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You searched for subject:(Drug targeting ). Showing records 1 – 30 of 218 total matches.

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University of Georgia

1. Shawer, Mohannad Mahmoud. Lipoprotein-resembling submicron emulsion for drug and gene delivery.

Degree: PhD, Pharmacy (Pharmaceutics), 2002, University of Georgia

 Several anticancer compounds that have shown excellent efficacy are known to have high incidence of toxicity. The main reason of such toxicity can be due… (more)

Subjects/Keywords: Drug targeting

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APA (6th Edition):

Shawer, M. M. (2002). Lipoprotein-resembling submicron emulsion for drug and gene delivery. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/shawer_mohannad_m_200205_phd

Chicago Manual of Style (16th Edition):

Shawer, Mohannad Mahmoud. “Lipoprotein-resembling submicron emulsion for drug and gene delivery.” 2002. Doctoral Dissertation, University of Georgia. Accessed August 15, 2020. http://purl.galileo.usg.edu/uga_etd/shawer_mohannad_m_200205_phd.

MLA Handbook (7th Edition):

Shawer, Mohannad Mahmoud. “Lipoprotein-resembling submicron emulsion for drug and gene delivery.” 2002. Web. 15 Aug 2020.

Vancouver:

Shawer MM. Lipoprotein-resembling submicron emulsion for drug and gene delivery. [Internet] [Doctoral dissertation]. University of Georgia; 2002. [cited 2020 Aug 15]. Available from: http://purl.galileo.usg.edu/uga_etd/shawer_mohannad_m_200205_phd.

Council of Science Editors:

Shawer MM. Lipoprotein-resembling submicron emulsion for drug and gene delivery. [Doctoral Dissertation]. University of Georgia; 2002. Available from: http://purl.galileo.usg.edu/uga_etd/shawer_mohannad_m_200205_phd


University of Alberta

2. Soudy, Rania Nayel. Engineering peptides for anticancer drug targeting and antimicrobial activity.

Degree: PhD, Faculty of Pharmacy and Pharmaceutical Sciences, 2012, University of Alberta

 Peptides hold great promise for clinical applications such as cancer and antimicrobial therapies. In cancer, conjugation of cancer treatments to tumor specific peptides improves their… (more)

Subjects/Keywords: anticancer; antimicrobial peptides; drug targeting

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APA (6th Edition):

Soudy, R. N. (2012). Engineering peptides for anticancer drug targeting and antimicrobial activity. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/pc289k40s

Chicago Manual of Style (16th Edition):

Soudy, Rania Nayel. “Engineering peptides for anticancer drug targeting and antimicrobial activity.” 2012. Doctoral Dissertation, University of Alberta. Accessed August 15, 2020. https://era.library.ualberta.ca/files/pc289k40s.

MLA Handbook (7th Edition):

Soudy, Rania Nayel. “Engineering peptides for anticancer drug targeting and antimicrobial activity.” 2012. Web. 15 Aug 2020.

Vancouver:

Soudy RN. Engineering peptides for anticancer drug targeting and antimicrobial activity. [Internet] [Doctoral dissertation]. University of Alberta; 2012. [cited 2020 Aug 15]. Available from: https://era.library.ualberta.ca/files/pc289k40s.

Council of Science Editors:

Soudy RN. Engineering peptides for anticancer drug targeting and antimicrobial activity. [Doctoral Dissertation]. University of Alberta; 2012. Available from: https://era.library.ualberta.ca/files/pc289k40s


University of Toronto

3. Lei, Eric Kun. Expanding the Applications of Mitochondrial Targeted Delivery Peptides.

Degree: PhD, 2018, University of Toronto

 Mitochondria play a critical role in the generation of cellular energy, the organization of metabolic pathways, and regulation of programmed cell death. The study of… (more)

Subjects/Keywords: Drug Targeting; Mitochondria; Peptide; 0487

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APA (6th Edition):

Lei, E. K. (2018). Expanding the Applications of Mitochondrial Targeted Delivery Peptides. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/89815

Chicago Manual of Style (16th Edition):

Lei, Eric Kun. “Expanding the Applications of Mitochondrial Targeted Delivery Peptides.” 2018. Doctoral Dissertation, University of Toronto. Accessed August 15, 2020. http://hdl.handle.net/1807/89815.

MLA Handbook (7th Edition):

Lei, Eric Kun. “Expanding the Applications of Mitochondrial Targeted Delivery Peptides.” 2018. Web. 15 Aug 2020.

Vancouver:

Lei EK. Expanding the Applications of Mitochondrial Targeted Delivery Peptides. [Internet] [Doctoral dissertation]. University of Toronto; 2018. [cited 2020 Aug 15]. Available from: http://hdl.handle.net/1807/89815.

Council of Science Editors:

Lei EK. Expanding the Applications of Mitochondrial Targeted Delivery Peptides. [Doctoral Dissertation]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/89815


University of Illinois – Chicago

4. Venugopal, Indu. Intrathecal Magnetic Drug Targeting for Treatment of Central Nervous System Diseases.

Degree: 2016, University of Illinois – Chicago

 Delivering drugs to the Central Nervous System is a formidable task due to barriers such as the blood brain barrier and blood-cerebrospinal fluid barrier, which… (more)

Subjects/Keywords: Intrathecal drug delivery; magnetic drug targeting

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APA (6th Edition):

Venugopal, I. (2016). Intrathecal Magnetic Drug Targeting for Treatment of Central Nervous System Diseases. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/21757

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):

Venugopal, Indu. “Intrathecal Magnetic Drug Targeting for Treatment of Central Nervous System Diseases.” 2016. Thesis, University of Illinois – Chicago. Accessed August 15, 2020. http://hdl.handle.net/10027/21757.

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

MLA Handbook (7th Edition):

Venugopal, Indu. “Intrathecal Magnetic Drug Targeting for Treatment of Central Nervous System Diseases.” 2016. Web. 15 Aug 2020.

Vancouver:

Venugopal I. Intrathecal Magnetic Drug Targeting for Treatment of Central Nervous System Diseases. [Internet] [Thesis]. University of Illinois – Chicago; 2016. [cited 2020 Aug 15]. Available from: http://hdl.handle.net/10027/21757.

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

Council of Science Editors:

Venugopal I. Intrathecal Magnetic Drug Targeting for Treatment of Central Nervous System Diseases. [Thesis]. University of Illinois – Chicago; 2016. Available from: http://hdl.handle.net/10027/21757

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


Temple University

5. Shabana, Ahmed Marawan. Development and biological evaluation of drug delivery nanosystems targeting hypoxic tumors.

Degree: PhD, 2018, Temple University

Pharmaceutical Sciences

Hypoxia is a characteristic pathophysiological feature of many solid tumors, which contributes significantly to resistance to chemotherapy and radiotherapy. It also induces numerous… (more)

Subjects/Keywords: Pharmaceutical sciences;

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APA (6th Edition):

Shabana, A. M. (2018). Development and biological evaluation of drug delivery nanosystems targeting hypoxic tumors. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,506376

Chicago Manual of Style (16th Edition):

Shabana, Ahmed Marawan. “Development and biological evaluation of drug delivery nanosystems targeting hypoxic tumors.” 2018. Doctoral Dissertation, Temple University. Accessed August 15, 2020. http://digital.library.temple.edu/u?/p245801coll10,506376.

