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You searched for subject:(Targeted Drug Delivery). Showing records 1 – 30 of 92 total matches.

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Wichita State University

1. 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 April 21, 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. 21 Apr 2019.

Vancouver:

Abedin F. Magnetic and albumin targeted drug delivery for breast cancer treatment . [Internet] [Masters thesis]. Wichita State University; 2011. [cited 2019 Apr 21]. 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


University of Waterloo

2. 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 April 21, 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. 21 Apr 2019.

Vancouver:

Tsai TH. Starch Nanoparticles for Targeted Anti-Cancer Drug Delivery. [Internet] [Thesis]. University of Waterloo; 2015. [cited 2019 Apr 21]. 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

3. 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 April 21, 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. 21 Apr 2019.

Vancouver:

Yang X. Development of Nanoparticle Systems for Therapeutic Drug Delivery. [Internet] [Doctoral dissertation]. The Ohio State University; 2009. [cited 2019 Apr 21]. 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


Case Western Reserve University

4. 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 April 21, 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. 21 Apr 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 Apr 21]. 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


Dublin City University

5. 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 April 21, 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. 21 Apr 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 Apr 21]. 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


University of Toronto

6. 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 April 21, 2019. http://hdl.handle.net/1807/33368.

MLA Handbook (7th Edition):

Chan, Dianna. “Polymeric Micelles for SiRNA and AON Delivery.” 2012. Web. 21 Apr 2019.

Vancouver:

Chan D. Polymeric Micelles for SiRNA and AON Delivery. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2019 Apr 21]. 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

7. 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 April 21, 2019. http://hdl.handle.net/11299/191471.

MLA Handbook (7th Edition):

Petersen, Matthew. “Degradable Polymersomes for Targeted Drug Delivery.” 2013. Web. 21 Apr 2019.

Vancouver:

Petersen M. Degradable Polymersomes for Targeted Drug Delivery. [Internet] [Doctoral dissertation]. University of Minnesota; 2013. [cited 2019 Apr 21]. 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


Brigham Young University

8. 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 April 21, 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. 21 Apr 2019.

Vancouver:

Hartley JM. Surface Modification of Liposomes Containing Nanoemulsions. [Internet] [Masters thesis]. Brigham Young University; 2011. [cited 2019 Apr 21]. 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 Alberta

9. 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 April 21, 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. 21 Apr 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 Apr 21]. 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

10. 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 April 21, 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. 21 Apr 2019.

Vancouver:

Garriga Font M. Micro-Crawlers in Confined Space: Volume Oscillating Hydrogels. [Internet] [Thesis]. University of Colorado; 2016. [cited 2019 Apr 21]. 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

11. 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… …utilization in human treatment. Discussion As reported earlier, nanomedical drug delivery can… …dendrimers. Nanocarriermediated drug delivery can utilize triggered drug release, passive targeting… …actively targeted nanomedicine. BIND-014, the first product developed with their Accurinsâ… …BIND-014, the encapsulated drug is Docetaxel, the active ingredient in Taxotere®, a… 

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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 April 21, 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. 21 Apr 2019.

Vancouver:

Vehmeijer LJC. Clinically Relevant Strategies of Actively Targeted Nanomedicine. [Internet] [Masters thesis]. Universiteit Utrecht; 2013. [cited 2019 Apr 21]. 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

12. 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 April 21, 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. 21 Apr 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 Apr 21]. 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


Cornell University

13. 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 April 21, 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. 21 Apr 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 Apr 21]. 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

14. 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 April 21, 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. 21 Apr 2019.

Vancouver:

Crawford L. Exploitation Of P-Glycoprotein At The Blood Brain Barrier For Targeted Drug Delivery . [Internet] [Thesis]. Cornell University; 2015. [cited 2019 Apr 21]. 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

15. 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 April 21, 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. 21 Apr 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 Apr 21]. 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

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

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 April 21, 2019. http://hdl.handle.net/11343/123601.

