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You searched for subject:(drug delivery systems). Showing records 121 – 150 of 395 total matches.

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Univerzitet u Beogradu

121. Babić, Marija M. 1984-. Sinteza i karakterizacija polimernih matrica na bazi 2-hidroksialkil akrilata i itakonske kiseline za kontrolisano otpuštanje oksaprozina.

Degree: Tehnološko-metalurški fakultet, 2016, Univerzitet u Beogradu

Tehnološko inženjerstvo-Hemijsko inženjerstvo / Technology Engineering-Chemical Engineering

U cilju unapređenja efikasnosti farmakoterapije razvojem sofisticiranih sistema za kontrolisano otpuštanje aktivnih supstanci u ovom radu su sintetisane… (more)

Subjects/Keywords: Hydrogels · Polimeric matrices · 2-Hydroxyethyl acrylate · 2-Hydroxypropyl acrylate · Itaconic acid · Drug delivery systems · Oxaprozin.

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APA (6th Edition):

Babić, M. M. 1. (2016). Sinteza i karakterizacija polimernih matrica na bazi 2-hidroksialkil akrilata i itakonske kiseline za kontrolisano otpuštanje oksaprozina. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:11264/bdef:Content/get

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

Chicago Manual of Style (16th Edition):

Babić, Marija M 1984-. “Sinteza i karakterizacija polimernih matrica na bazi 2-hidroksialkil akrilata i itakonske kiseline za kontrolisano otpuštanje oksaprozina.” 2016. Thesis, Univerzitet u Beogradu. Accessed June 25, 2019. https://fedorabg.bg.ac.rs/fedora/get/o:11264/bdef:Content/get.

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

MLA Handbook (7th Edition):

Babić, Marija M 1984-. “Sinteza i karakterizacija polimernih matrica na bazi 2-hidroksialkil akrilata i itakonske kiseline za kontrolisano otpuštanje oksaprozina.” 2016. Web. 25 Jun 2019.

Vancouver:

Babić MM1. Sinteza i karakterizacija polimernih matrica na bazi 2-hidroksialkil akrilata i itakonske kiseline za kontrolisano otpuštanje oksaprozina. [Internet] [Thesis]. Univerzitet u Beogradu; 2016. [cited 2019 Jun 25]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:11264/bdef:Content/get.

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

Council of Science Editors:

Babić MM1. Sinteza i karakterizacija polimernih matrica na bazi 2-hidroksialkil akrilata i itakonske kiseline za kontrolisano otpuštanje oksaprozina. [Thesis]. Univerzitet u Beogradu; 2016. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:11264/bdef:Content/get

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


RMIT University

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

Degree: 2015, RMIT University

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

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

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Kulhari, H. “Peptide and monoclonal antibody mediated targeting of nanoconjugates in cancer chemotherapy.” 2015. Thesis, RMIT University. Accessed June 25, 2019. http://researchbank.rmit.edu.au/view/rmit:161409.

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

MLA Handbook (7th Edition):

Kulhari, H. “Peptide and monoclonal antibody mediated targeting of nanoconjugates in cancer chemotherapy.” 2015. Web. 25 Jun 2019.

Vancouver:

Kulhari H. Peptide and monoclonal antibody mediated targeting of nanoconjugates in cancer chemotherapy. [Internet] [Thesis]. RMIT University; 2015. [cited 2019 Jun 25]. Available from: http://researchbank.rmit.edu.au/view/rmit:161409.

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

Council of Science Editors:

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

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


University of Alberta

123. 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 June 25, 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. 25 Jun 2019.

Vancouver:

Dong C. Polymer-coated liposomes: preparation, stability and release of acetylsalicylic acid. [Internet] [Doctoral dissertation]. University of Alberta; 1992. [cited 2019 Jun 25]. 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


Hong Kong University of Science and Technology

124. Cheung, Chi Yeung. Ultrasound-mediated intrascleral macromolecule delivery.

Degree: 2009, Hong Kong University of Science and Technology

 Delivering macromolecules to the posterior segment of eye non-invasively is always challenging as the eye has several barriers to protect it from being invaded. The… (more)

Subjects/Keywords: Posterior segment (Eye)  – Diseases  – Treatment; Macromolecules  – Therapeutic use; Ultrasonics in ophthalmology; Drug delivery systems

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APA (6th Edition):

Cheung, C. Y. (2009). Ultrasound-mediated intrascleral macromolecule delivery. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b1071219 ; http://repository.ust.hk/ir/bitstream/1783.1-6784/1/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):

Cheung, Chi Yeung. “Ultrasound-mediated intrascleral macromolecule delivery.” 2009. Thesis, Hong Kong University of Science and Technology. Accessed June 25, 2019. https://doi.org/10.14711/thesis-b1071219 ; http://repository.ust.hk/ir/bitstream/1783.1-6784/1/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):

Cheung, Chi Yeung. “Ultrasound-mediated intrascleral macromolecule delivery.” 2009. Web. 25 Jun 2019.

Vancouver:

Cheung CY. Ultrasound-mediated intrascleral macromolecule delivery. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2009. [cited 2019 Jun 25]. Available from: https://doi.org/10.14711/thesis-b1071219 ; http://repository.ust.hk/ir/bitstream/1783.1-6784/1/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:

Cheung CY. Ultrasound-mediated intrascleral macromolecule delivery. [Thesis]. Hong Kong University of Science and Technology; 2009. Available from: https://doi.org/10.14711/thesis-b1071219 ; http://repository.ust.hk/ir/bitstream/1783.1-6784/1/th_redirect.html

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


Ryerson University

125. Keshavarz, Meysam. Hybrid Silicon-Based Nanomaterials Synthesized Via Femtosecond Laser For Theranostics Applications.

Degree: 2017, Ryerson University

 Biocompatibility and bio-stability are two very important criteria of the materials being used in biology and biological related applications. Among biocompatible materials, Silicon has been… (more)

Subjects/Keywords: Nanosilicon; Nanobiotechnology  – Research; Cancer cells; Nanomedicine  – Research; Nanostructured materials  – Testing; Drug delivery systems

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APA (6th Edition):

Keshavarz, M. (2017). Hybrid Silicon-Based Nanomaterials Synthesized Via Femtosecond Laser For Theranostics Applications. (Thesis). Ryerson University. Retrieved from https://digital.library.ryerson.ca/islandora/object/RULA%3A6896

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):

Keshavarz, Meysam. “Hybrid Silicon-Based Nanomaterials Synthesized Via Femtosecond Laser For Theranostics Applications.” 2017. Thesis, Ryerson University. Accessed June 25, 2019. https://digital.library.ryerson.ca/islandora/object/RULA%3A6896.

