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You searched for subject:(targeted delivery). Showing records 1 – 30 of 144 total matches.

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University of Missouri – Kansas City

1. Boddu, Sai Hanuman Sagar, 1981-. Fomulation and Delivery of Drugs for Macular Edema and Retinoblastoma; Synthesis and In Vitro Characterization of Doxorubicin Loaded Surface Modified Nanoparticles Using PLGA-PEG-PLGA Polymer .

Degree: 2011, University of Missouri – Kansas City

 Macular edema (ME) is caused by central extravascular swelling of the macula resulting in a significant loss of visual activity. Corticosteroids are widely used in… (more)

Subjects/Keywords: Targeted Delivery; PLGA-PEG-FOL

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APA (6th Edition):

Boddu, Sai Hanuman Sagar, 1. (2011). Fomulation and Delivery of Drugs for Macular Edema and Retinoblastoma; Synthesis and In Vitro Characterization of Doxorubicin Loaded Surface Modified Nanoparticles Using PLGA-PEG-PLGA Polymer . (Thesis). University of Missouri – Kansas City. Retrieved from http://hdl.handle.net/10355/9588

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):

Boddu, Sai Hanuman Sagar, 1981-. “Fomulation and Delivery of Drugs for Macular Edema and Retinoblastoma; Synthesis and In Vitro Characterization of Doxorubicin Loaded Surface Modified Nanoparticles Using PLGA-PEG-PLGA Polymer .” 2011. Thesis, University of Missouri – Kansas City. Accessed July 22, 2019. http://hdl.handle.net/10355/9588.

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

MLA Handbook (7th Edition):

Boddu, Sai Hanuman Sagar, 1981-. “Fomulation and Delivery of Drugs for Macular Edema and Retinoblastoma; Synthesis and In Vitro Characterization of Doxorubicin Loaded Surface Modified Nanoparticles Using PLGA-PEG-PLGA Polymer .” 2011. Web. 22 Jul 2019.

Vancouver:

Boddu, Sai Hanuman Sagar 1. Fomulation and Delivery of Drugs for Macular Edema and Retinoblastoma; Synthesis and In Vitro Characterization of Doxorubicin Loaded Surface Modified Nanoparticles Using PLGA-PEG-PLGA Polymer . [Internet] [Thesis]. University of Missouri – Kansas City; 2011. [cited 2019 Jul 22]. Available from: http://hdl.handle.net/10355/9588.

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

Council of Science Editors:

Boddu, Sai Hanuman Sagar 1. Fomulation and Delivery of Drugs for Macular Edema and Retinoblastoma; Synthesis and In Vitro Characterization of Doxorubicin Loaded Surface Modified Nanoparticles Using PLGA-PEG-PLGA Polymer . [Thesis]. University of Missouri – Kansas City; 2011. Available from: http://hdl.handle.net/10355/9588

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


Wichita State University

2. Abedin, Farhana. Magnetic and albumin targeted drug delivery for breast cancer treatment .

Degree: 2011, Wichita State University

 This research work involves multifunctional magnetically targeted drug delivery microspheres for treatment against breast cancer. A combination therapy approach was followed by encapsulating two chemotherapeutics,… (more)

Subjects/Keywords: Targeted drug delivery; Magnetite nanoparticle; Breast cancer

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APA (6th Edition):

Abedin, F. (2011). Magnetic and albumin targeted drug delivery for breast cancer treatment . (Masters Thesis). Wichita State University. Retrieved from http://hdl.handle.net/10057/5054

Chicago Manual of Style (16th Edition):

Abedin, Farhana. “Magnetic and albumin targeted drug delivery for breast cancer treatment .” 2011. Masters Thesis, Wichita State University. Accessed July 22, 2019. http://hdl.handle.net/10057/5054.

MLA Handbook (7th Edition):

Abedin, Farhana. “Magnetic and albumin targeted drug delivery for breast cancer treatment .” 2011. Web. 22 Jul 2019.

Vancouver:

Abedin F. Magnetic and albumin targeted drug delivery for breast cancer treatment . [Internet] [Masters thesis]. Wichita State University; 2011. [cited 2019 Jul 22]. Available from: http://hdl.handle.net/10057/5054.

Council of Science Editors:

Abedin F. Magnetic and albumin targeted drug delivery for breast cancer treatment . [Masters Thesis]. Wichita State University; 2011. Available from: http://hdl.handle.net/10057/5054


Cornell University

3. Kang, Sungkwon. Engineering Leukocyte Integrins For Therapeutic Development Against Inflammatory Diseases .

Degree: 2012, Cornell University

 Inflammation is considered as a hallmark of host defense against infections and injuries. On the flipside, prolonged and non-resolving chronic inflammation is also associated with… (more)

Subjects/Keywords: protein engineering; leukocyte integrins; targeted delivery

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APA (6th Edition):

Kang, S. (2012). Engineering Leukocyte Integrins For Therapeutic Development Against Inflammatory Diseases . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/29487

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):

Kang, Sungkwon. “Engineering Leukocyte Integrins For Therapeutic Development Against Inflammatory Diseases .” 2012. Thesis, Cornell University. Accessed July 22, 2019. http://hdl.handle.net/1813/29487.

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

MLA Handbook (7th Edition):

Kang, Sungkwon. “Engineering Leukocyte Integrins For Therapeutic Development Against Inflammatory Diseases .” 2012. Web. 22 Jul 2019.

Vancouver:

Kang S. Engineering Leukocyte Integrins For Therapeutic Development Against Inflammatory Diseases . [Internet] [Thesis]. Cornell University; 2012. [cited 2019 Jul 22]. Available from: http://hdl.handle.net/1813/29487.

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

Council of Science Editors:

Kang S. Engineering Leukocyte Integrins For Therapeutic Development Against Inflammatory Diseases . [Thesis]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/29487

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


University of Waterloo

4. Tsai, Tsung Hao. Starch Nanoparticles for Targeted Anti-Cancer Drug Delivery.

Degree: 2015, University of Waterloo

 In the field of anti-cancer drug delivery, nanoparticles have become an active topic of research. Nanoparticles made of biodegradable materials such as polylactic acid, proteins,… (more)

Subjects/Keywords: Starch; Nanoparticle; Cancer; Targeted Drug Delivery

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APA (6th Edition):

Tsai, T. H. (2015). Starch Nanoparticles for Targeted Anti-Cancer Drug Delivery. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/9573

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):

Tsai, Tsung Hao. “Starch Nanoparticles for Targeted Anti-Cancer Drug Delivery.” 2015. Thesis, University of Waterloo. Accessed July 22, 2019. http://hdl.handle.net/10012/9573.

