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You searched for subject:(Pharmaceutics AND Drug Design). Showing records 1 – 30 of 205 total matches.

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Northeastern University

1. Panwar, Rajiv. Reduction of the cardiotoxicity of doxorubicin: demonstration by in vivo imaging with bispecific antibody/radiolabeled negatively charged polymers.

Degree: PhD, School of Pharmacy, 2012, Northeastern University

 ECG and serum CK-MB (creatinine kinase) or cardiac troponin analyses are the routine tests for the diagnosis of myocardial necrosis. Borderline CK-MB elevations and uninterpretable… (more)

Subjects/Keywords: Pharmaceutics and Drug delivery systems; Pharmaceutics and Drug Design; Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Panwar, R. (2012). Reduction of the cardiotoxicity of doxorubicin: demonstration by in vivo imaging with bispecific antibody/radiolabeled negatively charged polymers. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/d20002959

Chicago Manual of Style (16th Edition):

Panwar, Rajiv. “Reduction of the cardiotoxicity of doxorubicin: demonstration by in vivo imaging with bispecific antibody/radiolabeled negatively charged polymers.” 2012. Doctoral Dissertation, Northeastern University. Accessed February 18, 2020. http://hdl.handle.net/2047/d20002959.

MLA Handbook (7th Edition):

Panwar, Rajiv. “Reduction of the cardiotoxicity of doxorubicin: demonstration by in vivo imaging with bispecific antibody/radiolabeled negatively charged polymers.” 2012. Web. 18 Feb 2020.

Vancouver:

Panwar R. Reduction of the cardiotoxicity of doxorubicin: demonstration by in vivo imaging with bispecific antibody/radiolabeled negatively charged polymers. [Internet] [Doctoral dissertation]. Northeastern University; 2012. [cited 2020 Feb 18]. Available from: http://hdl.handle.net/2047/d20002959.

Council of Science Editors:

Panwar R. Reduction of the cardiotoxicity of doxorubicin: demonstration by in vivo imaging with bispecific antibody/radiolabeled negatively charged polymers. [Doctoral Dissertation]. Northeastern University; 2012. Available from: http://hdl.handle.net/2047/d20002959


University of Kentucky

2. Hou, Shurong. HUMAN BUTYRYLCHOLINESTERASE MUTANTS FOR COCAINE DETOXIFICATION.

Degree: 2014, University of Kentucky

 Cocaine is one of the most reinforcing drugs of abuse and has caused serious medical and social problems. There is no FDA-approved medication specific for… (more)

Subjects/Keywords: Protein drug; enzyme therapy; human butyrylcholinesterase; cocaine; drug abuse treatment; Pharmaceutics and Drug Design

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APA (6th Edition):

Hou, S. (2014). HUMAN BUTYRYLCHOLINESTERASE MUTANTS FOR COCAINE DETOXIFICATION. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/pharmacy_etds/38

Chicago Manual of Style (16th Edition):

Hou, Shurong. “HUMAN BUTYRYLCHOLINESTERASE MUTANTS FOR COCAINE DETOXIFICATION.” 2014. Doctoral Dissertation, University of Kentucky. Accessed February 18, 2020. https://uknowledge.uky.edu/pharmacy_etds/38.

MLA Handbook (7th Edition):

Hou, Shurong. “HUMAN BUTYRYLCHOLINESTERASE MUTANTS FOR COCAINE DETOXIFICATION.” 2014. Web. 18 Feb 2020.

Vancouver:

Hou S. HUMAN BUTYRYLCHOLINESTERASE MUTANTS FOR COCAINE DETOXIFICATION. [Internet] [Doctoral dissertation]. University of Kentucky; 2014. [cited 2020 Feb 18]. Available from: https://uknowledge.uky.edu/pharmacy_etds/38.

Council of Science Editors:

Hou S. HUMAN BUTYRYLCHOLINESTERASE MUTANTS FOR COCAINE DETOXIFICATION. [Doctoral Dissertation]. University of Kentucky; 2014. Available from: https://uknowledge.uky.edu/pharmacy_etds/38


University of Kentucky

3. Fang, Lei. COMPUTATIONAL MODELING, DESIGN, AND CHARACTERIZATION OF COCAINE-METABOLIZING ENZYMES FOR ANTI-COCAINE MEDICATION.

Degree: 2013, University of Kentucky

 Cocaine is a widely abused and addictive drug, resulting in serious medical and social problems in modern society. Currently, there is no FDA-approved medication specific… (more)

Subjects/Keywords: Protein drug design; Human butyrylcholinesterase; Bacterial cocaine esterase; Mutant; Anti-Cocaine; Pharmaceutics and Drug Design

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APA (6th Edition):

Fang, L. (2013). COMPUTATIONAL MODELING, DESIGN, AND CHARACTERIZATION OF COCAINE-METABOLIZING ENZYMES FOR ANTI-COCAINE MEDICATION. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/pharmacy_etds/39

Chicago Manual of Style (16th Edition):

Fang, Lei. “COMPUTATIONAL MODELING, DESIGN, AND CHARACTERIZATION OF COCAINE-METABOLIZING ENZYMES FOR ANTI-COCAINE MEDICATION.” 2013. Doctoral Dissertation, University of Kentucky. Accessed February 18, 2020. https://uknowledge.uky.edu/pharmacy_etds/39.

MLA Handbook (7th Edition):

Fang, Lei. “COMPUTATIONAL MODELING, DESIGN, AND CHARACTERIZATION OF COCAINE-METABOLIZING ENZYMES FOR ANTI-COCAINE MEDICATION.” 2013. Web. 18 Feb 2020.

Vancouver:

Fang L. COMPUTATIONAL MODELING, DESIGN, AND CHARACTERIZATION OF COCAINE-METABOLIZING ENZYMES FOR ANTI-COCAINE MEDICATION. [Internet] [Doctoral dissertation]. University of Kentucky; 2013. [cited 2020 Feb 18]. Available from: https://uknowledge.uky.edu/pharmacy_etds/39.

Council of Science Editors:

Fang L. COMPUTATIONAL MODELING, DESIGN, AND CHARACTERIZATION OF COCAINE-METABOLIZING ENZYMES FOR ANTI-COCAINE MEDICATION. [Doctoral Dissertation]. University of Kentucky; 2013. Available from: https://uknowledge.uky.edu/pharmacy_etds/39


Western Kentucky University

4. Wang, Ban. Synthesis of Bis(imino)pyridine Iron(II) Complexes and Development of Bis(imino)pyridine Iron(II) Catalyzed Carbene Transfer Reactions.

Degree: MS, Department of Chemistry, 2019, Western Kentucky University

  Metal catalysis of symmetric and asymmetric carbene transfer reactions has been widely applied in natural product synthesis and material science over years. Metal carbene… (more)

Subjects/Keywords: Organic Chemistry; Pharmaceutical Preparations; Pharmaceutics and Drug Design

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APA (6th Edition):

Wang, B. (2019). Synthesis of Bis(imino)pyridine Iron(II) Complexes and Development of Bis(imino)pyridine Iron(II) Catalyzed Carbene Transfer Reactions. (Masters Thesis). Western Kentucky University. Retrieved from https://digitalcommons.wku.edu/theses/3159

Chicago Manual of Style (16th Edition):

Wang, Ban. “Synthesis of Bis(imino)pyridine Iron(II) Complexes and Development of Bis(imino)pyridine Iron(II) Catalyzed Carbene Transfer Reactions.” 2019. Masters Thesis, Western Kentucky University. Accessed February 18, 2020. https://digitalcommons.wku.edu/theses/3159.

