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You searched for subject:(Polymeric drug delivery systems). Showing records 1 – 30 of 70049 total matches.

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Hong Kong University of Science and Technology

1. Zhou, Junli CBME. Polymeric nanoparticles for intracellular drug delivery.

Degree: 2015, Hong Kong University of Science and Technology

Polymeric nanoparticle is a competitive candidate in intracellular drug delivery. However, limited understanding of the effects of physicochemical parameters on particle-cell interaction and intracellular trafficking… (more)

Subjects/Keywords: Polymeric drug delivery systems; Polymers in medicine; Drug delivery systems; Nanostructured materials

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

APA (6th Edition):

Zhou, J. C. (2015). Polymeric nanoparticles for intracellular drug delivery. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b1552205 ; http://repository.ust.hk/ir/bitstream/1783.1-95280/1/th_redirect.html

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):

Zhou, Junli CBME. “Polymeric nanoparticles for intracellular drug delivery.” 2015. Thesis, Hong Kong University of Science and Technology. Accessed July 23, 2019. https://doi.org/10.14711/thesis-b1552205 ; http://repository.ust.hk/ir/bitstream/1783.1-95280/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Zhou, Junli CBME. “Polymeric nanoparticles for intracellular drug delivery.” 2015. Web. 23 Jul 2019.

Vancouver:

Zhou JC. Polymeric nanoparticles for intracellular drug delivery. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2015. [cited 2019 Jul 23]. Available from: https://doi.org/10.14711/thesis-b1552205 ; http://repository.ust.hk/ir/bitstream/1783.1-95280/1/th_redirect.html.

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

Council of Science Editors:

Zhou JC. Polymeric nanoparticles for intracellular drug delivery. [Thesis]. Hong Kong University of Science and Technology; 2015. Available from: https://doi.org/10.14711/thesis-b1552205 ; http://repository.ust.hk/ir/bitstream/1783.1-95280/1/th_redirect.html

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


University of North Texas

2. Nguyen, Duong Thuy. Self-assembly Polymeric Nanoparticles Composed of Polymers Crosslinked with Transition Metals for Use in Drug Delivery.

Degree: 2015, University of North Texas

 A major drawback of chemotherapy is the lack of selectively leading to damage in healthy tissue, which results in severe acute side effects to cancer… (more)

Subjects/Keywords: nanoparticle; drug delivery; transition metal; Polymeric drug delivery systems.; Nanoparticles.; Polymers in medicine.; Transition metals.

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APA (6th Edition):

Nguyen, D. T. (2015). Self-assembly Polymeric Nanoparticles Composed of Polymers Crosslinked with Transition Metals for Use in Drug Delivery. (Thesis). University of North Texas. Retrieved from https://digital.library.unt.edu/ark:/67531/metadc822738/

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):

Nguyen, Duong Thuy. “Self-assembly Polymeric Nanoparticles Composed of Polymers Crosslinked with Transition Metals for Use in Drug Delivery.” 2015. Thesis, University of North Texas. Accessed July 23, 2019. https://digital.library.unt.edu/ark:/67531/metadc822738/.

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

MLA Handbook (7th Edition):

Nguyen, Duong Thuy. “Self-assembly Polymeric Nanoparticles Composed of Polymers Crosslinked with Transition Metals for Use in Drug Delivery.” 2015. Web. 23 Jul 2019.

Vancouver:

Nguyen DT. Self-assembly Polymeric Nanoparticles Composed of Polymers Crosslinked with Transition Metals for Use in Drug Delivery. [Internet] [Thesis]. University of North Texas; 2015. [cited 2019 Jul 23]. Available from: https://digital.library.unt.edu/ark:/67531/metadc822738/.

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

Council of Science Editors:

Nguyen DT. Self-assembly Polymeric Nanoparticles Composed of Polymers Crosslinked with Transition Metals for Use in Drug Delivery. [Thesis]. University of North Texas; 2015. Available from: https://digital.library.unt.edu/ark:/67531/metadc822738/

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


University of Utah

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

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

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

Subjects/Keywords: Drug Delivery Systems; Polymeric Drugs

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Suh, Won-Hee. “Cell-specific targeting polymeric gene delivery carriers;.” 2001. Doctoral Dissertation, University of Utah. Accessed July 23, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/467/rec/121.

MLA Handbook (7th Edition):

Suh, Won-Hee. “Cell-specific targeting polymeric gene delivery carriers;.” 2001. Web. 23 Jul 2019.

Vancouver:

Suh W. Cell-specific targeting polymeric gene delivery carriers;. [Internet] [Doctoral dissertation]. University of Utah; 2001. [cited 2019 Jul 23]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/467/rec/121.

Council of Science Editors:

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


Columbia University

4. Nwadibia, Ekeoma C. Chemical Targeting of Specific Cell Types in Living Brain Tissue.

Degree: 2018, Columbia University

 This thesis details our early efforts towards the discovery of polymeric and macromolecular platforms for the targeted delivery of sensors and actuators to specific cell… (more)

Subjects/Keywords: Chemistry; Neurosciences; Polymeric drug delivery systems; Brain chemistry

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APA (6th Edition):

Nwadibia, E. C. (2018). Chemical Targeting of Specific Cell Types in Living Brain Tissue. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D812754J

Chicago Manual of Style (16th Edition):

Nwadibia, Ekeoma C. “Chemical Targeting of Specific Cell Types in Living Brain Tissue.” 2018. Doctoral Dissertation, Columbia University. Accessed July 23, 2019. https://doi.org/10.7916/D812754J.

MLA Handbook (7th Edition):

Nwadibia, Ekeoma C. “Chemical Targeting of Specific Cell Types in Living Brain Tissue.” 2018. Web. 23 Jul 2019.

Vancouver:

Nwadibia EC. Chemical Targeting of Specific Cell Types in Living Brain Tissue. [Internet] [Doctoral dissertation]. Columbia University; 2018. [cited 2019 Jul 23]. Available from: https://doi.org/10.7916/D812754J.

