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You searched for subject:(Division of Pharmacoengineering AND Molecular Pharmaceutics). Showing records 1 – 30 of 34 total matches.

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University of North Carolina

1. Joy, Melanie S. Disposition of Mycophenolic Acid and Its Glucuronide Metabolites in Subjects with Glomerulonephritis: Implications of Genes and Effects on Kidney Outcomes.

Degree: 2010, University of North Carolina

 Glomerulonephritis is the third most frequent cause of end-stage kidney disease in the U.S. population. Treatments include immunosuppressant agents such as mycophenolate mofetil. The purpose… (more)

Subjects/Keywords: Eshelman School of Pharmacy; Division of Pharmacoengineering and Molecular Pharmaceutics

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APA (6th Edition):

Joy, M. S. (2010). Disposition of Mycophenolic Acid and Its Glucuronide Metabolites in Subjects with Glomerulonephritis: Implications of Genes and Effects on Kidney Outcomes. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:ca77f175-d151-40eb-a822-7018cf594876

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):

Joy, Melanie S. “Disposition of Mycophenolic Acid and Its Glucuronide Metabolites in Subjects with Glomerulonephritis: Implications of Genes and Effects on Kidney Outcomes.” 2010. Thesis, University of North Carolina. Accessed November 28, 2020. https://cdr.lib.unc.edu/record/uuid:ca77f175-d151-40eb-a822-7018cf594876.

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

MLA Handbook (7th Edition):

Joy, Melanie S. “Disposition of Mycophenolic Acid and Its Glucuronide Metabolites in Subjects with Glomerulonephritis: Implications of Genes and Effects on Kidney Outcomes.” 2010. Web. 28 Nov 2020.

Vancouver:

Joy MS. Disposition of Mycophenolic Acid and Its Glucuronide Metabolites in Subjects with Glomerulonephritis: Implications of Genes and Effects on Kidney Outcomes. [Internet] [Thesis]. University of North Carolina; 2010. [cited 2020 Nov 28]. Available from: https://cdr.lib.unc.edu/record/uuid:ca77f175-d151-40eb-a822-7018cf594876.

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

Council of Science Editors:

Joy MS. Disposition of Mycophenolic Acid and Its Glucuronide Metabolites in Subjects with Glomerulonephritis: Implications of Genes and Effects on Kidney Outcomes. [Thesis]. University of North Carolina; 2010. Available from: https://cdr.lib.unc.edu/record/uuid:ca77f175-d151-40eb-a822-7018cf594876

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


University of North Carolina

2. Wang, Chenchen. Pulmonary delivery of isoxyl particles to treat Mycobacterium tuberculosis.

Degree: 2010, University of North Carolina

 Isoxyl is an effective drug to treat multi-drug resistant tuberculosis but its use was impaired by failure in clinical trials. Due to absence of reliable… (more)

Subjects/Keywords: Eshelman School of Pharmacy; Division of Pharmacoengineering and Molecular Pharmaceutics

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APA (6th Edition):

Wang, C. (2010). Pulmonary delivery of isoxyl particles to treat Mycobacterium tuberculosis. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:11d2d6cc-4f17-4808-b488-a766a9422dd8

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, Chenchen. “Pulmonary delivery of isoxyl particles to treat Mycobacterium tuberculosis.” 2010. Thesis, University of North Carolina. Accessed November 28, 2020. https://cdr.lib.unc.edu/record/uuid:11d2d6cc-4f17-4808-b488-a766a9422dd8.

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

MLA Handbook (7th Edition):

Wang, Chenchen. “Pulmonary delivery of isoxyl particles to treat Mycobacterium tuberculosis.” 2010. Web. 28 Nov 2020.

Vancouver:

Wang C. Pulmonary delivery of isoxyl particles to treat Mycobacterium tuberculosis. [Internet] [Thesis]. University of North Carolina; 2010. [cited 2020 Nov 28]. Available from: https://cdr.lib.unc.edu/record/uuid:11d2d6cc-4f17-4808-b488-a766a9422dd8.

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

Council of Science Editors:

Wang C. Pulmonary delivery of isoxyl particles to treat Mycobacterium tuberculosis. [Thesis]. University of North Carolina; 2010. Available from: https://cdr.lib.unc.edu/record/uuid:11d2d6cc-4f17-4808-b488-a766a9422dd8

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


University of North Carolina

3. Hackett, Michael J. Paclitaxel-2'-o-pentadecylhemiglutarate: a prodrug strategy for albumin based drug delivery.

Degree: 2011, University of North Carolina

 Delivery of antineoplastic agents to solid tumors remains a great challenge in formulation development. Preclinical successes often do not translate into clinical therapies due to… (more)

Subjects/Keywords: Eshelman School of Pharmacy; Division of Pharmacoengineering and Molecular Pharmaceutics

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APA (6th Edition):

Hackett, M. J. (2011). Paclitaxel-2'-o-pentadecylhemiglutarate: a prodrug strategy for albumin based drug delivery. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:570260a0-b394-46e6-a045-f4d04bb6f5f3

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):

Hackett, Michael J. “Paclitaxel-2'-o-pentadecylhemiglutarate: a prodrug strategy for albumin based drug delivery.” 2011. Thesis, University of North Carolina. Accessed November 28, 2020. https://cdr.lib.unc.edu/record/uuid:570260a0-b394-46e6-a045-f4d04bb6f5f3.

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

MLA Handbook (7th Edition):

Hackett, Michael J. “Paclitaxel-2'-o-pentadecylhemiglutarate: a prodrug strategy for albumin based drug delivery.” 2011. Web. 28 Nov 2020.

Vancouver:

Hackett MJ. Paclitaxel-2'-o-pentadecylhemiglutarate: a prodrug strategy for albumin based drug delivery. [Internet] [Thesis]. University of North Carolina; 2011. [cited 2020 Nov 28]. Available from: https://cdr.lib.unc.edu/record/uuid:570260a0-b394-46e6-a045-f4d04bb6f5f3.

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

Council of Science Editors:

Hackett MJ. Paclitaxel-2'-o-pentadecylhemiglutarate: a prodrug strategy for albumin based drug delivery. [Thesis]. University of North Carolina; 2011. Available from: https://cdr.lib.unc.edu/record/uuid:570260a0-b394-46e6-a045-f4d04bb6f5f3

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


University of North Carolina

4. Liu, Dongyun. Water-in-oil Microemulsions and Hydrogel Nanoparticles in Water-in-Oil Microemulsions for Local Intestinal Delivery of Peptides and Proteins.

Degree: 2013, University of North Carolina

 The objectives of the present studies were to develop water-in-oil (W/O) microemulsions (MEs) and hydrogel nanoparticles in W/O MEs for effective local intestinal delivery of… (more)

Subjects/Keywords: Eshelman School of Pharmacy; Division of Pharmacoengineering and Molecular Pharmaceutics

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APA (6th Edition):

Liu, D. (2013). Water-in-oil Microemulsions and Hydrogel Nanoparticles in Water-in-Oil Microemulsions for Local Intestinal Delivery of Peptides and Proteins. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:1510e2fe-cd00-489e-927f-b4f8e4582e7f

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):

Liu, Dongyun. “Water-in-oil Microemulsions and Hydrogel Nanoparticles in Water-in-Oil Microemulsions for Local Intestinal Delivery of Peptides and Proteins.” 2013. Thesis, University of North Carolina. Accessed November 28, 2020. https://cdr.lib.unc.edu/record/uuid:1510e2fe-cd00-489e-927f-b4f8e4582e7f.

