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You searched for subject:(Poloxamer). Showing records 1 – 19 of 19 total matches.

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1. SILVA, Camila Maria Barros da. Formulação de gel termossensível mucoadesivo contendo cloridrato de pilocarpina para tratamento de xerostomia .

Degree: 2017, Universidade Federal de Pernambuco

 O cloridrato de pilocarpina tem sido utilizado no tratamento da xerostomia, entretanto sua atuação sistêmica promove reações adversas indesejáveis. Tal problemática leva a necessidade da… (more)

Subjects/Keywords: Pilocarpina; Poloxamer; Xerostomia

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APA (6th Edition):

SILVA, C. M. B. d. (2017). Formulação de gel termossensível mucoadesivo contendo cloridrato de pilocarpina para tratamento de xerostomia . (Masters Thesis). Universidade Federal de Pernambuco. Retrieved from https://repositorio.ufpe.br/handle/123456789/26670

Chicago Manual of Style (16th Edition):

SILVA, Camila Maria Barros da. “Formulação de gel termossensível mucoadesivo contendo cloridrato de pilocarpina para tratamento de xerostomia .” 2017. Masters Thesis, Universidade Federal de Pernambuco. Accessed October 28, 2020. https://repositorio.ufpe.br/handle/123456789/26670.

MLA Handbook (7th Edition):

SILVA, Camila Maria Barros da. “Formulação de gel termossensível mucoadesivo contendo cloridrato de pilocarpina para tratamento de xerostomia .” 2017. Web. 28 Oct 2020.

Vancouver:

SILVA CMBd. Formulação de gel termossensível mucoadesivo contendo cloridrato de pilocarpina para tratamento de xerostomia . [Internet] [Masters thesis]. Universidade Federal de Pernambuco; 2017. [cited 2020 Oct 28]. Available from: https://repositorio.ufpe.br/handle/123456789/26670.

Council of Science Editors:

SILVA CMBd. Formulação de gel termossensível mucoadesivo contendo cloridrato de pilocarpina para tratamento de xerostomia . [Masters Thesis]. Universidade Federal de Pernambuco; 2017. Available from: https://repositorio.ufpe.br/handle/123456789/26670


University of Alberta

2. Chaudhary, Hetal R. The poloxamer 407 induced hyperlipidemic rat model and its effect on renal toxicity of calcineurin inhibitors.

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

 The present study characterized poloxamer 407 (P407) induced hyperlipidemia in rats and investigated its effect of on renal toxicity of the immunosuppressants tacrolimus and cyclosporine… (more)

Subjects/Keywords: Hyperlipidemia, Poloxamer 407, Cyclosporine, Tacrolimus

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APA (6th Edition):

Chaudhary, H. R. (2012). The poloxamer 407 induced hyperlipidemic rat model and its effect on renal toxicity of calcineurin inhibitors. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/js956h44z

Chicago Manual of Style (16th Edition):

Chaudhary, Hetal R. “The poloxamer 407 induced hyperlipidemic rat model and its effect on renal toxicity of calcineurin inhibitors.” 2012. Masters Thesis, University of Alberta. Accessed October 28, 2020. https://era.library.ualberta.ca/files/js956h44z.

MLA Handbook (7th Edition):

Chaudhary, Hetal R. “The poloxamer 407 induced hyperlipidemic rat model and its effect on renal toxicity of calcineurin inhibitors.” 2012. Web. 28 Oct 2020.

Vancouver:

Chaudhary HR. The poloxamer 407 induced hyperlipidemic rat model and its effect on renal toxicity of calcineurin inhibitors. [Internet] [Masters thesis]. University of Alberta; 2012. [cited 2020 Oct 28]. Available from: https://era.library.ualberta.ca/files/js956h44z.

Council of Science Editors:

Chaudhary HR. The poloxamer 407 induced hyperlipidemic rat model and its effect on renal toxicity of calcineurin inhibitors. [Masters Thesis]. University of Alberta; 2012. Available from: https://era.library.ualberta.ca/files/js956h44z

3. Salmon, Damien. Usage biopharmaceutique in vitro combiné des hydrogels thermoréversibles et d’une cellule de diffusion innovante : Combined in vitro biopharmaceutic use of thermoreversible hydrogels and an innovative diffusion cell.

Degree: Docteur es, Sciences du médicament, physico-chimie et ingénierie, 2016, Lyon

La biopharmacie s'intéresse au devenir du médicament au contact d'un épithélium. Cela conditionne la biodisponibilité du principe actif, rendant les études biopharmaceutiques indispensables au développement… (more)

Subjects/Keywords: Biopharmacie; Perméabilité; Épithélium; Hydrogel; Poloxamer; Biopharmacy; Permeability; Epithelium; Hydrogel; Poloxamer; 615.19

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APA (6th Edition):

Salmon, D. (2016). Usage biopharmaceutique in vitro combiné des hydrogels thermoréversibles et d’une cellule de diffusion innovante : Combined in vitro biopharmaceutic use of thermoreversible hydrogels and an innovative diffusion cell. (Doctoral Dissertation). Lyon. Retrieved from http://www.theses.fr/2016LYSE1056

Chicago Manual of Style (16th Edition):

Salmon, Damien. “Usage biopharmaceutique in vitro combiné des hydrogels thermoréversibles et d’une cellule de diffusion innovante : Combined in vitro biopharmaceutic use of thermoreversible hydrogels and an innovative diffusion cell.” 2016. Doctoral Dissertation, Lyon. Accessed October 28, 2020. http://www.theses.fr/2016LYSE1056.

