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You searched for subject:(controlled drug release). Showing records 1 – 30 of 119 total matches.

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University of Cambridge

1. 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 July 21, 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. 21 Jul 2019.

Vancouver:

Chia LSO. Investigating Controlled Release Pulmonary Drug Delivery Systems . [Internet] [Thesis]. University of Cambridge; 2018. [cited 2019 Jul 21]. 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


University of Cincinnati

2. 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 July 21, 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. 21 Jul 2019.

Vancouver:

Tolia G. Use of Silicone Adhesive for Improving Oral Controlled Delivery. [Internet] [Doctoral dissertation]. University of Cincinnati; 2018. [cited 2019 Jul 21]. 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 Cincinnati

3. Zhou, Zilan. Engineered Nanoparticle for Targeted and Controlled Drug Delivery.

Degree: PhD, Engineering and Applied Science: Chemical Engineering, 2017, University of Cincinnati

 Cancer is still a major threat to public health worldwide. Thanks to the extensive studies in cancer biology and growing understanding in cancer, many novel… (more)

Subjects/Keywords: Chemical Engineering; Drug delivery; controlled drug release; sequential delivery; combination therapy

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APA (6th Edition):

Zhou, Z. (2017). Engineered Nanoparticle for Targeted and Controlled Drug Delivery. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1505831582487098

Chicago Manual of Style (16th Edition):

Zhou, Zilan. “Engineered Nanoparticle for Targeted and Controlled Drug Delivery.” 2017. Doctoral Dissertation, University of Cincinnati. Accessed July 21, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1505831582487098.

MLA Handbook (7th Edition):

Zhou, Zilan. “Engineered Nanoparticle for Targeted and Controlled Drug Delivery.” 2017. Web. 21 Jul 2019.

Vancouver:

Zhou Z. Engineered Nanoparticle for Targeted and Controlled Drug Delivery. [Internet] [Doctoral dissertation]. University of Cincinnati; 2017. [cited 2019 Jul 21]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1505831582487098.

Council of Science Editors:

Zhou Z. Engineered Nanoparticle for Targeted and Controlled Drug Delivery. [Doctoral Dissertation]. University of Cincinnati; 2017. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1505831582487098


University of Georgia

4. McLean, Amy Katherine. Using controlled internal drug release (CIDR) inserts for estrus synchronization in dairy heifers.

Degree: MS, Animal and Dairy Science, 2003, University of Georgia

 In Experiment 1, 164 heifers were assigned to two treatment groups. Each received a CIDR insert for 7 days. Treatment 1 received prostaglandin (PGF2 á… (more)

Subjects/Keywords: Controlled Internal Drug Release (CIDR)

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APA (6th Edition):

McLean, A. K. (2003). Using controlled internal drug release (CIDR) inserts for estrus synchronization in dairy heifers. (Masters Thesis). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/mclean_amy_k_200312_ms

Chicago Manual of Style (16th Edition):

McLean, Amy Katherine. “Using controlled internal drug release (CIDR) inserts for estrus synchronization in dairy heifers.” 2003. Masters Thesis, University of Georgia. Accessed July 21, 2019. http://purl.galileo.usg.edu/uga_etd/mclean_amy_k_200312_ms.

MLA Handbook (7th Edition):

McLean, Amy Katherine. “Using controlled internal drug release (CIDR) inserts for estrus synchronization in dairy heifers.” 2003. Web. 21 Jul 2019.

Vancouver:

McLean AK. Using controlled internal drug release (CIDR) inserts for estrus synchronization in dairy heifers. [Internet] [Masters thesis]. University of Georgia; 2003. [cited 2019 Jul 21]. Available from: http://purl.galileo.usg.edu/uga_etd/mclean_amy_k_200312_ms.

Council of Science Editors:

McLean AK. Using controlled internal drug release (CIDR) inserts for estrus synchronization in dairy heifers. [Masters Thesis]. University of Georgia; 2003. Available from: http://purl.galileo.usg.edu/uga_etd/mclean_amy_k_200312_ms


University of Georgia

5. Fain, Jillian L. Evaluating the effectiveness of using the controlled internal drug release (CIDR) insert for synchronization of estrus and post-insemination progesterone therapy to improve reproductive performance of dairy cattle.

Degree: MS, Animal and Dairy Science, 2005, University of Georgia

 Study 1 combined the CIDR insert for ovulation synchronization and TAI. Animals received 50 µg GnRH (-9 d), CIDR (1.38 g progesterone) (-9 d), 25… (more)

Subjects/Keywords: Controlled Internal Drug Release (CIDR)

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APA (6th Edition):

Fain, J. L. (2005). Evaluating the effectiveness of using the controlled internal drug release (CIDR) insert for synchronization of estrus and post-insemination progesterone therapy to improve reproductive performance of dairy cattle. (Masters Thesis). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/fain_jillian_l_200512_ms

Chicago Manual of Style (16th Edition):

Fain, Jillian L. “Evaluating the effectiveness of using the controlled internal drug release (CIDR) insert for synchronization of estrus and post-insemination progesterone therapy to improve reproductive performance of dairy cattle.” 2005. Masters Thesis, University of Georgia. Accessed July 21, 2019. http://purl.galileo.usg.edu/uga_etd/fain_jillian_l_200512_ms.

MLA Handbook (7th Edition):

Fain, Jillian L. “Evaluating the effectiveness of using the controlled internal drug release (CIDR) insert for synchronization of estrus and post-insemination progesterone therapy to improve reproductive performance of dairy cattle.” 2005. Web. 21 Jul 2019.

Vancouver:

Fain JL. Evaluating the effectiveness of using the controlled internal drug release (CIDR) insert for synchronization of estrus and post-insemination progesterone therapy to improve reproductive performance of dairy cattle. [Internet] [Masters thesis]. University of Georgia; 2005. [cited 2019 Jul 21]. Available from: http://purl.galileo.usg.edu/uga_etd/fain_jillian_l_200512_ms.

