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You searched for subject:( Controlled release). Showing records 1 – 30 of 413 total matches.

[1] [2] [3] [4] [5] … [14]

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University of Georgia

1. Alem, Peter Otieno. Irrigation, fertilization and non-chemical plant growth regulation in greenhouse production.

Degree: PhD, Horticulture, 2014, University of Georgia

 Rising concerns over environmental impacts of excessive water and fertilizer use in the horticultural industry necessitate more efficient use of water and nutrients. Both substrate… (more)

Subjects/Keywords: Controlled release fertilizer

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APA (6th Edition):

Alem, P. O. (2014). Irrigation, fertilization and non-chemical plant growth regulation in greenhouse production. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/alem_peter_o_201408_phd

Chicago Manual of Style (16th Edition):

Alem, Peter Otieno. “Irrigation, fertilization and non-chemical plant growth regulation in greenhouse production.” 2014. Doctoral Dissertation, University of Georgia. Accessed October 22, 2019. http://purl.galileo.usg.edu/uga_etd/alem_peter_o_201408_phd.

MLA Handbook (7th Edition):

Alem, Peter Otieno. “Irrigation, fertilization and non-chemical plant growth regulation in greenhouse production.” 2014. Web. 22 Oct 2019.

Vancouver:

Alem PO. Irrigation, fertilization and non-chemical plant growth regulation in greenhouse production. [Internet] [Doctoral dissertation]. University of Georgia; 2014. [cited 2019 Oct 22]. Available from: http://purl.galileo.usg.edu/uga_etd/alem_peter_o_201408_phd.

Council of Science Editors:

Alem PO. Irrigation, fertilization and non-chemical plant growth regulation in greenhouse production. [Doctoral Dissertation]. University of Georgia; 2014. Available from: http://purl.galileo.usg.edu/uga_etd/alem_peter_o_201408_phd


University of Georgia

2. Williams, Mervin Lee. Viscosity of the continuous phase and other factors in the optimization of matrix microsphere formulations prepared by emulsion-solvent evaporation.

Degree: PhD, Pharmacy (Pharmaceutics), 2003, University of Georgia

 The objective of this study was to examine the effect of the continuous phase viscosity and other formulation factors on microsphere properties. Matrix microspheres were… (more)

Subjects/Keywords: controlled-release

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APA (6th Edition):

Williams, M. L. (2003). Viscosity of the continuous phase and other factors in the optimization of matrix microsphere formulations prepared by emulsion-solvent evaporation. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/williams_mervin_l_200312_phd

Chicago Manual of Style (16th Edition):

Williams, Mervin Lee. “Viscosity of the continuous phase and other factors in the optimization of matrix microsphere formulations prepared by emulsion-solvent evaporation.” 2003. Doctoral Dissertation, University of Georgia. Accessed October 22, 2019. http://purl.galileo.usg.edu/uga_etd/williams_mervin_l_200312_phd.

MLA Handbook (7th Edition):

Williams, Mervin Lee. “Viscosity of the continuous phase and other factors in the optimization of matrix microsphere formulations prepared by emulsion-solvent evaporation.” 2003. Web. 22 Oct 2019.

Vancouver:

Williams ML. Viscosity of the continuous phase and other factors in the optimization of matrix microsphere formulations prepared by emulsion-solvent evaporation. [Internet] [Doctoral dissertation]. University of Georgia; 2003. [cited 2019 Oct 22]. Available from: http://purl.galileo.usg.edu/uga_etd/williams_mervin_l_200312_phd.

Council of Science Editors:

Williams ML. Viscosity of the continuous phase and other factors in the optimization of matrix microsphere formulations prepared by emulsion-solvent evaporation. [Doctoral Dissertation]. University of Georgia; 2003. Available from: http://purl.galileo.usg.edu/uga_etd/williams_mervin_l_200312_phd

3. Papathanasiou, Konstantinos. Controlled release drug delivery systems for osteoporosis pharmaceuticals based on silica hydrogels.

Degree: 2017, University of Crete (UOC); Πανεπιστήμιο Κρήτης

Gel systems have found extensive applications in the medicinal/pharmaceutical field because of their ease of preparation, ability for modifications, and responsiveness to external chemical or… (more)

Subjects/Keywords: Ελεγχόμενη αποδέσμευση; Controlled release

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APA (6th Edition):

Papathanasiou, K. (2017). Controlled release drug delivery systems for osteoporosis pharmaceuticals based on silica hydrogels. (Thesis). University of Crete (UOC); Πανεπιστήμιο Κρήτης. Retrieved from http://hdl.handle.net/10442/hedi/40439

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):

Papathanasiou, Konstantinos. “Controlled release drug delivery systems for osteoporosis pharmaceuticals based on silica hydrogels.” 2017. Thesis, University of Crete (UOC); Πανεπιστήμιο Κρήτης. Accessed October 22, 2019. http://hdl.handle.net/10442/hedi/40439.

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

MLA Handbook (7th Edition):

Papathanasiou, Konstantinos. “Controlled release drug delivery systems for osteoporosis pharmaceuticals based on silica hydrogels.” 2017. Web. 22 Oct 2019.

Vancouver:

Papathanasiou K. Controlled release drug delivery systems for osteoporosis pharmaceuticals based on silica hydrogels. [Internet] [Thesis]. University of Crete (UOC); Πανεπιστήμιο Κρήτης; 2017. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/10442/hedi/40439.

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

Council of Science Editors:

Papathanasiou K. Controlled release drug delivery systems for osteoporosis pharmaceuticals based on silica hydrogels. [Thesis]. University of Crete (UOC); Πανεπιστήμιο Κρήτης; 2017. Available from: http://hdl.handle.net/10442/hedi/40439

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


Vanderbilt University

4. Nelson, Christopher Edward. Sustained local delivery of siRNA from an injectable scaffold.

Degree: MS, Biomedical Engineering, 2011, Vanderbilt University

Controlled gene silencing technologies have significant, unrealized potential for use in tissue regeneration applications. The design described herein provides a means to package and protect… (more)

Subjects/Keywords: controlled release; RNAi; polyurethane; siRNA

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APA (6th Edition):

Nelson, C. E. (2011). Sustained local delivery of siRNA from an injectable scaffold. (Masters Thesis). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu//available/etd-10272011-113508/ ;

Chicago Manual of Style (16th Edition):

Nelson, Christopher Edward. “Sustained local delivery of siRNA from an injectable scaffold.” 2011. Masters Thesis, Vanderbilt University. Accessed October 22, 2019. http://etd.library.vanderbilt.edu//available/etd-10272011-113508/ ;.

