancer treatments having little impact on disease course. The objective of this thesis is to… (more)

Subjects/Keywords: Nanosystems; Nanoparticles; Photoacoustics; Drug delivery; Chemotherapy; Nanocages; Nanoplates; Pancreatic cancer

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

APA (6th Edition):

Homan, K. A. (2010). Nanosystems for combined therapy and imaging of pancreatic cancer. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/ETD-UT-2010-12-2261

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):

Homan, Kimberly Ann. “Nanosystems for combined therapy and imaging of pancreatic cancer.” 2010. Thesis, University of Texas – Austin. Accessed March 23, 2019. http://hdl.handle.net/2152/ETD-UT-2010-12-2261.

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

MLA Handbook (7th Edition):

Homan, Kimberly Ann. “Nanosystems for combined therapy and imaging of pancreatic cancer.” 2010. Web. 23 Mar 2019.

Vancouver:

Homan KA. Nanosystems for combined therapy and imaging of pancreatic cancer. [Internet] [Thesis]. University of Texas – Austin; 2010. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/2152/ETD-UT-2010-12-2261.

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

Council of Science Editors:

Homan KA. Nanosystems for combined therapy and imaging of pancreatic cancer. [Thesis]. University of Texas – Austin; 2010. Available from: http://hdl.handle.net/2152/ETD-UT-2010-12-2261

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


University of Minnesota

30. Richardson, Eric Stephen. Intrapericardial delivery of anti-arrhythmic agents.

Degree: PhD, Biomedical Engineering, 2009, University of Minnesota

 Anti-arrhythmic agents are known for their narrow therapeutic window and common side effects. Delivery of anti-arrhythmic agents into the pericardium has shown to increase their… (more)

Subjects/Keywords: Anti-arrhythmic Agent; Drug Delivery; Pericardium; Biomedical Engineering

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

APA (6th Edition):

Richardson, E. S. (2009). Intrapericardial delivery of anti-arrhythmic agents. (Doctoral Dissertation). University of Minnesota. Retrieved from http://purl.umn.edu/52393

Chicago Manual of Style (16th Edition):

Richardson, Eric Stephen. “Intrapericardial delivery of anti-arrhythmic agents.” 2009. Doctoral Dissertation, University of Minnesota. Accessed March 23, 2019. http://purl.umn.edu/52393.

MLA Handbook (7th Edition):

Richardson, Eric Stephen. “Intrapericardial delivery of anti-arrhythmic agents.” 2009. Web. 23 Mar 2019.

Vancouver:

Richardson ES. Intrapericardial delivery of anti-arrhythmic agents. [Internet] [Doctoral dissertation]. University of Minnesota; 2009. [cited 2019 Mar 23]. Available from: http://purl.umn.edu/52393.

Council of Science Editors:

Richardson ES. Intrapericardial delivery of anti-arrhythmic agents. [Doctoral Dissertation]. University of Minnesota; 2009. Available from: http://purl.umn.edu/52393

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