MLA Handbook (7th Edition):

Shabana, Ahmed Marawan. “Development and biological evaluation of drug delivery nanosystems targeting hypoxic tumors.” 2018. Web. 15 Aug 2020.

Vancouver:

Shabana AM. Development and biological evaluation of drug delivery nanosystems targeting hypoxic tumors. [Internet] [Doctoral dissertation]. Temple University; 2018. [cited 2020 Aug 15]. Available from: http://digital.library.temple.edu/u?/p245801coll10,506376.

Council of Science Editors:

Shabana AM. Development and biological evaluation of drug delivery nanosystems targeting hypoxic tumors. [Doctoral Dissertation]. Temple University; 2018. Available from: http://digital.library.temple.edu/u?/p245801coll10,506376


Drexel University

6. Yang, Heng. Protein surface analysis by dimension reduction with applications in functional annotation and drug target prediction.

Degree: 2015, Drexel University

The protein structure initiatives have increased the number of experimentally determined protein tertiary structures, providing tremendous opportunities for detailed comparative analysis of proteins. Although protein… (more)

Subjects/Keywords: Biomedical engineering; Proteins – Structure; Drug targeting

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APA (6th Edition):

Yang, H. (2015). Protein surface analysis by dimension reduction with applications in functional annotation and drug target prediction. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:6404

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, Heng. “Protein surface analysis by dimension reduction with applications in functional annotation and drug target prediction.” 2015. Thesis, Drexel University. Accessed August 15, 2020. http://hdl.handle.net/1860/idea:6404.

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

MLA Handbook (7th Edition):

Yang, Heng. “Protein surface analysis by dimension reduction with applications in functional annotation and drug target prediction.” 2015. Web. 15 Aug 2020.

Vancouver:

Yang H. Protein surface analysis by dimension reduction with applications in functional annotation and drug target prediction. [Internet] [Thesis]. Drexel University; 2015. [cited 2020 Aug 15]. Available from: http://hdl.handle.net/1860/idea:6404.

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

Council of Science Editors:

Yang H. Protein surface analysis by dimension reduction with applications in functional annotation and drug target prediction. [Thesis]. Drexel University; 2015. Available from: http://hdl.handle.net/1860/idea:6404

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


Hong Kong University of Science and Technology

7. Zhong, Yiyang. Elaboration and characterization of the iron oxide magnetic electrospun diverse nanofibers and nanoparticles.

Degree: 2014, Hong Kong University of Science and Technology

 Magnetically controlled drug targeting is a very effective way of local or regional antitumor treatment. In traditional way, magnetic material is used as targeting part… (more)

Subjects/Keywords: Nanostructured materials ; Electrospinning ; Drug delivery systems ; Technological innovations ; Drug targeting

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APA (6th Edition):

Zhong, Y. (2014). Elaboration and characterization of the iron oxide magnetic electrospun diverse nanofibers and nanoparticles. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-70865 ; https://doi.org/10.14711/thesis-b1333636 ; http://repository.ust.hk/ir/bitstream/1783.1-70865/1/th_redirect.html

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):

Zhong, Yiyang. “Elaboration and characterization of the iron oxide magnetic electrospun diverse nanofibers and nanoparticles.” 2014. Thesis, Hong Kong University of Science and Technology. Accessed August 15, 2020. http://repository.ust.hk/ir/Record/1783.1-70865 ; https://doi.org/10.14711/thesis-b1333636 ; http://repository.ust.hk/ir/bitstream/1783.1-70865/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Zhong, Yiyang. “Elaboration and characterization of the iron oxide magnetic electrospun diverse nanofibers and nanoparticles.” 2014. Web. 15 Aug 2020.

Vancouver:

Zhong Y. Elaboration and characterization of the iron oxide magnetic electrospun diverse nanofibers and nanoparticles. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2014. [cited 2020 Aug 15]. Available from: http://repository.ust.hk/ir/Record/1783.1-70865 ; https://doi.org/10.14711/thesis-b1333636 ; http://repository.ust.hk/ir/bitstream/1783.1-70865/1/th_redirect.html.

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

Council of Science Editors:

Zhong Y. Elaboration and characterization of the iron oxide magnetic electrospun diverse nanofibers and nanoparticles. [Thesis]. Hong Kong University of Science and Technology; 2014. Available from: http://repository.ust.hk/ir/Record/1783.1-70865 ; https://doi.org/10.14711/thesis-b1333636 ; http://repository.ust.hk/ir/bitstream/1783.1-70865/1/th_redirect.html

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

8. Skarbek, Charles. Synthèse et évaluation pharmacologique d’analogues préactivés de l’ifosfamide : prodrogues et nanoparticules à visée antitumorale : Synthesis and pharmacological evaluation of preactivated ifosfamide analogs : prodrugs and nanoparticles designed against cancer.

Degree: Docteur es, Pharmacotechnie et biopharmacie, 2017, Université Paris-Saclay (ComUE)

L’ifosfamide (IFO) et le cyclophosphamide (CPM) sont des oxazaphosphorines, prodrogues nécessitant une bioactivation pour être actif. Dans le cas de l’IFO, sa biotransformation conduit à… (more)

Subjects/Keywords: Nanoparticules; Drug design; Ciblage; Nanoparticle; Drug design; Targeting

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APA (6th Edition):

Skarbek, C. (2017). Synthèse et évaluation pharmacologique d’analogues préactivés de l’ifosfamide : prodrogues et nanoparticules à visée antitumorale : Synthesis and pharmacological evaluation of preactivated ifosfamide analogs : prodrugs and nanoparticles designed against cancer. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2017SACLS247

Chicago Manual of Style (16th Edition):

Skarbek, Charles. “Synthèse et évaluation pharmacologique d’analogues préactivés de l’ifosfamide : prodrogues et nanoparticules à visée antitumorale : Synthesis and pharmacological evaluation of preactivated ifosfamide analogs : prodrugs and nanoparticles designed against cancer.” 2017. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed August 15, 2020. http://www.theses.fr/2017SACLS247.

MLA Handbook (7th Edition):

Skarbek, Charles. “Synthèse et évaluation pharmacologique d’analogues préactivés de l’ifosfamide : prodrogues et nanoparticules à visée antitumorale : Synthesis and pharmacological evaluation of preactivated ifosfamide analogs : prodrugs and nanoparticles designed against cancer.” 2017. Web. 15 Aug 2020.