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

MLA Handbook (7th Edition):

Keshavarz, Meysam. “Hybrid Silicon-Based Nanomaterials Synthesized Via Femtosecond Laser For Theranostics Applications.” 2017. Web. 25 Jun 2019.

Vancouver:

Keshavarz M. Hybrid Silicon-Based Nanomaterials Synthesized Via Femtosecond Laser For Theranostics Applications. [Internet] [Thesis]. Ryerson University; 2017. [cited 2019 Jun 25]. Available from: https://digital.library.ryerson.ca/islandora/object/RULA%3A6896.

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

Council of Science Editors:

Keshavarz M. Hybrid Silicon-Based Nanomaterials Synthesized Via Femtosecond Laser For Theranostics Applications. [Thesis]. Ryerson University; 2017. Available from: https://digital.library.ryerson.ca/islandora/object/RULA%3A6896

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


University of Manchester

126. Camarillo Lopez, Raul Horacio. Applying Native Chemical Ligation to the Development of Magnetically-responsive Drug Delivery Platforms for Biomedical Applications.

Degree: 2017, University of Manchester

 The potential of magnetic nanoparticle-vesicle assemblies (MNP-V) as remote controlled drug delivery platforms capable of inducing cellular responses under magnetic stimuli has been previously demonstrated… (more)

Subjects/Keywords: Native Chemical Ligation; Magnetic Nanoparticles; Drug Delivery Systems; Nanotechnology; Thiol-thioester exchange

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APA (6th Edition):

Camarillo Lopez, R. H. (2017). Applying Native Chemical Ligation to the Development of Magnetically-responsive Drug Delivery Platforms for Biomedical Applications. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:307668

Chicago Manual of Style (16th Edition):

Camarillo Lopez, Raul Horacio. “Applying Native Chemical Ligation to the Development of Magnetically-responsive Drug Delivery Platforms for Biomedical Applications.” 2017. Doctoral Dissertation, University of Manchester. Accessed June 25, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:307668.

MLA Handbook (7th Edition):

Camarillo Lopez, Raul Horacio. “Applying Native Chemical Ligation to the Development of Magnetically-responsive Drug Delivery Platforms for Biomedical Applications.” 2017. Web. 25 Jun 2019.

Vancouver:

Camarillo Lopez RH. Applying Native Chemical Ligation to the Development of Magnetically-responsive Drug Delivery Platforms for Biomedical Applications. [Internet] [Doctoral dissertation]. University of Manchester; 2017. [cited 2019 Jun 25]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:307668.

Council of Science Editors:

Camarillo Lopez RH. Applying Native Chemical Ligation to the Development of Magnetically-responsive Drug Delivery Platforms for Biomedical Applications. [Doctoral Dissertation]. University of Manchester; 2017. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:307668

127. 이, 원일. Correction of target-controlled infusion following the wrong selection of emulsion concentration of propofol.

Degree: 2015, Ajou University

Background: We investigated the correction methods following wrong-settings of emulsion concentrations of propofol as a countermeasure against erroneous target-controlled infusions (TCI). Methods: TCIs were started… (more)

Subjects/Keywords: Drug delivery systems; Infusion pumps; Intravenous infusion; Propofol; 약물 전달 시스템; 주입 펌프; 정맥 주입

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APA (6th Edition):

이, . (2015). Correction of target-controlled infusion following the wrong selection of emulsion concentration of propofol. (Thesis). Ajou University. Retrieved from http://repository.ajou.ac.kr/handle/201003/11841 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000019017

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):

이, 원일. “Correction of target-controlled infusion following the wrong selection of emulsion concentration of propofol.” 2015. Thesis, Ajou University. Accessed June 25, 2019. http://repository.ajou.ac.kr/handle/201003/11841 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000019017.

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

MLA Handbook (7th Edition):

이, 원일. “Correction of target-controlled infusion following the wrong selection of emulsion concentration of propofol.” 2015. Web. 25 Jun 2019.

Vancouver:

이 . Correction of target-controlled infusion following the wrong selection of emulsion concentration of propofol. [Internet] [Thesis]. Ajou University; 2015. [cited 2019 Jun 25]. Available from: http://repository.ajou.ac.kr/handle/201003/11841 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000019017.

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

Council of Science Editors:

이 . Correction of target-controlled infusion following the wrong selection of emulsion concentration of propofol. [Thesis]. Ajou University; 2015. Available from: http://repository.ajou.ac.kr/handle/201003/11841 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000019017

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


Drexel University

128. Allen, Kathleen Bridget. Stress and deformation of biological membranes during cellular outgrowth and cell and liposome injection: a numerical and experimental study.

Degree: 2008, Drexel University

Revealing the molecular events of neuronal growth is critical to obtaining a deeper understanding of nervous system development, neural injury response, and neural tissue engineering.… (more)

Subjects/Keywords: Mechanical engineering; Liposomes; Drug delivery systems

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APA (6th Edition):

Allen, K. B. (2008). Stress and deformation of biological membranes during cellular outgrowth and cell and liposome injection: a numerical and experimental study. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/2895

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):

Allen, Kathleen Bridget. “Stress and deformation of biological membranes during cellular outgrowth and cell and liposome injection: a numerical and experimental study.” 2008. Thesis, Drexel University. Accessed June 25, 2019. http://hdl.handle.net/1860/2895.

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

MLA Handbook (7th Edition):

Allen, Kathleen Bridget. “Stress and deformation of biological membranes during cellular outgrowth and cell and liposome injection: a numerical and experimental study.” 2008. Web. 25 Jun 2019.

Vancouver:

Allen KB. Stress and deformation of biological membranes during cellular outgrowth and cell and liposome injection: a numerical and experimental study. [Internet] [Thesis]. Drexel University; 2008. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/1860/2895.

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

Council of Science Editors:

Allen KB. Stress and deformation of biological membranes during cellular outgrowth and cell and liposome injection: a numerical and experimental study. [Thesis]. Drexel University; 2008. Available from: http://hdl.handle.net/1860/2895

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


Drexel University

129. Tuesca, Anthony D. Synthesis, characterization, and application of polyethylene glycol modified insulin for oral delivery using complexation hydrogels.

