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You searched for subject:(Sustained release). Showing records 1 – 30 of 71 total matches.

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University of Otago

1. Kojarunchitt, Thunjiradasiree. Sustained release thermoresponsive hydrogels for vaccine delivery .

Degree: 2013, University of Otago

 Purpose: Modern vaccine development has concentrated on the use of highly purified peptides and proteins as target antigens. While these subunit antigens exhibit good safety… (more)

Subjects/Keywords: Thermoresponsive hydrogels; Vaccine-sustained release

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APA (6th Edition):

Kojarunchitt, T. (2013). Sustained release thermoresponsive hydrogels for vaccine delivery . (Doctoral Dissertation). University of Otago. Retrieved from http://hdl.handle.net/10523/4377

Chicago Manual of Style (16th Edition):

Kojarunchitt, Thunjiradasiree. “Sustained release thermoresponsive hydrogels for vaccine delivery .” 2013. Doctoral Dissertation, University of Otago. Accessed August 15, 2018. http://hdl.handle.net/10523/4377.

MLA Handbook (7th Edition):

Kojarunchitt, Thunjiradasiree. “Sustained release thermoresponsive hydrogels for vaccine delivery .” 2013. Web. 15 Aug 2018.

Vancouver:

Kojarunchitt T. Sustained release thermoresponsive hydrogels for vaccine delivery . [Internet] [Doctoral dissertation]. University of Otago; 2013. [cited 2018 Aug 15]. Available from: http://hdl.handle.net/10523/4377.

Council of Science Editors:

Kojarunchitt T. Sustained release thermoresponsive hydrogels for vaccine delivery . [Doctoral Dissertation]. University of Otago; 2013. Available from: http://hdl.handle.net/10523/4377


Dalhousie University

2. Parikh, Ankit. Novel sustained release biodegradable drug delivery system for targeting chronic rhinosinusitis.

Degree: MS, College of Pharmacy, 2014, Dalhousie University

 Chronic rhinosinusitis (CRS) is a condition in which the nasal cavity and the paranasal sinuses become inflammed causing facial pressure, pain, headache, nasal obstruction and… (more)

Subjects/Keywords: sustained release; biodegradable; microparticles; implant; hydrogel; sponge; chronic rhinosinusitis

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APA (6th Edition):

Parikh, A. (2014). Novel sustained release biodegradable drug delivery system for targeting chronic rhinosinusitis. (Masters Thesis). Dalhousie University. Retrieved from http://hdl.handle.net/10222/53977

Chicago Manual of Style (16th Edition):

Parikh, Ankit. “Novel sustained release biodegradable drug delivery system for targeting chronic rhinosinusitis.” 2014. Masters Thesis, Dalhousie University. Accessed August 15, 2018. http://hdl.handle.net/10222/53977.

MLA Handbook (7th Edition):

Parikh, Ankit. “Novel sustained release biodegradable drug delivery system for targeting chronic rhinosinusitis.” 2014. Web. 15 Aug 2018.

Vancouver:

Parikh A. Novel sustained release biodegradable drug delivery system for targeting chronic rhinosinusitis. [Internet] [Masters thesis]. Dalhousie University; 2014. [cited 2018 Aug 15]. Available from: http://hdl.handle.net/10222/53977.

Council of Science Editors:

Parikh A. Novel sustained release biodegradable drug delivery system for targeting chronic rhinosinusitis. [Masters Thesis]. Dalhousie University; 2014. Available from: http://hdl.handle.net/10222/53977


Addis Ababa University

3. MULUKEN, NIGATU. MYRRH RESIN (Commiphora myrrha) AS RATE CONTROLLING EXCIPIENT IN SUSTAINED RELEASE MATRIX TABLETS OF THEOPHYLLINE: EVALUATION, FORMULATION AND OPTIMIZATION STUDY .

Degree: 2014, Addis Ababa University

 Myrrh is an oleo-gum resin, obtained from the stem of various species of Commiphora, Family Burseraceae. The chief source is Commiphora myrrha. Myrrh is phytotoxically… (more)

Subjects/Keywords: Myrrh resin; theophylline; sustained release; matrix tablet; optimization; central composite design

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APA (6th Edition):

MULUKEN, N. (2014). MYRRH RESIN (Commiphora myrrha) AS RATE CONTROLLING EXCIPIENT IN SUSTAINED RELEASE MATRIX TABLETS OF THEOPHYLLINE: EVALUATION, FORMULATION AND OPTIMIZATION STUDY . (Thesis). Addis Ababa University. Retrieved from http://etd.aau.edu.et/dspace/handle/123456789/6068

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):

MULUKEN, NIGATU. “MYRRH RESIN (Commiphora myrrha) AS RATE CONTROLLING EXCIPIENT IN SUSTAINED RELEASE MATRIX TABLETS OF THEOPHYLLINE: EVALUATION, FORMULATION AND OPTIMIZATION STUDY .” 2014. Thesis, Addis Ababa University. Accessed August 15, 2018. http://etd.aau.edu.et/dspace/handle/123456789/6068.

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

MLA Handbook (7th Edition):

MULUKEN, NIGATU. “MYRRH RESIN (Commiphora myrrha) AS RATE CONTROLLING EXCIPIENT IN SUSTAINED RELEASE MATRIX TABLETS OF THEOPHYLLINE: EVALUATION, FORMULATION AND OPTIMIZATION STUDY .” 2014. Web. 15 Aug 2018.

Vancouver:

MULUKEN N. MYRRH RESIN (Commiphora myrrha) AS RATE CONTROLLING EXCIPIENT IN SUSTAINED RELEASE MATRIX TABLETS OF THEOPHYLLINE: EVALUATION, FORMULATION AND OPTIMIZATION STUDY . [Internet] [Thesis]. Addis Ababa University; 2014. [cited 2018 Aug 15]. Available from: http://etd.aau.edu.et/dspace/handle/123456789/6068.

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

Council of Science Editors:

MULUKEN N. MYRRH RESIN (Commiphora myrrha) AS RATE CONTROLLING EXCIPIENT IN SUSTAINED RELEASE MATRIX TABLETS OF THEOPHYLLINE: EVALUATION, FORMULATION AND OPTIMIZATION STUDY . [Thesis]. Addis Ababa University; 2014. Available from: http://etd.aau.edu.et/dspace/handle/123456789/6068

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


Addis Ababa University

4. Lidia, Tesfaye. ENHANCING THE DISSOLUTION AND SUSTAINING THE RELEASE OF DICLOFENAC SODIUM USING THE METHOD LIQUISOLID TECHNOLOGY .

Degree: 2014, Addis Ababa University

 Various methods of modifying solubility and dissolution properties of drugs have been developed over the years. Methods such as liquisolid technology, which can be used… (more)

Subjects/Keywords: Liquisolid compact; Diclofenac Sodium; Solubility; Dissolution; Sustained release.

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APA (6th Edition):

Lidia, T. (2014). ENHANCING THE DISSOLUTION AND SUSTAINING THE RELEASE OF DICLOFENAC SODIUM USING THE METHOD LIQUISOLID TECHNOLOGY . (Thesis). Addis Ababa University. Retrieved from http://etd.aau.edu.et/dspace/handle/123456789/6084

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):

Lidia, Tesfaye. “ENHANCING THE DISSOLUTION AND SUSTAINING THE RELEASE OF DICLOFENAC SODIUM USING THE METHOD LIQUISOLID TECHNOLOGY .” 2014. Thesis, Addis Ababa University. Accessed August 15, 2018. http://etd.aau.edu.et/dspace/handle/123456789/6084.

