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You searched for subject:(Simple Micelle Systems Poorly Water soluble Drugs Solubilization Thermodynamic Model Surface Activity). Showing records 1 – 30 of 160653 total matches.

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University of Kentucky

1. Feng, Shaoxin. STUDIES ON DRUG SOLUBILIZATION MECHANISM IN SIMPLE MICELLE SYSTEMS.

Degree: 2009, University of Kentucky

 Poor aqueous solubilities of drug candidates limit the biopharmaceutical usefulness in either oral or parenteral dosage forms. Lipid assemblies, such as micelles, may provide a… (more)

Subjects/Keywords: Simple Micelle Systems|Poorly Water-soluble Drugs|Solubilization|Thermodynamic Model|Surface Activity; Pharmacy and Pharmaceutical Sciences

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

APA (6th Edition):

Feng, S. (2009). STUDIES ON DRUG SOLUBILIZATION MECHANISM IN SIMPLE MICELLE SYSTEMS. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/gradschool_diss/787

Chicago Manual of Style (16th Edition):

Feng, Shaoxin. “STUDIES ON DRUG SOLUBILIZATION MECHANISM IN SIMPLE MICELLE SYSTEMS.” 2009. Doctoral Dissertation, University of Kentucky. Accessed January 21, 2020. https://uknowledge.uky.edu/gradschool_diss/787.

MLA Handbook (7th Edition):

Feng, Shaoxin. “STUDIES ON DRUG SOLUBILIZATION MECHANISM IN SIMPLE MICELLE SYSTEMS.” 2009. Web. 21 Jan 2020.

Vancouver:

Feng S. STUDIES ON DRUG SOLUBILIZATION MECHANISM IN SIMPLE MICELLE SYSTEMS. [Internet] [Doctoral dissertation]. University of Kentucky; 2009. [cited 2020 Jan 21]. Available from: https://uknowledge.uky.edu/gradschool_diss/787.

Council of Science Editors:

Feng S. STUDIES ON DRUG SOLUBILIZATION MECHANISM IN SIMPLE MICELLE SYSTEMS. [Doctoral Dissertation]. University of Kentucky; 2009. Available from: https://uknowledge.uky.edu/gradschool_diss/787


University of Otago

2. Loebmann, Korbinian Arthur Maria. Co-amorphous drug formulations .

Degree: 2013, University of Otago

 Poor aqueous solubility of an active pharmaceutical ingredient (API) is one of the most pressing problems in pharmaceutical research and development because up to 90%… (more)

Subjects/Keywords: co-amorphous; dissolution; amino acids; glass transition; molecular interactions; poorly water soluble drugs

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APA (6th Edition):

Loebmann, K. A. M. (2013). Co-amorphous drug formulations . (Doctoral Dissertation). University of Otago. Retrieved from http://hdl.handle.net/10523/4112

Chicago Manual of Style (16th Edition):

Loebmann, Korbinian Arthur Maria. “Co-amorphous drug formulations .” 2013. Doctoral Dissertation, University of Otago. Accessed January 21, 2020. http://hdl.handle.net/10523/4112.

MLA Handbook (7th Edition):

Loebmann, Korbinian Arthur Maria. “Co-amorphous drug formulations .” 2013. Web. 21 Jan 2020.

Vancouver:

Loebmann KAM. Co-amorphous drug formulations . [Internet] [Doctoral dissertation]. University of Otago; 2013. [cited 2020 Jan 21]. Available from: http://hdl.handle.net/10523/4112.

Council of Science Editors:

Loebmann KAM. Co-amorphous drug formulations . [Doctoral Dissertation]. University of Otago; 2013. Available from: http://hdl.handle.net/10523/4112


University of Texas – Austin

3. Bennett, Ryan Cole. Thermal processing cyclodextrins and thermoplastic polymers for bioavailability enhancement of poorly water-soluble drugs.