Degree: 2008, Drexel University

Therapeutic proteins and peptides represent a major area of research in current pharmaceutical and biotechnology companies. Due to their inherent instability, the vast majority of… (more)

Subjects/Keywords: Chemical engineering; Colloids; Drug delivery systems

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APA (6th Edition):

Tuesca, A. D. (2008). Synthesis, characterization, and application of polyethylene glycol modified insulin for oral delivery using complexation hydrogels. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/2715

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):

Tuesca, Anthony D. “Synthesis, characterization, and application of polyethylene glycol modified insulin for oral delivery using complexation hydrogels.” 2008. Thesis, Drexel University. Accessed June 25, 2019. http://hdl.handle.net/1860/2715.

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

MLA Handbook (7th Edition):

Tuesca, Anthony D. “Synthesis, characterization, and application of polyethylene glycol modified insulin for oral delivery using complexation hydrogels.” 2008. Web. 25 Jun 2019.

Vancouver:

Tuesca AD. Synthesis, characterization, and application of polyethylene glycol modified insulin for oral delivery using complexation hydrogels. [Internet] [Thesis]. Drexel University; 2008. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/1860/2715.

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

Council of Science Editors:

Tuesca AD. Synthesis, characterization, and application of polyethylene glycol modified insulin for oral delivery using complexation hydrogels. [Thesis]. Drexel University; 2008. Available from: http://hdl.handle.net/1860/2715

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


Drexel University

130. Hans, Meredith L. Synthesis, characterization, and application of biodegradable polymeric prodrug micelles for long-term drug delivery.

Degree: 2005, Drexel University

Long-term drug delivery has several advantages such increasing bioavialability of drugs, reduction of pharmaceutical side effects, and increased patient compliance. Nanoparticles, such as block copolymer… (more)

Subjects/Keywords: Chemical engineering; Drug delivery systems; Polymers

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APA (6th Edition):

Hans, M. L. (2005). Synthesis, characterization, and application of biodegradable polymeric prodrug micelles for long-term drug delivery. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/879

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):

Hans, Meredith L. “Synthesis, characterization, and application of biodegradable polymeric prodrug micelles for long-term drug delivery.” 2005. Thesis, Drexel University. Accessed June 25, 2019. http://hdl.handle.net/1860/879.

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

MLA Handbook (7th Edition):

Hans, Meredith L. “Synthesis, characterization, and application of biodegradable polymeric prodrug micelles for long-term drug delivery.” 2005. Web. 25 Jun 2019.

Vancouver:

Hans ML. Synthesis, characterization, and application of biodegradable polymeric prodrug micelles for long-term drug delivery. [Internet] [Thesis]. Drexel University; 2005. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/1860/879.

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

Council of Science Editors:

Hans ML. Synthesis, characterization, and application of biodegradable polymeric prodrug micelles for long-term drug delivery. [Thesis]. Drexel University; 2005. Available from: http://hdl.handle.net/1860/879

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


Uniwersytet im. Adama Mickiewicza w Poznaniu

131. Tomaszewska, Joanna. Synteza i zastosowanie nowych fluorowanych oraz niefluorowanych monosacharydów – bloków budulcowych do syntezy podjednostek kwasu hialuronowego .

Degree: 2017, Uniwersytet im. Adama Mickiewicza w Poznaniu

 Syntetycznie dostępne węglowodany cieszą się obecnie dużym zainteresowaniem w rozwoju nowych układów dostarczania leków, jak również inhibitorach enzymów. Synteza podjednostek kwasu hialuronowego (HA) (Rysunek 1)… (more)

Subjects/Keywords: kwas hialuronowy; hyaluronic acid; chemii „click”; click chemistry; systemy dostarczania leków; drug delivery systems

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APA (6th Edition):

Tomaszewska, J. (2017). Synteza i zastosowanie nowych fluorowanych oraz niefluorowanych monosacharydów – bloków budulcowych do syntezy podjednostek kwasu hialuronowego . (Doctoral Dissertation). Uniwersytet im. Adama Mickiewicza w Poznaniu. Retrieved from http://hdl.handle.net/10593/19768

Chicago Manual of Style (16th Edition):

Tomaszewska, Joanna. “Synteza i zastosowanie nowych fluorowanych oraz niefluorowanych monosacharydów – bloków budulcowych do syntezy podjednostek kwasu hialuronowego .” 2017. Doctoral Dissertation, Uniwersytet im. Adama Mickiewicza w Poznaniu. Accessed June 25, 2019. http://hdl.handle.net/10593/19768.

MLA Handbook (7th Edition):

Tomaszewska, Joanna. “Synteza i zastosowanie nowych fluorowanych oraz niefluorowanych monosacharydów – bloków budulcowych do syntezy podjednostek kwasu hialuronowego .” 2017. Web. 25 Jun 2019.

Vancouver:

Tomaszewska J. Synteza i zastosowanie nowych fluorowanych oraz niefluorowanych monosacharydów – bloków budulcowych do syntezy podjednostek kwasu hialuronowego . [Internet] [Doctoral dissertation]. Uniwersytet im. Adama Mickiewicza w Poznaniu; 2017. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/10593/19768.

Council of Science Editors:

Tomaszewska J. Synteza i zastosowanie nowych fluorowanych oraz niefluorowanych monosacharydów – bloków budulcowych do syntezy podjednostek kwasu hialuronowego . [Doctoral Dissertation]. Uniwersytet im. Adama Mickiewicza w Poznaniu; 2017. Available from: http://hdl.handle.net/10593/19768


Michigan State University

132. Fisher, Laura Marie. Engineered polysaccharide carboxylate matrices for ocular drug delivery.

Degree: MS, Department of Chemical Engineering and Material Science, 2004, Michigan State University

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

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APA (6th Edition):

Fisher, L. M. (2004). Engineered polysaccharide carboxylate matrices for ocular drug delivery. (Masters Thesis). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:32853

Chicago Manual of Style (16th Edition):

Fisher, Laura Marie. “Engineered polysaccharide carboxylate matrices for ocular drug delivery.” 2004. Masters Thesis, Michigan State University. Accessed June 25, 2019. http://etd.lib.msu.edu/islandora/object/etd:32853.

MLA Handbook (7th Edition):

Fisher, Laura Marie. “Engineered polysaccharide carboxylate matrices for ocular drug delivery.” 2004. Web. 25 Jun 2019.

