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You searched for subject:(Oral Drug Delivery). Showing records 1 – 30 of 49 total matches.

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1. Goldenshtein, Victoria. Effect Of Mucin On Hydrodynamic Diameter And Zeta Potential Of Polymeric Nanospheres.

Degree: Biomedical Engineering, 2017, Brown University

 The degree of interaction between nanoencapsulated material and gastrointestinal mucin can be an important determinant in efficiency of absorption of orally delivered therapeutics. Mucus lining… (more)

Subjects/Keywords: Oral Drug Delivery

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

APA (6th Edition):

Goldenshtein, V. (2017). Effect Of Mucin On Hydrodynamic Diameter And Zeta Potential Of Polymeric Nanospheres. (Thesis). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:733342/

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):

Goldenshtein, Victoria. “Effect Of Mucin On Hydrodynamic Diameter And Zeta Potential Of Polymeric Nanospheres.” 2017. Thesis, Brown University. Accessed March 23, 2019. https://repository.library.brown.edu/studio/item/bdr:733342/.

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

MLA Handbook (7th Edition):

Goldenshtein, Victoria. “Effect Of Mucin On Hydrodynamic Diameter And Zeta Potential Of Polymeric Nanospheres.” 2017. Web. 23 Mar 2019.

Vancouver:

Goldenshtein V. Effect Of Mucin On Hydrodynamic Diameter And Zeta Potential Of Polymeric Nanospheres. [Internet] [Thesis]. Brown University; 2017. [cited 2019 Mar 23]. Available from: https://repository.library.brown.edu/studio/item/bdr:733342/.

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

Council of Science Editors:

Goldenshtein V. Effect Of Mucin On Hydrodynamic Diameter And Zeta Potential Of Polymeric Nanospheres. [Thesis]. Brown University; 2017. Available from: https://repository.library.brown.edu/studio/item/bdr:733342/

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


University of Utah

2. Hubbard, Dallin Andrew. Transepithelial transport of pamam dendrimers across isolated intestinal tissue.

Degree: PhD, Bioengineering, 2016, University of Utah

 Poly(amido amine) (PAMAM) dendrimers have shown potential to carry poorly absorbed drugs across the intestinal barrier and into systemic circulation, reducing the need for intravenous… (more)

Subjects/Keywords: dendrimer; drug delivery; oral delivery; Ussing

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APA (6th Edition):

Hubbard, D. A. (2016). Transepithelial transport of pamam dendrimers across isolated intestinal tissue. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/4102/rec/2779

Chicago Manual of Style (16th Edition):

Hubbard, Dallin Andrew. “Transepithelial transport of pamam dendrimers across isolated intestinal tissue.” 2016. Doctoral Dissertation, University of Utah. Accessed March 23, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/4102/rec/2779.

MLA Handbook (7th Edition):

Hubbard, Dallin Andrew. “Transepithelial transport of pamam dendrimers across isolated intestinal tissue.” 2016. Web. 23 Mar 2019.

Vancouver:

Hubbard DA. Transepithelial transport of pamam dendrimers across isolated intestinal tissue. [Internet] [Doctoral dissertation]. University of Utah; 2016. [cited 2019 Mar 23]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/4102/rec/2779.

Council of Science Editors:

Hubbard DA. Transepithelial transport of pamam dendrimers across isolated intestinal tissue. [Doctoral Dissertation]. University of Utah; 2016. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/4102/rec/2779

3. Bhandary, Sarita. Design Development and evaluation of Gastro Intestinal Muco Adhesive Patch System GIMAPS for Oral Drug delivery.

Degree: Pharmacy, 2013, INFLIBNET

A new gastrointestinal mucoadhesive patch system (GIMAPS) has been newlinedesigned for the oral drug delivery of Duloxetine hydrochloride (DLX). The system newlineconsists of four layered… (more)

Subjects/Keywords: Gastro Intestinal Muco Adhesive; Oral Drug delivery

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APA (6th Edition):

Bhandary, S. (2013). Design Development and evaluation of Gastro Intestinal Muco Adhesive Patch System GIMAPS for Oral Drug delivery. (Thesis). INFLIBNET. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/9095

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):

Bhandary, Sarita. “Design Development and evaluation of Gastro Intestinal Muco Adhesive Patch System GIMAPS for Oral Drug delivery.” 2013. Thesis, INFLIBNET. Accessed March 23, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/9095.

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

MLA Handbook (7th Edition):

Bhandary, Sarita. “Design Development and evaluation of Gastro Intestinal Muco Adhesive Patch System GIMAPS for Oral Drug delivery.” 2013. Web. 23 Mar 2019.

Vancouver:

Bhandary S. Design Development and evaluation of Gastro Intestinal Muco Adhesive Patch System GIMAPS for Oral Drug delivery. [Internet] [Thesis]. INFLIBNET; 2013. [cited 2019 Mar 23]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/9095.

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

Council of Science Editors:

Bhandary S. Design Development and evaluation of Gastro Intestinal Muco Adhesive Patch System GIMAPS for Oral Drug delivery. [Thesis]. INFLIBNET; 2013. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/9095

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


University of Hong Kong

4. Kam, Kin-wai. A systematic review of factors improving medication safety of oral medication via enteral feeding tubes in institutions.

Degree: MPH, 2014, University of Hong Kong

Objective: Medication safety is always having great concern in healthcare. Giving oral medication through enteral feeding tubes is not uncommon and is a well-known area… (more)

Subjects/Keywords: Drug delivery devices; Enteral feeding; Oral medication

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APA (6th Edition):

Kam, K. (2014). A systematic review of factors improving medication safety of oral medication via enteral feeding tubes in institutions. (Masters Thesis). University of Hong Kong. Retrieved from Kam, K. [甘健威]. (2014). A systematic review of factors improving medication safety of oral medication via enteral feeding tubes in institutions. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5320369 ; http://dx.doi.org/10.5353/th_b5320369 ; http://hdl.handle.net/10722/206916

Chicago Manual of Style (16th Edition):

Kam, Kin-wai. “A systematic review of factors improving medication safety of oral medication via enteral feeding tubes in institutions.” 2014. Masters Thesis, University of Hong Kong. Accessed March 23, 2019. Kam, K. [甘健威]. (2014). A systematic review of factors improving medication safety of oral medication via enteral feeding tubes in institutions. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5320369 ; http://dx.doi.org/10.5353/th_b5320369 ; http://hdl.handle.net/10722/206916.