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

MLA Handbook (7th Edition):

Lidia, Tesfaye. “ENHANCING THE DISSOLUTION AND SUSTAINING THE RELEASE OF DICLOFENAC SODIUM USING THE METHOD LIQUISOLID TECHNOLOGY .” 2014. Web. 15 Aug 2018.

Vancouver:

Lidia T. ENHANCING THE DISSOLUTION AND SUSTAINING THE RELEASE OF DICLOFENAC SODIUM USING THE METHOD LIQUISOLID TECHNOLOGY . [Internet] [Thesis]. Addis Ababa University; 2014. [cited 2018 Aug 15]. Available from: http://etd.aau.edu.et/dspace/handle/123456789/6084.

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

Council of Science Editors:

Lidia T. ENHANCING THE DISSOLUTION AND SUSTAINING THE RELEASE OF DICLOFENAC SODIUM USING THE METHOD LIQUISOLID TECHNOLOGY . [Thesis]. Addis Ababa University; 2014. Available from: http://etd.aau.edu.et/dspace/handle/123456789/6084

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


Addis Ababa University

5. Yohaness, Mulualem. Preparation and Evaluation of Dual Modified Ethiopian Yam (Dioscorea abyssinica) Starch for Sustained Release Tablet Formulation .

Degree: 2013, Addis Ababa University

 Starch has been the subject of intensive research over many decades due to the fact that native starches are diverse, biodegradable, applications are enormous and… (more)

Subjects/Keywords: Dioscorea abyssinica; Boyna starch; Cross-linking; Acetylation; Dual modification; Sustained release.

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APA (6th Edition):

Yohaness, M. (2013). Preparation and Evaluation of Dual Modified Ethiopian Yam (Dioscorea abyssinica) Starch for Sustained Release Tablet Formulation . (Thesis). Addis Ababa University. Retrieved from http://etd.aau.edu.et/dspace/handle/123456789/6092

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):

Yohaness, Mulualem. “Preparation and Evaluation of Dual Modified Ethiopian Yam (Dioscorea abyssinica) Starch for Sustained Release Tablet Formulation .” 2013. Thesis, Addis Ababa University. Accessed August 15, 2018. http://etd.aau.edu.et/dspace/handle/123456789/6092.

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

MLA Handbook (7th Edition):

Yohaness, Mulualem. “Preparation and Evaluation of Dual Modified Ethiopian Yam (Dioscorea abyssinica) Starch for Sustained Release Tablet Formulation .” 2013. Web. 15 Aug 2018.

Vancouver:

Yohaness M. Preparation and Evaluation of Dual Modified Ethiopian Yam (Dioscorea abyssinica) Starch for Sustained Release Tablet Formulation . [Internet] [Thesis]. Addis Ababa University; 2013. [cited 2018 Aug 15]. Available from: http://etd.aau.edu.et/dspace/handle/123456789/6092.

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

Council of Science Editors:

Yohaness M. Preparation and Evaluation of Dual Modified Ethiopian Yam (Dioscorea abyssinica) Starch for Sustained Release Tablet Formulation . [Thesis]. Addis Ababa University; 2013. Available from: http://etd.aau.edu.et/dspace/handle/123456789/6092

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


University of Otago

6. Pirayavaraporn, Chompak. The effect of moisture during thermal treatment of directly compressed Eudragit ®RLPO matrices .

Degree: 2012, University of Otago

 Purpose: This thesis investigated of the effect of moisture on a polymeric matrix system. The effect of moisture on compaction and coalescence behaviours, which are… (more)

Subjects/Keywords: Matrix systems; Moisture; Eudragit; Methacrylates; Sustained release tablets; Coalescence; Humidity

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APA (6th Edition):

Pirayavaraporn, C. (2012). The effect of moisture during thermal treatment of directly compressed Eudragit ®RLPO matrices . (Doctoral Dissertation). University of Otago. Retrieved from http://hdl.handle.net/10523/2512

Chicago Manual of Style (16th Edition):

Pirayavaraporn, Chompak. “The effect of moisture during thermal treatment of directly compressed Eudragit ®RLPO matrices .” 2012. Doctoral Dissertation, University of Otago. Accessed August 15, 2018. http://hdl.handle.net/10523/2512.

MLA Handbook (7th Edition):

Pirayavaraporn, Chompak. “The effect of moisture during thermal treatment of directly compressed Eudragit ®RLPO matrices .” 2012. Web. 15 Aug 2018.

Vancouver:

Pirayavaraporn C. The effect of moisture during thermal treatment of directly compressed Eudragit ®RLPO matrices . [Internet] [Doctoral dissertation]. University of Otago; 2012. [cited 2018 Aug 15]. Available from: http://hdl.handle.net/10523/2512.

Council of Science Editors:

Pirayavaraporn C. The effect of moisture during thermal treatment of directly compressed Eudragit ®RLPO matrices . [Doctoral Dissertation]. University of Otago; 2012. Available from: http://hdl.handle.net/10523/2512


University of Waterloo

7. Alsehli, Mosa. Arborescent Polypeptides for Sustained Drug Delivery Applications.

Degree: 2017, University of Waterloo

 This Ph.D. dissertation describes the synthesis of arborescent copolymers of generations G1 and G2 designed to serve as drug delivery nanocarriers for cancer treatment. Poly(γ-benzyl… (more)

Subjects/Keywords: arborescent poly(benzyl L-glutamate); sustained release; drug delivery; Doxorubicin

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APA (6th Edition):

Alsehli, M. (2017). Arborescent Polypeptides for Sustained Drug Delivery Applications. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/12122

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):

Alsehli, Mosa. “Arborescent Polypeptides for Sustained Drug Delivery Applications.” 2017. Thesis, University of Waterloo. Accessed August 15, 2018. http://hdl.handle.net/10012/12122.

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

MLA Handbook (7th Edition):

Alsehli, Mosa. “Arborescent Polypeptides for Sustained Drug Delivery Applications.” 2017. Web. 15 Aug 2018.

Vancouver:

Alsehli M. Arborescent Polypeptides for Sustained Drug Delivery Applications. [Internet] [Thesis]. University of Waterloo; 2017. [cited 2018 Aug 15]. Available from: http://hdl.handle.net/10012/12122.

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

Council of Science Editors:

Alsehli M. Arborescent Polypeptides for Sustained Drug Delivery Applications. [Thesis]. University of Waterloo; 2017. Available from: http://hdl.handle.net/10012/12122

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


University of Western Ontario

8. Zhang, Yunhan. Dry Powder Coating of Pharmaceutical Pellets with a Novel Rotary Fluidized Bed.

Degree: 2016, University of Western Ontario

 The conventional coating of pharmaceutical pellets is achieved by liquid-based coating techniques using a fluidized bed or a pan coater. However, many restrictions and drawbacks… (more)

Subjects/Keywords: pellets coating; dry powder coating; rotary fluidized bed; drug release; fast release; sustained release; delayed release; Eudragit® EPO; Eudragit® RS/RL; Acryl-EZE

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APA (6th Edition):

Zhang, Y. (2016). Dry Powder Coating of Pharmaceutical Pellets with a Novel Rotary Fluidized Bed. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/3664

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):

Zhang, Yunhan. “Dry Powder Coating of Pharmaceutical Pellets with a Novel Rotary Fluidized Bed.” 2016. Thesis, University of Western Ontario. Accessed August 15, 2018. https://ir.lib.uwo.ca/etd/3664.