MLA Handbook (7th Edition):

Nelson, Christopher Edward. “Sustained local delivery of siRNA from an injectable scaffold.” 2011. Web. 22 Oct 2019.

Vancouver:

Nelson CE. Sustained local delivery of siRNA from an injectable scaffold. [Internet] [Masters thesis]. Vanderbilt University; 2011. [cited 2019 Oct 22]. Available from: http://etd.library.vanderbilt.edu//available/etd-10272011-113508/ ;.

Council of Science Editors:

Nelson CE. Sustained local delivery of siRNA from an injectable scaffold. [Masters Thesis]. Vanderbilt University; 2011. Available from: http://etd.library.vanderbilt.edu//available/etd-10272011-113508/ ;


University of Guelph

5. Wang, Wenjing. Carriers for Controlled Release of Allyl Isothiocyanate, Diacetyl and Cinnamaldehyde for Antimicrobial Active Packaging .

Degree: 2016, University of Guelph

 Antimicrobial volatiles are gaining increasing interest for active packaging applications. However, many hurdles remain unresolved, especially on delivering antimicrobial compounds in a controlled manner to… (more)

Subjects/Keywords: antimicrobial packaging; controlled release

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APA (6th Edition):

Wang, W. (2016). Carriers for Controlled Release of Allyl Isothiocyanate, Diacetyl and Cinnamaldehyde for Antimicrobial Active Packaging . (Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9714

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):

Wang, Wenjing. “Carriers for Controlled Release of Allyl Isothiocyanate, Diacetyl and Cinnamaldehyde for Antimicrobial Active Packaging .” 2016. Thesis, University of Guelph. Accessed October 22, 2019. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9714.

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

MLA Handbook (7th Edition):

Wang, Wenjing. “Carriers for Controlled Release of Allyl Isothiocyanate, Diacetyl and Cinnamaldehyde for Antimicrobial Active Packaging .” 2016. Web. 22 Oct 2019.

Vancouver:

Wang W. Carriers for Controlled Release of Allyl Isothiocyanate, Diacetyl and Cinnamaldehyde for Antimicrobial Active Packaging . [Internet] [Thesis]. University of Guelph; 2016. [cited 2019 Oct 22]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9714.

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

Council of Science Editors:

Wang W. Carriers for Controlled Release of Allyl Isothiocyanate, Diacetyl and Cinnamaldehyde for Antimicrobial Active Packaging . [Thesis]. University of Guelph; 2016. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9714

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


Nelson Mandela Metropolitan University

6. Barnard, Carla. Investigating the effect of various film-forming polymers on the evaporation rate of a volatile component in a cosmetic formulation.

Degree: Faculty of Science, 2010, Nelson Mandela Metropolitan University

 The topical application of many substances, including drugs, enzymes, moisturizers and fragrances, contributes largely to the cosmetic and pharmaceutical industries. These components are often volatile… (more)

Subjects/Keywords: Cosmetic delivery systems; Controlled release preparations; Cosmetics; Polymers; Drugs  – Controlled release

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APA (6th Edition):

Barnard, C. (2010). Investigating the effect of various film-forming polymers on the evaporation rate of a volatile component in a cosmetic formulation. (Thesis). Nelson Mandela Metropolitan University. Retrieved from http://hdl.handle.net/10948/1498

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):

Barnard, Carla. “Investigating the effect of various film-forming polymers on the evaporation rate of a volatile component in a cosmetic formulation.” 2010. Thesis, Nelson Mandela Metropolitan University. Accessed October 22, 2019. http://hdl.handle.net/10948/1498.

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

MLA Handbook (7th Edition):

Barnard, Carla. “Investigating the effect of various film-forming polymers on the evaporation rate of a volatile component in a cosmetic formulation.” 2010. Web. 22 Oct 2019.

Vancouver:

Barnard C. Investigating the effect of various film-forming polymers on the evaporation rate of a volatile component in a cosmetic formulation. [Internet] [Thesis]. Nelson Mandela Metropolitan University; 2010. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/10948/1498.

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

Council of Science Editors:

Barnard C. Investigating the effect of various film-forming polymers on the evaporation rate of a volatile component in a cosmetic formulation. [Thesis]. Nelson Mandela Metropolitan University; 2010. Available from: http://hdl.handle.net/10948/1498

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


University of Georgia

7. Collier, Jarrod. An in vitro batch release dissolution test for the evaluation of controlled release drugs.

Degree: MS, Pharmacy (Pharmaceutics), 2003, University of Georgia

 The means by which a drug is introduced into the body is almost as important as the drug itself. It is imperative that drug concentration… (more)

Subjects/Keywords: Controlled release drugs

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APA (6th Edition):

Collier, J. (2003). An in vitro batch release dissolution test for the evaluation of controlled release drugs. (Masters Thesis). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/collier_jarrod_w_200308_ms

Chicago Manual of Style (16th Edition):

Collier, Jarrod. “An in vitro batch release dissolution test for the evaluation of controlled release drugs.” 2003. Masters Thesis, University of Georgia. Accessed October 22, 2019. http://purl.galileo.usg.edu/uga_etd/collier_jarrod_w_200308_ms.

MLA Handbook (7th Edition):

Collier, Jarrod. “An in vitro batch release dissolution test for the evaluation of controlled release drugs.” 2003. Web. 22 Oct 2019.

Vancouver:

Collier J. An in vitro batch release dissolution test for the evaluation of controlled release drugs. [Internet] [Masters thesis]. University of Georgia; 2003. [cited 2019 Oct 22]. Available from: http://purl.galileo.usg.edu/uga_etd/collier_jarrod_w_200308_ms.

Council of Science Editors:

Collier J. An in vitro batch release dissolution test for the evaluation of controlled release drugs. [Masters Thesis]. University of Georgia; 2003. Available from: http://purl.galileo.usg.edu/uga_etd/collier_jarrod_w_200308_ms


University of Alberta

8. Lao, Io San Elka. Formulation of sustained release microparticles of a bacterial nutrient and an antihistamine.

Degree: MS, Faculty of Pharmacy and Pharmaceutical Sciences, 1993, University of Alberta

Subjects/Keywords: Controlled release preparations.

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APA (6th Edition):

Lao, I. S. E. (1993). Formulation of sustained release microparticles of a bacterial nutrient and an antihistamine. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/6682x5924

Chicago Manual of Style (16th Edition):

Lao, Io San Elka. “Formulation of sustained release microparticles of a bacterial nutrient and an antihistamine.” 1993. Masters Thesis, University of Alberta. Accessed October 22, 2019. https://era.library.ualberta.ca/files/6682x5924.