Council of Science Editors:

Nwadibia EC. Chemical Targeting of Specific Cell Types in Living Brain Tissue. [Doctoral Dissertation]. Columbia University; 2018. Available from: https://doi.org/10.7916/D812754J

5. Krit Suknuntha. Characterization of polymer blends as mucoadhesive materials for gastroretentive drug delivery system .

Degree: คณะเภสัชศาสตร์ ภาควิชาเทคโนโลยีเภสัชกรรม, 2012, Prince of Songkla University

Subjects/Keywords: Polymeric composites; Drug delivery systems

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

APA (6th Edition):

Suknuntha, K. (2012). Characterization of polymer blends as mucoadhesive materials for gastroretentive drug delivery system . (Thesis). Prince of Songkla University. Retrieved from http://kb.psu.ac.th/psukb/handle/2010/8788

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):

Suknuntha, Krit. “Characterization of polymer blends as mucoadhesive materials for gastroretentive drug delivery system .” 2012. Thesis, Prince of Songkla University. Accessed July 23, 2019. http://kb.psu.ac.th/psukb/handle/2010/8788.

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

MLA Handbook (7th Edition):

Suknuntha, Krit. “Characterization of polymer blends as mucoadhesive materials for gastroretentive drug delivery system .” 2012. Web. 23 Jul 2019.

Vancouver:

Suknuntha K. Characterization of polymer blends as mucoadhesive materials for gastroretentive drug delivery system . [Internet] [Thesis]. Prince of Songkla University; 2012. [cited 2019 Jul 23]. Available from: http://kb.psu.ac.th/psukb/handle/2010/8788.

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

Council of Science Editors:

Suknuntha K. Characterization of polymer blends as mucoadhesive materials for gastroretentive drug delivery system . [Thesis]. Prince of Songkla University; 2012. Available from: http://kb.psu.ac.th/psukb/handle/2010/8788

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


University of Alberta

6. Zhang, Qi. Targeted Delivery of Arsenic Compounds to Tumor Cells Using Polymeric Micelles.

Degree: PhD, Medical Sciences-Laboratory Medicine and Pathology, 2016, University of Alberta

 Arsenic trioxide (ATO), dissolved in water as arsenous acid or inorganic arsenite (AsIII), is an effective chemotherapeutic agent against acute promyelocytic leukemia (APL). It has… (more)

Subjects/Keywords: Drug delivery; Arsenic; Polymeric micelle

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APA (6th Edition):

Zhang, Q. (2016). Targeted Delivery of Arsenic Compounds to Tumor Cells Using Polymeric Micelles. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/cjd472w75n

Chicago Manual of Style (16th Edition):

Zhang, Qi. “Targeted Delivery of Arsenic Compounds to Tumor Cells Using Polymeric Micelles.” 2016. Doctoral Dissertation, University of Alberta. Accessed July 23, 2019. https://era.library.ualberta.ca/files/cjd472w75n.

MLA Handbook (7th Edition):

Zhang, Qi. “Targeted Delivery of Arsenic Compounds to Tumor Cells Using Polymeric Micelles.” 2016. Web. 23 Jul 2019.

Vancouver:

Zhang Q. Targeted Delivery of Arsenic Compounds to Tumor Cells Using Polymeric Micelles. [Internet] [Doctoral dissertation]. University of Alberta; 2016. [cited 2019 Jul 23]. Available from: https://era.library.ualberta.ca/files/cjd472w75n.

Council of Science Editors:

Zhang Q. Targeted Delivery of Arsenic Compounds to Tumor Cells Using Polymeric Micelles. [Doctoral Dissertation]. University of Alberta; 2016. Available from: https://era.library.ualberta.ca/files/cjd472w75n


Texas A&M University

7. Lim, Young. Development of Polyphosphoester-Based Polymeric Nanoparticles as Delivery Carriers for Silver-Based Antimicrobial Agents for Treatment of Infectious Diseases.

Degree: 2015, Texas A&M University

 The development of well-defined polymeric nanoparticles (NPs) as delivery carriers for antimicrobials targeting human infectious diseases requires rational design of the polymer template, an efficient… (more)

Subjects/Keywords: Polymeric Nanoparticle; Drug delivery

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APA (6th Edition):

Lim, Y. (2015). Development of Polyphosphoester-Based Polymeric Nanoparticles as Delivery Carriers for Silver-Based Antimicrobial Agents for Treatment of Infectious Diseases. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/155529

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):

Lim, Young. “Development of Polyphosphoester-Based Polymeric Nanoparticles as Delivery Carriers for Silver-Based Antimicrobial Agents for Treatment of Infectious Diseases.” 2015. Thesis, Texas A&M University. Accessed July 23, 2019. http://hdl.handle.net/1969.1/155529.

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

MLA Handbook (7th Edition):

Lim, Young. “Development of Polyphosphoester-Based Polymeric Nanoparticles as Delivery Carriers for Silver-Based Antimicrobial Agents for Treatment of Infectious Diseases.” 2015. Web. 23 Jul 2019.

Vancouver:

Lim Y. Development of Polyphosphoester-Based Polymeric Nanoparticles as Delivery Carriers for Silver-Based Antimicrobial Agents for Treatment of Infectious Diseases. [Internet] [Thesis]. Texas A&M University; 2015. [cited 2019 Jul 23]. Available from: http://hdl.handle.net/1969.1/155529.

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

Council of Science Editors:

Lim Y. Development of Polyphosphoester-Based Polymeric Nanoparticles as Delivery Carriers for Silver-Based Antimicrobial Agents for Treatment of Infectious Diseases. [Thesis]. Texas A&M University; 2015. Available from: http://hdl.handle.net/1969.1/155529

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


University of New South Wales

8. Du, Alice. Investigation on the effect of crosslinking density and use of mucoadhesive glycopolymers on nanoparticle treatment of prostate cancer.