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

MLA Handbook (7th Edition):

Zhang, Yunhan. “Dry Powder Coating of Pharmaceutical Pellets with a Novel Rotary Fluidized Bed.” 2016. Web. 15 Aug 2018.

Vancouver:

Zhang Y. Dry Powder Coating of Pharmaceutical Pellets with a Novel Rotary Fluidized Bed. [Internet] [Thesis]. University of Western Ontario; 2016. [cited 2018 Aug 15]. Available from: https://ir.lib.uwo.ca/etd/3664.

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

Council of Science Editors:

Zhang Y. Dry Powder Coating of Pharmaceutical Pellets with a Novel Rotary Fluidized Bed. [Thesis]. University of Western Ontario; 2016. Available from: https://ir.lib.uwo.ca/etd/3664

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


Northeastern University

9. O'Neil, Jacklyn. Controlling drug delivery for the application of extended or sustained-release drug products for parenteral administration.

Degree: MS, Department of Chemistry and Chemical Biology, 2010, Northeastern University

 New therapeutic agents are constantly being developed in order to treat new and current disease states. Many of these new compounds display a narrower therapeutic… (more)

Subjects/Keywords: drug delivery systems; sustained release; extended release; Drugs – Toxicology; Pharmacokinetics – Case studies; Drug delivery systems – Case studies; Chemistry; Medical Biochemistry

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APA (6th Edition):

O'Neil, J. (2010). Controlling drug delivery for the application of extended or sustained-release drug products for parenteral administration. (Masters Thesis). Northeastern University. Retrieved from http://hdl.handle.net/2047/d20000132

Chicago Manual of Style (16th Edition):

O'Neil, Jacklyn. “Controlling drug delivery for the application of extended or sustained-release drug products for parenteral administration.” 2010. Masters Thesis, Northeastern University. Accessed August 15, 2018. http://hdl.handle.net/2047/d20000132.

MLA Handbook (7th Edition):

O'Neil, Jacklyn. “Controlling drug delivery for the application of extended or sustained-release drug products for parenteral administration.” 2010. Web. 15 Aug 2018.

Vancouver:

O'Neil J. Controlling drug delivery for the application of extended or sustained-release drug products for parenteral administration. [Internet] [Masters thesis]. Northeastern University; 2010. [cited 2018 Aug 15]. Available from: http://hdl.handle.net/2047/d20000132.

Council of Science Editors:

O'Neil J. Controlling drug delivery for the application of extended or sustained-release drug products for parenteral administration. [Masters Thesis]. Northeastern University; 2010. Available from: http://hdl.handle.net/2047/d20000132


University of Debrecen

10. Dyatlov, Nikita. Formulation and investigation of Paracetamol sustained release Matrix tablets and their potential influence on fever in childhood .

Degree: DE – Gyógyszerésztudományi Kar, University of Debrecen

 This research consists of 2 parts : theoretical (where I researched and read numerous articles about mechanisms of fever regulation, pharmaceutical management of febrile response… (more)

Subjects/Keywords: matrix tablet; paracetamol; sustained release; modified release; fever

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APA (6th Edition):

Dyatlov, N. (n.d.). Formulation and investigation of Paracetamol sustained release Matrix tablets and their potential influence on fever in childhood . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/240826

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Dyatlov, Nikita. “Formulation and investigation of Paracetamol sustained release Matrix tablets and their potential influence on fever in childhood .” Thesis, University of Debrecen. Accessed August 15, 2018. http://hdl.handle.net/2437/240826.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Dyatlov, Nikita. “Formulation and investigation of Paracetamol sustained release Matrix tablets and their potential influence on fever in childhood .” Web. 15 Aug 2018.

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

Vancouver:

Dyatlov N. Formulation and investigation of Paracetamol sustained release Matrix tablets and their potential influence on fever in childhood . [Internet] [Thesis]. University of Debrecen; [cited 2018 Aug 15]. Available from: http://hdl.handle.net/2437/240826.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

Dyatlov N. Formulation and investigation of Paracetamol sustained release Matrix tablets and their potential influence on fever in childhood . [Thesis]. University of Debrecen; Available from: http://hdl.handle.net/2437/240826

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

11. Rezende, Fabiano de Araújo. Revestimento de grânulos farmacêuticos em leito fluidizado.

Degree: Mestrado, Medicamentos e Cosméticos, 2007, University of São Paulo

Operações de revestimento são amplamente utilizadas em diversos setores industriais, tais como químico, agrícola, alimentício e farmacêutico. Dentre as principais razões para a aplicação de… (more)

Subjects/Keywords: acetaminophen.; fluidized-bed; granules coating; leito fluidizado; liberação modificada; paracetamol.; revestimento de grânulos; sustained-release

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APA (6th Edition):

Rezende, F. d. A. (2007). Revestimento de grânulos farmacêuticos em leito fluidizado. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/60/60137/tde-02102008-163334/ ;

Chicago Manual of Style (16th Edition):

Rezende, Fabiano de Araújo. “Revestimento de grânulos farmacêuticos em leito fluidizado.” 2007. Masters Thesis, University of São Paulo. Accessed August 15, 2018. http://www.teses.usp.br/teses/disponiveis/60/60137/tde-02102008-163334/ ;.

MLA Handbook (7th Edition):

Rezende, Fabiano de Araújo. “Revestimento de grânulos farmacêuticos em leito fluidizado.” 2007. Web. 15 Aug 2018.

Vancouver:

Rezende FdA. Revestimento de grânulos farmacêuticos em leito fluidizado. [Internet] [Masters thesis]. University of São Paulo; 2007. [cited 2018 Aug 15]. Available from: http://www.teses.usp.br/teses/disponiveis/60/60137/tde-02102008-163334/ ;.

Council of Science Editors:

Rezende FdA. Revestimento de grânulos farmacêuticos em leito fluidizado. [Masters Thesis]. University of São Paulo; 2007. Available from: http://www.teses.usp.br/teses/disponiveis/60/60137/tde-02102008-163334/ ;

12. Shah, Kirit R. Sustained delayed release of anti inflammatory drugs; -.

Degree: Pharmacy, 2015, Gujarat University

None newline

-

Advisors/Committee Members: Jani Girish K.

Subjects/Keywords: anti inflammatory drugs; delayed release; Sustained

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APA (6th Edition):

Shah, K. R. (2015). Sustained delayed release of anti inflammatory drugs; -. (Thesis). Gujarat University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/33494

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):

Shah, Kirit R. “Sustained delayed release of anti inflammatory drugs; -.” 2015. Thesis, Gujarat University. Accessed August 15, 2018. http://shodhganga.inflibnet.ac.in/handle/10603/33494.

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

MLA Handbook (7th Edition):

Shah, Kirit R. “Sustained delayed release of anti inflammatory drugs; -.” 2015. Web. 15 Aug 2018.

Vancouver:

Shah KR. Sustained delayed release of anti inflammatory drugs; -. [Internet] [Thesis]. Gujarat University; 2015. [cited 2018 Aug 15]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/33494.

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

Council of Science Editors:

Shah KR. Sustained delayed release of anti inflammatory drugs; -. [Thesis]. Gujarat University; 2015. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/33494

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


University of Adelaide

13. Yan, Liang. Studies of self-assembled substituted poly(acrylate) networks as potential sustained drug delivery systems and of fluorescent conjugated polymer nanoparticles in cell imaging.

