Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

You searched for subject:(Targeted drug delivery). Showing records 1 – 30 of 127 total matches.

[1] [2] [3] [4] [5]

Search Limiters

Last 2 Years | English Only

Degrees

Levels

▼ Search Limiters


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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 January 16, 2021. http://hdl.handle.net/10057/5054.

MLA Handbook (7th Edition):

Abedin, Farhana. “Magnetic and albumin targeted drug delivery for breast cancer treatment .” 2011. Web. 16 Jan 2021.

Vancouver:

Abedin F. Magnetic and albumin targeted drug delivery for breast cancer treatment . [Internet] [Masters thesis]. Wichita State University; 2011. [cited 2021 Jan 16]. 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 Minnesota

2. Harris, Michael. Self-Assembled Single Stranded DNA-Amphiphiles for Targeted Drug Delivery.

Degree: PhD, Chemical Engineering, 2018, University of Minnesota

 The use of targeted drug delivery has significantly improved the field of medicine in the last 30 years. At the same time, the field of… (more)

Subjects/Keywords: Amphiphile; Cancer; DNA Aptamer; Targeted Drug Delivery

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Harris, M. (2018). Self-Assembled Single Stranded DNA-Amphiphiles for Targeted Drug Delivery. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/206266

Chicago Manual of Style (16th Edition):

Harris, Michael. “Self-Assembled Single Stranded DNA-Amphiphiles for Targeted Drug Delivery.” 2018. Doctoral Dissertation, University of Minnesota. Accessed January 16, 2021. http://hdl.handle.net/11299/206266.

MLA Handbook (7th Edition):

Harris, Michael. “Self-Assembled Single Stranded DNA-Amphiphiles for Targeted Drug Delivery.” 2018. Web. 16 Jan 2021.

Vancouver:

Harris M. Self-Assembled Single Stranded DNA-Amphiphiles for Targeted Drug Delivery. [Internet] [Doctoral dissertation]. University of Minnesota; 2018. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/11299/206266.

Council of Science Editors:

Harris M. Self-Assembled Single Stranded DNA-Amphiphiles for Targeted Drug Delivery. [Doctoral Dissertation]. University of Minnesota; 2018. Available from: http://hdl.handle.net/11299/206266


University of Waterloo

3. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 January 16, 2021. 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. 16 Jan 2021.

Vancouver:

Tsai TH. Starch Nanoparticles for Targeted Anti-Cancer Drug Delivery. [Internet] [Thesis]. University of Waterloo; 2015. [cited 2021 Jan 16]. 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

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

Degree: PhD, Chemistry, 2011, Case Western Reserve University School of Graduate Studies

 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Cheng, Y. (2011). Gold Nanoparticles as Drug Delivery Vectors for Photodynamic Therapy of Cancers. (Doctoral Dissertation). Case Western Reserve University School of Graduate Studies. 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 School of Graduate Studies. Accessed January 16, 2021. 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. 16 Jan 2021.

Vancouver:

Cheng Y. Gold Nanoparticles as Drug Delivery Vectors for Photodynamic Therapy of Cancers. [Internet] [Doctoral dissertation]. Case Western Reserve University School of Graduate Studies; 2011. [cited 2021 Jan 16]. 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 School of Graduate Studies; 2011. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1301503263


University of Toronto

5. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 January 16, 2021. http://hdl.handle.net/1807/33368.

MLA Handbook (7th Edition):

Chan, Dianna. “Polymeric Micelles for SiRNA and AON Delivery.” 2012. Web. 16 Jan 2021.

Vancouver:

Chan D. Polymeric Micelles for SiRNA and AON Delivery. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2021 Jan 16]. 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

6. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 January 16, 2021. http://hdl.handle.net/11299/191471.

MLA Handbook (7th Edition):

Petersen, Matthew. “Degradable Polymersomes for Targeted Drug Delivery.” 2013. Web. 16 Jan 2021.

Vancouver:

Petersen M. Degradable Polymersomes for Targeted Drug Delivery. [Internet] [Doctoral dissertation]. University of Minnesota; 2013. [cited 2021 Jan 16]. 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

7. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 January 16, 2021. 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. 16 Jan 2021.

Vancouver:

Hartley JM. Surface Modification of Liposomes Containing Nanoemulsions. [Internet] [Masters thesis]. Brigham Young University; 2011. [cited 2021 Jan 16]. 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 Texas – Austin

8. -8314-1719. Design and synthesis of novel sigma receptor ligands through scaffold minimization and their application towards targeted drug delivery.