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

MLA Handbook (7th Edition):

Liu, Dongyun. “Water-in-oil Microemulsions and Hydrogel Nanoparticles in Water-in-Oil Microemulsions for Local Intestinal Delivery of Peptides and Proteins.” 2013. Web. 28 Nov 2020.

Vancouver:

Liu D. Water-in-oil Microemulsions and Hydrogel Nanoparticles in Water-in-Oil Microemulsions for Local Intestinal Delivery of Peptides and Proteins. [Internet] [Thesis]. University of North Carolina; 2013. [cited 2020 Nov 28]. Available from: https://cdr.lib.unc.edu/record/uuid:1510e2fe-cd00-489e-927f-b4f8e4582e7f.

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

Council of Science Editors:

Liu D. Water-in-oil Microemulsions and Hydrogel Nanoparticles in Water-in-Oil Microemulsions for Local Intestinal Delivery of Peptides and Proteins. [Thesis]. University of North Carolina; 2013. Available from: https://cdr.lib.unc.edu/record/uuid:1510e2fe-cd00-489e-927f-b4f8e4582e7f

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


University of North Carolina

5. Jiang, Yuhang. Block Ionomer Complex Formulations For In Vivo Protein Delivery.

Degree: 2016, University of North Carolina

 Complex coacervation between therapeutic proteins and hydrophilic ionic-neutral block-copolymers leads to the formation of core-shell structured nanoparticles gently packaging the proteins in its core (reviewed… (more)

Subjects/Keywords: Eshelman School of Pharmacy; Division of Pharmacoengineering and Molecular Pharmaceutics

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APA (6th Edition):

Jiang, Y. (2016). Block Ionomer Complex Formulations For In Vivo Protein Delivery. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:4d9d0222-dbaf-4c49-ab1b-bca855350e05

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):

Jiang, Yuhang. “Block Ionomer Complex Formulations For In Vivo Protein Delivery.” 2016. Thesis, University of North Carolina. Accessed November 28, 2020. https://cdr.lib.unc.edu/record/uuid:4d9d0222-dbaf-4c49-ab1b-bca855350e05.

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

MLA Handbook (7th Edition):

Jiang, Yuhang. “Block Ionomer Complex Formulations For In Vivo Protein Delivery.” 2016. Web. 28 Nov 2020.

Vancouver:

Jiang Y. Block Ionomer Complex Formulations For In Vivo Protein Delivery. [Internet] [Thesis]. University of North Carolina; 2016. [cited 2020 Nov 28]. Available from: https://cdr.lib.unc.edu/record/uuid:4d9d0222-dbaf-4c49-ab1b-bca855350e05.

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

Council of Science Editors:

Jiang Y. Block Ionomer Complex Formulations For In Vivo Protein Delivery. [Thesis]. University of North Carolina; 2016. Available from: https://cdr.lib.unc.edu/record/uuid:4d9d0222-dbaf-4c49-ab1b-bca855350e05

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


University of North Carolina

6. Fu, Jing. THE ROLE OF CARBOXYLESTERASES IN THE BIOTRANSFORMATION OF A RADIONUCLIDE DECORPORATION AGENT DTPA PENTA-ETHYL ESTER PRODRUG.

Degree: 2016, University of North Carolina

 A penta-ethyl ester prodrug of diethylenetriaminepentaacetic acid (C2E5) was developed for radionuclide decorporation. Previous studies of C2E5 delivered by oral and transdermal routes in rats… (more)

Subjects/Keywords: Eshelman School of Pharmacy; Division of Pharmacoengineering and Molecular Pharmaceutics

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APA (6th Edition):

Fu, J. (2016). THE ROLE OF CARBOXYLESTERASES IN THE BIOTRANSFORMATION OF A RADIONUCLIDE DECORPORATION AGENT DTPA PENTA-ETHYL ESTER PRODRUG. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:e0182e8b-02fe-40a0-8552-28e0ed133cbc

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):

Fu, Jing. “THE ROLE OF CARBOXYLESTERASES IN THE BIOTRANSFORMATION OF A RADIONUCLIDE DECORPORATION AGENT DTPA PENTA-ETHYL ESTER PRODRUG.” 2016. Thesis, University of North Carolina. Accessed November 28, 2020. https://cdr.lib.unc.edu/record/uuid:e0182e8b-02fe-40a0-8552-28e0ed133cbc.

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

MLA Handbook (7th Edition):

Fu, Jing. “THE ROLE OF CARBOXYLESTERASES IN THE BIOTRANSFORMATION OF A RADIONUCLIDE DECORPORATION AGENT DTPA PENTA-ETHYL ESTER PRODRUG.” 2016. Web. 28 Nov 2020.

Vancouver:

Fu J. THE ROLE OF CARBOXYLESTERASES IN THE BIOTRANSFORMATION OF A RADIONUCLIDE DECORPORATION AGENT DTPA PENTA-ETHYL ESTER PRODRUG. [Internet] [Thesis]. University of North Carolina; 2016. [cited 2020 Nov 28]. Available from: https://cdr.lib.unc.edu/record/uuid:e0182e8b-02fe-40a0-8552-28e0ed133cbc.

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

Council of Science Editors:

Fu J. THE ROLE OF CARBOXYLESTERASES IN THE BIOTRANSFORMATION OF A RADIONUCLIDE DECORPORATION AGENT DTPA PENTA-ETHYL ESTER PRODRUG. [Thesis]. University of North Carolina; 2016. Available from: https://cdr.lib.unc.edu/record/uuid:e0182e8b-02fe-40a0-8552-28e0ed133cbc

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


University of North Carolina

7. Bulaklak, Karen. Uncovering the role of microRNA-206 in Duchenne muscular dystrophy.

Degree: 2017, University of North Carolina

 Duchenne muscular dystrophy (DMD) is a severe muscle wasting disorder for which there is no cure. It is caused by a defect in the dystrophin… (more)

Subjects/Keywords: Eshelman School of Pharmacy; Division of Pharmacoengineering and Molecular Pharmaceutics

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APA (6th Edition):

Bulaklak, K. (2017). Uncovering the role of microRNA-206 in Duchenne muscular dystrophy. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:21730dc1-f75d-40ba-a745-741f663f9671

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):

Bulaklak, Karen. “Uncovering the role of microRNA-206 in Duchenne muscular dystrophy.” 2017. Thesis, University of North Carolina. Accessed November 28, 2020. https://cdr.lib.unc.edu/record/uuid:21730dc1-f75d-40ba-a745-741f663f9671.

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

MLA Handbook (7th Edition):

Bulaklak, Karen. “Uncovering the role of microRNA-206 in Duchenne muscular dystrophy.” 2017. Web. 28 Nov 2020.

Vancouver:

Bulaklak K. Uncovering the role of microRNA-206 in Duchenne muscular dystrophy. [Internet] [Thesis]. University of North Carolina; 2017. [cited 2020 Nov 28]. Available from: https://cdr.lib.unc.edu/record/uuid:21730dc1-f75d-40ba-a745-741f663f9671.