MLA Handbook (7th Edition):

Wang, Ban. “Synthesis of Bis(imino)pyridine Iron(II) Complexes and Development of Bis(imino)pyridine Iron(II) Catalyzed Carbene Transfer Reactions.” 2019. Web. 18 Feb 2020.

Vancouver:

Wang B. Synthesis of Bis(imino)pyridine Iron(II) Complexes and Development of Bis(imino)pyridine Iron(II) Catalyzed Carbene Transfer Reactions. [Internet] [Masters thesis]. Western Kentucky University; 2019. [cited 2020 Feb 18]. Available from: https://digitalcommons.wku.edu/theses/3159.

Council of Science Editors:

Wang B. Synthesis of Bis(imino)pyridine Iron(II) Complexes and Development of Bis(imino)pyridine Iron(II) Catalyzed Carbene Transfer Reactions. [Masters Thesis]. Western Kentucky University; 2019. Available from: https://digitalcommons.wku.edu/theses/3159


University of Kentucky

5. Ghosh, Priyanka. Formulation Optimization for Pore Lifetime Enhancement and Sustained Drug Delivery Across Microneedle Treated Skin.

Degree: 2013, University of Kentucky

 Microneedle (MN) enhanced drug delivery is a safe, effective and efficient enhancement method for delivery of drug molecules across the skin. The “poke (press) and… (more)

Subjects/Keywords: microneedles; naltrexone; transdermal; formulation stratigies; micropore lifetime; Pharmaceutics and Drug Design

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APA (6th Edition):

Ghosh, P. (2013). Formulation Optimization for Pore Lifetime Enhancement and Sustained Drug Delivery Across Microneedle Treated Skin. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/pharmacy_etds/22

Chicago Manual of Style (16th Edition):

Ghosh, Priyanka. “Formulation Optimization for Pore Lifetime Enhancement and Sustained Drug Delivery Across Microneedle Treated Skin.” 2013. Doctoral Dissertation, University of Kentucky. Accessed February 18, 2020. https://uknowledge.uky.edu/pharmacy_etds/22.

MLA Handbook (7th Edition):

Ghosh, Priyanka. “Formulation Optimization for Pore Lifetime Enhancement and Sustained Drug Delivery Across Microneedle Treated Skin.” 2013. Web. 18 Feb 2020.

Vancouver:

Ghosh P. Formulation Optimization for Pore Lifetime Enhancement and Sustained Drug Delivery Across Microneedle Treated Skin. [Internet] [Doctoral dissertation]. University of Kentucky; 2013. [cited 2020 Feb 18]. Available from: https://uknowledge.uky.edu/pharmacy_etds/22.

Council of Science Editors:

Ghosh P. Formulation Optimization for Pore Lifetime Enhancement and Sustained Drug Delivery Across Microneedle Treated Skin. [Doctoral Dissertation]. University of Kentucky; 2013. Available from: https://uknowledge.uky.edu/pharmacy_etds/22


University of Kentucky

6. Ao, Lin. Investigating Mechanisms Determining Cancer Cell Sensitivity to Carfilzomib and Novel Strategies to Overcome Resistance.

Degree: 2016, University of Kentucky

 Proteasome inhibitors (PIs) are a class of FDA-approved anti-cancer agents which includes the first-generation PI bortezomib (BTZ) and second-generation carfilzomib (CFZ). Drug resistance is a… (more)

Subjects/Keywords: proteasome inhibitor; carfilzomib; resistance; cancer; Pharmaceutics and Drug Design

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APA (6th Edition):

Ao, L. (2016). Investigating Mechanisms Determining Cancer Cell Sensitivity to Carfilzomib and Novel Strategies to Overcome Resistance. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/pharmacy_etds/68

Chicago Manual of Style (16th Edition):

Ao, Lin. “Investigating Mechanisms Determining Cancer Cell Sensitivity to Carfilzomib and Novel Strategies to Overcome Resistance.” 2016. Doctoral Dissertation, University of Kentucky. Accessed February 18, 2020. https://uknowledge.uky.edu/pharmacy_etds/68.

MLA Handbook (7th Edition):

Ao, Lin. “Investigating Mechanisms Determining Cancer Cell Sensitivity to Carfilzomib and Novel Strategies to Overcome Resistance.” 2016. Web. 18 Feb 2020.

Vancouver:

Ao L. Investigating Mechanisms Determining Cancer Cell Sensitivity to Carfilzomib and Novel Strategies to Overcome Resistance. [Internet] [Doctoral dissertation]. University of Kentucky; 2016. [cited 2020 Feb 18]. Available from: https://uknowledge.uky.edu/pharmacy_etds/68.

Council of Science Editors:

Ao L. Investigating Mechanisms Determining Cancer Cell Sensitivity to Carfilzomib and Novel Strategies to Overcome Resistance. [Doctoral Dissertation]. University of Kentucky; 2016. Available from: https://uknowledge.uky.edu/pharmacy_etds/68


New Jersey Institute of Technology

7. Walker, Annmarie C. Comparative analysis of the dissolution performance of aspirin tablets in the usp apparatus 2 and in a minivessel dissolution system.

Degree: MSin Pharmaceutical Engineering - (M.S.), Chemical, Biological and Pharmaceutical Engineering, 2017, New Jersey Institute of Technology

  Dissolution testing is a critical component of quality control procedures in the pharmaceutical industry in order to ensure that the final solid dosage forms… (more)

Subjects/Keywords: Pharmaceutical industry; Quality control; Chemical Engineering; Pharmaceutics and Drug Design

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APA (6th Edition):

Walker, A. C. (2017). Comparative analysis of the dissolution performance of aspirin tablets in the usp apparatus 2 and in a minivessel dissolution system. (Thesis). New Jersey Institute of Technology. Retrieved from https://digitalcommons.njit.edu/theses/46

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):

Walker, Annmarie C. “Comparative analysis of the dissolution performance of aspirin tablets in the usp apparatus 2 and in a minivessel dissolution system.” 2017. Thesis, New Jersey Institute of Technology. Accessed February 18, 2020. https://digitalcommons.njit.edu/theses/46.

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

MLA Handbook (7th Edition):

Walker, Annmarie C. “Comparative analysis of the dissolution performance of aspirin tablets in the usp apparatus 2 and in a minivessel dissolution system.” 2017. Web. 18 Feb 2020.

Vancouver:

Walker AC. Comparative analysis of the dissolution performance of aspirin tablets in the usp apparatus 2 and in a minivessel dissolution system. [Internet] [Thesis]. New Jersey Institute of Technology; 2017. [cited 2020 Feb 18]. Available from: https://digitalcommons.njit.edu/theses/46.

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

Council of Science Editors:

Walker AC. Comparative analysis of the dissolution performance of aspirin tablets in the usp apparatus 2 and in a minivessel dissolution system. [Thesis]. New Jersey Institute of Technology; 2017. Available from: https://digitalcommons.njit.edu/theses/46

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


New Jersey Institute of Technology

8. Wijayasekara, Dilanji Bhagya. Minimum agitation speed for solid suspension and mixing time in a torispherical -bottomed pharmaceutical stirred tank under different baffling conditions.

