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You searched for subject:(Stimulus responsive). Showing records 1 – 13 of 13 total matches.

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University of New South Wales

1. Quek, Jing Yang. Self-Assembly of Stimulus-Responsive Water Soluble RAFT (Co)Polymers.

Degree: Centre for Advanced Macromolecular Design, 2014, University of New South Wales

 In this thesis, homopolymers and well-defined AB diblock copolymers that are stimulus responsive were prepared via a combination of reversible-addition fragmentation chain transfer (RAFT) polymerization… (more)

Subjects/Keywords: Self-Assembly; Stimulus-Responsive; RAFT Polymerization

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APA (6th Edition):

Quek, J. Y. (2014). Self-Assembly of Stimulus-Responsive Water Soluble RAFT (Co)Polymers. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/53532 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12227/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Quek, Jing Yang. “Self-Assembly of Stimulus-Responsive Water Soluble RAFT (Co)Polymers.” 2014. Doctoral Dissertation, University of New South Wales. Accessed October 18, 2019. http://handle.unsw.edu.au/1959.4/53532 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12227/SOURCE02?view=true.

MLA Handbook (7th Edition):

Quek, Jing Yang. “Self-Assembly of Stimulus-Responsive Water Soluble RAFT (Co)Polymers.” 2014. Web. 18 Oct 2019.

Vancouver:

Quek JY. Self-Assembly of Stimulus-Responsive Water Soluble RAFT (Co)Polymers. [Internet] [Doctoral dissertation]. University of New South Wales; 2014. [cited 2019 Oct 18]. Available from: http://handle.unsw.edu.au/1959.4/53532 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12227/SOURCE02?view=true.

Council of Science Editors:

Quek JY. Self-Assembly of Stimulus-Responsive Water Soluble RAFT (Co)Polymers. [Doctoral Dissertation]. University of New South Wales; 2014. Available from: http://handle.unsw.edu.au/1959.4/53532 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12227/SOURCE02?view=true


University of Toronto

2. Chen, Haotian. One Step Formation of Heterogeneous Tubular Biomaterials and Stimulus Responsive Hydrogels.

Degree: 2014, University of Toronto

Tubular structures are fundamental constituents of plant, animal and human tissues. Synthetically prepared biomaterial tubular constructs have a variety of applications that include engineered blood… (more)

Subjects/Keywords: Bioprinting; Hydrogels; Soft materials; Spatial heterogeneities; Stimulus Responsive; Tubular structures; 0541

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APA (6th Edition):

Chen, H. (2014). One Step Formation of Heterogeneous Tubular Biomaterials and Stimulus Responsive Hydrogels. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/68576

Chicago Manual of Style (16th Edition):

Chen, Haotian. “One Step Formation of Heterogeneous Tubular Biomaterials and Stimulus Responsive Hydrogels.” 2014. Masters Thesis, University of Toronto. Accessed October 18, 2019. http://hdl.handle.net/1807/68576.

MLA Handbook (7th Edition):

Chen, Haotian. “One Step Formation of Heterogeneous Tubular Biomaterials and Stimulus Responsive Hydrogels.” 2014. Web. 18 Oct 2019.

Vancouver:

Chen H. One Step Formation of Heterogeneous Tubular Biomaterials and Stimulus Responsive Hydrogels. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1807/68576.

Council of Science Editors:

Chen H. One Step Formation of Heterogeneous Tubular Biomaterials and Stimulus Responsive Hydrogels. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/68576


University of Michigan

3. Carter, Kelsey King. Streamlined Gelator Discovery Through the Analysis of Intermolecular Interactions in the Solid State.