Degree: PhD, Pharmaceutical Sciences, 2014, University of Texas – Austin

 With the advent and utility of high throughput screening, the number of drug substances in the developmental pipeline of pharmaceutical industries that are poorly water-soluble(more)

Subjects/Keywords: Thermal processing; Poorly water-soluble drug

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APA (6th Edition):

Bennett, R. C. (2014). Thermal processing cyclodextrins and thermoplastic polymers for bioavailability enhancement of poorly water-soluble drugs. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/31551

Chicago Manual of Style (16th Edition):

Bennett, Ryan Cole. “Thermal processing cyclodextrins and thermoplastic polymers for bioavailability enhancement of poorly water-soluble drugs.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed January 21, 2020. http://hdl.handle.net/2152/31551.

MLA Handbook (7th Edition):

Bennett, Ryan Cole. “Thermal processing cyclodextrins and thermoplastic polymers for bioavailability enhancement of poorly water-soluble drugs.” 2014. Web. 21 Jan 2020.

Vancouver:

Bennett RC. Thermal processing cyclodextrins and thermoplastic polymers for bioavailability enhancement of poorly water-soluble drugs. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2020 Jan 21]. Available from: http://hdl.handle.net/2152/31551.

Council of Science Editors:

Bennett RC. Thermal processing cyclodextrins and thermoplastic polymers for bioavailability enhancement of poorly water-soluble drugs. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/31551


Temple University

4. Narvekar, Mayuri. DEVELOPMENT AND CHARACTERIZATION OF POLYMER-OIL NANOSTRUCTURED CARRIER (PONC) FOR CONTROLLED DELIVERY OF ALL-TRANS RETINOIC ACID (ATRA).

Degree: PhD, 2014, Temple University

Pharmaceutical Sciences

The commonly used PLGA-based delivery systems are often limited by their inadequate drug loading and release properties. This study reports the integration of… (more)

Subjects/Keywords: Pharmaceutical sciences; Nanotechnology;

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APA (6th Edition):

Narvekar, M. (2014). DEVELOPMENT AND CHARACTERIZATION OF POLYMER-OIL NANOSTRUCTURED CARRIER (PONC) FOR CONTROLLED DELIVERY OF ALL-TRANS RETINOIC ACID (ATRA). (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,245651

Chicago Manual of Style (16th Edition):

Narvekar, Mayuri. “DEVELOPMENT AND CHARACTERIZATION OF POLYMER-OIL NANOSTRUCTURED CARRIER (PONC) FOR CONTROLLED DELIVERY OF ALL-TRANS RETINOIC ACID (ATRA).” 2014. Doctoral Dissertation, Temple University. Accessed January 21, 2020. http://digital.library.temple.edu/u?/p245801coll10,245651.

MLA Handbook (7th Edition):

Narvekar, Mayuri. “DEVELOPMENT AND CHARACTERIZATION OF POLYMER-OIL NANOSTRUCTURED CARRIER (PONC) FOR CONTROLLED DELIVERY OF ALL-TRANS RETINOIC ACID (ATRA).” 2014. Web. 21 Jan 2020.

Vancouver:

Narvekar M. DEVELOPMENT AND CHARACTERIZATION OF POLYMER-OIL NANOSTRUCTURED CARRIER (PONC) FOR CONTROLLED DELIVERY OF ALL-TRANS RETINOIC ACID (ATRA). [Internet] [Doctoral dissertation]. Temple University; 2014. [cited 2020 Jan 21]. Available from: http://digital.library.temple.edu/u?/p245801coll10,245651.

Council of Science Editors:

Narvekar M. DEVELOPMENT AND CHARACTERIZATION OF POLYMER-OIL NANOSTRUCTURED CARRIER (PONC) FOR CONTROLLED DELIVERY OF ALL-TRANS RETINOIC ACID (ATRA). [Doctoral Dissertation]. Temple University; 2014. Available from: http://digital.library.temple.edu/u?/p245801coll10,245651


New Jersey Institute of Technology

5. Afolabi, Afolawemi. Batch and continuous production of stable dense suspensions of drug nanoparticles in a wet stirred media mill.