Degree: MSin Pharmaceutical Engineering - (M.S.), Chemical, Biological and Pharmaceutical Engineering, 2010, New Jersey Institute of Technology

  The minimum agitation speed, NS, required to just suspend solid particles dispersed in water was experimentally determined in this work for a glass-lined type… (more)

Subjects/Keywords: Solid particle suspension; Agitation speed; Chemical Engineering; Pharmaceutics and Drug Design

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APA (6th Edition):

Wijayasekara, D. B. (2010). Minimum agitation speed for solid suspension and mixing time in a torispherical -bottomed pharmaceutical stirred tank under different baffling conditions. (Thesis). New Jersey Institute of Technology. Retrieved from https://digitalcommons.njit.edu/theses/65

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):

Wijayasekara, Dilanji Bhagya. “Minimum agitation speed for solid suspension and mixing time in a torispherical -bottomed pharmaceutical stirred tank under different baffling conditions.” 2010. Thesis, New Jersey Institute of Technology. Accessed February 18, 2020. https://digitalcommons.njit.edu/theses/65.

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

MLA Handbook (7th Edition):

Wijayasekara, Dilanji Bhagya. “Minimum agitation speed for solid suspension and mixing time in a torispherical -bottomed pharmaceutical stirred tank under different baffling conditions.” 2010. Web. 18 Feb 2020.

Vancouver:

Wijayasekara DB. Minimum agitation speed for solid suspension and mixing time in a torispherical -bottomed pharmaceutical stirred tank under different baffling conditions. [Internet] [Thesis]. New Jersey Institute of Technology; 2010. [cited 2020 Feb 18]. Available from: https://digitalcommons.njit.edu/theses/65.

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

Council of Science Editors:

Wijayasekara DB. Minimum agitation speed for solid suspension and mixing time in a torispherical -bottomed pharmaceutical stirred tank under different baffling conditions. [Thesis]. New Jersey Institute of Technology; 2010. Available from: https://digitalcommons.njit.edu/theses/65

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


New Jersey Institute of Technology

9. Arulmozhi, Anandhavalavan. Dissolution testing of prednisone and salicylic acid calibrator tablets at different tablet locations.

Degree: MSin Pharmaceutical Engineering - (M.S.), Chemical, Biological and Pharmaceutical Engineering, 2011, New Jersey Institute of Technology

  Dissolution testing is routinely carried out in the pharmaceutical industry to determine the rate of dissolution of solid dosage forms. This test is one… (more)

Subjects/Keywords: Dissolution testing; Tablet location; Chemical Engineering; Pharmaceutics and Drug Design

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APA (6th Edition):

Arulmozhi, A. (2011). Dissolution testing of prednisone and salicylic acid calibrator tablets at different tablet locations. (Thesis). New Jersey Institute of Technology. Retrieved from https://digitalcommons.njit.edu/theses/86

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):

Arulmozhi, Anandhavalavan. “Dissolution testing of prednisone and salicylic acid calibrator tablets at different tablet locations.” 2011. Thesis, New Jersey Institute of Technology. Accessed February 18, 2020. https://digitalcommons.njit.edu/theses/86.

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

MLA Handbook (7th Edition):

Arulmozhi, Anandhavalavan. “Dissolution testing of prednisone and salicylic acid calibrator tablets at different tablet locations.” 2011. Web. 18 Feb 2020.

Vancouver:

Arulmozhi A. Dissolution testing of prednisone and salicylic acid calibrator tablets at different tablet locations. [Internet] [Thesis]. New Jersey Institute of Technology; 2011. [cited 2020 Feb 18]. Available from: https://digitalcommons.njit.edu/theses/86.

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

Council of Science Editors:

Arulmozhi A. Dissolution testing of prednisone and salicylic acid calibrator tablets at different tablet locations. [Thesis]. New Jersey Institute of Technology; 2011. Available from: https://digitalcommons.njit.edu/theses/86

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


New Jersey Institute of Technology

10. Parekh, Shrutiben Rameshbhai. Dissolution of disintegrating solid dosage forms in a modified dissolution testing apparatus 2.

Degree: MSin Pharmaceutical Engineering - (M.S.), Chemical, Biological and Pharmaceutical Engineering, 2011, New Jersey Institute of Technology

  Dissolution tests are routinely carried out in the pharmaceutical industry to determine the dissolution rate of solid dosage forms. Dissolution testing serves as a… (more)

Subjects/Keywords: Dissolution tests; Dissolution profiles; Chemical Engineering; Pharmaceutics and Drug Design

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APA (6th Edition):

Parekh, S. R. (2011). Dissolution of disintegrating solid dosage forms in a modified dissolution testing apparatus 2. (Thesis). New Jersey Institute of Technology. Retrieved from https://digitalcommons.njit.edu/theses/93

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):

Parekh, Shrutiben Rameshbhai. “Dissolution of disintegrating solid dosage forms in a modified dissolution testing apparatus 2.” 2011. Thesis, New Jersey Institute of Technology. Accessed February 18, 2020. https://digitalcommons.njit.edu/theses/93.

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

MLA Handbook (7th Edition):

Parekh, Shrutiben Rameshbhai. “Dissolution of disintegrating solid dosage forms in a modified dissolution testing apparatus 2.” 2011. Web. 18 Feb 2020.

Vancouver:

Parekh SR. Dissolution of disintegrating solid dosage forms in a modified dissolution testing apparatus 2. [Internet] [Thesis]. New Jersey Institute of Technology; 2011. [cited 2020 Feb 18]. Available from: https://digitalcommons.njit.edu/theses/93.

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

Council of Science Editors:

Parekh SR. Dissolution of disintegrating solid dosage forms in a modified dissolution testing apparatus 2. [Thesis]. New Jersey Institute of Technology; 2011. Available from: https://digitalcommons.njit.edu/theses/93

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


New Jersey Institute of Technology

11. Wei, Ran. Transdermal and transbuccal delivery of lidocaine and nicotine : combined effects of iontophoresis and chemical enhancers.

Degree: MSin Pharmaceutical Engineering - (M.S.), Chemical, Biological and Pharmaceutical Engineering, 2011, New Jersey Institute of Technology

  This study focused on the effects of iontophoresis and chemical enhancers on drug release. The transport of Lidocaine HCl (LHCl) and Nicotine Hydrogen Tartrate… (more)

Subjects/Keywords: Iontophoresis; Enhancer; Transdermal; Transbuccal; Chemical Engineering; Pharmaceutics and Drug Design

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APA (6th Edition):

Wei, R. (2011). Transdermal and transbuccal delivery of lidocaine and nicotine : combined effects of iontophoresis and chemical enhancers. (Thesis). New Jersey Institute of Technology. Retrieved from https://digitalcommons.njit.edu/theses/97

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):

Wei, Ran. “Transdermal and transbuccal delivery of lidocaine and nicotine : combined effects of iontophoresis and chemical enhancers.” 2011. Thesis, New Jersey Institute of Technology. Accessed February 18, 2020. https://digitalcommons.njit.edu/theses/97.

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

MLA Handbook (7th Edition):

Wei, Ran. “Transdermal and transbuccal delivery of lidocaine and nicotine : combined effects of iontophoresis and chemical enhancers.” 2011. Web. 18 Feb 2020.

Vancouver:

Wei R. Transdermal and transbuccal delivery of lidocaine and nicotine : combined effects of iontophoresis and chemical enhancers. [Internet] [Thesis]. New Jersey Institute of Technology; 2011. [cited 2020 Feb 18]. Available from: https://digitalcommons.njit.edu/theses/97.

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

Council of Science Editors:

Wei R. Transdermal and transbuccal delivery of lidocaine and nicotine : combined effects of iontophoresis and chemical enhancers. [Thesis]. New Jersey Institute of Technology; 2011. Available from: https://digitalcommons.njit.edu/theses/97

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


New Jersey Institute of Technology

12. Zhou, Anqi. Experimental determination of the mixing requirements for solid suspension in pharmaceutical stirred tank reactors.