MLA Handbook (7th Edition):

Salmon, Damien. “Usage biopharmaceutique in vitro combiné des hydrogels thermoréversibles et d’une cellule de diffusion innovante : Combined in vitro biopharmaceutic use of thermoreversible hydrogels and an innovative diffusion cell.” 2016. Web. 28 Oct 2020.

Vancouver:

Salmon D. Usage biopharmaceutique in vitro combiné des hydrogels thermoréversibles et d’une cellule de diffusion innovante : Combined in vitro biopharmaceutic use of thermoreversible hydrogels and an innovative diffusion cell. [Internet] [Doctoral dissertation]. Lyon; 2016. [cited 2020 Oct 28]. Available from: http://www.theses.fr/2016LYSE1056.

Council of Science Editors:

Salmon D. Usage biopharmaceutique in vitro combiné des hydrogels thermoréversibles et d’une cellule de diffusion innovante : Combined in vitro biopharmaceutic use of thermoreversible hydrogels and an innovative diffusion cell. [Doctoral Dissertation]. Lyon; 2016. Available from: http://www.theses.fr/2016LYSE1056


Clemson University

4. Klep, Oleksandr. Programming of Retention Capacity and Release Capabilities of Propargyl Acrylate Nanoparticles Decorated with Poloxamer Copolymer.

Degree: PhD, School of Materials Science and Engineering, 2018, Clemson University

 Nanoparticle based drug delivery offers an advantage over free drug deliv-ery as it allows the manufacturer to introduce various control mechanisms either for targeted delivery… (more)

Subjects/Keywords: Drug delivery; FRET; Grafting density; Nanocomposite; Poloxamer; Sensor

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APA (6th Edition):

Klep, O. (2018). Programming of Retention Capacity and Release Capabilities of Propargyl Acrylate Nanoparticles Decorated with Poloxamer Copolymer. (Doctoral Dissertation). Clemson University. Retrieved from https://tigerprints.clemson.edu/all_dissertations/2133

Chicago Manual of Style (16th Edition):

Klep, Oleksandr. “Programming of Retention Capacity and Release Capabilities of Propargyl Acrylate Nanoparticles Decorated with Poloxamer Copolymer.” 2018. Doctoral Dissertation, Clemson University. Accessed October 28, 2020. https://tigerprints.clemson.edu/all_dissertations/2133.

MLA Handbook (7th Edition):

Klep, Oleksandr. “Programming of Retention Capacity and Release Capabilities of Propargyl Acrylate Nanoparticles Decorated with Poloxamer Copolymer.” 2018. Web. 28 Oct 2020.

Vancouver:

Klep O. Programming of Retention Capacity and Release Capabilities of Propargyl Acrylate Nanoparticles Decorated with Poloxamer Copolymer. [Internet] [Doctoral dissertation]. Clemson University; 2018. [cited 2020 Oct 28]. Available from: https://tigerprints.clemson.edu/all_dissertations/2133.

Council of Science Editors:

Klep O. Programming of Retention Capacity and Release Capabilities of Propargyl Acrylate Nanoparticles Decorated with Poloxamer Copolymer. [Doctoral Dissertation]. Clemson University; 2018. Available from: https://tigerprints.clemson.edu/all_dissertations/2133

5. Kreidel, Rogério Nepomuceno. Desenvolvimento e caracterização de dispersões sólidas de nimodipino empregando PEG 6000 ou Poloxamer 407.

Degree: Mestrado, Produção e Controle Farmacêuticos, 2010, University of São Paulo

O nimodipino é um bloqueador de canais de cálcio usado principalmente na terapia da hemorragia subaracnóidea e no tratamento de distúrbios cognitivos. É praticamente insolúvel… (more)

Subjects/Keywords: Dispersões sólidas; Dissolução; Dissolution; Estabilidade dos medicamentos; Farmacotécnica; Nimodipine; Nimodipino; Pharmacotechniques; Polietilenoglicol; Poloxamer; Poloxamer; Polyethylene glycol; Solid dispersions; Solubilidade; Solubility; Stability of drugs

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APA (6th Edition):

Kreidel, R. N. (2010). Desenvolvimento e caracterização de dispersões sólidas de nimodipino empregando PEG 6000 ou Poloxamer 407. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/9/9139/tde-07042010-173035/ ;

Chicago Manual of Style (16th Edition):

Kreidel, Rogério Nepomuceno. “Desenvolvimento e caracterização de dispersões sólidas de nimodipino empregando PEG 6000 ou Poloxamer 407.” 2010. Masters Thesis, University of São Paulo. Accessed October 28, 2020. http://www.teses.usp.br/teses/disponiveis/9/9139/tde-07042010-173035/ ;.