MLA Handbook (7th Edition):

Lao, Io San Elka. “Formulation of sustained release microparticles of a bacterial nutrient and an antihistamine.” 1993. Web. 22 Oct 2019.

Vancouver:

Lao ISE. Formulation of sustained release microparticles of a bacterial nutrient and an antihistamine. [Internet] [Masters thesis]. University of Alberta; 1993. [cited 2019 Oct 22]. Available from: https://era.library.ualberta.ca/files/6682x5924.

Council of Science Editors:

Lao ISE. Formulation of sustained release microparticles of a bacterial nutrient and an antihistamine. [Masters Thesis]. University of Alberta; 1993. Available from: https://era.library.ualberta.ca/files/6682x5924


Case Western Reserve University

9. Zheng, Zijie. IN SITU FORMING PHOTODEGRADABLE HYDROGEL FOR CONTROLLED DELIVERY OF siRNA.

Degree: MSs, Biomedical Engineering, 2015, Case Western Reserve University

 Cells adapt themselves to the dynamic extracellular environment by responding to numerous signal stimuli. Strategies for engineering stimulus-responsive biomaterials as drug delivery vehicles may mimic… (more)

Subjects/Keywords: Biomedical Engineering; siRNA, photodegradable, hydrogel, controlled release

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APA (6th Edition):

Zheng, Z. (2015). IN SITU FORMING PHOTODEGRADABLE HYDROGEL FOR CONTROLLED DELIVERY OF siRNA. (Masters Thesis). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1434560306

Chicago Manual of Style (16th Edition):

Zheng, Zijie. “IN SITU FORMING PHOTODEGRADABLE HYDROGEL FOR CONTROLLED DELIVERY OF siRNA.” 2015. Masters Thesis, Case Western Reserve University. Accessed October 22, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1434560306.

MLA Handbook (7th Edition):

Zheng, Zijie. “IN SITU FORMING PHOTODEGRADABLE HYDROGEL FOR CONTROLLED DELIVERY OF siRNA.” 2015. Web. 22 Oct 2019.

Vancouver:

Zheng Z. IN SITU FORMING PHOTODEGRADABLE HYDROGEL FOR CONTROLLED DELIVERY OF siRNA. [Internet] [Masters thesis]. Case Western Reserve University; 2015. [cited 2019 Oct 22]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1434560306.

Council of Science Editors:

Zheng Z. IN SITU FORMING PHOTODEGRADABLE HYDROGEL FOR CONTROLLED DELIVERY OF siRNA. [Masters Thesis]. Case Western Reserve University; 2015. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1434560306


Cornell University

10. Weiser, Jennifer. The Design, Synthesis, And Characterization Of Poly(Carbonate-Ester)S Based On Dihydroxyacetone For Use As Potential Biomaterials.

Degree: 2013, Cornell University

 The creation of new devices and materials with desirable biomedical characteristics, such as biocompatibility and easily tunable physico-chemical parameters, has played a key role in… (more)

Subjects/Keywords: Dihydroxyacetone; controlled release; bicinchoninic acid assay

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APA (6th Edition):

Weiser, J. (2013). The Design, Synthesis, And Characterization Of Poly(Carbonate-Ester)S Based On Dihydroxyacetone For Use As Potential Biomaterials. (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/33877

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):

Weiser, Jennifer. “The Design, Synthesis, And Characterization Of Poly(Carbonate-Ester)S Based On Dihydroxyacetone For Use As Potential Biomaterials. ” 2013. Thesis, Cornell University. Accessed October 22, 2019. http://hdl.handle.net/1813/33877.

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

MLA Handbook (7th Edition):

Weiser, Jennifer. “The Design, Synthesis, And Characterization Of Poly(Carbonate-Ester)S Based On Dihydroxyacetone For Use As Potential Biomaterials. ” 2013. Web. 22 Oct 2019.

Vancouver:

Weiser J. The Design, Synthesis, And Characterization Of Poly(Carbonate-Ester)S Based On Dihydroxyacetone For Use As Potential Biomaterials. [Internet] [Thesis]. Cornell University; 2013. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/1813/33877.

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

Council of Science Editors:

Weiser J. The Design, Synthesis, And Characterization Of Poly(Carbonate-Ester)S Based On Dihydroxyacetone For Use As Potential Biomaterials. [Thesis]. Cornell University; 2013. Available from: http://hdl.handle.net/1813/33877

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


Oregon State University

11. Sahajwalla, Chandrahas G. New product formulation and multiple dose pharmacokinetics of acetaminophen.

Degree: PhD, Pharmacy, 1987, Oregon State University

 Four different treatments of acetaminophen were administered to eight healthy volunteers in multiple doses (five doses). Saliva acetaminophen concentration-time profiles were determined. Non-compartmental pharmacokinetic parameters… (more)

Subjects/Keywords: Acetaminophen  – Controlled release

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APA (6th Edition):

Sahajwalla, C. G. (1987). New product formulation and multiple dose pharmacokinetics of acetaminophen. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/40856

Chicago Manual of Style (16th Edition):

Sahajwalla, Chandrahas G. “New product formulation and multiple dose pharmacokinetics of acetaminophen.” 1987. Doctoral Dissertation, Oregon State University. Accessed October 22, 2019. http://hdl.handle.net/1957/40856.

MLA Handbook (7th Edition):

Sahajwalla, Chandrahas G. “New product formulation and multiple dose pharmacokinetics of acetaminophen.” 1987. Web. 22 Oct 2019.

Vancouver:

Sahajwalla CG. New product formulation and multiple dose pharmacokinetics of acetaminophen. [Internet] [Doctoral dissertation]. Oregon State University; 1987. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/1957/40856.

Council of Science Editors:

Sahajwalla CG. New product formulation and multiple dose pharmacokinetics of acetaminophen. [Doctoral Dissertation]. Oregon State University; 1987. Available from: http://hdl.handle.net/1957/40856


Oregon State University

12. Borin, Marie T. New product formulations and pharmacokinetics of acetaminophen.

Degree: PhD, Pharmacy, 1985, Oregon State University

Subjects/Keywords: Acetaminophen  – Controlled release

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APA (6th Edition):

Borin, M. T. (1985). New product formulations and pharmacokinetics of acetaminophen. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/40857

Chicago Manual of Style (16th Edition):

Borin, Marie T. “New product formulations and pharmacokinetics of acetaminophen.” 1985. Doctoral Dissertation, Oregon State University. Accessed October 22, 2019. http://hdl.handle.net/1957/40857.