Degree: MSin Pharmaceutical Engineering - (M.S.), Chemical, Biological and Pharmaceutical Engineering, 2014, New Jersey Institute of Technology

  Glass and glass-lined, stirred-tank reactors are of significant importance in the pharmaceutical and related industries. Because of fabrication issues, a retreat blade impeller (RBI)… (more)

Subjects/Keywords: Retreat blade impeller; Agitation systems; Chemical Engineering; Pharmaceutics and Drug Design

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APA (6th Edition):

Zhou, A. (2014). Experimental determination of the mixing requirements for solid suspension in pharmaceutical stirred tank reactors. (Thesis). New Jersey Institute of Technology. Retrieved from https://digitalcommons.njit.edu/theses/206

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):

Zhou, Anqi. “Experimental determination of the mixing requirements for solid suspension in pharmaceutical stirred tank reactors.” 2014. Thesis, New Jersey Institute of Technology. Accessed February 18, 2020. https://digitalcommons.njit.edu/theses/206.

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

MLA Handbook (7th Edition):

Zhou, Anqi. “Experimental determination of the mixing requirements for solid suspension in pharmaceutical stirred tank reactors.” 2014. Web. 18 Feb 2020.

Vancouver:

Zhou A. Experimental determination of the mixing requirements for solid suspension in pharmaceutical stirred tank reactors. [Internet] [Thesis]. New Jersey Institute of Technology; 2014. [cited 2020 Feb 18]. Available from: https://digitalcommons.njit.edu/theses/206.

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

Council of Science Editors:

Zhou A. Experimental determination of the mixing requirements for solid suspension in pharmaceutical stirred tank reactors. [Thesis]. New Jersey Institute of Technology; 2014. Available from: https://digitalcommons.njit.edu/theses/206

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


University of Western Ontario

13. Rytelewski, Mateusz. Overcoming Innate and Acquired Therapy Resistance by Targeting DNA Repair in Human Cancer Cells.

Degree: 2015, University of Western Ontario

 Genomic instability and a high mutation rate lead to heterogeneity in human tumors. Mathematical modelling predicts that these characteristics promote acquired resistance to cytotoxic and… (more)

Subjects/Keywords: cancer therapy resistance; DNA repair; BRCA2; chemotherapy; ovarian cancer; antisense; Neoplasms; Pharmaceutics and Drug Design

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APA (6th Edition):

Rytelewski, M. (2015). Overcoming Innate and Acquired Therapy Resistance by Targeting DNA Repair in Human Cancer Cells. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/3438

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):

Rytelewski, Mateusz. “Overcoming Innate and Acquired Therapy Resistance by Targeting DNA Repair in Human Cancer Cells.” 2015. Thesis, University of Western Ontario. Accessed February 18, 2020. https://ir.lib.uwo.ca/etd/3438.

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

MLA Handbook (7th Edition):

Rytelewski, Mateusz. “Overcoming Innate and Acquired Therapy Resistance by Targeting DNA Repair in Human Cancer Cells.” 2015. Web. 18 Feb 2020.

Vancouver:

Rytelewski M. Overcoming Innate and Acquired Therapy Resistance by Targeting DNA Repair in Human Cancer Cells. [Internet] [Thesis]. University of Western Ontario; 2015. [cited 2020 Feb 18]. Available from: https://ir.lib.uwo.ca/etd/3438.

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

Council of Science Editors:

Rytelewski M. Overcoming Innate and Acquired Therapy Resistance by Targeting DNA Repair in Human Cancer Cells. [Thesis]. University of Western Ontario; 2015. Available from: https://ir.lib.uwo.ca/etd/3438

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


University of Colorado

14. Xu, Yemin. Mechanisms of Protein Stability in Lyophilized Samples.

Degree: PhD, Chemistry & Biochemistry, 2014, University of Colorado

  Lyophilization is often the choice for therapeutic proteins when an aqueous formulation is not sufficiently stable to achieve the desired shelf life. Lyophilization incorporates… (more)

Subjects/Keywords: Interface; Lyophilization; Mobility; Protein formulation; Stability; Structure; Medicinal and Pharmaceutical Chemistry; Pharmaceutics and Drug Design

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APA (6th Edition):

Xu, Y. (2014). Mechanisms of Protein Stability in Lyophilized Samples. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/110

Chicago Manual of Style (16th Edition):

Xu, Yemin. “Mechanisms of Protein Stability in Lyophilized Samples.” 2014. Doctoral Dissertation, University of Colorado. Accessed February 18, 2020. https://scholar.colorado.edu/chem_gradetds/110.

MLA Handbook (7th Edition):

Xu, Yemin. “Mechanisms of Protein Stability in Lyophilized Samples.” 2014. Web. 18 Feb 2020.

Vancouver:

Xu Y. Mechanisms of Protein Stability in Lyophilized Samples. [Internet] [Doctoral dissertation]. University of Colorado; 2014. [cited 2020 Feb 18]. Available from: https://scholar.colorado.edu/chem_gradetds/110.

Council of Science Editors:

Xu Y. Mechanisms of Protein Stability in Lyophilized Samples. [Doctoral Dissertation]. University of Colorado; 2014. Available from: https://scholar.colorado.edu/chem_gradetds/110


University of Kentucky

15. Jordan, Carolyn T. DESIGN AND ANALYSIS OF CURCUMIN CONJUGATED POLY(BETA-AMINO ESTER) NETWORKS FOR CONTROLLED RELEASE IN OXIDATIVE STRESS ENVIRONMENTS.

Degree: 2018, University of Kentucky

 Oxidative stress, the imbalance of free radical generation with antioxidant defenses, leads to cellular inflammation, apoptosis and cell death. This compromised environment results in debilitating… (more)

Subjects/Keywords: Oxidative Stress; Antioxidant Therapeutics; Responsive Polymers; Curcumin; Oral Mucositis; Pharmaceutics and Drug Design; Polymer Science

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

APA (6th Edition):

Jordan, C. T. (2018). DESIGN AND ANALYSIS OF CURCUMIN CONJUGATED POLY(BETA-AMINO ESTER) NETWORKS FOR CONTROLLED RELEASE IN OXIDATIVE STRESS ENVIRONMENTS. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/cme_etds/84

Chicago Manual of Style (16th Edition):

Jordan, Carolyn T. “DESIGN AND ANALYSIS OF CURCUMIN CONJUGATED POLY(BETA-AMINO ESTER) NETWORKS FOR CONTROLLED RELEASE IN OXIDATIVE STRESS ENVIRONMENTS.” 2018. Doctoral Dissertation, University of Kentucky. Accessed February 18, 2020. https://uknowledge.uky.edu/cme_etds/84.

MLA Handbook (7th Edition):

Jordan, Carolyn T. “DESIGN AND ANALYSIS OF CURCUMIN CONJUGATED POLY(BETA-AMINO ESTER) NETWORKS FOR CONTROLLED RELEASE IN OXIDATIVE STRESS ENVIRONMENTS.” 2018. Web. 18 Feb 2020.

Vancouver:

Jordan CT. DESIGN AND ANALYSIS OF CURCUMIN CONJUGATED POLY(BETA-AMINO ESTER) NETWORKS FOR CONTROLLED RELEASE IN OXIDATIVE STRESS ENVIRONMENTS. [Internet] [Doctoral dissertation]. University of Kentucky; 2018. [cited 2020 Feb 18]. Available from: https://uknowledge.uky.edu/cme_etds/84.