MLA Handbook (7th Edition):

Kreidel, Rogério Nepomuceno. “Desenvolvimento e caracterização de dispersões sólidas de nimodipino empregando PEG 6000 ou Poloxamer 407.” 2010. Web. 28 Oct 2020.

Vancouver:

Kreidel RN. Desenvolvimento e caracterização de dispersões sólidas de nimodipino empregando PEG 6000 ou Poloxamer 407. [Internet] [Masters thesis]. University of São Paulo; 2010. [cited 2020 Oct 28]. Available from: http://www.teses.usp.br/teses/disponiveis/9/9139/tde-07042010-173035/ ;.

Council of Science Editors:

Kreidel RN. Desenvolvimento e caracterização de dispersões sólidas de nimodipino empregando PEG 6000 ou Poloxamer 407. [Masters Thesis]. University of São Paulo; 2010. Available from: http://www.teses.usp.br/teses/disponiveis/9/9139/tde-07042010-173035/ ;


University of Guelph

6. Laniesse, Delphine. Pharmacology and antinociception of a sustained-released butorphanol – poloxamer 407 formulation in Amazon parrots.

Degree: Associate Diploma in Agriculture, Agriculture, 2016, University of Guelph

 Butorphanol is an opioid drug used for pain management in Psittacidae. It has a short duration of action (2-3h) when administered IM or IV. In… (more)

Subjects/Keywords: avian; butorphanol; analgesia; poloxamer; P407; pharmacokinetic; pharmacodynamic; nociception; antinociception; rheology; amazon parrot; bird; opioid

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APA (6th Edition):

Laniesse, D. (2016). Pharmacology and antinociception of a sustained-released butorphanol – poloxamer 407 formulation in Amazon parrots. (Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9674

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):

Laniesse, Delphine. “Pharmacology and antinociception of a sustained-released butorphanol – poloxamer 407 formulation in Amazon parrots.” 2016. Thesis, University of Guelph. Accessed October 28, 2020. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9674.

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

MLA Handbook (7th Edition):

Laniesse, Delphine. “Pharmacology and antinociception of a sustained-released butorphanol – poloxamer 407 formulation in Amazon parrots.” 2016. Web. 28 Oct 2020.

Vancouver:

Laniesse D. Pharmacology and antinociception of a sustained-released butorphanol – poloxamer 407 formulation in Amazon parrots. [Internet] [Thesis]. University of Guelph; 2016. [cited 2020 Oct 28]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9674.

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

Council of Science Editors:

Laniesse D. Pharmacology and antinociception of a sustained-released butorphanol – poloxamer 407 formulation in Amazon parrots. [Thesis]. University of Guelph; 2016. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9674

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

7. Zeng, Ni. Formulation et caractérisation d'une forme buccale mucoadhésive thermogélifiante pour administration de sulfate de salbutamol : Formulation and characterization of a thermogelling mucoadhesive buccal form for salbutamol sulfate administration.

Degree: Docteur es, Pharmacologie, 2015, Sorbonne Paris Cité

Le traitement de l’asthme concerne une large population et fait appel très majoritairement à une administration par voie pulmonaire. Cette voie présente certains inconvénients qui… (more)

Subjects/Keywords: Salbutamol; Poloxamère; Gomme xanthane; Appareil à flux continu; Cytotoxicité; Mucoadhésion; Salbutamol; Poloxamer; Xanthan gum; Flow through apparatus; Cytotoxicity; Mucoadhesion; 615.6

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

APA (6th Edition):

Zeng, N. (2015). Formulation et caractérisation d'une forme buccale mucoadhésive thermogélifiante pour administration de sulfate de salbutamol : Formulation and characterization of a thermogelling mucoadhesive buccal form for salbutamol sulfate administration. (Doctoral Dissertation). Sorbonne Paris Cité. Retrieved from http://www.theses.fr/2015USPCP602

Chicago Manual of Style (16th Edition):

Zeng, Ni. “Formulation et caractérisation d'une forme buccale mucoadhésive thermogélifiante pour administration de sulfate de salbutamol : Formulation and characterization of a thermogelling mucoadhesive buccal form for salbutamol sulfate administration.” 2015. Doctoral Dissertation, Sorbonne Paris Cité. Accessed October 28, 2020. http://www.theses.fr/2015USPCP602.

MLA Handbook (7th Edition):

Zeng, Ni. “Formulation et caractérisation d'une forme buccale mucoadhésive thermogélifiante pour administration de sulfate de salbutamol : Formulation and characterization of a thermogelling mucoadhesive buccal form for salbutamol sulfate administration.” 2015. Web. 28 Oct 2020.

Vancouver:

Zeng N. Formulation et caractérisation d'une forme buccale mucoadhésive thermogélifiante pour administration de sulfate de salbutamol : Formulation and characterization of a thermogelling mucoadhesive buccal form for salbutamol sulfate administration. [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; 2015. [cited 2020 Oct 28]. Available from: http://www.theses.fr/2015USPCP602.