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

Council of Science Editors:

Bulaklak K. Uncovering the role of microRNA-206 in Duchenne muscular dystrophy. [Thesis]. University of North Carolina; 2017. Available from: https://cdr.lib.unc.edu/record/uuid:21730dc1-f75d-40ba-a745-741f663f9671

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


University of North Carolina

8. Ma, Ping. Drug-Loaded Lipid Nanoparticles for Improved Cancer Treatment: Engineering, In-Vitro, and In-Vivo Evaluation.

Degree: 2012, University of North Carolina

 The objectives of these studies were to develop lipid-based nanoparticles (NPs) of anthracyclines (idarubicin, IDA and doxorubicin, DOX) and taxanes (paclitaxel, PX) for improved cancer… (more)

Subjects/Keywords: Eshelman School of Pharmacy; Division of Pharmacoengineering and Molecular Pharmaceutics

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APA (6th Edition):

Ma, P. (2012). Drug-Loaded Lipid Nanoparticles for Improved Cancer Treatment: Engineering, In-Vitro, and In-Vivo Evaluation. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:4b0af895-2390-44e4-b590-37538273a195

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):

Ma, Ping. “Drug-Loaded Lipid Nanoparticles for Improved Cancer Treatment: Engineering, In-Vitro, and In-Vivo Evaluation.” 2012. Thesis, University of North Carolina. Accessed November 28, 2020. https://cdr.lib.unc.edu/record/uuid:4b0af895-2390-44e4-b590-37538273a195.

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

MLA Handbook (7th Edition):

Ma, Ping. “Drug-Loaded Lipid Nanoparticles for Improved Cancer Treatment: Engineering, In-Vitro, and In-Vivo Evaluation.” 2012. Web. 28 Nov 2020.

Vancouver:

Ma P. Drug-Loaded Lipid Nanoparticles for Improved Cancer Treatment: Engineering, In-Vitro, and In-Vivo Evaluation. [Internet] [Thesis]. University of North Carolina; 2012. [cited 2020 Nov 28]. Available from: https://cdr.lib.unc.edu/record/uuid:4b0af895-2390-44e4-b590-37538273a195.

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

Council of Science Editors:

Ma P. Drug-Loaded Lipid Nanoparticles for Improved Cancer Treatment: Engineering, In-Vitro, and In-Vivo Evaluation. [Thesis]. University of North Carolina; 2012. Available from: https://cdr.lib.unc.edu/record/uuid:4b0af895-2390-44e4-b590-37538273a195

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


University of North Carolina

9. Minocha, Shalini. Investigations into the Mechanisms of Cell Death: The Common Link between Anticancer Nanotherapeutics and Nanotoxicology.

Degree: 2012, University of North Carolina

 Nanotoxicology and anticancer nanotherapeutics are essentially two sides of the same coin. The nanotoxicology discipline deals with the nanoparticle (NP)-induced toxicity and mechanisms of cell… (more)

Subjects/Keywords: Eshelman School of Pharmacy; Division of Pharmacoengineering and Molecular Pharmaceutics

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APA (6th Edition):

Minocha, S. (2012). Investigations into the Mechanisms of Cell Death: The Common Link between Anticancer Nanotherapeutics and Nanotoxicology. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:66f33bb2-2426-4a19-9275-0a53fd093ba4

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):

Minocha, Shalini. “Investigations into the Mechanisms of Cell Death: The Common Link between Anticancer Nanotherapeutics and Nanotoxicology.” 2012. Thesis, University of North Carolina. Accessed November 28, 2020. https://cdr.lib.unc.edu/record/uuid:66f33bb2-2426-4a19-9275-0a53fd093ba4.

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

MLA Handbook (7th Edition):

Minocha, Shalini. “Investigations into the Mechanisms of Cell Death: The Common Link between Anticancer Nanotherapeutics and Nanotoxicology.” 2012. Web. 28 Nov 2020.

Vancouver:

Minocha S. Investigations into the Mechanisms of Cell Death: The Common Link between Anticancer Nanotherapeutics and Nanotoxicology. [Internet] [Thesis]. University of North Carolina; 2012. [cited 2020 Nov 28]. Available from: https://cdr.lib.unc.edu/record/uuid:66f33bb2-2426-4a19-9275-0a53fd093ba4.

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

Council of Science Editors:

Minocha S. Investigations into the Mechanisms of Cell Death: The Common Link between Anticancer Nanotherapeutics and Nanotoxicology. [Thesis]. University of North Carolina; 2012. Available from: https://cdr.lib.unc.edu/record/uuid:66f33bb2-2426-4a19-9275-0a53fd093ba4

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


University of North Carolina

10. Tseng, Yu-Cheng. LCP Nanoparticle for Tumor and Lymph Node Metastasis Imaging.

Degree: 2013, University of North Carolina

 A lipid/calcium/phosphate (LCP) nanoparticle formulation (particle diameter ~25 nm) has previously been developed to delivery siRNA with superior efficiency. In this work, 111In was formulated… (more)

Subjects/Keywords: Eshelman School of Pharmacy; Division of Pharmacoengineering and Molecular Pharmaceutics

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APA (6th Edition):

Tseng, Y. (2013). LCP Nanoparticle for Tumor and Lymph Node Metastasis Imaging. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:d58dc4de-47eb-46c6-89e9-54f7f8f9f6d1

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):

Tseng, Yu-Cheng. “LCP Nanoparticle for Tumor and Lymph Node Metastasis Imaging.” 2013. Thesis, University of North Carolina. Accessed November 28, 2020. https://cdr.lib.unc.edu/record/uuid:d58dc4de-47eb-46c6-89e9-54f7f8f9f6d1.

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

MLA Handbook (7th Edition):

Tseng, Yu-Cheng. “LCP Nanoparticle for Tumor and Lymph Node Metastasis Imaging.” 2013. Web. 28 Nov 2020.

Vancouver:

Tseng Y. LCP Nanoparticle for Tumor and Lymph Node Metastasis Imaging. [Internet] [Thesis]. University of North Carolina; 2013. [cited 2020 Nov 28]. Available from: https://cdr.lib.unc.edu/record/uuid:d58dc4de-47eb-46c6-89e9-54f7f8f9f6d1.

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

Council of Science Editors:

Tseng Y. LCP Nanoparticle for Tumor and Lymph Node Metastasis Imaging. [Thesis]. University of North Carolina; 2013. Available from: https://cdr.lib.unc.edu/record/uuid:d58dc4de-47eb-46c6-89e9-54f7f8f9f6d1

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


University of North Carolina

11. Peng, Lei. Taxane conjugate nanoparticles for improved non-small cell lung cancer treatment in a novel orthotopic mouse model.

Degree: 2014, University of North Carolina

 The objectives of these studies were to develop lipid-based nanoparticles (NPs) to deliver taxane conjugates for improved non-small cell lung cancer (NSCLC) treatment. The chemotherapy… (more)

Subjects/Keywords: Eshelman School of Pharmacy; Division of Pharmacoengineering and Molecular Pharmaceutics

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APA (6th Edition):

Peng, L. (2014). Taxane conjugate nanoparticles for improved non-small cell lung cancer treatment in a novel orthotopic mouse model. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:d05ff7e3-c57f-4b28-a4e0-9b359f67cf67

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):

Peng, Lei. “Taxane conjugate nanoparticles for improved non-small cell lung cancer treatment in a novel orthotopic mouse model.” 2014. Thesis, University of North Carolina. Accessed November 28, 2020. https://cdr.lib.unc.edu/record/uuid:d05ff7e3-c57f-4b28-a4e0-9b359f67cf67.