MLA Handbook (7th Edition):

Kam, Kin-wai. “A systematic review of factors improving medication safety of oral medication via enteral feeding tubes in institutions.” 2014. Web. 23 Mar 2019.

Vancouver:

Kam K. A systematic review of factors improving medication safety of oral medication via enteral feeding tubes in institutions. [Internet] [Masters thesis]. University of Hong Kong; 2014. [cited 2019 Mar 23]. Available from: Kam, K. [甘健威]. (2014). A systematic review of factors improving medication safety of oral medication via enteral feeding tubes in institutions. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5320369 ; http://dx.doi.org/10.5353/th_b5320369 ; http://hdl.handle.net/10722/206916.

Council of Science Editors:

Kam K. A systematic review of factors improving medication safety of oral medication via enteral feeding tubes in institutions. [Masters Thesis]. University of Hong Kong; 2014. Available from: Kam, K. [甘健威]. (2014). A systematic review of factors improving medication safety of oral medication via enteral feeding tubes in institutions. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5320369 ; http://dx.doi.org/10.5353/th_b5320369 ; http://hdl.handle.net/10722/206916


Dublin City University

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

Degree: School of Biotechnology, 2015, Dublin City University

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

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

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

McDonald, Bernard. “Development of an oral drug delivery platform formulation for the targeted delivery of celecoxib for the chemoprevention and treatment of colorectal cancer.” 2015. Thesis, Dublin City University. Accessed March 23, 2019. http://doras.dcu.ie/20409/.

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

MLA Handbook (7th Edition):

McDonald, Bernard. “Development of an oral drug delivery platform formulation for the targeted delivery of celecoxib for the chemoprevention and treatment of colorectal cancer.” 2015. Web. 23 Mar 2019.

Vancouver:

McDonald B. Development of an oral drug delivery platform formulation for the targeted delivery of celecoxib for the chemoprevention and treatment of colorectal cancer. [Internet] [Thesis]. Dublin City University; 2015. [cited 2019 Mar 23]. Available from: http://doras.dcu.ie/20409/.

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

Council of Science Editors:

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

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

6. Ipsita, Biswal. Formulation and development of Bi-layer solid dosage form of losartan potassium containing an immediate release layer and a slow release layer; -.

Degree: Pharmacy, 2012, Shiksha o Anusandhan University

Losartan potassium (LP) is a type of medicine called an Angiotensin II receptor antagonist. It works by preventing the action of a hormone in the… (more)

Subjects/Keywords: Pharmacy; Drug delivery routes; Oral Delivery Systems; Tablets; Hypertension

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APA (6th Edition):

Ipsita, B. (2012). Formulation and development of Bi-layer solid dosage form of losartan potassium containing an immediate release layer and a slow release layer; -. (Thesis). Shiksha o Anusandhan University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/12333

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):

Ipsita, Biswal. “Formulation and development of Bi-layer solid dosage form of losartan potassium containing an immediate release layer and a slow release layer; -.” 2012. Thesis, Shiksha o Anusandhan University. Accessed March 23, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/12333.

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

MLA Handbook (7th Edition):

Ipsita, Biswal. “Formulation and development of Bi-layer solid dosage form of losartan potassium containing an immediate release layer and a slow release layer; -.” 2012. Web. 23 Mar 2019.

Vancouver:

Ipsita B. Formulation and development of Bi-layer solid dosage form of losartan potassium containing an immediate release layer and a slow release layer; -. [Internet] [Thesis]. Shiksha o Anusandhan University; 2012. [cited 2019 Mar 23]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/12333.

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

Council of Science Editors:

Ipsita B. Formulation and development of Bi-layer solid dosage form of losartan potassium containing an immediate release layer and a slow release layer; -. [Thesis]. Shiksha o Anusandhan University; 2012. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/12333

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


University of Iowa

7. Bhatt, Bhavik Janankkumar. Regenerated cellulose for controlled oral drug delivery.

Degree: PhD, Pharmacy, 2012, University of Iowa

  The performance of regenerated cellulose (RC) films and capsules was investigated for their applications in oral controlled drug delivery. Regenerated cellulose films were prepared… (more)

Subjects/Keywords: Capsules; Film technology; Oral drug delivery; Osmotic drug delivery; Regenerated Cellulose; Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Bhatt, B. J. (2012). Regenerated cellulose for controlled oral drug delivery. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/4577

Chicago Manual of Style (16th Edition):

Bhatt, Bhavik Janankkumar. “Regenerated cellulose for controlled oral drug delivery.” 2012. Doctoral Dissertation, University of Iowa. Accessed March 23, 2019. https://ir.uiowa.edu/etd/4577.

MLA Handbook (7th Edition):

Bhatt, Bhavik Janankkumar. “Regenerated cellulose for controlled oral drug delivery.” 2012. Web. 23 Mar 2019.

Vancouver:

Bhatt BJ. Regenerated cellulose for controlled oral drug delivery. [Internet] [Doctoral dissertation]. University of Iowa; 2012. [cited 2019 Mar 23]. Available from: https://ir.uiowa.edu/etd/4577.

Council of Science Editors:

Bhatt BJ. Regenerated cellulose for controlled oral drug delivery. [Doctoral Dissertation]. University of Iowa; 2012. Available from: https://ir.uiowa.edu/etd/4577


Texas A&M University

8. Yu, Xiao. Progress toward a Colon Targeting Nanoparticle Based Drug Delivery System.

Degree: 2012, Texas A&M University

 Hydrophobic drug paclitaxel nanoparticles (PAX NPs) and pH sensitive hydrogels were prepared in this study to build a colon targeting nanoparticle based drug delivery system… (more)

Subjects/Keywords: nanoparticles; hydrogel; colon targeting; oral drug delivery; controlled releases

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APA (6th Edition):

Yu, X. (2012). Progress toward a Colon Targeting Nanoparticle Based Drug Delivery System. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2012-05-11053

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):

Yu, Xiao. “Progress toward a Colon Targeting Nanoparticle Based Drug Delivery System.” 2012. Thesis, Texas A&M University. Accessed March 23, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-2012-05-11053.

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

MLA Handbook (7th Edition):

Yu, Xiao. “Progress toward a Colon Targeting Nanoparticle Based Drug Delivery System.” 2012. Web. 23 Mar 2019.

Vancouver:

Yu X. Progress toward a Colon Targeting Nanoparticle Based Drug Delivery System. [Internet] [Thesis]. Texas A&M University; 2012. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2012-05-11053.