Vancouver:

Skarbek C. Synthèse et évaluation pharmacologique d’analogues préactivés de l’ifosfamide : prodrogues et nanoparticules à visée antitumorale : Synthesis and pharmacological evaluation of preactivated ifosfamide analogs : prodrugs and nanoparticles designed against cancer. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2017. [cited 2020 Aug 15]. Available from: http://www.theses.fr/2017SACLS247.

Council of Science Editors:

Skarbek C. Synthèse et évaluation pharmacologique d’analogues préactivés de l’ifosfamide : prodrogues et nanoparticules à visée antitumorale : Synthesis and pharmacological evaluation of preactivated ifosfamide analogs : prodrugs and nanoparticles designed against cancer. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2017. Available from: http://www.theses.fr/2017SACLS247


Northeastern University

9. Sriraman, Shravan Kumar. Combination liposome-based anti-cancer preparations.

Degree: PhD, School of Pharmacy, 2016, Northeastern University

 Cancer is a complex disease that is continuously evolving in order to overcome current treatment approaches. Due to the inefficiency of current treatments, there has… (more)

Subjects/Keywords: cancer; combination; nanoparticles; targeting; Liposomes; Therapeutic use; Drug carriers (Pharmacy); Drug targeting; Nanomedicine; Ovaries; Cancer; Animal models; Transferrin; Folic acid

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APA (6th Edition):

Sriraman, S. K. (2016). Combination liposome-based anti-cancer preparations. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/D20198346

Chicago Manual of Style (16th Edition):

Sriraman, Shravan Kumar. “Combination liposome-based anti-cancer preparations.” 2016. Doctoral Dissertation, Northeastern University. Accessed August 15, 2020. http://hdl.handle.net/2047/D20198346.

MLA Handbook (7th Edition):

Sriraman, Shravan Kumar. “Combination liposome-based anti-cancer preparations.” 2016. Web. 15 Aug 2020.

Vancouver:

Sriraman SK. Combination liposome-based anti-cancer preparations. [Internet] [Doctoral dissertation]. Northeastern University; 2016. [cited 2020 Aug 15]. Available from: http://hdl.handle.net/2047/D20198346.

Council of Science Editors:

Sriraman SK. Combination liposome-based anti-cancer preparations. [Doctoral Dissertation]. Northeastern University; 2016. Available from: http://hdl.handle.net/2047/D20198346


University of Utah

10. Jensen, Keith Dale. Internalization and fate of HPMA copolymers and antisense-HPMA copolymer conjugates in Hep G2 cells;.

Degree: PhD, Pharmaceutics & Pharmaceutical Chemistry;, 2002, University of Utah

 To better understand the fate of macromolecules in cells and begin to alter that fate, we studied a antisense oligonucleotide designed to inhibit the hepatitis… (more)

Subjects/Keywords: Drug Targeting; Polymeric Drug Delivery Systems

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APA (6th Edition):

Jensen, K. D. (2002). Internalization and fate of HPMA copolymers and antisense-HPMA copolymer conjugates in Hep G2 cells;. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/292/rec/709

Chicago Manual of Style (16th Edition):

Jensen, Keith Dale. “Internalization and fate of HPMA copolymers and antisense-HPMA copolymer conjugates in Hep G2 cells;.” 2002. Doctoral Dissertation, University of Utah. Accessed August 15, 2020. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/292/rec/709.

MLA Handbook (7th Edition):

Jensen, Keith Dale. “Internalization and fate of HPMA copolymers and antisense-HPMA copolymer conjugates in Hep G2 cells;.” 2002. Web. 15 Aug 2020.

Vancouver:

Jensen KD. Internalization and fate of HPMA copolymers and antisense-HPMA copolymer conjugates in Hep G2 cells;. [Internet] [Doctoral dissertation]. University of Utah; 2002. [cited 2020 Aug 15]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/292/rec/709.

Council of Science Editors:

Jensen KD. Internalization and fate of HPMA copolymers and antisense-HPMA copolymer conjugates in Hep G2 cells;. [Doctoral Dissertation]. University of Utah; 2002. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/292/rec/709


University of Akron

11. Shah, Kush. Receptor-Mediated Targeting to Enhance Therapeutic Efficacy of Chemotherapeutic Agents.

Degree: PhD, Integrated Bioscience, 2014, University of Akron

  Dr. Paul Ehlrich introduced the concept of targeted drug delivery in 1904. With the advancement in technology, and molecular biology techniques, several new targeting(more)

Subjects/Keywords: Biomedical Engineering; Biomedical Research; Drug Delivery; Drug Targeting; Hyaluronan; L-tyrosine Polyphosphate; Nanoparticles; Resveratrol; MOMIPP

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APA (6th Edition):

Shah, K. (2014). Receptor-Mediated Targeting to Enhance Therapeutic Efficacy of Chemotherapeutic Agents. (Doctoral Dissertation). University of Akron. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=akron1390926627

Chicago Manual of Style (16th Edition):

Shah, Kush. “Receptor-Mediated Targeting to Enhance Therapeutic Efficacy of Chemotherapeutic Agents.” 2014. Doctoral Dissertation, University of Akron. Accessed August 15, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=akron1390926627.

MLA Handbook (7th Edition):

Shah, Kush. “Receptor-Mediated Targeting to Enhance Therapeutic Efficacy of Chemotherapeutic Agents.” 2014. Web. 15 Aug 2020.

Vancouver:

Shah K. Receptor-Mediated Targeting to Enhance Therapeutic Efficacy of Chemotherapeutic Agents. [Internet] [Doctoral dissertation]. University of Akron; 2014. [cited 2020 Aug 15]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=akron1390926627.

Council of Science Editors:

Shah K. Receptor-Mediated Targeting to Enhance Therapeutic Efficacy of Chemotherapeutic Agents. [Doctoral Dissertation]. University of Akron; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=akron1390926627


University of Sydney

12. Glenister, Alexandra. Glucose conjugation to increase the uptake of metal complexes by cancer cells .

Degree: 2017, University of Sydney

 To improve the efficacy of anticancer chemotherapy it is necessary to develop targeted treatments, which can be achieved by exploiting differences between normal and cancerous… (more)

Subjects/Keywords: drug design; cancer targeting; prodrug; Warburg effect; cobalt (III) complexes

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APA (6th Edition):

Glenister, A. (2017). Glucose conjugation to increase the uptake of metal complexes by cancer cells . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/16849

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):

Glenister, Alexandra. “Glucose conjugation to increase the uptake of metal complexes by cancer cells .” 2017. Thesis, University of Sydney. Accessed August 15, 2020. http://hdl.handle.net/2123/16849.

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

MLA Handbook (7th Edition):

Glenister, Alexandra. “Glucose conjugation to increase the uptake of metal complexes by cancer cells .” 2017. Web. 15 Aug 2020.