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

MLA Handbook (7th Edition):

Peng, Lei. “Taxane conjugate nanoparticles for improved non-small cell lung cancer treatment in a novel orthotopic mouse model.” 2014. Web. 28 Nov 2020.

Vancouver:

Peng L. Taxane conjugate nanoparticles for improved non-small cell lung cancer treatment in a novel orthotopic mouse model. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Nov 28]. Available from: https://cdr.lib.unc.edu/record/uuid:d05ff7e3-c57f-4b28-a4e0-9b359f67cf67.

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

Council of Science Editors:

Peng L. Taxane conjugate nanoparticles for improved non-small cell lung cancer treatment in a novel orthotopic mouse model. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:d05ff7e3-c57f-4b28-a4e0-9b359f67cf67

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


University of North Carolina

12. Wang, Sheena Hailin. Novel Delivery Systems for Nasal Adminstration of Anthrax Vaccine.

Degree: 2010, University of North Carolina

 There is current biodefense interest in protection against Anthrax. The inhaled form of anthrax is difficult to diagnose and can be fatal without prompt antibiotic… (more)

Subjects/Keywords: Eshelman School of Pharmacy; Division of Pharmacoengineering and Molecular Pharmaceutics

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APA (6th Edition):

Wang, S. H. (2010). Novel Delivery Systems for Nasal Adminstration of Anthrax Vaccine. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:e11bd47b-2e80-4f59-9081-67532f2e71a1

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, Sheena Hailin. “Novel Delivery Systems for Nasal Adminstration of Anthrax Vaccine.” 2010. Thesis, University of North Carolina. Accessed November 28, 2020. https://cdr.lib.unc.edu/record/uuid:e11bd47b-2e80-4f59-9081-67532f2e71a1.

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

MLA Handbook (7th Edition):

Wang, Sheena Hailin. “Novel Delivery Systems for Nasal Adminstration of Anthrax Vaccine.” 2010. Web. 28 Nov 2020.

Vancouver:

Wang SH. Novel Delivery Systems for Nasal Adminstration of Anthrax Vaccine. [Internet] [Thesis]. University of North Carolina; 2010. [cited 2020 Nov 28]. Available from: https://cdr.lib.unc.edu/record/uuid:e11bd47b-2e80-4f59-9081-67532f2e71a1.

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

Council of Science Editors:

Wang SH. Novel Delivery Systems for Nasal Adminstration of Anthrax Vaccine. [Thesis]. University of North Carolina; 2010. Available from: https://cdr.lib.unc.edu/record/uuid:e11bd47b-2e80-4f59-9081-67532f2e71a1

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


University of North Carolina

13. Feng, Lan. Oil-filled Lipid Nanoparticles Containing Docetaxel Conjugates for Controlled Drug Release.

Degree: 2012, University of North Carolina

 It has always been challenging to deliver anticancer agents effectively, safely and selectively to solid tumors. Taxotere, as the only marketed dosage form of docetaxel… (more)

Subjects/Keywords: Eshelman School of Pharmacy; Division of Pharmacoengineering and Molecular Pharmaceutics

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APA (6th Edition):

Feng, L. (2012). Oil-filled Lipid Nanoparticles Containing Docetaxel Conjugates for Controlled Drug Release. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:6190c5d5-a7bb-420e-b87b-0de2487bd5bf

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):

Feng, Lan. “Oil-filled Lipid Nanoparticles Containing Docetaxel Conjugates for Controlled Drug Release.” 2012. Thesis, University of North Carolina. Accessed November 28, 2020. https://cdr.lib.unc.edu/record/uuid:6190c5d5-a7bb-420e-b87b-0de2487bd5bf.

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

MLA Handbook (7th Edition):

Feng, Lan. “Oil-filled Lipid Nanoparticles Containing Docetaxel Conjugates for Controlled Drug Release.” 2012. Web. 28 Nov 2020.

Vancouver:

Feng L. Oil-filled Lipid Nanoparticles Containing Docetaxel Conjugates for Controlled Drug Release. [Internet] [Thesis]. University of North Carolina; 2012. [cited 2020 Nov 28]. Available from: https://cdr.lib.unc.edu/record/uuid:6190c5d5-a7bb-420e-b87b-0de2487bd5bf.

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

Council of Science Editors:

Feng L. Oil-filled Lipid Nanoparticles Containing Docetaxel Conjugates for Controlled Drug Release. [Thesis]. University of North Carolina; 2012. Available from: https://cdr.lib.unc.edu/record/uuid:6190c5d5-a7bb-420e-b87b-0de2487bd5bf

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


University of North Carolina

14. Pu, Dongqiuye. Quantitative structure-toxicity relationship modeling of organic compounds and nanoparticles.

Degree: 2012, University of North Carolina

 Safety issues are considered the single largest reason for today’s drug development failures. It is both costly and time-consuming for toxicological evaluation of materials. This… (more)

Subjects/Keywords: Eshelman School of Pharmacy; Division of Pharmacoengineering and Molecular Pharmaceutics

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APA (6th Edition):

Pu, D. (2012). Quantitative structure-toxicity relationship modeling of organic compounds and nanoparticles. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:a660ee98-4916-420c-9eb2-60b139eecd80

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):

Pu, Dongqiuye. “Quantitative structure-toxicity relationship modeling of organic compounds and nanoparticles.” 2012. Thesis, University of North Carolina. Accessed November 28, 2020. https://cdr.lib.unc.edu/record/uuid:a660ee98-4916-420c-9eb2-60b139eecd80.

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

MLA Handbook (7th Edition):

Pu, Dongqiuye. “Quantitative structure-toxicity relationship modeling of organic compounds and nanoparticles.” 2012. Web. 28 Nov 2020.

Vancouver:

Pu D. Quantitative structure-toxicity relationship modeling of organic compounds and nanoparticles. [Internet] [Thesis]. University of North Carolina; 2012. [cited 2020 Nov 28]. Available from: https://cdr.lib.unc.edu/record/uuid:a660ee98-4916-420c-9eb2-60b139eecd80.

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

Council of Science Editors:

Pu D. Quantitative structure-toxicity relationship modeling of organic compounds and nanoparticles. [Thesis]. University of North Carolina; 2012. Available from: https://cdr.lib.unc.edu/record/uuid:a660ee98-4916-420c-9eb2-60b139eecd80

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


University of North Carolina

15. Glatt, Dylan. MONOCLONAL ANTIBODY-MEDIATED TUMOR TARGETING AND DRUG DELIVERY TO SOLID TUMORS.

Degree: 2016, University of North Carolina

 Antibody-drug conjugates (ADCs) are an emerging class of targeted anticancer therapeutics. Premised on Paul Ehrlich’s magic bullet hypothesis and clinical need to improve the tumor… (more)

Subjects/Keywords: Eshelman School of Pharmacy; Division of Pharmacoengineering and Molecular Pharmaceutics

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APA (6th Edition):

Glatt, D. (2016). MONOCLONAL ANTIBODY-MEDIATED TUMOR TARGETING AND DRUG DELIVERY TO SOLID TUMORS. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:1cd75d93-72b9-4e2a-8229-5b509f559781

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):

Glatt, Dylan. “MONOCLONAL ANTIBODY-MEDIATED TUMOR TARGETING AND DRUG DELIVERY TO SOLID TUMORS.” 2016. Thesis, University of North Carolina. Accessed November 28, 2020. https://cdr.lib.unc.edu/record/uuid:1cd75d93-72b9-4e2a-8229-5b509f559781.