Degree: Centre for Advanced Macromolecular Design, 2017, University of New South Wales

Polymeric micelles have the potential to be the next generation of “smart” delivery vehicles for drug delivery, especially for anti-cancer therapy. Polymeric micelles can be… (more)

Subjects/Keywords: drug delivery; polymeric nanoparticles; glycopolymers

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APA (6th Edition):

Du, A. (2017). Investigation on the effect of crosslinking density and use of mucoadhesive glycopolymers on nanoparticle treatment of prostate cancer. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/57599 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:44165/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Du, Alice. “Investigation on the effect of crosslinking density and use of mucoadhesive glycopolymers on nanoparticle treatment of prostate cancer.” 2017. Doctoral Dissertation, University of New South Wales. Accessed July 23, 2019. http://handle.unsw.edu.au/1959.4/57599 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:44165/SOURCE02?view=true.

MLA Handbook (7th Edition):

Du, Alice. “Investigation on the effect of crosslinking density and use of mucoadhesive glycopolymers on nanoparticle treatment of prostate cancer.” 2017. Web. 23 Jul 2019.

Vancouver:

Du A. Investigation on the effect of crosslinking density and use of mucoadhesive glycopolymers on nanoparticle treatment of prostate cancer. [Internet] [Doctoral dissertation]. University of New South Wales; 2017. [cited 2019 Jul 23]. Available from: http://handle.unsw.edu.au/1959.4/57599 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:44165/SOURCE02?view=true.

Council of Science Editors:

Du A. Investigation on the effect of crosslinking density and use of mucoadhesive glycopolymers on nanoparticle treatment of prostate cancer. [Doctoral Dissertation]. University of New South Wales; 2017. Available from: http://handle.unsw.edu.au/1959.4/57599 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:44165/SOURCE02?view=true


University of Utah

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

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

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

Subjects/Keywords: Drug Targeting; Polymeric Drug Delivery Systems

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Jensen, Keith Dale. “Internalization and fate of HPMA copolymers and antisense-HPMA copolymer conjugates in Hep G2 cells;.” 2002. Doctoral Dissertation, University of Utah. Accessed July 23, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/292/rec/709.

MLA Handbook (7th Edition):

Jensen, Keith Dale. “Internalization and fate of HPMA copolymers and antisense-HPMA copolymer conjugates in Hep G2 cells;.” 2002. Web. 23 Jul 2019.

Vancouver:

Jensen KD. Internalization and fate of HPMA copolymers and antisense-HPMA copolymer conjugates in Hep G2 cells;. [Internet] [Doctoral dissertation]. University of Utah; 2002. [cited 2019 Jul 23]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/292/rec/709.

Council of Science Editors:

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


Hong Kong University of Science and Technology

10. Yeung, Wai Kit SENG. Protease-responsive polymer vesicle by peptide-polymer hybrid.

Degree: 2015, Hong Kong University of Science and Technology

 Protease-sensitive polymer vesicles are a potential carriers for stimuli-responsive drug delivery. There are only few protease-sensitive polymer vesicles developed. This thesis aims to prepare protease-sensitive… (more)

Subjects/Keywords: Drug carriers (Pharmacy); Polymers in medicine; Polymeric drugs; Drug delivery systems; Peptide drugs

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APA (6th Edition):

Yeung, W. K. S. (2015). Protease-responsive polymer vesicle by peptide-polymer hybrid. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b1552140 ; http://repository.ust.hk/ir/bitstream/1783.1-95275/1/th_redirect.html

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):

Yeung, Wai Kit SENG. “Protease-responsive polymer vesicle by peptide-polymer hybrid.” 2015. Thesis, Hong Kong University of Science and Technology. Accessed July 23, 2019. https://doi.org/10.14711/thesis-b1552140 ; http://repository.ust.hk/ir/bitstream/1783.1-95275/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Yeung, Wai Kit SENG. “Protease-responsive polymer vesicle by peptide-polymer hybrid.” 2015. Web. 23 Jul 2019.

Vancouver:

Yeung WKS. Protease-responsive polymer vesicle by peptide-polymer hybrid. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2015. [cited 2019 Jul 23]. Available from: https://doi.org/10.14711/thesis-b1552140 ; http://repository.ust.hk/ir/bitstream/1783.1-95275/1/th_redirect.html.

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

Council of Science Editors:

Yeung WKS. Protease-responsive polymer vesicle by peptide-polymer hybrid. [Thesis]. Hong Kong University of Science and Technology; 2015. Available from: https://doi.org/10.14711/thesis-b1552140 ; http://repository.ust.hk/ir/bitstream/1783.1-95275/1/th_redirect.html

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


University of Western Sydney

11. Whitty, Elizabeth G. Assessment of the "smart" polymer poly(acrylic acid) for drug delivery.

Degree: 2015, University of Western Sydney

 Anticancer drug delivery systems are currently in the spotlight of anticancer research in order to address the harmful side effects commonly associated with anticancer drug(more)

Subjects/Keywords: polymers in medicine; drug delivery systems; antineoplastic agents; administration; polymeric drug delivery systems; Thesis (M.Sc. (Hons.)) – University of Western Sydney, 2015

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APA (6th Edition):

Whitty, E. G. (2015). Assessment of the "smart" polymer poly(acrylic acid) for drug delivery. (Thesis). University of Western Sydney. Retrieved from http://hdl.handle.net/1959.7/uws:36580

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):

Whitty, Elizabeth G. “Assessment of the "smart" polymer poly(acrylic acid) for drug delivery.” 2015. Thesis, University of Western Sydney. Accessed July 23, 2019. http://hdl.handle.net/1959.7/uws:36580.

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

MLA Handbook (7th Edition):

Whitty, Elizabeth G. “Assessment of the "smart" polymer poly(acrylic acid) for drug delivery.” 2015. Web. 23 Jul 2019.

Vancouver:

Whitty EG. Assessment of the "smart" polymer poly(acrylic acid) for drug delivery. [Internet] [Thesis]. University of Western Sydney; 2015. [cited 2019 Jul 23]. Available from: http://hdl.handle.net/1959.7/uws:36580.

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

Council of Science Editors:

Whitty EG. Assessment of the "smart" polymer poly(acrylic acid) for drug delivery. [Thesis]. University of Western Sydney; 2015. Available from: http://hdl.handle.net/1959.7/uws:36580

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


University of Alberta

12. Dong, Cunji. Polymer-coated liposomes: preparation, stability and release of acetylsalicylic acid.

Degree: PhD, Department of Pharmacy and Pharmaceutical Sciences, 1992, University of Alberta

Subjects/Keywords: Polymers.; Liposomes.; Polymeric drug delivery systems.