Degree: PhD, Chemical, Biological and Pharmaceutical Engineering, 2013, New Jersey Institute of Technology

  One way to improve the bioavailability of poorly water-soluble drugs is to reduce particle size of drug crystals down to nanoscale via wet stirred… (more)

Subjects/Keywords: Poorly water soluble drugs; Sub 100 nm and media wear; Nanoparticles; Wet stirred media milling; Microhydrodynamics; Rehbinder effect; Chemical Engineering

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APA (6th Edition):

Afolabi, A. (2013). Batch and continuous production of stable dense suspensions of drug nanoparticles in a wet stirred media mill. (Doctoral Dissertation). New Jersey Institute of Technology. Retrieved from https://digitalcommons.njit.edu/dissertations/391

Chicago Manual of Style (16th Edition):

Afolabi, Afolawemi. “Batch and continuous production of stable dense suspensions of drug nanoparticles in a wet stirred media mill.” 2013. Doctoral Dissertation, New Jersey Institute of Technology. Accessed January 21, 2020. https://digitalcommons.njit.edu/dissertations/391.

MLA Handbook (7th Edition):

Afolabi, Afolawemi. “Batch and continuous production of stable dense suspensions of drug nanoparticles in a wet stirred media mill.” 2013. Web. 21 Jan 2020.

Vancouver:

Afolabi A. Batch and continuous production of stable dense suspensions of drug nanoparticles in a wet stirred media mill. [Internet] [Doctoral dissertation]. New Jersey Institute of Technology; 2013. [cited 2020 Jan 21]. Available from: https://digitalcommons.njit.edu/dissertations/391.

Council of Science Editors:

Afolabi A. Batch and continuous production of stable dense suspensions of drug nanoparticles in a wet stirred media mill. [Doctoral Dissertation]. New Jersey Institute of Technology; 2013. Available from: https://digitalcommons.njit.edu/dissertations/391


New Jersey Institute of Technology

6. Li, Meng. Assessment of nanocomposites vs. amorphous solid dispersions for dissolution enhancement of bcs class ii drugs.

Degree: PhD, Chemical, Biological and Pharmaceutical Engineering, 2017, New Jersey Institute of Technology

  Nanoparticle-based formulations (nanocomposites) and amorphous solid dispersions, shortly ASDs, are two major pharmaceutical formulation platforms used for the bioavailability enhancement of poorly water-soluble drugs.… (more)

Subjects/Keywords: Bioavailability enhancement; Poorly water-soluble drugs; Nanoparticles; Amorphous solid dispersion; Wet media milling; Spray drying/Hot melt extrusion; Chemical Engineering

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APA (6th Edition):

Li, M. (2017). Assessment of nanocomposites vs. amorphous solid dispersions for dissolution enhancement of bcs class ii drugs. (Doctoral Dissertation). New Jersey Institute of Technology. Retrieved from https://digitalcommons.njit.edu/dissertations/45

Chicago Manual of Style (16th Edition):

Li, Meng. “Assessment of nanocomposites vs. amorphous solid dispersions for dissolution enhancement of bcs class ii drugs.” 2017. Doctoral Dissertation, New Jersey Institute of Technology. Accessed January 21, 2020. https://digitalcommons.njit.edu/dissertations/45.

MLA Handbook (7th Edition):

Li, Meng. “Assessment of nanocomposites vs. amorphous solid dispersions for dissolution enhancement of bcs class ii drugs.” 2017. Web. 21 Jan 2020.

Vancouver:

Li M. Assessment of nanocomposites vs. amorphous solid dispersions for dissolution enhancement of bcs class ii drugs. [Internet] [Doctoral dissertation]. New Jersey Institute of Technology; 2017. [cited 2020 Jan 21]. Available from: https://digitalcommons.njit.edu/dissertations/45.

Council of Science Editors:

Li M. Assessment of nanocomposites vs. amorphous solid dispersions for dissolution enhancement of bcs class ii drugs. [Doctoral Dissertation]. New Jersey Institute of Technology; 2017. Available from: https://digitalcommons.njit.edu/dissertations/45


Freie Universität Berlin

7. Darwich, May. Löslichkeits-/Bioverfügbarkeitsverbesserung von schwer löslichen Wirkstoffen und ihre Formulierung in Arzneiformen mit kontrollierter Freisetzung.