Council of Science Editors:

Jordan CT. DESIGN AND ANALYSIS OF CURCUMIN CONJUGATED POLY(BETA-AMINO ESTER) NETWORKS FOR CONTROLLED RELEASE IN OXIDATIVE STRESS ENVIRONMENTS. [Doctoral Dissertation]. University of Kentucky; 2018. Available from: https://uknowledge.uky.edu/cme_etds/84


University of Kentucky

16. Chen, Xiabin. DEVELOPMENT OF COCAINE HYDROLASE FOR THERAPEUTIC TREATMENT OF COCAINE ABUSE.

Degree: 2016, University of Kentucky

 Cocaine abuse is a world-wide public health and social problem without a U.S. Food and Drug Administration (FDA)-approved medication. An ideal anti-cocaine medication would accelerate… (more)

Subjects/Keywords: Cocaine abuse; benzoylecgonine; enzyme therapy; protein engineering; butyrylcholinesterase; LC-MS/MS; Pharmaceutics and Drug Design

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APA (6th Edition):

Chen, X. (2016). DEVELOPMENT OF COCAINE HYDROLASE FOR THERAPEUTIC TREATMENT OF COCAINE ABUSE. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/pharmacy_etds/59

Chicago Manual of Style (16th Edition):

Chen, Xiabin. “DEVELOPMENT OF COCAINE HYDROLASE FOR THERAPEUTIC TREATMENT OF COCAINE ABUSE.” 2016. Doctoral Dissertation, University of Kentucky. Accessed February 18, 2020. https://uknowledge.uky.edu/pharmacy_etds/59.

MLA Handbook (7th Edition):

Chen, Xiabin. “DEVELOPMENT OF COCAINE HYDROLASE FOR THERAPEUTIC TREATMENT OF COCAINE ABUSE.” 2016. Web. 18 Feb 2020.

Vancouver:

Chen X. DEVELOPMENT OF COCAINE HYDROLASE FOR THERAPEUTIC TREATMENT OF COCAINE ABUSE. [Internet] [Doctoral dissertation]. University of Kentucky; 2016. [cited 2020 Feb 18]. Available from: https://uknowledge.uky.edu/pharmacy_etds/59.

Council of Science Editors:

Chen X. DEVELOPMENT OF COCAINE HYDROLASE FOR THERAPEUTIC TREATMENT OF COCAINE ABUSE. [Doctoral Dissertation]. University of Kentucky; 2016. Available from: https://uknowledge.uky.edu/pharmacy_etds/59


University of Kentucky

17. Li, Hui. RNA AS A UNIQUE POLYMER TO BUILD CONTROLLABLE NANOSTRUCTURES FOR NANOMEDICINE AND NANOTECHNOLOGY.

Degree: 2016, University of Kentucky

 RNA nanotechnology is an emerging field that involves the design, construction and functionalization of nanostructures composed mainly of RNA for applications in biomedical and material… (more)

Subjects/Keywords: RNA Nanotechnology; pRNA; Three-way Junction; Nanostructures; Nanomedicine; Nanomedicine; Pharmaceutics and Drug Design

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APA (6th Edition):

Li, H. (2016). RNA AS A UNIQUE POLYMER TO BUILD CONTROLLABLE NANOSTRUCTURES FOR NANOMEDICINE AND NANOTECHNOLOGY. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/pharmacy_etds/67

Chicago Manual of Style (16th Edition):

Li, Hui. “RNA AS A UNIQUE POLYMER TO BUILD CONTROLLABLE NANOSTRUCTURES FOR NANOMEDICINE AND NANOTECHNOLOGY.” 2016. Doctoral Dissertation, University of Kentucky. Accessed February 18, 2020. https://uknowledge.uky.edu/pharmacy_etds/67.

MLA Handbook (7th Edition):

Li, Hui. “RNA AS A UNIQUE POLYMER TO BUILD CONTROLLABLE NANOSTRUCTURES FOR NANOMEDICINE AND NANOTECHNOLOGY.” 2016. Web. 18 Feb 2020.

Vancouver:

Li H. RNA AS A UNIQUE POLYMER TO BUILD CONTROLLABLE NANOSTRUCTURES FOR NANOMEDICINE AND NANOTECHNOLOGY. [Internet] [Doctoral dissertation]. University of Kentucky; 2016. [cited 2020 Feb 18]. Available from: https://uknowledge.uky.edu/pharmacy_etds/67.

Council of Science Editors:

Li H. RNA AS A UNIQUE POLYMER TO BUILD CONTROLLABLE NANOSTRUCTURES FOR NANOMEDICINE AND NANOTECHNOLOGY. [Doctoral Dissertation]. University of Kentucky; 2016. Available from: https://uknowledge.uky.edu/pharmacy_etds/67


Northeastern University

18. Gordon, Justin Brad. A study of the loss of acidic drug plasma protein binding sites in mouse serum albumin and loss prevention with a serine protease inhibitor adduct.

Degree: MS, Department of Biology, 2013, Northeastern University

 Rapid equilibrium dialysis (RED) plasma protein binding is a validated and widely used assay in the pharmaceutical industry that has produced consistent results at Millennium… (more)

Subjects/Keywords: plasma protein binding; rapid equilbrium dialysis; serum albumin; Biology; Pharmaceutics and Drug Design

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APA (6th Edition):

Gordon, J. B. (2013). A study of the loss of acidic drug plasma protein binding sites in mouse serum albumin and loss prevention with a serine protease inhibitor adduct. (Masters Thesis). Northeastern University. Retrieved from http://hdl.handle.net/2047/d20003094

Chicago Manual of Style (16th Edition):

Gordon, Justin Brad. “A study of the loss of acidic drug plasma protein binding sites in mouse serum albumin and loss prevention with a serine protease inhibitor adduct.” 2013. Masters Thesis, Northeastern University. Accessed February 18, 2020. http://hdl.handle.net/2047/d20003094.

MLA Handbook (7th Edition):

Gordon, Justin Brad. “A study of the loss of acidic drug plasma protein binding sites in mouse serum albumin and loss prevention with a serine protease inhibitor adduct.” 2013. Web. 18 Feb 2020.

Vancouver:

Gordon JB. A study of the loss of acidic drug plasma protein binding sites in mouse serum albumin and loss prevention with a serine protease inhibitor adduct. [Internet] [Masters thesis]. Northeastern University; 2013. [cited 2020 Feb 18]. Available from: http://hdl.handle.net/2047/d20003094.

Council of Science Editors:

Gordon JB. A study of the loss of acidic drug plasma protein binding sites in mouse serum albumin and loss prevention with a serine protease inhibitor adduct. [Masters Thesis]. Northeastern University; 2013. Available from: http://hdl.handle.net/2047/d20003094


University of Kentucky

19. Zheng, Xirong. Pharmacokinetic and Pharmacodynamic Evaluation of Cocaine Hydrolases for the Treatment of Cocaine Overdose and Cocaine Addiction Using Rodent Models.

Degree: 2019, University of Kentucky

 Overdose and addiction are two medical complications of cocaine abuse. To date, there is no FDA approved pharmacotherapy specific for cocaine abuse. Cocaine hydrolases (CocHs)… (more)

Subjects/Keywords: cocaine overdose; cocaine addiction; cocaine hydrolase; mathematical model; Pharmaceutics and Drug Design

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

APA (6th Edition):

Zheng, X. (2019). Pharmacokinetic and Pharmacodynamic Evaluation of Cocaine Hydrolases for the Treatment of Cocaine Overdose and Cocaine Addiction Using Rodent Models. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/pharmacy_etds/102

Chicago Manual of Style (16th Edition):

Zheng, Xirong. “Pharmacokinetic and Pharmacodynamic Evaluation of Cocaine Hydrolases for the Treatment of Cocaine Overdose and Cocaine Addiction Using Rodent Models.” 2019. Doctoral Dissertation, University of Kentucky. Accessed February 18, 2020. https://uknowledge.uky.edu/pharmacy_etds/102.