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APA (6th Edition):

Dong, C. (1992). Polymer-coated liposomes: preparation, stability and release of acetylsalicylic acid. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/dv13zv93n

Chicago Manual of Style (16th Edition):

Dong, Cunji. “Polymer-coated liposomes: preparation, stability and release of acetylsalicylic acid.” 1992. Doctoral Dissertation, University of Alberta. Accessed July 23, 2019. https://era.library.ualberta.ca/files/dv13zv93n.

MLA Handbook (7th Edition):

Dong, Cunji. “Polymer-coated liposomes: preparation, stability and release of acetylsalicylic acid.” 1992. Web. 23 Jul 2019.

Vancouver:

Dong C. Polymer-coated liposomes: preparation, stability and release of acetylsalicylic acid. [Internet] [Doctoral dissertation]. University of Alberta; 1992. [cited 2019 Jul 23]. Available from: https://era.library.ualberta.ca/files/dv13zv93n.

Council of Science Editors:

Dong C. Polymer-coated liposomes: preparation, stability and release of acetylsalicylic acid. [Doctoral Dissertation]. University of Alberta; 1992. Available from: https://era.library.ualberta.ca/files/dv13zv93n


University of Texas – Austin

13. Thomas, Joshua Brock. Lightly crosslinked poly(ethylene glycol)-tethered, pH-responsive biomaterials.

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

Subjects/Keywords: Drugs – Controlled release; Polymeric drug delivery systems; Polymeric drugs

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APA (6th Edition):

Thomas, J. B. (2006). Lightly crosslinked poly(ethylene glycol)-tethered, pH-responsive biomaterials. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/2940

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):

Thomas, Joshua Brock. “Lightly crosslinked poly(ethylene glycol)-tethered, pH-responsive biomaterials.” 2006. Thesis, University of Texas – Austin. Accessed July 23, 2019. http://hdl.handle.net/2152/2940.

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

MLA Handbook (7th Edition):

Thomas, Joshua Brock. “Lightly crosslinked poly(ethylene glycol)-tethered, pH-responsive biomaterials.” 2006. Web. 23 Jul 2019.

Vancouver:

Thomas JB. Lightly crosslinked poly(ethylene glycol)-tethered, pH-responsive biomaterials. [Internet] [Thesis]. University of Texas – Austin; 2006. [cited 2019 Jul 23]. Available from: http://hdl.handle.net/2152/2940.

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

Council of Science Editors:

Thomas JB. Lightly crosslinked poly(ethylene glycol)-tethered, pH-responsive biomaterials. [Thesis]. University of Texas – Austin; 2006. Available from: http://hdl.handle.net/2152/2940

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


Northeastern University

14. Jain, Shardool. Macrophage targeted tuftsin-modified alginate nanoparticles as non-viral delivery system for anti-inflammatory gene therapy in the treatment of rheumatoid arthritis.

Degree: PhD, School of Pharmacy, 2014, Northeastern University

 The goal of this project is to develop and characterize a macrophage targeted alginate polymer based gene delivery system for the treatment of rheumatoid arthritis… (more)

Subjects/Keywords: targeted delivery; Polymeric drug delivery systems; Nanoparticles; Therapeutic use; Gene therapy; Rheumatoid arthritis; Treatment; Rheumatoid arthritis; Animal models; Alginates; Macrophages

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APA (6th Edition):

Jain, S. (2014). Macrophage targeted tuftsin-modified alginate nanoparticles as non-viral delivery system for anti-inflammatory gene therapy in the treatment of rheumatoid arthritis. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/D20204485

Chicago Manual of Style (16th Edition):

Jain, Shardool. “Macrophage targeted tuftsin-modified alginate nanoparticles as non-viral delivery system for anti-inflammatory gene therapy in the treatment of rheumatoid arthritis.” 2014. Doctoral Dissertation, Northeastern University. Accessed July 23, 2019. http://hdl.handle.net/2047/D20204485.

MLA Handbook (7th Edition):

Jain, Shardool. “Macrophage targeted tuftsin-modified alginate nanoparticles as non-viral delivery system for anti-inflammatory gene therapy in the treatment of rheumatoid arthritis.” 2014. Web. 23 Jul 2019.

Vancouver:

Jain S. Macrophage targeted tuftsin-modified alginate nanoparticles as non-viral delivery system for anti-inflammatory gene therapy in the treatment of rheumatoid arthritis. [Internet] [Doctoral dissertation]. Northeastern University; 2014. [cited 2019 Jul 23]. Available from: http://hdl.handle.net/2047/D20204485.

Council of Science Editors:

Jain S. Macrophage targeted tuftsin-modified alginate nanoparticles as non-viral delivery system for anti-inflammatory gene therapy in the treatment of rheumatoid arthritis. [Doctoral Dissertation]. Northeastern University; 2014. Available from: http://hdl.handle.net/2047/D20204485


The Ohio State University

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

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

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

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

MLA Handbook (7th Edition):

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

Vancouver:

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

Council of Science Editors:

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


University of Utah

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

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

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

Subjects/Keywords: Drug delivery systems

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Preston, J. “Processing of MRI data for simulation and monitoring of drug delivery.” 2009. Masters Thesis, University of Utah. Accessed July 23, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1224/rec/934.

MLA Handbook (7th Edition):

Preston, J. “Processing of MRI data for simulation and monitoring of drug delivery.” 2009. Web. 23 Jul 2019.

Vancouver:

Preston J. Processing of MRI data for simulation and monitoring of drug delivery. [Internet] [Masters thesis]. University of Utah; 2009. [cited 2019 Jul 23]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1224/rec/934.

Council of Science Editors:

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


Oregon State University

17. Doddapaneni, Bhuvana S. Development of Micellar and Nanoparticle Structures based on Polyester Diblock Copolymer Platform for the Treatment of Metastatic Tumors.