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

Council of Science Editors:

Yu X. Progress toward a Colon Targeting Nanoparticle Based Drug Delivery System. [Thesis]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2012-05-11053

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


University of Minnesota

9. Ting, Jeffrey. Tunable Polymers as Specialized Excipients for Oral Drug Delivery.

Degree: PhD, Chemical Engineering, 2016, University of Minnesota

 For the continued advancement of modern pills and tablets in oral drug administration, spray–dried dispersions (solid–solid mixtures of amorphous drugs and polymers) have the potential… (more)

Subjects/Keywords: drug delivery; medicine; oral administration; polymers; solid dispersions; solubilizers

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APA (6th Edition):

Ting, J. (2016). Tunable Polymers as Specialized Excipients for Oral Drug Delivery. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/191427

Chicago Manual of Style (16th Edition):

Ting, Jeffrey. “Tunable Polymers as Specialized Excipients for Oral Drug Delivery.” 2016. Doctoral Dissertation, University of Minnesota. Accessed March 23, 2019. http://hdl.handle.net/11299/191427.

MLA Handbook (7th Edition):

Ting, Jeffrey. “Tunable Polymers as Specialized Excipients for Oral Drug Delivery.” 2016. Web. 23 Mar 2019.

Vancouver:

Ting J. Tunable Polymers as Specialized Excipients for Oral Drug Delivery. [Internet] [Doctoral dissertation]. University of Minnesota; 2016. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/11299/191427.

Council of Science Editors:

Ting J. Tunable Polymers as Specialized Excipients for Oral Drug Delivery. [Doctoral Dissertation]. University of Minnesota; 2016. Available from: http://hdl.handle.net/11299/191427


Northeastern University

10. Buyukozturk, Fulden. Mechanistic studies and modeling of self-emulsifying drug delivery systems for the oral delivery of hydrophobic drugs.

Degree: PhD, Department of Chemical Engineering, 2012, Northeastern University

 The oral route for drug delivery is not possible for approximately 50% of currently marketed drug compounds due to low solubility in water. Lipid based… (more)

Subjects/Keywords: Mechanistic Modeling; Oral Drug Delivery; SEDDS; Biochemical and Biomolecular Engineering; Medicinal-Pharmaceutical Chemistry

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APA (6th Edition):

Buyukozturk, F. (2012). Mechanistic studies and modeling of self-emulsifying drug delivery systems for the oral delivery of hydrophobic drugs. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/d20002833

Chicago Manual of Style (16th Edition):

Buyukozturk, Fulden. “Mechanistic studies and modeling of self-emulsifying drug delivery systems for the oral delivery of hydrophobic drugs.” 2012. Doctoral Dissertation, Northeastern University. Accessed March 23, 2019. http://hdl.handle.net/2047/d20002833.

MLA Handbook (7th Edition):

Buyukozturk, Fulden. “Mechanistic studies and modeling of self-emulsifying drug delivery systems for the oral delivery of hydrophobic drugs.” 2012. Web. 23 Mar 2019.

Vancouver:

Buyukozturk F. Mechanistic studies and modeling of self-emulsifying drug delivery systems for the oral delivery of hydrophobic drugs. [Internet] [Doctoral dissertation]. Northeastern University; 2012. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/2047/d20002833.

Council of Science Editors:

Buyukozturk F. Mechanistic studies and modeling of self-emulsifying drug delivery systems for the oral delivery of hydrophobic drugs. [Doctoral Dissertation]. Northeastern University; 2012. Available from: http://hdl.handle.net/2047/d20002833


University of California – Berkeley

11. Fischer, Kathleen Elizabeth. Silicon Nanowires for Bioadhesion and Drug Delivery.

Degree: Bioengineering, 2010, University of California – Berkeley

 Mucosal tissues have great potential for delivery of therapeutic macromolecules, but drug absorption is often thwarted by chemical and physical barriers, such as the mucus… (more)

Subjects/Keywords: Biomedical Engineering; Nanotechnology; Pharmaceutical Sciences; bioadhesion; cytoadhesion; microspheres; nanoengineered surfaces; nanowires; oral drug delivery

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APA (6th Edition):

Fischer, K. E. (2010). Silicon Nanowires for Bioadhesion and Drug Delivery. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/5nr9v8zh

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):

Fischer, Kathleen Elizabeth. “Silicon Nanowires for Bioadhesion and Drug Delivery.” 2010. Thesis, University of California – Berkeley. Accessed March 23, 2019. http://www.escholarship.org/uc/item/5nr9v8zh.

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

MLA Handbook (7th Edition):

Fischer, Kathleen Elizabeth. “Silicon Nanowires for Bioadhesion and Drug Delivery.” 2010. Web. 23 Mar 2019.

Vancouver:

Fischer KE. Silicon Nanowires for Bioadhesion and Drug Delivery. [Internet] [Thesis]. University of California – Berkeley; 2010. [cited 2019 Mar 23]. Available from: http://www.escholarship.org/uc/item/5nr9v8zh.

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

Council of Science Editors:

Fischer KE. Silicon Nanowires for Bioadhesion and Drug Delivery. [Thesis]. University of California – Berkeley; 2010. Available from: http://www.escholarship.org/uc/item/5nr9v8zh

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


Virginia Tech

12. Marks, Joyann Audrene. Synthesis and Applications of Cellulose Derivatives for Drug Delivery.

Degree: PhD, Learning Sciences and Technologies, 2015, Virginia Tech

 In an effort to produce new derivatives of cellulose for drug delivery applications, methods were developed to regioselectively modify C-6 halo cellulose esters to produce… (more)

Subjects/Keywords: pairwise blends; amorphous solid dispersion; oral drug delivery; cellulose esters; bioavailability; cationic cellulose; extrusion

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APA (6th Edition):

Marks, J. A. (2015). Synthesis and Applications of Cellulose Derivatives for Drug Delivery. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/75307

Chicago Manual of Style (16th Edition):

Marks, Joyann Audrene. “Synthesis and Applications of Cellulose Derivatives for Drug Delivery.” 2015. Doctoral Dissertation, Virginia Tech. Accessed March 23, 2019. http://hdl.handle.net/10919/75307.

MLA Handbook (7th Edition):

Marks, Joyann Audrene. “Synthesis and Applications of Cellulose Derivatives for Drug Delivery.” 2015. Web. 23 Mar 2019.

Vancouver:

Marks JA. Synthesis and Applications of Cellulose Derivatives for Drug Delivery. [Internet] [Doctoral dissertation]. Virginia Tech; 2015. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/10919/75307.