MLA Handbook (7th Edition):

Zheng, Xirong. “Pharmacokinetic and Pharmacodynamic Evaluation of Cocaine Hydrolases for the Treatment of Cocaine Overdose and Cocaine Addiction Using Rodent Models.” 2019. Web. 18 Feb 2020.

Vancouver:

Zheng X. Pharmacokinetic and Pharmacodynamic Evaluation of Cocaine Hydrolases for the Treatment of Cocaine Overdose and Cocaine Addiction Using Rodent Models. [Internet] [Doctoral dissertation]. University of Kentucky; 2019. [cited 2020 Feb 18]. Available from: https://uknowledge.uky.edu/pharmacy_etds/102.

Council of Science Editors:

Zheng X. Pharmacokinetic and Pharmacodynamic Evaluation of Cocaine Hydrolases for the Treatment of Cocaine Overdose and Cocaine Addiction Using Rodent Models. [Doctoral Dissertation]. University of Kentucky; 2019. Available from: https://uknowledge.uky.edu/pharmacy_etds/102


New Jersey Institute of Technology

20. Sun, Chuan. Effect of tablet compression on the dissolution of aspirin tablets using a novel off-center paddle impeller (opi) dissolution testing system.

Degree: MSin Pharmaceutical Engineering - (M.S.), Chemical, Biological and Pharmaceutical Engineering, 2013, New Jersey Institute of Technology

  In the pharmaceutical industry, dissolution testing is routinely carried out to determine the dissolution rate of oral solid dosage forms. Among several testing devices,… (more)

Subjects/Keywords: Dissolution testing; Dissolution rate; Off-center paddle impeller; Chemical Engineering; Pharmaceutics and Drug Design

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APA (6th Edition):

Sun, C. (2013). Effect of tablet compression on the dissolution of aspirin tablets using a novel off-center paddle impeller (opi) dissolution testing system. (Thesis). New Jersey Institute of Technology. Retrieved from https://digitalcommons.njit.edu/theses/160

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):

Sun, Chuan. “Effect of tablet compression on the dissolution of aspirin tablets using a novel off-center paddle impeller (opi) dissolution testing system.” 2013. Thesis, New Jersey Institute of Technology. Accessed February 18, 2020. https://digitalcommons.njit.edu/theses/160.

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

MLA Handbook (7th Edition):

Sun, Chuan. “Effect of tablet compression on the dissolution of aspirin tablets using a novel off-center paddle impeller (opi) dissolution testing system.” 2013. Web. 18 Feb 2020.

Vancouver:

Sun C. Effect of tablet compression on the dissolution of aspirin tablets using a novel off-center paddle impeller (opi) dissolution testing system. [Internet] [Thesis]. New Jersey Institute of Technology; 2013. [cited 2020 Feb 18]. Available from: https://digitalcommons.njit.edu/theses/160.

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

Council of Science Editors:

Sun C. Effect of tablet compression on the dissolution of aspirin tablets using a novel off-center paddle impeller (opi) dissolution testing system. [Thesis]. New Jersey Institute of Technology; 2013. Available from: https://digitalcommons.njit.edu/theses/160

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


New Jersey Institute of Technology

21. Qiu, Hui. QSAR modeling of chemical penetration enhancers using novel replacement algorithms.

Degree: MSin Pharmaceutical Bioprocessing - (M.S.), Chemical, Biological and Pharmaceutical Engineering, 2013, New Jersey Institute of Technology

  The applications of transdermal delivery are limited because of the resistance of the skin to drug diffusion. Only potent drugs, with molecular weight less… (more)

Subjects/Keywords: Transdermal delivery; Chemical penetration enhancers; Chemical penetration enhancer structures; Chemical Engineering; Pharmaceutics and Drug Design

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APA (6th Edition):

Qiu, H. (2013). QSAR modeling of chemical penetration enhancers using novel replacement algorithms. (Thesis). New Jersey Institute of Technology. Retrieved from https://digitalcommons.njit.edu/theses/162

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):

Qiu, Hui. “QSAR modeling of chemical penetration enhancers using novel replacement algorithms.” 2013. Thesis, New Jersey Institute of Technology. Accessed February 18, 2020. https://digitalcommons.njit.edu/theses/162.

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

MLA Handbook (7th Edition):

Qiu, Hui. “QSAR modeling of chemical penetration enhancers using novel replacement algorithms.” 2013. Web. 18 Feb 2020.

Vancouver:

Qiu H. QSAR modeling of chemical penetration enhancers using novel replacement algorithms. [Internet] [Thesis]. New Jersey Institute of Technology; 2013. [cited 2020 Feb 18]. Available from: https://digitalcommons.njit.edu/theses/162.

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

Council of Science Editors:

Qiu H. QSAR modeling of chemical penetration enhancers using novel replacement algorithms. [Thesis]. New Jersey Institute of Technology; 2013. Available from: https://digitalcommons.njit.edu/theses/162

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


New Jersey Institute of Technology

22. Kim, Alyssa Misoo. Engineering spores to display g protein-coupled receptors for directed evolution.

Degree: MSin Pharmaceutical Engineering - (M.S.), Chemical, Biological and Pharmaceutical Engineering, 2013, New Jersey Institute of Technology

  All human cells are surrounded by a plasma membrane made from a phospholipid bilayer, which is responsible for maintaining a biologically active species, while… (more)

Subjects/Keywords: Protein engineering; G protein-coupled receptors; Chemical Engineering; Pharmaceutics and Drug Design

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APA (6th Edition):

Kim, A. M. (2013). Engineering spores to display g protein-coupled receptors for directed evolution. (Thesis). New Jersey Institute of Technology. Retrieved from https://digitalcommons.njit.edu/theses/174

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, Alyssa Misoo. “Engineering spores to display g protein-coupled receptors for directed evolution.” 2013. Thesis, New Jersey Institute of Technology. Accessed February 18, 2020. https://digitalcommons.njit.edu/theses/174.

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

MLA Handbook (7th Edition):

Kim, Alyssa Misoo. “Engineering spores to display g protein-coupled receptors for directed evolution.” 2013. Web. 18 Feb 2020.

Vancouver:

Kim AM. Engineering spores to display g protein-coupled receptors for directed evolution. [Internet] [Thesis]. New Jersey Institute of Technology; 2013. [cited 2020 Feb 18]. Available from: https://digitalcommons.njit.edu/theses/174.

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

Council of Science Editors:

Kim AM. Engineering spores to display g protein-coupled receptors for directed evolution. [Thesis]. New Jersey Institute of Technology; 2013. Available from: https://digitalcommons.njit.edu/theses/174

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


New Jersey Institute of Technology

23. Song, Yufeng. Effect of impeller submergence on power dissipation and solids suspension in mixing systems equipped with pitch-blade turbines.

Degree: MSin Pharmaceutical Engineering - (M.S.), Chemical, Biological and Pharmaceutical Engineering, 2015, New Jersey Institute of Technology

  Mixing and dispersion of solids in a liquid is a process frequently encountered in the pharmaceutical industry and often conducted in cylindrical baffled tanks… (more)

Subjects/Keywords: Impeller submergence; Power dissipation; Solids suspension; Mixing systems; Chemical Engineering; Pharmaceutics and Drug Design

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APA (6th Edition):

Song, Y. (2015). Effect of impeller submergence on power dissipation and solids suspension in mixing systems equipped with pitch-blade turbines. (Thesis). New Jersey Institute of Technology. Retrieved from https://digitalcommons.njit.edu/theses/246

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):

Song, Yufeng. “Effect of impeller submergence on power dissipation and solids suspension in mixing systems equipped with pitch-blade turbines.” 2015. Thesis, New Jersey Institute of Technology. Accessed February 18, 2020. https://digitalcommons.njit.edu/theses/246.