Council of Science Editors:

Zeng N. Formulation et caractérisation d'une forme buccale mucoadhésive thermogélifiante pour administration de sulfate de salbutamol : Formulation and characterization of a thermogelling mucoadhesive buccal form for salbutamol sulfate administration. [Doctoral Dissertation]. Sorbonne Paris Cité; 2015. Available from: http://www.theses.fr/2015USPCP602

8. Zeng, Ni. Formulation et caractérisation d'une forme buccale mucoadhésive thermogélifiante pour administration de sulfate de salbutamol : Formulation and characterization of a thermogelling mucoadhesive buccal form for salbutamol sulfate administration.

Degree: Docteur es, Pharmacologie, 2015, Université Paris Descartes – Paris V

Le traitement de l’asthme concerne une large population et fait appel très majoritairement à une administration par voie pulmonaire. Cette voie présente certains inconvénients qui… (more)

Subjects/Keywords: Salbutamol; Poloxamère; Gomme xanthane; Appareil à flux continu; Cytotoxicité; Mucoadhésion; Salbutamol; Poloxamer; Xanthan gum; Flow through apparatus; Cytotoxicity; Mucoadhesion; 615.6

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

APA (6th Edition):

Zeng, N. (2015). Formulation et caractérisation d'une forme buccale mucoadhésive thermogélifiante pour administration de sulfate de salbutamol : Formulation and characterization of a thermogelling mucoadhesive buccal form for salbutamol sulfate administration. (Doctoral Dissertation). Université Paris Descartes – Paris V. Retrieved from http://www.theses.fr/2015PA05P602

Chicago Manual of Style (16th Edition):

Zeng, Ni. “Formulation et caractérisation d'une forme buccale mucoadhésive thermogélifiante pour administration de sulfate de salbutamol : Formulation and characterization of a thermogelling mucoadhesive buccal form for salbutamol sulfate administration.” 2015. Doctoral Dissertation, Université Paris Descartes – Paris V. Accessed October 28, 2020. http://www.theses.fr/2015PA05P602.

MLA Handbook (7th Edition):

Zeng, Ni. “Formulation et caractérisation d'une forme buccale mucoadhésive thermogélifiante pour administration de sulfate de salbutamol : Formulation and characterization of a thermogelling mucoadhesive buccal form for salbutamol sulfate administration.” 2015. Web. 28 Oct 2020.

Vancouver:

Zeng N. Formulation et caractérisation d'une forme buccale mucoadhésive thermogélifiante pour administration de sulfate de salbutamol : Formulation and characterization of a thermogelling mucoadhesive buccal form for salbutamol sulfate administration. [Internet] [Doctoral dissertation]. Université Paris Descartes – Paris V; 2015. [cited 2020 Oct 28]. Available from: http://www.theses.fr/2015PA05P602.

Council of Science Editors:

Zeng N. Formulation et caractérisation d'une forme buccale mucoadhésive thermogélifiante pour administration de sulfate de salbutamol : Formulation and characterization of a thermogelling mucoadhesive buccal form for salbutamol sulfate administration. [Doctoral Dissertation]. Université Paris Descartes – Paris V; 2015. Available from: http://www.theses.fr/2015PA05P602

9. Violet, Fabien. Développement d’une protéine à libération prolongée, mise au point du procédé d’encapsulation sans solvant halogéné et optimisation du profil de libération. : Development of microencapsulation process without toxic solvent, application to sustained protein release.

Degree: Docteur es, Pharmacie, 2015, Angers

La régénération tissulaire est une voie prometteuse de thérapie dans le cadre des maladies dégénératives. Dans ce but sont conçus les microcarriers pharmacologiquement actifs (PAM).… (more)

Subjects/Keywords: Microsphère; Protéine; Libération prolongée; Prilling; Plga; Poloxamère; Hsp27; Héparine; Microsphere; Protein; Drug Delivery; Prilling; Plga; Poloxamer; Hsp27; Heparin; 610

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

APA (6th Edition):

Violet, F. (2015). Développement d’une protéine à libération prolongée, mise au point du procédé d’encapsulation sans solvant halogéné et optimisation du profil de libération. : Development of microencapsulation process without toxic solvent, application to sustained protein release. (Doctoral Dissertation). Angers. Retrieved from http://www.theses.fr/2015ANGE0040

Chicago Manual of Style (16th Edition):

Violet, Fabien. “Développement d’une protéine à libération prolongée, mise au point du procédé d’encapsulation sans solvant halogéné et optimisation du profil de libération. : Development of microencapsulation process without toxic solvent, application to sustained protein release.” 2015. Doctoral Dissertation, Angers. Accessed October 28, 2020. http://www.theses.fr/2015ANGE0040.

MLA Handbook (7th Edition):

Violet, Fabien. “Développement d’une protéine à libération prolongée, mise au point du procédé d’encapsulation sans solvant halogéné et optimisation du profil de libération. : Development of microencapsulation process without toxic solvent, application to sustained protein release.” 2015. Web. 28 Oct 2020.

Vancouver:

Violet F. Développement d’une protéine à libération prolongée, mise au point du procédé d’encapsulation sans solvant halogéné et optimisation du profil de libération. : Development of microencapsulation process without toxic solvent, application to sustained protein release. [Internet] [Doctoral dissertation]. Angers; 2015. [cited 2020 Oct 28]. Available from: http://www.theses.fr/2015ANGE0040.