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

MLA Handbook (7th Edition):

Tsai, Tsung Hao. “Starch Nanoparticles for Targeted Anti-Cancer Drug Delivery.” 2015. Web. 22 Jul 2019.

Vancouver:

Tsai TH. Starch Nanoparticles for Targeted Anti-Cancer Drug Delivery. [Internet] [Thesis]. University of Waterloo; 2015. [cited 2019 Jul 22]. Available from: http://hdl.handle.net/10012/9573.

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

Council of Science Editors:

Tsai TH. Starch Nanoparticles for Targeted Anti-Cancer Drug Delivery. [Thesis]. University of Waterloo; 2015. Available from: http://hdl.handle.net/10012/9573

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


The Ohio State University

5. Yang, Xiaojuan. Development of Nanoparticle Systems for Therapeutic Drug Delivery.

Degree: PhD, Pharmacy, 2009, The Ohio State University

 Among various drug delivery systems, nanoparticles have shown some unique advantages. In this dissertation, a series of lipid and polymer-based nanoparticle systems were designed and… (more)

Subjects/Keywords: Pharmaceuticals; nanoparticle; drug delivery system; TfR-targeted delivery; nucleic acid delivery; chemotherapy drug delivery

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APA (6th Edition):

Yang, X. (2009). Development of Nanoparticle Systems for Therapeutic Drug Delivery. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1248972068

Chicago Manual of Style (16th Edition):

Yang, Xiaojuan. “Development of Nanoparticle Systems for Therapeutic Drug Delivery.” 2009. Doctoral Dissertation, The Ohio State University. Accessed July 22, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1248972068.

MLA Handbook (7th Edition):

Yang, Xiaojuan. “Development of Nanoparticle Systems for Therapeutic Drug Delivery.” 2009. Web. 22 Jul 2019.

Vancouver:

Yang X. Development of Nanoparticle Systems for Therapeutic Drug Delivery. [Internet] [Doctoral dissertation]. The Ohio State University; 2009. [cited 2019 Jul 22]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1248972068.

Council of Science Editors:

Yang X. Development of Nanoparticle Systems for Therapeutic Drug Delivery. [Doctoral Dissertation]. The Ohio State University; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1248972068


Dublin City University

6. McDonald, Bernard. Development of an oral drug delivery platform formulation for the targeted delivery of celecoxib for the chemoprevention and treatment of colorectal cancer.

Degree: School of Biotechnology, 2015, Dublin City University

 The anti-inflammatory drug celecoxib (CLX) has been shown to exert protective effects in colorectal cancer (CRC) therapy. The primary objective of this study was to… (more)

Subjects/Keywords: Biology; Pharmacology; Biochemistry; Colorectal cancer; Chemoprevention; Oral drug delivery; Targeted delivery

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APA (6th Edition):

McDonald, B. (2015). Development of an oral drug delivery platform formulation for the targeted delivery of celecoxib for the chemoprevention and treatment of colorectal cancer. (Thesis). Dublin City University. Retrieved from http://doras.dcu.ie/20409/

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):

McDonald, Bernard. “Development of an oral drug delivery platform formulation for the targeted delivery of celecoxib for the chemoprevention and treatment of colorectal cancer.” 2015. Thesis, Dublin City University. Accessed July 22, 2019. http://doras.dcu.ie/20409/.

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

MLA Handbook (7th Edition):

McDonald, Bernard. “Development of an oral drug delivery platform formulation for the targeted delivery of celecoxib for the chemoprevention and treatment of colorectal cancer.” 2015. Web. 22 Jul 2019.

Vancouver:

McDonald B. Development of an oral drug delivery platform formulation for the targeted delivery of celecoxib for the chemoprevention and treatment of colorectal cancer. [Internet] [Thesis]. Dublin City University; 2015. [cited 2019 Jul 22]. Available from: http://doras.dcu.ie/20409/.

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

Council of Science Editors:

McDonald B. Development of an oral drug delivery platform formulation for the targeted delivery of celecoxib for the chemoprevention and treatment of colorectal cancer. [Thesis]. Dublin City University; 2015. Available from: http://doras.dcu.ie/20409/

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


Case Western Reserve University

7. Cheng, Yu. Gold Nanoparticles as Drug Delivery Vectors for Photodynamic Therapy of Cancers.

Degree: PhD, Chemistry, 2011, Case Western Reserve University

 Gold nanoparticle-drug conjugates have attracted increasing attention in drug delivery for photodynamic cancer therapy. The nanoparticle acts as a water-soluble and bio-compatible platform that allows… (more)

Subjects/Keywords: Chemistry; gold nanoparticles; drug delivery; cancer; photodynamic therapy; targeted drug delivery

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APA (6th Edition):

Cheng, Y. (2011). Gold Nanoparticles as Drug Delivery Vectors for Photodynamic Therapy of Cancers. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1301503263

Chicago Manual of Style (16th Edition):

Cheng, Yu. “Gold Nanoparticles as Drug Delivery Vectors for Photodynamic Therapy of Cancers.” 2011. Doctoral Dissertation, Case Western Reserve University. Accessed July 22, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1301503263.

MLA Handbook (7th Edition):

Cheng, Yu. “Gold Nanoparticles as Drug Delivery Vectors for Photodynamic Therapy of Cancers.” 2011. Web. 22 Jul 2019.

Vancouver:

Cheng Y. Gold Nanoparticles as Drug Delivery Vectors for Photodynamic Therapy of Cancers. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2011. [cited 2019 Jul 22]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1301503263.

Council of Science Editors:

Cheng Y. Gold Nanoparticles as Drug Delivery Vectors for Photodynamic Therapy of Cancers. [Doctoral Dissertation]. Case Western Reserve University; 2011. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1301503263


University of Southern Mississippi

8. Shi, Yongliang. Self-Assembled Gold Nanoplexes for Cancer-Targeted siRNA Delivery.

Degree: MS, Chemistry and Biochemistry, 2014, University of Southern Mississippi

  Through layer-by-layer method, the authors have constructed three Au nanoplexes: AuPEI/RNA/PEI, AuPEI/RNA/PEI-mPEG, and AuPEI/NA/PEI-PEG-FA. All the nanoplexes are characterized by UV-vis spectrometry, DLS, and… (more)

Subjects/Keywords: gold nanoparticles; siRNA delivery; cancer-targeted delivery; Biotechnology; Medical Biochemistry; Nanomedicine

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APA (6th Edition):

Shi, Y. (2014). Self-Assembled Gold Nanoplexes for Cancer-Targeted siRNA Delivery. (Masters Thesis). University of Southern Mississippi. Retrieved from https://aquila.usm.edu/masters_theses/37

Chicago Manual of Style (16th Edition):

Shi, Yongliang. “Self-Assembled Gold Nanoplexes for Cancer-Targeted siRNA Delivery.” 2014. Masters Thesis, University of Southern Mississippi. Accessed July 22, 2019. https://aquila.usm.edu/masters_theses/37.