Council of Science Editors:

Fain JL. Evaluating the effectiveness of using the controlled internal drug release (CIDR) insert for synchronization of estrus and post-insemination progesterone therapy to improve reproductive performance of dairy cattle. [Masters Thesis]. University of Georgia; 2005. Available from: http://purl.galileo.usg.edu/uga_etd/fain_jillian_l_200512_ms


Queensland University of Technology

6. Hsieh, Mike Hou-Ning. Mathematical modelling of controlled drug release from polymer micro-spheres : incorporating the effects of swelling, diffusion and dissolution via moving boundary problems.

Degree: 2012, Queensland University of Technology

Controlled drug delivery is a key topic in modern pharmacotherapy, where controlled drug delivery devices are required to prolong the period of release, maintain a… (more)

Subjects/Keywords: mathematical modelling; controlled drug release; polymer micro-spheres; swelling; boundary problems

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APA (6th Edition):

Hsieh, M. H. (2012). Mathematical modelling of controlled drug release from polymer micro-spheres : incorporating the effects of swelling, diffusion and dissolution via moving boundary problems. (Thesis). Queensland University of Technology. Retrieved from https://eprints.qut.edu.au/60306/

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):

Hsieh, Mike Hou-Ning. “Mathematical modelling of controlled drug release from polymer micro-spheres : incorporating the effects of swelling, diffusion and dissolution via moving boundary problems.” 2012. Thesis, Queensland University of Technology. Accessed July 21, 2019. https://eprints.qut.edu.au/60306/.

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

MLA Handbook (7th Edition):

Hsieh, Mike Hou-Ning. “Mathematical modelling of controlled drug release from polymer micro-spheres : incorporating the effects of swelling, diffusion and dissolution via moving boundary problems.” 2012. Web. 21 Jul 2019.

Vancouver:

Hsieh MH. Mathematical modelling of controlled drug release from polymer micro-spheres : incorporating the effects of swelling, diffusion and dissolution via moving boundary problems. [Internet] [Thesis]. Queensland University of Technology; 2012. [cited 2019 Jul 21]. Available from: https://eprints.qut.edu.au/60306/.

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

Council of Science Editors:

Hsieh MH. Mathematical modelling of controlled drug release from polymer micro-spheres : incorporating the effects of swelling, diffusion and dissolution via moving boundary problems. [Thesis]. Queensland University of Technology; 2012. Available from: https://eprints.qut.edu.au/60306/

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


Queen Mary, University of London

7. Ma, Jia. Processing of polymer-based systems for improved performance and controlled release.

Degree: PhD, 2011, Queen Mary, University of London

 This thesis focuses on improved processing methods for enhanced mechanical properties in polymer nanocomposites, and controlled drug release in polymer based delivery systems. Supercritical carbon… (more)

Subjects/Keywords: 668.9; Chemistry; polymer nanocomposites; Polymer based delivery systems; controlled drug release

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APA (6th Edition):

Ma, J. (2011). Processing of polymer-based systems for improved performance and controlled release. (Doctoral Dissertation). Queen Mary, University of London. Retrieved from http://qmro.qmul.ac.uk/xmlui/handle/123456789/15048 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.542016

Chicago Manual of Style (16th Edition):

Ma, Jia. “Processing of polymer-based systems for improved performance and controlled release.” 2011. Doctoral Dissertation, Queen Mary, University of London. Accessed July 21, 2019. http://qmro.qmul.ac.uk/xmlui/handle/123456789/15048 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.542016.

MLA Handbook (7th Edition):

Ma, Jia. “Processing of polymer-based systems for improved performance and controlled release.” 2011. Web. 21 Jul 2019.

Vancouver:

Ma J. Processing of polymer-based systems for improved performance and controlled release. [Internet] [Doctoral dissertation]. Queen Mary, University of London; 2011. [cited 2019 Jul 21]. Available from: http://qmro.qmul.ac.uk/xmlui/handle/123456789/15048 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.542016.

Council of Science Editors:

Ma J. Processing of polymer-based systems for improved performance and controlled release. [Doctoral Dissertation]. Queen Mary, University of London; 2011. Available from: http://qmro.qmul.ac.uk/xmlui/handle/123456789/15048 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.542016


McMaster University

8. Mateen, Rabia. MOLECULAR RECOGNITION EVENTS IN POLYMER-BASED SYSTEMS.

Degree: PhD, 2019, McMaster University

 Molecular recognition is an important tool for developing tunable controlled release systems and fabricating biosensors with increased selectivity and sensitivity. The development of polymer-based materials… (more)

Subjects/Keywords: molecular recognition; polymers; hydrogels; biosensing; drug discovery; controlled release devices

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APA (6th Edition):

Mateen, R. (2019). MOLECULAR RECOGNITION EVENTS IN POLYMER-BASED SYSTEMS. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/23958

Chicago Manual of Style (16th Edition):

Mateen, Rabia. “MOLECULAR RECOGNITION EVENTS IN POLYMER-BASED SYSTEMS.” 2019. Doctoral Dissertation, McMaster University. Accessed July 21, 2019. http://hdl.handle.net/11375/23958.

MLA Handbook (7th Edition):

Mateen, Rabia. “MOLECULAR RECOGNITION EVENTS IN POLYMER-BASED SYSTEMS.” 2019. Web. 21 Jul 2019.

Vancouver:

Mateen R. MOLECULAR RECOGNITION EVENTS IN POLYMER-BASED SYSTEMS. [Internet] [Doctoral dissertation]. McMaster University; 2019. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/11375/23958.

Council of Science Editors:

Mateen R. MOLECULAR RECOGNITION EVENTS IN POLYMER-BASED SYSTEMS. [Doctoral Dissertation]. McMaster University; 2019. Available from: http://hdl.handle.net/11375/23958


Georgia Tech

9. Srinivasan, Sangeetha. Conditioning dendritic cell responses using engineered biomaterials for immunotherapy.

Degree: PhD, Biomedical Engineering (Joint GT/Emory Department), 2016, Georgia Tech

 Pivotal discoveries in the field of immunology over the last five decades have changed the way new therapies are designed for applications as varied as… (more)

Subjects/Keywords: Biomaterial; Immunotherapy; Dendritic cells; Microparticles; Scaffold; Controlled release; Drug delivery; Autoimmune

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APA (6th Edition):

Srinivasan, S. (2016). Conditioning dendritic cell responses using engineered biomaterials for immunotherapy. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/59153

Chicago Manual of Style (16th Edition):

Srinivasan, Sangeetha. “Conditioning dendritic cell responses using engineered biomaterials for immunotherapy.” 2016. Doctoral Dissertation, Georgia Tech. Accessed July 21, 2019. http://hdl.handle.net/1853/59153.