Degree: 2016, Freie Universität Berlin

 Durch eine schlechte Wasserlöslichkeit ergeben sich erhebliche Herausforderungen, wie die verminderte orale Resorption und Bioverfügbarkeit. Um die Probleme der geringen Löslichkeit zu überwinden, wurden verschiedene… (more)

Subjects/Keywords: solubility enhancement; poorly water-soluble drugs; modified release formulations; 500 Naturwissenschaften und Mathematik::540 Chemie::540 Chemie und zugeordnete Wissenschaften

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APA (6th Edition):

Darwich, M. (2016). Löslichkeits-/Bioverfügbarkeitsverbesserung von schwer löslichen Wirkstoffen und ihre Formulierung in Arzneiformen mit kontrollierter Freisetzung. (Thesis). Freie Universität Berlin. Retrieved from https://refubium.fu-berlin.de/handle/fub188/10487

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):

Darwich, May. “Löslichkeits-/Bioverfügbarkeitsverbesserung von schwer löslichen Wirkstoffen und ihre Formulierung in Arzneiformen mit kontrollierter Freisetzung.” 2016. Thesis, Freie Universität Berlin. Accessed January 21, 2020. https://refubium.fu-berlin.de/handle/fub188/10487.

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

MLA Handbook (7th Edition):

Darwich, May. “Löslichkeits-/Bioverfügbarkeitsverbesserung von schwer löslichen Wirkstoffen und ihre Formulierung in Arzneiformen mit kontrollierter Freisetzung.” 2016. Web. 21 Jan 2020.

Vancouver:

Darwich M. Löslichkeits-/Bioverfügbarkeitsverbesserung von schwer löslichen Wirkstoffen und ihre Formulierung in Arzneiformen mit kontrollierter Freisetzung. [Internet] [Thesis]. Freie Universität Berlin; 2016. [cited 2020 Jan 21]. Available from: https://refubium.fu-berlin.de/handle/fub188/10487.

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

Council of Science Editors:

Darwich M. Löslichkeits-/Bioverfügbarkeitsverbesserung von schwer löslichen Wirkstoffen und ihre Formulierung in Arzneiformen mit kontrollierter Freisetzung. [Thesis]. Freie Universität Berlin; 2016. Available from: https://refubium.fu-berlin.de/handle/fub188/10487

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


University College Cork

8. O'Shea, Joseph P. Mechanistic understanding of bioenabling formulation approaches to improve oral bioavailability using porcine in vivo and in silico models.

Degree: 2018, University College Cork

 Objectives: Mesoporous silicas (SLC) have demonstrated considerable potential to improve bioavailability of poorly soluble drugs by facilitating rapid dissolution and generating supersaturation. The addition of… (more)

Subjects/Keywords: Poorly water soluble drugs (PWSD); Pig model; Biorelevant dissolution testing; In vitro in vivo correlations (IVIVC); Physiologically based pharmacokinetic modelling; Lipid based formulations; Food effect; Mesoporous silica; Bioenabling formulations; Formulation screening; Oral drug absorption; Preclinical animal model

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APA (6th Edition):

O'Shea, J. P. (2018). Mechanistic understanding of bioenabling formulation approaches to improve oral bioavailability using porcine in vivo and in silico models. (Thesis). University College Cork. Retrieved from http://hdl.handle.net/10468/6710

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):

O'Shea, Joseph P. “Mechanistic understanding of bioenabling formulation approaches to improve oral bioavailability using porcine in vivo and in silico models.” 2018. Thesis, University College Cork. Accessed January 21, 2020. http://hdl.handle.net/10468/6710.

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

MLA Handbook (7th Edition):

O'Shea, Joseph P. “Mechanistic understanding of bioenabling formulation approaches to improve oral bioavailability using porcine in vivo and in silico models.” 2018. Web. 21 Jan 2020.

Vancouver:

O'Shea JP. Mechanistic understanding of bioenabling formulation approaches to improve oral bioavailability using porcine in vivo and in silico models. [Internet] [Thesis]. University College Cork; 2018. [cited 2020 Jan 21]. Available from: http://hdl.handle.net/10468/6710.