Council of Science Editors:

Violet F. Développement d’une protéine à libération prolongée, mise au point du procédé d’encapsulation sans solvant halogéné et optimisation du profil de libération. : Development of microencapsulation process without toxic solvent, application to sustained protein release. [Doctoral Dissertation]. Angers; 2015. Available from: http://www.theses.fr/2015ANGE0040


Freie Universität Berlin

10. Heilmann, Sarah. In vitro characterisation of nanastructured carrier systems.

Degree: 2012, Freie Universität Berlin

 Pain caused by severe skin wounds asks for the treatment with systemically applied opioids which is associated with severe and encumbering adverse effects like respiratory… (more)

Subjects/Keywords: morphine; solid lipid nanoparticles; poloxamer hydrogels; release studies; skin absorption; 500 Naturwissenschaften und Mathematik::540 Chemie

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APA (6th Edition):

Heilmann, S. (2012). In vitro characterisation of nanastructured carrier systems. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-9195

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):

Heilmann, Sarah. “In vitro characterisation of nanastructured carrier systems.” 2012. Thesis, Freie Universität Berlin. Accessed October 28, 2020. http://dx.doi.org/10.17169/refubium-9195.

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

MLA Handbook (7th Edition):

Heilmann, Sarah. “In vitro characterisation of nanastructured carrier systems.” 2012. Web. 28 Oct 2020.

Vancouver:

Heilmann S. In vitro characterisation of nanastructured carrier systems. [Internet] [Thesis]. Freie Universität Berlin; 2012. [cited 2020 Oct 28]. Available from: http://dx.doi.org/10.17169/refubium-9195.

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

Council of Science Editors:

Heilmann S. In vitro characterisation of nanastructured carrier systems. [Thesis]. Freie Universität Berlin; 2012. Available from: http://dx.doi.org/10.17169/refubium-9195

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

11. Zeng, Ni. Formulation et caractérisation d'une forme buccale mucoadhésive thermogélifiante pour administration de sulfate de salbutamol : Formulation and characterization of a thermogelling mucoadhesive buccal form for salbutamol sulfate administration.

Degree: Docteur es, Pharmacologie, 2015, Sorbonne Paris Cité

Le traitement de l’asthme concerne une large population et fait appel très majoritairement à une administration par voie pulmonaire. Cette voie présente certains inconvénients qui… (more)

Subjects/Keywords: Salbutamol; Poloxamère; Gomme xanthane; Appareil à flux continu; Cytotoxicité; Mucoadhésion; Salbutamol; Poloxamer; Xanthan gum; Flow through apparatus; Cytotoxicity; Mucoadhesion; 615.6

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

APA (6th Edition):

Zeng, N. (2015). Formulation et caractérisation d'une forme buccale mucoadhésive thermogélifiante pour administration de sulfate de salbutamol : Formulation and characterization of a thermogelling mucoadhesive buccal form for salbutamol sulfate administration. (Doctoral Dissertation). Sorbonne Paris Cité. Retrieved from http://www.theses.fr/2015USPCB075

Chicago Manual of Style (16th Edition):

Zeng, Ni. “Formulation et caractérisation d'une forme buccale mucoadhésive thermogélifiante pour administration de sulfate de salbutamol : Formulation and characterization of a thermogelling mucoadhesive buccal form for salbutamol sulfate administration.” 2015. Doctoral Dissertation, Sorbonne Paris Cité. Accessed October 28, 2020. http://www.theses.fr/2015USPCB075.

MLA Handbook (7th Edition):

Zeng, Ni. “Formulation et caractérisation d'une forme buccale mucoadhésive thermogélifiante pour administration de sulfate de salbutamol : Formulation and characterization of a thermogelling mucoadhesive buccal form for salbutamol sulfate administration.” 2015. Web. 28 Oct 2020.

Vancouver:

Zeng N. Formulation et caractérisation d'une forme buccale mucoadhésive thermogélifiante pour administration de sulfate de salbutamol : Formulation and characterization of a thermogelling mucoadhesive buccal form for salbutamol sulfate administration. [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; 2015. [cited 2020 Oct 28]. Available from: http://www.theses.fr/2015USPCB075.

Council of Science Editors:

Zeng N. Formulation et caractérisation d'une forme buccale mucoadhésive thermogélifiante pour administration de sulfate de salbutamol : Formulation and characterization of a thermogelling mucoadhesive buccal form for salbutamol sulfate administration. [Doctoral Dissertation]. Sorbonne Paris Cité; 2015. Available from: http://www.theses.fr/2015USPCB075


Georgia Tech

12. Sengupta, Aritra. Intracellular drug delivery using laser activated carbon nanoparticles.

Degree: PhD, Chemical and Biomolecular Engineering, 2014, Georgia Tech

 We demonstrate intracellular delivery of various molecules by inducing controlled and reversible cell damage through pulsed laser irradiation of carbon black (CB) nanoparticles. We then… (more)

Subjects/Keywords: Laser; Nanosecond; Carbon black; Intracellular; Drug delivery; Photoacoustics; Pluronics; Poloxamer; siRNA; EGFR; In-vivo; In-vitro

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APA (6th Edition):

Sengupta, A. (2014). Intracellular drug delivery using laser activated carbon nanoparticles. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/53996

Chicago Manual of Style (16th Edition):

Sengupta, Aritra. “Intracellular drug delivery using laser activated carbon nanoparticles.” 2014. Doctoral Dissertation, Georgia Tech. Accessed October 28, 2020. http://hdl.handle.net/1853/53996.