Degree: MA, Chemistry, 2019, University of Texas – Austin

 Sigma receptors are a class of proteins in which both subtypes (sigma 1 and sigma 2) have been implicated in the pathology of most central… (more)

Subjects/Keywords: Sigma receptors; Sigma receptor ligands; Scaffold minimization; Targeted drug delivery; Ligand-targeted cancer therapeutic

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

-8314-1719. (2019). Design and synthesis of novel sigma receptor ligands through scaffold minimization and their application towards targeted drug delivery. (Masters Thesis). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/2770

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Chicago Manual of Style (16th Edition):

-8314-1719. “Design and synthesis of novel sigma receptor ligands through scaffold minimization and their application towards targeted drug delivery.” 2019. Masters Thesis, University of Texas – Austin. Accessed January 16, 2021. http://dx.doi.org/10.26153/tsw/2770.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

MLA Handbook (7th Edition):

-8314-1719. “Design and synthesis of novel sigma receptor ligands through scaffold minimization and their application towards targeted drug delivery.” 2019. Web. 16 Jan 2021.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

-8314-1719. Design and synthesis of novel sigma receptor ligands through scaffold minimization and their application towards targeted drug delivery. [Internet] [Masters thesis]. University of Texas – Austin; 2019. [cited 2021 Jan 16]. Available from: http://dx.doi.org/10.26153/tsw/2770.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

-8314-1719. Design and synthesis of novel sigma receptor ligands through scaffold minimization and their application towards targeted drug delivery. [Masters Thesis]. University of Texas – Austin; 2019. Available from: http://dx.doi.org/10.26153/tsw/2770

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete


UCLA

9. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 January 16, 2021. 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. 16 Jan 2021.

Vancouver:

Yanes RE. Study of Mesoporous Silica Nanoparticles' (MSNs) intracellular trafficking and their application as drug delivery vehicles. [Internet] [Thesis]. UCLA; 2013. [cited 2021 Jan 16]. 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


University of Rochester

10. Wang, Yuchen (1991 - ). Development of controlled release systems for fracture-targeted therapeutic delivery.

Degree: PhD, 2018, University of Rochester

 Fracture healing is a major clinical challenge, with a 10-20% impaired healing rate, resulting in significantly prolonged hospitalization, decreased quality of life, and substantial healthcare… (more)

Subjects/Keywords: Fracture healing; Targeted drug delivery; Controlled release; Nanoparticles; siRNA; Hydrogels

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Wang, Y. (. -. ). (2018). Development of controlled release systems for fracture-targeted therapeutic delivery. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/33504

Chicago Manual of Style (16th Edition):

Wang, Yuchen (1991 - ). “Development of controlled release systems for fracture-targeted therapeutic delivery.” 2018. Doctoral Dissertation, University of Rochester. Accessed January 16, 2021. http://hdl.handle.net/1802/33504.

MLA Handbook (7th Edition):

Wang, Yuchen (1991 - ). “Development of controlled release systems for fracture-targeted therapeutic delivery.” 2018. Web. 16 Jan 2021.

Vancouver:

Wang Y(-). Development of controlled release systems for fracture-targeted therapeutic delivery. [Internet] [Doctoral dissertation]. University of Rochester; 2018. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1802/33504.

Council of Science Editors:

Wang Y(-). Development of controlled release systems for fracture-targeted therapeutic delivery. [Doctoral Dissertation]. University of Rochester; 2018. Available from: http://hdl.handle.net/1802/33504


University of Alberta

11. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 January 16, 2021. 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. 16 Jan 2021.

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 2021 Jan 16]. 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

12. 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… 

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 January 16, 2021. 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. 16 Jan 2021.

Vancouver:

Vehmeijer LJC. Clinically Relevant Strategies of Actively Targeted Nanomedicine. [Internet] [Masters thesis]. Universiteit Utrecht; 2013. [cited 2021 Jan 16]. 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


Cornell University

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

Degree: PhD, Chemical Engineering, 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Crawford, Lindsey. “Exploitation Of P-Glycoprotein At The Blood Brain Barrier For Targeted Drug Delivery.” 2015. Doctoral Dissertation, Cornell University. Accessed January 16, 2021. http://hdl.handle.net/1813/41124.

MLA Handbook (7th Edition):

Crawford, Lindsey. “Exploitation Of P-Glycoprotein At The Blood Brain Barrier For Targeted Drug Delivery.” 2015. Web. 16 Jan 2021.