MLA Handbook (7th Edition):

Srinivasan, Sangeetha. “Conditioning dendritic cell responses using engineered biomaterials for immunotherapy.” 2016. Web. 21 Jul 2019.

Vancouver:

Srinivasan S. Conditioning dendritic cell responses using engineered biomaterials for immunotherapy. [Internet] [Doctoral dissertation]. Georgia Tech; 2016. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/1853/59153.

Council of Science Editors:

Srinivasan S. Conditioning dendritic cell responses using engineered biomaterials for immunotherapy. [Doctoral Dissertation]. Georgia Tech; 2016. Available from: http://hdl.handle.net/1853/59153

10. SILVA, Dayanne Tomaz Casimiro da. Desenvolvimento de sistemas de dispersões sólidas para liberação pH dependente do tamoxifeno .

Degree: 2016, Universidade Federal de Pernambuco

 O Tamoxifeno (TMX) utilizado no tratamento do câncer de mama, apresenta diversas desvantagens, elevada toxicidade, baixa solubilidade e precipitação no ambiente gástrico na forma de… (more)

Subjects/Keywords: Polímeros; Liberação controlada de fármacos; Dissolução; Polymers; Controlled drug release; Dissolution

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APA (6th Edition):

SILVA, D. T. C. d. (2016). Desenvolvimento de sistemas de dispersões sólidas para liberação pH dependente do tamoxifeno . (Thesis). Universidade Federal de Pernambuco. Retrieved from https://repositorio.ufpe.br/handle/123456789/18371

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):

SILVA, Dayanne Tomaz Casimiro da. “Desenvolvimento de sistemas de dispersões sólidas para liberação pH dependente do tamoxifeno .” 2016. Thesis, Universidade Federal de Pernambuco. Accessed July 21, 2019. https://repositorio.ufpe.br/handle/123456789/18371.

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

MLA Handbook (7th Edition):

SILVA, Dayanne Tomaz Casimiro da. “Desenvolvimento de sistemas de dispersões sólidas para liberação pH dependente do tamoxifeno .” 2016. Web. 21 Jul 2019.

Vancouver:

SILVA DTCd. Desenvolvimento de sistemas de dispersões sólidas para liberação pH dependente do tamoxifeno . [Internet] [Thesis]. Universidade Federal de Pernambuco; 2016. [cited 2019 Jul 21]. Available from: https://repositorio.ufpe.br/handle/123456789/18371.

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

Council of Science Editors:

SILVA DTCd. Desenvolvimento de sistemas de dispersões sólidas para liberação pH dependente do tamoxifeno . [Thesis]. Universidade Federal de Pernambuco; 2016. Available from: https://repositorio.ufpe.br/handle/123456789/18371

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


University of Waikato

11. Babu, Kavitha Mary Vadakkel. The Development of a Novel Controlled Release Drug Delivery System .

Degree: 2007, University of Waikato

 The aim of this research was to formulate, characterise and assess the feasibility of a novel drug delivery system known as the in situ gelling… (more)

Subjects/Keywords: Controlled Release Drug Delivery; Parenteral

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APA (6th Edition):

Babu, K. M. V. (2007). The Development of a Novel Controlled Release Drug Delivery System . (Doctoral Dissertation). University of Waikato. Retrieved from http://hdl.handle.net/10289/2590

Chicago Manual of Style (16th Edition):

Babu, Kavitha Mary Vadakkel. “The Development of a Novel Controlled Release Drug Delivery System .” 2007. Doctoral Dissertation, University of Waikato. Accessed July 21, 2019. http://hdl.handle.net/10289/2590.

MLA Handbook (7th Edition):

Babu, Kavitha Mary Vadakkel. “The Development of a Novel Controlled Release Drug Delivery System .” 2007. Web. 21 Jul 2019.

Vancouver:

Babu KMV. The Development of a Novel Controlled Release Drug Delivery System . [Internet] [Doctoral dissertation]. University of Waikato; 2007. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/10289/2590.

Council of Science Editors:

Babu KMV. The Development of a Novel Controlled Release Drug Delivery System . [Doctoral Dissertation]. University of Waikato; 2007. Available from: http://hdl.handle.net/10289/2590


University of Rochester

12. Van Hove, Amy H. (1987 - ). Enzymatically-responsive poly(ethylene glycol) hydrogels for the controlled delivery of therapeutic peptides.

Degree: PhD, 2015, University of Rochester

 Therapeutic angiogenesis holds great potential for treatment of ischemic tissues and in tissue engineering, where insufficient vascularization limits construct size, complexity, and anastomosis with host… (more)

Subjects/Keywords: Controlled release; Drug delivery; Hydrogel; Peptide; Poly(ethylene glycol); Stimuli-responsive

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APA (6th Edition):

Van Hove, A. H. (. -. ). (2015). Enzymatically-responsive poly(ethylene glycol) hydrogels for the controlled delivery of therapeutic peptides. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/29655

Chicago Manual of Style (16th Edition):

Van Hove, Amy H (1987 - ). “Enzymatically-responsive poly(ethylene glycol) hydrogels for the controlled delivery of therapeutic peptides.” 2015. Doctoral Dissertation, University of Rochester. Accessed July 21, 2019. http://hdl.handle.net/1802/29655.

MLA Handbook (7th Edition):

Van Hove, Amy H (1987 - ). “Enzymatically-responsive poly(ethylene glycol) hydrogels for the controlled delivery of therapeutic peptides.” 2015. Web. 21 Jul 2019.