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

Council of Science Editors:

O'Shea JP. Mechanistic understanding of bioenabling formulation approaches to improve oral bioavailability using porcine in vivo and in silico models. [Thesis]. University College Cork; 2018. Available from: http://hdl.handle.net/10468/6710

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


Université Catholique de Louvain

9. Duhem, Nicolas. New derivatives of vitamin E as nanovectors for poorly soluble drugs and anticancer agents.

Degree: 2013, Université Catholique de Louvain

 The aim of this work was to develop novel vitamin E conjugates for the vectorization of active pharmaceutical ingredients through nanotechnologies. The physico-chemical and biological… (more)

Subjects/Keywords: nanoparticle; polymeric micelle; self-assembled prodrug; vitamin E; poorly soluble drug; doxorubicin

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APA (6th Edition):

Duhem, N. (2013). New derivatives of vitamin E as nanovectors for poorly soluble drugs and anticancer agents. (Thesis). Université Catholique de Louvain. Retrieved from http://hdl.handle.net/2078.1/135380

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):

Duhem, Nicolas. “New derivatives of vitamin E as nanovectors for poorly soluble drugs and anticancer agents.” 2013. Thesis, Université Catholique de Louvain. Accessed January 21, 2020. http://hdl.handle.net/2078.1/135380.

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

MLA Handbook (7th Edition):

Duhem, Nicolas. “New derivatives of vitamin E as nanovectors for poorly soluble drugs and anticancer agents.” 2013. Web. 21 Jan 2020.

Vancouver:

Duhem N. New derivatives of vitamin E as nanovectors for poorly soluble drugs and anticancer agents. [Internet] [Thesis]. Université Catholique de Louvain; 2013. [cited 2020 Jan 21]. Available from: http://hdl.handle.net/2078.1/135380.

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

Council of Science Editors:

Duhem N. New derivatives of vitamin E as nanovectors for poorly soluble drugs and anticancer agents. [Thesis]. Université Catholique de Louvain; 2013. Available from: http://hdl.handle.net/2078.1/135380

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


University of Tennessee – Knoxville

10. Jiang, Xueguang. Synthesis and Solution Behavior of Doubly Responsive Hydrophilic Block Copolymers.

Degree: 2010, University of Tennessee – Knoxville

 This dissertation presents the synthesis of stimuli-sensitive hydrophilic polymers, particularly doubly responsive hydrophilic block copolymers, by controlled radical polymerizations and the study of their solution… (more)

Subjects/Keywords: Thermosensitive; water-soluble; micelle; gel; stimuli-responsive

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APA (6th Edition):

Jiang, X. (2010). Synthesis and Solution Behavior of Doubly Responsive Hydrophilic Block Copolymers. (Doctoral Dissertation). University of Tennessee – Knoxville. Retrieved from https://trace.tennessee.edu/utk_graddiss/809

Chicago Manual of Style (16th Edition):

Jiang, Xueguang. “Synthesis and Solution Behavior of Doubly Responsive Hydrophilic Block Copolymers.” 2010. Doctoral Dissertation, University of Tennessee – Knoxville. Accessed January 21, 2020. https://trace.tennessee.edu/utk_graddiss/809.

MLA Handbook (7th Edition):

Jiang, Xueguang. “Synthesis and Solution Behavior of Doubly Responsive Hydrophilic Block Copolymers.” 2010. Web. 21 Jan 2020.

Vancouver:

Jiang X. Synthesis and Solution Behavior of Doubly Responsive Hydrophilic Block Copolymers. [Internet] [Doctoral dissertation]. University of Tennessee – Knoxville; 2010. [cited 2020 Jan 21]. Available from: https://trace.tennessee.edu/utk_graddiss/809.

Council of Science Editors:

Jiang X. Synthesis and Solution Behavior of Doubly Responsive Hydrophilic Block Copolymers. [Doctoral Dissertation]. University of Tennessee – Knoxville; 2010. Available from: https://trace.tennessee.edu/utk_graddiss/809


University of Texas – Austin

11. -6334-3030. Application of hot-melt extrusion in the manufacturing of amorphous solid dispersions containing thermally labile drugs.

Degree: PhD, Pharmaceutical Sciences, 2017, University of Texas – Austin

 Hot-melt extrusion has gained favor over traditional pharmaceutical formulation techniques in bioavailability/solubility enhancement because it is a solvent-free and continuous operation process that does not… (more)

Subjects/Keywords: Chemical stability; Amorphous; Solid dispersion; Poorly water-soluble drugs; Hot-melt extrusion; Thermally labile drugs; Solubility enhancement; Bioavailability enhancement; Flory-Huggins theory; Gliclazide

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APA (6th Edition):

-6334-3030. (2017). Application of hot-melt extrusion in the manufacturing of amorphous solid dispersions containing thermally labile drugs. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/47149

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

Chicago Manual of Style (16th Edition):

-6334-3030. “Application of hot-melt extrusion in the manufacturing of amorphous solid dispersions containing thermally labile drugs.” 2017. Doctoral Dissertation, University of Texas – Austin. Accessed January 21, 2020. http://hdl.handle.net/2152/47149.