Council of Science Editors:

Marks JA. Synthesis and Applications of Cellulose Derivatives for Drug Delivery. [Doctoral Dissertation]. Virginia Tech; 2015. Available from: http://hdl.handle.net/10919/75307


Virginia Tech

13. Liu, Haoyu. Synthesis and Structure-property Evaluation of Novel Cellulosic Polymers as Amorphous Solid Dispersion Matrices for Enhanced Oral Drug Delivery.

Degree: PhD, Learning Sciences and Technologies, 2014, Virginia Tech

 The use of amorphous solid dispersions (ASDs) is an effective and increasingly widely adopted approach for solubility and bioavailability enhancement of hydrophobic drugs. Cellulose derivatives… (more)

Subjects/Keywords: cellulose ω-carboxyesters; amorphous solid dispersion; amphiphilicity; structure-property relationship; oral drug delivery

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APA (6th Edition):

Liu, H. (2014). Synthesis and Structure-property Evaluation of Novel Cellulosic Polymers as Amorphous Solid Dispersion Matrices for Enhanced Oral Drug Delivery. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/54934

Chicago Manual of Style (16th Edition):

Liu, Haoyu. “Synthesis and Structure-property Evaluation of Novel Cellulosic Polymers as Amorphous Solid Dispersion Matrices for Enhanced Oral Drug Delivery.” 2014. Doctoral Dissertation, Virginia Tech. Accessed March 23, 2019. http://hdl.handle.net/10919/54934.

MLA Handbook (7th Edition):

Liu, Haoyu. “Synthesis and Structure-property Evaluation of Novel Cellulosic Polymers as Amorphous Solid Dispersion Matrices for Enhanced Oral Drug Delivery.” 2014. Web. 23 Mar 2019.

Vancouver:

Liu H. Synthesis and Structure-property Evaluation of Novel Cellulosic Polymers as Amorphous Solid Dispersion Matrices for Enhanced Oral Drug Delivery. [Internet] [Doctoral dissertation]. Virginia Tech; 2014. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/10919/54934.

Council of Science Editors:

Liu H. Synthesis and Structure-property Evaluation of Novel Cellulosic Polymers as Amorphous Solid Dispersion Matrices for Enhanced Oral Drug Delivery. [Doctoral Dissertation]. Virginia Tech; 2014. Available from: http://hdl.handle.net/10919/54934


Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ)

14. Samaridou, Eleni. Ανάπτυξη νανοφορέων για τη στοματική και οφθαλμική χορήγηση θεραπευτικών βιομορίων.

Degree: 2015, Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ)

 The primary aim of this thesis was the development of mucus permeating nanocarriers according to alternative mucus penetration strategies (e.g., controlled release of mucolytic agents,… (more)

Subjects/Keywords: Στοματική χορήγηση βιομορίων; Οφθαλμική χορήγηση βιομορίων; Νανοφορείς; ΒΛΕΝΝΑ; Βλεννολυτικοί παράγοντες; Διάβαση της βλέννας; C ΠΕΠΤΙΔΙΟ - ΙΝΣΟΥΛΙΝΗ; Oral drug delivery; Ocular drug delivery; Nanobased drug delivery systems; Mucus permeation; Oral delivery of insulin

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APA (6th Edition):

Samaridou, E. (2015). Ανάπτυξη νανοφορέων για τη στοματική και οφθαλμική χορήγηση θεραπευτικών βιομορίων. (Thesis). Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ). Retrieved from http://hdl.handle.net/10442/hedi/36672

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):

Samaridou, Eleni. “Ανάπτυξη νανοφορέων για τη στοματική και οφθαλμική χορήγηση θεραπευτικών βιομορίων.” 2015. Thesis, Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ). Accessed March 23, 2019. http://hdl.handle.net/10442/hedi/36672.

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

MLA Handbook (7th Edition):

Samaridou, Eleni. “Ανάπτυξη νανοφορέων για τη στοματική και οφθαλμική χορήγηση θεραπευτικών βιομορίων.” 2015. Web. 23 Mar 2019.

Vancouver:

Samaridou E. Ανάπτυξη νανοφορέων για τη στοματική και οφθαλμική χορήγηση θεραπευτικών βιομορίων. [Internet] [Thesis]. Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ); 2015. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/10442/hedi/36672.

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

Council of Science Editors:

Samaridou E. Ανάπτυξη νανοφορέων για τη στοματική και οφθαλμική χορήγηση θεραπευτικών βιομορίων. [Thesis]. Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ); 2015. Available from: http://hdl.handle.net/10442/hedi/36672

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


University of Kentucky

15. Authimoolam, Sundar Prasanth. STABILITY OF AFFINITY BASED LAYER-BY-LAYER POLYMERIC SELF-ASSEMBLIES FOR ORAL WOUND APPLICATIONS.

Degree: 2011, University of Kentucky

Oral mucositis is a painful and debilitating chronic inflammatory condition that can result from chemo and/or radiotherapy. While current treatment strategies which provide temporary relief… (more)

Subjects/Keywords: Oral mucositis; Biotin-Streptavidin; Layer-by-Layer; Poly (acrylic acid); Oral drug delivery; Biochemical and Biomolecular Engineering; Chemical Engineering

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APA (6th Edition):

Authimoolam, S. P. (2011). STABILITY OF AFFINITY BASED LAYER-BY-LAYER POLYMERIC SELF-ASSEMBLIES FOR ORAL WOUND APPLICATIONS. (Masters Thesis). University of Kentucky. Retrieved from http://uknowledge.uky.edu/cme_etds/3

Chicago Manual of Style (16th Edition):

Authimoolam, Sundar Prasanth. “STABILITY OF AFFINITY BASED LAYER-BY-LAYER POLYMERIC SELF-ASSEMBLIES FOR ORAL WOUND APPLICATIONS.” 2011. Masters Thesis, University of Kentucky. Accessed March 23, 2019. http://uknowledge.uky.edu/cme_etds/3.

MLA Handbook (7th Edition):

Authimoolam, Sundar Prasanth. “STABILITY OF AFFINITY BASED LAYER-BY-LAYER POLYMERIC SELF-ASSEMBLIES FOR ORAL WOUND APPLICATIONS.” 2011. Web. 23 Mar 2019.

Vancouver:

Authimoolam SP. STABILITY OF AFFINITY BASED LAYER-BY-LAYER POLYMERIC SELF-ASSEMBLIES FOR ORAL WOUND APPLICATIONS. [Internet] [Masters thesis]. University of Kentucky; 2011. [cited 2019 Mar 23]. Available from: http://uknowledge.uky.edu/cme_etds/3.