Vancouver:

Van Hove AH(-). Enzymatically-responsive poly(ethylene glycol) hydrogels for the controlled delivery of therapeutic peptides. [Internet] [Doctoral dissertation]. University of Rochester; 2015. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/1802/29655.

Council of Science Editors:

Van Hove AH(-). Enzymatically-responsive poly(ethylene glycol) hydrogels for the controlled delivery of therapeutic peptides. [Doctoral Dissertation]. University of Rochester; 2015. Available from: http://hdl.handle.net/1802/29655


University of Southern California

13. Wang, Wan. Development of protein polymer therapeutics for the eye.

Degree: PhD, Pharmaceutical Sciences, 2014, University of Southern California

 Collecting visual information from the surroundings and transmitting the signals to the brain, the eye plays a crucial role in our daily life. Visual impairment… (more)

Subjects/Keywords: bioavailability; cell uptake; controlled release; drug delivery; elastin‐like polypeptides; ocular

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APA (6th Edition):

Wang, W. (2014). Development of protein polymer therapeutics for the eye. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/429068/rec/1964

Chicago Manual of Style (16th Edition):

Wang, Wan. “Development of protein polymer therapeutics for the eye.” 2014. Doctoral Dissertation, University of Southern California. Accessed July 21, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/429068/rec/1964.

MLA Handbook (7th Edition):

Wang, Wan. “Development of protein polymer therapeutics for the eye.” 2014. Web. 21 Jul 2019.

Vancouver:

Wang W. Development of protein polymer therapeutics for the eye. [Internet] [Doctoral dissertation]. University of Southern California; 2014. [cited 2019 Jul 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/429068/rec/1964.

Council of Science Editors:

Wang W. Development of protein polymer therapeutics for the eye. [Doctoral Dissertation]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/429068/rec/1964


Arizona State University

14. Labiano, Alpha Chavez. Evaluation of Nanoporous Carbon Thin Films for Drug Loading and Controlled Release.

Degree: MS, Chemical Engineering, 2011, Arizona State University

 Mesoporous materials that possess large surface area, tunable pore size, and ordered structures are attractive features for many applications such as adsorption, protein separation, enzyme… (more)

Subjects/Keywords: Chemical engineering; carbon; controlled release; drug delivery; films; nanoporous

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APA (6th Edition):

Labiano, A. C. (2011). Evaluation of Nanoporous Carbon Thin Films for Drug Loading and Controlled Release. (Masters Thesis). Arizona State University. Retrieved from http://repository.asu.edu/items/14389

Chicago Manual of Style (16th Edition):

Labiano, Alpha Chavez. “Evaluation of Nanoporous Carbon Thin Films for Drug Loading and Controlled Release.” 2011. Masters Thesis, Arizona State University. Accessed July 21, 2019. http://repository.asu.edu/items/14389.

MLA Handbook (7th Edition):

Labiano, Alpha Chavez. “Evaluation of Nanoporous Carbon Thin Films for Drug Loading and Controlled Release.” 2011. Web. 21 Jul 2019.

Vancouver:

Labiano AC. Evaluation of Nanoporous Carbon Thin Films for Drug Loading and Controlled Release. [Internet] [Masters thesis]. Arizona State University; 2011. [cited 2019 Jul 21]. Available from: http://repository.asu.edu/items/14389.

Council of Science Editors:

Labiano AC. Evaluation of Nanoporous Carbon Thin Films for Drug Loading and Controlled Release. [Masters Thesis]. Arizona State University; 2011. Available from: http://repository.asu.edu/items/14389


University of Texas – Austin

15. Du, Ju. Polymer-based antibiotics formulation for the treatment of lung infections.

Degree: Pharmaceutical Sciences, 2015, University of Texas – Austin

 Delivering antibiotics through pulmonary is a promising approach for treatment of cystic fibrosis (CF). For the current marketed antibiotic formulations, however, the requirement of multiple… (more)

Subjects/Keywords: Antibiotic; Pulmonary; Controlled drug release; Polymer; Lung infections; Polymer based antiobiotics; Lung infection treatment; Controlled pulmonary release

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APA (6th Edition):

Du, J. (2015). Polymer-based antibiotics formulation for the treatment of lung infections. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/47197

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):

Du, Ju. “Polymer-based antibiotics formulation for the treatment of lung infections.” 2015. Thesis, University of Texas – Austin. Accessed July 21, 2019. http://hdl.handle.net/2152/47197.

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

MLA Handbook (7th Edition):

Du, Ju. “Polymer-based antibiotics formulation for the treatment of lung infections.” 2015. Web. 21 Jul 2019.

Vancouver:

Du J. Polymer-based antibiotics formulation for the treatment of lung infections. [Internet] [Thesis]. University of Texas – Austin; 2015. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/2152/47197.

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

Council of Science Editors:

Du J. Polymer-based antibiotics formulation for the treatment of lung infections. [Thesis]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/47197

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

16. Kirksak Assawadarakorn. Evaluation of tobacco pipe as dry power inhaler device .

Degree: Faculty of Pharmaceutical Sciences (Pharmaceutical Sciences), 2007, Prince of Songkla University

Subjects/Keywords: Controlled release technology; Controlled release preparations; Drug delivery systems

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APA (6th Edition):

Assawadarakorn, K. (2007). Evaluation of tobacco pipe as dry power inhaler device . (Thesis). Prince of Songkla University. Retrieved from http://kb.psu.ac.th/psukb/handle/2553/1464

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):

Assawadarakorn, Kirksak. “Evaluation of tobacco pipe as dry power inhaler device .” 2007. Thesis, Prince of Songkla University. Accessed July 21, 2019. http://kb.psu.ac.th/psukb/handle/2553/1464.

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

MLA Handbook (7th Edition):

Assawadarakorn, Kirksak. “Evaluation of tobacco pipe as dry power inhaler device .” 2007. Web. 21 Jul 2019.

Vancouver:

Assawadarakorn K. Evaluation of tobacco pipe as dry power inhaler device . [Internet] [Thesis]. Prince of Songkla University; 2007. [cited 2019 Jul 21]. Available from: http://kb.psu.ac.th/psukb/handle/2553/1464.