Degree: 2016, University of Adelaide

 Polymer networks are promising biomaterials for drug delivery as they have porous structures and are often biocompatible. The general aspects of the host-guest complexation capability… (more)

Subjects/Keywords: host-guest complexation; self-assembly; poly(acrylate) networks; sustained release; conjugated polymer nanoparticles; fluorescence

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APA (6th Edition):

Yan, L. (2016). Studies of self-assembled substituted poly(acrylate) networks as potential sustained drug delivery systems and of fluorescent conjugated polymer nanoparticles in cell imaging. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/103611

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):

Yan, Liang. “Studies of self-assembled substituted poly(acrylate) networks as potential sustained drug delivery systems and of fluorescent conjugated polymer nanoparticles in cell imaging.” 2016. Thesis, University of Adelaide. Accessed August 15, 2018. http://hdl.handle.net/2440/103611.

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

MLA Handbook (7th Edition):

Yan, Liang. “Studies of self-assembled substituted poly(acrylate) networks as potential sustained drug delivery systems and of fluorescent conjugated polymer nanoparticles in cell imaging.” 2016. Web. 15 Aug 2018.

Vancouver:

Yan L. Studies of self-assembled substituted poly(acrylate) networks as potential sustained drug delivery systems and of fluorescent conjugated polymer nanoparticles in cell imaging. [Internet] [Thesis]. University of Adelaide; 2016. [cited 2018 Aug 15]. Available from: http://hdl.handle.net/2440/103611.

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

Council of Science Editors:

Yan L. Studies of self-assembled substituted poly(acrylate) networks as potential sustained drug delivery systems and of fluorescent conjugated polymer nanoparticles in cell imaging. [Thesis]. University of Adelaide; 2016. Available from: http://hdl.handle.net/2440/103611

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


Universidade do Rio Grande do Sul

14. Baja, Karine Gehlen. Farmacocinética do cloridrato de tramadol administrado por via oral em cães com a mutação nt230(del4) no gene MDR1.

Degree: 2013, Universidade do Rio Grande do Sul

 A P-glicoproteína (P-gp) é uma transportadora transmembrana de múltiplos fármacos, produto do gene MDR1 (ABCB1). A P-gp contribui para a função de barreira de vários… (more)

Subjects/Keywords: Tramadol; MDR1; P-glycoprotein; Farmacocinética; Genetic mutation; Farmacogenética; Gogs; Genes MDR; Cães; Sustained release tramadol

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

APA (6th Edition):

Baja, K. G. (2013). Farmacocinética do cloridrato de tramadol administrado por via oral em cães com a mutação nt230(del4) no gene MDR1. (Thesis). Universidade do Rio Grande do Sul. Retrieved from http://hdl.handle.net/10183/79520

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):

Baja, Karine Gehlen. “Farmacocinética do cloridrato de tramadol administrado por via oral em cães com a mutação nt230(del4) no gene MDR1.” 2013. Thesis, Universidade do Rio Grande do Sul. Accessed August 15, 2018. http://hdl.handle.net/10183/79520.

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

MLA Handbook (7th Edition):

Baja, Karine Gehlen. “Farmacocinética do cloridrato de tramadol administrado por via oral em cães com a mutação nt230(del4) no gene MDR1.” 2013. Web. 15 Aug 2018.

Vancouver:

Baja KG. Farmacocinética do cloridrato de tramadol administrado por via oral em cães com a mutação nt230(del4) no gene MDR1. [Internet] [Thesis]. Universidade do Rio Grande do Sul; 2013. [cited 2018 Aug 15]. Available from: http://hdl.handle.net/10183/79520.

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

Council of Science Editors:

Baja KG. Farmacocinética do cloridrato de tramadol administrado por via oral em cães com a mutação nt230(del4) no gene MDR1. [Thesis]. Universidade do Rio Grande do Sul; 2013. Available from: http://hdl.handle.net/10183/79520

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


Université Paris-Sud – Paris XI

15. Giacalone, Giovanna. Implant chargé en nanoparticules pour la libération contrôlée et le ciblage lymphatique de nucléotides et d’analogues nucléotidiques : Multi-stage delivery of nucleotides and nucleotide analogs to lymph nodes and leukocytes.

Degree: Docteur es, Pharmacotechnie et biopharmacie, 2014, Université Paris-Sud – Paris XI

Les nucléotides naturels et les analogues nucléotidiques présentent des activités pharmacologiques importantes : par exemple, le nucléotide adénosine triphosphate (ATP) présente un intérêt pour le… (more)

Subjects/Keywords: Nanoparticules; ATP; Chitosane; Libération prolongée; PLGA; Vectorisation; Nanoparticles; ATP; Chitosan; PLGA; Sustained release; Drug delivery

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APA (6th Edition):

Giacalone, G. (2014). Implant chargé en nanoparticules pour la libération contrôlée et le ciblage lymphatique de nucléotides et d’analogues nucléotidiques : Multi-stage delivery of nucleotides and nucleotide analogs to lymph nodes and leukocytes. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2014PA114845

Chicago Manual of Style (16th Edition):

Giacalone, Giovanna. “Implant chargé en nanoparticules pour la libération contrôlée et le ciblage lymphatique de nucléotides et d’analogues nucléotidiques : Multi-stage delivery of nucleotides and nucleotide analogs to lymph nodes and leukocytes.” 2014. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed August 15, 2018. http://www.theses.fr/2014PA114845.

MLA Handbook (7th Edition):

Giacalone, Giovanna. “Implant chargé en nanoparticules pour la libération contrôlée et le ciblage lymphatique de nucléotides et d’analogues nucléotidiques : Multi-stage delivery of nucleotides and nucleotide analogs to lymph nodes and leukocytes.” 2014. Web. 15 Aug 2018.

Vancouver:

Giacalone G. Implant chargé en nanoparticules pour la libération contrôlée et le ciblage lymphatique de nucléotides et d’analogues nucléotidiques : Multi-stage delivery of nucleotides and nucleotide analogs to lymph nodes and leukocytes. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2014. [cited 2018 Aug 15]. Available from: http://www.theses.fr/2014PA114845.

Council of Science Editors:

Giacalone G. Implant chargé en nanoparticules pour la libération contrôlée et le ciblage lymphatique de nucléotides et d’analogues nucléotidiques : Multi-stage delivery of nucleotides and nucleotide analogs to lymph nodes and leukocytes. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2014. Available from: http://www.theses.fr/2014PA114845


Queens University

16. Allison, Stephanie. Delivery of oseltamivir phosphate and gemcibatine from implantable poly (D,L-lactic-co-glycolic acid) cylinders for the treatment of pancreatic cancer .

Degree: Chemical Engineering, 2015, Queens University

 The aim of the study was to develop implantable poly (D,L-lactic-co-glycolic acid) (PLGA) cylinders capable of releasing oseltamivir phosphate (OP) and gemcitabine (GEM) over 30… (more)

Subjects/Keywords: Drug delivery; Pancreatic cancer; Poly (D,L-lactic-co-glycolic acid); Sustained release

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APA (6th Edition):

Allison, S. (2015). Delivery of oseltamivir phosphate and gemcibatine from implantable poly (D,L-lactic-co-glycolic acid) cylinders for the treatment of pancreatic cancer . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/13572

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):

Allison, Stephanie. “Delivery of oseltamivir phosphate and gemcibatine from implantable poly (D,L-lactic-co-glycolic acid) cylinders for the treatment of pancreatic cancer .” 2015. Thesis, Queens University. Accessed August 15, 2018. http://hdl.handle.net/1974/13572.