MLA Handbook (7th Edition):

Shirbin, Steven Josef. “Synthetic polypeptides for biomedical and bioactive applications.” 2016. Web. 21 Apr 2019.

Vancouver:

Shirbin SJ. Synthetic polypeptides for biomedical and bioactive applications. [Internet] [Doctoral dissertation]. University of Melbourne; 2016. [cited 2019 Apr 21]. 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


University of Waterloo

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

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 April 21, 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. 21 Apr 2019.

Vancouver:

Bahsoun NE. Double Emulsion Mucoadhesive Nanoparticles for Hydrophilic Ocular Drug Delivery. [Internet] [Thesis]. University of Waterloo; 2018. [cited 2019 Apr 21]. 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


Université Catholique de Louvain

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

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 April 21, 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. 21 Apr 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 Apr 21]. 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 Pennsylvania

19. Greineder, Colin F. Augmenting the Protein C Pathway with Endothelial Targeted Biotherapeutics: Strategies to Promote Partnering of TM and EPCR.

Degree: 2014, University of Pennsylvania

 The design of targeted recombinant biotherapeutics is a rapidly growing area of translational biomedical research, with particular relevance to acute and life-threatening conditions, in which… (more)

Subjects/Keywords: Endothelial Protein C Receptor; Endothelium; Targeted Drug Delivery; Thrombomodulin; Biomedical; Pharmacology

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APA (6th Edition):

Greineder, C. F. (2014). Augmenting the Protein C Pathway with Endothelial Targeted Biotherapeutics: Strategies to Promote Partnering of TM and EPCR. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/1296

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):

Greineder, Colin F. “Augmenting the Protein C Pathway with Endothelial Targeted Biotherapeutics: Strategies to Promote Partnering of TM and EPCR.” 2014. Thesis, University of Pennsylvania. Accessed April 21, 2019. https://repository.upenn.edu/edissertations/1296.

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

MLA Handbook (7th Edition):

Greineder, Colin F. “Augmenting the Protein C Pathway with Endothelial Targeted Biotherapeutics: Strategies to Promote Partnering of TM and EPCR.” 2014. Web. 21 Apr 2019.

Vancouver:

Greineder CF. Augmenting the Protein C Pathway with Endothelial Targeted Biotherapeutics: Strategies to Promote Partnering of TM and EPCR. [Internet] [Thesis]. University of Pennsylvania; 2014. [cited 2019 Apr 21]. Available from: https://repository.upenn.edu/edissertations/1296.

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

Council of Science Editors:

Greineder CF. Augmenting the Protein C Pathway with Endothelial Targeted Biotherapeutics: Strategies to Promote Partnering of TM and EPCR. [Thesis]. University of Pennsylvania; 2014. Available from: https://repository.upenn.edu/edissertations/1296

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


University of Pennsylvania

20. Gao, Chen. Engineering Bioactive Materials From Recombinant Oleosin Towards Drug Delivery Applications.

Degree: 2018, University of Pennsylvania

Drug carrier plays a critical role in achieving therapeutic effect in human or animals. Existing commercial drug carriers are mostly chemically synthesized, making the materials… (more)

Subjects/Keywords: oleosin; recombinant protein; self assembly; targeted drug delivery; Chemical Engineering

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

APA (6th Edition):

Gao, C. (2018). Engineering Bioactive Materials From Recombinant Oleosin Towards Drug Delivery Applications. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/2776

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):

Gao, Chen. “Engineering Bioactive Materials From Recombinant Oleosin Towards Drug Delivery Applications.” 2018. Thesis, University of Pennsylvania. Accessed April 21, 2019. https://repository.upenn.edu/edissertations/2776.

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

MLA Handbook (7th Edition):

Gao, Chen. “Engineering Bioactive Materials From Recombinant Oleosin Towards Drug Delivery Applications.” 2018. Web. 21 Apr 2019.