Council of Science Editors:

Authimoolam SP. STABILITY OF AFFINITY BASED LAYER-BY-LAYER POLYMERIC SELF-ASSEMBLIES FOR ORAL WOUND APPLICATIONS. [Masters Thesis]. University of Kentucky; 2011. Available from: http://uknowledge.uky.edu/cme_etds/3

16. Nekkanti, Vijay Kumar. Formulation development and biopharmaceutical assessment of nanoparticle technology based oral drug delivery system; -.

Degree: Pharmacy, 2010, Jawaharlal Nehru Technological University

Poorly water-soluble drugs such as Candesartan cilexetil and Camptothecin analog offer challenges in developing a drug product with adequate bioavailability. The bioavailability of these drugs… (more)

Subjects/Keywords: Drug Nanoparticles; Piston gap Technologies; Differential Scanning Calorimetry (DSC); X-ray Powder Diffraction (XRPD); Pharmacy; oral drug delivery system

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APA (6th Edition):

Nekkanti, V. K. (2010). Formulation development and biopharmaceutical assessment of nanoparticle technology based oral drug delivery system; -. (Thesis). Jawaharlal Nehru Technological University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/4521

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):

Nekkanti, Vijay Kumar. “Formulation development and biopharmaceutical assessment of nanoparticle technology based oral drug delivery system; -.” 2010. Thesis, Jawaharlal Nehru Technological University. Accessed March 23, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/4521.

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

MLA Handbook (7th Edition):

Nekkanti, Vijay Kumar. “Formulation development and biopharmaceutical assessment of nanoparticle technology based oral drug delivery system; -.” 2010. Web. 23 Mar 2019.

Vancouver:

Nekkanti VK. Formulation development and biopharmaceutical assessment of nanoparticle technology based oral drug delivery system; -. [Internet] [Thesis]. Jawaharlal Nehru Technological University; 2010. [cited 2019 Mar 23]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/4521.

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

Council of Science Editors:

Nekkanti VK. Formulation development and biopharmaceutical assessment of nanoparticle technology based oral drug delivery system; -. [Thesis]. Jawaharlal Nehru Technological University; 2010. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/4521

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


University of Michigan

17. Nieto, Kari. Long-Acting Release Implants for Local Fenretinide Delivery and Oral Cancer Chemoprevention.

Degree: PhD, Pharmaceutical Sciences, 2017, University of Michigan

 The synthetic vitamin A derivative, fenretinide (4HPR) was developed in the 1970’s as a means to induce retinoid cancer preventive effects in cells and tissues… (more)

Subjects/Keywords: Local Drug Delivery; Oral Cancer Chemoprevention; Drug-Tissue Penetration Enhancement; Fenretinide; Long-Acting Release Implants; Science (General); Science

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

APA (6th Edition):

Nieto, K. (2017). Long-Acting Release Implants for Local Fenretinide Delivery and Oral Cancer Chemoprevention. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/140855

Chicago Manual of Style (16th Edition):

Nieto, Kari. “Long-Acting Release Implants for Local Fenretinide Delivery and Oral Cancer Chemoprevention.” 2017. Doctoral Dissertation, University of Michigan. Accessed March 23, 2019. http://hdl.handle.net/2027.42/140855.

MLA Handbook (7th Edition):

Nieto, Kari. “Long-Acting Release Implants for Local Fenretinide Delivery and Oral Cancer Chemoprevention.” 2017. Web. 23 Mar 2019.

Vancouver:

Nieto K. Long-Acting Release Implants for Local Fenretinide Delivery and Oral Cancer Chemoprevention. [Internet] [Doctoral dissertation]. University of Michigan; 2017. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/2027.42/140855.

Council of Science Editors:

Nieto K. Long-Acting Release Implants for Local Fenretinide Delivery and Oral Cancer Chemoprevention. [Doctoral Dissertation]. University of Michigan; 2017. Available from: http://hdl.handle.net/2027.42/140855


Virginia Tech

18. Pavurala, Naresh. Oral Drug Delivery  – Molecular Design and Transport Modeling.

Degree: PhD, Chemical Engineering, 2013, Virginia Tech

 One of the major challenges faced by the pharmaceutical industry is to accelerate the product innovation process and reduce the time-to-market for new drug developments.… (more)

Subjects/Keywords: Oral drug delivery; drug release model; ACAT model; pharmacokinetic model; simulation; optimization; molecular design; structure-property models; novel polymers; release kinetics; oral dosage form; tablet design

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

APA (6th Edition):

Pavurala, N. (2013). Oral Drug Delivery  – Molecular Design and Transport Modeling. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/53505

Chicago Manual of Style (16th Edition):

Pavurala, Naresh. “Oral Drug Delivery  – Molecular Design and Transport Modeling.” 2013. Doctoral Dissertation, Virginia Tech. Accessed March 23, 2019. http://hdl.handle.net/10919/53505.

MLA Handbook (7th Edition):

Pavurala, Naresh. “Oral Drug Delivery  – Molecular Design and Transport Modeling.” 2013. Web. 23 Mar 2019.

Vancouver:

Pavurala N. Oral Drug Delivery  – Molecular Design and Transport Modeling. [Internet] [Doctoral dissertation]. Virginia Tech; 2013. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/10919/53505.

Council of Science Editors:

Pavurala N. Oral Drug Delivery  – Molecular Design and Transport Modeling. [Doctoral Dissertation]. Virginia Tech; 2013. Available from: http://hdl.handle.net/10919/53505


Northeastern University

19. Attarwala, Husain. Multi-compartmental oral delivery systems for silencing intestinal tissue transglutaminase-2 and interleukin-15 genes in the treatment of celiac disease.

Degree: PhD, Pharmaceutics and Drug Delivery Program, 2016, Northeastern University

 Celiac disease is caused by an immune response against cereal gluten peptides in the small intestine. The dietary ingestion of gluten triggers a cascade of… (more)

Subjects/Keywords: gelatin nanoparticles; interleukin-15; multi-compartmental delivery systems; oral siRNA delivery; transglutaminase-2; Gene silencing; Small interfering RNA; Drug delivery systems; Transglutaminases; Cytokines; Nanoparticles; Celiac disease; Treatment

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APA (6th Edition):

Attarwala, H. (2016). Multi-compartmental oral delivery systems for silencing intestinal tissue transglutaminase-2 and interleukin-15 genes in the treatment of celiac disease. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/D20213355

Chicago Manual of Style (16th Edition):

Attarwala, Husain. “Multi-compartmental oral delivery systems for silencing intestinal tissue transglutaminase-2 and interleukin-15 genes in the treatment of celiac disease.” 2016. Doctoral Dissertation, Northeastern University. Accessed March 23, 2019. http://hdl.handle.net/2047/D20213355.