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

Council of Science Editors:

Assawadarakorn K. Evaluation of tobacco pipe as dry power inhaler device . [Thesis]. Prince of Songkla University; 2007. Available from: http://kb.psu.ac.th/psukb/handle/2553/1464

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

17. Pijush Kumar Paul. Preparation and Characterization of Biomimetic Molecularly Imprinted Polymer for Controlled Release Drug Delivery System of Oral Insulin .

Degree: คณะเภสัชศาสตร์ ภาควิชาเภสัชเคมี, 2017, Prince of Songkla University

Subjects/Keywords: Insulin Controlled release; Controlled release preparations; Drug delivery systems

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APA (6th Edition):

Paul, P. K. (2017). Preparation and Characterization of Biomimetic Molecularly Imprinted Polymer for Controlled Release Drug Delivery System of Oral Insulin . (Thesis). Prince of Songkla University. Retrieved from http://kb.psu.ac.th/psukb/handle/2016/12189

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):

Paul, Pijush Kumar. “Preparation and Characterization of Biomimetic Molecularly Imprinted Polymer for Controlled Release Drug Delivery System of Oral Insulin .” 2017. Thesis, Prince of Songkla University. Accessed July 21, 2019. http://kb.psu.ac.th/psukb/handle/2016/12189.

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

MLA Handbook (7th Edition):

Paul, Pijush Kumar. “Preparation and Characterization of Biomimetic Molecularly Imprinted Polymer for Controlled Release Drug Delivery System of Oral Insulin .” 2017. Web. 21 Jul 2019.

Vancouver:

Paul PK. Preparation and Characterization of Biomimetic Molecularly Imprinted Polymer for Controlled Release Drug Delivery System of Oral Insulin . [Internet] [Thesis]. Prince of Songkla University; 2017. [cited 2019 Jul 21]. Available from: http://kb.psu.ac.th/psukb/handle/2016/12189.

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

Council of Science Editors:

Paul PK. Preparation and Characterization of Biomimetic Molecularly Imprinted Polymer for Controlled Release Drug Delivery System of Oral Insulin . [Thesis]. Prince of Songkla University; 2017. Available from: http://kb.psu.ac.th/psukb/handle/2016/12189

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


Duke University

18. Luginbuhl, Kelli Michelle. Recombinantly Engineered Polypeptides for Drug Delivery .

Degree: 2017, Duke University

  Novel drug delivery methods aims to improve the therapeutic efficacy by enhancing the molecule’s pharmacokinetic profile as well as increasing its accumulation at the… (more)

Subjects/Keywords: Biomedical engineering; Materials Science; Controlled release; Drug delivery; Drug depot; Glucagon-like peptide-1

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APA (6th Edition):

Luginbuhl, K. M. (2017). Recombinantly Engineered Polypeptides for Drug Delivery . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/16310

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):

Luginbuhl, Kelli Michelle. “Recombinantly Engineered Polypeptides for Drug Delivery .” 2017. Thesis, Duke University. Accessed July 21, 2019. http://hdl.handle.net/10161/16310.

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

MLA Handbook (7th Edition):

Luginbuhl, Kelli Michelle. “Recombinantly Engineered Polypeptides for Drug Delivery .” 2017. Web. 21 Jul 2019.

Vancouver:

Luginbuhl KM. Recombinantly Engineered Polypeptides for Drug Delivery . [Internet] [Thesis]. Duke University; 2017. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/10161/16310.

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

Council of Science Editors:

Luginbuhl KM. Recombinantly Engineered Polypeptides for Drug Delivery . [Thesis]. Duke University; 2017. Available from: http://hdl.handle.net/10161/16310

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


Universitat Politècnica de València

19. Giménez Morales, Cristina. Design of new bio-gated nanodevices for advanced communication processes and targeted controlled release of therapeutic agents .

Degree: 2016, Universitat Politècnica de València

 [EN] The present PhD thesis, which is entitled "Design of new bio-gated nanodevices for advanced communication processes and targeted controlled release of therapeutic agents" is… (more)

Subjects/Keywords: Mesoporous silica nanoparticles; Hybrid materials; Drug delivery system; Controlled drug delivery; Intracellular release

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APA (6th Edition):

Giménez Morales, C. (2016). Design of new bio-gated nanodevices for advanced communication processes and targeted controlled release of therapeutic agents . (Doctoral Dissertation). Universitat Politècnica de València. Retrieved from http://hdl.handle.net/10251/62822

Chicago Manual of Style (16th Edition):

Giménez Morales, Cristina. “Design of new bio-gated nanodevices for advanced communication processes and targeted controlled release of therapeutic agents .” 2016. Doctoral Dissertation, Universitat Politècnica de València. Accessed July 21, 2019. http://hdl.handle.net/10251/62822.

MLA Handbook (7th Edition):

Giménez Morales, Cristina. “Design of new bio-gated nanodevices for advanced communication processes and targeted controlled release of therapeutic agents .” 2016. Web. 21 Jul 2019.

Vancouver:

Giménez Morales C. Design of new bio-gated nanodevices for advanced communication processes and targeted controlled release of therapeutic agents . [Internet] [Doctoral dissertation]. Universitat Politècnica de València; 2016. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/10251/62822.

Council of Science Editors:

Giménez Morales C. Design of new bio-gated nanodevices for advanced communication processes and targeted controlled release of therapeutic agents . [Doctoral Dissertation]. Universitat Politècnica de València; 2016. Available from: http://hdl.handle.net/10251/62822


Universitat Politècnica de València

20. De la Torre Paredes, Cristina. Nanotechnology and supramolecular chemistry in controlled release and molecular recognition proceses for biomedical applications" .