Degree: PhD, Chemistry, 2014, University of Michigan

 Low molecular weight gels are self-assembled materials comprised of a fiberous structure that is able to immobilize a liquid phase. Gels can be triggered by… (more)

Subjects/Keywords: self-assembly; gelation; stimulus-responsive materials; Chemistry; Science

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APA (6th Edition):

Carter, K. K. (2014). Streamlined Gelator Discovery Through the Analysis of Intermolecular Interactions in the Solid State. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/110414

Chicago Manual of Style (16th Edition):

Carter, Kelsey King. “Streamlined Gelator Discovery Through the Analysis of Intermolecular Interactions in the Solid State.” 2014. Doctoral Dissertation, University of Michigan. Accessed October 18, 2019. http://hdl.handle.net/2027.42/110414.

MLA Handbook (7th Edition):

Carter, Kelsey King. “Streamlined Gelator Discovery Through the Analysis of Intermolecular Interactions in the Solid State.” 2014. Web. 18 Oct 2019.

Vancouver:

Carter KK. Streamlined Gelator Discovery Through the Analysis of Intermolecular Interactions in the Solid State. [Internet] [Doctoral dissertation]. University of Michigan; 2014. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2027.42/110414.

Council of Science Editors:

Carter KK. Streamlined Gelator Discovery Through the Analysis of Intermolecular Interactions in the Solid State. [Doctoral Dissertation]. University of Michigan; 2014. Available from: http://hdl.handle.net/2027.42/110414


Penn State University

4. Kaweesi, Henry. Studies toward (i) a depolymerizable poly(vinylcarbamate) and (ii) a turn-off fluorescent sensor for β-D-galactosidase.

Degree: MS, Chemistry, 2013, Penn State University

 Poly(carbamates) that depolymerize from head-to-tail through azaquinone methide intermediates show slow rates of depolymerization, particularly in non-polar solvents. Previous research in the Phillips group has… (more)

Subjects/Keywords: depolymerization; poly(carbamates); stimulus responsive end-cap; fluorescence; turn-off sensor; anthracene diboronic acid

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APA (6th Edition):

Kaweesi, H. (2013). Studies toward (i) a depolymerizable poly(vinylcarbamate) and (ii) a turn-off fluorescent sensor for β-D-galactosidase. (Masters Thesis). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/19349

Chicago Manual of Style (16th Edition):

Kaweesi, Henry. “Studies toward (i) a depolymerizable poly(vinylcarbamate) and (ii) a turn-off fluorescent sensor for β-D-galactosidase.” 2013. Masters Thesis, Penn State University. Accessed October 18, 2019. https://etda.libraries.psu.edu/catalog/19349.

MLA Handbook (7th Edition):

Kaweesi, Henry. “Studies toward (i) a depolymerizable poly(vinylcarbamate) and (ii) a turn-off fluorescent sensor for β-D-galactosidase.” 2013. Web. 18 Oct 2019.

Vancouver:

Kaweesi H. Studies toward (i) a depolymerizable poly(vinylcarbamate) and (ii) a turn-off fluorescent sensor for β-D-galactosidase. [Internet] [Masters thesis]. Penn State University; 2013. [cited 2019 Oct 18]. Available from: https://etda.libraries.psu.edu/catalog/19349.

Council of Science Editors:

Kaweesi H. Studies toward (i) a depolymerizable poly(vinylcarbamate) and (ii) a turn-off fluorescent sensor for β-D-galactosidase. [Masters Thesis]. Penn State University; 2013. Available from: https://etda.libraries.psu.edu/catalog/19349


University of Toledo

5. Lawrence, Patrick G. Ionically Crosslinked Polymer Networks for Underwater Adhesion and Long-Term Controlled Release.

Degree: MS, Chemical Engineering, 2014, University of Toledo

 Underwater adhesives have several potential applications in industry as well as in medicine. Much of the recent research in this area has focused on adhesive… (more)

Subjects/Keywords: Chemical Engineering; Chemistry; Materials Science; Polymers; Polymer Chemistry; Ionic Crosslinking; Polyelectrolytes; Underwater Adhesion; Stimulus-Responsive; Controlled Release

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APA (6th Edition):

Lawrence, P. G. (2014). Ionically Crosslinked Polymer Networks for Underwater Adhesion and Long-Term Controlled Release. (Masters Thesis). University of Toledo. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=toledo1417437994

Chicago Manual of Style (16th Edition):

Lawrence, Patrick G. “Ionically Crosslinked Polymer Networks for Underwater Adhesion and Long-Term Controlled Release.” 2014. Masters Thesis, University of Toledo. Accessed October 18, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1417437994.