Vancouver:

Fisher LM. Engineered polysaccharide carboxylate matrices for ocular drug delivery. [Internet] [Masters thesis]. Michigan State University; 2004. [cited 2019 Jun 25]. Available from: http://etd.lib.msu.edu/islandora/object/etd:32853.

Council of Science Editors:

Fisher LM. Engineered polysaccharide carboxylate matrices for ocular drug delivery. [Masters Thesis]. Michigan State University; 2004. Available from: http://etd.lib.msu.edu/islandora/object/etd:32853


Tartu University

133. Künnapuu, Kadri. Modification of the cell-penetrating peptide PepFect14 for targeted tumor gene delivery and reduced toxicity .

Degree: 2018, Tartu University

 Viimastel aastakümnetel on geeniteraapia alal toimunud olulised edasiminekud, mis on teinud võimalikuks haiguste ravimise geenitasandil vigast geeni asendades või selle ekspressiooni maha surudes. Terapeutilistel eesmärkidel… (more)

Subjects/Keywords: cell-penetrating peptides; nucleic acids; drug delivery systems; tissue compatibility; tumors; toxity; gene therapy

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

APA (6th Edition):

Künnapuu, K. (2018). Modification of the cell-penetrating peptide PepFect14 for targeted tumor gene delivery and reduced toxicity . (Thesis). Tartu University. Retrieved from http://hdl.handle.net/10062/62840

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):

Künnapuu, Kadri. “Modification of the cell-penetrating peptide PepFect14 for targeted tumor gene delivery and reduced toxicity .” 2018. Thesis, Tartu University. Accessed June 25, 2019. http://hdl.handle.net/10062/62840.

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

MLA Handbook (7th Edition):

Künnapuu, Kadri. “Modification of the cell-penetrating peptide PepFect14 for targeted tumor gene delivery and reduced toxicity .” 2018. Web. 25 Jun 2019.

Vancouver:

Künnapuu K. Modification of the cell-penetrating peptide PepFect14 for targeted tumor gene delivery and reduced toxicity . [Internet] [Thesis]. Tartu University; 2018. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/10062/62840.

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

Council of Science Editors:

Künnapuu K. Modification of the cell-penetrating peptide PepFect14 for targeted tumor gene delivery and reduced toxicity . [Thesis]. Tartu University; 2018. Available from: http://hdl.handle.net/10062/62840

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


Rutgers University

134. Wang, Yang, 1978-. Hypoxia inducible factor: targeted anticancer prodrug.

Degree: PhD, Pharmaceutical Science, 2007, Rutgers University

In vitro and in vivo antitumor effect of the combination of an inducer of cell death (anticancer drug) and a suppressor of cellular resistance (antisense… (more)

Subjects/Keywords: Cancer – Treatment; Prodrugs; Drug delivery systems

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APA (6th Edition):

Wang, Yang, 1. (2007). Hypoxia inducible factor: targeted anticancer prodrug. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.17105

Chicago Manual of Style (16th Edition):

Wang, Yang, 1978-. “Hypoxia inducible factor: targeted anticancer prodrug.” 2007. Doctoral Dissertation, Rutgers University. Accessed June 25, 2019. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.17105.

MLA Handbook (7th Edition):

Wang, Yang, 1978-. “Hypoxia inducible factor: targeted anticancer prodrug.” 2007. Web. 25 Jun 2019.

Vancouver:

Wang, Yang 1. Hypoxia inducible factor: targeted anticancer prodrug. [Internet] [Doctoral dissertation]. Rutgers University; 2007. [cited 2019 Jun 25]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.17105.

Council of Science Editors:

Wang, Yang 1. Hypoxia inducible factor: targeted anticancer prodrug. [Doctoral Dissertation]. Rutgers University; 2007. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.17105

135. Sahay, Abhishek, 1983-. Drop on demand technology as a mini manufacturing platform for drug delivery and personalized medicine.

Degree: MS, Biomedical Engineering, 2012, Rutgers University

 There is need to develop a process and technology through which small tailored dosages can be delivered with precision and accuracy. This has led to… (more)

Subjects/Keywords: Drug delivery systems; Pharmaceutical technology

…controlled release delivery and precise dosage formulations for small-scale manufacturing systems… …incorporated into a future drug delivery platform. 3 One of the major problems that need to be… …administration and the Dosage Form (drug delivery system) – the wrong choice of delivery… …dependent on the drug /formulation delivery platform. Microdispensing and, in particular, Drop on… …delivery of customizable drug architecture due to its innovative and modular design. enables… 

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APA (6th Edition):

Sahay, Abhishek, 1. (2012). Drop on demand technology as a mini manufacturing platform for drug delivery and personalized medicine. (Masters Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000064169

Chicago Manual of Style (16th Edition):

Sahay, Abhishek, 1983-. “Drop on demand technology as a mini manufacturing platform for drug delivery and personalized medicine.” 2012. Masters Thesis, Rutgers University. Accessed June 25, 2019. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000064169.

MLA Handbook (7th Edition):

Sahay, Abhishek, 1983-. “Drop on demand technology as a mini manufacturing platform for drug delivery and personalized medicine.” 2012. Web. 25 Jun 2019.

Vancouver:

Sahay, Abhishek 1. Drop on demand technology as a mini manufacturing platform for drug delivery and personalized medicine. [Internet] [Masters thesis]. Rutgers University; 2012. [cited 2019 Jun 25]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000064169.

Council of Science Editors:

Sahay, Abhishek 1. Drop on demand technology as a mini manufacturing platform for drug delivery and personalized medicine. [Masters Thesis]. Rutgers University; 2012. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000064169

136. Kutscher, Hilliard L., 1978-. Pharmacokinetics and toxicodynamics of intravenously administered rigid microparticles that passively target the pulmonary circulation of rodents.

Degree: Pharmaceutical Science, 2012, Rutgers University

Subjects/Keywords: Drug delivery systems; Pulmonary circulation

…used as drug delivery systems for a number of years to increase circulation of an active… …filtration function can be exploited to trap MP drug delivery systems designed to take advantage of… …as sustained release drug delivery devices for the administration of therapeutics by… …optimal drug delivery system based upon a microembolization strategy requires a precise… …substantially in different species. 7 2.2.1. Pulmonary targeted drug delivery system for the… 

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APA (6th Edition):

Kutscher, Hilliard L., 1. (2012). Pharmacokinetics and toxicodynamics of intravenously administered rigid microparticles that passively target the pulmonary circulation of rodents. (Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000066851

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):

Kutscher, Hilliard L., 1978-. “Pharmacokinetics and toxicodynamics of intravenously administered rigid microparticles that passively target the pulmonary circulation of rodents.” 2012. Thesis, Rutgers University. Accessed June 25, 2019. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000066851.