Vancouver:

Glenister A. Glucose conjugation to increase the uptake of metal complexes by cancer cells . [Internet] [Thesis]. University of Sydney; 2017. [cited 2020 Aug 15]. Available from: http://hdl.handle.net/2123/16849.

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

Council of Science Editors:

Glenister A. Glucose conjugation to increase the uptake of metal complexes by cancer cells . [Thesis]. University of Sydney; 2017. Available from: http://hdl.handle.net/2123/16849

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


University of Alberta

13. Wang, guilin. Bisphosphonate-modified nanoparticles as drug delivery systems for bone diseases.

Degree: PhD, Department of Chemical and Materials Engineering, 2011, University of Alberta

 The objective of this thesis is to design nanoparticle (NP)-based drug delivery systems suitable for treatment of bone diseases. Two types of nanocarriers, (1) polymer… (more)

Subjects/Keywords: liposome; bone morphogenetic protein-2; nanoparticles; bone targeting; bisphosphonate; drug delivery

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APA (6th Edition):

Wang, g. (2011). Bisphosphonate-modified nanoparticles as drug delivery systems for bone diseases. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/1544bp45j

Chicago Manual of Style (16th Edition):

Wang, guilin. “Bisphosphonate-modified nanoparticles as drug delivery systems for bone diseases.” 2011. Doctoral Dissertation, University of Alberta. Accessed August 15, 2020. https://era.library.ualberta.ca/files/1544bp45j.

MLA Handbook (7th Edition):

Wang, guilin. “Bisphosphonate-modified nanoparticles as drug delivery systems for bone diseases.” 2011. Web. 15 Aug 2020.

Vancouver:

Wang g. Bisphosphonate-modified nanoparticles as drug delivery systems for bone diseases. [Internet] [Doctoral dissertation]. University of Alberta; 2011. [cited 2020 Aug 15]. Available from: https://era.library.ualberta.ca/files/1544bp45j.

Council of Science Editors:

Wang g. Bisphosphonate-modified nanoparticles as drug delivery systems for bone diseases. [Doctoral Dissertation]. University of Alberta; 2011. Available from: https://era.library.ualberta.ca/files/1544bp45j


Durban University of Technology

14. Odayar, Kriya. Active targeting of cancer cells using gemcitabine conjugated platinum nanoparticles.

Degree: 2017, Durban University of Technology

Submitted in fulfillment of the requirements of the Degree of Master's in Biotechnology, Durban University of Technology, 2017.

Nanotechnology is explained as the science of… (more)

Subjects/Keywords: Biotechnology; Nanotechnology; Nanoparticles; Drug targeting; Cancer cells; Antineoplastic agents; Cancer – Chemotherapy

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APA (6th Edition):

Odayar, K. (2017). Active targeting of cancer cells using gemcitabine conjugated platinum nanoparticles. (Thesis). Durban University of Technology. Retrieved from http://hdl.handle.net/10321/2642

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):

Odayar, Kriya. “Active targeting of cancer cells using gemcitabine conjugated platinum nanoparticles.” 2017. Thesis, Durban University of Technology. Accessed August 15, 2020. http://hdl.handle.net/10321/2642.

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

MLA Handbook (7th Edition):

Odayar, Kriya. “Active targeting of cancer cells using gemcitabine conjugated platinum nanoparticles.” 2017. Web. 15 Aug 2020.

Vancouver:

Odayar K. Active targeting of cancer cells using gemcitabine conjugated platinum nanoparticles. [Internet] [Thesis]. Durban University of Technology; 2017. [cited 2020 Aug 15]. Available from: http://hdl.handle.net/10321/2642.

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

Council of Science Editors:

Odayar K. Active targeting of cancer cells using gemcitabine conjugated platinum nanoparticles. [Thesis]. Durban University of Technology; 2017. Available from: http://hdl.handle.net/10321/2642

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

15. Vehmeijer, L.J.C. Clinically Relevant Strategies of Actively Targeted Nanomedicine.

Degree: 2013, Universiteit Utrecht

 Nanocarriers, particles in the size range of 1 to 1000 nanometer, are the application of nanotechnology to drug delivery. Delivery of therapeutic agents through these… (more)

Subjects/Keywords: nanomedicine; nanocarrier; nanoparticle; active targeting; ligand; drug delivery; actively targeted

…qualities, such as the size, drug loading, drug release or differential targeting, allows for… …dendrimers. Nanocarriermediated drug delivery can utilize triggered drug release, passive targeting… …release polymers and a stealth protective layer covered in targeting ligands127. In the case of… …BIND-014, the encapsulated drug is Docetaxel, the active ingredient in Taxotere®, a… …biodegradable PLGA-PEG polymer that can be conjugated to targeting ligands, which in this case targets… 

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APA (6th Edition):

Vehmeijer, L. J. C. (2013). Clinically Relevant Strategies of Actively Targeted Nanomedicine. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/288151

Chicago Manual of Style (16th Edition):

Vehmeijer, L J C. “Clinically Relevant Strategies of Actively Targeted Nanomedicine.” 2013. Masters Thesis, Universiteit Utrecht. Accessed August 15, 2020. http://dspace.library.uu.nl:8080/handle/1874/288151.

MLA Handbook (7th Edition):

Vehmeijer, L J C. “Clinically Relevant Strategies of Actively Targeted Nanomedicine.” 2013. Web. 15 Aug 2020.

Vancouver:

Vehmeijer LJC. Clinically Relevant Strategies of Actively Targeted Nanomedicine. [Internet] [Masters thesis]. Universiteit Utrecht; 2013. [cited 2020 Aug 15]. Available from: http://dspace.library.uu.nl:8080/handle/1874/288151.

Council of Science Editors:

Vehmeijer LJC. Clinically Relevant Strategies of Actively Targeted Nanomedicine. [Masters Thesis]. Universiteit Utrecht; 2013. Available from: http://dspace.library.uu.nl:8080/handle/1874/288151


Texas A&M University

16. Yu, Xiao. Progress toward a Colon Targeting Nanoparticle Based Drug Delivery System.

Degree: PhD, Chemical Engineering, 2012, Texas A&M University

 Hydrophobic drug paclitaxel nanoparticles (PAX NPs) and pH sensitive hydrogels were prepared in this study to build a colon targeting nanoparticle based drug delivery system… (more)

Subjects/Keywords: nanoparticles; hydrogel; colon targeting; oral drug delivery; controlled releases

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APA (6th Edition):

Yu, X. (2012). Progress toward a Colon Targeting Nanoparticle Based Drug Delivery System. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2012-05-11053

Chicago Manual of Style (16th Edition):

Yu, Xiao. “Progress toward a Colon Targeting Nanoparticle Based Drug Delivery System.” 2012. Doctoral Dissertation, Texas A&M University. Accessed August 15, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2012-05-11053.