MLA Handbook (7th Edition):

Sengupta, Aritra. “Intracellular drug delivery using laser activated carbon nanoparticles.” 2014. Web. 28 Oct 2020.

Vancouver:

Sengupta A. Intracellular drug delivery using laser activated carbon nanoparticles. [Internet] [Doctoral dissertation]. Georgia Tech; 2014. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/1853/53996.

Council of Science Editors:

Sengupta A. Intracellular drug delivery using laser activated carbon nanoparticles. [Doctoral Dissertation]. Georgia Tech; 2014. Available from: http://hdl.handle.net/1853/53996


University of Vienna

13. Kerleta, Vera. The impact of the interplay between nonionics and the cell membrane on the nanoparticle-cell association and stability of Caco-2 cells.

Degree: 2010, University of Vienna

Nanopartikel (NP) sind etwa 10- 100mal kleiner als eine Eukaryontenzelle und können in diese aufgenommen werden. Bei Aufnahmestudien werden derzeit werden Fluoreszenz-markierte NP eingesetzt, die… (more)

Subjects/Keywords: 30.30 Naturwissenschaften in Beziehung zu anderen Fachgebieten; 44.40 Pharmazie, Pharmazeutika; Caco-2 Zellen / Zellmembran / PLGA, Nanopartikel / Tenside / Poloxamer 188 / Polysorbat 20 / Polysorbat 80 / Flow Zytometer / Mikroaspiration; Caco-2 cells / cell membrane / PLGA / nanoparticles / surfactant / Poloxamer 188 / Polysorbate 20 / Polysorbate 80 / flow cytometry / microaspiration

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APA (6th Edition):

Kerleta, V. (2010). The impact of the interplay between nonionics and the cell membrane on the nanoparticle-cell association and stability of Caco-2 cells. (Thesis). University of Vienna. Retrieved from http://othes.univie.ac.at/9530/

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):

Kerleta, Vera. “The impact of the interplay between nonionics and the cell membrane on the nanoparticle-cell association and stability of Caco-2 cells.” 2010. Thesis, University of Vienna. Accessed October 28, 2020. http://othes.univie.ac.at/9530/.

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

MLA Handbook (7th Edition):

Kerleta, Vera. “The impact of the interplay between nonionics and the cell membrane on the nanoparticle-cell association and stability of Caco-2 cells.” 2010. Web. 28 Oct 2020.

Vancouver:

Kerleta V. The impact of the interplay between nonionics and the cell membrane on the nanoparticle-cell association and stability of Caco-2 cells. [Internet] [Thesis]. University of Vienna; 2010. [cited 2020 Oct 28]. Available from: http://othes.univie.ac.at/9530/.

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

Council of Science Editors:

Kerleta V. The impact of the interplay between nonionics and the cell membrane on the nanoparticle-cell association and stability of Caco-2 cells. [Thesis]. University of Vienna; 2010. Available from: http://othes.univie.ac.at/9530/

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


Université de Montréal

14. Lacerda, Clemente Augusto. Culture des ostéoblastes dans un gel de Pluronic F-127 : effet sur la viabilité et le phénotype cellulaire.

Degree: 2005, Université de Montréal

Subjects/Keywords: Poloxamer; Pluronic F-127 (BASF); Ostéoblastes; Injectable; Thermo sensible; Gel

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

APA (6th Edition):

Lacerda, C. A. (2005). Culture des ostéoblastes dans un gel de Pluronic F-127 : effet sur la viabilité et le phénotype cellulaire. (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/17689

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):

Lacerda, Clemente Augusto. “Culture des ostéoblastes dans un gel de Pluronic F-127 : effet sur la viabilité et le phénotype cellulaire.” 2005. Thesis, Université de Montréal. Accessed October 28, 2020. http://hdl.handle.net/1866/17689.

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

MLA Handbook (7th Edition):

Lacerda, Clemente Augusto. “Culture des ostéoblastes dans un gel de Pluronic F-127 : effet sur la viabilité et le phénotype cellulaire.” 2005. Web. 28 Oct 2020.

Vancouver:

Lacerda CA. Culture des ostéoblastes dans un gel de Pluronic F-127 : effet sur la viabilité et le phénotype cellulaire. [Internet] [Thesis]. Université de Montréal; 2005. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/1866/17689.

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

Council of Science Editors:

Lacerda CA. Culture des ostéoblastes dans un gel de Pluronic F-127 : effet sur la viabilité et le phénotype cellulaire. [Thesis]. Université de Montréal; 2005. Available from: http://hdl.handle.net/1866/17689

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


University of Waterloo

15. Shortall, Samantha Marisha. Mixed Micelle Characterization of Pluronic and Gemini Surfactant – Based Gene Therapy Carriers and a Connection to Transfection Efficiency.