Degree: PhD, Pharmacy, 2016, Oregon State University

 Poor aqueous solubility of a large number of newly discovered chemical entities is posing a significant challenge for the formulation industry and is delaying their… (more)

Subjects/Keywords: Drug delivery systems

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APA (6th Edition):

Doddapaneni, B. S. (2016). Development of Micellar and Nanoparticle Structures based on Polyester Diblock Copolymer Platform for the Treatment of Metastatic Tumors. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/59410

Chicago Manual of Style (16th Edition):

Doddapaneni, Bhuvana S. “Development of Micellar and Nanoparticle Structures based on Polyester Diblock Copolymer Platform for the Treatment of Metastatic Tumors.” 2016. Doctoral Dissertation, Oregon State University. Accessed July 23, 2019. http://hdl.handle.net/1957/59410.

MLA Handbook (7th Edition):

Doddapaneni, Bhuvana S. “Development of Micellar and Nanoparticle Structures based on Polyester Diblock Copolymer Platform for the Treatment of Metastatic Tumors.” 2016. Web. 23 Jul 2019.

Vancouver:

Doddapaneni BS. Development of Micellar and Nanoparticle Structures based on Polyester Diblock Copolymer Platform for the Treatment of Metastatic Tumors. [Internet] [Doctoral dissertation]. Oregon State University; 2016. [cited 2019 Jul 23]. Available from: http://hdl.handle.net/1957/59410.

Council of Science Editors:

Doddapaneni BS. Development of Micellar and Nanoparticle Structures based on Polyester Diblock Copolymer Platform for the Treatment of Metastatic Tumors. [Doctoral Dissertation]. Oregon State University; 2016. Available from: http://hdl.handle.net/1957/59410


Rutgers University

18. Demirdirek, Bahar. Synthesis and evaluation of amphiphilic scorpion-like and star macromolecules for biomedical applications.

Degree: MS, Chemistry and Chemical Biology, 2009, Rutgers University

 Self-assembled and unimolecular amphiphilic macromolecules with pseudo-double branched and single tails were synthesized. Degradation behavior, drug loading efficiency, drug release rate and stability of macromolecules… (more)

Subjects/Keywords: Drug delivery systems

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APA (6th Edition):

Demirdirek, B. (2009). Synthesis and evaluation of amphiphilic scorpion-like and star macromolecules for biomedical applications. (Masters Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000050505

Chicago Manual of Style (16th Edition):

Demirdirek, Bahar. “Synthesis and evaluation of amphiphilic scorpion-like and star macromolecules for biomedical applications.” 2009. Masters Thesis, Rutgers University. Accessed July 23, 2019. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000050505.

MLA Handbook (7th Edition):

Demirdirek, Bahar. “Synthesis and evaluation of amphiphilic scorpion-like and star macromolecules for biomedical applications.” 2009. Web. 23 Jul 2019.

Vancouver:

Demirdirek B. Synthesis and evaluation of amphiphilic scorpion-like and star macromolecules for biomedical applications. [Internet] [Masters thesis]. Rutgers University; 2009. [cited 2019 Jul 23]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000050505.

Council of Science Editors:

Demirdirek B. Synthesis and evaluation of amphiphilic scorpion-like and star macromolecules for biomedical applications. [Masters Thesis]. Rutgers University; 2009. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000050505


Rutgers University

19. del Rosario, Leilani Singson. Preparation and evaluation of amphiphilic macromolecules-based conjugates and micelles for anticancer drug delivery:.

Degree: PhD, Chemistry and Chemical Biology, 2009, Rutgers University

Micelles assembled from amphiphilic macromolecules (AM) or drug-conjugated AMs were evaluated as anticancer drug carriers in terms of drug content, sustained/controlled drug release and cytotoxicity… (more)

Subjects/Keywords: Drug delivery systems

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APA (6th Edition):

del Rosario, L. S. (2009). Preparation and evaluation of amphiphilic macromolecules-based conjugates and micelles for anticancer drug delivery:. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051195

Chicago Manual of Style (16th Edition):

del Rosario, Leilani Singson. “Preparation and evaluation of amphiphilic macromolecules-based conjugates and micelles for anticancer drug delivery:.” 2009. Doctoral Dissertation, Rutgers University. Accessed July 23, 2019. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051195.

MLA Handbook (7th Edition):

del Rosario, Leilani Singson. “Preparation and evaluation of amphiphilic macromolecules-based conjugates and micelles for anticancer drug delivery:.” 2009. Web. 23 Jul 2019.

Vancouver:

del Rosario LS. Preparation and evaluation of amphiphilic macromolecules-based conjugates and micelles for anticancer drug delivery:. [Internet] [Doctoral dissertation]. Rutgers University; 2009. [cited 2019 Jul 23]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051195.

Council of Science Editors:

del Rosario LS. Preparation and evaluation of amphiphilic macromolecules-based conjugates and micelles for anticancer drug delivery:. [Doctoral Dissertation]. Rutgers University; 2009. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051195

20. Rajpara, Seeta. Visualizing Nanoparticles: Integration of Methods Used for Biological and Polymeric Interfaces.

Degree: 2016, Brown University

 One of the major challenges in the field of controlled drug delivery systems involves overcoming the poor bioavailability of some therapeutic compounds. Polymeric microspheres can… (more)

Subjects/Keywords: drug delivery systems

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APA (6th Edition):

Rajpara, S. (2016). Visualizing Nanoparticles: Integration of Methods Used for Biological and Polymeric Interfaces. (Thesis). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:818054/

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):

Rajpara, Seeta. “Visualizing Nanoparticles: Integration of Methods Used for Biological and Polymeric Interfaces.” 2016. Thesis, Brown University. Accessed July 23, 2019. https://repository.library.brown.edu/studio/item/bdr:818054/.

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

MLA Handbook (7th Edition):

Rajpara, Seeta. “Visualizing Nanoparticles: Integration of Methods Used for Biological and Polymeric Interfaces.” 2016. Web. 23 Jul 2019.

Vancouver:

Rajpara S. Visualizing Nanoparticles: Integration of Methods Used for Biological and Polymeric Interfaces. [Internet] [Thesis]. Brown University; 2016. [cited 2019 Jul 23]. Available from: https://repository.library.brown.edu/studio/item/bdr:818054/.