MLA Handbook (7th Edition):

Attarwala, Husain. “Multi-compartmental oral delivery systems for silencing intestinal tissue transglutaminase-2 and interleukin-15 genes in the treatment of celiac disease.” 2016. Web. 23 Mar 2019.

Vancouver:

Attarwala H. Multi-compartmental oral delivery systems for silencing intestinal tissue transglutaminase-2 and interleukin-15 genes in the treatment of celiac disease. [Internet] [Doctoral dissertation]. Northeastern University; 2016. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/2047/D20213355.

Council of Science Editors:

Attarwala H. Multi-compartmental oral delivery systems for silencing intestinal tissue transglutaminase-2 and interleukin-15 genes in the treatment of celiac disease. [Doctoral Dissertation]. Northeastern University; 2016. Available from: http://hdl.handle.net/2047/D20213355


University of Utah

20. Singhal, Dharmendra. Enzymatic barrier to oral and central nervous system delivery of anti-HIV nucleoside reverse transcriptase inhibitors;.

Degree: PhD, Pharmaceutics & Pharmaceutical Chemistry;, 1996, University of Utah

 Most of the dideoxynucleoside reverse transcriptase inhibitors used for treating HIV infection in humans exhibit very low central nervous system (CNS) uptake due to unknown… (more)

Subjects/Keywords: Oral Drug Delivery; HIV: Immune Deficiency; AIDS; Pharmacology: Pharmaceuticals

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APA (6th Edition):

Singhal, D. (1996). Enzymatic barrier to oral and central nervous system delivery of anti-HIV nucleoside reverse transcriptase inhibitors;. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/32/rec/454

Chicago Manual of Style (16th Edition):

Singhal, Dharmendra. “Enzymatic barrier to oral and central nervous system delivery of anti-HIV nucleoside reverse transcriptase inhibitors;.” 1996. Doctoral Dissertation, University of Utah. Accessed March 23, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/32/rec/454.

MLA Handbook (7th Edition):

Singhal, Dharmendra. “Enzymatic barrier to oral and central nervous system delivery of anti-HIV nucleoside reverse transcriptase inhibitors;.” 1996. Web. 23 Mar 2019.

Vancouver:

Singhal D. Enzymatic barrier to oral and central nervous system delivery of anti-HIV nucleoside reverse transcriptase inhibitors;. [Internet] [Doctoral dissertation]. University of Utah; 1996. [cited 2019 Mar 23]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/32/rec/454.

Council of Science Editors:

Singhal D. Enzymatic barrier to oral and central nervous system delivery of anti-HIV nucleoside reverse transcriptase inhibitors;. [Doctoral Dissertation]. University of Utah; 1996. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/32/rec/454

21. Kshirsagar Sanjay J. Design and development of oral dosage forms for colon-specific drug delivery.

Degree: Pharmaceutical Sciences, 2011, Jawaharlal Nehru Technological University

None

References included

Advisors/Committee Members: Bhalekar, Mangesh R.

Subjects/Keywords: Pharmaceutical Sciences; Oral dosage; Colon-specific drug delivery

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APA (6th Edition):

J, K. S. (2011). Design and development of oral dosage forms for colon-specific drug delivery. (Thesis). Jawaharlal Nehru Technological University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/8337

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):

J, Kshirsagar Sanjay. “Design and development of oral dosage forms for colon-specific drug delivery.” 2011. Thesis, Jawaharlal Nehru Technological University. Accessed March 23, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/8337.

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

MLA Handbook (7th Edition):

J, Kshirsagar Sanjay. “Design and development of oral dosage forms for colon-specific drug delivery.” 2011. Web. 23 Mar 2019.

Vancouver:

J KS. Design and development of oral dosage forms for colon-specific drug delivery. [Internet] [Thesis]. Jawaharlal Nehru Technological University; 2011. [cited 2019 Mar 23]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/8337.

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

Council of Science Editors:

J KS. Design and development of oral dosage forms for colon-specific drug delivery. [Thesis]. Jawaharlal Nehru Technological University; 2011. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/8337

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

22. Bharani Madasu. Comparative evaluation of different cyclodextrins and methods of preparations for improving oral bioavailability of BCS class II drugs Saquinavir and Ritonavir; -.

Degree: pharmacy, 2013, Andhra University

None

References given chapter wise

Advisors/Committee Members: Ramana Murthy, K V.

Subjects/Keywords: pharmacy; oral drug delivery; Cyclodextrins; Saquinavir; Ritonavir; cyclodextrins

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APA (6th Edition):

Madasu, B. (2013). Comparative evaluation of different cyclodextrins and methods of preparations for improving oral bioavailability of BCS class II drugs Saquinavir and Ritonavir; -. (Thesis). Andhra University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/8719

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):

Madasu, Bharani. “Comparative evaluation of different cyclodextrins and methods of preparations for improving oral bioavailability of BCS class II drugs Saquinavir and Ritonavir; -.” 2013. Thesis, Andhra University. Accessed March 23, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/8719.

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

MLA Handbook (7th Edition):

Madasu, Bharani. “Comparative evaluation of different cyclodextrins and methods of preparations for improving oral bioavailability of BCS class II drugs Saquinavir and Ritonavir; -.” 2013. Web. 23 Mar 2019.

Vancouver:

Madasu B. Comparative evaluation of different cyclodextrins and methods of preparations for improving oral bioavailability of BCS class II drugs Saquinavir and Ritonavir; -. [Internet] [Thesis]. Andhra University; 2013. [cited 2019 Mar 23]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/8719.

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

Council of Science Editors:

Madasu B. Comparative evaluation of different cyclodextrins and methods of preparations for improving oral bioavailability of BCS class II drugs Saquinavir and Ritonavir; -. [Thesis]. Andhra University; 2013. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/8719

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

23. Sarangdhar, Asane Govind. Designing and development of Antiprotozoal Mucoadhesive oral drug delivery system;.

Degree: 2010, Jawaharlal Nehru Technological University

Subjects/Keywords: Pharmaceutical Science; Oral drug delivery system; Model Drugs

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APA (6th Edition):

Sarangdhar, A. G. (2010). Designing and development of Antiprotozoal Mucoadhesive oral drug delivery system;. (Thesis). Jawaharlal Nehru Technological University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/2179

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):

Sarangdhar, Asane Govind. “Designing and development of Antiprotozoal Mucoadhesive oral drug delivery system;.” 2010. Thesis, Jawaharlal Nehru Technological University. Accessed March 23, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/2179.