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

MLA Handbook (7th Edition):

-6334-3030. “Application of hot-melt extrusion in the manufacturing of amorphous solid dispersions containing thermally labile drugs.” 2017. Web. 21 Jan 2020.

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

Vancouver:

-6334-3030. Application of hot-melt extrusion in the manufacturing of amorphous solid dispersions containing thermally labile drugs. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2017. [cited 2020 Jan 21]. Available from: http://hdl.handle.net/2152/47149.

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

Council of Science Editors:

-6334-3030. Application of hot-melt extrusion in the manufacturing of amorphous solid dispersions containing thermally labile drugs. [Doctoral Dissertation]. University of Texas – Austin; 2017. Available from: http://hdl.handle.net/2152/47149

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


Euskal Herriko Unibertsitatea / Universidad del País Vasco

12. Beloqui García, Ana. Nanostructured lipid carriers as vehicles for the delivery of poorly water-soluble drugs .

Degree: 2013, Euskal Herriko Unibertsitatea / Universidad del País Vasco

 El objetivo de esta tesis ha sido el desarrollo de una formulación basada en NLCs para la administración de fármacos poco solubles, tanto por vía… (more)

Subjects/Keywords: poorly-soluble; drugs; absortion; Caco-2; M cell; biodistribution; nanoparticles

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APA (6th Edition):

Beloqui García, A. (2013). Nanostructured lipid carriers as vehicles for the delivery of poorly water-soluble drugs . (Doctoral Dissertation). Euskal Herriko Unibertsitatea / Universidad del País Vasco. Retrieved from http://hdl.handle.net/10810/18371

Chicago Manual of Style (16th Edition):

Beloqui García, Ana. “Nanostructured lipid carriers as vehicles for the delivery of poorly water-soluble drugs .” 2013. Doctoral Dissertation, Euskal Herriko Unibertsitatea / Universidad del País Vasco. Accessed January 21, 2020. http://hdl.handle.net/10810/18371.

MLA Handbook (7th Edition):

Beloqui García, Ana. “Nanostructured lipid carriers as vehicles for the delivery of poorly water-soluble drugs .” 2013. Web. 21 Jan 2020.

Vancouver:

Beloqui García A. Nanostructured lipid carriers as vehicles for the delivery of poorly water-soluble drugs . [Internet] [Doctoral dissertation]. Euskal Herriko Unibertsitatea / Universidad del País Vasco; 2013. [cited 2020 Jan 21]. Available from: http://hdl.handle.net/10810/18371.

Council of Science Editors:

Beloqui García A. Nanostructured lipid carriers as vehicles for the delivery of poorly water-soluble drugs . [Doctoral Dissertation]. Euskal Herriko Unibertsitatea / Universidad del País Vasco; 2013. Available from: http://hdl.handle.net/10810/18371


University of Toronto

13. Lugtu-Pe, Jamie Anne. Controlled Release as a Strategy to Prevent Solution-mediated Phase Transformation in Amorphous Solid Dispersions: Effect of Dosage Form Design.

Degree: 2014, University of Toronto

The purpose of this study was to define the limits of developing a controlled-release amorphous solid dispersion (CRSD) system intended for enhancing the bioavailability of… (more)

Subjects/Keywords: controlled release; dosage form design; poorly soluble drugs; solid dispersion; 0572

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APA (6th Edition):

Lugtu-Pe, J. A. (2014). Controlled Release as a Strategy to Prevent Solution-mediated Phase Transformation in Amorphous Solid Dispersions: Effect of Dosage Form Design. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/81085

Chicago Manual of Style (16th Edition):

Lugtu-Pe, Jamie Anne. “Controlled Release as a Strategy to Prevent Solution-mediated Phase Transformation in Amorphous Solid Dispersions: Effect of Dosage Form Design.” 2014. Masters Thesis, University of Toronto. Accessed January 21, 2020. http://hdl.handle.net/1807/81085.