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

Council of Science Editors:

Rajpara S. Visualizing Nanoparticles: Integration of Methods Used for Biological and Polymeric Interfaces. [Thesis]. Brown University; 2016. Available from: https://repository.library.brown.edu/studio/item/bdr:818054/

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


University of Oklahoma

21. Bio, Moses Kwabena. A NEW STRATEGY FOR PHOTO-TRIGGERED RELEASE OF DRUGS BY VISIBLE/NEAR IR LIGHT: PHOTO-UNCLICK CHEMISTRY.

Degree: PhD, 2012, University of Oklahoma

 A prodrug of drug-linker-photosensitizer CA4-L-PS was prepared to prove the photo-unclick chemistry in cells. The results obtained were consistent with our expectation. While the prodrug… (more)

Subjects/Keywords: Drug delivery systems

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APA (6th Edition):

Bio, M. K. (2012). A NEW STRATEGY FOR PHOTO-TRIGGERED RELEASE OF DRUGS BY VISIBLE/NEAR IR LIGHT: PHOTO-UNCLICK CHEMISTRY. (Doctoral Dissertation). University of Oklahoma. Retrieved from http://hdl.handle.net/11244/319135

Chicago Manual of Style (16th Edition):

Bio, Moses Kwabena. “A NEW STRATEGY FOR PHOTO-TRIGGERED RELEASE OF DRUGS BY VISIBLE/NEAR IR LIGHT: PHOTO-UNCLICK CHEMISTRY.” 2012. Doctoral Dissertation, University of Oklahoma. Accessed July 23, 2019. http://hdl.handle.net/11244/319135.

MLA Handbook (7th Edition):

Bio, Moses Kwabena. “A NEW STRATEGY FOR PHOTO-TRIGGERED RELEASE OF DRUGS BY VISIBLE/NEAR IR LIGHT: PHOTO-UNCLICK CHEMISTRY.” 2012. Web. 23 Jul 2019.

Vancouver:

Bio MK. A NEW STRATEGY FOR PHOTO-TRIGGERED RELEASE OF DRUGS BY VISIBLE/NEAR IR LIGHT: PHOTO-UNCLICK CHEMISTRY. [Internet] [Doctoral dissertation]. University of Oklahoma; 2012. [cited 2019 Jul 23]. Available from: http://hdl.handle.net/11244/319135.

Council of Science Editors:

Bio MK. A NEW STRATEGY FOR PHOTO-TRIGGERED RELEASE OF DRUGS BY VISIBLE/NEAR IR LIGHT: PHOTO-UNCLICK CHEMISTRY. [Doctoral Dissertation]. University of Oklahoma; 2012. Available from: http://hdl.handle.net/11244/319135

22. Surakarn Paichamnan. Preparation of Chitosan Films and microspheres by Cross-Linking reaction using de-proteinated Epoxidized natural rubber for skin drug delivery .

Degree: คณะเภสัชศาสตร์ ภาควิชาเภสัชเคมี, 2014, Prince of Songkla University

Subjects/Keywords: Drug delivery systems; Plant polymers Biotechnology; Polymerization; Polymeric drug delivery systems

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APA (6th Edition):

Paichamnan, S. (2014). Preparation of Chitosan Films and microspheres by Cross-Linking reaction using de-proteinated Epoxidized natural rubber for skin drug delivery . (Thesis). Prince of Songkla University. Retrieved from http://kb.psu.ac.th/psukb/handle/2010/10223

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):

Paichamnan, Surakarn. “Preparation of Chitosan Films and microspheres by Cross-Linking reaction using de-proteinated Epoxidized natural rubber for skin drug delivery .” 2014. Thesis, Prince of Songkla University. Accessed July 23, 2019. http://kb.psu.ac.th/psukb/handle/2010/10223.

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

MLA Handbook (7th Edition):

Paichamnan, Surakarn. “Preparation of Chitosan Films and microspheres by Cross-Linking reaction using de-proteinated Epoxidized natural rubber for skin drug delivery .” 2014. Web. 23 Jul 2019.

Vancouver:

Paichamnan S. Preparation of Chitosan Films and microspheres by Cross-Linking reaction using de-proteinated Epoxidized natural rubber for skin drug delivery . [Internet] [Thesis]. Prince of Songkla University; 2014. [cited 2019 Jul 23]. Available from: http://kb.psu.ac.th/psukb/handle/2010/10223.

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

Council of Science Editors:

Paichamnan S. Preparation of Chitosan Films and microspheres by Cross-Linking reaction using de-proteinated Epoxidized natural rubber for skin drug delivery . [Thesis]. Prince of Songkla University; 2014. Available from: http://kb.psu.ac.th/psukb/handle/2010/10223

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


Michigan State University

23. Cao, Ping. Development and synthesis of novel poly(beta-amino acid) drug delivery systems.

Degree: MS, Department of Chemistry, 2004, Michigan State University

Subjects/Keywords: Polymeric drug delivery systems; Drug delivery systems; Polymers in medicine; Polymers – Therapeutic use

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APA (6th Edition):

Cao, P. (2004). Development and synthesis of novel poly(beta-amino acid) drug delivery systems. (Masters Thesis). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:32888

Chicago Manual of Style (16th Edition):

Cao, Ping. “Development and synthesis of novel poly(beta-amino acid) drug delivery systems.” 2004. Masters Thesis, Michigan State University. Accessed July 23, 2019. http://etd.lib.msu.edu/islandora/object/etd:32888.

MLA Handbook (7th Edition):

Cao, Ping. “Development and synthesis of novel poly(beta-amino acid) drug delivery systems.” 2004. Web. 23 Jul 2019.

Vancouver:

Cao P. Development and synthesis of novel poly(beta-amino acid) drug delivery systems. [Internet] [Masters thesis]. Michigan State University; 2004. [cited 2019 Jul 23]. Available from: http://etd.lib.msu.edu/islandora/object/etd:32888.