Vancouver:

Crawford L. Exploitation Of P-Glycoprotein At The Blood Brain Barrier For Targeted Drug Delivery. [Internet] [Doctoral dissertation]. Cornell University; 2015. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1813/41124.

Council of Science Editors:

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


Cornell University

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

Degree: PhD, Biomedical Engineering, 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/38837

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. Doctoral Dissertation, Cornell University. Accessed January 16, 2021. http://hdl.handle.net/1813/38837.

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. 16 Jan 2021.

Vancouver:

Leelawattanachai J. Influence Of Size And Specificity On Pharmacokinetics, Biodistribution, And Tumor Targeting Of Widely Used Biologics: Fundamental Understanding To Applications. [Internet] [Doctoral dissertation]. Cornell University; 2014. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1813/38837.

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. [Doctoral Dissertation]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/38837


University of Oxford

15. Skaripa-Koukelli, Eirini. Towards the synthesis and delivery of a halogenated MCT1 substrate.

Degree: PhD, 2020, University of Oxford

 The monocarboxylate transporter 1 (MCT1) has received special attention as a potential therapeutic target in cancer thanks to its role in lactate shuttling. In breast… (more)

Subjects/Keywords: Drug delivery systems; tumour metabolism; targeted radionuclide therapy

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Skaripa-Koukelli, E. (2020). Towards the synthesis and delivery of a halogenated MCT1 substrate. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:644745d6-9ce1-4039-a6fa-6f46196c3c8f ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.808306

Chicago Manual of Style (16th Edition):

Skaripa-Koukelli, Eirini. “Towards the synthesis and delivery of a halogenated MCT1 substrate.” 2020. Doctoral Dissertation, University of Oxford. Accessed January 16, 2021. http://ora.ox.ac.uk/objects/uuid:644745d6-9ce1-4039-a6fa-6f46196c3c8f ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.808306.

MLA Handbook (7th Edition):

Skaripa-Koukelli, Eirini. “Towards the synthesis and delivery of a halogenated MCT1 substrate.” 2020. Web. 16 Jan 2021.

Vancouver:

Skaripa-Koukelli E. Towards the synthesis and delivery of a halogenated MCT1 substrate. [Internet] [Doctoral dissertation]. University of Oxford; 2020. [cited 2021 Jan 16]. Available from: http://ora.ox.ac.uk/objects/uuid:644745d6-9ce1-4039-a6fa-6f46196c3c8f ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.808306.

Council of Science Editors:

Skaripa-Koukelli E. Towards the synthesis and delivery of a halogenated MCT1 substrate. [Doctoral Dissertation]. University of Oxford; 2020. Available from: http://ora.ox.ac.uk/objects/uuid:644745d6-9ce1-4039-a6fa-6f46196c3c8f ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.808306


University of Waterloo

16. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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 January 16, 2021. 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. 16 Jan 2021.

Vancouver:

Bahsoun NE. Double Emulsion Mucoadhesive Nanoparticles for Hydrophilic Ocular Drug Delivery. [Internet] [Thesis]. University of Waterloo; 2018. [cited 2021 Jan 16]. 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


Temple University

17. 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;

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 January 16, 2021. 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. 16 Jan 2021.

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 2021 Jan 16]. 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


New Jersey Institute of Technology

18. Lu, Weilong. Magnetic targeted drug delivery system in gene therapy.

Degree: MSin Materials Science and Engineering - (M.S.), Committee for the Interdisciplinary Program in Materials Science and Engineering, 2012, New Jersey Institute of Technology

Drug delivery system is a method to transport the drug of the required amount accurately to the targeted diseased part. Recently, the concept of… (more)

Subjects/Keywords: Magnetic targeted drug delivery system; Gene therapy; Materials Science and Engineering

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Lu, W. (2012). Magnetic targeted drug delivery system in gene therapy. (Thesis). New Jersey Institute of Technology. Retrieved from https://digitalcommons.njit.edu/theses/134

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):

Lu, Weilong. “Magnetic targeted drug delivery system in gene therapy.” 2012. Thesis, New Jersey Institute of Technology. Accessed January 16, 2021. https://digitalcommons.njit.edu/theses/134.

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

MLA Handbook (7th Edition):

Lu, Weilong. “Magnetic targeted drug delivery system in gene therapy.” 2012. Web. 16 Jan 2021.