MLA Handbook (7th Edition):

Borin, Marie T. “New product formulations and pharmacokinetics of acetaminophen.” 1985. Web. 22 Oct 2019.

Vancouver:

Borin MT. New product formulations and pharmacokinetics of acetaminophen. [Internet] [Doctoral dissertation]. Oregon State University; 1985. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/1957/40857.

Council of Science Editors:

Borin MT. New product formulations and pharmacokinetics of acetaminophen. [Doctoral Dissertation]. Oregon State University; 1985. Available from: http://hdl.handle.net/1957/40857


Oregon State University

13. Fahmy, Sahar Abd El-Sattar. Development of novel spray coated soft elastic gelatin capsule sustained release formulations of nifedipine, bioavailability and bioequivalence of verapamil HCL controlled release formulations, pharmacokinetics of terbinafine after single oral doses in raptors.

Degree: PhD, Pharmacy, 2004, Oregon State University

 This dissertation describes the development of a new sustained release formulation of nifedipine. The new formulation was developed by coating commercially available immediate release soft… (more)

Subjects/Keywords: Nifedipine  – Controlled release

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APA (6th Edition):

Fahmy, S. A. E. (2004). Development of novel spray coated soft elastic gelatin capsule sustained release formulations of nifedipine, bioavailability and bioequivalence of verapamil HCL controlled release formulations, pharmacokinetics of terbinafine after single oral doses in raptors. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/29795

Chicago Manual of Style (16th Edition):

Fahmy, Sahar Abd El-Sattar. “Development of novel spray coated soft elastic gelatin capsule sustained release formulations of nifedipine, bioavailability and bioequivalence of verapamil HCL controlled release formulations, pharmacokinetics of terbinafine after single oral doses in raptors.” 2004. Doctoral Dissertation, Oregon State University. Accessed October 22, 2019. http://hdl.handle.net/1957/29795.

MLA Handbook (7th Edition):

Fahmy, Sahar Abd El-Sattar. “Development of novel spray coated soft elastic gelatin capsule sustained release formulations of nifedipine, bioavailability and bioequivalence of verapamil HCL controlled release formulations, pharmacokinetics of terbinafine after single oral doses in raptors.” 2004. Web. 22 Oct 2019.

Vancouver:

Fahmy SAE. Development of novel spray coated soft elastic gelatin capsule sustained release formulations of nifedipine, bioavailability and bioequivalence of verapamil HCL controlled release formulations, pharmacokinetics of terbinafine after single oral doses in raptors. [Internet] [Doctoral dissertation]. Oregon State University; 2004. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/1957/29795.

Council of Science Editors:

Fahmy SAE. Development of novel spray coated soft elastic gelatin capsule sustained release formulations of nifedipine, bioavailability and bioequivalence of verapamil HCL controlled release formulations, pharmacokinetics of terbinafine after single oral doses in raptors. [Doctoral Dissertation]. Oregon State University; 2004. Available from: http://hdl.handle.net/1957/29795


Oregon State University

14. Rakkanka, Vipaporn. A novel self-sealing chewable sustained release tablet of acetaminophen ; Development and evaluation of novel itraconazole oral formulations ; A novel zero order release matrix tablet.

Degree: PhD, Pharmacy, 2003, Oregon State University

Subjects/Keywords: Acetaminophen  – Controlled release

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APA (6th Edition):

Rakkanka, V. (2003). A novel self-sealing chewable sustained release tablet of acetaminophen ; Development and evaluation of novel itraconazole oral formulations ; A novel zero order release matrix tablet. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/30894

Chicago Manual of Style (16th Edition):

Rakkanka, Vipaporn. “A novel self-sealing chewable sustained release tablet of acetaminophen ; Development and evaluation of novel itraconazole oral formulations ; A novel zero order release matrix tablet.” 2003. Doctoral Dissertation, Oregon State University. Accessed October 22, 2019. http://hdl.handle.net/1957/30894.

MLA Handbook (7th Edition):

Rakkanka, Vipaporn. “A novel self-sealing chewable sustained release tablet of acetaminophen ; Development and evaluation of novel itraconazole oral formulations ; A novel zero order release matrix tablet.” 2003. Web. 22 Oct 2019.

Vancouver:

Rakkanka V. A novel self-sealing chewable sustained release tablet of acetaminophen ; Development and evaluation of novel itraconazole oral formulations ; A novel zero order release matrix tablet. [Internet] [Doctoral dissertation]. Oregon State University; 2003. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/1957/30894.

Council of Science Editors:

Rakkanka V. A novel self-sealing chewable sustained release tablet of acetaminophen ; Development and evaluation of novel itraconazole oral formulations ; A novel zero order release matrix tablet. [Doctoral Dissertation]. Oregon State University; 2003. Available from: http://hdl.handle.net/1957/30894


Oregon State University

15. Kalns, John Eric. Pharmacokinetics and pharmacodynamics of: 1) Oral sustained release acetaminophen suspension in children; 2) Potassium chloride in adults.

Degree: PhD, Pharmacy, 1993, Oregon State University

Subjects/Keywords: Acetaminophen  – Controlled release

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APA (6th Edition):

Kalns, J. E. (1993). Pharmacokinetics and pharmacodynamics of: 1) Oral sustained release acetaminophen suspension in children; 2) Potassium chloride in adults. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/35827

Chicago Manual of Style (16th Edition):

Kalns, John Eric. “Pharmacokinetics and pharmacodynamics of: 1) Oral sustained release acetaminophen suspension in children; 2) Potassium chloride in adults.” 1993. Doctoral Dissertation, Oregon State University. Accessed October 22, 2019. http://hdl.handle.net/1957/35827.

MLA Handbook (7th Edition):

Kalns, John Eric. “Pharmacokinetics and pharmacodynamics of: 1) Oral sustained release acetaminophen suspension in children; 2) Potassium chloride in adults.” 1993. Web. 22 Oct 2019.

Vancouver:

Kalns JE. Pharmacokinetics and pharmacodynamics of: 1) Oral sustained release acetaminophen suspension in children; 2) Potassium chloride in adults. [Internet] [Doctoral dissertation]. Oregon State University; 1993. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/1957/35827.