Vancouver:

Gao C. Engineering Bioactive Materials From Recombinant Oleosin Towards Drug Delivery Applications. [Internet] [Thesis]. University of Pennsylvania; 2018. [cited 2019 Apr 21]. Available from: https://repository.upenn.edu/edissertations/2776.

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

Council of Science Editors:

Gao C. Engineering Bioactive Materials From Recombinant Oleosin Towards Drug Delivery Applications. [Thesis]. University of Pennsylvania; 2018. Available from: https://repository.upenn.edu/edissertations/2776

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


Virginia Tech

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

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 April 21, 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. 21 Apr 2019.

Vancouver:

Colacino K. The Potential of Cellulose Nanocrystals in the Detection and Treatment of Cancer. [Internet] [Doctoral dissertation]. Virginia Tech; 2013. [cited 2019 Apr 21]. 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


University of Michigan

22. Misra, Asish C. Multicompartmental Carriers for Medical Applications.

Degree: PhD, Biomedical Engineering, 2016, University of Michigan

Targeted particulate carrier based therapies have the potential to vastly improve current treatment modalities in medicine by concentrating a therapeutic at its desired target, and… (more)

Subjects/Keywords: multicompartmental particles; carriers for medical applications; targeted drug delivery; targeted therapy; nanoparticles; microparticles; Biomedical Engineering; Engineering

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

APA (6th Edition):

Misra, A. C. (2016). Multicompartmental Carriers for Medical Applications. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/120726

Chicago Manual of Style (16th Edition):

Misra, Asish C. “Multicompartmental Carriers for Medical Applications.” 2016. Doctoral Dissertation, University of Michigan. Accessed April 21, 2019. http://hdl.handle.net/2027.42/120726.

MLA Handbook (7th Edition):

Misra, Asish C. “Multicompartmental Carriers for Medical Applications.” 2016. Web. 21 Apr 2019.

Vancouver:

Misra AC. Multicompartmental Carriers for Medical Applications. [Internet] [Doctoral dissertation]. University of Michigan; 2016. [cited 2019 Apr 21]. Available from: http://hdl.handle.net/2027.42/120726.

Council of Science Editors:

Misra AC. Multicompartmental Carriers for Medical Applications. [Doctoral Dissertation]. University of Michigan; 2016. Available from: http://hdl.handle.net/2027.42/120726


University of Wisconsin – Milwaukee

23. Loeser, Vera Franziska. Modeling of Anticancer Drug Delivery By Temperature-Sensitive Liposomes.

Degree: MS, Mathematics, 2017, University of Wisconsin – Milwaukee

  Cytotoxic anticancer drugs are used to treat cancer, particularly tumors. These drugs themselves do not distinguish between healthy and tumor cells and attack all… (more)

Subjects/Keywords: Doxorubicin; Drug Delivery; Mathematical Modeling; Targeted Therapy; Temperature-Sensitive Liposomes; Tumor; Mathematics; Oncology

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APA (6th Edition):

Loeser, V. F. (2017). Modeling of Anticancer Drug Delivery By Temperature-Sensitive Liposomes. (Thesis). University of Wisconsin – Milwaukee. Retrieved from https://dc.uwm.edu/etd/1509

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):

Loeser, Vera Franziska. “Modeling of Anticancer Drug Delivery By Temperature-Sensitive Liposomes.” 2017. Thesis, University of Wisconsin – Milwaukee. Accessed April 21, 2019. https://dc.uwm.edu/etd/1509.

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

MLA Handbook (7th Edition):

Loeser, Vera Franziska. “Modeling of Anticancer Drug Delivery By Temperature-Sensitive Liposomes.” 2017. Web. 21 Apr 2019.

Vancouver:

Loeser VF. Modeling of Anticancer Drug Delivery By Temperature-Sensitive Liposomes. [Internet] [Thesis]. University of Wisconsin – Milwaukee; 2017. [cited 2019 Apr 21]. Available from: https://dc.uwm.edu/etd/1509.