MLA Handbook (7th Edition):

Shi, Yongliang. “Self-Assembled Gold Nanoplexes for Cancer-Targeted siRNA Delivery.” 2014. Web. 22 Jul 2019.

Vancouver:

Shi Y. Self-Assembled Gold Nanoplexes for Cancer-Targeted siRNA Delivery. [Internet] [Masters thesis]. University of Southern Mississippi; 2014. [cited 2019 Jul 22]. Available from: https://aquila.usm.edu/masters_theses/37.

Council of Science Editors:

Shi Y. Self-Assembled Gold Nanoplexes for Cancer-Targeted siRNA Delivery. [Masters Thesis]. University of Southern Mississippi; 2014. Available from: https://aquila.usm.edu/masters_theses/37


University of Toronto

9. Chan, Dianna. Polymeric Micelles for SiRNA and AON Delivery.

Degree: 2012, University of Toronto

Immuno-nanoparticles of poly(ᴅ,ʟ-lactide-co-2-methyl-2-carboxytrimethylene carbonate)-g-poly(ethylene glycol) (poly(LA-co-TMCC)-g-PEG) have been used to target breast cancer cells through the specific binding of trastuzumab antibodies to over-expressed human epidermal… (more)

Subjects/Keywords: polymer nanoparticles; targeted delivery; gene therapy; drug delivery; 0542

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APA (6th Edition):

Chan, D. (2012). Polymeric Micelles for SiRNA and AON Delivery. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/33368

Chicago Manual of Style (16th Edition):

Chan, Dianna. “Polymeric Micelles for SiRNA and AON Delivery.” 2012. Masters Thesis, University of Toronto. Accessed July 22, 2019. http://hdl.handle.net/1807/33368.

MLA Handbook (7th Edition):

Chan, Dianna. “Polymeric Micelles for SiRNA and AON Delivery.” 2012. Web. 22 Jul 2019.

Vancouver:

Chan D. Polymeric Micelles for SiRNA and AON Delivery. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2019 Jul 22]. Available from: http://hdl.handle.net/1807/33368.

Council of Science Editors:

Chan D. Polymeric Micelles for SiRNA and AON Delivery. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/33368


University of Minnesota

10. Petersen, Matthew. Degradable Polymersomes for Targeted Drug Delivery.

Degree: PhD, Material Science and Engineering, 2013, University of Minnesota

 Chemotherapy today is often accompanied by major side effects due to delivery of toxic drugs to healthy tissue in addition to diseased cells. Targeted drug… (more)

Subjects/Keywords: Block Copolymers; Degradable Polymers; Drug Delivery; Polymersomes; Self Assembly; Targeted Delivery

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APA (6th Edition):

Petersen, M. (2013). Degradable Polymersomes for Targeted Drug Delivery. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/191471

Chicago Manual of Style (16th Edition):

Petersen, Matthew. “Degradable Polymersomes for Targeted Drug Delivery.” 2013. Doctoral Dissertation, University of Minnesota. Accessed July 22, 2019. http://hdl.handle.net/11299/191471.

MLA Handbook (7th Edition):

Petersen, Matthew. “Degradable Polymersomes for Targeted Drug Delivery.” 2013. Web. 22 Jul 2019.

Vancouver:

Petersen M. Degradable Polymersomes for Targeted Drug Delivery. [Internet] [Doctoral dissertation]. University of Minnesota; 2013. [cited 2019 Jul 22]. Available from: http://hdl.handle.net/11299/191471.

Council of Science Editors:

Petersen M. Degradable Polymersomes for Targeted Drug Delivery. [Doctoral Dissertation]. University of Minnesota; 2013. Available from: http://hdl.handle.net/11299/191471

11. Tzeng, Stephany Yi. Polymeric Nanoparticle-Based DNA AND siRNA Delivery for Cancer Treatment and Stem Cell Engineering.

Degree: 2014, Johns Hopkins University

 The fields of biomaterials, nanobiotechnology, and gene and drug delivery have all progressed over the past decades and have rapidly become a focus of research… (more)

Subjects/Keywords: nanomedicine; nanoparticles; polymeric gene delivery; non-viral gene delivery; DNA delivery; siRNA delivery; targeted cancer therapy

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APA (6th Edition):

Tzeng, S. Y. (2014). Polymeric Nanoparticle-Based DNA AND siRNA Delivery for Cancer Treatment and Stem Cell Engineering. (Thesis). Johns Hopkins University. Retrieved from http://jhir.library.jhu.edu/handle/1774.2/36968

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):

Tzeng, Stephany Yi. “Polymeric Nanoparticle-Based DNA AND siRNA Delivery for Cancer Treatment and Stem Cell Engineering.” 2014. Thesis, Johns Hopkins University. Accessed July 22, 2019. http://jhir.library.jhu.edu/handle/1774.2/36968.

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

MLA Handbook (7th Edition):

Tzeng, Stephany Yi. “Polymeric Nanoparticle-Based DNA AND siRNA Delivery for Cancer Treatment and Stem Cell Engineering.” 2014. Web. 22 Jul 2019.

Vancouver:

Tzeng SY. Polymeric Nanoparticle-Based DNA AND siRNA Delivery for Cancer Treatment and Stem Cell Engineering. [Internet] [Thesis]. Johns Hopkins University; 2014. [cited 2019 Jul 22]. Available from: http://jhir.library.jhu.edu/handle/1774.2/36968.

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

Council of Science Editors:

Tzeng SY. Polymeric Nanoparticle-Based DNA AND siRNA Delivery for Cancer Treatment and Stem Cell Engineering. [Thesis]. Johns Hopkins University; 2014. Available from: http://jhir.library.jhu.edu/handle/1774.2/36968

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


Brigham Young University

12. Hartley, Jonathan Michael. Surface Modification of Liposomes Containing Nanoemulsions.

Degree: MS, 2011, Brigham Young University

  Many attempts have been made to make cancer therapy more selective and less detrimental to the health of the patients. Nanoparticles have emerged as… (more)

Subjects/Keywords: liposomes; nanoemulsions; drug delivery; ultrasound; targeted drug delivery; vesosomes; eLiposome; Chemical Engineering

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APA (6th Edition):

Hartley, J. M. (2011). Surface Modification of Liposomes Containing Nanoemulsions. (Masters Thesis). Brigham Young University. Retrieved from https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=3845&context=etd

Chicago Manual of Style (16th Edition):

Hartley, Jonathan Michael. “Surface Modification of Liposomes Containing Nanoemulsions.” 2011. Masters Thesis, Brigham Young University. Accessed July 22, 2019. https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=3845&context=etd.