Council of Science Editors:

Kalns JE. Pharmacokinetics and pharmacodynamics of: 1) Oral sustained release acetaminophen suspension in children; 2) Potassium chloride in adults. [Doctoral Dissertation]. Oregon State University; 1993. Available from: http://hdl.handle.net/1957/35827


Oregon State University

16. Kapsi, Shivakumar G. Development and in vivo testing of a gastric retention device (GRD) in dogs: Product formulations and in vitro-in vivo evaluation of a) immediate release formulation of itraconazole, b) controlled-release formulation of ketoprofen in adults.

Degree: PhD, Pharmacy, 1998, Oregon State University

 This thesis describes 1) development of a gastric retention device (GRD) to increase gastric retention time of certain drugs, 2) product formulations of an immediate… (more)

Subjects/Keywords: Drugs  – Controlled release

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APA (6th Edition):

Kapsi, S. G. (1998). Development and in vivo testing of a gastric retention device (GRD) in dogs: Product formulations and in vitro-in vivo evaluation of a) immediate release formulation of itraconazole, b) controlled-release formulation of ketoprofen in adults. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/33331

Chicago Manual of Style (16th Edition):

Kapsi, Shivakumar G. “Development and in vivo testing of a gastric retention device (GRD) in dogs: Product formulations and in vitro-in vivo evaluation of a) immediate release formulation of itraconazole, b) controlled-release formulation of ketoprofen in adults.” 1998. Doctoral Dissertation, Oregon State University. Accessed October 22, 2019. http://hdl.handle.net/1957/33331.

MLA Handbook (7th Edition):

Kapsi, Shivakumar G. “Development and in vivo testing of a gastric retention device (GRD) in dogs: Product formulations and in vitro-in vivo evaluation of a) immediate release formulation of itraconazole, b) controlled-release formulation of ketoprofen in adults.” 1998. Web. 22 Oct 2019.

Vancouver:

Kapsi SG. Development and in vivo testing of a gastric retention device (GRD) in dogs: Product formulations and in vitro-in vivo evaluation of a) immediate release formulation of itraconazole, b) controlled-release formulation of ketoprofen in adults. [Internet] [Doctoral dissertation]. Oregon State University; 1998. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/1957/33331.

Council of Science Editors:

Kapsi SG. Development and in vivo testing of a gastric retention device (GRD) in dogs: Product formulations and in vitro-in vivo evaluation of a) immediate release formulation of itraconazole, b) controlled-release formulation of ketoprofen in adults. [Doctoral Dissertation]. Oregon State University; 1998. Available from: http://hdl.handle.net/1957/33331


Oregon State University

17. Yang, Ning-Ning. Product formulations and in vitro-in vivo evaluation of a novel "Tablet-in-a-Bottle" suspension formulation of amoxicillin and clavulanic acid.

Degree: MS, Pharmacy, 1997, Oregon State University

 This thesis describes a novel "Tablet-in-a-Bottle" oral suspension formulation. Ingredients with unstable physical or chemical characteristics can be placed in a core tablet, and then… (more)

Subjects/Keywords: Amoxicillin  – Controlled release

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APA (6th Edition):

Yang, N. (1997). Product formulations and in vitro-in vivo evaluation of a novel "Tablet-in-a-Bottle" suspension formulation of amoxicillin and clavulanic acid. (Masters Thesis). Oregon State University. Retrieved from http://hdl.handle.net/1957/33676

Chicago Manual of Style (16th Edition):

Yang, Ning-Ning. “Product formulations and in vitro-in vivo evaluation of a novel "Tablet-in-a-Bottle" suspension formulation of amoxicillin and clavulanic acid.” 1997. Masters Thesis, Oregon State University. Accessed October 22, 2019. http://hdl.handle.net/1957/33676.

MLA Handbook (7th Edition):

Yang, Ning-Ning. “Product formulations and in vitro-in vivo evaluation of a novel "Tablet-in-a-Bottle" suspension formulation of amoxicillin and clavulanic acid.” 1997. Web. 22 Oct 2019.

Vancouver:

Yang N. Product formulations and in vitro-in vivo evaluation of a novel "Tablet-in-a-Bottle" suspension formulation of amoxicillin and clavulanic acid. [Internet] [Masters thesis]. Oregon State University; 1997. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/1957/33676.

Council of Science Editors:

Yang N. Product formulations and in vitro-in vivo evaluation of a novel "Tablet-in-a-Bottle" suspension formulation of amoxicillin and clavulanic acid. [Masters Thesis]. Oregon State University; 1997. Available from: http://hdl.handle.net/1957/33676


Oregon State University

18. Ge, Yan, 1962-. Development and evaluation of a sustained release amoxicillin dosage form.

Degree: MS, Pharmacy, 1994, Oregon State University

Subjects/Keywords: Amoxicillin  – Controlled release

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APA (6th Edition):

Ge, Yan, 1. (1994). Development and evaluation of a sustained release amoxicillin dosage form. (Masters Thesis). Oregon State University. Retrieved from http://hdl.handle.net/1957/35255

Chicago Manual of Style (16th Edition):

Ge, Yan, 1962-. “Development and evaluation of a sustained release amoxicillin dosage form.” 1994. Masters Thesis, Oregon State University. Accessed October 22, 2019. http://hdl.handle.net/1957/35255.

MLA Handbook (7th Edition):

Ge, Yan, 1962-. “Development and evaluation of a sustained release amoxicillin dosage form.” 1994. Web. 22 Oct 2019.

Vancouver:

Ge, Yan 1. Development and evaluation of a sustained release amoxicillin dosage form. [Internet] [Masters thesis]. Oregon State University; 1994. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/1957/35255.

Council of Science Editors:

Ge, Yan 1. Development and evaluation of a sustained release amoxicillin dosage form. [Masters Thesis]. Oregon State University; 1994. Available from: http://hdl.handle.net/1957/35255


Oregon State University

19. Piepmeier, Edward H. Formulation of an oral acetylsalicylic acid suspension and pharmacokinetics of parenteral thrombomodulin analogues.

Degree: PhD, Pharmacy, 1991, Oregon State University

 Sustained concentrations of active compound were maintained in vitro and in vivo for an oral and a parenteral dosage form respectively. The vehicle of a… (more)

Subjects/Keywords: Aspirin  – Controlled release

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APA (6th Edition):

Piepmeier, E. H. (1991). Formulation of an oral acetylsalicylic acid suspension and pharmacokinetics of parenteral thrombomodulin analogues. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/37514

Chicago Manual of Style (16th Edition):

Piepmeier, Edward H. “Formulation of an oral acetylsalicylic acid suspension and pharmacokinetics of parenteral thrombomodulin analogues.” 1991. Doctoral Dissertation, Oregon State University. Accessed October 22, 2019. http://hdl.handle.net/1957/37514.