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

MLA Handbook (7th Edition):

Song, Yufeng. “Effect of impeller submergence on power dissipation and solids suspension in mixing systems equipped with pitch-blade turbines.” 2015. Web. 18 Feb 2020.

Vancouver:

Song Y. Effect of impeller submergence on power dissipation and solids suspension in mixing systems equipped with pitch-blade turbines. [Internet] [Thesis]. New Jersey Institute of Technology; 2015. [cited 2020 Feb 18]. Available from: https://digitalcommons.njit.edu/theses/246.

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

Council of Science Editors:

Song Y. Effect of impeller submergence on power dissipation and solids suspension in mixing systems equipped with pitch-blade turbines. [Thesis]. New Jersey Institute of Technology; 2015. Available from: https://digitalcommons.njit.edu/theses/246

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


New Jersey Institute of Technology

24. Tang, Yingxi. Experimental determination of solids suspension with angled impeller in a pharmaceutical mixing vessel.

Degree: MSin Pharmaceutical Engineering - (M.S.), Chemical, Biological and Pharmaceutical Engineering, 2015, New Jersey Institute of Technology

  Angled-mounted impellers are commonly used in a number of pharmaceutical industry applications, from laboratory reactors to full-scale tanks. In these systems, the impeller is… (more)

Subjects/Keywords: Angled-mounted impellers; Minimum agitation speed; Solids suspension; Chemical Engineering; Pharmaceutics and Drug Design

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APA (6th Edition):

Tang, Y. (2015). Experimental determination of solids suspension with angled impeller in a pharmaceutical mixing vessel. (Thesis). New Jersey Institute of Technology. Retrieved from https://digitalcommons.njit.edu/theses/247

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):

Tang, Yingxi. “Experimental determination of solids suspension with angled impeller in a pharmaceutical mixing vessel.” 2015. Thesis, New Jersey Institute of Technology. Accessed February 18, 2020. https://digitalcommons.njit.edu/theses/247.

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

MLA Handbook (7th Edition):

Tang, Yingxi. “Experimental determination of solids suspension with angled impeller in a pharmaceutical mixing vessel.” 2015. Web. 18 Feb 2020.

Vancouver:

Tang Y. Experimental determination of solids suspension with angled impeller in a pharmaceutical mixing vessel. [Internet] [Thesis]. New Jersey Institute of Technology; 2015. [cited 2020 Feb 18]. Available from: https://digitalcommons.njit.edu/theses/247.

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

Council of Science Editors:

Tang Y. Experimental determination of solids suspension with angled impeller in a pharmaceutical mixing vessel. [Thesis]. New Jersey Institute of Technology; 2015. Available from: https://digitalcommons.njit.edu/theses/247

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


New Jersey Institute of Technology

25. Ma, Ji. Computational and experimental determination of the hydrodynamics in a stirred unbaffled vessel provided with angle-mounted axial impellers.

Degree: MSin Pharmaceutical Engineering - (M.S.), Chemical, Biological and Pharmaceutical Engineering, 2015, New Jersey Institute of Technology

  In most industrial applications, stirred tanks and reactors are typically provided with baffles to improve their mixing characteristics. However, in a number of pharmaceutical… (more)

Subjects/Keywords: Hydrodynamics; Unbaffled vessel; Angle-mounted impellers; Chemical Engineering; Pharmaceutics and Drug Design

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APA (6th Edition):

Ma, J. (2015). Computational and experimental determination of the hydrodynamics in a stirred unbaffled vessel provided with angle-mounted axial impellers. (Thesis). New Jersey Institute of Technology. Retrieved from https://digitalcommons.njit.edu/theses/258

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, Ji. “Computational and experimental determination of the hydrodynamics in a stirred unbaffled vessel provided with angle-mounted axial impellers.” 2015. Thesis, New Jersey Institute of Technology. Accessed February 18, 2020. https://digitalcommons.njit.edu/theses/258.

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

MLA Handbook (7th Edition):

Ma, Ji. “Computational and experimental determination of the hydrodynamics in a stirred unbaffled vessel provided with angle-mounted axial impellers.” 2015. Web. 18 Feb 2020.

Vancouver:

Ma J. Computational and experimental determination of the hydrodynamics in a stirred unbaffled vessel provided with angle-mounted axial impellers. [Internet] [Thesis]. New Jersey Institute of Technology; 2015. [cited 2020 Feb 18]. Available from: https://digitalcommons.njit.edu/theses/258.

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

Council of Science Editors:

Ma J. Computational and experimental determination of the hydrodynamics in a stirred unbaffled vessel provided with angle-mounted axial impellers. [Thesis]. New Jersey Institute of Technology; 2015. Available from: https://digitalcommons.njit.edu/theses/258

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


Northeastern University

26. Doshi, Aatman Satish. In vitro evaluations of bisphosphonate therapy in refractory cancer by targeting tumor-associated macrophages.

Degree: MS, School of Pharmacy, 2013, Northeastern University

 The main aim of this MS thesis project was to develop a targeted drug delivery system which is capable of targeting tumor-associated macrophages (TAMs). Alendronate… (more)

Subjects/Keywords: Anti-cancer; Formulations; In vitro assays; Liposomes; Pharmaceutics and Drug Design; Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Doshi, A. S. (2013). In vitro evaluations of bisphosphonate therapy in refractory cancer by targeting tumor-associated macrophages. (Masters Thesis). Northeastern University. Retrieved from http://hdl.handle.net/2047/d20004932

Chicago Manual of Style (16th Edition):

Doshi, Aatman Satish. “In vitro evaluations of bisphosphonate therapy in refractory cancer by targeting tumor-associated macrophages.” 2013. Masters Thesis, Northeastern University. Accessed February 18, 2020. http://hdl.handle.net/2047/d20004932.

MLA Handbook (7th Edition):

Doshi, Aatman Satish. “In vitro evaluations of bisphosphonate therapy in refractory cancer by targeting tumor-associated macrophages.” 2013. Web. 18 Feb 2020.

Vancouver:

Doshi AS. In vitro evaluations of bisphosphonate therapy in refractory cancer by targeting tumor-associated macrophages. [Internet] [Masters thesis]. Northeastern University; 2013. [cited 2020 Feb 18]. Available from: http://hdl.handle.net/2047/d20004932.

Council of Science Editors:

Doshi AS. In vitro evaluations of bisphosphonate therapy in refractory cancer by targeting tumor-associated macrophages. [Masters Thesis]. Northeastern University; 2013. Available from: http://hdl.handle.net/2047/d20004932


University of Kentucky

27. Mishra, Murli. EXPLORATION OF THE SRX-PRX AXIS AS A SMALL-MOLECULE TARGET.

Degree: 2016, University of Kentucky

 Lung cancer is a leading cause of cancer-related mortality irrespective of gender. The Sulfiredoxin (Srx) and Peroxiredoxin (Prx) are a group of thiol-based antioxidant proteins… (more)

Subjects/Keywords: Sulfiredoxin; Peroxiredoxin; Drug-discovery; Lung cancer; Carcinogenesis; Metastasis inhibitor; Bioinformatics; Medicinal and Pharmaceutical Chemistry; Medicinal Chemistry and Pharmaceutics; Pharmaceutics and Drug Design; Pharmacology; Toxicology

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APA (6th Edition):

Mishra, M. (2016). EXPLORATION OF THE SRX-PRX AXIS AS A SMALL-MOLECULE TARGET. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/toxicology_etds/14

Chicago Manual of Style (16th Edition):

Mishra, Murli. “EXPLORATION OF THE SRX-PRX AXIS AS A SMALL-MOLECULE TARGET.” 2016. Doctoral Dissertation, University of Kentucky. Accessed February 18, 2020. https://uknowledge.uky.edu/toxicology_etds/14.