MLA Handbook (7th Edition):

Lawrence, Patrick G. “Ionically Crosslinked Polymer Networks for Underwater Adhesion and Long-Term Controlled Release.” 2014. Web. 18 Oct 2019.

Vancouver:

Lawrence PG. Ionically Crosslinked Polymer Networks for Underwater Adhesion and Long-Term Controlled Release. [Internet] [Masters thesis]. University of Toledo; 2014. [cited 2019 Oct 18]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1417437994.

Council of Science Editors:

Lawrence PG. Ionically Crosslinked Polymer Networks for Underwater Adhesion and Long-Term Controlled Release. [Masters Thesis]. University of Toledo; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1417437994


Rice University

6. Gomez, Eric Jordan. Optogenetic strategies for stimulus-responsive viral gene delivery.

Degree: PhD, Engineering, 2016, Rice University

 Heightened interest in the field of gene therapy has led to the development of multitudes of gene vector candidates. Most, if not all, modern vector… (more)

Subjects/Keywords: Gene therapy; AAV; viral gene delivery; optogenetics; Phytochrome; stimulus-responsive; gene delivery; protein engineering; adeno-associated virus

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APA (6th Edition):

Gomez, E. J. (2016). Optogenetic strategies for stimulus-responsive viral gene delivery. (Doctoral Dissertation). Rice University. Retrieved from http://hdl.handle.net/1911/96553

Chicago Manual of Style (16th Edition):

Gomez, Eric Jordan. “Optogenetic strategies for stimulus-responsive viral gene delivery.” 2016. Doctoral Dissertation, Rice University. Accessed October 18, 2019. http://hdl.handle.net/1911/96553.

MLA Handbook (7th Edition):

Gomez, Eric Jordan. “Optogenetic strategies for stimulus-responsive viral gene delivery.” 2016. Web. 18 Oct 2019.

Vancouver:

Gomez EJ. Optogenetic strategies for stimulus-responsive viral gene delivery. [Internet] [Doctoral dissertation]. Rice University; 2016. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1911/96553.

Council of Science Editors:

Gomez EJ. Optogenetic strategies for stimulus-responsive viral gene delivery. [Doctoral Dissertation]. Rice University; 2016. Available from: http://hdl.handle.net/1911/96553


Rice University

7. Evans, Annicka Carter. Developing stimulus-responsive adeno-associated virus vectors for cancer-targeted gene therapy.

Degree: PhD, Bioengineering, 2018, Rice University

 The most significant challenge to current gene therapy trials is ensuring delivery to exclusively diseased sites. Both non-viral and viral vectors have broad natural tropisms… (more)

Subjects/Keywords: adeno-associated virus; AAV; gene therapy; biocomputing nanoparticles; stimulus-responsive; targeted therapeutics; protease-responsive; protease; oxidative stress; Nrf2; Keap1; n-terminal externalization

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APA (6th Edition):

Evans, A. C. (2018). Developing stimulus-responsive adeno-associated virus vectors for cancer-targeted gene therapy. (Doctoral Dissertation). Rice University. Retrieved from http://hdl.handle.net/1911/105353

Chicago Manual of Style (16th Edition):

Evans, Annicka Carter. “Developing stimulus-responsive adeno-associated virus vectors for cancer-targeted gene therapy.” 2018. Doctoral Dissertation, Rice University. Accessed October 18, 2019. http://hdl.handle.net/1911/105353.

MLA Handbook (7th Edition):

Evans, Annicka Carter. “Developing stimulus-responsive adeno-associated virus vectors for cancer-targeted gene therapy.” 2018. Web. 18 Oct 2019.