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

MLA Handbook (7th Edition):

Sarangdhar, Asane Govind. “Designing and development of Antiprotozoal Mucoadhesive oral drug delivery system;.” 2010. Web. 23 Mar 2019.

Vancouver:

Sarangdhar AG. Designing and development of Antiprotozoal Mucoadhesive oral drug delivery system;. [Internet] [Thesis]. Jawaharlal Nehru Technological University; 2010. [cited 2019 Mar 23]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/2179.

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

Council of Science Editors:

Sarangdhar AG. Designing and development of Antiprotozoal Mucoadhesive oral drug delivery system;. [Thesis]. Jawaharlal Nehru Technological University; 2010. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/2179

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


Wright State University

24. Flannery, Tiffany L. Enhanced Neurogenesis In Subventricular Zone Of Rats That Voluntarily Ingest Fluoxetine And Simavastatin Combination Treatment.

Degree: MS, Biological Sciences, 2017, Wright State University

 Stroke is one of the leading causes of deaths as the risk factors, both controllable and uncontrollable, are many. We first concentrated on a stress-free… (more)

Subjects/Keywords: Biology; Anatomy and Physiology; Pharmacology; Neurobiology; neurogenesis; rat; subventricular zone; fluoxetine; simvastatin; voluntary oral drug delivery; sham surgery

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APA (6th Edition):

Flannery, T. L. (2017). Enhanced Neurogenesis In Subventricular Zone Of Rats That Voluntarily Ingest Fluoxetine And Simavastatin Combination Treatment. (Masters Thesis). Wright State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=wright1484566200182717

Chicago Manual of Style (16th Edition):

Flannery, Tiffany L. “Enhanced Neurogenesis In Subventricular Zone Of Rats That Voluntarily Ingest Fluoxetine And Simavastatin Combination Treatment.” 2017. Masters Thesis, Wright State University. Accessed March 23, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=wright1484566200182717.

MLA Handbook (7th Edition):

Flannery, Tiffany L. “Enhanced Neurogenesis In Subventricular Zone Of Rats That Voluntarily Ingest Fluoxetine And Simavastatin Combination Treatment.” 2017. Web. 23 Mar 2019.

Vancouver:

Flannery TL. Enhanced Neurogenesis In Subventricular Zone Of Rats That Voluntarily Ingest Fluoxetine And Simavastatin Combination Treatment. [Internet] [Masters thesis]. Wright State University; 2017. [cited 2019 Mar 23]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1484566200182717.

Council of Science Editors:

Flannery TL. Enhanced Neurogenesis In Subventricular Zone Of Rats That Voluntarily Ingest Fluoxetine And Simavastatin Combination Treatment. [Masters Thesis]. Wright State University; 2017. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1484566200182717


University of Otago

25. Parayath, Neha Nitin. Styrene maleic acid micelles as a nanocarrier system for oral anticancer drug delivery .

Degree: University of Otago

 ABSTRACT The oral route is the preferred mode of drug administration due to its non-invasive nature, economical benefits, and the potential to improve patients’ quality… (more)

Subjects/Keywords: Nanomedicine; Drug Delivery; Oral Administration; Nanomicelles; Colon Cancer

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APA (6th Edition):

Parayath, N. N. (n.d.). Styrene maleic acid micelles as a nanocarrier system for oral anticancer drug delivery . (Doctoral Dissertation). University of Otago. Retrieved from http://hdl.handle.net/10523/6274

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Chicago Manual of Style (16th Edition):

Parayath, Neha Nitin. “Styrene maleic acid micelles as a nanocarrier system for oral anticancer drug delivery .” Doctoral Dissertation, University of Otago. Accessed March 23, 2019. http://hdl.handle.net/10523/6274.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

MLA Handbook (7th Edition):

Parayath, Neha Nitin. “Styrene maleic acid micelles as a nanocarrier system for oral anticancer drug delivery .” Web. 23 Mar 2019.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Parayath NN. Styrene maleic acid micelles as a nanocarrier system for oral anticancer drug delivery . [Internet] [Doctoral dissertation]. University of Otago; [cited 2019 Mar 23]. Available from: http://hdl.handle.net/10523/6274.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Council of Science Editors:

Parayath NN. Styrene maleic acid micelles as a nanocarrier system for oral anticancer drug delivery . [Doctoral Dissertation]. University of Otago; Available from: http://hdl.handle.net/10523/6274

Note: this citation may be lacking information needed for this citation format:
No year of publication.


University of Illinois – Chicago

26. Shen, Hao. Continuous Production of Stable Polymeric Nanoparticles for Oral Drug Delivery.

Degree: 2013, University of Illinois – Chicago

 Minimal bioavailability of hydrophobic compounds limits their biomedical and biological applications. In this thesis, we have developed a continuous and scalable process to generate stable… (more)

Subjects/Keywords: polymeric nanoparticles: oral drug delivery; flash nanoprecipitation; multi-inlet vortex mixer; spray drying; chemoprevention, morphine tolerance and dependence

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APA (6th Edition):

Shen, H. (2013). Continuous Production of Stable Polymeric Nanoparticles for Oral Drug Delivery. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/10360

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):

Shen, Hao. “Continuous Production of Stable Polymeric Nanoparticles for Oral Drug Delivery.” 2013. Thesis, University of Illinois – Chicago. Accessed March 23, 2019. http://hdl.handle.net/10027/10360.

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

MLA Handbook (7th Edition):

Shen, Hao. “Continuous Production of Stable Polymeric Nanoparticles for Oral Drug Delivery.” 2013. Web. 23 Mar 2019.

Vancouver:

Shen H. Continuous Production of Stable Polymeric Nanoparticles for Oral Drug Delivery. [Internet] [Thesis]. University of Illinois – Chicago; 2013. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/10027/10360.