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

MLA Handbook (7th Edition):

Kutscher, Hilliard L., 1978-. “Pharmacokinetics and toxicodynamics of intravenously administered rigid microparticles that passively target the pulmonary circulation of rodents.” 2012. Web. 25 Jun 2019.

Vancouver:

Kutscher, Hilliard L. 1. Pharmacokinetics and toxicodynamics of intravenously administered rigid microparticles that passively target the pulmonary circulation of rodents. [Internet] [Thesis]. Rutgers University; 2012. [cited 2019 Jun 25]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000066851.

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

Council of Science Editors:

Kutscher, Hilliard L. 1. Pharmacokinetics and toxicodynamics of intravenously administered rigid microparticles that passively target the pulmonary circulation of rodents. [Thesis]. Rutgers University; 2012. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000066851

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


Deakin University

137. Mahidhara, V.N.L.Ganesh. Orally administered anti-cancer nanocarriers loaded with therapeutic proteins.

Degree: 2012, Deakin University

  Anti-cancerous ability of orally fed therapeutic proteins was potentiated by further strengthening their digestive resistance by means of nano encapsulation. In this regard, formulation of… (more)

Subjects/Keywords: alginate enclosed chitosan coated ceramic nanocarriers; cancer therapy; drug delivery systems; nanotechnology

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APA (6th Edition):

Mahidhara, V. N. L. G. (2012). Orally administered anti-cancer nanocarriers loaded with therapeutic proteins. (Thesis). Deakin University. Retrieved from http://hdl.handle.net/10536/DRO/DU:30073444

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):

Mahidhara, V N L Ganesh. “Orally administered anti-cancer nanocarriers loaded with therapeutic proteins.” 2012. Thesis, Deakin University. Accessed June 25, 2019. http://hdl.handle.net/10536/DRO/DU:30073444.

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

MLA Handbook (7th Edition):

Mahidhara, V N L Ganesh. “Orally administered anti-cancer nanocarriers loaded with therapeutic proteins.” 2012. Web. 25 Jun 2019.

Vancouver:

Mahidhara VNLG. Orally administered anti-cancer nanocarriers loaded with therapeutic proteins. [Internet] [Thesis]. Deakin University; 2012. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/10536/DRO/DU:30073444.

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

Council of Science Editors:

Mahidhara VNLG. Orally administered anti-cancer nanocarriers loaded with therapeutic proteins. [Thesis]. Deakin University; 2012. Available from: http://hdl.handle.net/10536/DRO/DU:30073444

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


Deakin University

138. She, Xiaodong. Tailored hollow mesoporous silica nanoplatforms with biological labels for colon targeted drug deliver systems.

Degree: 2014, Deakin University

 Hollow mesoporous silica nanoparticles (HMSNs) were synthesized via a new strategy. HMSNs have a high drug loading, controlled release behaviour, and specifically targeting when bioconjugated… (more)

Subjects/Keywords: Hollow mesoporous silica nanoparticles (HMSNs); drug delivery systems; chemotherapy; colon cancer; colon cancer therapy

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APA (6th Edition):

She, X. (2014). Tailored hollow mesoporous silica nanoplatforms with biological labels for colon targeted drug deliver systems. (Thesis). Deakin University. Retrieved from http://hdl.handle.net/10536/DRO/DU:30073697

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):

She, Xiaodong. “Tailored hollow mesoporous silica nanoplatforms with biological labels for colon targeted drug deliver systems.” 2014. Thesis, Deakin University. Accessed June 25, 2019. http://hdl.handle.net/10536/DRO/DU:30073697.

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

MLA Handbook (7th Edition):

She, Xiaodong. “Tailored hollow mesoporous silica nanoplatforms with biological labels for colon targeted drug deliver systems.” 2014. Web. 25 Jun 2019.

Vancouver:

She X. Tailored hollow mesoporous silica nanoplatforms with biological labels for colon targeted drug deliver systems. [Internet] [Thesis]. Deakin University; 2014. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/10536/DRO/DU:30073697.

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

Council of Science Editors:

She X. Tailored hollow mesoporous silica nanoplatforms with biological labels for colon targeted drug deliver systems. [Thesis]. Deakin University; 2014. Available from: http://hdl.handle.net/10536/DRO/DU:30073697

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


Columbia University

139. Suryaprakash, Smruthi. Engineering mesenchymal stem cells for enhanced cancer therapy.

Degree: 2018, Columbia University

 Glioblastoma is the most common adult malignant primary brain tumor with one of the worst prognosis. With a survival of 10 to 12 months, glioblastoma… (more)

Subjects/Keywords: Biomedical engineering; Mesenchymal stem cells; Glioblastoma multiforme; Cancer – Treatment – Research; Drug delivery systems

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APA (6th Edition):

Suryaprakash, S. (2018). Engineering mesenchymal stem cells for enhanced cancer therapy. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D82Z2HF3

Chicago Manual of Style (16th Edition):

Suryaprakash, Smruthi. “Engineering mesenchymal stem cells for enhanced cancer therapy.” 2018. Doctoral Dissertation, Columbia University. Accessed June 25, 2019. https://doi.org/10.7916/D82Z2HF3.

MLA Handbook (7th Edition):

Suryaprakash, Smruthi. “Engineering mesenchymal stem cells for enhanced cancer therapy.” 2018. Web. 25 Jun 2019.

Vancouver:

Suryaprakash S. Engineering mesenchymal stem cells for enhanced cancer therapy. [Internet] [Doctoral dissertation]. Columbia University; 2018. [cited 2019 Jun 25]. Available from: https://doi.org/10.7916/D82Z2HF3.

Council of Science Editors:

Suryaprakash S. Engineering mesenchymal stem cells for enhanced cancer therapy. [Doctoral Dissertation]. Columbia University; 2018. Available from: https://doi.org/10.7916/D82Z2HF3


Columbia University

140. Downs, Matthew. Focused Ultrasound Mediated Blood-Brain Barrier Opening in Non-Human Primates: Safety, Efficacy and Drug Delivery.