Vancouver:

Evans AC. Developing stimulus-responsive adeno-associated virus vectors for cancer-targeted gene therapy. [Internet] [Doctoral dissertation]. Rice University; 2018. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1911/105353.

Council of Science Editors:

Evans AC. Developing stimulus-responsive adeno-associated virus vectors for cancer-targeted gene therapy. [Doctoral Dissertation]. Rice University; 2018. Available from: http://hdl.handle.net/1911/105353


Rice University

8. Evans, Annicka Carter. Developing stimulus-responsive adeno-associated virus vectors for cancer-targeted gene therapy.

Degree: PhD, Bioengineering, 2018, Rice University

 The most significant challenge to current gene therapy trials is ensuring delivery to exclusively diseased sites. Both non-viral and viral vectors have broad natural tropisms… (more)

Subjects/Keywords: adeno-associated virus; AAV; gene therapy; biocomputing nanoparticles; stimulus-responsive; targeted therapeutics; protease-responsive; protease; oxidative stress; Nrf2; Keap1; n-terminal externalization

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APA (6th Edition):

Evans, A. C. (2018). Developing stimulus-responsive adeno-associated virus vectors for cancer-targeted gene therapy. (Doctoral Dissertation). Rice University. Retrieved from http://hdl.handle.net/1911/105355

Chicago Manual of Style (16th Edition):

Evans, Annicka Carter. “Developing stimulus-responsive adeno-associated virus vectors for cancer-targeted gene therapy.” 2018. Doctoral Dissertation, Rice University. Accessed October 18, 2019. http://hdl.handle.net/1911/105355.

MLA Handbook (7th Edition):

Evans, Annicka Carter. “Developing stimulus-responsive adeno-associated virus vectors for cancer-targeted gene therapy.” 2018. Web. 18 Oct 2019.

Vancouver:

Evans AC. Developing stimulus-responsive adeno-associated virus vectors for cancer-targeted gene therapy. [Internet] [Doctoral dissertation]. Rice University; 2018. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1911/105355.

Council of Science Editors:

Evans AC. Developing stimulus-responsive adeno-associated virus vectors for cancer-targeted gene therapy. [Doctoral Dissertation]. Rice University; 2018. Available from: http://hdl.handle.net/1911/105355


Rice University

9. Evans, Annicka Carter. Developing stimulus-responsive adeno-associated virus vectors for cancer-targeted gene therapy.

Degree: PhD, Bioengineering, 2018, Rice University

 The most significant challenge to current gene therapy trials is ensuring delivery to exclusively diseased sites. Both non-viral and viral vectors have broad natural tropisms… (more)

Subjects/Keywords: adeno-associated virus; AAV; gene therapy; biocomputing nanoparticles; stimulus-responsive; targeted therapeutics; protease-responsive; protease; oxidative stress; Nrf2; Keap1; n-terminal externalization

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

APA (6th Edition):

Evans, A. C. (2018). Developing stimulus-responsive adeno-associated virus vectors for cancer-targeted gene therapy. (Doctoral Dissertation). Rice University. Retrieved from http://hdl.handle.net/1911/105352

Chicago Manual of Style (16th Edition):

Evans, Annicka Carter. “Developing stimulus-responsive adeno-associated virus vectors for cancer-targeted gene therapy.” 2018. Doctoral Dissertation, Rice University. Accessed October 18, 2019. http://hdl.handle.net/1911/105352.

MLA Handbook (7th Edition):

Evans, Annicka Carter. “Developing stimulus-responsive adeno-associated virus vectors for cancer-targeted gene therapy.” 2018. Web. 18 Oct 2019.

Vancouver:

Evans AC. Developing stimulus-responsive adeno-associated virus vectors for cancer-targeted gene therapy. [Internet] [Doctoral dissertation]. Rice University; 2018. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1911/105352.