MLA Handbook (7th Edition):

Hartley, Jonathan Michael. “Surface Modification of Liposomes Containing Nanoemulsions.” 2011. Web. 22 Jul 2019.

Vancouver:

Hartley JM. Surface Modification of Liposomes Containing Nanoemulsions. [Internet] [Masters thesis]. Brigham Young University; 2011. [cited 2019 Jul 22]. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=3845&context=etd.

Council of Science Editors:

Hartley JM. Surface Modification of Liposomes Containing Nanoemulsions. [Masters Thesis]. Brigham Young University; 2011. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=3845&context=etd


University of Iowa

13. Tu, Mai H. Lipooligosaccharide-modified polymeric particles for targeted pulmonary drug delivery.

Degree: PhD, Pharmaceutical Sciences and Experimental Therapeutics, 2015, University of Iowa

Targeted delivery of drugs directly to the lung epithelium is a promising, though challenging, strategy for the treatment of diseases that affect the lung… (more)

Subjects/Keywords: lipooligosaccharide; lung cells; nanoparticle; pharmacy; pulmonary delivery; targeted delivery; Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Tu, M. H. (2015). Lipooligosaccharide-modified polymeric particles for targeted pulmonary drug delivery. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/5666

Chicago Manual of Style (16th Edition):

Tu, Mai H. “Lipooligosaccharide-modified polymeric particles for targeted pulmonary drug delivery.” 2015. Doctoral Dissertation, University of Iowa. Accessed July 22, 2019. https://ir.uiowa.edu/etd/5666.

MLA Handbook (7th Edition):

Tu, Mai H. “Lipooligosaccharide-modified polymeric particles for targeted pulmonary drug delivery.” 2015. Web. 22 Jul 2019.

Vancouver:

Tu MH. Lipooligosaccharide-modified polymeric particles for targeted pulmonary drug delivery. [Internet] [Doctoral dissertation]. University of Iowa; 2015. [cited 2019 Jul 22]. Available from: https://ir.uiowa.edu/etd/5666.

Council of Science Editors:

Tu MH. Lipooligosaccharide-modified polymeric particles for targeted pulmonary drug delivery. [Doctoral Dissertation]. University of Iowa; 2015. Available from: https://ir.uiowa.edu/etd/5666


University of Utah

14. Owen, Shawn C. Cryptofluorescent cobalamin bioconjugate for the visualization of tumor margins.

Degree: PhD, Pharmaceutics & Pharmaceutical Chemistry;, 2010, University of Utah

 Cryptofluorescent cobalamin bioconjugates were designed, synthesized, and evaluated for the potential to delineate tumor margins during surgical procedures, and therefore facilitate complete tumor resection. The… (more)

Subjects/Keywords: Breast cancer; Cobalamin; Fluorescence; Molecular imaging; Targeted delivery

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APA (6th Edition):

Owen, S. C. (2010). Cryptofluorescent cobalamin bioconjugate for the visualization of tumor margins. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1486/rec/273

Chicago Manual of Style (16th Edition):

Owen, Shawn C. “Cryptofluorescent cobalamin bioconjugate for the visualization of tumor margins.” 2010. Doctoral Dissertation, University of Utah. Accessed July 22, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1486/rec/273.

MLA Handbook (7th Edition):

Owen, Shawn C. “Cryptofluorescent cobalamin bioconjugate for the visualization of tumor margins.” 2010. Web. 22 Jul 2019.

Vancouver:

Owen SC. Cryptofluorescent cobalamin bioconjugate for the visualization of tumor margins. [Internet] [Doctoral dissertation]. University of Utah; 2010. [cited 2019 Jul 22]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1486/rec/273.

Council of Science Editors:

Owen SC. Cryptofluorescent cobalamin bioconjugate for the visualization of tumor margins. [Doctoral Dissertation]. University of Utah; 2010. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1486/rec/273


University of Alberta

15. Redman, Gillian. Inhaled Aerosols Targeted via Magnetic Alignment of High Aspect Ratio Particles: An In Vivo and Optimization Study.

Degree: Masters of Science, Department of Mechanical Engineering, 2011, University of Alberta

 An in vivo study with 19 rabbits was completed. Half of the exposed rabbits had a magnetic field placed externally over their right lung. Magnetic… (more)

Subjects/Keywords: Targeted Drug Delivery; Pharmaceutical Aerosols; High Aspect Ratio Particles

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APA (6th Edition):

Redman, G. (2011). Inhaled Aerosols Targeted via Magnetic Alignment of High Aspect Ratio Particles: An In Vivo and Optimization Study. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/v118rf360

Chicago Manual of Style (16th Edition):

Redman, Gillian. “Inhaled Aerosols Targeted via Magnetic Alignment of High Aspect Ratio Particles: An In Vivo and Optimization Study.” 2011. Masters Thesis, University of Alberta. Accessed July 22, 2019. https://era.library.ualberta.ca/files/v118rf360.

MLA Handbook (7th Edition):

Redman, Gillian. “Inhaled Aerosols Targeted via Magnetic Alignment of High Aspect Ratio Particles: An In Vivo and Optimization Study.” 2011. Web. 22 Jul 2019.

Vancouver:

Redman G. Inhaled Aerosols Targeted via Magnetic Alignment of High Aspect Ratio Particles: An In Vivo and Optimization Study. [Internet] [Masters thesis]. University of Alberta; 2011. [cited 2019 Jul 22]. Available from: https://era.library.ualberta.ca/files/v118rf360.

Council of Science Editors:

Redman G. Inhaled Aerosols Targeted via Magnetic Alignment of High Aspect Ratio Particles: An In Vivo and Optimization Study. [Masters Thesis]. University of Alberta; 2011. Available from: https://era.library.ualberta.ca/files/v118rf360


University of Colorado

16. Garriga Font, Marti. Micro-Crawlers in Confined Space: Volume Oscillating Hydrogels.

Degree: ME, 2016, University of Colorado

  Recent research has shown that certain polymer hydrogels with simple elongated geometries are capable of moving in a crawling fashion, their motion mechanics inspired… (more)

Subjects/Keywords: robots; polymer hydrogels; targeted drug delivery; Mechanical Engineering

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APA (6th Edition):

Garriga Font, M. (2016). Micro-Crawlers in Confined Space: Volume Oscillating Hydrogels. (Thesis). University of Colorado. Retrieved from http://scholar.colorado.edu/cven_gradetds/45

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):

Garriga Font, Marti. “Micro-Crawlers in Confined Space: Volume Oscillating Hydrogels.” 2016. Thesis, University of Colorado. Accessed July 22, 2019. http://scholar.colorado.edu/cven_gradetds/45.