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

Council of Science Editors:

Shen H. Continuous Production of Stable Polymeric Nanoparticles for Oral Drug Delivery. [Thesis]. University of Illinois – Chicago; 2013. Available from: http://hdl.handle.net/10027/10360

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


Clemson University

27. Blichmann, Paul. ORAL DELIVERY OF PEPTIDE DRUGS FOR MITIGATION OF CROHN'S DISEASE.

Degree: MS, Bioengineering, 2012, Clemson University

  Protein drugs are typically administered intravenously, but this practice has clear disadvantages such as widespread circulation and swift clearance from the body. Orally delivered… (more)

Subjects/Keywords: colon targeting; controlled release; Inflammatory Bowel Disease; MUC1 targeting; oral drug delivery; peptide drugs; Biomedical Engineering and Bioengineering

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

APA (6th Edition):

Blichmann, P. (2012). ORAL DELIVERY OF PEPTIDE DRUGS FOR MITIGATION OF CROHN'S DISEASE. (Masters Thesis). Clemson University. Retrieved from https://tigerprints.clemson.edu/all_theses/1486

Chicago Manual of Style (16th Edition):

Blichmann, Paul. “ORAL DELIVERY OF PEPTIDE DRUGS FOR MITIGATION OF CROHN'S DISEASE.” 2012. Masters Thesis, Clemson University. Accessed March 23, 2019. https://tigerprints.clemson.edu/all_theses/1486.

MLA Handbook (7th Edition):

Blichmann, Paul. “ORAL DELIVERY OF PEPTIDE DRUGS FOR MITIGATION OF CROHN'S DISEASE.” 2012. Web. 23 Mar 2019.

Vancouver:

Blichmann P. ORAL DELIVERY OF PEPTIDE DRUGS FOR MITIGATION OF CROHN'S DISEASE. [Internet] [Masters thesis]. Clemson University; 2012. [cited 2019 Mar 23]. Available from: https://tigerprints.clemson.edu/all_theses/1486.

Council of Science Editors:

Blichmann P. ORAL DELIVERY OF PEPTIDE DRUGS FOR MITIGATION OF CROHN'S DISEASE. [Masters Thesis]. Clemson University; 2012. Available from: https://tigerprints.clemson.edu/all_theses/1486


Wayne State University

28. Bharatwaj, Balaji. Polymeric nanocarriers for the regional and systemic delivery of therapeutics to and through the lungs.

Degree: PhD, Chemical Engineering and Materials Science, 2012, Wayne State University

  The lungs are considered as one of the fastest portals of entry to the bloodstream and oral inhalation (OI) has long been accepted as… (more)

Subjects/Keywords: Dendrimers, Oral Inhalation, PEGylation, Polymeric Nanocarriers, Pulmonary Drug Delivery, Transport Modulation; Chemical Engineering; Nanoscience and Nanotechnology

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

APA (6th Edition):

Bharatwaj, B. (2012). Polymeric nanocarriers for the regional and systemic delivery of therapeutics to and through the lungs. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/426

Chicago Manual of Style (16th Edition):

Bharatwaj, Balaji. “Polymeric nanocarriers for the regional and systemic delivery of therapeutics to and through the lungs.” 2012. Doctoral Dissertation, Wayne State University. Accessed March 23, 2019. https://digitalcommons.wayne.edu/oa_dissertations/426.

MLA Handbook (7th Edition):

Bharatwaj, Balaji. “Polymeric nanocarriers for the regional and systemic delivery of therapeutics to and through the lungs.” 2012. Web. 23 Mar 2019.

Vancouver:

Bharatwaj B. Polymeric nanocarriers for the regional and systemic delivery of therapeutics to and through the lungs. [Internet] [Doctoral dissertation]. Wayne State University; 2012. [cited 2019 Mar 23]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/426.

Council of Science Editors:

Bharatwaj B. Polymeric nanocarriers for the regional and systemic delivery of therapeutics to and through the lungs. [Doctoral Dissertation]. Wayne State University; 2012. Available from: https://digitalcommons.wayne.edu/oa_dissertations/426


Virginia Tech

29. Dong, Yifan. Design and Synthesis of Cellulose Ether Derivatives for Oral Drug Delivery.

Degree: PhD, Chemistry, 2017, Virginia Tech

 Chemical modification of naturally occurring cellulose into ester and ether derivatives has been of growing interest due to inexhaustible cellulose resources, and to excellent properties… (more)

Subjects/Keywords: cellulose ethers; design and synthesis; oral drug delivery; olefin cross-metathesis; thiol-Michael addition; amorphous solid dispersion

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

APA (6th Edition):

Dong, Y. (2017). Design and Synthesis of Cellulose Ether Derivatives for Oral Drug Delivery. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/86141

Chicago Manual of Style (16th Edition):

Dong, Yifan. “Design and Synthesis of Cellulose Ether Derivatives for Oral Drug Delivery.” 2017. Doctoral Dissertation, Virginia Tech. Accessed March 23, 2019. http://hdl.handle.net/10919/86141.

MLA Handbook (7th Edition):

Dong, Yifan. “Design and Synthesis of Cellulose Ether Derivatives for Oral Drug Delivery.” 2017. Web. 23 Mar 2019.

Vancouver:

Dong Y. Design and Synthesis of Cellulose Ether Derivatives for Oral Drug Delivery. [Internet] [Doctoral dissertation]. Virginia Tech; 2017. [cited 2019 Mar 23]. Available from: http://hdl.handle.net/10919/86141.

Council of Science Editors:

Dong Y. Design and Synthesis of Cellulose Ether Derivatives for Oral Drug Delivery. [Doctoral Dissertation]. Virginia Tech; 2017. Available from: http://hdl.handle.net/10919/86141

30. Joshi, Amita. Oral modified multiparticulate drug delivery system for the treatment of tuberculosis;.

Degree: 2010, Nirma University

References p.152-156, Summary p. 157-161 Advisors/Committee Members: Nivsarkar, Manish.

Subjects/Keywords: Oral multiparticulate drug delivery system; Drug delivery system; Drugs; Hydrodynamically balanced systems; Floating drug delivery system; Fixed Dose Combination; Tuberculosis

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

APA (6th Edition):

Joshi, A. (2010). Oral modified multiparticulate drug delivery system for the treatment of tuberculosis;. (Thesis). Nirma University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/2369

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):

Joshi, Amita. “Oral modified multiparticulate drug delivery system for the treatment of tuberculosis;.” 2010. Thesis, Nirma University. Accessed March 23, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/2369.

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

MLA Handbook (7th Edition):

Joshi, Amita. “Oral modified multiparticulate drug delivery system for the treatment of tuberculosis;.” 2010. Web. 23 Mar 2019.

Vancouver:

Joshi A. Oral modified multiparticulate drug delivery system for the treatment of tuberculosis;. [Internet] [Thesis]. Nirma University; 2010. [cited 2019 Mar 23]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/2369.

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

Council of Science Editors:

Joshi A. Oral modified multiparticulate drug delivery system for the treatment of tuberculosis;. [Thesis]. Nirma University; 2010. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/2369

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

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