MLA Handbook (7th Edition):

Yu, Xiao. “Progress toward a Colon Targeting Nanoparticle Based Drug Delivery System.” 2012. Web. 15 Aug 2020.

Vancouver:

Yu X. Progress toward a Colon Targeting Nanoparticle Based Drug Delivery System. [Internet] [Doctoral dissertation]. Texas A&M University; 2012. [cited 2020 Aug 15]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2012-05-11053.

Council of Science Editors:

Yu X. Progress toward a Colon Targeting Nanoparticle Based Drug Delivery System. [Doctoral Dissertation]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2012-05-11053


University of Rochester

17. Baranello, Michael Pasquale. Functionalized poly(styrene-alt maleic anhydride)-b-poly(styrene) micelles for targeted delivery of parthenolide to leukemia cells.

Degree: PhD, 2015, University of Rochester

 Small molecule anticancer agents present many challenges for systemic drug delivery including rapid blood clearance, nonspecific extravasation and accumulation, and inability to overcome multidrug resistant… (more)

Subjects/Keywords: AML; Drug delivery; Micelles; Nanoparticles; Parthenolide; Targeting; Leukemia

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APA (6th Edition):

Baranello, M. P. (2015). Functionalized poly(styrene-alt maleic anhydride)-b-poly(styrene) micelles for targeted delivery of parthenolide to leukemia cells. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/30053

Chicago Manual of Style (16th Edition):

Baranello, Michael Pasquale. “Functionalized poly(styrene-alt maleic anhydride)-b-poly(styrene) micelles for targeted delivery of parthenolide to leukemia cells.” 2015. Doctoral Dissertation, University of Rochester. Accessed August 15, 2020. http://hdl.handle.net/1802/30053.

MLA Handbook (7th Edition):

Baranello, Michael Pasquale. “Functionalized poly(styrene-alt maleic anhydride)-b-poly(styrene) micelles for targeted delivery of parthenolide to leukemia cells.” 2015. Web. 15 Aug 2020.

Vancouver:

Baranello MP. Functionalized poly(styrene-alt maleic anhydride)-b-poly(styrene) micelles for targeted delivery of parthenolide to leukemia cells. [Internet] [Doctoral dissertation]. University of Rochester; 2015. [cited 2020 Aug 15]. Available from: http://hdl.handle.net/1802/30053.

Council of Science Editors:

Baranello MP. Functionalized poly(styrene-alt maleic anhydride)-b-poly(styrene) micelles for targeted delivery of parthenolide to leukemia cells. [Doctoral Dissertation]. University of Rochester; 2015. Available from: http://hdl.handle.net/1802/30053


University of New South Wales

18. Tjandra, Kristel. Cell-targeting peptides for selective drug delivery to tumour cells.

Degree: Chemistry, 2018, University of New South Wales

 Cancer stands out as a disease that could benefit immensely from targeted drug delivery. The presence of molecular biomarkers that differentiate cancer cells from their… (more)

Subjects/Keywords: Polymersome; Drug delivery; Peptide; Multivalency; Cancer; Targeting; Bioconjugation

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APA (6th Edition):

Tjandra, K. (2018). Cell-targeting peptides for selective drug delivery to tumour cells. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/61937 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:57812/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Tjandra, Kristel. “Cell-targeting peptides for selective drug delivery to tumour cells.” 2018. Doctoral Dissertation, University of New South Wales. Accessed August 15, 2020. http://handle.unsw.edu.au/1959.4/61937 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:57812/SOURCE02?view=true.

MLA Handbook (7th Edition):

Tjandra, Kristel. “Cell-targeting peptides for selective drug delivery to tumour cells.” 2018. Web. 15 Aug 2020.

Vancouver:

Tjandra K. Cell-targeting peptides for selective drug delivery to tumour cells. [Internet] [Doctoral dissertation]. University of New South Wales; 2018. [cited 2020 Aug 15]. Available from: http://handle.unsw.edu.au/1959.4/61937 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:57812/SOURCE02?view=true.

Council of Science Editors:

Tjandra K. Cell-targeting peptides for selective drug delivery to tumour cells. [Doctoral Dissertation]. University of New South Wales; 2018. Available from: http://handle.unsw.edu.au/1959.4/61937 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:57812/SOURCE02?view=true


Université Catholique de Louvain

19. Schleich, Nathalie. Dual paclitaxel/superparamagnetic iron oxide-loaded PLGA-based nanoparticles for cancer therapy and magnetic resonance imaging.

Degree: 2015, Université Catholique de Louvain

Theranostic nanoparticles (NP) have the potential to revolutionize cancer diagnosis and therapy. We aimed to develop dual paclitaxel/SPIO-loaded PLGA-based NP for cancer therapy and magnetic… (more)

Subjects/Keywords: Cancer; Targeted drug delivery; MRI; Theranostic; Magnetic targeting; Nanomedicine

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APA (6th Edition):

Schleich, N. (2015). Dual paclitaxel/superparamagnetic iron oxide-loaded PLGA-based nanoparticles for cancer therapy and magnetic resonance imaging. (Thesis). Université Catholique de Louvain. Retrieved from http://hdl.handle.net/2078.1/156338

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):

Schleich, Nathalie. “Dual paclitaxel/superparamagnetic iron oxide-loaded PLGA-based nanoparticles for cancer therapy and magnetic resonance imaging.” 2015. Thesis, Université Catholique de Louvain. Accessed August 15, 2020. http://hdl.handle.net/2078.1/156338.

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

MLA Handbook (7th Edition):

Schleich, Nathalie. “Dual paclitaxel/superparamagnetic iron oxide-loaded PLGA-based nanoparticles for cancer therapy and magnetic resonance imaging.” 2015. Web. 15 Aug 2020.

Vancouver:

Schleich N. Dual paclitaxel/superparamagnetic iron oxide-loaded PLGA-based nanoparticles for cancer therapy and magnetic resonance imaging. [Internet] [Thesis]. Université Catholique de Louvain; 2015. [cited 2020 Aug 15]. Available from: http://hdl.handle.net/2078.1/156338.

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

Council of Science Editors:

Schleich N. Dual paclitaxel/superparamagnetic iron oxide-loaded PLGA-based nanoparticles for cancer therapy and magnetic resonance imaging. [Thesis]. Université Catholique de Louvain; 2015. Available from: http://hdl.handle.net/2078.1/156338

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


University of Bath

20. Sahm, Ulrike Gisela. Interaction of naturally occurring and synthetic MSH peptides with peripheral and CNS melanocortin receptors.