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

MLA Handbook (7th Edition):

Glatt, Dylan. “MONOCLONAL ANTIBODY-MEDIATED TUMOR TARGETING AND DRUG DELIVERY TO SOLID TUMORS.” 2016. Web. 28 Nov 2020.

Vancouver:

Glatt D. MONOCLONAL ANTIBODY-MEDIATED TUMOR TARGETING AND DRUG DELIVERY TO SOLID TUMORS. [Internet] [Thesis]. University of North Carolina; 2016. [cited 2020 Nov 28]. Available from: https://cdr.lib.unc.edu/record/uuid:1cd75d93-72b9-4e2a-8229-5b509f559781.

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

Council of Science Editors:

Glatt D. MONOCLONAL ANTIBODY-MEDIATED TUMOR TARGETING AND DRUG DELIVERY TO SOLID TUMORS. [Thesis]. University of North Carolina; 2016. Available from: https://cdr.lib.unc.edu/record/uuid:1cd75d93-72b9-4e2a-8229-5b509f559781

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


University of North Carolina

16. Miao, Lei. THE ROLE OF TUMOR DESMOPLASIA IN NANOPARTICLE DELIVERY OF DRUGS AND GENES.

Degree: 2016, University of North Carolina

 In desmoplastic tumors, stroma cells capture nanoparticles (NPs), preventing them from reaching tumor cells, resulting in compromised anti-tumor efficacy. This dissertation focuses on understanding the… (more)

Subjects/Keywords: Eshelman School of Pharmacy; Division of Pharmacoengineering and Molecular Pharmaceutics

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APA (6th Edition):

Miao, L. (2016). THE ROLE OF TUMOR DESMOPLASIA IN NANOPARTICLE DELIVERY OF DRUGS AND GENES. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:7ff690db-7d76-44e8-9a15-0ea6f3084b66

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):

Miao, Lei. “THE ROLE OF TUMOR DESMOPLASIA IN NANOPARTICLE DELIVERY OF DRUGS AND GENES.” 2016. Thesis, University of North Carolina. Accessed November 28, 2020. https://cdr.lib.unc.edu/record/uuid:7ff690db-7d76-44e8-9a15-0ea6f3084b66.

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

MLA Handbook (7th Edition):

Miao, Lei. “THE ROLE OF TUMOR DESMOPLASIA IN NANOPARTICLE DELIVERY OF DRUGS AND GENES.” 2016. Web. 28 Nov 2020.

Vancouver:

Miao L. THE ROLE OF TUMOR DESMOPLASIA IN NANOPARTICLE DELIVERY OF DRUGS AND GENES. [Internet] [Thesis]. University of North Carolina; 2016. [cited 2020 Nov 28]. Available from: https://cdr.lib.unc.edu/record/uuid:7ff690db-7d76-44e8-9a15-0ea6f3084b66.

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

Council of Science Editors:

Miao L. THE ROLE OF TUMOR DESMOPLASIA IN NANOPARTICLE DELIVERY OF DRUGS AND GENES. [Thesis]. University of North Carolina; 2016. Available from: https://cdr.lib.unc.edu/record/uuid:7ff690db-7d76-44e8-9a15-0ea6f3084b66

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


University of North Carolina

17. Kapadia, Chintan. Engineering PRINT® Nanoparticle Subunit Vaccine to Induce Antitumor Immune Response.

Degree: 2016, University of North Carolina

 Educating our immune system via vaccination is an attractive approach to combat cancer. Tumor-specific cytotoxic T cells (CTLs) such as CD8+ effector T cells play… (more)

Subjects/Keywords: Eshelman School of Pharmacy; Division of Pharmacoengineering and Molecular Pharmaceutics

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APA (6th Edition):

Kapadia, C. (2016). Engineering PRINT® Nanoparticle Subunit Vaccine to Induce Antitumor Immune Response. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:735110cf-2501-47c9-b894-3d44aba3a7cb

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):

Kapadia, Chintan. “Engineering PRINT® Nanoparticle Subunit Vaccine to Induce Antitumor Immune Response.” 2016. Thesis, University of North Carolina. Accessed November 28, 2020. https://cdr.lib.unc.edu/record/uuid:735110cf-2501-47c9-b894-3d44aba3a7cb.

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

MLA Handbook (7th Edition):

Kapadia, Chintan. “Engineering PRINT® Nanoparticle Subunit Vaccine to Induce Antitumor Immune Response.” 2016. Web. 28 Nov 2020.

Vancouver:

Kapadia C. Engineering PRINT® Nanoparticle Subunit Vaccine to Induce Antitumor Immune Response. [Internet] [Thesis]. University of North Carolina; 2016. [cited 2020 Nov 28]. Available from: https://cdr.lib.unc.edu/record/uuid:735110cf-2501-47c9-b894-3d44aba3a7cb.

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

Council of Science Editors:

Kapadia C. Engineering PRINT® Nanoparticle Subunit Vaccine to Induce Antitumor Immune Response. [Thesis]. University of North Carolina; 2016. Available from: https://cdr.lib.unc.edu/record/uuid:735110cf-2501-47c9-b894-3d44aba3a7cb

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


University of North Carolina

18. Rahhal, Tojan. Engineering PRINT® Particles for Pulmonary Delivery of Therapeutics.

Degree: 2016, University of North Carolina

 Pulmonary drug delivery is an attractive new approach to the traditional parenteral route of administration due to its non-invasive nature, convenience, and increased patient compliance.… (more)

Subjects/Keywords: Eshelman School of Pharmacy; Division of Pharmacoengineering and Molecular Pharmaceutics

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APA (6th Edition):

Rahhal, T. (2016). Engineering PRINT® Particles for Pulmonary Delivery of Therapeutics. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:cdfaecbe-d711-4632-8c93-700e85c26de5

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):

Rahhal, Tojan. “Engineering PRINT® Particles for Pulmonary Delivery of Therapeutics.” 2016. Thesis, University of North Carolina. Accessed November 28, 2020. https://cdr.lib.unc.edu/record/uuid:cdfaecbe-d711-4632-8c93-700e85c26de5.

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

MLA Handbook (7th Edition):

Rahhal, Tojan. “Engineering PRINT® Particles for Pulmonary Delivery of Therapeutics.” 2016. Web. 28 Nov 2020.

Vancouver:

Rahhal T. Engineering PRINT® Particles for Pulmonary Delivery of Therapeutics. [Internet] [Thesis]. University of North Carolina; 2016. [cited 2020 Nov 28]. Available from: https://cdr.lib.unc.edu/record/uuid:cdfaecbe-d711-4632-8c93-700e85c26de5.

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

Council of Science Editors:

Rahhal T. Engineering PRINT® Particles for Pulmonary Delivery of Therapeutics. [Thesis]. University of North Carolina; 2016. Available from: https://cdr.lib.unc.edu/record/uuid:cdfaecbe-d711-4632-8c93-700e85c26de5

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


University of North Carolina

19. Kim, Myung Soo. Exosome Mediated Delivery of Paclitaxel for the Treatment of Multi-Drug Resistant Pulmonary Metastases.