Degree: 2020, University of Waterloo

 Non-viral gene therapy formulation development often relies on a rational design approach, where vector components are selected based on individual characteristics known to favour transfection… (more)

Subjects/Keywords: gene delivery; gemini surfactant; poloxamer; mixed micellization; Pluronic; 16-3-16; N,N’-bis(dimethylhexadecyl)-1,3-propanediammonium dibromide; interaction parameter; transfection efficiency; non-viral

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APA (6th Edition):

Shortall, S. M. (2020). Mixed Micelle Characterization of Pluronic and Gemini Surfactant – Based Gene Therapy Carriers and a Connection to Transfection Efficiency. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/16309

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):

Shortall, Samantha Marisha. “Mixed Micelle Characterization of Pluronic and Gemini Surfactant – Based Gene Therapy Carriers and a Connection to Transfection Efficiency.” 2020. Thesis, University of Waterloo. Accessed October 28, 2020. http://hdl.handle.net/10012/16309.

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

MLA Handbook (7th Edition):

Shortall, Samantha Marisha. “Mixed Micelle Characterization of Pluronic and Gemini Surfactant – Based Gene Therapy Carriers and a Connection to Transfection Efficiency.” 2020. Web. 28 Oct 2020.

Vancouver:

Shortall SM. Mixed Micelle Characterization of Pluronic and Gemini Surfactant – Based Gene Therapy Carriers and a Connection to Transfection Efficiency. [Internet] [Thesis]. University of Waterloo; 2020. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/10012/16309.

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

Council of Science Editors:

Shortall SM. Mixed Micelle Characterization of Pluronic and Gemini Surfactant – Based Gene Therapy Carriers and a Connection to Transfection Efficiency. [Thesis]. University of Waterloo; 2020. Available from: http://hdl.handle.net/10012/16309

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


University of Helsinki

16. Piipponen, Anu. Menetelmiä nanokiteiden liukenemisnopeuden tutkimiseksi.

Degree: Farmaceutiska fakulteten, 2016, University of Helsinki

 Farmaseuttiset nanokiteet ovat alle mikrometrin kokoisia puhtaasta lääkeaineesta ja stabilisaattorista koostuvia kiteitä. Niiden suurin etu yli mikrometrin suuruisiin kiteisiin nähden on niiden nopeampi liukeneminen. Liukenemisnopeuden… (more)

Subjects/Keywords: DLS; nanocrystal; indometacin; wet milling; dissolution; light scattering; dialysis; poloxamer 188; liukenemisnopeus; valonsironta; nanokide; indometasiini; märkäjauhatus; dialyysi; poloksameeri 188; Farmaceutisk teknologi; Pharmacy Technology; Farmasian teknologia

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

APA (6th Edition):

Piipponen, A. (2016). Menetelmiä nanokiteiden liukenemisnopeuden tutkimiseksi. (Masters Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/167524

Chicago Manual of Style (16th Edition):

Piipponen, Anu. “Menetelmiä nanokiteiden liukenemisnopeuden tutkimiseksi.” 2016. Masters Thesis, University of Helsinki. Accessed October 28, 2020. http://hdl.handle.net/10138/167524.

MLA Handbook (7th Edition):

Piipponen, Anu. “Menetelmiä nanokiteiden liukenemisnopeuden tutkimiseksi.” 2016. Web. 28 Oct 2020.

Vancouver:

Piipponen A. Menetelmiä nanokiteiden liukenemisnopeuden tutkimiseksi. [Internet] [Masters thesis]. University of Helsinki; 2016. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/10138/167524.

Council of Science Editors:

Piipponen A. Menetelmiä nanokiteiden liukenemisnopeuden tutkimiseksi. [Masters Thesis]. University of Helsinki; 2016. Available from: http://hdl.handle.net/10138/167524

17. Punnamaraju, Sri Ramya. The Evaluation of the Sedimentation Behavior of Magnesium Hydroxide in the Never Dried State.

Degree: MSP, College of Pharmacy, 2012, University of Toledo Health Science Campus

 The objective of this study is to prepare and evaluate the effect of Poloxamer 407 on the sedimentation behavior of never dried magnesium hydroxide suspensions.… (more)

Subjects/Keywords: Pharmaceuticals; Sedimentation; Poloxamer; never dried suspensions; hindered settling

…88 7.4 Hindered settling parameters for Mg (OH)2 suspended in 0.5% Poloxamer… …88 7.5 Hindered settling parameters for Mg (OH)2 suspended in 0.075% Poloxamer… …91 7.7 Qavg and ε values for Mg (OH)2 suspended in 0.025% Poloxamer… …91 7.8 Qavg and ε values for Mg (OH)2 suspended in 0.5% Poloxamer… …91 7.9 Qavg and ε values for Mg (OH)2 suspended in 0.075% Poloxamer… 

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APA (6th Edition):

Punnamaraju, S. R. (2012). The Evaluation of the Sedimentation Behavior of Magnesium Hydroxide in the Never Dried State. (Masters Thesis). University of Toledo Health Science Campus. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=mco1352945106

Chicago Manual of Style (16th Edition):

Punnamaraju, Sri Ramya. “The Evaluation of the Sedimentation Behavior of Magnesium Hydroxide in the Never Dried State.” 2012. Masters Thesis, University of Toledo Health Science Campus. Accessed October 28, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=mco1352945106.