Vancouver:

Lu W. Magnetic targeted drug delivery system in gene therapy. [Internet] [Thesis]. New Jersey Institute of Technology; 2012. [cited 2021 Jan 16]. Available from: https://digitalcommons.njit.edu/theses/134.

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

Council of Science Editors:

Lu W. Magnetic targeted drug delivery system in gene therapy. [Thesis]. New Jersey Institute of Technology; 2012. Available from: https://digitalcommons.njit.edu/theses/134

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


University of Colorado

19. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Garriga Font, M. (2016). Micro-Crawlers in Confined Space: Volume Oscillating Hydrogels. (Thesis). University of Colorado. Retrieved from https://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 January 16, 2021. https://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. 16 Jan 2021.

Vancouver:

Garriga Font M. Micro-Crawlers in Confined Space: Volume Oscillating Hydrogels. [Internet] [Thesis]. University of Colorado; 2016. [cited 2021 Jan 16]. Available from: https://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: https://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


Université Catholique de Louvain

20. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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 January 16, 2021. 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. 16 Jan 2021.

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 2021 Jan 16]. 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 Wolverhampton

21. Wali, Aisha Roshan Mohamed. Designing a safe dendronised polymeric nanocarrier for hydrophobic drugs or gene delivery in cancer therapy.

Degree: PhD, 2018, University of Wolverhampton

 The hardship of cancer is continuously increasing and is rapidly spreading globally. At present, almost one-third of newly discovered potential therapeutics have poor pharmacokinetics and… (more)

Subjects/Keywords: cancer; targeted drug delivery; nanoparticles; micelles; dendrons; amphiphilic polysaccharide; doxorubicin; curcumin

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Wali, A. R. M. (2018). Designing a safe dendronised polymeric nanocarrier for hydrophobic drugs or gene delivery in cancer therapy. (Doctoral Dissertation). University of Wolverhampton. Retrieved from http://hdl.handle.net/2436/622665

Chicago Manual of Style (16th Edition):

Wali, Aisha Roshan Mohamed. “Designing a safe dendronised polymeric nanocarrier for hydrophobic drugs or gene delivery in cancer therapy.” 2018. Doctoral Dissertation, University of Wolverhampton. Accessed January 16, 2021. http://hdl.handle.net/2436/622665.

MLA Handbook (7th Edition):

Wali, Aisha Roshan Mohamed. “Designing a safe dendronised polymeric nanocarrier for hydrophobic drugs or gene delivery in cancer therapy.” 2018. Web. 16 Jan 2021.

Vancouver:

Wali ARM. Designing a safe dendronised polymeric nanocarrier for hydrophobic drugs or gene delivery in cancer therapy. [Internet] [Doctoral dissertation]. University of Wolverhampton; 2018. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/2436/622665.

Council of Science Editors:

Wali ARM. Designing a safe dendronised polymeric nanocarrier for hydrophobic drugs or gene delivery in cancer therapy. [Doctoral Dissertation]. University of Wolverhampton; 2018. Available from: http://hdl.handle.net/2436/622665


University of Pennsylvania

22. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 January 16, 2021. 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. 16 Jan 2021.

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 2021 Jan 16]. 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


Virginia Tech

23. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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 January 16, 2021. 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. 16 Jan 2021.

Vancouver:

Colacino K. The Potential of Cellulose Nanocrystals in the Detection and Treatment of Cancer. [Internet] [Doctoral dissertation]. Virginia Tech; 2013. [cited 2021 Jan 16]. 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

24. Williams, Jon. Theranostics Based On Linear Dendritic Block Copolymers.

Degree: PhD, Chemistry, 2019, University of Mississippi

 When combining imaging and therapeutic motifs, known as theranostics, amphiphilic diblock copolymers have a strong precedent of success. These polymers can self-assemble into a variety… (more)

Subjects/Keywords: Dendrimers; PISA; RAFT; Self-Assembly; Targeted Drug Delivery; Vesicles; Organic Chemistry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Williams, J. (2019). Theranostics Based On Linear Dendritic Block Copolymers. (Doctoral Dissertation). University of Mississippi. Retrieved from https://egrove.olemiss.edu/etd/1971

Chicago Manual of Style (16th Edition):

Williams, Jon. “Theranostics Based On Linear Dendritic Block Copolymers.” 2019. Doctoral Dissertation, University of Mississippi. Accessed January 16, 2021. https://egrove.olemiss.edu/etd/1971.

MLA Handbook (7th Edition):

Williams, Jon. “Theranostics Based On Linear Dendritic Block Copolymers.” 2019. Web. 16 Jan 2021.