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

MLA Handbook (7th Edition):

Allison, Stephanie. “Delivery of oseltamivir phosphate and gemcibatine from implantable poly (D,L-lactic-co-glycolic acid) cylinders for the treatment of pancreatic cancer .” 2015. Web. 15 Aug 2018.

Vancouver:

Allison S. Delivery of oseltamivir phosphate and gemcibatine from implantable poly (D,L-lactic-co-glycolic acid) cylinders for the treatment of pancreatic cancer . [Internet] [Thesis]. Queens University; 2015. [cited 2018 Aug 15]. Available from: http://hdl.handle.net/1974/13572.

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

Council of Science Editors:

Allison S. Delivery of oseltamivir phosphate and gemcibatine from implantable poly (D,L-lactic-co-glycolic acid) cylinders for the treatment of pancreatic cancer . [Thesis]. Queens University; 2015. Available from: http://hdl.handle.net/1974/13572

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


Iowa State University

17. Zhang, Bingqi. Self-assembled pentablock copolymers for selective and sustained gene delivery.

Degree: 2011, Iowa State University

 The poly(diethylaminoethyl methacrylate) (PDEAEM) - Pluronic F127 - PDEAEM pentablock copolymer (PB) gene delivery vector system has been found to possess an inherent selectivity in… (more)

Subjects/Keywords: gene delivery; intracellular trafficking; Pluronic; poly(diethylaminoethyl methacrylate); sustained release; targeting; Biological Engineering; Chemical Engineering

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APA (6th Edition):

Zhang, B. (2011). Self-assembled pentablock copolymers for selective and sustained gene delivery. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/11204

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):

Zhang, Bingqi. “Self-assembled pentablock copolymers for selective and sustained gene delivery.” 2011. Thesis, Iowa State University. Accessed August 15, 2018. https://lib.dr.iastate.edu/etd/11204.

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

MLA Handbook (7th Edition):

Zhang, Bingqi. “Self-assembled pentablock copolymers for selective and sustained gene delivery.” 2011. Web. 15 Aug 2018.

Vancouver:

Zhang B. Self-assembled pentablock copolymers for selective and sustained gene delivery. [Internet] [Thesis]. Iowa State University; 2011. [cited 2018 Aug 15]. Available from: https://lib.dr.iastate.edu/etd/11204.

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

Council of Science Editors:

Zhang B. Self-assembled pentablock copolymers for selective and sustained gene delivery. [Thesis]. Iowa State University; 2011. Available from: https://lib.dr.iastate.edu/etd/11204

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

18. Solfiell, David J. Gold Nanoparticles and Drug Delivery.

Degree: MS(M.S.), Chemistry, 2014, U of Massachusetts : Masters

  Nanoparticles are important tools in biotechnology and biomedical research. Gold nanoparticles (AuNPs) have emerged as a particularly important class of nanobiotechnological tools as a… (more)

Subjects/Keywords: Gold Nanoparticles; Drug Delivery; Hydrophobicity; Protein Delivery; Sustained Release; siRNA; Organic Chemistry

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APA (6th Edition):

Solfiell, D. J. (2014). Gold Nanoparticles and Drug Delivery. (Masters Thesis). U of Massachusetts : Masters. Retrieved from http://scholarworks.umass.edu/theses/1200

Chicago Manual of Style (16th Edition):

Solfiell, David J. “Gold Nanoparticles and Drug Delivery.” 2014. Masters Thesis, U of Massachusetts : Masters. Accessed August 15, 2018. http://scholarworks.umass.edu/theses/1200.

MLA Handbook (7th Edition):

Solfiell, David J. “Gold Nanoparticles and Drug Delivery.” 2014. Web. 15 Aug 2018.

Vancouver:

Solfiell DJ. Gold Nanoparticles and Drug Delivery. [Internet] [Masters thesis]. U of Massachusetts : Masters; 2014. [cited 2018 Aug 15]. Available from: http://scholarworks.umass.edu/theses/1200.

Council of Science Editors:

Solfiell DJ. Gold Nanoparticles and Drug Delivery. [Masters Thesis]. U of Massachusetts : Masters; 2014. Available from: http://scholarworks.umass.edu/theses/1200

19. M. Muthukumaran. Formulation and evaluation of sustained release mucoadhesive bilayer tablets of the active medicament using statistical optimization technique;.

Degree: Pharmaceutical Sciences, 2015, Jawaharlal Nehru Technological University, Anantapuram

No newline

conclusion - 155-157, references- 158-172

Advisors/Committee Members: Dr. D. Dhachinamurthy and Dr. K. B. Chandra Sekhar.

Subjects/Keywords: Bilayer Tablets; Optimization Techniques; Pharmaceutical Sciences; Sustained Release

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APA (6th Edition):

Muthukumaran, M. (2015). Formulation and evaluation of sustained release mucoadhesive bilayer tablets of the active medicament using statistical optimization technique;. (Thesis). Jawaharlal Nehru Technological University, Anantapuram. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/45235

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):

Muthukumaran, M.. “Formulation and evaluation of sustained release mucoadhesive bilayer tablets of the active medicament using statistical optimization technique;.” 2015. Thesis, Jawaharlal Nehru Technological University, Anantapuram. Accessed August 15, 2018. http://shodhganga.inflibnet.ac.in/handle/10603/45235.

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

MLA Handbook (7th Edition):

Muthukumaran, M.. “Formulation and evaluation of sustained release mucoadhesive bilayer tablets of the active medicament using statistical optimization technique;.” 2015. Web. 15 Aug 2018.

Vancouver:

Muthukumaran M. Formulation and evaluation of sustained release mucoadhesive bilayer tablets of the active medicament using statistical optimization technique;. [Internet] [Thesis]. Jawaharlal Nehru Technological University, Anantapuram; 2015. [cited 2018 Aug 15]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/45235.

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

Council of Science Editors:

Muthukumaran M. Formulation and evaluation of sustained release mucoadhesive bilayer tablets of the active medicament using statistical optimization technique;. [Thesis]. Jawaharlal Nehru Technological University, Anantapuram; 2015. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/45235

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

20. Lira, Ana Amélia Moreira. Desenvolvimento, caracterização e avaliação de sistemas microestruturados para veiculação de ácido retinóico na pele.

Degree: PhD, Medicamentos e Cosméticos, 2007, University of São Paulo

Este trabalho propôe o desenvolvimento de micropartículas para veiculação deste fármaco na pele, aumentando a estabilidade da molécula e proporcionando uma liberação sustentada, o que… (more)

Subjects/Keywords: Acid Chitosan Sodium; Ácido retinóico; Alginate; Cutaneous Penetration.; Liberação Sustentada; Microparticles; Micropartículas; Penetração Cutânea; Quitosana Alginato; Retinoic; Sustained release

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

APA (6th Edition):

Lira, A. A. M. (2007). Desenvolvimento, caracterização e avaliação de sistemas microestruturados para veiculação de ácido retinóico na pele. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/60/60137/tde-01122010-105253/ ;

Chicago Manual of Style (16th Edition):

Lira, Ana Amélia Moreira. “Desenvolvimento, caracterização e avaliação de sistemas microestruturados para veiculação de ácido retinóico na pele.” 2007. Doctoral Dissertation, University of São Paulo. Accessed August 15, 2018. http://www.teses.usp.br/teses/disponiveis/60/60137/tde-01122010-105253/ ;.