MLA Handbook (7th Edition):

Piepmeier, Edward H. “Formulation of an oral acetylsalicylic acid suspension and pharmacokinetics of parenteral thrombomodulin analogues.” 1991. Web. 22 Oct 2019.

Vancouver:

Piepmeier EH. Formulation of an oral acetylsalicylic acid suspension and pharmacokinetics of parenteral thrombomodulin analogues. [Internet] [Doctoral dissertation]. Oregon State University; 1991. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/1957/37514.

Council of Science Editors:

Piepmeier EH. Formulation of an oral acetylsalicylic acid suspension and pharmacokinetics of parenteral thrombomodulin analogues. [Doctoral Dissertation]. Oregon State University; 1991. Available from: http://hdl.handle.net/1957/37514


Oregon State University

20. Le, Hang Thi. Preparing sustained release dosage forms of nifedipine by hot-melt coating method: Preparing sustained release dosage form of nifedipine by hot-melt coating method.

Degree: MS, Pharmacy, 2004, Oregon State University

Subjects/Keywords: Drugs  – Controlled release

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APA (6th Edition):

Le, H. T. (2004). Preparing sustained release dosage forms of nifedipine by hot-melt coating method: Preparing sustained release dosage form of nifedipine by hot-melt coating method. (Masters Thesis). Oregon State University. Retrieved from http://hdl.handle.net/1957/22780

Chicago Manual of Style (16th Edition):

Le, Hang Thi. “Preparing sustained release dosage forms of nifedipine by hot-melt coating method: Preparing sustained release dosage form of nifedipine by hot-melt coating method.” 2004. Masters Thesis, Oregon State University. Accessed October 22, 2019. http://hdl.handle.net/1957/22780.

MLA Handbook (7th Edition):

Le, Hang Thi. “Preparing sustained release dosage forms of nifedipine by hot-melt coating method: Preparing sustained release dosage form of nifedipine by hot-melt coating method.” 2004. Web. 22 Oct 2019.

Vancouver:

Le HT. Preparing sustained release dosage forms of nifedipine by hot-melt coating method: Preparing sustained release dosage form of nifedipine by hot-melt coating method. [Internet] [Masters thesis]. Oregon State University; 2004. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/1957/22780.

Council of Science Editors:

Le HT. Preparing sustained release dosage forms of nifedipine by hot-melt coating method: Preparing sustained release dosage form of nifedipine by hot-melt coating method. [Masters Thesis]. Oregon State University; 2004. Available from: http://hdl.handle.net/1957/22780


University of Cambridge

21. Chia, Leonard Sze Onn. Investigating Controlled Release Pulmonary Drug Delivery Systems .

Degree: 2018, University of Cambridge

 The therapeutic effect of pulmonary drug delivery systems is limited by its rapid clearance from the lungs by robust clearance mechanisms. By controlling the release(more)

Subjects/Keywords: Pulmonary Delivery; Drug Delivery; Controlled Release

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APA (6th Edition):

Chia, L. S. O. (2018). Investigating Controlled Release Pulmonary Drug Delivery Systems . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/273209

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):

Chia, Leonard Sze Onn. “Investigating Controlled Release Pulmonary Drug Delivery Systems .” 2018. Thesis, University of Cambridge. Accessed October 22, 2019. https://www.repository.cam.ac.uk/handle/1810/273209.

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

MLA Handbook (7th Edition):

Chia, Leonard Sze Onn. “Investigating Controlled Release Pulmonary Drug Delivery Systems .” 2018. Web. 22 Oct 2019.

Vancouver:

Chia LSO. Investigating Controlled Release Pulmonary Drug Delivery Systems . [Internet] [Thesis]. University of Cambridge; 2018. [cited 2019 Oct 22]. Available from: https://www.repository.cam.ac.uk/handle/1810/273209.

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

Council of Science Editors:

Chia LSO. Investigating Controlled Release Pulmonary Drug Delivery Systems . [Thesis]. University of Cambridge; 2018. Available from: https://www.repository.cam.ac.uk/handle/1810/273209

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


Colorado School of Mines

22. Adams, Marisa L. Release of bioactive agents from mesoporous silica nanoparticles for biological applications.

Degree: MS(M.S.), Chemistry, 2018, Colorado School of Mines

 The high surface area, pore volume, and biocompatible/ biodegradable silica matrix of mesoporous silica nanoparticles (MSN) has led to extensive investigation into these materials as… (more)

Subjects/Keywords: Mesoporous silica nanoparticles; Controlled release; Oral mucosa

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APA (6th Edition):

Adams, M. L. (2018). Release of bioactive agents from mesoporous silica nanoparticles for biological applications. (Masters Thesis). Colorado School of Mines. Retrieved from http://hdl.handle.net/11124/172826

Chicago Manual of Style (16th Edition):

Adams, Marisa L. “Release of bioactive agents from mesoporous silica nanoparticles for biological applications.” 2018. Masters Thesis, Colorado School of Mines. Accessed October 22, 2019. http://hdl.handle.net/11124/172826.

MLA Handbook (7th Edition):

Adams, Marisa L. “Release of bioactive agents from mesoporous silica nanoparticles for biological applications.” 2018. Web. 22 Oct 2019.

Vancouver:

Adams ML. Release of bioactive agents from mesoporous silica nanoparticles for biological applications. [Internet] [Masters thesis]. Colorado School of Mines; 2018. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/11124/172826.

Council of Science Editors:

Adams ML. Release of bioactive agents from mesoporous silica nanoparticles for biological applications. [Masters Thesis]. Colorado School of Mines; 2018. Available from: http://hdl.handle.net/11124/172826


University of Waterloo

23. Xu, Jiang. Synthesis of Polymeric Nanoparticles for the Controlled Release of Hydrophobic and Hydrophillic Theraputic Compounds.

Degree: 2016, University of Waterloo

 Polymeric nanoparticle (NP) drug carriers present a promising technology for controlled release since they are capable of improving the encapsulation efficiency and stability of the… (more)

Subjects/Keywords: Polymeric nanoparticles; controlled release; microfluidics; nanoprecipitation; nanotechnology

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APA (6th Edition):

Xu, J. (2016). Synthesis of Polymeric Nanoparticles for the Controlled Release of Hydrophobic and Hydrophillic Theraputic Compounds. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/10778

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):

Xu, Jiang. “Synthesis of Polymeric Nanoparticles for the Controlled Release of Hydrophobic and Hydrophillic Theraputic Compounds.” 2016. Thesis, University of Waterloo. Accessed October 22, 2019. http://hdl.handle.net/10012/10778.