Vancouver:

Williams J. Theranostics Based On Linear Dendritic Block Copolymers. [Internet] [Doctoral dissertation]. University of Mississippi; 2019. [cited 2021 Jan 16]. Available from: https://egrove.olemiss.edu/etd/1971.

Council of Science Editors:

Williams J. Theranostics Based On Linear Dendritic Block Copolymers. [Doctoral Dissertation]. University of Mississippi; 2019. Available from: https://egrove.olemiss.edu/etd/1971

25. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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 January 16, 2021. http://hdl.handle.net/11343/123601.

MLA Handbook (7th Edition):

Shirbin, Steven Josef. “Synthetic polypeptides for biomedical and bioactive applications.” 2016. Web. 16 Jan 2021.

Vancouver:

Shirbin SJ. Synthetic polypeptides for biomedical and bioactive applications. [Internet] [Doctoral dissertation]. University of Melbourne; 2016. [cited 2021 Jan 16]. 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 Missouri – Columbia

26. Houston, Zachary H. Hydrolytic stability of carbamate and carbonate closomers for the design of a multifaceted drug delivery system.

Degree: 2011, University of Missouri – Columbia

 [ACCESS RESTRICTED TO THE UNIVERSITY OF MISSOURI AT REQUEST OF AUTHOR.] Twelve-fold substituted polyhedral boranes (closomers) are of therapeutic and diagnostic interest in the applications… (more)

Subjects/Keywords: targeted drug delivery; closomers; hydrolysis; organic-aqueous solvent mixture

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Houston, Z. H. (2011). Hydrolytic stability of carbamate and carbonate closomers for the design of a multifaceted drug delivery system. (Thesis). University of Missouri – Columbia. Retrieved from http://hdl.handle.net/10355/14588

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):

Houston, Zachary H. “Hydrolytic stability of carbamate and carbonate closomers for the design of a multifaceted drug delivery system.” 2011. Thesis, University of Missouri – Columbia. Accessed January 16, 2021. http://hdl.handle.net/10355/14588.

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

MLA Handbook (7th Edition):

Houston, Zachary H. “Hydrolytic stability of carbamate and carbonate closomers for the design of a multifaceted drug delivery system.” 2011. Web. 16 Jan 2021.

Vancouver:

Houston ZH. Hydrolytic stability of carbamate and carbonate closomers for the design of a multifaceted drug delivery system. [Internet] [Thesis]. University of Missouri – Columbia; 2011. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/10355/14588.

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

Council of Science Editors:

Houston ZH. Hydrolytic stability of carbamate and carbonate closomers for the design of a multifaceted drug delivery system. [Thesis]. University of Missouri – Columbia; 2011. Available from: http://hdl.handle.net/10355/14588

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


University of Pennsylvania

27. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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 January 16, 2021. 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. 16 Jan 2021.

Vancouver:

Gao C. Engineering Bioactive Materials From Recombinant Oleosin Towards Drug Delivery Applications. [Internet] [Thesis]. University of Pennsylvania; 2018. [cited 2021 Jan 16]. 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

28. Garripelli, Vivek Kumar. Development of Novel Thermosensitive Polymers for Bioresponsive Drug Delivery.

Degree: PhD, Pharmaceutical Sciences, 2012, University of Mississippi

 Stimuli-responsive polymers have already showed tremendous promise in controlled and self-regulated drug delivery. Successful construction of responsive polymers requires amalgamation of chemical, physical and biological… (more)

Subjects/Keywords: Bioresponsive Drug Delivery; Nanocomposite Thermogel; Pluronic; Protein Delivery; Thermosensitive Polymer; Tumor Targeted Drug Delivery; Pharmacy and Pharmaceutical Sciences

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Garripelli, V. K. (2012). Development of Novel Thermosensitive Polymers for Bioresponsive Drug Delivery. (Doctoral Dissertation). University of Mississippi. Retrieved from https://egrove.olemiss.edu/etd/117

Chicago Manual of Style (16th Edition):

Garripelli, Vivek Kumar. “Development of Novel Thermosensitive Polymers for Bioresponsive Drug Delivery.” 2012. Doctoral Dissertation, University of Mississippi. Accessed January 16, 2021. https://egrove.olemiss.edu/etd/117.

MLA Handbook (7th Edition):

Garripelli, Vivek Kumar. “Development of Novel Thermosensitive Polymers for Bioresponsive Drug Delivery.” 2012. Web. 16 Jan 2021.