Degree: 2016, University of North Carolina

 Exosomes have recently come into focus as “natural nanoparticles” for use as drug delivery vehicles because they lack many drawbacks inherent to other nanoformulations. Many… (more)

Subjects/Keywords: Eshelman School of Pharmacy; Division of Pharmacoengineering and Molecular Pharmaceutics

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APA (6th Edition):

Kim, M. S. (2016). Exosome Mediated Delivery of Paclitaxel for the Treatment of Multi-Drug Resistant Pulmonary Metastases. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:8a99fea7-72ca-449e-824f-50fd55864faa

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):

Kim, Myung Soo. “Exosome Mediated Delivery of Paclitaxel for the Treatment of Multi-Drug Resistant Pulmonary Metastases.” 2016. Thesis, University of North Carolina. Accessed November 28, 2020. https://cdr.lib.unc.edu/record/uuid:8a99fea7-72ca-449e-824f-50fd55864faa.

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

MLA Handbook (7th Edition):

Kim, Myung Soo. “Exosome Mediated Delivery of Paclitaxel for the Treatment of Multi-Drug Resistant Pulmonary Metastases.” 2016. Web. 28 Nov 2020.

Vancouver:

Kim MS. Exosome Mediated Delivery of Paclitaxel for the Treatment of Multi-Drug Resistant Pulmonary Metastases. [Internet] [Thesis]. University of North Carolina; 2016. [cited 2020 Nov 28]. Available from: https://cdr.lib.unc.edu/record/uuid:8a99fea7-72ca-449e-824f-50fd55864faa.

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

Council of Science Editors:

Kim MS. Exosome Mediated Delivery of Paclitaxel for the Treatment of Multi-Drug Resistant Pulmonary Metastases. [Thesis]. University of North Carolina; 2016. Available from: https://cdr.lib.unc.edu/record/uuid:8a99fea7-72ca-449e-824f-50fd55864faa

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


University of North Carolina

20. Yang, Angela. Exploring and harnessing PEG-immune system interactions to engineer targeted stealth nanoparticles.

Degree: 2016, University of North Carolina

 Effective nanoparticle drug delivery to tumor cells typically relies on prolonged systemic circulation of the nanoparticles to allow for extravasation and accumulation in tumor tissue,… (more)

Subjects/Keywords: Eshelman School of Pharmacy; Division of Pharmacoengineering and Molecular Pharmaceutics

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APA (6th Edition):

Yang, A. (2016). Exploring and harnessing PEG-immune system interactions to engineer targeted stealth nanoparticles. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:fdf758dc-4a02-4ec8-9397-4746e2e2bb58

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, Angela. “Exploring and harnessing PEG-immune system interactions to engineer targeted stealth nanoparticles.” 2016. Thesis, University of North Carolina. Accessed November 28, 2020. https://cdr.lib.unc.edu/record/uuid:fdf758dc-4a02-4ec8-9397-4746e2e2bb58.

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

MLA Handbook (7th Edition):

Yang, Angela. “Exploring and harnessing PEG-immune system interactions to engineer targeted stealth nanoparticles.” 2016. Web. 28 Nov 2020.

Vancouver:

Yang A. Exploring and harnessing PEG-immune system interactions to engineer targeted stealth nanoparticles. [Internet] [Thesis]. University of North Carolina; 2016. [cited 2020 Nov 28]. Available from: https://cdr.lib.unc.edu/record/uuid:fdf758dc-4a02-4ec8-9397-4746e2e2bb58.

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

Council of Science Editors:

Yang A. Exploring and harnessing PEG-immune system interactions to engineer targeted stealth nanoparticles. [Thesis]. University of North Carolina; 2016. Available from: https://cdr.lib.unc.edu/record/uuid:fdf758dc-4a02-4ec8-9397-4746e2e2bb58

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


University of North Carolina

21. Shen, Tammy. Development and Characterization of PRINT® Particles as Drug Delivery Vehicles in the Lung.

Degree: 2014, University of North Carolina

 The aim of this dissertation is to develop and investigate the utility of the Particle Replication in Non-wetting Templates (PRINT®) technology as a toolbox to… (more)

Subjects/Keywords: Pharmaceutical chemistry; Eshelman School of Pharmacy; Division of Pharmacoengineering and Molecular Pharmaceutics

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APA (6th Edition):

Shen, T. (2014). Development and Characterization of PRINT® Particles as Drug Delivery Vehicles in the Lung. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:d5a9cf1d-c7cf-4588-9866-f367a0c30c1b

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

Chicago Manual of Style (16th Edition):

Shen, Tammy. “Development and Characterization of PRINT® Particles as Drug Delivery Vehicles in the Lung.” 2014. Thesis, University of North Carolina. Accessed November 28, 2020. https://cdr.lib.unc.edu/record/uuid:d5a9cf1d-c7cf-4588-9866-f367a0c30c1b.

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

MLA Handbook (7th Edition):

Shen, Tammy. “Development and Characterization of PRINT® Particles as Drug Delivery Vehicles in the Lung.” 2014. Web. 28 Nov 2020.

Vancouver:

Shen T. Development and Characterization of PRINT® Particles as Drug Delivery Vehicles in the Lung. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Nov 28]. Available from: https://cdr.lib.unc.edu/record/uuid:d5a9cf1d-c7cf-4588-9866-f367a0c30c1b.

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

Council of Science Editors:

Shen T. Development and Characterization of PRINT® Particles as Drug Delivery Vehicles in the Lung. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:d5a9cf1d-c7cf-4588-9866-f367a0c30c1b

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


University of North Carolina

22. Huckle, James. C2E2: An Orally Administered Radionuclide Decorporation Agent.

Degree: 2014, University of North Carolina

 The increasing threats of nuclear terrorism have made the development of medical countermeasures a priority for international security. Injectable formulations of diethylenetriaminepentaacetic acid (DTPA) have… (more)

Subjects/Keywords: Pharmaceutical chemistry; Eshelman School of Pharmacy; Division of Pharmacoengineering and Molecular Pharmaceutics

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APA (6th Edition):

Huckle, J. (2014). C2E2: An Orally Administered Radionuclide Decorporation Agent. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:d95fdb33-74de-4d99-9379-4a75b7a1b2fe

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):

Huckle, James. “C2E2: An Orally Administered Radionuclide Decorporation Agent.” 2014. Thesis, University of North Carolina. Accessed November 28, 2020. https://cdr.lib.unc.edu/record/uuid:d95fdb33-74de-4d99-9379-4a75b7a1b2fe.

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

MLA Handbook (7th Edition):

Huckle, James. “C2E2: An Orally Administered Radionuclide Decorporation Agent.” 2014. Web. 28 Nov 2020.

Vancouver:

Huckle J. C2E2: An Orally Administered Radionuclide Decorporation Agent. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Nov 28]. Available from: https://cdr.lib.unc.edu/record/uuid:d95fdb33-74de-4d99-9379-4a75b7a1b2fe.