MLA Handbook (7th Edition):

Lugtu-Pe, Jamie Anne. “Controlled Release as a Strategy to Prevent Solution-mediated Phase Transformation in Amorphous Solid Dispersions: Effect of Dosage Form Design.” 2014. Web. 21 Jan 2020.

Vancouver:

Lugtu-Pe JA. Controlled Release as a Strategy to Prevent Solution-mediated Phase Transformation in Amorphous Solid Dispersions: Effect of Dosage Form Design. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2020 Jan 21]. Available from: http://hdl.handle.net/1807/81085.

Council of Science Editors:

Lugtu-Pe JA. Controlled Release as a Strategy to Prevent Solution-mediated Phase Transformation in Amorphous Solid Dispersions: Effect of Dosage Form Design. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/81085


University of Toronto

14. Lugtu-Pe, Jamie Anne. Controlled Release as a Strategy to Prevent Solution-mediated Phase Transformation in Amorphous Solid Dispersions: Effect of Dosage Form Design.

Degree: 2014, University of Toronto

The purpose of this study was to define the limits of developing a controlled-release amorphous solid dispersion (CRSD) system intended for enhancing the bioavailability of… (more)

Subjects/Keywords: controlled release; dosage form design; poorly soluble drugs; solid dispersion; 0572

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APA (6th Edition):

Lugtu-Pe, J. A. (2014). Controlled Release as a Strategy to Prevent Solution-mediated Phase Transformation in Amorphous Solid Dispersions: Effect of Dosage Form Design. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/81086

Chicago Manual of Style (16th Edition):

Lugtu-Pe, Jamie Anne. “Controlled Release as a Strategy to Prevent Solution-mediated Phase Transformation in Amorphous Solid Dispersions: Effect of Dosage Form Design.” 2014. Masters Thesis, University of Toronto. Accessed January 21, 2020. http://hdl.handle.net/1807/81086.

MLA Handbook (7th Edition):

Lugtu-Pe, Jamie Anne. “Controlled Release as a Strategy to Prevent Solution-mediated Phase Transformation in Amorphous Solid Dispersions: Effect of Dosage Form Design.” 2014. Web. 21 Jan 2020.

Vancouver:

Lugtu-Pe JA. Controlled Release as a Strategy to Prevent Solution-mediated Phase Transformation in Amorphous Solid Dispersions: Effect of Dosage Form Design. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2020 Jan 21]. Available from: http://hdl.handle.net/1807/81086.

Council of Science Editors:

Lugtu-Pe JA. Controlled Release as a Strategy to Prevent Solution-mediated Phase Transformation in Amorphous Solid Dispersions: Effect of Dosage Form Design. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/81086


University of Bradford

15. Bansiwal, Mukesh. Investigation of drug ionic liquid salts for topical delivery systems.

Degree: PhD, 2017, University of Bradford

 Pharmaceutical companies and FDA (Federal Drug Administration) rules rely heavily on crystalline active pharmaceutical ingredients delivered as tablets and powders in the form of neutral… (more)

Subjects/Keywords: Ionic liquids (ILs); Poorly water soluble drugs; Topical drug delivery; Partitioning; Ion-pairing; Carbomer; Oligomer; Benzalkonium ILs; Ionic liquids with mixed anions; Hydrogel; NSAIDs; Sulfacetamide; Pharmaceutical performance

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APA (6th Edition):

Bansiwal, M. (2017). Investigation of drug ionic liquid salts for topical delivery systems. (Doctoral Dissertation). University of Bradford. Retrieved from http://hdl.handle.net/10454/17161

Chicago Manual of Style (16th Edition):

Bansiwal, Mukesh. “Investigation of drug ionic liquid salts for topical delivery systems.” 2017. Doctoral Dissertation, University of Bradford. Accessed January 21, 2020. http://hdl.handle.net/10454/17161.

MLA Handbook (7th Edition):

Bansiwal, Mukesh. “Investigation of drug ionic liquid salts for topical delivery systems.” 2017. Web. 21 Jan 2020.

Vancouver:

Bansiwal M. Investigation of drug ionic liquid salts for topical delivery systems. [Internet] [Doctoral dissertation]. University of Bradford; 2017. [cited 2020 Jan 21]. Available from: http://hdl.handle.net/10454/17161.