Degree: PhD, 1994, University of Bath

Subjects/Keywords: 572; Drug targeting; Malignant melonoma

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APA (6th Edition):

Sahm, U. G. (1994). Interaction of naturally occurring and synthetic MSH peptides with peripheral and CNS melanocortin receptors. (Doctoral Dissertation). University of Bath. Retrieved from https://researchportal.bath.ac.uk/en/studentthesis/interaction-of-naturally-occurring-and-synthetic-msh-peptides-with-peripheral-and-cns-melanocortin-receptors(f3b24791-f459-4537-9a37-673391695e7a).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.385312

Chicago Manual of Style (16th Edition):

Sahm, Ulrike Gisela. “Interaction of naturally occurring and synthetic MSH peptides with peripheral and CNS melanocortin receptors.” 1994. Doctoral Dissertation, University of Bath. Accessed August 15, 2020. https://researchportal.bath.ac.uk/en/studentthesis/interaction-of-naturally-occurring-and-synthetic-msh-peptides-with-peripheral-and-cns-melanocortin-receptors(f3b24791-f459-4537-9a37-673391695e7a).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.385312.

MLA Handbook (7th Edition):

Sahm, Ulrike Gisela. “Interaction of naturally occurring and synthetic MSH peptides with peripheral and CNS melanocortin receptors.” 1994. Web. 15 Aug 2020.

Vancouver:

Sahm UG. Interaction of naturally occurring and synthetic MSH peptides with peripheral and CNS melanocortin receptors. [Internet] [Doctoral dissertation]. University of Bath; 1994. [cited 2020 Aug 15]. Available from: https://researchportal.bath.ac.uk/en/studentthesis/interaction-of-naturally-occurring-and-synthetic-msh-peptides-with-peripheral-and-cns-melanocortin-receptors(f3b24791-f459-4537-9a37-673391695e7a).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.385312.

Council of Science Editors:

Sahm UG. Interaction of naturally occurring and synthetic MSH peptides with peripheral and CNS melanocortin receptors. [Doctoral Dissertation]. University of Bath; 1994. Available from: https://researchportal.bath.ac.uk/en/studentthesis/interaction-of-naturally-occurring-and-synthetic-msh-peptides-with-peripheral-and-cns-melanocortin-receptors(f3b24791-f459-4537-9a37-673391695e7a).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.385312


Freie Universität Berlin

21. Zhang, Yujuan. Untersuchung der Proteinadsorption an Nanocarriern für das intravenöse Drug- Targeting.

Degree: 2013, Freie Universität Berlin

 The study of drug targeting is for the purpose of reducing side effects and achieving selective effectiveness of drugs in vivo. The determining factor for… (more)

Subjects/Keywords: protein adsorption pattern; nanocarriers; drug targeting; 600 Technik, Medizin, angewandte Wissenschaften

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APA (6th Edition):

Zhang, Y. (2013). Untersuchung der Proteinadsorption an Nanocarriern für das intravenöse Drug- Targeting. (Thesis). Freie Universität Berlin. Retrieved from https://refubium.fu-berlin.de/handle/fub188/13598

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

Chicago Manual of Style (16th Edition):

Zhang, Yujuan. “Untersuchung der Proteinadsorption an Nanocarriern für das intravenöse Drug- Targeting.” 2013. Thesis, Freie Universität Berlin. Accessed August 15, 2020. https://refubium.fu-berlin.de/handle/fub188/13598.

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

MLA Handbook (7th Edition):

Zhang, Yujuan. “Untersuchung der Proteinadsorption an Nanocarriern für das intravenöse Drug- Targeting.” 2013. Web. 15 Aug 2020.

Vancouver:

Zhang Y. Untersuchung der Proteinadsorption an Nanocarriern für das intravenöse Drug- Targeting. [Internet] [Thesis]. Freie Universität Berlin; 2013. [cited 2020 Aug 15]. Available from: https://refubium.fu-berlin.de/handle/fub188/13598.

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

Council of Science Editors:

Zhang Y. Untersuchung der Proteinadsorption an Nanocarriern für das intravenöse Drug- Targeting. [Thesis]. Freie Universität Berlin; 2013. Available from: https://refubium.fu-berlin.de/handle/fub188/13598

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


University of Southern California

22. Shi, Pu. Integrin-mediated targeting of protein polymer nanoparticles carrying a cytostatic macrolide.

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

 Chapter 1: Cytotoxicity, low water solubility, rapid clearance from circulation, and off‐target side‐effects are common drawbacks of conventional small‐molecule drugs. To overcome these shortcomings, many… (more)

Subjects/Keywords: drug delivery; elastin-like polypeptide; nanoparticle; tumor targeting

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APA (6th Edition):

Shi, P. (2014). Integrin-mediated targeting of protein polymer nanoparticles carrying a cytostatic macrolide. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/453262/rec/3559

Chicago Manual of Style (16th Edition):

Shi, Pu. “Integrin-mediated targeting of protein polymer nanoparticles carrying a cytostatic macrolide.” 2014. Doctoral Dissertation, University of Southern California. Accessed August 15, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/453262/rec/3559.

MLA Handbook (7th Edition):

Shi, Pu. “Integrin-mediated targeting of protein polymer nanoparticles carrying a cytostatic macrolide.” 2014. Web. 15 Aug 2020.

Vancouver:

Shi P. Integrin-mediated targeting of protein polymer nanoparticles carrying a cytostatic macrolide. [Internet] [Doctoral dissertation]. University of Southern California; 2014. [cited 2020 Aug 15]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/453262/rec/3559.

Council of Science Editors:

Shi P. Integrin-mediated targeting of protein polymer nanoparticles carrying a cytostatic macrolide. [Doctoral Dissertation]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/453262/rec/3559


Colorado State University

23. Fowles, Jared S. Utilization of a canine cancer cell line (FACC) panel in comparative and translational studies of gene expression and drug sensitivity.

Degree: PhD, Cell and Molecular Biology, 2015, Colorado State University

 Canine cancer is the leading cause of death in adult dogs. The use of the canine cancer model in translational research is growing in popularity… (more)

Subjects/Keywords: drug sensitivity; osteosarcoma; prediction models; melanoma; canine cancer; pathway targeting

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APA (6th Edition):

Fowles, J. S. (2015). Utilization of a canine cancer cell line (FACC) panel in comparative and translational studies of gene expression and drug sensitivity. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/167117

Chicago Manual of Style (16th Edition):

Fowles, Jared S. “Utilization of a canine cancer cell line (FACC) panel in comparative and translational studies of gene expression and drug sensitivity.” 2015. Doctoral Dissertation, Colorado State University. Accessed August 15, 2020. http://hdl.handle.net/10217/167117.

MLA Handbook (7th Edition):

Fowles, Jared S. “Utilization of a canine cancer cell line (FACC) panel in comparative and translational studies of gene expression and drug sensitivity.” 2015. Web. 15 Aug 2020.

Vancouver:

Fowles JS. Utilization of a canine cancer cell line (FACC) panel in comparative and translational studies of gene expression and drug sensitivity. [Internet] [Doctoral dissertation]. Colorado State University; 2015. [cited 2020 Aug 15]. Available from: http://hdl.handle.net/10217/167117.