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

Council of Science Editors:

Loeser VF. Modeling of Anticancer Drug Delivery By Temperature-Sensitive Liposomes. [Thesis]. University of Wisconsin – Milwaukee; 2017. Available from: https://dc.uwm.edu/etd/1509

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


Texas Medical Center

24. Srinivasan, Srimeenakshi. TARGETING BREAST CANCER WITH BACTERIOPHAGE ASSOCIATED SILICON PARTICLES.

Degree: PhD, 2014, Texas Medical Center

  Nanoparticle based therapeutics have been successfully used in the treatment of breast cancer. Development of nanovectors targeted to cancer cells or elements in the… (more)

Subjects/Keywords: Nanomedicine; Porous Silicon; Breast Cancer; Targeted Drug Delivery; Medicine and Health Sciences; Nanomedicine

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APA (6th Edition):

Srinivasan, S. (2014). TARGETING BREAST CANCER WITH BACTERIOPHAGE ASSOCIATED SILICON PARTICLES. (Doctoral Dissertation). Texas Medical Center. Retrieved from http://digitalcommons.library.tmc.edu/utgsbs_dissertations/449

Chicago Manual of Style (16th Edition):

Srinivasan, Srimeenakshi. “TARGETING BREAST CANCER WITH BACTERIOPHAGE ASSOCIATED SILICON PARTICLES.” 2014. Doctoral Dissertation, Texas Medical Center. Accessed April 21, 2019. http://digitalcommons.library.tmc.edu/utgsbs_dissertations/449.

MLA Handbook (7th Edition):

Srinivasan, Srimeenakshi. “TARGETING BREAST CANCER WITH BACTERIOPHAGE ASSOCIATED SILICON PARTICLES.” 2014. Web. 21 Apr 2019.

Vancouver:

Srinivasan S. TARGETING BREAST CANCER WITH BACTERIOPHAGE ASSOCIATED SILICON PARTICLES. [Internet] [Doctoral dissertation]. Texas Medical Center; 2014. [cited 2019 Apr 21]. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/449.

Council of Science Editors:

Srinivasan S. TARGETING BREAST CANCER WITH BACTERIOPHAGE ASSOCIATED SILICON PARTICLES. [Doctoral Dissertation]. Texas Medical Center; 2014. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/449


Univerzitet u Beogradu

25. Bulatović, Mirna Z., 1985-. Ispitivanje antitumorskog delovanja 6-[trifenilstanil]-1-heksanola vezanog za mezoporozni nanomaterijal SBA-15 u modelu mišjeg melanoma in vitro i in vivo.

Degree: Biološki fakultet, 2016, Univerzitet u Beogradu

Biologija tumora - Eksperimentalna onkologija / Tumor biology - Experimental oncology

Uprkos razvoju imunoterapije i ciljanih terapija, globalna incidenca melanoma nastavlja da raste. Konvencionalna hemoterapija,… (more)

Subjects/Keywords: melanoma; chemotherapy; targeted drug delivery; mesoporous silica; organotin compounds; differentiation; cellular senescence

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APA (6th Edition):

Bulatović, Mirna Z., 1. (2016). Ispitivanje antitumorskog delovanja 6-[trifenilstanil]-1-heksanola vezanog za mezoporozni nanomaterijal SBA-15 u modelu mišjeg melanoma in vitro i in vivo. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:10940/bdef:Content/get

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):

Bulatović, Mirna Z., 1985-. “Ispitivanje antitumorskog delovanja 6-[trifenilstanil]-1-heksanola vezanog za mezoporozni nanomaterijal SBA-15 u modelu mišjeg melanoma in vitro i in vivo.” 2016. Thesis, Univerzitet u Beogradu. Accessed April 21, 2019. https://fedorabg.bg.ac.rs/fedora/get/o:10940/bdef:Content/get.