Council of Science Editors:

Evans AC. Developing stimulus-responsive adeno-associated virus vectors for cancer-targeted gene therapy. [Doctoral Dissertation]. Rice University; 2018. Available from: http://hdl.handle.net/1911/105352


Rice University

10. Evans, Annicka Carter. Developing stimulus-responsive adeno-associated virus vectors for cancer-targeted gene therapy.

Degree: PhD, Engineering, 2018, Rice University

 The most significant challenge to current gene therapy trials is ensuring delivery to exclusively diseased sites. Both non-viral and viral vectors have broad natural tropisms… (more)

Subjects/Keywords: adeno-associated virus; AAV; gene therapy; biocomputing nanoparticles; stimulus-responsive; targeted therapeutics; protease-responsive; protease; oxidative stress; Nrf2; Keap1; n-terminal externalization

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APA (6th Edition):

Evans, A. C. (2018). Developing stimulus-responsive adeno-associated virus vectors for cancer-targeted gene therapy. (Doctoral Dissertation). Rice University. Retrieved from http://hdl.handle.net/1911/105351

Chicago Manual of Style (16th Edition):

Evans, Annicka Carter. “Developing stimulus-responsive adeno-associated virus vectors for cancer-targeted gene therapy.” 2018. Doctoral Dissertation, Rice University. Accessed October 18, 2019. http://hdl.handle.net/1911/105351.

MLA Handbook (7th Edition):

Evans, Annicka Carter. “Developing stimulus-responsive adeno-associated virus vectors for cancer-targeted gene therapy.” 2018. Web. 18 Oct 2019.

Vancouver:

Evans AC. Developing stimulus-responsive adeno-associated virus vectors for cancer-targeted gene therapy. [Internet] [Doctoral dissertation]. Rice University; 2018. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1911/105351.

Council of Science Editors:

Evans AC. Developing stimulus-responsive adeno-associated virus vectors for cancer-targeted gene therapy. [Doctoral Dissertation]. Rice University; 2018. Available from: http://hdl.handle.net/1911/105351


University of Texas – Austin

11. -0255-8318. Stimulus-responsive delivery systems for enabling the oral delivery of protein therapeutics exhibiting high isoelectric point.

Degree: PhD, Chemical Engineering, 2015, University of Texas – Austin

 Protein therapeutics offer numerous advantages over small molecule drugs and are rapidly becoming one of the most prominent classes of therapeutics. Unfortunately, they are delivered… (more)

Subjects/Keywords: Hydrogels; Protein therapeutics; Protein therapy; Drug delivery; Oral delivery; Aptamers; PH-responsive; Stimulus-responsive; Ionic strength; Isoelectric point; PEGylation; Conjugation; Bioconjugation; Intestinal absorption; Intestinal transport; Itaconic acid; N-vinylpyrrolidone; Methacrylic acid; Mesh size; Crosslinking density; SELEX; In vivo; Closed-loop

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APA (6th Edition):

-0255-8318. (2015). Stimulus-responsive delivery systems for enabling the oral delivery of protein therapeutics exhibiting high isoelectric point. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/30484

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Chicago Manual of Style (16th Edition):

-0255-8318. “Stimulus-responsive delivery systems for enabling the oral delivery of protein therapeutics exhibiting high isoelectric point.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed October 18, 2019. http://hdl.handle.net/2152/30484.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

MLA Handbook (7th Edition):

-0255-8318. “Stimulus-responsive delivery systems for enabling the oral delivery of protein therapeutics exhibiting high isoelectric point.” 2015. Web. 18 Oct 2019.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

-0255-8318. Stimulus-responsive delivery systems for enabling the oral delivery of protein therapeutics exhibiting high isoelectric point. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2152/30484.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

-0255-8318. Stimulus-responsive delivery systems for enabling the oral delivery of protein therapeutics exhibiting high isoelectric point. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/30484

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete


Duke University

12. Chang, Debby Pei-Shan. Mechanical and Tribological Study of a Stimulus Responsive Hydrogel, pNIPAAm, and a Mucinous Glycoprotein, Lubricin .