Degree: 2015, Columbia University

 The blood-brain barrier (BBB) is physiologically essential for brain homeostasis. While it protects the brain from noxious agents, it prevents almost all currently available drugs… (more)

Subjects/Keywords: Brain – Diseases – Treatment; High-intensity focused ultrasound; Drug delivery systems; Blood-brain barrier; Biomedical engineering

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APA (6th Edition):

Downs, M. (2015). Focused Ultrasound Mediated Blood-Brain Barrier Opening in Non-Human Primates: Safety, Efficacy and Drug Delivery. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D82B8XC7

Chicago Manual of Style (16th Edition):

Downs, Matthew. “Focused Ultrasound Mediated Blood-Brain Barrier Opening in Non-Human Primates: Safety, Efficacy and Drug Delivery.” 2015. Doctoral Dissertation, Columbia University. Accessed June 25, 2019. https://doi.org/10.7916/D82B8XC7.

MLA Handbook (7th Edition):

Downs, Matthew. “Focused Ultrasound Mediated Blood-Brain Barrier Opening in Non-Human Primates: Safety, Efficacy and Drug Delivery.” 2015. Web. 25 Jun 2019.

Vancouver:

Downs M. Focused Ultrasound Mediated Blood-Brain Barrier Opening in Non-Human Primates: Safety, Efficacy and Drug Delivery. [Internet] [Doctoral dissertation]. Columbia University; 2015. [cited 2019 Jun 25]. Available from: https://doi.org/10.7916/D82B8XC7.

Council of Science Editors:

Downs M. Focused Ultrasound Mediated Blood-Brain Barrier Opening in Non-Human Primates: Safety, Efficacy and Drug Delivery. [Doctoral Dissertation]. Columbia University; 2015. Available from: https://doi.org/10.7916/D82B8XC7


University of Johannesburg

141. Tshweu, Lesego L. Development of spray-dried polycaprolactone-drug loaded nanoparticles towards improving current HIV chemotherapy.

Degree: 2013, University of Johannesburg

M.Sc. (Chemistry)

Human immunodeficiency virus (HIV) is continuously rewriting medical history as one of the diseases affecting humankind. Current treatments available for HIV, namely antiretrovirals… (more)

Subjects/Keywords: HIV infections - Chemotherapy; Antiretroviral agents; Polycaprolactone; Nanoparticles; Drug delivery systems; Spray drying

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APA (6th Edition):

Tshweu, L. L. (2013). Development of spray-dried polycaprolactone-drug loaded nanoparticles towards improving current HIV chemotherapy. (Thesis). University of Johannesburg. Retrieved from http://hdl.handle.net/10210/8576

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):

Tshweu, Lesego L. “Development of spray-dried polycaprolactone-drug loaded nanoparticles towards improving current HIV chemotherapy.” 2013. Thesis, University of Johannesburg. Accessed June 25, 2019. http://hdl.handle.net/10210/8576.

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

MLA Handbook (7th Edition):

Tshweu, Lesego L. “Development of spray-dried polycaprolactone-drug loaded nanoparticles towards improving current HIV chemotherapy.” 2013. Web. 25 Jun 2019.

Vancouver:

Tshweu LL. Development of spray-dried polycaprolactone-drug loaded nanoparticles towards improving current HIV chemotherapy. [Internet] [Thesis]. University of Johannesburg; 2013. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/10210/8576.

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

Council of Science Editors:

Tshweu LL. Development of spray-dried polycaprolactone-drug loaded nanoparticles towards improving current HIV chemotherapy. [Thesis]. University of Johannesburg; 2013. Available from: http://hdl.handle.net/10210/8576

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


Rochester Institute of Technology

142. Barman, Poulami. The Interaction of peptides with functionalized carbon nanotubes.

Degree: Thomas H. Gosnell School of Life Sciences (COS), 2009, Rochester Institute of Technology

 A literature study was conducted to review peptide adhesion to carbon nanotubes and they were found to be important in the drug designing industries. To… (more)

Subjects/Keywords: Binding free energy; Drug delivery systems; Interaction; Peptides; Single walled carbon nanotubes; Vasopressin

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APA (6th Edition):

Barman, P. (2009). The Interaction of peptides with functionalized carbon nanotubes. (Thesis). Rochester Institute of Technology. Retrieved from https://scholarworks.rit.edu/theses/4059

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):

Barman, Poulami. “The Interaction of peptides with functionalized carbon nanotubes.” 2009. Thesis, Rochester Institute of Technology. Accessed June 25, 2019. https://scholarworks.rit.edu/theses/4059.

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

MLA Handbook (7th Edition):

Barman, Poulami. “The Interaction of peptides with functionalized carbon nanotubes.” 2009. Web. 25 Jun 2019.

Vancouver:

Barman P. The Interaction of peptides with functionalized carbon nanotubes. [Internet] [Thesis]. Rochester Institute of Technology; 2009. [cited 2019 Jun 25]. Available from: https://scholarworks.rit.edu/theses/4059.

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

Council of Science Editors:

Barman P. The Interaction of peptides with functionalized carbon nanotubes. [Thesis]. Rochester Institute of Technology; 2009. Available from: https://scholarworks.rit.edu/theses/4059

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


University of Bridgeport

143. Mi, Fei. Design and Simulation of an Electrostatically-Driven MEMS Micro-Mixer .

Degree: 2015, University of Bridgeport

 Bio MEMS ( Biology Micro-electro-mechanical Systems) focus on some micro-fabricated devices including electrical and mechanical parts to study the biological system such as new polymer-based… (more)

Subjects/Keywords: Bio-micro-electro-mechanical-systems (BioMEMS); Drug delivery; Electromechanical active micro-mixer; ANSYS simulation

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APA (6th Edition):

Mi, F. (2015). Design and Simulation of an Electrostatically-Driven MEMS Micro-Mixer . (Thesis). University of Bridgeport. Retrieved from https://scholarworks.bridgeport.edu/xmlui/handle/123456789/1475

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):

Mi, Fei. “Design and Simulation of an Electrostatically-Driven MEMS Micro-Mixer .” 2015. Thesis, University of Bridgeport. Accessed June 25, 2019. https://scholarworks.bridgeport.edu/xmlui/handle/123456789/1475.

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

MLA Handbook (7th Edition):

Mi, Fei. “Design and Simulation of an Electrostatically-Driven MEMS Micro-Mixer .” 2015. Web. 25 Jun 2019.