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

MLA Handbook (7th Edition):

Xu, Jiang. “Synthesis of Polymeric Nanoparticles for the Controlled Release of Hydrophobic and Hydrophillic Theraputic Compounds.” 2016. Web. 22 Oct 2019.

Vancouver:

Xu J. Synthesis of Polymeric Nanoparticles for the Controlled Release of Hydrophobic and Hydrophillic Theraputic Compounds. [Internet] [Thesis]. University of Waterloo; 2016. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/10012/10778.

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

Council of Science Editors:

Xu J. Synthesis of Polymeric Nanoparticles for the Controlled Release of Hydrophobic and Hydrophillic Theraputic Compounds. [Thesis]. University of Waterloo; 2016. Available from: http://hdl.handle.net/10012/10778

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

24. Pajaree Sakdiset. Development of Ethosome Containing Indomethacin for Transdermal Delivery .

Degree: คณะเภสัชศาสตร์ ภาควิชาเทคโนโลยีเภสัชกรรม, 2010, Prince of Songkla University

Subjects/Keywords: Drugs Controlled release

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APA (6th Edition):

Sakdiset, P. (2010). Development of Ethosome Containing Indomethacin for Transdermal Delivery . (Thesis). Prince of Songkla University. Retrieved from http://kb.psu.ac.th/psukb/handle/2016/10293

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):

Sakdiset, Pajaree. “Development of Ethosome Containing Indomethacin for Transdermal Delivery .” 2010. Thesis, Prince of Songkla University. Accessed October 22, 2019. http://kb.psu.ac.th/psukb/handle/2016/10293.

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

MLA Handbook (7th Edition):

Sakdiset, Pajaree. “Development of Ethosome Containing Indomethacin for Transdermal Delivery .” 2010. Web. 22 Oct 2019.

Vancouver:

Sakdiset P. Development of Ethosome Containing Indomethacin for Transdermal Delivery . [Internet] [Thesis]. Prince of Songkla University; 2010. [cited 2019 Oct 22]. Available from: http://kb.psu.ac.th/psukb/handle/2016/10293.

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

Council of Science Editors:

Sakdiset P. Development of Ethosome Containing Indomethacin for Transdermal Delivery . [Thesis]. Prince of Songkla University; 2010. Available from: http://kb.psu.ac.th/psukb/handle/2016/10293

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


University of Waterloo

25. Tse, John. Gelatin Methacrylate as a Controlled Release Vehicle for Treatment of Recurrent Corneal Erosion.

Degree: 2018, University of Waterloo

 Patients with recurrent corneal erosions (RCE) experience unpredictable and painful episodes, caused by the loss of superficial corneal epithelial cells. The erratic nature of RCE… (more)

Subjects/Keywords: Recurrent Corneal Erosion; GelMA; Controlled Release

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APA (6th Edition):

Tse, J. (2018). Gelatin Methacrylate as a Controlled Release Vehicle for Treatment of Recurrent Corneal Erosion. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/13710

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):

Tse, John. “Gelatin Methacrylate as a Controlled Release Vehicle for Treatment of Recurrent Corneal Erosion.” 2018. Thesis, University of Waterloo. Accessed October 22, 2019. http://hdl.handle.net/10012/13710.

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

MLA Handbook (7th Edition):

Tse, John. “Gelatin Methacrylate as a Controlled Release Vehicle for Treatment of Recurrent Corneal Erosion.” 2018. Web. 22 Oct 2019.

Vancouver:

Tse J. Gelatin Methacrylate as a Controlled Release Vehicle for Treatment of Recurrent Corneal Erosion. [Internet] [Thesis]. University of Waterloo; 2018. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/10012/13710.

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

Council of Science Editors:

Tse J. Gelatin Methacrylate as a Controlled Release Vehicle for Treatment of Recurrent Corneal Erosion. [Thesis]. University of Waterloo; 2018. Available from: http://hdl.handle.net/10012/13710

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


University of Toledo

26. Baawad, Abdullah. Release of Low Acyl Gellan Gum in a Controlled Release System.

Degree: MS, Chemical Engineering, 2018, University of Toledo

 The release of low acyl gellan gum from a controlled release system was evaluated at 0, 0.5, 1% concentration of tri-calcium phosphate. Release rates of… (more)

Subjects/Keywords: Chemical Engineering; controlled release; gellan gum; release rate

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APA (6th Edition):

Baawad, A. (2018). Release of Low Acyl Gellan Gum in a Controlled Release System. (Masters Thesis). University of Toledo. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=toledo1544823979777171

Chicago Manual of Style (16th Edition):

Baawad, Abdullah. “Release of Low Acyl Gellan Gum in a Controlled Release System.” 2018. Masters Thesis, University of Toledo. Accessed October 22, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1544823979777171.

MLA Handbook (7th Edition):

Baawad, Abdullah. “Release of Low Acyl Gellan Gum in a Controlled Release System.” 2018. Web. 22 Oct 2019.

Vancouver:

Baawad A. Release of Low Acyl Gellan Gum in a Controlled Release System. [Internet] [Masters thesis]. University of Toledo; 2018. [cited 2019 Oct 22]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1544823979777171.

Council of Science Editors:

Baawad A. Release of Low Acyl Gellan Gum in a Controlled Release System. [Masters Thesis]. University of Toledo; 2018. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1544823979777171


Georgia Tech

27. Padmore, Trudy J. Controlled release of GLP-1 from affinity-based protein microspheres and quantitative analysis of the role of fiber length on phagocytosis and inflammatory response by macrophages.

Degree: PhD, Chemical and Biomolecular Engineering, 2016, Georgia Tech

 Peptide drugs are highly specific and efficacious; interest in them remains high despite the challenges of rapid clearance and degradation. To overcome these limitations peptide… (more)

Subjects/Keywords: GLP-1; Controlled release; Affinity-based release; Protein microspheres; Fiber length; Length models

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APA (6th Edition):

Padmore, T. J. (2016). Controlled release of GLP-1 from affinity-based protein microspheres and quantitative analysis of the role of fiber length on phagocytosis and inflammatory response by macrophages. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/56336

Chicago Manual of Style (16th Edition):

Padmore, Trudy J. “Controlled release of GLP-1 from affinity-based protein microspheres and quantitative analysis of the role of fiber length on phagocytosis and inflammatory response by macrophages.” 2016. Doctoral Dissertation, Georgia Tech. Accessed October 22, 2019. http://hdl.handle.net/1853/56336.