Degree: 2018, Universitat Politècnica de València

 La presente tesis doctoral, titulada "Nanotecnología y química supramolecular en procesos de liberación controlada y reconocimiento molecular para aplicaciones biomédicas", se centra en dos temas… (more)

Subjects/Keywords: Mesoporous silica nanoparticles; Hybrid materials; Drug delivery system; Controlled drug delivery; Intracellular release

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APA (6th Edition):

De la Torre Paredes, C. (2018). Nanotechnology and supramolecular chemistry in controlled release and molecular recognition proceses for biomedical applications" . (Doctoral Dissertation). Universitat Politècnica de València. Retrieved from http://hdl.handle.net/10251/94043

Chicago Manual of Style (16th Edition):

De la Torre Paredes, Cristina. “Nanotechnology and supramolecular chemistry in controlled release and molecular recognition proceses for biomedical applications" .” 2018. Doctoral Dissertation, Universitat Politècnica de València. Accessed July 21, 2019. http://hdl.handle.net/10251/94043.

MLA Handbook (7th Edition):

De la Torre Paredes, Cristina. “Nanotechnology and supramolecular chemistry in controlled release and molecular recognition proceses for biomedical applications" .” 2018. Web. 21 Jul 2019.

Vancouver:

De la Torre Paredes C. Nanotechnology and supramolecular chemistry in controlled release and molecular recognition proceses for biomedical applications" . [Internet] [Doctoral dissertation]. Universitat Politècnica de València; 2018. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/10251/94043.

Council of Science Editors:

De la Torre Paredes C. Nanotechnology and supramolecular chemistry in controlled release and molecular recognition proceses for biomedical applications" . [Doctoral Dissertation]. Universitat Politècnica de València; 2018. Available from: http://hdl.handle.net/10251/94043


University of Texas – Austin

21. Rastogi, Ashish. Design, development, and evaluation of a scalable micro perforated drug delivery device capable of long-term zero order release.

Degree: Pharmacy, 2009, University of Texas – Austin

 Chronic diseases can often be managed by constantly delivering therapeutic amounts of drug for prolonged periods. A controlled release for extended duration would replace the… (more)

Subjects/Keywords: Implantable drug delivery systems; Controlled release of drugs; Zero order drug release rate; Perforated microtubes; Polyimide microtubes

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APA (6th Edition):

Rastogi, A. (2009). Design, development, and evaluation of a scalable micro perforated drug delivery device capable of long-term zero order release. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/7542

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):

Rastogi, Ashish. “Design, development, and evaluation of a scalable micro perforated drug delivery device capable of long-term zero order release.” 2009. Thesis, University of Texas – Austin. Accessed July 21, 2019. http://hdl.handle.net/2152/7542.

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

MLA Handbook (7th Edition):

Rastogi, Ashish. “Design, development, and evaluation of a scalable micro perforated drug delivery device capable of long-term zero order release.” 2009. Web. 21 Jul 2019.

Vancouver:

Rastogi A. Design, development, and evaluation of a scalable micro perforated drug delivery device capable of long-term zero order release. [Internet] [Thesis]. University of Texas – Austin; 2009. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/2152/7542.

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

Council of Science Editors:

Rastogi A. Design, development, and evaluation of a scalable micro perforated drug delivery device capable of long-term zero order release. [Thesis]. University of Texas – Austin; 2009. Available from: http://hdl.handle.net/2152/7542

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

22. Oberto Grangeiro da Silva. Hidroxiapatita mesoporosa pura e modificada organicamente com grupos nitrogenados síntese, caracterização e uso como carreadora de fármacos.

Degree: 2010, Universidade Federal da Paraíba

Materiais mesoporosos apresentam um arranjo de poros ordenados e uma distribuição de poros muito estreita aliada a altas áreas superficiais, que são características estruturais interessantes… (more)

Subjects/Keywords: Hidroxiapatita; Sólidos mesoporosos; Liberação Controlada de Fármacos; QUIMICA; Mesoporous solids; Hydroxyapatite; Controlled Drug Release

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APA (6th Edition):

Silva, O. G. d. (2010). Hidroxiapatita mesoporosa pura e modificada organicamente com grupos nitrogenados síntese, caracterização e uso como carreadora de fármacos. (Thesis). Universidade Federal da Paraíba. Retrieved from http://bdtd.biblioteca.ufpb.br/tde_busca/arquivo.php?codArquivo=1721

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):

Silva, Oberto Grangeiro da. “Hidroxiapatita mesoporosa pura e modificada organicamente com grupos nitrogenados síntese, caracterização e uso como carreadora de fármacos.” 2010. Thesis, Universidade Federal da Paraíba. Accessed July 21, 2019. http://bdtd.biblioteca.ufpb.br/tde_busca/arquivo.php?codArquivo=1721.

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

MLA Handbook (7th Edition):

Silva, Oberto Grangeiro da. “Hidroxiapatita mesoporosa pura e modificada organicamente com grupos nitrogenados síntese, caracterização e uso como carreadora de fármacos.” 2010. Web. 21 Jul 2019.

Vancouver:

Silva OGd. Hidroxiapatita mesoporosa pura e modificada organicamente com grupos nitrogenados síntese, caracterização e uso como carreadora de fármacos. [Internet] [Thesis]. Universidade Federal da Paraíba; 2010. [cited 2019 Jul 21]. Available from: http://bdtd.biblioteca.ufpb.br/tde_busca/arquivo.php?codArquivo=1721.

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

Council of Science Editors:

Silva OGd. Hidroxiapatita mesoporosa pura e modificada organicamente com grupos nitrogenados síntese, caracterização e uso como carreadora de fármacos. [Thesis]. Universidade Federal da Paraíba; 2010. Available from: http://bdtd.biblioteca.ufpb.br/tde_busca/arquivo.php?codArquivo=1721

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


Temple University

23. Owaisat, Suzan. A novel oral dosage form with drug independent formulation and variable controlled release.

Degree: PhD, 2015, Temple University

Pharmaceutical Sciences

A unique dosage form which uses a hydrophilic polymer was developed to provide for a predicable release of several drugs. This drug release(more)

Subjects/Keywords: Pharmaceutical sciences;

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APA (6th Edition):

Owaisat, S. (2015). A novel oral dosage form with drug independent formulation and variable controlled release. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,342831

Chicago Manual of Style (16th Edition):

Owaisat, Suzan. “A novel oral dosage form with drug independent formulation and variable controlled release.” 2015. Doctoral Dissertation, Temple University. Accessed July 21, 2019. http://digital.library.temple.edu/u?/p245801coll10,342831.