Vancouver:

Mi F. Design and Simulation of an Electrostatically-Driven MEMS Micro-Mixer . [Internet] [Thesis]. University of Bridgeport; 2015. [cited 2019 Jun 25]. Available from: https://scholarworks.bridgeport.edu/xmlui/handle/123456789/1475.

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

Council of Science Editors:

Mi F. Design and Simulation of an Electrostatically-Driven MEMS Micro-Mixer . [Thesis]. University of Bridgeport; 2015. Available from: https://scholarworks.bridgeport.edu/xmlui/handle/123456789/1475

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


University of Iowa

144. Yoo, Jun. Synthesis of new biodegradable polysulfenamides for applications in medicine.

Degree: PhD, Chemistry, 2011, University of Iowa

  The first polysulfenamides were synthesized with S-N and N-S-N bonds along the backbone. We demonstrated that sulfenamides were stable in polar protic and aprotic… (more)

Subjects/Keywords: Biocompatible polymers; Biodegradable polymers; Comb block copolymers; Drug delivery systems; Microparticles; Polysulfenamides; Chemistry

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APA (6th Edition):

Yoo, J. (2011). Synthesis of new biodegradable polysulfenamides for applications in medicine. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/1114

Chicago Manual of Style (16th Edition):

Yoo, Jun. “Synthesis of new biodegradable polysulfenamides for applications in medicine.” 2011. Doctoral Dissertation, University of Iowa. Accessed June 25, 2019. https://ir.uiowa.edu/etd/1114.

MLA Handbook (7th Edition):

Yoo, Jun. “Synthesis of new biodegradable polysulfenamides for applications in medicine.” 2011. Web. 25 Jun 2019.

Vancouver:

Yoo J. Synthesis of new biodegradable polysulfenamides for applications in medicine. [Internet] [Doctoral dissertation]. University of Iowa; 2011. [cited 2019 Jun 25]. Available from: https://ir.uiowa.edu/etd/1114.

Council of Science Editors:

Yoo J. Synthesis of new biodegradable polysulfenamides for applications in medicine. [Doctoral Dissertation]. University of Iowa; 2011. Available from: https://ir.uiowa.edu/etd/1114


University of North Texas

145. Hinojosa, Barbara R. Nanoparticles Engineered to Bind Serum Albumin: Microwave Assisted Synthesis, Characterization, and Functionalization of Fluorescently-Labeled, Acrylate-Based, Polymer Nanoparticles.

Degree: 2010, University of North Texas

 The potential use of polymeric, functionalized nanoparticles (NPs) as drug delivery vectors was explored. Covalent conjugation of albumin to the surface of NPs via maleimide… (more)

Subjects/Keywords: Polymer nanoparticles; polymerization; circulation time; increasing; Nanoparticles.; Serum albumin.; Acrylates.; Drug delivery systems.

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APA (6th Edition):

Hinojosa, B. R. (2010). Nanoparticles Engineered to Bind Serum Albumin: Microwave Assisted Synthesis, Characterization, and Functionalization of Fluorescently-Labeled, Acrylate-Based, Polymer Nanoparticles. (Thesis). University of North Texas. Retrieved from https://digital.library.unt.edu/ark:/67531/metadc30466/

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):

Hinojosa, Barbara R. “Nanoparticles Engineered to Bind Serum Albumin: Microwave Assisted Synthesis, Characterization, and Functionalization of Fluorescently-Labeled, Acrylate-Based, Polymer Nanoparticles.” 2010. Thesis, University of North Texas. Accessed June 25, 2019. https://digital.library.unt.edu/ark:/67531/metadc30466/.

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

MLA Handbook (7th Edition):

Hinojosa, Barbara R. “Nanoparticles Engineered to Bind Serum Albumin: Microwave Assisted Synthesis, Characterization, and Functionalization of Fluorescently-Labeled, Acrylate-Based, Polymer Nanoparticles.” 2010. Web. 25 Jun 2019.

Vancouver:

Hinojosa BR. Nanoparticles Engineered to Bind Serum Albumin: Microwave Assisted Synthesis, Characterization, and Functionalization of Fluorescently-Labeled, Acrylate-Based, Polymer Nanoparticles. [Internet] [Thesis]. University of North Texas; 2010. [cited 2019 Jun 25]. Available from: https://digital.library.unt.edu/ark:/67531/metadc30466/.

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

Council of Science Editors:

Hinojosa BR. Nanoparticles Engineered to Bind Serum Albumin: Microwave Assisted Synthesis, Characterization, and Functionalization of Fluorescently-Labeled, Acrylate-Based, Polymer Nanoparticles. [Thesis]. University of North Texas; 2010. Available from: https://digital.library.unt.edu/ark:/67531/metadc30466/

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


University of Texas Southwestern Medical Center

146. Schaffer, Nathaniel Elliot. DAF-12: A Novel Drug Target in Parasitic Nematodes.

Degree: 2014, University of Texas Southwestern Medical Center

 The nuclear receptor DAF-12, first identified in C. elegans, controls nematode species' entry into and exit from metabolically hypoactive resting states. In all of the… (more)

Subjects/Keywords: Antinematodal Agents; Drug Delivery Systems; Helminth Proteins; Nematoda; Receptors, Cytoplasmic and Nuclear

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APA (6th Edition):

Schaffer, N. E. (2014). DAF-12: A Novel Drug Target in Parasitic Nematodes. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/6590

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):

Schaffer, Nathaniel Elliot. “DAF-12: A Novel Drug Target in Parasitic Nematodes.” 2014. Thesis, University of Texas Southwestern Medical Center. Accessed June 25, 2019. http://hdl.handle.net/2152.5/6590.

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

MLA Handbook (7th Edition):

Schaffer, Nathaniel Elliot. “DAF-12: A Novel Drug Target in Parasitic Nematodes.” 2014. Web. 25 Jun 2019.

Vancouver:

Schaffer NE. DAF-12: A Novel Drug Target in Parasitic Nematodes. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2014. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/2152.5/6590.

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

Council of Science Editors:

Schaffer NE. DAF-12: A Novel Drug Target in Parasitic Nematodes. [Thesis]. University of Texas Southwestern Medical Center; 2014. Available from: http://hdl.handle.net/2152.5/6590

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


Northeastern University

147. Sawant, Rishikesh Manohar. Polyethylene glycol (PEG) as a key component of long-circulating delivery systems for therapy and imaging.