MLA Handbook (7th Edition):

Padmore, Trudy J. “Controlled release of GLP-1 from affinity-based protein microspheres and quantitative analysis of the role of fiber length on phagocytosis and inflammatory response by macrophages.” 2016. Web. 22 Oct 2019.

Vancouver:

Padmore TJ. Controlled release of GLP-1 from affinity-based protein microspheres and quantitative analysis of the role of fiber length on phagocytosis and inflammatory response by macrophages. [Internet] [Doctoral dissertation]. Georgia Tech; 2016. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/1853/56336.

Council of Science Editors:

Padmore TJ. Controlled release of GLP-1 from affinity-based protein microspheres and quantitative analysis of the role of fiber length on phagocytosis and inflammatory response by macrophages. [Doctoral Dissertation]. Georgia Tech; 2016. Available from: http://hdl.handle.net/1853/56336


The Ohio State University

28. Ostrom, Aaron Kale. Comparing the effect of controlled-release, slow-release, and water-soluble fertilizers on plant growth and nutrient leaching.

Degree: MS, Horticulture and Crop Science, 2011, The Ohio State University

 In the first experiment of this thesis, four different fertilizers were applied at three rates each in order to investigate their effect on growth and… (more)

Subjects/Keywords: Horticulture; floriculture; new guinea impatiens; slow-release fertilizer; controlled-release fertilizer; nutrient leaching

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APA (6th Edition):

Ostrom, A. K. (2011). Comparing the effect of controlled-release, slow-release, and water-soluble fertilizers on plant growth and nutrient leaching. (Masters Thesis). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1299641954

Chicago Manual of Style (16th Edition):

Ostrom, Aaron Kale. “Comparing the effect of controlled-release, slow-release, and water-soluble fertilizers on plant growth and nutrient leaching.” 2011. Masters Thesis, The Ohio State University. Accessed October 22, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1299641954.

MLA Handbook (7th Edition):

Ostrom, Aaron Kale. “Comparing the effect of controlled-release, slow-release, and water-soluble fertilizers on plant growth and nutrient leaching.” 2011. Web. 22 Oct 2019.

Vancouver:

Ostrom AK. Comparing the effect of controlled-release, slow-release, and water-soluble fertilizers on plant growth and nutrient leaching. [Internet] [Masters thesis]. The Ohio State University; 2011. [cited 2019 Oct 22]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1299641954.

Council of Science Editors:

Ostrom AK. Comparing the effect of controlled-release, slow-release, and water-soluble fertilizers on plant growth and nutrient leaching. [Masters Thesis]. The Ohio State University; 2011. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1299641954


University of Cincinnati

29. Tolia, Gaurav. Use of Silicone Adhesive for Improving Oral Controlled Delivery.

Degree: PhD, Pharmacy: Pharmaceutical Sciences/Biopharmaceutics, 2018, University of Cincinnati

Controlled release oral dosage form offers great advantages over conventional dosage form by providing steady drug plasma concentration, decreasing the frequency of administration, and providing… (more)

Subjects/Keywords: Pharmaceuticals; Controlled release; Drug delivery; Silicone polymer; Drug release; Matrix tablet; Polymer properties

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APA (6th Edition):

Tolia, G. (2018). Use of Silicone Adhesive for Improving Oral Controlled Delivery. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1521190743860228

Chicago Manual of Style (16th Edition):

Tolia, Gaurav. “Use of Silicone Adhesive for Improving Oral Controlled Delivery.” 2018. Doctoral Dissertation, University of Cincinnati. Accessed October 22, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1521190743860228.

MLA Handbook (7th Edition):

Tolia, Gaurav. “Use of Silicone Adhesive for Improving Oral Controlled Delivery.” 2018. Web. 22 Oct 2019.

Vancouver:

Tolia G. Use of Silicone Adhesive for Improving Oral Controlled Delivery. [Internet] [Doctoral dissertation]. University of Cincinnati; 2018. [cited 2019 Oct 22]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1521190743860228.

Council of Science Editors:

Tolia G. Use of Silicone Adhesive for Improving Oral Controlled Delivery. [Doctoral Dissertation]. University of Cincinnati; 2018. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1521190743860228


University of Lund

30. Fredenberg, Susanne. Poly(Lactide-co-Glycolide) in Controlled-Release Pharmaceuticals - Release Mechanisms.

Degree: 2011, University of Lund

Controlled-release formulations reduce the frequency of injections and better maintain plasma concentrations within the therapeutic window. Poly(D,L-lactide-co-glycolide) (PLG) is currently the most frequently used biodegradable… (more)

Subjects/Keywords: Kemiteknik; PLGA; Poly(lactide-co-glycolide); Release mechanism; Diffusion; Controlled Release; Degradation; Protein

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APA (6th Edition):

Fredenberg, S. (2011). Poly(Lactide-co-Glycolide) in Controlled-Release Pharmaceuticals - Release Mechanisms. (Doctoral Dissertation). University of Lund. Retrieved from http://lup.lub.lu.se/record/1788976 ; http://portal.research.lu.se/ws/files/5775852/1788978.pdf

Chicago Manual of Style (16th Edition):

Fredenberg, Susanne. “Poly(Lactide-co-Glycolide) in Controlled-Release Pharmaceuticals - Release Mechanisms.” 2011. Doctoral Dissertation, University of Lund. Accessed October 22, 2019. http://lup.lub.lu.se/record/1788976 ; http://portal.research.lu.se/ws/files/5775852/1788978.pdf.

MLA Handbook (7th Edition):

Fredenberg, Susanne. “Poly(Lactide-co-Glycolide) in Controlled-Release Pharmaceuticals - Release Mechanisms.” 2011. Web. 22 Oct 2019.

Vancouver:

Fredenberg S. Poly(Lactide-co-Glycolide) in Controlled-Release Pharmaceuticals - Release Mechanisms. [Internet] [Doctoral dissertation]. University of Lund; 2011. [cited 2019 Oct 22]. Available from: http://lup.lub.lu.se/record/1788976 ; http://portal.research.lu.se/ws/files/5775852/1788978.pdf.

Council of Science Editors:

Fredenberg S. Poly(Lactide-co-Glycolide) in Controlled-Release Pharmaceuticals - Release Mechanisms. [Doctoral Dissertation]. University of Lund; 2011. Available from: http://lup.lub.lu.se/record/1788976 ; http://portal.research.lu.se/ws/files/5775852/1788978.pdf

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