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

Council of Science Editors:

Huckle J. C2E2: An Orally Administered Radionuclide Decorporation Agent. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:d95fdb33-74de-4d99-9379-4a75b7a1b2fe

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


University of North Carolina

23. Byrne, James. Iontophoretic delivery of cytotoxic agents for the treatment of solid tumors.

Degree: 2014, University of North Carolina

 Parenteral and oral routes have been the traditional methods of administering cytotoxic agents to cancer patients. Unfortunately, the maximum potential effect of these cytotoxic agents… (more)

Subjects/Keywords: Pharmaceutical chemistry; Biomedical engineering; Eshelman School of Pharmacy; Division of Pharmacoengineering and Molecular Pharmaceutics

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APA (6th Edition):

Byrne, J. (2014). Iontophoretic delivery of cytotoxic agents for the treatment of solid tumors. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:14c1a94a-f257-42f1-a9e2-6cd983683bb9

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):

Byrne, James. “Iontophoretic delivery of cytotoxic agents for the treatment of solid tumors.” 2014. Thesis, University of North Carolina. Accessed November 28, 2020. https://cdr.lib.unc.edu/record/uuid:14c1a94a-f257-42f1-a9e2-6cd983683bb9.

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

MLA Handbook (7th Edition):

Byrne, James. “Iontophoretic delivery of cytotoxic agents for the treatment of solid tumors.” 2014. Web. 28 Nov 2020.

Vancouver:

Byrne J. Iontophoretic delivery of cytotoxic agents for the treatment of solid tumors. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Nov 28]. Available from: https://cdr.lib.unc.edu/record/uuid:14c1a94a-f257-42f1-a9e2-6cd983683bb9.

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

Council of Science Editors:

Byrne J. Iontophoretic delivery of cytotoxic agents for the treatment of solid tumors. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:14c1a94a-f257-42f1-a9e2-6cd983683bb9

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


University of North Carolina

24. Roode, Luke. Sub-TumorDistribution Of PRINT Nanoparticles And Its Application For Nucleic Acid Delivery.

Degree: 2014, University of North Carolina

 Nanoparticle accumulation is typically measured at the organ level. However, much basic in vitro and in vivo research points to differences in nanoparticle internalization and… (more)

Subjects/Keywords: Pharmaceutical chemistry; Nanotechnology; Pharmacology; Eshelman School of Pharmacy; Division of Pharmacoengineering and Molecular Pharmaceutics

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

APA (6th Edition):

Roode, L. (2014). Sub-TumorDistribution Of PRINT Nanoparticles And Its Application For Nucleic Acid Delivery. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:8abb0098-73f9-4e8d-b6f5-6c0e71ccc1b6

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):

Roode, Luke. “Sub-TumorDistribution Of PRINT Nanoparticles And Its Application For Nucleic Acid Delivery.” 2014. Thesis, University of North Carolina. Accessed November 28, 2020. https://cdr.lib.unc.edu/record/uuid:8abb0098-73f9-4e8d-b6f5-6c0e71ccc1b6.

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

MLA Handbook (7th Edition):

Roode, Luke. “Sub-TumorDistribution Of PRINT Nanoparticles And Its Application For Nucleic Acid Delivery.” 2014. Web. 28 Nov 2020.

Vancouver:

Roode L. Sub-TumorDistribution Of PRINT Nanoparticles And Its Application For Nucleic Acid Delivery. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Nov 28]. Available from: https://cdr.lib.unc.edu/record/uuid:8abb0098-73f9-4e8d-b6f5-6c0e71ccc1b6.

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

Council of Science Editors:

Roode L. Sub-TumorDistribution Of PRINT Nanoparticles And Its Application For Nucleic Acid Delivery. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:8abb0098-73f9-4e8d-b6f5-6c0e71ccc1b6

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


University of North Carolina

25. He, Zhijian. Poly(2-oxazoline)s as new drug delivery systems.

Degree: 2015, University of North Carolina

 Taxane drugs, a class of important cancer chemotherapeutics, are often associated with excipient-related hypersensitivity, severe neurotoxicity, peripheral neuropathy, drug resistance and other limitations that influence… (more)

Subjects/Keywords: Pharmaceutical chemistry; Pharmacology; Polymers; Chemistry; Eshelman School of Pharmacy; Division of Pharmacoengineering and Molecular Pharmaceutics

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

APA (6th Edition):

He, Z. (2015). Poly(2-oxazoline)s as new drug delivery systems. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:993684be-62e3-4139-96e0-ab733ab55a5e

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):

He, Zhijian. “Poly(2-oxazoline)s as new drug delivery systems.” 2015. Thesis, University of North Carolina. Accessed November 28, 2020. https://cdr.lib.unc.edu/record/uuid:993684be-62e3-4139-96e0-ab733ab55a5e.

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

MLA Handbook (7th Edition):

He, Zhijian. “Poly(2-oxazoline)s as new drug delivery systems.” 2015. Web. 28 Nov 2020.

Vancouver:

He Z. Poly(2-oxazoline)s as new drug delivery systems. [Internet] [Thesis]. University of North Carolina; 2015. [cited 2020 Nov 28]. Available from: https://cdr.lib.unc.edu/record/uuid:993684be-62e3-4139-96e0-ab733ab55a5e.

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

Council of Science Editors:

He Z. Poly(2-oxazoline)s as new drug delivery systems. [Thesis]. University of North Carolina; 2015. Available from: https://cdr.lib.unc.edu/record/uuid:993684be-62e3-4139-96e0-ab733ab55a5e

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


University of North Carolina

26. Telko, Martin Jan. Investigation of electrostatic charging phenomena in dry powder inhalers and the effect on deposition.

Degree: 2009, University of North Carolina

 Dry powder inhalers (DPI) are an important drug delivery option, for the treatment of respiratory diseases, and, increasingly, for the delivery of systemically acting drugs… (more)

Subjects/Keywords: Eshelman School of Pharmacy; Division of Pharmacoengineering and Molecular Pharmaceutics

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APA (6th Edition):

Telko, M. J. (2009). Investigation of electrostatic charging phenomena in dry powder inhalers and the effect on deposition. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:7c6e0216-d3f7-4f5c-8278-35fad2ecd8d4

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):

Telko, Martin Jan. “Investigation of electrostatic charging phenomena in dry powder inhalers and the effect on deposition.” 2009. Thesis, University of North Carolina. Accessed November 28, 2020. https://cdr.lib.unc.edu/record/uuid:7c6e0216-d3f7-4f5c-8278-35fad2ecd8d4.

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

MLA Handbook (7th Edition):

Telko, Martin Jan. “Investigation of electrostatic charging phenomena in dry powder inhalers and the effect on deposition.” 2009. Web. 28 Nov 2020.

Vancouver:

Telko MJ. Investigation of electrostatic charging phenomena in dry powder inhalers and the effect on deposition. [Internet] [Thesis]. University of North Carolina; 2009. [cited 2020 Nov 28]. Available from: https://cdr.lib.unc.edu/record/uuid:7c6e0216-d3f7-4f5c-8278-35fad2ecd8d4.