Council of Science Editors:

Cao P. Development and synthesis of novel poly(beta-amino acid) drug delivery systems. [Masters Thesis]. Michigan State University; 2004. Available from: http://etd.lib.msu.edu/islandora/object/etd:32888


Georgia Tech

24. Kao, Chen-Yu. Local and sustained delivery of hydrophobic drugs to the spinal cord with polyketal microparticles.

Degree: PhD, Biomedical Engineering, 2009, Georgia Tech

 Amyotrophic lateral sclerosis (ALS) is a devastating disease. Currently, there is no cure for this disease, and effective treatment strategies are greatly needed. Calpain activation… (more)

Subjects/Keywords: Microparticle; Polyketal; Sustained release; Amyotrophic lateral sclerosis; Intrapinal cord injection; Drug delivery; Hydrophobic; Calpain inhibitors; Calpain; Polymeric drug delivery systems; Polymers in medicine; Biomedical materials

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APA (6th Edition):

Kao, C. (2009). Local and sustained delivery of hydrophobic drugs to the spinal cord with polyketal microparticles. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/37304

Chicago Manual of Style (16th Edition):

Kao, Chen-Yu. “Local and sustained delivery of hydrophobic drugs to the spinal cord with polyketal microparticles.” 2009. Doctoral Dissertation, Georgia Tech. Accessed July 23, 2019. http://hdl.handle.net/1853/37304.

MLA Handbook (7th Edition):

Kao, Chen-Yu. “Local and sustained delivery of hydrophobic drugs to the spinal cord with polyketal microparticles.” 2009. Web. 23 Jul 2019.

Vancouver:

Kao C. Local and sustained delivery of hydrophobic drugs to the spinal cord with polyketal microparticles. [Internet] [Doctoral dissertation]. Georgia Tech; 2009. [cited 2019 Jul 23]. Available from: http://hdl.handle.net/1853/37304.

Council of Science Editors:

Kao C. Local and sustained delivery of hydrophobic drugs to the spinal cord with polyketal microparticles. [Doctoral Dissertation]. Georgia Tech; 2009. Available from: http://hdl.handle.net/1853/37304

25. Barcellos, Juliana Palma Abriata. Potencialidade do uso de sistemas nanoestruturados contendo ácido ursólico para a otimização da terapia da doenças de Chagas.

Degree: Mestrado, Medicamentos e Cosméticos, 2014, University of São Paulo

A doença de Chagas é causada pelo Trypanosoma cruzi e acomete milhões de pessoas, principalmente as de baixa renda em países subdesenvolvidos. É considerada uma… (more)

Subjects/Keywords: ácido ursólico; drug delivery systems; nanopartículas poliméricas; nanoprecipitação; nanoprecipitation; policaprolactona; polycaprolactone; polymeric nanoparticles; sistemas de liberação de fármacos; ursolic acid

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APA (6th Edition):

Barcellos, J. P. A. (2014). Potencialidade do uso de sistemas nanoestruturados contendo ácido ursólico para a otimização da terapia da doenças de Chagas. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/60/60137/tde-09042014-082744/ ;

Chicago Manual of Style (16th Edition):

Barcellos, Juliana Palma Abriata. “Potencialidade do uso de sistemas nanoestruturados contendo ácido ursólico para a otimização da terapia da doenças de Chagas.” 2014. Masters Thesis, University of São Paulo. Accessed July 23, 2019. http://www.teses.usp.br/teses/disponiveis/60/60137/tde-09042014-082744/ ;.

MLA Handbook (7th Edition):

Barcellos, Juliana Palma Abriata. “Potencialidade do uso de sistemas nanoestruturados contendo ácido ursólico para a otimização da terapia da doenças de Chagas.” 2014. Web. 23 Jul 2019.

Vancouver:

Barcellos JPA. Potencialidade do uso de sistemas nanoestruturados contendo ácido ursólico para a otimização da terapia da doenças de Chagas. [Internet] [Masters thesis]. University of São Paulo; 2014. [cited 2019 Jul 23]. Available from: http://www.teses.usp.br/teses/disponiveis/60/60137/tde-09042014-082744/ ;.

Council of Science Editors:

Barcellos JPA. Potencialidade do uso de sistemas nanoestruturados contendo ácido ursólico para a otimização da terapia da doenças de Chagas. [Masters Thesis]. University of São Paulo; 2014. Available from: http://www.teses.usp.br/teses/disponiveis/60/60137/tde-09042014-082744/ ;


Drexel University

26. Liu, Xinyin. Drug delivery systems based on polymer blends: synthesis, characterization, and application.

Degree: 2003, Drexel University

Polymer blending is the physical mixing of two or more existing polymers. Itoffers an effective way to produce new polymeric materials with combined excellent properties.… (more)

Subjects/Keywords: Polymeric drug delivery systems; Polymers in medicine

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APA (6th Edition):

Liu, X. (2003). Drug delivery systems based on polymer blends: synthesis, characterization, and application. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/218

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):

Liu, Xinyin. “Drug delivery systems based on polymer blends: synthesis, characterization, and application.” 2003. Thesis, Drexel University. Accessed July 23, 2019. http://hdl.handle.net/1860/218.

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

MLA Handbook (7th Edition):

Liu, Xinyin. “Drug delivery systems based on polymer blends: synthesis, characterization, and application.” 2003. Web. 23 Jul 2019.

Vancouver:

Liu X. Drug delivery systems based on polymer blends: synthesis, characterization, and application. [Internet] [Thesis]. Drexel University; 2003. [cited 2019 Jul 23]. Available from: http://hdl.handle.net/1860/218.

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

Council of Science Editors:

Liu X. Drug delivery systems based on polymer blends: synthesis, characterization, and application. [Thesis]. Drexel University; 2003. Available from: http://hdl.handle.net/1860/218

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

27. Batheja, Priya B., 1975-. Polymeric nanospheres for skin penetration enhancement: in vitro and in vivo assessment in skin models.