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

MLA Handbook (7th Edition):

Garriga Font, Marti. “Micro-Crawlers in Confined Space: Volume Oscillating Hydrogels.” 2016. Web. 22 Jul 2019.

Vancouver:

Garriga Font M. Micro-Crawlers in Confined Space: Volume Oscillating Hydrogels. [Internet] [Thesis]. University of Colorado; 2016. [cited 2019 Jul 22]. Available from: http://scholar.colorado.edu/cven_gradetds/45.

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

Council of Science Editors:

Garriga Font M. Micro-Crawlers in Confined Space: Volume Oscillating Hydrogels. [Thesis]. University of Colorado; 2016. Available from: http://scholar.colorado.edu/cven_gradetds/45

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


Georgia Tech

17. Sodji, Quaovi Hemeka. Improving histone deacetylase inhibition therapy through isoform selectivity and targeted delivery.

Degree: PhD, Chemistry and Biochemistry, 2014, Georgia Tech

 Histone deacetylase (HDAC) inhibition has recently emerged as a novel therapy for cancer treatment. However, currently approved histone deacetylase inhibitors (HDACi) are pan-inhibitors thus inhibiting… (more)

Subjects/Keywords: Histone deacetylase (HDAC); HDAC inhibitors; Isoform selectivity; Targeted delivery

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APA (6th Edition):

Sodji, Q. H. (2014). Improving histone deacetylase inhibition therapy through isoform selectivity and targeted delivery. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/53445

Chicago Manual of Style (16th Edition):

Sodji, Quaovi Hemeka. “Improving histone deacetylase inhibition therapy through isoform selectivity and targeted delivery.” 2014. Doctoral Dissertation, Georgia Tech. Accessed July 22, 2019. http://hdl.handle.net/1853/53445.

MLA Handbook (7th Edition):

Sodji, Quaovi Hemeka. “Improving histone deacetylase inhibition therapy through isoform selectivity and targeted delivery.” 2014. Web. 22 Jul 2019.

Vancouver:

Sodji QH. Improving histone deacetylase inhibition therapy through isoform selectivity and targeted delivery. [Internet] [Doctoral dissertation]. Georgia Tech; 2014. [cited 2019 Jul 22]. Available from: http://hdl.handle.net/1853/53445.

Council of Science Editors:

Sodji QH. Improving histone deacetylase inhibition therapy through isoform selectivity and targeted delivery. [Doctoral Dissertation]. Georgia Tech; 2014. Available from: http://hdl.handle.net/1853/53445

18. Vehmeijer, L.J.C. Clinically Relevant Strategies of Actively Targeted Nanomedicine.

Degree: 2013, Universiteit Utrecht

 Nanocarriers, particles in the size range of 1 to 1000 nanometer, are the application of nanotechnology to drug delivery. Delivery of therapeutic agents through these… (more)

Subjects/Keywords: nanomedicine; nanocarrier; nanoparticle; active targeting; ligand; drug delivery; actively targeted

…target219, actively targeted delivery of doxorubicin could prove problematic. Notably, the two of… …actively targeted nanomedicine. BIND-014, the first product developed with their Accurinsâ… …wide range of different products. These include chemotherapeutics and molecularly targeted… …and 136 non-encapsulated Dtxl . 8 CALAA-01, a transferrin-targeted nanoparticle in… …example of Calando Pharmaceuticals’ RONDEL™ (RNAi/Oligonucleotide Nanoparticle Delivery… 

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APA (6th Edition):

Vehmeijer, L. J. C. (2013). Clinically Relevant Strategies of Actively Targeted Nanomedicine. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/288151

Chicago Manual of Style (16th Edition):

Vehmeijer, L J C. “Clinically Relevant Strategies of Actively Targeted Nanomedicine.” 2013. Masters Thesis, Universiteit Utrecht. Accessed July 22, 2019. http://dspace.library.uu.nl:8080/handle/1874/288151.

MLA Handbook (7th Edition):

Vehmeijer, L J C. “Clinically Relevant Strategies of Actively Targeted Nanomedicine.” 2013. Web. 22 Jul 2019.

Vancouver:

Vehmeijer LJC. Clinically Relevant Strategies of Actively Targeted Nanomedicine. [Internet] [Masters thesis]. Universiteit Utrecht; 2013. [cited 2019 Jul 22]. Available from: http://dspace.library.uu.nl:8080/handle/1874/288151.

Council of Science Editors:

Vehmeijer LJC. Clinically Relevant Strategies of Actively Targeted Nanomedicine. [Masters Thesis]. Universiteit Utrecht; 2013. Available from: http://dspace.library.uu.nl:8080/handle/1874/288151


UCLA

19. Yanes, Rolando Eduardo. Study of Mesoporous Silica Nanoparticles' (MSNs) intracellular trafficking and their application as drug delivery vehicles.

Degree: Microbiology, Immunology, & Molecular Genetics, 2013, UCLA

 Mesoporous silica nanoparticles (MSNs) are attractive drug delivery vehicle candidates due to their biocompatibility, stability, high surface area and efficient cellular uptake. In this dissertation,… (more)

Subjects/Keywords: Nanotechnology; Cellular biology; Exocytosis; Mesoporous Silica Nanoparticles; Targeted drug delivery

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APA (6th Edition):

Yanes, R. E. (2013). Study of Mesoporous Silica Nanoparticles' (MSNs) intracellular trafficking and their application as drug delivery vehicles. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/3zv804km

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):

Yanes, Rolando Eduardo. “Study of Mesoporous Silica Nanoparticles' (MSNs) intracellular trafficking and their application as drug delivery vehicles.” 2013. Thesis, UCLA. Accessed July 22, 2019. http://www.escholarship.org/uc/item/3zv804km.

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

MLA Handbook (7th Edition):

Yanes, Rolando Eduardo. “Study of Mesoporous Silica Nanoparticles' (MSNs) intracellular trafficking and their application as drug delivery vehicles.” 2013. Web. 22 Jul 2019.

Vancouver:

Yanes RE. Study of Mesoporous Silica Nanoparticles' (MSNs) intracellular trafficking and their application as drug delivery vehicles. [Internet] [Thesis]. UCLA; 2013. [cited 2019 Jul 22]. Available from: http://www.escholarship.org/uc/item/3zv804km.