Council of Science Editors:

Fowles JS. Utilization of a canine cancer cell line (FACC) panel in comparative and translational studies of gene expression and drug sensitivity. [Doctoral Dissertation]. Colorado State University; 2015. Available from: http://hdl.handle.net/10217/167117


University of Arizona

24. Stamm, Matthew T. Particle Dynamics and Particle-Cell Interaction in Microfluidic Systems .

Degree: 2013, University of Arizona

 Particle-laden flow in a microchannel resulting in aggregation of microparticles was investigated to determine the dependence of the cluster growth rate on the following parameters:… (more)

Subjects/Keywords: cell targeting; cerasome; drug delivery; microfluidics; Mechanical Engineering; cancer

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APA (6th Edition):

Stamm, M. T. (2013). Particle Dynamics and Particle-Cell Interaction in Microfluidic Systems . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/308886

Chicago Manual of Style (16th Edition):

Stamm, Matthew T. “Particle Dynamics and Particle-Cell Interaction in Microfluidic Systems .” 2013. Doctoral Dissertation, University of Arizona. Accessed August 15, 2020. http://hdl.handle.net/10150/308886.

MLA Handbook (7th Edition):

Stamm, Matthew T. “Particle Dynamics and Particle-Cell Interaction in Microfluidic Systems .” 2013. Web. 15 Aug 2020.

Vancouver:

Stamm MT. Particle Dynamics and Particle-Cell Interaction in Microfluidic Systems . [Internet] [Doctoral dissertation]. University of Arizona; 2013. [cited 2020 Aug 15]. Available from: http://hdl.handle.net/10150/308886.

Council of Science Editors:

Stamm MT. Particle Dynamics and Particle-Cell Interaction in Microfluidic Systems . [Doctoral Dissertation]. University of Arizona; 2013. Available from: http://hdl.handle.net/10150/308886


Kansas State University

25. Sriadibhatla, Soma Sekhar. Synthesis and characterization of Alendronate functionalized Poly (l-lactide) polymers for engineering bone tumor targeting nanoparticles.

Degree: MS, Department of Chemistry, 2016, Kansas State University

 Nanomedicine-based therapeutics have exhibited clear benefits when compared to unmodified drugs, which include improved pharmacokinetics, drug retention, targeting efficiency, and minimizes toxicity. Every year thousands… (more)

Subjects/Keywords: Poly(l-lactide); Nanomedicine; Bone tumor; Drug delivery; Targeting; Bisphosphonates

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APA (6th Edition):

Sriadibhatla, S. S. (2016). Synthesis and characterization of Alendronate functionalized Poly (l-lactide) polymers for engineering bone tumor targeting nanoparticles. (Masters Thesis). Kansas State University. Retrieved from http://hdl.handle.net/2097/34511

Chicago Manual of Style (16th Edition):

Sriadibhatla, Soma Sekhar. “Synthesis and characterization of Alendronate functionalized Poly (l-lactide) polymers for engineering bone tumor targeting nanoparticles.” 2016. Masters Thesis, Kansas State University. Accessed August 15, 2020. http://hdl.handle.net/2097/34511.

MLA Handbook (7th Edition):

Sriadibhatla, Soma Sekhar. “Synthesis and characterization of Alendronate functionalized Poly (l-lactide) polymers for engineering bone tumor targeting nanoparticles.” 2016. Web. 15 Aug 2020.

Vancouver:

Sriadibhatla SS. Synthesis and characterization of Alendronate functionalized Poly (l-lactide) polymers for engineering bone tumor targeting nanoparticles. [Internet] [Masters thesis]. Kansas State University; 2016. [cited 2020 Aug 15]. Available from: http://hdl.handle.net/2097/34511.

Council of Science Editors:

Sriadibhatla SS. Synthesis and characterization of Alendronate functionalized Poly (l-lactide) polymers for engineering bone tumor targeting nanoparticles. [Masters Thesis]. Kansas State University; 2016. Available from: http://hdl.handle.net/2097/34511


University of Notre Dame

26. David T. Omstead. Optimizing the Selective Delivery of Chemotherapeutics to Multiple Myeloma through the Design of Peptide-Targeted Liposomes</h1>.

Degree: Chemical and Biomolecular Engineering, 2020, University of Notre Dame

  This dissertation will describe the design, characterization, biodistribution, and efficacy of peptide-targeted liposomes for use in selective treatment of multiple myeloma. Multiple myeloma (MM)… (more)

Subjects/Keywords: Cancer; Liposomes; iRGD; Multivalency; CD138; Dual-targeting; Multiple Myeloma; Nanoparticles; VLA-4; LPAM-1; Selectivity; Peptide-targeting; CD38; Drug Delivery

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APA (6th Edition):

Omstead, D. T. (2020). Optimizing the Selective Delivery of Chemotherapeutics to Multiple Myeloma through the Design of Peptide-Targeted Liposomes</h1>. (Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/8336h131q0x

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):

Omstead, David T.. “Optimizing the Selective Delivery of Chemotherapeutics to Multiple Myeloma through the Design of Peptide-Targeted Liposomes</h1>.” 2020. Thesis, University of Notre Dame. Accessed August 15, 2020. https://curate.nd.edu/show/8336h131q0x.

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

MLA Handbook (7th Edition):

Omstead, David T.. “Optimizing the Selective Delivery of Chemotherapeutics to Multiple Myeloma through the Design of Peptide-Targeted Liposomes</h1>.” 2020. Web. 15 Aug 2020.

Vancouver:

Omstead DT. Optimizing the Selective Delivery of Chemotherapeutics to Multiple Myeloma through the Design of Peptide-Targeted Liposomes</h1>. [Internet] [Thesis]. University of Notre Dame; 2020. [cited 2020 Aug 15]. Available from: https://curate.nd.edu/show/8336h131q0x.

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

Council of Science Editors:

Omstead DT. Optimizing the Selective Delivery of Chemotherapeutics to Multiple Myeloma through the Design of Peptide-Targeted Liposomes</h1>. [Thesis]. University of Notre Dame; 2020. Available from: https://curate.nd.edu/show/8336h131q0x

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


Clemson University

27. Blichmann, Paul. ORAL DELIVERY OF PEPTIDE DRUGS FOR MITIGATION OF CROHN'S DISEASE.

Degree: MS, Bioengineering, 2012, Clemson University

  Protein drugs are typically administered intravenously, but this practice has clear disadvantages such as widespread circulation and swift clearance from the body. Orally delivered… (more)

Subjects/Keywords: colon targeting; controlled release; Inflammatory Bowel Disease; MUC1 targeting; oral drug delivery; peptide drugs; Biomedical Engineering and Bioengineering

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APA (6th Edition):

Blichmann, P. (2012). ORAL DELIVERY OF PEPTIDE DRUGS FOR MITIGATION OF CROHN'S DISEASE. (Masters Thesis). Clemson University. Retrieved from https://tigerprints.clemson.edu/all_theses/1486

Chicago Manual of Style (16th Edition):

Blichmann, Paul. “ORAL DELIVERY OF PEPTIDE DRUGS FOR MITIGATION OF CROHN'S DISEASE.” 2012. Masters Thesis, Clemson University. Accessed August 15, 2020. https://tigerprints.clemson.edu/all_theses/1486.