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

MLA Handbook (7th Edition):

Bulatović, Mirna Z., 1985-. “Ispitivanje antitumorskog delovanja 6-[trifenilstanil]-1-heksanola vezanog za mezoporozni nanomaterijal SBA-15 u modelu mišjeg melanoma in vitro i in vivo.” 2016. Web. 21 Apr 2019.

Vancouver:

Bulatović, Mirna Z. 1. Ispitivanje antitumorskog delovanja 6-[trifenilstanil]-1-heksanola vezanog za mezoporozni nanomaterijal SBA-15 u modelu mišjeg melanoma in vitro i in vivo. [Internet] [Thesis]. Univerzitet u Beogradu; 2016. [cited 2019 Apr 21]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:10940/bdef:Content/get.

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

Council of Science Editors:

Bulatović, Mirna Z. 1. Ispitivanje antitumorskog delovanja 6-[trifenilstanil]-1-heksanola vezanog za mezoporozni nanomaterijal SBA-15 u modelu mišjeg melanoma in vitro i in vivo. [Thesis]. Univerzitet u Beogradu; 2016. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:10940/bdef:Content/get

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


RMIT University

26. Kulhari, H. Peptide and monoclonal antibody mediated targeting of nanoconjugates in cancer chemotherapy.

Degree: 2015, RMIT University

 Cancer is one of the most common causes of the death. Currently used anticancer drugs have shown to be effective against various cancers. However, these… (more)

Subjects/Keywords: Fields of Research; Nanoparticles; Peptide; Antibody; Cancer chemotherapy; Nanomedicines; Targeted drug delivery systems

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APA (6th Edition):

Kulhari, H. (2015). Peptide and monoclonal antibody mediated targeting of nanoconjugates in cancer chemotherapy. (Thesis). RMIT University. Retrieved from http://researchbank.rmit.edu.au/view/rmit:161409

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):

Kulhari, H. “Peptide and monoclonal antibody mediated targeting of nanoconjugates in cancer chemotherapy.” 2015. Thesis, RMIT University. Accessed April 21, 2019. http://researchbank.rmit.edu.au/view/rmit:161409.

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

MLA Handbook (7th Edition):

Kulhari, H. “Peptide and monoclonal antibody mediated targeting of nanoconjugates in cancer chemotherapy.” 2015. Web. 21 Apr 2019.

Vancouver:

Kulhari H. Peptide and monoclonal antibody mediated targeting of nanoconjugates in cancer chemotherapy. [Internet] [Thesis]. RMIT University; 2015. [cited 2019 Apr 21]. Available from: http://researchbank.rmit.edu.au/view/rmit:161409.

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

Council of Science Editors:

Kulhari H. Peptide and monoclonal antibody mediated targeting of nanoconjugates in cancer chemotherapy. [Thesis]. RMIT University; 2015. Available from: http://researchbank.rmit.edu.au/view/rmit:161409

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

27. Hansen, Caroline Elizabeth. A platelet-mediated paradigm for the targeted delivery of microencapsulated, clot-augmenting biotherapeutics.

Degree: PhD, Chemistry and Biochemistry, 2017, Georgia Tech

 Reported herein is a paradigm-shifting, targeted drug delivery system that leverages the patient’s own platelets to sense and actuate targeted delivery of a clot-augmenting therapeutic… (more)

Subjects/Keywords: Targeted drug delivery; Platelet contraction

…SUMMARY Reported herein is a paradigm-shifting, targeted drug delivery system that leverages… …contraction. This cell-mediated, targeted drug delivery system utilizes polyelectrolyte multilayer… …clotting environment, which has yet to be used to perform targeted drug delivery. This work… …could drastically advance future “smart” targeted drug delivery strategies in the context of… …The overall objective of this thesis was to develop a targeted drug delivery paradigm that… 

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

APA (6th Edition):

Hansen, C. E. (2017). A platelet-mediated paradigm for the targeted delivery of microencapsulated, clot-augmenting biotherapeutics. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/58716

Chicago Manual of Style (16th Edition):

Hansen, Caroline Elizabeth. “A platelet-mediated paradigm for the targeted delivery of microencapsulated, clot-augmenting biotherapeutics.” 2017. Doctoral Dissertation, Georgia Tech. Accessed April 21, 2019. http://hdl.handle.net/1853/58716.