MLA Handbook (7th Edition):

Lira, Ana Amélia Moreira. “Desenvolvimento, caracterização e avaliação de sistemas microestruturados para veiculação de ácido retinóico na pele.” 2007. Web. 15 Aug 2018.

Vancouver:

Lira AAM. Desenvolvimento, caracterização e avaliação de sistemas microestruturados para veiculação de ácido retinóico na pele. [Internet] [Doctoral dissertation]. University of São Paulo; 2007. [cited 2018 Aug 15]. Available from: http://www.teses.usp.br/teses/disponiveis/60/60137/tde-01122010-105253/ ;.

Council of Science Editors:

Lira AAM. Desenvolvimento, caracterização e avaliação de sistemas microestruturados para veiculação de ácido retinóico na pele. [Doctoral Dissertation]. University of São Paulo; 2007. Available from: http://www.teses.usp.br/teses/disponiveis/60/60137/tde-01122010-105253/ ;


Univerzitet u Beogradu

21. Čalija, Bojan R., 1982-. Funkcionalnost hitozana u formulaciji alginat-hitozan mikročestica kao nosača za nesteroidne antiinflamatorne lekove.

Degree: Farmaceutski fakultet, 2014, Univerzitet u Beogradu

Farmacija - Farmaceutska tehnologija / Pharmacy - Pharmaceutical technology

Prednosti mikročestica u odnosu na konvencionalne nosače lekovitih supstanci ogledaju se u sferičnom obliku, velikom odnosu… (more)

Subjects/Keywords: chitosan; chitosan oligosaccharide; sodium alginate; polyelectrolyte complex; microparticles; naproxen; nonsteroidal antiinflamatory drugs; sustained release; pH sensitivity; experimental design

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APA (6th Edition):

Čalija, Bojan R., 1. (2014). Funkcionalnost hitozana u formulaciji alginat-hitozan mikročestica kao nosača za nesteroidne antiinflamatorne lekove. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:7198/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):

Čalija, Bojan R., 1982-. “Funkcionalnost hitozana u formulaciji alginat-hitozan mikročestica kao nosača za nesteroidne antiinflamatorne lekove.” 2014. Thesis, Univerzitet u Beogradu. Accessed August 15, 2018. https://fedorabg.bg.ac.rs/fedora/get/o:7198/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):

Čalija, Bojan R., 1982-. “Funkcionalnost hitozana u formulaciji alginat-hitozan mikročestica kao nosača za nesteroidne antiinflamatorne lekove.” 2014. Web. 15 Aug 2018.

Vancouver:

Čalija, Bojan R. 1. Funkcionalnost hitozana u formulaciji alginat-hitozan mikročestica kao nosača za nesteroidne antiinflamatorne lekove. [Internet] [Thesis]. Univerzitet u Beogradu; 2014. [cited 2018 Aug 15]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:7198/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:

Čalija, Bojan R. 1. Funkcionalnost hitozana u formulaciji alginat-hitozan mikročestica kao nosača za nesteroidne antiinflamatorne lekove. [Thesis]. Univerzitet u Beogradu; 2014. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:7198/bdef:Content/get

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


University of Akron

22. Ditto, Andrew James. Biodegradable Nanoparticles for Use as an Inhalable Antimicrobial and as a Receptor Targeted Delivery Device.

Degree: PhD, Biomedical Engineering, 2010, University of Akron

 Drug delivery challenges include drug instability, insolubility, dosing, toxicity, and targeting, which can be addressed by encapsulation into degradable nanoparticles that can be modified for… (more)

Subjects/Keywords: Biomedical Research; nanoparticles; drug delivery; antimicrobial; targeted; targeting; folic acid; L-tyrosine; degradable; sustained release; silver; SCC; LTP

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APA (6th Edition):

Ditto, A. J. (2010). Biodegradable Nanoparticles for Use as an Inhalable Antimicrobial and as a Receptor Targeted Delivery Device. (Doctoral Dissertation). University of Akron. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=akron1280335303

Chicago Manual of Style (16th Edition):

Ditto, Andrew James. “Biodegradable Nanoparticles for Use as an Inhalable Antimicrobial and as a Receptor Targeted Delivery Device.” 2010. Doctoral Dissertation, University of Akron. Accessed August 15, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=akron1280335303.

MLA Handbook (7th Edition):

Ditto, Andrew James. “Biodegradable Nanoparticles for Use as an Inhalable Antimicrobial and as a Receptor Targeted Delivery Device.” 2010. Web. 15 Aug 2018.

Vancouver:

Ditto AJ. Biodegradable Nanoparticles for Use as an Inhalable Antimicrobial and as a Receptor Targeted Delivery Device. [Internet] [Doctoral dissertation]. University of Akron; 2010. [cited 2018 Aug 15]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=akron1280335303.

Council of Science Editors:

Ditto AJ. Biodegradable Nanoparticles for Use as an Inhalable Antimicrobial and as a Receptor Targeted Delivery Device. [Doctoral Dissertation]. University of Akron; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=akron1280335303


Virginia Tech

23. Taori, Vijay P. Poly(glycoamidoamine)s: Understanding their Structure and Structure-Bioactivity Relationships.

Degree: PhD, Chemistry, 2010, Virginia Tech

 In order to achieve efficient therapeutic effect, it is important to understand the structure of biomaterials that are used in the therapeutic delivery system. This… (more)

Subjects/Keywords: Layer-by-layer; Poly(glycoamidoamine); Polymer degradation; amide Hydrolysis; Guanidine; Non-viral DNA Delivery; Sustained release; Structure-bioactivity relationship

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

APA (6th Edition):

Taori, V. P. (2010). Poly(glycoamidoamine)s: Understanding their Structure and Structure-Bioactivity Relationships. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/77982

Chicago Manual of Style (16th Edition):

Taori, Vijay P. “Poly(glycoamidoamine)s: Understanding their Structure and Structure-Bioactivity Relationships.” 2010. Doctoral Dissertation, Virginia Tech. Accessed August 15, 2018. http://hdl.handle.net/10919/77982.

MLA Handbook (7th Edition):

Taori, Vijay P. “Poly(glycoamidoamine)s: Understanding their Structure and Structure-Bioactivity Relationships.” 2010. Web. 15 Aug 2018.

Vancouver:

Taori VP. Poly(glycoamidoamine)s: Understanding their Structure and Structure-Bioactivity Relationships. [Internet] [Doctoral dissertation]. Virginia Tech; 2010. [cited 2018 Aug 15]. Available from: http://hdl.handle.net/10919/77982.

Council of Science Editors:

Taori VP. Poly(glycoamidoamine)s: Understanding their Structure and Structure-Bioactivity Relationships. [Doctoral Dissertation]. Virginia Tech; 2010. Available from: http://hdl.handle.net/10919/77982


University of Otago

24. Bobbala, Sharan Kumar Reddy. Novel Injectable Thermoresponsive Hydrogels For Sustained Release Vaccines .

Degree: University of Otago

 Purpose: Current vaccine development has focussed on the use of subunit vaccines that utilise highly purified protein and peptide antigens. Subunit antigens are safe to… (more)

Subjects/Keywords: Thermoresponsive hydrogels; Nanoparticles; Vaccine delivery; Sustained release

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

APA (6th Edition):

Bobbala, S. K. R. (n.d.). Novel Injectable Thermoresponsive Hydrogels For Sustained Release Vaccines . (Doctoral Dissertation). University of Otago. Retrieved from http://hdl.handle.net/10523/6006

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

Chicago Manual of Style (16th Edition):

Bobbala, Sharan Kumar Reddy. “Novel Injectable Thermoresponsive Hydrogels For Sustained Release Vaccines .” Doctoral Dissertation, University of Otago. Accessed August 15, 2018. http://hdl.handle.net/10523/6006.