Vancouver:

Garripelli VK. Development of Novel Thermosensitive Polymers for Bioresponsive Drug Delivery. [Internet] [Doctoral dissertation]. University of Mississippi; 2012. [cited 2021 Jan 16]. Available from: https://egrove.olemiss.edu/etd/117.

Council of Science Editors:

Garripelli VK. Development of Novel Thermosensitive Polymers for Bioresponsive Drug Delivery. [Doctoral Dissertation]. University of Mississippi; 2012. Available from: https://egrove.olemiss.edu/etd/117


University of Oxford

29. Lyon, P. C. Targeted release from lyso-thermosensitive liposomal doxorubicin (ThermoDox®) using focused ultrasound in patients with liver tumours.

Degree: PhD, 2016, University of Oxford

 The TARDOX study is a Phase I first-in-man proof-of-concept study which aims to demonstrate the safety and feasibility of targeted delivery of a thermo-sensitive liposome… (more)

Subjects/Keywords: 610.28; Ultrasound-targeted drug delivery; Liposomal drug delivery systems; HIFU; LTLD; Lyso-thermosensitive liposomal doxorubicin; Targeted drug delivery; Hyperthermia; Thermodox; Focused ultrasound

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Lyon, P. C. (2016). Targeted release from lyso-thermosensitive liposomal doxorubicin (ThermoDox®) using focused ultrasound in patients with liver tumours. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:4817361a-e7f8-4773-ac81-8445ace05301 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.729944

Chicago Manual of Style (16th Edition):

Lyon, P C. “Targeted release from lyso-thermosensitive liposomal doxorubicin (ThermoDox®) using focused ultrasound in patients with liver tumours.” 2016. Doctoral Dissertation, University of Oxford. Accessed January 16, 2021. http://ora.ox.ac.uk/objects/uuid:4817361a-e7f8-4773-ac81-8445ace05301 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.729944.

MLA Handbook (7th Edition):

Lyon, P C. “Targeted release from lyso-thermosensitive liposomal doxorubicin (ThermoDox®) using focused ultrasound in patients with liver tumours.” 2016. Web. 16 Jan 2021.

Vancouver:

Lyon PC. Targeted release from lyso-thermosensitive liposomal doxorubicin (ThermoDox®) using focused ultrasound in patients with liver tumours. [Internet] [Doctoral dissertation]. University of Oxford; 2016. [cited 2021 Jan 16]. Available from: http://ora.ox.ac.uk/objects/uuid:4817361a-e7f8-4773-ac81-8445ace05301 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.729944.

Council of Science Editors:

Lyon PC. Targeted release from lyso-thermosensitive liposomal doxorubicin (ThermoDox®) using focused ultrasound in patients with liver tumours. [Doctoral Dissertation]. University of Oxford; 2016. Available from: http://ora.ox.ac.uk/objects/uuid:4817361a-e7f8-4773-ac81-8445ace05301 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.729944


University of Rochester

30. Newman, Maureen R. Bone-targeted polymer delivery of osteoanabolics for bone regeneration.

Degree: PhD, 2018, University of Rochester

 Bone is a dynamic organ with ~4% the total surface constitutively undergoing active remodeling. Under normal homeostatic conditions, bone resorption balances bone formation. Due to… (more)

Subjects/Keywords: Bone; Peptide; Polymer therapeutic; Small molecule drug; Targeted drug delivery; Tartrate-resistance acid phosphatase

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Newman, M. R. (2018). Bone-targeted polymer delivery of osteoanabolics for bone regeneration. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/34277

Chicago Manual of Style (16th Edition):

Newman, Maureen R. “Bone-targeted polymer delivery of osteoanabolics for bone regeneration.” 2018. Doctoral Dissertation, University of Rochester. Accessed January 16, 2021. http://hdl.handle.net/1802/34277.

MLA Handbook (7th Edition):

Newman, Maureen R. “Bone-targeted polymer delivery of osteoanabolics for bone regeneration.” 2018. Web. 16 Jan 2021.

Vancouver:

Newman MR. Bone-targeted polymer delivery of osteoanabolics for bone regeneration. [Internet] [Doctoral dissertation]. University of Rochester; 2018. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1802/34277.

Council of Science Editors:

Newman MR. Bone-targeted polymer delivery of osteoanabolics for bone regeneration. [Doctoral Dissertation]. University of Rochester; 2018. Available from: http://hdl.handle.net/1802/34277

[1] [2] [3] [4] [5]

.