Degree: 2009, Duke University

  Friction is the resistive force that arises when two contacting surfaces move relative to each other. Frictional interactions are important from both engineering and… (more)

Subjects/Keywords: Engineering, Materials Science; Engineering, Biomedical; Engineering, Mechanical; cartilage lubrication; friction force microscopy; joint lubrication; lubricin; PRG; stimulus responsive hydrogel

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APA (6th Edition):

Chang, D. P. (2009). Mechanical and Tribological Study of a Stimulus Responsive Hydrogel, pNIPAAm, and a Mucinous Glycoprotein, Lubricin . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/1359

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):

Chang, Debby Pei-Shan. “Mechanical and Tribological Study of a Stimulus Responsive Hydrogel, pNIPAAm, and a Mucinous Glycoprotein, Lubricin .” 2009. Thesis, Duke University. Accessed October 18, 2019. http://hdl.handle.net/10161/1359.

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

MLA Handbook (7th Edition):

Chang, Debby Pei-Shan. “Mechanical and Tribological Study of a Stimulus Responsive Hydrogel, pNIPAAm, and a Mucinous Glycoprotein, Lubricin .” 2009. Web. 18 Oct 2019.

Vancouver:

Chang DP. Mechanical and Tribological Study of a Stimulus Responsive Hydrogel, pNIPAAm, and a Mucinous Glycoprotein, Lubricin . [Internet] [Thesis]. Duke University; 2009. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/10161/1359.

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

Council of Science Editors:

Chang DP. Mechanical and Tribological Study of a Stimulus Responsive Hydrogel, pNIPAAm, and a Mucinous Glycoprotein, Lubricin . [Thesis]. Duke University; 2009. Available from: http://hdl.handle.net/10161/1359

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

13. Elliott, Lindsay C. Single molecule tracking studies of lower critical solution temperature transition behavior in poly(N-isopropylacrylamide).

Degree: PhD, 0335, 2011, University of Illinois – Urbana-Champaign

 In this thesis project, single molecule tracking, SMT, experiments in poly(n-isopropylacrylamide, pNIPAAm, were carried out using probe fluorophores that had partitioned into the polymer. When… (more)

Subjects/Keywords: Single molecule tracking (SMT); atom transfer radical polymerization (ATRP); poly(N-isopropylacrylamide) (pNIPAAm); stimulus responsive polymer (SRP); temperature sensitive hydrogel; free volume change; lower critical solution temperature (LCST); confinement level calculations; time series analysis; statistical analysis of lateral diffusion and multistate kinetics; radius of gyration evolution

…components. Ebara et al. used stimulus-responsive pNIPAAmbased copolymers to expose or mask… …initial papers on stimulus-responsive polymers with a report of a discontinuous phase transition… …publications about hydrogels and stimulus-responsive polymers shown in Figure 1.1. Figure 1.1… …biocompatibility;16,17 and κ-carrageenan, derived from red seaweed, which is K+ responsive and… …assembled devices with temperature-responsive 2 components to separate, isolate, react, and… 

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APA (6th Edition):

Elliott, L. C. (2011). Single molecule tracking studies of lower critical solution temperature transition behavior in poly(N-isopropylacrylamide). (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/24149

Chicago Manual of Style (16th Edition):

Elliott, Lindsay C. “Single molecule tracking studies of lower critical solution temperature transition behavior in poly(N-isopropylacrylamide).” 2011. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed October 18, 2019. http://hdl.handle.net/2142/24149.

MLA Handbook (7th Edition):

Elliott, Lindsay C. “Single molecule tracking studies of lower critical solution temperature transition behavior in poly(N-isopropylacrylamide).” 2011. Web. 18 Oct 2019.

Vancouver:

Elliott LC. Single molecule tracking studies of lower critical solution temperature transition behavior in poly(N-isopropylacrylamide). [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2011. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2142/24149.

Council of Science Editors:

Elliott LC. Single molecule tracking studies of lower critical solution temperature transition behavior in poly(N-isopropylacrylamide). [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/24149

.