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

MLA Handbook (7th Edition):

Bobbala, Sharan Kumar Reddy. “Novel Injectable Thermoresponsive Hydrogels For Sustained Release Vaccines .” Web. 15 Aug 2018.

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

Vancouver:

Bobbala SKR. Novel Injectable Thermoresponsive Hydrogels For Sustained Release Vaccines . [Internet] [Doctoral dissertation]. University of Otago; [cited 2018 Aug 15]. Available from: http://hdl.handle.net/10523/6006.

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

Council of Science Editors:

Bobbala SKR. Novel Injectable Thermoresponsive Hydrogels For Sustained Release Vaccines . [Doctoral Dissertation]. University of Otago; Available from: http://hdl.handle.net/10523/6006

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

25. Camargo-Pardo, Javier-Andrés. Systèmes injectables biodégradables pour la libération prolongée d'ivermectine : Injectable biodegradable systems for ivermectine sustained release.

Degree: Docteur es, Sciences de la Vie et de la Santé, 2010, Université Henri Poincaré – Nancy I

Des systèmes injectables de formation in situ ont été utilisés dans les dernières années pour l'obtention de formulations de préparation facile et permettant la libération… (more)

Subjects/Keywords: In situ; Isi; Ism; Libération prolongée; Biocompatible; Biodégradable; Ivermectine; Hsp; In situ; Isi; Ism; Sustained release; Biocompatible; Biodegradable; Ivermectin; Hsp

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

APA (6th Edition):

Camargo-Pardo, J. (2010). Systèmes injectables biodégradables pour la libération prolongée d'ivermectine : Injectable biodegradable systems for ivermectine sustained release. (Doctoral Dissertation). Université Henri Poincaré – Nancy I. Retrieved from http://www.theses.fr/2010NAN10068

Chicago Manual of Style (16th Edition):

Camargo-Pardo, Javier-Andrés. “Systèmes injectables biodégradables pour la libération prolongée d'ivermectine : Injectable biodegradable systems for ivermectine sustained release.” 2010. Doctoral Dissertation, Université Henri Poincaré – Nancy I. Accessed August 15, 2018. http://www.theses.fr/2010NAN10068.

MLA Handbook (7th Edition):

Camargo-Pardo, Javier-Andrés. “Systèmes injectables biodégradables pour la libération prolongée d'ivermectine : Injectable biodegradable systems for ivermectine sustained release.” 2010. Web. 15 Aug 2018.

Vancouver:

Camargo-Pardo J. Systèmes injectables biodégradables pour la libération prolongée d'ivermectine : Injectable biodegradable systems for ivermectine sustained release. [Internet] [Doctoral dissertation]. Université Henri Poincaré – Nancy I; 2010. [cited 2018 Aug 15]. Available from: http://www.theses.fr/2010NAN10068.

Council of Science Editors:

Camargo-Pardo J. Systèmes injectables biodégradables pour la libération prolongée d'ivermectine : Injectable biodegradable systems for ivermectine sustained release. [Doctoral Dissertation]. Université Henri Poincaré – Nancy I; 2010. Available from: http://www.theses.fr/2010NAN10068

26. Cantin, Oriane. PEO hot melt extrudates for controlled drug delivery : Extrudats à base d'oxyde de poly éthylène pour la libération contrôlée.

Degree: Docteur es, Sciences pharmaceutiques, 2016, Université Lille II – Droit et Santé

Parmi les procédés de fabrication continue, l’extrusion par fusion à chaud est une technique dont l’intérêt dans le domaine pharmaceutique est grandissant. Ce procédé permet… (more)

Subjects/Keywords: Oxyde de poly éthylène; Extrusion par fusion à chaud; Libération contrôlée; Poly ethylene oxide; Hot melt extrusion; Sustained release; PEO; PEG

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APA (6th Edition):

Cantin, O. (2016). PEO hot melt extrudates for controlled drug delivery : Extrudats à base d'oxyde de poly éthylène pour la libération contrôlée. (Doctoral Dissertation). Université Lille II – Droit et Santé. Retrieved from http://www.theses.fr/2016LIL2S035

Chicago Manual of Style (16th Edition):

Cantin, Oriane. “PEO hot melt extrudates for controlled drug delivery : Extrudats à base d'oxyde de poly éthylène pour la libération contrôlée.” 2016. Doctoral Dissertation, Université Lille II – Droit et Santé. Accessed August 15, 2018. http://www.theses.fr/2016LIL2S035.

MLA Handbook (7th Edition):

Cantin, Oriane. “PEO hot melt extrudates for controlled drug delivery : Extrudats à base d'oxyde de poly éthylène pour la libération contrôlée.” 2016. Web. 15 Aug 2018.

Vancouver:

Cantin O. PEO hot melt extrudates for controlled drug delivery : Extrudats à base d'oxyde de poly éthylène pour la libération contrôlée. [Internet] [Doctoral dissertation]. Université Lille II – Droit et Santé 2016. [cited 2018 Aug 15]. Available from: http://www.theses.fr/2016LIL2S035.

Council of Science Editors:

Cantin O. PEO hot melt extrudates for controlled drug delivery : Extrudats à base d'oxyde de poly éthylène pour la libération contrôlée. [Doctoral Dissertation]. Université Lille II – Droit et Santé 2016. Available from: http://www.theses.fr/2016LIL2S035


Massey University

27. Booty, Samuel James. Ionically cross-linked alginate hydrogels as drug delivery systems for analgesics in broiler chickens.

Degree: Masters of Science, Chemistry, 2017, Massey University

 Treating birds with analgesic drugs requires continuous injections of near lethal concentrations to maintain the therapeutic dose in the blood plasma. This is due to… (more)

Subjects/Keywords: Colloids; Alginates; Analgesics; Controlled release; Drug delivery systems; Broilers (Poultry); Research Subject Categories::TECHNOLOGY::Chemical engineering::Other chemical engineering; Sodium salicylate; Sodium aspirin; Sustained release; Broiler chicken

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APA (6th Edition):

Booty, S. J. (2017). Ionically cross-linked alginate hydrogels as drug delivery systems for analgesics in broiler chickens. (Masters Thesis). Massey University. Retrieved from http://hdl.handle.net/10179/12167

Chicago Manual of Style (16th Edition):

Booty, Samuel James. “Ionically cross-linked alginate hydrogels as drug delivery systems for analgesics in broiler chickens.” 2017. Masters Thesis, Massey University. Accessed August 15, 2018. http://hdl.handle.net/10179/12167.

MLA Handbook (7th Edition):

Booty, Samuel James. “Ionically cross-linked alginate hydrogels as drug delivery systems for analgesics in broiler chickens.” 2017. Web. 15 Aug 2018.