Degree: PhD, Pharmaceutical Science, 2010, Rutgers University

Research and development in the field of topical and transdermal delivery has been particularly challenging due to the tough penetration barrier provided by the stratum… (more)

Subjects/Keywords: Polymeric drug delivery systems; Transdermal medication

…Transdermal drug delivery systems (TDDS) have offered several clinical advantages over… …systems. In the recent years, the use of polymeric/biomaterial based carriers for skin delivery… …deliver the drug transdermally.(21) Polymeric nanoparticles for skin delivery have… …drug delivery and the market growth for topical and transdermal delivery systems, we decided… …50 Formulation development for delivery of polymeric nanospheres to skin layers… 

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APA (6th Edition):

Batheja, Priya B., 1. (2010). Polymeric nanospheres for skin penetration enhancement: in vitro and in vivo assessment in skin models. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000052097

Chicago Manual of Style (16th Edition):

Batheja, Priya B., 1975-. “Polymeric nanospheres for skin penetration enhancement: in vitro and in vivo assessment in skin models.” 2010. Doctoral Dissertation, Rutgers University. Accessed July 23, 2019. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000052097.

MLA Handbook (7th Edition):

Batheja, Priya B., 1975-. “Polymeric nanospheres for skin penetration enhancement: in vitro and in vivo assessment in skin models.” 2010. Web. 23 Jul 2019.

Vancouver:

Batheja, Priya B. 1. Polymeric nanospheres for skin penetration enhancement: in vitro and in vivo assessment in skin models. [Internet] [Doctoral dissertation]. Rutgers University; 2010. [cited 2019 Jul 23]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000052097.

Council of Science Editors:

Batheja, Priya B. 1. Polymeric nanospheres for skin penetration enhancement: in vitro and in vivo assessment in skin models. [Doctoral Dissertation]. Rutgers University; 2010. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000052097

28. Nikitczuk, Kevin P., 1983-. Polymer based immune modulation for the generation of an anti-tumor immune response.

Degree: Biomedical Engineering, 2011, Rutgers University

Subjects/Keywords: Polymeric drug delivery systems; Tumors—Immunological aspects

…of polymer based delivery systems has allowed them to be used to deliver chemotherapeutic… …delivery of encapsulated components to cell. These PLGA delivery systems help prevent enzymatic… …between the innate and adaptive systems. APCs of the innate immune response, for example… …approach, e.g. with a single drug, will not be adequate in most cases. A combinatorial approach… …antibodies, viral vaccines, cell based therapies, and polymer delivery systems17,18,19. In general… 

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APA (6th Edition):

Nikitczuk, Kevin P., 1. (2011). Polymer based immune modulation for the generation of an anti-tumor immune response. (Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063542

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):

Nikitczuk, Kevin P., 1983-. “Polymer based immune modulation for the generation of an anti-tumor immune response.” 2011. Thesis, Rutgers University. Accessed July 23, 2019. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063542.

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

MLA Handbook (7th Edition):

Nikitczuk, Kevin P., 1983-. “Polymer based immune modulation for the generation of an anti-tumor immune response.” 2011. Web. 23 Jul 2019.

Vancouver:

Nikitczuk, Kevin P. 1. Polymer based immune modulation for the generation of an anti-tumor immune response. [Internet] [Thesis]. Rutgers University; 2011. [cited 2019 Jul 23]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063542.

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

Council of Science Editors:

Nikitczuk, Kevin P. 1. Polymer based immune modulation for the generation of an anti-tumor immune response. [Thesis]. Rutgers University; 2011. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063542

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


University of Texas – Austin

29. Crowley, Michael McDonald. Physicochemical and mechanical characterization of hot-melt extruded dosage forms.

Degree: Pharmacy, 2003, University of Texas – Austin

 The physicochemical and mechanical properties and the mechanisms of drug release from drug delivery systems prepared by hotmelt extrusion were investigated. The influence of processing… (more)

Subjects/Keywords: Drug delivery systems; Polymeric drugs; Drugs – Controlled release

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

APA (6th Edition):

Crowley, M. M. (2003). Physicochemical and mechanical characterization of hot-melt extruded dosage forms. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/528

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):

Crowley, Michael McDonald. “Physicochemical and mechanical characterization of hot-melt extruded dosage forms.” 2003. Thesis, University of Texas – Austin. Accessed July 23, 2019. http://hdl.handle.net/2152/528.

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

MLA Handbook (7th Edition):

Crowley, Michael McDonald. “Physicochemical and mechanical characterization of hot-melt extruded dosage forms.” 2003. Web. 23 Jul 2019.

Vancouver:

Crowley MM. Physicochemical and mechanical characterization of hot-melt extruded dosage forms. [Internet] [Thesis]. University of Texas – Austin; 2003. [cited 2019 Jul 23]. Available from: http://hdl.handle.net/2152/528.

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

Council of Science Editors:

Crowley MM. Physicochemical and mechanical characterization of hot-melt extruded dosage forms. [Thesis]. University of Texas – Austin; 2003. Available from: http://hdl.handle.net/2152/528

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


University of Texas – Austin

30. Zhu, Yucun. Properties of polymeric drug delivery systems prepared by hot-melt extrusion.

Degree: Pharmacy, 2002, University of Texas – Austin

 The purpose of this research project was to investigate the physicochemical and drug release properties of polymeric drug delivery systems prepared by hot-melt extrusion containing… (more)

Subjects/Keywords: Polymeric drugs; Drug delivery systems; Drugs – Controlled release

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Zhu, Y. (2002). Properties of polymeric drug delivery systems prepared by hot-melt extrusion. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/1092

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):

Zhu, Yucun. “Properties of polymeric drug delivery systems prepared by hot-melt extrusion.” 2002. Thesis, University of Texas – Austin. Accessed July 23, 2019. http://hdl.handle.net/2152/1092.

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

MLA Handbook (7th Edition):

Zhu, Yucun. “Properties of polymeric drug delivery systems prepared by hot-melt extrusion.” 2002. Web. 23 Jul 2019.

Vancouver:

Zhu Y. Properties of polymeric drug delivery systems prepared by hot-melt extrusion. [Internet] [Thesis]. University of Texas – Austin; 2002. [cited 2019 Jul 23]. Available from: http://hdl.handle.net/2152/1092.

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

Council of Science Editors:

Zhu Y. Properties of polymeric drug delivery systems prepared by hot-melt extrusion. [Thesis]. University of Texas – Austin; 2002. Available from: http://hdl.handle.net/2152/1092

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

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