MLA Handbook (7th Edition):

Mishra, Murli. “EXPLORATION OF THE SRX-PRX AXIS AS A SMALL-MOLECULE TARGET.” 2016. Web. 18 Feb 2020.

Vancouver:

Mishra M. EXPLORATION OF THE SRX-PRX AXIS AS A SMALL-MOLECULE TARGET. [Internet] [Doctoral dissertation]. University of Kentucky; 2016. [cited 2020 Feb 18]. Available from: https://uknowledge.uky.edu/toxicology_etds/14.

Council of Science Editors:

Mishra M. EXPLORATION OF THE SRX-PRX AXIS AS A SMALL-MOLECULE TARGET. [Doctoral Dissertation]. University of Kentucky; 2016. Available from: https://uknowledge.uky.edu/toxicology_etds/14


University of Western Ontario

28. Bulmer, Cody. Encapsulation and Controlled Release of rHu-Erythropoietin from Chitosan Biopolymer Nanoparticles.

Degree: 2012, University of Western Ontario

 The objective of this research project was to develop a drug delivery system for recombinant human erythropoietin (rHu-EPO), a glycoprotein hormone used in the treatment… (more)

Subjects/Keywords: Chitosan; Drug delivery; Erythropoietin; Ionotropic gelation; Nanoparticles; Response surface modeling; Biomaterials; Nanoscience and Nanotechnology; Pharmaceutics and Drug Design

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

APA (6th Edition):

Bulmer, C. (2012). Encapsulation and Controlled Release of rHu-Erythropoietin from Chitosan Biopolymer Nanoparticles. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/553

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):

Bulmer, Cody. “Encapsulation and Controlled Release of rHu-Erythropoietin from Chitosan Biopolymer Nanoparticles.” 2012. Thesis, University of Western Ontario. Accessed February 18, 2020. https://ir.lib.uwo.ca/etd/553.

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

MLA Handbook (7th Edition):

Bulmer, Cody. “Encapsulation and Controlled Release of rHu-Erythropoietin from Chitosan Biopolymer Nanoparticles.” 2012. Web. 18 Feb 2020.

Vancouver:

Bulmer C. Encapsulation and Controlled Release of rHu-Erythropoietin from Chitosan Biopolymer Nanoparticles. [Internet] [Thesis]. University of Western Ontario; 2012. [cited 2020 Feb 18]. Available from: https://ir.lib.uwo.ca/etd/553.

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

Council of Science Editors:

Bulmer C. Encapsulation and Controlled Release of rHu-Erythropoietin from Chitosan Biopolymer Nanoparticles. [Thesis]. University of Western Ontario; 2012. Available from: https://ir.lib.uwo.ca/etd/553

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


East Tennessee State University

29. Cooper, Dustin. An Investigation into Formulation and Therapeutic Effectiveness of Nanoparticle Drug Delivery for Select Pharmaceutical Agents.

Degree: PhD, Biomedical Sciences, 2016, East Tennessee State University

Drug based nanoparticle (NP) formulations have gained considerable attention over the past decade for their use in various drug delivery systems. NPs have been… (more)

Subjects/Keywords: Nanoparticle; Formulation; Drug Delivery; Polymer; DMAB; PVA; Celecoxib; Diclofenac; PLGA; Zeta Potential; Nanomedicine; Pharmaceutics and Drug Design

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

APA (6th Edition):

Cooper, D. (2016). An Investigation into Formulation and Therapeutic Effectiveness of Nanoparticle Drug Delivery for Select Pharmaceutical Agents. (Doctoral Dissertation). East Tennessee State University. Retrieved from https://dc.etsu.edu/etd/3024

Chicago Manual of Style (16th Edition):

Cooper, Dustin. “An Investigation into Formulation and Therapeutic Effectiveness of Nanoparticle Drug Delivery for Select Pharmaceutical Agents.” 2016. Doctoral Dissertation, East Tennessee State University. Accessed February 18, 2020. https://dc.etsu.edu/etd/3024.

MLA Handbook (7th Edition):

Cooper, Dustin. “An Investigation into Formulation and Therapeutic Effectiveness of Nanoparticle Drug Delivery for Select Pharmaceutical Agents.” 2016. Web. 18 Feb 2020.

Vancouver:

Cooper D. An Investigation into Formulation and Therapeutic Effectiveness of Nanoparticle Drug Delivery for Select Pharmaceutical Agents. [Internet] [Doctoral dissertation]. East Tennessee State University; 2016. [cited 2020 Feb 18]. Available from: https://dc.etsu.edu/etd/3024.

Council of Science Editors:

Cooper D. An Investigation into Formulation and Therapeutic Effectiveness of Nanoparticle Drug Delivery for Select Pharmaceutical Agents. [Doctoral Dissertation]. East Tennessee State University; 2016. Available from: https://dc.etsu.edu/etd/3024


University of Kentucky

30. Sarpal, Kanika. PHASE BEHAVIOR OF AMORPHOUS SOLID DISPERSIONS: MISCIBILITY AND MOLECULAR INTERACTIONS.

Degree: 2019, University of Kentucky

 Over the past few decades, amorphous solid dispersions (ASDs) have been of great interest to pharmaceutical scientists to address bioavailability issues associated with poorly water-soluble… (more)

Subjects/Keywords: Amorphous solid dispersions; Solid-state nuclear magnetic resonance spectroscopy; Drug-polymer miscibility; Hydrogen bonding; Physical stability; Pharmaceutics and Drug Design

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

APA (6th Edition):

Sarpal, K. (2019). PHASE BEHAVIOR OF AMORPHOUS SOLID DISPERSIONS: MISCIBILITY AND MOLECULAR INTERACTIONS. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/pharmacy_etds/98

Chicago Manual of Style (16th Edition):

Sarpal, Kanika. “PHASE BEHAVIOR OF AMORPHOUS SOLID DISPERSIONS: MISCIBILITY AND MOLECULAR INTERACTIONS.” 2019. Doctoral Dissertation, University of Kentucky. Accessed February 18, 2020. https://uknowledge.uky.edu/pharmacy_etds/98.

MLA Handbook (7th Edition):

Sarpal, Kanika. “PHASE BEHAVIOR OF AMORPHOUS SOLID DISPERSIONS: MISCIBILITY AND MOLECULAR INTERACTIONS.” 2019. Web. 18 Feb 2020.

Vancouver:

Sarpal K. PHASE BEHAVIOR OF AMORPHOUS SOLID DISPERSIONS: MISCIBILITY AND MOLECULAR INTERACTIONS. [Internet] [Doctoral dissertation]. University of Kentucky; 2019. [cited 2020 Feb 18]. Available from: https://uknowledge.uky.edu/pharmacy_etds/98.

Council of Science Editors:

Sarpal K. PHASE BEHAVIOR OF AMORPHOUS SOLID DISPERSIONS: MISCIBILITY AND MOLECULAR INTERACTIONS. [Doctoral Dissertation]. University of Kentucky; 2019. Available from: https://uknowledge.uky.edu/pharmacy_etds/98

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