Vancouver:

Booty SJ. Ionically cross-linked alginate hydrogels as drug delivery systems for analgesics in broiler chickens. [Internet] [Masters thesis]. Massey University; 2017. [cited 2018 Aug 15]. Available from: http://hdl.handle.net/10179/12167.

Council of Science Editors:

Booty SJ. Ionically cross-linked alginate hydrogels as drug delivery systems for analgesics in broiler chickens. [Masters Thesis]. Massey University; 2017. Available from: http://hdl.handle.net/10179/12167


Kyoto University

28. Ito, Ran. Adipogenesis using human adipose tissue-derived stem cells sustaining release of basic fibroblast growth factor .

Degree: 2014, Kyoto University

Subjects/Keywords: Adipogenesis; adipose tissue-derived stem cell(ASC); controlled release; sustained release; bFGF; gelatin

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APA (6th Edition):

Ito, R. (2014). Adipogenesis using human adipose tissue-derived stem cells sustaining release of basic fibroblast growth factor . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/188645

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):

Ito, Ran. “Adipogenesis using human adipose tissue-derived stem cells sustaining release of basic fibroblast growth factor .” 2014. Thesis, Kyoto University. Accessed August 15, 2018. http://hdl.handle.net/2433/188645.

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

MLA Handbook (7th Edition):

Ito, Ran. “Adipogenesis using human adipose tissue-derived stem cells sustaining release of basic fibroblast growth factor .” 2014. Web. 15 Aug 2018.

Vancouver:

Ito R. Adipogenesis using human adipose tissue-derived stem cells sustaining release of basic fibroblast growth factor . [Internet] [Thesis]. Kyoto University; 2014. [cited 2018 Aug 15]. Available from: http://hdl.handle.net/2433/188645.

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

Council of Science Editors:

Ito R. Adipogenesis using human adipose tissue-derived stem cells sustaining release of basic fibroblast growth factor . [Thesis]. Kyoto University; 2014. Available from: http://hdl.handle.net/2433/188645

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


Université Paris-Sud – Paris XI

29. Pivette, Perrine. Microsphères lipidiques obtenues par prilling : du polymorphisme des constituants à la compréhension du mécanisme de libération d'un principe actif hydrosoluble : Lipidic microspheres obtained by a prilling process : from constituents polymorphism to the understanding of the release mechanism of a water soluble drug.

Degree: Docteur es, Pharmacotechnie et biopharmacie, 2011, Université Paris-Sud – Paris XI

Le travail de recherche mené au cours de cette thèse a été effectué dans le cadre d’une collaboration industrielle et a porté sur l’étude des… (more)

Subjects/Keywords: Compritol®; Cinétique de libération; Libération prolongée; Paraffine parafluid; Polymorphisme; Prilling; Compritol®; Sustained Release; Release Mechanism; X-ray diffraction; Lipid excipient; Microspheres; Paraffin; Polymorphism; Prilling

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APA (6th Edition):

Pivette, P. (2011). Microsphères lipidiques obtenues par prilling : du polymorphisme des constituants à la compréhension du mécanisme de libération d'un principe actif hydrosoluble : Lipidic microspheres obtained by a prilling process : from constituents polymorphism to the understanding of the release mechanism of a water soluble drug. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2011PA114811

Chicago Manual of Style (16th Edition):

Pivette, Perrine. “Microsphères lipidiques obtenues par prilling : du polymorphisme des constituants à la compréhension du mécanisme de libération d'un principe actif hydrosoluble : Lipidic microspheres obtained by a prilling process : from constituents polymorphism to the understanding of the release mechanism of a water soluble drug.” 2011. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed August 15, 2018. http://www.theses.fr/2011PA114811.

MLA Handbook (7th Edition):

Pivette, Perrine. “Microsphères lipidiques obtenues par prilling : du polymorphisme des constituants à la compréhension du mécanisme de libération d'un principe actif hydrosoluble : Lipidic microspheres obtained by a prilling process : from constituents polymorphism to the understanding of the release mechanism of a water soluble drug.” 2011. Web. 15 Aug 2018.

Vancouver:

Pivette P. Microsphères lipidiques obtenues par prilling : du polymorphisme des constituants à la compréhension du mécanisme de libération d'un principe actif hydrosoluble : Lipidic microspheres obtained by a prilling process : from constituents polymorphism to the understanding of the release mechanism of a water soluble drug. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2011. [cited 2018 Aug 15]. Available from: http://www.theses.fr/2011PA114811.

Council of Science Editors:

Pivette P. Microsphères lipidiques obtenues par prilling : du polymorphisme des constituants à la compréhension du mécanisme de libération d'un principe actif hydrosoluble : Lipidic microspheres obtained by a prilling process : from constituents polymorphism to the understanding of the release mechanism of a water soluble drug. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2011. Available from: http://www.theses.fr/2011PA114811


Université Paris-Sud – Paris XI

30. Hamoudi, Mounira Chérifa. Évaluation d'une forme galénique à base d'alpha cyclodextrine et d'huile végétale pour l'administration par voie orale de molécules actives peu solubles dans l'eau : Beads made of cyclodextrin and oil for oral delivery of lipophilic drugs.

Degree: Docteur es, Pharmacotechnie et physico-chimie, 2012, Université Paris-Sud – Paris XI

L’objectif général de cette thèse a été d’étudier le potentiel de billes à base de molécules d’α-cyclodextrine et d’huile de soja, pour l’administration orale de… (more)

Subjects/Keywords: Billes; Emulsion séche; Libération immédiate; Séchage à l'étuve; Cyclodextrin beads; Soybean oil; Dry emulsion; Oral delivery; Progesterone; Indomethacin; Fast release; Sustained release; Oven-drying; Freeze-drying

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

APA (6th Edition):

Hamoudi, M. C. (2012). Évaluation d'une forme galénique à base d'alpha cyclodextrine et d'huile végétale pour l'administration par voie orale de molécules actives peu solubles dans l'eau : Beads made of cyclodextrin and oil for oral delivery of lipophilic drugs. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2012PA114826

Chicago Manual of Style (16th Edition):

Hamoudi, Mounira Chérifa. “Évaluation d'une forme galénique à base d'alpha cyclodextrine et d'huile végétale pour l'administration par voie orale de molécules actives peu solubles dans l'eau : Beads made of cyclodextrin and oil for oral delivery of lipophilic drugs.” 2012. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed August 15, 2018. http://www.theses.fr/2012PA114826.

MLA Handbook (7th Edition):

Hamoudi, Mounira Chérifa. “Évaluation d'une forme galénique à base d'alpha cyclodextrine et d'huile végétale pour l'administration par voie orale de molécules actives peu solubles dans l'eau : Beads made of cyclodextrin and oil for oral delivery of lipophilic drugs.” 2012. Web. 15 Aug 2018.

Vancouver:

Hamoudi MC. Évaluation d'une forme galénique à base d'alpha cyclodextrine et d'huile végétale pour l'administration par voie orale de molécules actives peu solubles dans l'eau : Beads made of cyclodextrin and oil for oral delivery of lipophilic drugs. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2012. [cited 2018 Aug 15]. Available from: http://www.theses.fr/2012PA114826.

Council of Science Editors:

Hamoudi MC. Évaluation d'une forme galénique à base d'alpha cyclodextrine et d'huile végétale pour l'administration par voie orale de molécules actives peu solubles dans l'eau : Beads made of cyclodextrin and oil for oral delivery of lipophilic drugs. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2012. Available from: http://www.theses.fr/2012PA114826

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