MLA Handbook (7th Edition):

Blichmann, Paul. “ORAL DELIVERY OF PEPTIDE DRUGS FOR MITIGATION OF CROHN'S DISEASE.” 2012. Web. 15 Aug 2020.

Vancouver:

Blichmann P. ORAL DELIVERY OF PEPTIDE DRUGS FOR MITIGATION OF CROHN'S DISEASE. [Internet] [Masters thesis]. Clemson University; 2012. [cited 2020 Aug 15]. Available from: https://tigerprints.clemson.edu/all_theses/1486.

Council of Science Editors:

Blichmann P. ORAL DELIVERY OF PEPTIDE DRUGS FOR MITIGATION OF CROHN'S DISEASE. [Masters Thesis]. Clemson University; 2012. Available from: https://tigerprints.clemson.edu/all_theses/1486


Case Western Reserve University

28. Weinberg, Brent D. Intratumoral Chemotherapy for Liver Cancer Using Biodegradable Polymer Implants.

Degree: PhD, Biomedical Engineering, 2007, Case Western Reserve University

 Cancer is the second leading cause of death in the United States, behind only heart disease. Many cancers, particularly solid tumors, are inaccessible to surgery,… (more)

Subjects/Keywords: Engineering, Biomedical; radiofrequency ablation; liver cancer; biodegradable implant; mathematical modeling; chemotherapy; drug targeting

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APA (6th Edition):

Weinberg, B. D. (2007). Intratumoral Chemotherapy for Liver Cancer Using Biodegradable Polymer Implants. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1176749922

Chicago Manual of Style (16th Edition):

Weinberg, Brent D. “Intratumoral Chemotherapy for Liver Cancer Using Biodegradable Polymer Implants.” 2007. Doctoral Dissertation, Case Western Reserve University. Accessed August 15, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=case1176749922.

MLA Handbook (7th Edition):

Weinberg, Brent D. “Intratumoral Chemotherapy for Liver Cancer Using Biodegradable Polymer Implants.” 2007. Web. 15 Aug 2020.

Vancouver:

Weinberg BD. Intratumoral Chemotherapy for Liver Cancer Using Biodegradable Polymer Implants. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2007. [cited 2020 Aug 15]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1176749922.

Council of Science Editors:

Weinberg BD. Intratumoral Chemotherapy for Liver Cancer Using Biodegradable Polymer Implants. [Doctoral Dissertation]. Case Western Reserve University; 2007. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1176749922


North Carolina State University

29. Kelley, Richard Lee. Plant virus nanoparticles as targeting agents: New tools for cell biology.

Degree: MS, Chemistry, 2009, North Carolina State University

 ABSTRACT KELLEY, RICHARD LEE. Plant virus nanoparticles as targeting agents: New tools for cell biology. (Under the direction of Stefan Franzen) In order to develop… (more)

Subjects/Keywords: cell targeting; drug carrier; red clover necrotic mosaic virus; plant viral nanoparticle; pharmaceutical

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

APA (6th Edition):

Kelley, R. L. (2009). Plant virus nanoparticles as targeting agents: New tools for cell biology. (Thesis). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/1894

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):

Kelley, Richard Lee. “Plant virus nanoparticles as targeting agents: New tools for cell biology.” 2009. Thesis, North Carolina State University. Accessed August 15, 2020. http://www.lib.ncsu.edu/resolver/1840.16/1894.

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

MLA Handbook (7th Edition):

Kelley, Richard Lee. “Plant virus nanoparticles as targeting agents: New tools for cell biology.” 2009. Web. 15 Aug 2020.

Vancouver:

Kelley RL. Plant virus nanoparticles as targeting agents: New tools for cell biology. [Internet] [Thesis]. North Carolina State University; 2009. [cited 2020 Aug 15]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/1894.

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

Council of Science Editors:

Kelley RL. Plant virus nanoparticles as targeting agents: New tools for cell biology. [Thesis]. North Carolina State University; 2009. Available from: http://www.lib.ncsu.edu/resolver/1840.16/1894

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

30. A.F. RAPOSO MOREIRA DIAS. SYNTHESIS OF RGD PEPTIDOMIMETIC-DRUG CONJUGATES FOR THE TUMOR-TARGETED DELIVERY OF CYTOTOXIC AGENTS.

Degree: 2018, Università degli Studi di Milano

 Integrins are a large family of heterodimeric transmembrane glycoprotein receptors, composed by two non-covalently associated subunits (α and β). Integrins αVβ3 and αVβ5 are overexpressed… (more)

Subjects/Keywords: tumor targeting; integrins; multivalency; small molecule-drug conjugates; Settore CHIM/06 - Chimica Organica

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

APA (6th Edition):

DIAS, A. R. M. (2018). SYNTHESIS OF RGD PEPTIDOMIMETIC-DRUG CONJUGATES FOR THE TUMOR-TARGETED DELIVERY OF CYTOTOXIC AGENTS. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/583313

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):

DIAS, A.F. RAPOSO MOREIRA. “SYNTHESIS OF RGD PEPTIDOMIMETIC-DRUG CONJUGATES FOR THE TUMOR-TARGETED DELIVERY OF CYTOTOXIC AGENTS.” 2018. Thesis, Università degli Studi di Milano. Accessed August 15, 2020. http://hdl.handle.net/2434/583313.

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

MLA Handbook (7th Edition):

DIAS, A.F. RAPOSO MOREIRA. “SYNTHESIS OF RGD PEPTIDOMIMETIC-DRUG CONJUGATES FOR THE TUMOR-TARGETED DELIVERY OF CYTOTOXIC AGENTS.” 2018. Web. 15 Aug 2020.

Vancouver:

DIAS ARM. SYNTHESIS OF RGD PEPTIDOMIMETIC-DRUG CONJUGATES FOR THE TUMOR-TARGETED DELIVERY OF CYTOTOXIC AGENTS. [Internet] [Thesis]. Università degli Studi di Milano; 2018. [cited 2020 Aug 15]. Available from: http://hdl.handle.net/2434/583313.

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

Council of Science Editors:

DIAS ARM. SYNTHESIS OF RGD PEPTIDOMIMETIC-DRUG CONJUGATES FOR THE TUMOR-TARGETED DELIVERY OF CYTOTOXIC AGENTS. [Thesis]. Università degli Studi di Milano; 2018. Available from: http://hdl.handle.net/2434/583313

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

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