MLA Handbook (7th Edition):

Owaisat, Suzan. “A novel oral dosage form with drug independent formulation and variable controlled release.” 2015. Web. 21 Jul 2019.

Vancouver:

Owaisat S. A novel oral dosage form with drug independent formulation and variable controlled release. [Internet] [Doctoral dissertation]. Temple University; 2015. [cited 2019 Jul 21]. Available from: http://digital.library.temple.edu/u?/p245801coll10,342831.

Council of Science Editors:

Owaisat S. A novel oral dosage form with drug independent formulation and variable controlled release. [Doctoral Dissertation]. Temple University; 2015. Available from: http://digital.library.temple.edu/u?/p245801coll10,342831

24. Patel, Keyur V. Studies in design and characterization of controlled release antihypertensive drug formulations prepared using bio compatible polymers; -.

Degree: Pharmacology, 1997, Gujarat University

None

Rafarance p.202-216

Advisors/Committee Members: Gohel, M C.

Subjects/Keywords: compatible polymers; controlled release; drug formulations

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APA (6th Edition):

Patel, K. V. (1997). Studies in design and characterization of controlled release antihypertensive drug formulations prepared using bio compatible polymers; -. (Thesis). Gujarat University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/35805

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):

Patel, Keyur V. “Studies in design and characterization of controlled release antihypertensive drug formulations prepared using bio compatible polymers; -.” 1997. Thesis, Gujarat University. Accessed July 21, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/35805.

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

MLA Handbook (7th Edition):

Patel, Keyur V. “Studies in design and characterization of controlled release antihypertensive drug formulations prepared using bio compatible polymers; -.” 1997. Web. 21 Jul 2019.

Vancouver:

Patel KV. Studies in design and characterization of controlled release antihypertensive drug formulations prepared using bio compatible polymers; -. [Internet] [Thesis]. Gujarat University; 1997. [cited 2019 Jul 21]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/35805.

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

Council of Science Editors:

Patel KV. Studies in design and characterization of controlled release antihypertensive drug formulations prepared using bio compatible polymers; -. [Thesis]. Gujarat University; 1997. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/35805

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


EPFL

25. Nassajian Moghadam, Mohamadreza. Self-heating hydrogel for mechanically-controlled drug release.

Degree: 2015, EPFL

 Due to our active lifestyle, knee cartilage is at risk for focal defects. Unfortunately, the native healing properties of the articular cartilage are very limited.… (more)

Subjects/Keywords: drug delivery system; controlled release; hydrogel; viscous dissipation; mechanical loading; thermosensitive nanoparticles

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APA (6th Edition):

Nassajian Moghadam, M. (2015). Self-heating hydrogel for mechanically-controlled drug release. (Thesis). EPFL. Retrieved from http://infoscience.epfl.ch/record/205894

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):

Nassajian Moghadam, Mohamadreza. “Self-heating hydrogel for mechanically-controlled drug release.” 2015. Thesis, EPFL. Accessed July 21, 2019. http://infoscience.epfl.ch/record/205894.

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

MLA Handbook (7th Edition):

Nassajian Moghadam, Mohamadreza. “Self-heating hydrogel for mechanically-controlled drug release.” 2015. Web. 21 Jul 2019.

Vancouver:

Nassajian Moghadam M. Self-heating hydrogel for mechanically-controlled drug release. [Internet] [Thesis]. EPFL; 2015. [cited 2019 Jul 21]. Available from: http://infoscience.epfl.ch/record/205894.

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

Council of Science Editors:

Nassajian Moghadam M. Self-heating hydrogel for mechanically-controlled drug release. [Thesis]. EPFL; 2015. Available from: http://infoscience.epfl.ch/record/205894

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


University of Western Ontario

26. Yang, Qingliang. Powder Coating for Pharmaceutical Solid Dosage Forms.

Degree: 2016, University of Western Ontario

 During the past 50 years, pharmaceutical coating has gone through the transition from sugar coating to organic solvent coating and aqueous coating. Since the 1990s,… (more)

Subjects/Keywords: Pharmaceutical solid dosage forms; powder coating; tablets; pellets; osmotic drug delivery system; controlled release

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APA (6th Edition):

Yang, Q. (2016). Powder Coating for Pharmaceutical Solid Dosage Forms. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/3964

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):

Yang, Qingliang. “Powder Coating for Pharmaceutical Solid Dosage Forms.” 2016. Thesis, University of Western Ontario. Accessed July 21, 2019. https://ir.lib.uwo.ca/etd/3964.

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

MLA Handbook (7th Edition):

Yang, Qingliang. “Powder Coating for Pharmaceutical Solid Dosage Forms.” 2016. Web. 21 Jul 2019.

Vancouver:

Yang Q. Powder Coating for Pharmaceutical Solid Dosage Forms. [Internet] [Thesis]. University of Western Ontario; 2016. [cited 2019 Jul 21]. Available from: https://ir.lib.uwo.ca/etd/3964.

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

Council of Science Editors:

Yang Q. Powder Coating for Pharmaceutical Solid Dosage Forms. [Thesis]. University of Western Ontario; 2016. Available from: https://ir.lib.uwo.ca/etd/3964

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


McMaster University

27. Campbell, Scott Brice. ’Smart’, Injectable, Magnetic Nanocomposite Hydrogels for Biomedical Applications with a Focus on Externally-Mediated Release.

Degree: PhD, 2017, McMaster University

The capability of precisely controlling the kinetics of therapeutic delivery at the optimal location and rate for a given patient would have great potential to… (more)

Subjects/Keywords: drug delivery; remote controlled release; hydrogels; microgels; iron oxide nanoparticles; microinjector; magnetic

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APA (6th Edition):

Campbell, S. B. (2017). ’Smart’, Injectable, Magnetic Nanocomposite Hydrogels for Biomedical Applications with a Focus on Externally-Mediated Release. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/20953

Chicago Manual of Style (16th Edition):

Campbell, Scott Brice. “’Smart’, Injectable, Magnetic Nanocomposite Hydrogels for Biomedical Applications with a Focus on Externally-Mediated Release.” 2017. Doctoral Dissertation, McMaster University. Accessed July 21, 2019. http://hdl.handle.net/11375/20953.