Degree: PhD, School of Pharmacy, 2008, Northeastern University

 The undesired side-effects of many therapies and diagnostics result from their accumulation in the non-target tissues. There is a clear need to design pharmaceutical delivery(more)

Subjects/Keywords: Health science; Drug delivery systems; Nanotechnology; Polymeric drug delivery systems; Drug delivery systems; Pharmacy and Pharmaceutical Sciences

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

APA (6th Edition):

Sawant, R. M. (2008). Polyethylene glycol (PEG) as a key component of long-circulating delivery systems for therapy and imaging. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/d1001701x

Chicago Manual of Style (16th Edition):

Sawant, Rishikesh Manohar. “Polyethylene glycol (PEG) as a key component of long-circulating delivery systems for therapy and imaging.” 2008. Doctoral Dissertation, Northeastern University. Accessed June 25, 2019. http://hdl.handle.net/2047/d1001701x.

MLA Handbook (7th Edition):

Sawant, Rishikesh Manohar. “Polyethylene glycol (PEG) as a key component of long-circulating delivery systems for therapy and imaging.” 2008. Web. 25 Jun 2019.

Vancouver:

Sawant RM. Polyethylene glycol (PEG) as a key component of long-circulating delivery systems for therapy and imaging. [Internet] [Doctoral dissertation]. Northeastern University; 2008. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/2047/d1001701x.

Council of Science Editors:

Sawant RM. Polyethylene glycol (PEG) as a key component of long-circulating delivery systems for therapy and imaging. [Doctoral Dissertation]. Northeastern University; 2008. Available from: http://hdl.handle.net/2047/d1001701x


University of Utah

148. Li, Xiaoling. Biodegradable polymeric prodrugs of antihypertensive agents;.

Degree: PhD, Pharmaceutics & Pharmaceutical Chemistry;, 1991, University of Utah

 Biodegradable polymeric prodrugs of antihypertensive agents were developed by covalently binding minoxidil, clonidine, prazosin, and CGS 16617 to poly(alpha-amino acids) via labile linkages. The amide… (more)

Subjects/Keywords: Drug Carrierse; Drug Delivery Systems; Prodrugs; Polymers

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

APA (6th Edition):

Li, X. (1991). Biodegradable polymeric prodrugs of antihypertensive agents;. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/26/rec/101

Chicago Manual of Style (16th Edition):

Li, Xiaoling. “Biodegradable polymeric prodrugs of antihypertensive agents;.” 1991. Doctoral Dissertation, University of Utah. Accessed June 25, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/26/rec/101.

MLA Handbook (7th Edition):

Li, Xiaoling. “Biodegradable polymeric prodrugs of antihypertensive agents;.” 1991. Web. 25 Jun 2019.

Vancouver:

Li X. Biodegradable polymeric prodrugs of antihypertensive agents;. [Internet] [Doctoral dissertation]. University of Utah; 1991. [cited 2019 Jun 25]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/26/rec/101.

Council of Science Editors:

Li X. Biodegradable polymeric prodrugs of antihypertensive agents;. [Doctoral Dissertation]. University of Utah; 1991. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/26/rec/101


University of Alberta

149. Mehra, Tarun. A liposomal sustained released system for cytosine arabinoside.

Degree: MS, Department of Pharmacology, 1990, University of Alberta

Subjects/Keywords: Drug carriers (Pharmacy); Drug delivery systems.; Liposomes.; Cytosine arabinoside.

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

APA (6th Edition):

Mehra, T. (1990). A liposomal sustained released system for cytosine arabinoside. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/0v8382895

Chicago Manual of Style (16th Edition):

Mehra, Tarun. “A liposomal sustained released system for cytosine arabinoside.” 1990. Masters Thesis, University of Alberta. Accessed June 25, 2019. https://era.library.ualberta.ca/files/0v8382895.

MLA Handbook (7th Edition):

Mehra, Tarun. “A liposomal sustained released system for cytosine arabinoside.” 1990. Web. 25 Jun 2019.

Vancouver:

Mehra T. A liposomal sustained released system for cytosine arabinoside. [Internet] [Masters thesis]. University of Alberta; 1990. [cited 2019 Jun 25]. Available from: https://era.library.ualberta.ca/files/0v8382895.

Council of Science Editors:

Mehra T. A liposomal sustained released system for cytosine arabinoside. [Masters Thesis]. University of Alberta; 1990. Available from: https://era.library.ualberta.ca/files/0v8382895


Rhodes University

150. Wa Kasongo, Kasongo. An investigation into the feasibility of incorporating didanosine into innovative solid lipid nanocarriers.

Degree: PhD, Faculty of Pharmacy, Pharmacy, 2010, Rhodes University

 The research undertaken in these studies aimed to investigate the feasibility of developing and manufacturing innovative solid lipid carriers, such as solid lipid nanoparticles (SLN)… (more)

Subjects/Keywords: Antiretroviral agents; HIV infections  – Drug testing; Didanosine; Nanoparticles; Drug delivery systems; Nanostructured materials; Lipids  – Therapeutic use

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

APA (6th Edition):

Wa Kasongo, K. (2010). An investigation into the feasibility of incorporating didanosine into innovative solid lipid nanocarriers. (Doctoral Dissertation). Rhodes University. Retrieved from http://hdl.handle.net/10962/d1003278

Chicago Manual of Style (16th Edition):

Wa Kasongo, Kasongo. “An investigation into the feasibility of incorporating didanosine into innovative solid lipid nanocarriers.” 2010. Doctoral Dissertation, Rhodes University. Accessed June 25, 2019. http://hdl.handle.net/10962/d1003278.

MLA Handbook (7th Edition):

Wa Kasongo, Kasongo. “An investigation into the feasibility of incorporating didanosine into innovative solid lipid nanocarriers.” 2010. Web. 25 Jun 2019.

Vancouver:

Wa Kasongo K. An investigation into the feasibility of incorporating didanosine into innovative solid lipid nanocarriers. [Internet] [Doctoral dissertation]. Rhodes University; 2010. [cited 2019 Jun 25]. Available from: http://hdl.handle.net/10962/d1003278.

Council of Science Editors:

Wa Kasongo K. An investigation into the feasibility of incorporating didanosine into innovative solid lipid nanocarriers. [Doctoral Dissertation]. Rhodes University; 2010. Available from: http://hdl.handle.net/10962/d1003278

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