MLA Handbook (7th Edition):

Punnamaraju, Sri Ramya. “The Evaluation of the Sedimentation Behavior of Magnesium Hydroxide in the Never Dried State.” 2012. Web. 28 Oct 2020.

Vancouver:

Punnamaraju SR. The Evaluation of the Sedimentation Behavior of Magnesium Hydroxide in the Never Dried State. [Internet] [Masters thesis]. University of Toledo Health Science Campus; 2012. [cited 2020 Oct 28]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=mco1352945106.

Council of Science Editors:

Punnamaraju SR. The Evaluation of the Sedimentation Behavior of Magnesium Hydroxide in the Never Dried State. [Masters Thesis]. University of Toledo Health Science Campus; 2012. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=mco1352945106

18. Gandra, Sarath Chandra Reddy. The Preparation and Characterization of Poloxamer-based Temperature-sensitive Hydrogels for Topical Drug Delivery.

Degree: MSP, College of Pharmacy, 2013, University of Toledo Health Science Campus

 Stimuli-sensitive hydrogels change their swelling behavior and drug release by sensing changes in the surrounding environment. One example is temperature-sensitive hydrogels which change their swelling… (more)

Subjects/Keywords: Pharmacy Sciences; Poloxamer; Temperature sensitive; Rheology; Mechanical Properties

…detail below. 1.4 Temperature-sensitive poloxamer-based hydrogels Temperature-sensitive… …and characterization of thermosensitive hydrogels. 8 Poloxamer block co-polymers are… …x28;organic/ aqueous /polar/non-polar). The aqueous solutions of poloxamer are very… …marketed poloxamers with their pluronic name (18). Poloxamer a b Molecular weight… …14600 F127 NF Poloxamer 407 is a commonly used co-polymer in pharmaceutical formulations… 

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APA (6th Edition):

Gandra, S. C. R. (2013). The Preparation and Characterization of Poloxamer-based Temperature-sensitive Hydrogels for Topical Drug Delivery. (Masters Thesis). University of Toledo Health Science Campus. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=mco1373375178

Chicago Manual of Style (16th Edition):

Gandra, Sarath Chandra Reddy. “The Preparation and Characterization of Poloxamer-based Temperature-sensitive Hydrogels for Topical Drug Delivery.” 2013. Masters Thesis, University of Toledo Health Science Campus. Accessed October 28, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=mco1373375178.

MLA Handbook (7th Edition):

Gandra, Sarath Chandra Reddy. “The Preparation and Characterization of Poloxamer-based Temperature-sensitive Hydrogels for Topical Drug Delivery.” 2013. Web. 28 Oct 2020.

Vancouver:

Gandra SCR. The Preparation and Characterization of Poloxamer-based Temperature-sensitive Hydrogels for Topical Drug Delivery. [Internet] [Masters thesis]. University of Toledo Health Science Campus; 2013. [cited 2020 Oct 28]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=mco1373375178.

Council of Science Editors:

Gandra SCR. The Preparation and Characterization of Poloxamer-based Temperature-sensitive Hydrogels for Topical Drug Delivery. [Masters Thesis]. University of Toledo Health Science Campus; 2013. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=mco1373375178


University of Sydney

19. Cheluvappa, Rajkumar. Pathophysiology of Liver Sinusoidal Endothelial Cells .

Degree: 2008, University of Sydney

 Owing to its strategic position in the liver sinusoid, pathologic and morphologic alterations of the Liver Sinusoidal Endothelial Cell (LSEC) have far-reaching repercussions for the… (more)

Subjects/Keywords: Liver; Pimonidazole; Hypoxia; Vascular endothelial growth factor; Vascular endothelial growth factor-receptor 2; Aging; Poloxamer 407; hepatocyte; immunohistochemistry; electron microscopy; liver sinusoidal endothelial cell; fenestrations; oxidative stress; Pseudomonas aeruginosa; pyocyanin; transplantation

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APA (6th Edition):

Cheluvappa, R. (2008). Pathophysiology of Liver Sinusoidal Endothelial Cells . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/2802

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):

Cheluvappa, Rajkumar. “Pathophysiology of Liver Sinusoidal Endothelial Cells .” 2008. Thesis, University of Sydney. Accessed October 28, 2020. http://hdl.handle.net/2123/2802.

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

MLA Handbook (7th Edition):

Cheluvappa, Rajkumar. “Pathophysiology of Liver Sinusoidal Endothelial Cells .” 2008. Web. 28 Oct 2020.

Vancouver:

Cheluvappa R. Pathophysiology of Liver Sinusoidal Endothelial Cells . [Internet] [Thesis]. University of Sydney; 2008. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/2123/2802.

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

Council of Science Editors:

Cheluvappa R. Pathophysiology of Liver Sinusoidal Endothelial Cells . [Thesis]. University of Sydney; 2008. Available from: http://hdl.handle.net/2123/2802

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

.