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

Council of Science Editors:

Yanes RE. Study of Mesoporous Silica Nanoparticles' (MSNs) intracellular trafficking and their application as drug delivery vehicles. [Thesis]. UCLA; 2013. Available from: http://www.escholarship.org/uc/item/3zv804km

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


Virginia Tech

20. Colacino, Katelyn. The Potential of Cellulose Nanocrystals in the Detection and Treatment of Cancer.

Degree: PhD, Biomedical Engineering, 2013, Virginia Tech

 Conventional methods of cancer therapy have been severely limited by inefficient delivery of therapeutic doses without incidence of harsh and toxic side effects in normal… (more)

Subjects/Keywords: Folate Receptor; Early Cancer Detection; Targeted Drug Delivery; Irreversible Electroporation

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APA (6th Edition):

Colacino, K. (2013). The Potential of Cellulose Nanocrystals in the Detection and Treatment of Cancer. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/51212

Chicago Manual of Style (16th Edition):

Colacino, Katelyn. “The Potential of Cellulose Nanocrystals in the Detection and Treatment of Cancer.” 2013. Doctoral Dissertation, Virginia Tech. Accessed July 22, 2019. http://hdl.handle.net/10919/51212.

MLA Handbook (7th Edition):

Colacino, Katelyn. “The Potential of Cellulose Nanocrystals in the Detection and Treatment of Cancer.” 2013. Web. 22 Jul 2019.

Vancouver:

Colacino K. The Potential of Cellulose Nanocrystals in the Detection and Treatment of Cancer. [Internet] [Doctoral dissertation]. Virginia Tech; 2013. [cited 2019 Jul 22]. Available from: http://hdl.handle.net/10919/51212.

Council of Science Editors:

Colacino K. The Potential of Cellulose Nanocrystals in the Detection and Treatment of Cancer. [Doctoral Dissertation]. Virginia Tech; 2013. Available from: http://hdl.handle.net/10919/51212


Cornell University

21. Leelawattanachai, Jeerapond. Influence Of Size And Specificity On Pharmacokinetics, Biodistribution, And Tumor Targeting Of Widely Used Biologics: Fundamental Understanding To Applications .

Degree: 2014, Cornell University

 Specific and efficient targeting to tumors as well as many other diseases is a key to the success in several therapeutic interventions. The specificity offers… (more)

Subjects/Keywords: targeted drug delivery systems; pharmacokinetics and biodistribution; BIOLOGICS

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APA (6th Edition):

Leelawattanachai, J. (2014). Influence Of Size And Specificity On Pharmacokinetics, Biodistribution, And Tumor Targeting Of Widely Used Biologics: Fundamental Understanding To Applications . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/38837

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):

Leelawattanachai, Jeerapond. “Influence Of Size And Specificity On Pharmacokinetics, Biodistribution, And Tumor Targeting Of Widely Used Biologics: Fundamental Understanding To Applications .” 2014. Thesis, Cornell University. Accessed July 22, 2019. http://hdl.handle.net/1813/38837.

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

MLA Handbook (7th Edition):

Leelawattanachai, Jeerapond. “Influence Of Size And Specificity On Pharmacokinetics, Biodistribution, And Tumor Targeting Of Widely Used Biologics: Fundamental Understanding To Applications .” 2014. Web. 22 Jul 2019.

Vancouver:

Leelawattanachai J. Influence Of Size And Specificity On Pharmacokinetics, Biodistribution, And Tumor Targeting Of Widely Used Biologics: Fundamental Understanding To Applications . [Internet] [Thesis]. Cornell University; 2014. [cited 2019 Jul 22]. Available from: http://hdl.handle.net/1813/38837.

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

Council of Science Editors:

Leelawattanachai J. Influence Of Size And Specificity On Pharmacokinetics, Biodistribution, And Tumor Targeting Of Widely Used Biologics: Fundamental Understanding To Applications . [Thesis]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/38837

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


Cornell University

22. Crawford, Lindsey. Exploitation Of P-Glycoprotein At The Blood Brain Barrier For Targeted Drug Delivery .

Degree: 2015, Cornell University

 Drug development for the central nervous system (CNS) has struggled to reach clinical approval. One reason many drugs do not advance into clinical applications is… (more)

Subjects/Keywords: P-glycoprotein; Targeted Drug Delivery; Blood Brain Barrier

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APA (6th Edition):

Crawford, L. (2015). Exploitation Of P-Glycoprotein At The Blood Brain Barrier For Targeted Drug Delivery . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/41124

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):

Crawford, Lindsey. “Exploitation Of P-Glycoprotein At The Blood Brain Barrier For Targeted Drug Delivery .” 2015. Thesis, Cornell University. Accessed July 22, 2019. http://hdl.handle.net/1813/41124.

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

MLA Handbook (7th Edition):

Crawford, Lindsey. “Exploitation Of P-Glycoprotein At The Blood Brain Barrier For Targeted Drug Delivery .” 2015. Web. 22 Jul 2019.

Vancouver:

Crawford L. Exploitation Of P-Glycoprotein At The Blood Brain Barrier For Targeted Drug Delivery . [Internet] [Thesis]. Cornell University; 2015. [cited 2019 Jul 22]. Available from: http://hdl.handle.net/1813/41124.

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

Council of Science Editors:

Crawford L. Exploitation Of P-Glycoprotein At The Blood Brain Barrier For Targeted Drug Delivery . [Thesis]. Cornell University; 2015. Available from: http://hdl.handle.net/1813/41124

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


Temple University

23. Hooshdaran, Bahman. DUAL INHIBITION OF CATHEPSIN G AND CHYMASE AFTER ISCHEMIA REPERFUSION: THE ROLE OF INFLAMMATORY SERINE PROTEASES IN ISCHEMIA REPERFUSION INJURY.

Degree: PhD, 2017, Temple University

Bioengineering

Acute myocardial infarction (AMI) is a leading cause of morbidity and mortality in the world (4). Restoration of coronary flow to the ischemic myocardium… (more)

Subjects/Keywords: Engineering; Bioengineering;

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APA (6th Edition):

Hooshdaran, B. (2017). DUAL INHIBITION OF CATHEPSIN G AND CHYMASE AFTER ISCHEMIA REPERFUSION: THE ROLE OF INFLAMMATORY SERINE PROTEASES IN ISCHEMIA REPERFUSION INJURY. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,475423

Chicago Manual of Style (16th Edition):

Hooshdaran, Bahman. “DUAL INHIBITION OF CATHEPSIN G AND CHYMASE AFTER ISCHEMIA REPERFUSION: THE ROLE OF INFLAMMATORY SERINE PROTEASES IN ISCHEMIA REPERFUSION INJURY.” 2017. Doctoral Dissertation, Temple University. Accessed July 22, 2019. http://digital.library.temple.edu/u?/p245801coll10,475423.