MLA Handbook (7th Edition):

Hansen, Caroline Elizabeth. “A platelet-mediated paradigm for the targeted delivery of microencapsulated, clot-augmenting biotherapeutics.” 2017. Web. 21 Apr 2019.

Vancouver:

Hansen CE. A platelet-mediated paradigm for the targeted delivery of microencapsulated, clot-augmenting biotherapeutics. [Internet] [Doctoral dissertation]. Georgia Tech; 2017. [cited 2019 Apr 21]. Available from: http://hdl.handle.net/1853/58716.

Council of Science Editors:

Hansen CE. A platelet-mediated paradigm for the targeted delivery of microencapsulated, clot-augmenting biotherapeutics. [Doctoral Dissertation]. Georgia Tech; 2017. Available from: http://hdl.handle.net/1853/58716

28. Κουτσιούκη, Καλλιόπη. Ανάπτυξη πολυλειτουργικών νανοκαψακίων φορτωμένα με αντικαρκινικά φάρμακα για τη στοχευμένη φαρμακοθεραπεία καρκινικών όγκων.

Degree: 2015, University of Patras

 Η Πακλιταξέλη αποτελεί ένα από τα πιο ευρέως διαδεδομένα χημειοθεραπευτικά φάρμακα και ενδείκνυται κυρίως σε καρκίνο του πνεύμονα, του μαστού, των ωοθηκών, καθώς και σε… (more)

Subjects/Keywords: Μαγνητικά νανοκαψάκια; Πακλιταξέλη; Στοχευμένη χορήγηση; 616.994 061; Magnetic nanocapsules; Paclitaxel; Targeted drug delivery

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

APA (6th Edition):

Κουτσιούκη, . (2015). Ανάπτυξη πολυλειτουργικών νανοκαψακίων φορτωμένα με αντικαρκινικά φάρμακα για τη στοχευμένη φαρμακοθεραπεία καρκινικών όγκων. (Masters Thesis). University of Patras. Retrieved from http://hdl.handle.net/10889/8788

Chicago Manual of Style (16th Edition):

Κουτσιούκη, Καλλιόπη. “Ανάπτυξη πολυλειτουργικών νανοκαψακίων φορτωμένα με αντικαρκινικά φάρμακα για τη στοχευμένη φαρμακοθεραπεία καρκινικών όγκων.” 2015. Masters Thesis, University of Patras. Accessed April 21, 2019. http://hdl.handle.net/10889/8788.

MLA Handbook (7th Edition):

Κουτσιούκη, Καλλιόπη. “Ανάπτυξη πολυλειτουργικών νανοκαψακίων φορτωμένα με αντικαρκινικά φάρμακα για τη στοχευμένη φαρμακοθεραπεία καρκινικών όγκων.” 2015. Web. 21 Apr 2019.

Vancouver:

Κουτσιούκη . Ανάπτυξη πολυλειτουργικών νανοκαψακίων φορτωμένα με αντικαρκινικά φάρμακα για τη στοχευμένη φαρμακοθεραπεία καρκινικών όγκων. [Internet] [Masters thesis]. University of Patras; 2015. [cited 2019 Apr 21]. Available from: http://hdl.handle.net/10889/8788.

Council of Science Editors:

Κουτσιούκη . Ανάπτυξη πολυλειτουργικών νανοκαψακίων φορτωμένα με αντικαρκινικά φάρμακα για τη στοχευμένη φαρμακοθεραπεία καρκινικών όγκων. [Masters Thesis]. University of Patras; 2015. Available from: http://hdl.handle.net/10889/8788


University of Oklahoma

29. Qu, Xuewei. Development of phage display-derived targeted cancer therapy and net-work scaffold for 3D cancer cell culture.