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

Council of Science Editors:

Telko MJ. Investigation of electrostatic charging phenomena in dry powder inhalers and the effect on deposition. [Thesis]. University of North Carolina; 2009. Available from: https://cdr.lib.unc.edu/record/uuid:7c6e0216-d3f7-4f5c-8278-35fad2ecd8d4

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


University of North Carolina

27. An, John Sunghoon. Utility of two distinct macromolecular carriers for nucleic acid delivery.

Degree: 2008, University of North Carolina

 The major crux of nucleic acid-based therapy is that nucleic acids are not naturally occurring outside the cell. The systems biology of humans has evolved… (more)

Subjects/Keywords: Eshelman School of Pharmacy; Division of Pharmacoengineering and Molecular Pharmaceutics

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APA (6th Edition):

An, J. S. (2008). Utility of two distinct macromolecular carriers for nucleic acid delivery. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:0dcf0e75-d316-47e7-b961-8bfd1dbd1721

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):

An, John Sunghoon. “Utility of two distinct macromolecular carriers for nucleic acid delivery.” 2008. Thesis, University of North Carolina. Accessed November 28, 2020. https://cdr.lib.unc.edu/record/uuid:0dcf0e75-d316-47e7-b961-8bfd1dbd1721.

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

MLA Handbook (7th Edition):

An, John Sunghoon. “Utility of two distinct macromolecular carriers for nucleic acid delivery.” 2008. Web. 28 Nov 2020.

Vancouver:

An JS. Utility of two distinct macromolecular carriers for nucleic acid delivery. [Internet] [Thesis]. University of North Carolina; 2008. [cited 2020 Nov 28]. Available from: https://cdr.lib.unc.edu/record/uuid:0dcf0e75-d316-47e7-b961-8bfd1dbd1721.

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

Council of Science Editors:

An JS. Utility of two distinct macromolecular carriers for nucleic acid delivery. [Thesis]. University of North Carolina; 2008. Available from: https://cdr.lib.unc.edu/record/uuid:0dcf0e75-d316-47e7-b961-8bfd1dbd1721

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


University of North Carolina

28. Hung, Hsin-I. Combined Gene Therapy of siRNA and Apoptosis Inducing Factor Generated from a Single Transcriptional Event.

Degree: 2008, University of North Carolina

 The goal of this project is to test the hypothesis that a single transcriptional event driven by RNA polymerase II promoter driven siRNA expression plasmid… (more)

Subjects/Keywords: Eshelman School of Pharmacy; Division of Pharmacoengineering and Molecular Pharmaceutics

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APA (6th Edition):

Hung, H. (2008). Combined Gene Therapy of siRNA and Apoptosis Inducing Factor Generated from a Single Transcriptional Event. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:718ec1d2-c263-448f-8991-5e1ffd771d8f

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):

Hung, Hsin-I. “Combined Gene Therapy of siRNA and Apoptosis Inducing Factor Generated from a Single Transcriptional Event.” 2008. Thesis, University of North Carolina. Accessed November 28, 2020. https://cdr.lib.unc.edu/record/uuid:718ec1d2-c263-448f-8991-5e1ffd771d8f.

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

MLA Handbook (7th Edition):

Hung, Hsin-I. “Combined Gene Therapy of siRNA and Apoptosis Inducing Factor Generated from a Single Transcriptional Event.” 2008. Web. 28 Nov 2020.

Vancouver:

Hung H. Combined Gene Therapy of siRNA and Apoptosis Inducing Factor Generated from a Single Transcriptional Event. [Internet] [Thesis]. University of North Carolina; 2008. [cited 2020 Nov 28]. Available from: https://cdr.lib.unc.edu/record/uuid:718ec1d2-c263-448f-8991-5e1ffd771d8f.

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

Council of Science Editors:

Hung H. Combined Gene Therapy of siRNA and Apoptosis Inducing Factor Generated from a Single Transcriptional Event. [Thesis]. University of North Carolina; 2008. Available from: https://cdr.lib.unc.edu/record/uuid:718ec1d2-c263-448f-8991-5e1ffd771d8f

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


University of North Carolina

29. Lu, Dongmei. Aerosol Delivery of Recombinant Antigen 85B in Microparticle Vaccine Systems for Protection Against Tuberculosis.

Degree: 2007, University of North Carolina

 The only available tuberculosis vaccine, bacille Calmette Guérin (BCG) has highly variable efficacy. Antigen 85B (Ag85B) is a protein secreted by Mycobacterium tuberculosis (MTB) in… (more)

Subjects/Keywords: Eshelman School of Pharmacy; Division of Pharmacoengineering and Molecular Pharmaceutics

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

APA (6th Edition):

Lu, D. (2007). Aerosol Delivery of Recombinant Antigen 85B in Microparticle Vaccine Systems for Protection Against Tuberculosis. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:77ddb011-ef82-479c-87e6-96b1ad9e4d9a

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):

Lu, Dongmei. “Aerosol Delivery of Recombinant Antigen 85B in Microparticle Vaccine Systems for Protection Against Tuberculosis.” 2007. Thesis, University of North Carolina. Accessed November 28, 2020. https://cdr.lib.unc.edu/record/uuid:77ddb011-ef82-479c-87e6-96b1ad9e4d9a.

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

MLA Handbook (7th Edition):

Lu, Dongmei. “Aerosol Delivery of Recombinant Antigen 85B in Microparticle Vaccine Systems for Protection Against Tuberculosis.” 2007. Web. 28 Nov 2020.

Vancouver:

Lu D. Aerosol Delivery of Recombinant Antigen 85B in Microparticle Vaccine Systems for Protection Against Tuberculosis. [Internet] [Thesis]. University of North Carolina; 2007. [cited 2020 Nov 28]. Available from: https://cdr.lib.unc.edu/record/uuid:77ddb011-ef82-479c-87e6-96b1ad9e4d9a.

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

Council of Science Editors:

Lu D. Aerosol Delivery of Recombinant Antigen 85B in Microparticle Vaccine Systems for Protection Against Tuberculosis. [Thesis]. University of North Carolina; 2007. Available from: https://cdr.lib.unc.edu/record/uuid:77ddb011-ef82-479c-87e6-96b1ad9e4d9a

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


University of North Carolina

30. Lee, Jin. Polymeric nanogels as gene carriers.

Degree: 2007, University of North Carolina

 Developing efficient and safe vectors is one of the main challenges in gene therapy. Multiple fatal incidences in applying virus have brought safety issues to… (more)

Subjects/Keywords: Eshelman School of Pharmacy; Division of Pharmacoengineering and Molecular Pharmaceutics

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

APA (6th Edition):

Lee, J. (2007). Polymeric nanogels as gene carriers. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:0c4098b6-89e1-49bc-81d4-25242ec30b45

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):

Lee, Jin. “Polymeric nanogels as gene carriers.” 2007. Thesis, University of North Carolina. Accessed November 28, 2020. https://cdr.lib.unc.edu/record/uuid:0c4098b6-89e1-49bc-81d4-25242ec30b45.

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

MLA Handbook (7th Edition):

Lee, Jin. “Polymeric nanogels as gene carriers.” 2007. Web. 28 Nov 2020.

Vancouver:

Lee J. Polymeric nanogels as gene carriers. [Internet] [Thesis]. University of North Carolina; 2007. [cited 2020 Nov 28]. Available from: https://cdr.lib.unc.edu/record/uuid:0c4098b6-89e1-49bc-81d4-25242ec30b45.

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

Council of Science Editors:

Lee J. Polymeric nanogels as gene carriers. [Thesis]. University of North Carolina; 2007. Available from: https://cdr.lib.unc.edu/record/uuid:0c4098b6-89e1-49bc-81d4-25242ec30b45

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

[1] [2]

.