MLA Handbook (7th Edition):

Hooshdaran, Bahman. “DUAL INHIBITION OF CATHEPSIN G AND CHYMASE AFTER ISCHEMIA REPERFUSION: THE ROLE OF INFLAMMATORY SERINE PROTEASES IN ISCHEMIA REPERFUSION INJURY.” 2017. Web. 22 Jul 2019.

Vancouver:

Hooshdaran B. DUAL INHIBITION OF CATHEPSIN G AND CHYMASE AFTER ISCHEMIA REPERFUSION: THE ROLE OF INFLAMMATORY SERINE PROTEASES IN ISCHEMIA REPERFUSION INJURY. [Internet] [Doctoral dissertation]. Temple University; 2017. [cited 2019 Jul 22]. Available from: http://digital.library.temple.edu/u?/p245801coll10,475423.

Council of Science Editors:

Hooshdaran B. DUAL INHIBITION OF CATHEPSIN G AND CHYMASE AFTER ISCHEMIA REPERFUSION: THE ROLE OF INFLAMMATORY SERINE PROTEASES IN ISCHEMIA REPERFUSION INJURY. [Doctoral Dissertation]. Temple University; 2017. Available from: http://digital.library.temple.edu/u?/p245801coll10,475423

24. Shirbin, Steven Josef. Synthetic polypeptides for biomedical and bioactive applications.

Degree: 2016, University of Melbourne

 Synthetic polypeptides are bioinspired mimics of natural polypeptides, readily prepared through controlled synthetic polymerization processes. Their use has offered chemists and biologists around the world… (more)

Subjects/Keywords: synthetic polypeptides; targeted drug delivery; tissue engineering; antimicrobial; bioactive; biomedical

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APA (6th Edition):

Shirbin, S. J. (2016). Synthetic polypeptides for biomedical and bioactive applications. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/123601

Chicago Manual of Style (16th Edition):

Shirbin, Steven Josef. “Synthetic polypeptides for biomedical and bioactive applications.” 2016. Doctoral Dissertation, University of Melbourne. Accessed July 22, 2019. http://hdl.handle.net/11343/123601.

MLA Handbook (7th Edition):

Shirbin, Steven Josef. “Synthetic polypeptides for biomedical and bioactive applications.” 2016. Web. 22 Jul 2019.

Vancouver:

Shirbin SJ. Synthetic polypeptides for biomedical and bioactive applications. [Internet] [Doctoral dissertation]. University of Melbourne; 2016. [cited 2019 Jul 22]. Available from: http://hdl.handle.net/11343/123601.

Council of Science Editors:

Shirbin SJ. Synthetic polypeptides for biomedical and bioactive applications. [Doctoral Dissertation]. University of Melbourne; 2016. Available from: http://hdl.handle.net/11343/123601


Université Catholique de Louvain

25. Schleich, Nathalie. Dual paclitaxel/superparamagnetic iron oxide-loaded PLGA-based nanoparticles for cancer therapy and magnetic resonance imaging.

Degree: 2015, Université Catholique de Louvain

Theranostic nanoparticles (NP) have the potential to revolutionize cancer diagnosis and therapy. We aimed to develop dual paclitaxel/SPIO-loaded PLGA-based NP for cancer therapy and magnetic… (more)

Subjects/Keywords: Cancer; Targeted drug delivery; MRI; Theranostic; Magnetic targeting; Nanomedicine

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APA (6th Edition):

Schleich, N. (2015). Dual paclitaxel/superparamagnetic iron oxide-loaded PLGA-based nanoparticles for cancer therapy and magnetic resonance imaging. (Thesis). Université Catholique de Louvain. Retrieved from http://hdl.handle.net/2078.1/156338

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):

Schleich, Nathalie. “Dual paclitaxel/superparamagnetic iron oxide-loaded PLGA-based nanoparticles for cancer therapy and magnetic resonance imaging.” 2015. Thesis, Université Catholique de Louvain. Accessed July 22, 2019. http://hdl.handle.net/2078.1/156338.

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

MLA Handbook (7th Edition):

Schleich, Nathalie. “Dual paclitaxel/superparamagnetic iron oxide-loaded PLGA-based nanoparticles for cancer therapy and magnetic resonance imaging.” 2015. Web. 22 Jul 2019.

Vancouver:

Schleich N. Dual paclitaxel/superparamagnetic iron oxide-loaded PLGA-based nanoparticles for cancer therapy and magnetic resonance imaging. [Internet] [Thesis]. Université Catholique de Louvain; 2015. [cited 2019 Jul 22]. Available from: http://hdl.handle.net/2078.1/156338.

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

Council of Science Editors:

Schleich N. Dual paclitaxel/superparamagnetic iron oxide-loaded PLGA-based nanoparticles for cancer therapy and magnetic resonance imaging. [Thesis]. Université Catholique de Louvain; 2015. Available from: http://hdl.handle.net/2078.1/156338

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


University of California – Irvine

26. Wang, Mingqiu. Kinetic Studies of Multivalent Nanoparticle Adhesion.

Degree: Biomedical Engineering, 2018, University of California – Irvine

Targeted delivery of functional nanoparticles (NPs) holds tremendous potential in diagnostics and therapeutics of vascular diseases and cancer. One of the major attributes is their… (more)

Subjects/Keywords: Biomedical engineering; kinetics; modeling; multivalent adhesion; nanoparticle; targeted delivery

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APA (6th Edition):

Wang, M. (2018). Kinetic Studies of Multivalent Nanoparticle Adhesion. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/3r478040

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

Chicago Manual of Style (16th Edition):

Wang, Mingqiu. “Kinetic Studies of Multivalent Nanoparticle Adhesion.” 2018. Thesis, University of California – Irvine. Accessed July 22, 2019. http://www.escholarship.org/uc/item/3r478040.

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

MLA Handbook (7th Edition):

Wang, Mingqiu. “Kinetic Studies of Multivalent Nanoparticle Adhesion.” 2018. Web. 22 Jul 2019.

Vancouver:

Wang M. Kinetic Studies of Multivalent Nanoparticle Adhesion. [Internet] [Thesis]. University of California – Irvine; 2018. [cited 2019 Jul 22]. Available from: http://www.escholarship.org/uc/item/3r478040.

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

Council of Science Editors:

Wang M. Kinetic Studies of Multivalent Nanoparticle Adhesion. [Thesis]. University of California – Irvine; 2018. Available from: http://www.escholarship.org/uc/item/3r478040

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


Kansas State University

27. Nguyen, Tuyen Duong Thanh. Engineering nanoparticles using chemical and biological approaches for tumor targeted delivery.