Degree: PhD, 2018, University of Oklahoma

 Precision medicine emphasizes the patient-specific formulation for treating diseases, especially cancer. For targeted cancer treatment, however, since the expression level of tumor receptors on each… (more)

Subjects/Keywords: Phage display; targeted cancer therapy; nano material drug delivery; in vitro tumor culture

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

APA (6th Edition):

Qu, X. (2018). Development of phage display-derived targeted cancer therapy and net-work scaffold for 3D cancer cell culture. (Doctoral Dissertation). University of Oklahoma. Retrieved from http://hdl.handle.net/11244/316765

Chicago Manual of Style (16th Edition):

Qu, Xuewei. “Development of phage display-derived targeted cancer therapy and net-work scaffold for 3D cancer cell culture.” 2018. Doctoral Dissertation, University of Oklahoma. Accessed April 21, 2019. http://hdl.handle.net/11244/316765.

MLA Handbook (7th Edition):

Qu, Xuewei. “Development of phage display-derived targeted cancer therapy and net-work scaffold for 3D cancer cell culture.” 2018. Web. 21 Apr 2019.

Vancouver:

Qu X. Development of phage display-derived targeted cancer therapy and net-work scaffold for 3D cancer cell culture. [Internet] [Doctoral dissertation]. University of Oklahoma; 2018. [cited 2019 Apr 21]. Available from: http://hdl.handle.net/11244/316765.

Council of Science Editors:

Qu X. Development of phage display-derived targeted cancer therapy and net-work scaffold for 3D cancer cell culture. [Doctoral Dissertation]. University of Oklahoma; 2018. Available from: http://hdl.handle.net/11244/316765


University of Toronto

30. Mardyani, Sawitri. Nanoparticles for Cancer Detection and Therapy: Towards Diagnostic Applications of Quantum Dots and Rational Design of Drug Delivery Vehicles.

Degree: 2011, University of Toronto

This thesis describes observations, techniques and strategies, which contribute towards the development of nanoparticle based detection and treatment of cancer. Quantum dots and biorecognition molecules… (more)

Subjects/Keywords: nanoparticles; cancer detection; cancer therapy; targeted drug delivery; quantum dots; phage display; 0541

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

APA (6th Edition):

Mardyani, S. (2011). Nanoparticles for Cancer Detection and Therapy: Towards Diagnostic Applications of Quantum Dots and Rational Design of Drug Delivery Vehicles. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/29803

Chicago Manual of Style (16th Edition):

Mardyani, Sawitri. “Nanoparticles for Cancer Detection and Therapy: Towards Diagnostic Applications of Quantum Dots and Rational Design of Drug Delivery Vehicles.” 2011. Doctoral Dissertation, University of Toronto. Accessed April 21, 2019. http://hdl.handle.net/1807/29803.

MLA Handbook (7th Edition):

Mardyani, Sawitri. “Nanoparticles for Cancer Detection and Therapy: Towards Diagnostic Applications of Quantum Dots and Rational Design of Drug Delivery Vehicles.” 2011. Web. 21 Apr 2019.

Vancouver:

Mardyani S. Nanoparticles for Cancer Detection and Therapy: Towards Diagnostic Applications of Quantum Dots and Rational Design of Drug Delivery Vehicles. [Internet] [Doctoral dissertation]. University of Toronto; 2011. [cited 2019 Apr 21]. Available from: http://hdl.handle.net/1807/29803.

Council of Science Editors:

Mardyani S. Nanoparticles for Cancer Detection and Therapy: Towards Diagnostic Applications of Quantum Dots and Rational Design of Drug Delivery Vehicles. [Doctoral Dissertation]. University of Toronto; 2011. Available from: http://hdl.handle.net/1807/29803

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