MLA Handbook (7th Edition):

Campbell, Scott Brice. “’Smart’, Injectable, Magnetic Nanocomposite Hydrogels for Biomedical Applications with a Focus on Externally-Mediated Release.” 2017. Web. 21 Jul 2019.

Vancouver:

Campbell SB. ’Smart’, Injectable, Magnetic Nanocomposite Hydrogels for Biomedical Applications with a Focus on Externally-Mediated Release. [Internet] [Doctoral dissertation]. McMaster University; 2017. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/11375/20953.

Council of Science Editors:

Campbell SB. ’Smart’, Injectable, Magnetic Nanocomposite Hydrogels for Biomedical Applications with a Focus on Externally-Mediated Release. [Doctoral Dissertation]. McMaster University; 2017. Available from: http://hdl.handle.net/11375/20953


Queensland University of Technology

28. Bock, Nathalie. Delivery of therapeutic molecules using electrosprayed polymeric particles for applications in tissue engineering.

Degree: 2014, Queensland University of Technology

 This thesis has developed an innovative technology, electrospraying, that allows biodegradable microparticles to deliver pharmaceuticals that aid bone regeneration. The establishment, characterisation and optimisation of… (more)

Subjects/Keywords: Electrospraying; Drug Delivery; Microparticles; Growth Factors; Tissue Engineering; Controlled Release; Electrospinning; Microspheres; Encapsulation; Protein

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APA (6th Edition):

Bock, N. (2014). Delivery of therapeutic molecules using electrosprayed polymeric particles for applications in tissue engineering. (Thesis). Queensland University of Technology. Retrieved from https://eprints.qut.edu.au/74514/

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):

Bock, Nathalie. “Delivery of therapeutic molecules using electrosprayed polymeric particles for applications in tissue engineering.” 2014. Thesis, Queensland University of Technology. Accessed July 21, 2019. https://eprints.qut.edu.au/74514/.

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

MLA Handbook (7th Edition):

Bock, Nathalie. “Delivery of therapeutic molecules using electrosprayed polymeric particles for applications in tissue engineering.” 2014. Web. 21 Jul 2019.

Vancouver:

Bock N. Delivery of therapeutic molecules using electrosprayed polymeric particles for applications in tissue engineering. [Internet] [Thesis]. Queensland University of Technology; 2014. [cited 2019 Jul 21]. Available from: https://eprints.qut.edu.au/74514/.

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

Council of Science Editors:

Bock N. Delivery of therapeutic molecules using electrosprayed polymeric particles for applications in tissue engineering. [Thesis]. Queensland University of Technology; 2014. Available from: https://eprints.qut.edu.au/74514/

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


Virginia Tech

29. Huang, Wei. Assembly, characterization and evaluation of a 3rd generation nanoparticle based drug carrier for metastatic breast cancer treatment.

Degree: PhD, Biological Systems Engineering, 2013, Virginia Tech

 Cancer is one of the leading causes of death in the world. For women in the U.S. and the European countries, breast cancer is the… (more)

Subjects/Keywords: metastatic breast cancer; nanohorn; immunoliposome; nanoparticle based drug carrier; double controlled release

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

APA (6th Edition):

Huang, W. (2013). Assembly, characterization and evaluation of a 3rd generation nanoparticle based drug carrier for metastatic breast cancer treatment. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/50932

Chicago Manual of Style (16th Edition):

Huang, Wei. “Assembly, characterization and evaluation of a 3rd generation nanoparticle based drug carrier for metastatic breast cancer treatment.” 2013. Doctoral Dissertation, Virginia Tech. Accessed July 21, 2019. http://hdl.handle.net/10919/50932.

MLA Handbook (7th Edition):

Huang, Wei. “Assembly, characterization and evaluation of a 3rd generation nanoparticle based drug carrier for metastatic breast cancer treatment.” 2013. Web. 21 Jul 2019.

Vancouver:

Huang W. Assembly, characterization and evaluation of a 3rd generation nanoparticle based drug carrier for metastatic breast cancer treatment. [Internet] [Doctoral dissertation]. Virginia Tech; 2013. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/10919/50932.

Council of Science Editors:

Huang W. Assembly, characterization and evaluation of a 3rd generation nanoparticle based drug carrier for metastatic breast cancer treatment. [Doctoral Dissertation]. Virginia Tech; 2013. Available from: http://hdl.handle.net/10919/50932


University of Adelaide

30. Valizadeh Kiamahalleh, Meisam. Nanoporous layered graphene hydrogel for controlled drug delivery.

Degree: 2015, University of Adelaide

 Graphene-related materials with tuneable pore sizes in the nanoscale range offer the potential to address significant challenges in biomolecule separation, controlled delivery of drugs, selective… (more)

Subjects/Keywords: graphene; peptide; self-assembly; hydrogel; nanoporous; adsorption; drug delivery; controlled release; anticancer; iocompatibility; cytotoxicity

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

APA (6th Edition):

Valizadeh Kiamahalleh, M. (2015). Nanoporous layered graphene hydrogel for controlled drug delivery. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/106439

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):

Valizadeh Kiamahalleh, Meisam. “Nanoporous layered graphene hydrogel for controlled drug delivery.” 2015. Thesis, University of Adelaide. Accessed July 21, 2019. http://hdl.handle.net/2440/106439.

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

MLA Handbook (7th Edition):

Valizadeh Kiamahalleh, Meisam. “Nanoporous layered graphene hydrogel for controlled drug delivery.” 2015. Web. 21 Jul 2019.

Vancouver:

Valizadeh Kiamahalleh M. Nanoporous layered graphene hydrogel for controlled drug delivery. [Internet] [Thesis]. University of Adelaide; 2015. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/2440/106439.

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

Council of Science Editors:

Valizadeh Kiamahalleh M. Nanoporous layered graphene hydrogel for controlled drug delivery. [Thesis]. University of Adelaide; 2015. Available from: http://hdl.handle.net/2440/106439

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

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