Degree: PhD, Department of Chemistry, 2019, Kansas State University

 Nanotechnology offers exciting options for the site-selective delivery of chemotherapeutics and diagnostic agents using nanoparticles. Varieties of organic and inorganic nanomaterials have been explored extensively… (more)

Subjects/Keywords: nanomedicine; MRI contrast agents; Biomimetic; Cancer; Targeted delivery; polymeric nanoparticles

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APA (6th Edition):

Nguyen, T. D. T. (2019). Engineering nanoparticles using chemical and biological approaches for tumor targeted delivery. (Doctoral Dissertation). Kansas State University. Retrieved from http://hdl.handle.net/2097/39466

Chicago Manual of Style (16th Edition):

Nguyen, Tuyen Duong Thanh. “Engineering nanoparticles using chemical and biological approaches for tumor targeted delivery.” 2019. Doctoral Dissertation, Kansas State University. Accessed July 22, 2019. http://hdl.handle.net/2097/39466.

MLA Handbook (7th Edition):

Nguyen, Tuyen Duong Thanh. “Engineering nanoparticles using chemical and biological approaches for tumor targeted delivery.” 2019. Web. 22 Jul 2019.

Vancouver:

Nguyen TDT. Engineering nanoparticles using chemical and biological approaches for tumor targeted delivery. [Internet] [Doctoral dissertation]. Kansas State University; 2019. [cited 2019 Jul 22]. Available from: http://hdl.handle.net/2097/39466.

Council of Science Editors:

Nguyen TDT. Engineering nanoparticles using chemical and biological approaches for tumor targeted delivery. [Doctoral Dissertation]. Kansas State University; 2019. Available from: http://hdl.handle.net/2097/39466


University of Waterloo

28. Bahsoun, Noor El-Huda. Double Emulsion Mucoadhesive Nanoparticles for Hydrophilic Ocular Drug Delivery.

Degree: 2018, University of Waterloo

 Common eye diseases such as conjunctivitis affect around 6 million people annually. Although eye drops are the most common treatment for these diseases, topical administration… (more)

Subjects/Keywords: drug delivery; hydrophilic; nanoparticle; targeted; ocular; mucoadhesive; double emulsion

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APA (6th Edition):

Bahsoun, N. E. (2018). Double Emulsion Mucoadhesive Nanoparticles for Hydrophilic Ocular Drug Delivery. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/13754

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):

Bahsoun, Noor El-Huda. “Double Emulsion Mucoadhesive Nanoparticles for Hydrophilic Ocular Drug Delivery.” 2018. Thesis, University of Waterloo. Accessed July 22, 2019. http://hdl.handle.net/10012/13754.

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

MLA Handbook (7th Edition):

Bahsoun, Noor El-Huda. “Double Emulsion Mucoadhesive Nanoparticles for Hydrophilic Ocular Drug Delivery.” 2018. Web. 22 Jul 2019.

Vancouver:

Bahsoun NE. Double Emulsion Mucoadhesive Nanoparticles for Hydrophilic Ocular Drug Delivery. [Internet] [Thesis]. University of Waterloo; 2018. [cited 2019 Jul 22]. Available from: http://hdl.handle.net/10012/13754.

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

Council of Science Editors:

Bahsoun NE. Double Emulsion Mucoadhesive Nanoparticles for Hydrophilic Ocular Drug Delivery. [Thesis]. University of Waterloo; 2018. Available from: http://hdl.handle.net/10012/13754

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


University of Waterloo

29. Linley, Stuart. Polymeric Coatings for Targeted Nanoparticle Delivery to Subsurface Contaminants.

Degree: 2019, University of Waterloo

 Terrestrial oil spills account for the majority of oil spills world wide and present a challenging remediation problem owing to the inaccessibility of subsurface petroleum… (more)

Subjects/Keywords: colloid transport; Pluronic; targeted delivery; crude oil; subsurface; binding; detection

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APA (6th Edition):

Linley, S. (2019). Polymeric Coatings for Targeted Nanoparticle Delivery to Subsurface Contaminants. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/14608

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):

Linley, Stuart. “Polymeric Coatings for Targeted Nanoparticle Delivery to Subsurface Contaminants.” 2019. Thesis, University of Waterloo. Accessed July 22, 2019. http://hdl.handle.net/10012/14608.

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

MLA Handbook (7th Edition):

Linley, Stuart. “Polymeric Coatings for Targeted Nanoparticle Delivery to Subsurface Contaminants.” 2019. Web. 22 Jul 2019.

Vancouver:

Linley S. Polymeric Coatings for Targeted Nanoparticle Delivery to Subsurface Contaminants. [Internet] [Thesis]. University of Waterloo; 2019. [cited 2019 Jul 22]. Available from: http://hdl.handle.net/10012/14608.

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

Council of Science Editors:

Linley S. Polymeric Coatings for Targeted Nanoparticle Delivery to Subsurface Contaminants. [Thesis]. University of Waterloo; 2019. Available from: http://hdl.handle.net/10012/14608

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


University of Minnesota

30. Levine, Rachel. Exploring Critical Vehicle Parameters for the Design of Multitargeted Nanoparticles for Cancer Specific Gene Delivery.

Degree: PhD, Chemical Engineering, 2015, University of Minnesota

 The greatest obstacle to clinical application of cancer gene therapy is lack of effective delivery tools. Gene delivery vehicles must protect against degradation, avoid immunogenic… (more)

Subjects/Keywords: Dual Targeting; Gene Delivery; Peptide Amphiphile; Stealth Liposomes; Targeted Therapies

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

APA (6th Edition):

Levine, R. (2015). Exploring Critical Vehicle Parameters for the Design of Multitargeted Nanoparticles for Cancer Specific Gene Delivery. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/188940

Chicago Manual of Style (16th Edition):

Levine, Rachel. “Exploring Critical Vehicle Parameters for the Design of Multitargeted Nanoparticles for Cancer Specific Gene Delivery.” 2015. Doctoral Dissertation, University of Minnesota. Accessed July 22, 2019. http://hdl.handle.net/11299/188940.

MLA Handbook (7th Edition):

Levine, Rachel. “Exploring Critical Vehicle Parameters for the Design of Multitargeted Nanoparticles for Cancer Specific Gene Delivery.” 2015. Web. 22 Jul 2019.

Vancouver:

Levine R. Exploring Critical Vehicle Parameters for the Design of Multitargeted Nanoparticles for Cancer Specific Gene Delivery. [Internet] [Doctoral dissertation]. University of Minnesota; 2015. [cited 2019 Jul 22]. Available from: http://hdl.handle.net/11299/188940.

Council of Science Editors:

Levine R. Exploring Critical Vehicle Parameters for the Design of Multitargeted Nanoparticles for Cancer Specific Gene Delivery. [Doctoral Dissertation]. University of Minnesota; 2015. Available from: http://hdl.handle.net/11299/188940

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