Council of Science Editors:

Bansiwal M. Investigation of drug ionic liquid salts for topical delivery systems. [Doctoral Dissertation]. University of Bradford; 2017. Available from: http://hdl.handle.net/10454/17161


University of Toledo Health Science Campus

16. Patel, Niraja Kiritkumar. Development and Characterization of Ternary Solid Dispersion Granules of Poorly Water Soluble Drugs: Diflunisal and Mefenamic acid.

Degree: MSP, College of Pharmacy, 2011, University of Toledo Health Science Campus

  The objective of this study was to increase the solubility of two poorly water soluble drugs, namely Diflunisal USP and Mefenamic Acid USP, by… (more)

Subjects/Keywords: Pharmaceuticals; Pharmacy Sciences; poorly water soluble; Ternery solid dispersion granules; Diflunisal.Mefenamic Acid

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APA (6th Edition):

Patel, N. K. (2011). Development and Characterization of Ternary Solid Dispersion Granules of Poorly Water Soluble Drugs: Diflunisal and Mefenamic acid. (Masters Thesis). University of Toledo Health Science Campus. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=mco1311094362

Chicago Manual of Style (16th Edition):

Patel, Niraja Kiritkumar. “Development and Characterization of Ternary Solid Dispersion Granules of Poorly Water Soluble Drugs: Diflunisal and Mefenamic acid.” 2011. Masters Thesis, University of Toledo Health Science Campus. Accessed January 21, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=mco1311094362.

MLA Handbook (7th Edition):

Patel, Niraja Kiritkumar. “Development and Characterization of Ternary Solid Dispersion Granules of Poorly Water Soluble Drugs: Diflunisal and Mefenamic acid.” 2011. Web. 21 Jan 2020.

Vancouver:

Patel NK. Development and Characterization of Ternary Solid Dispersion Granules of Poorly Water Soluble Drugs: Diflunisal and Mefenamic acid. [Internet] [Masters thesis]. University of Toledo Health Science Campus; 2011. [cited 2020 Jan 21]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=mco1311094362.

Council of Science Editors:

Patel NK. Development and Characterization of Ternary Solid Dispersion Granules of Poorly Water Soluble Drugs: Diflunisal and Mefenamic acid. [Masters Thesis]. University of Toledo Health Science Campus; 2011. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=mco1311094362


University of Sydney

17. Saffari, Morteza. Enhancements in Spray-Dried Powder Functionality, Using Multistage Fluidized-Bed Drying and a New Templating Process .

Degree: 2015, University of Sydney

 Spray drying is a technique that is widely applied to produce dry powders from their liquid or slurry states in the food and pharmaceutical industries.… (more)

Subjects/Keywords: highly porous excipients; spray drying; fluidized-bed drying; templating process; poorly water-soluble drug; crystallization

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APA (6th Edition):

Saffari, M. (2015). Enhancements in Spray-Dried Powder Functionality, Using Multistage Fluidized-Bed Drying and a New Templating Process . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/14711

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):

Saffari, Morteza. “Enhancements in Spray-Dried Powder Functionality, Using Multistage Fluidized-Bed Drying and a New Templating Process .” 2015. Thesis, University of Sydney. Accessed January 21, 2020. http://hdl.handle.net/2123/14711.

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

MLA Handbook (7th Edition):

Saffari, Morteza. “Enhancements in Spray-Dried Powder Functionality, Using Multistage Fluidized-Bed Drying and a New Templating Process .” 2015. Web. 21 Jan 2020.

Vancouver:

Saffari M. Enhancements in Spray-Dried Powder Functionality, Using Multistage Fluidized-Bed Drying and a New Templating Process . [Internet] [Thesis]. University of Sydney; 2015. [cited 2020 Jan 21]. Available from: http://hdl.handle.net/2123/14711.

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

Council of Science Editors:

Saffari M. Enhancements in Spray-Dried Powder Functionality, Using Multistage Fluidized-Bed Drying and a New Templating Process . [Thesis]. University of Sydney; 2015. Available from: http://hdl.handle.net/2123/14711

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

18. 伊藤, 弘一. 微粒子形成による難水溶性医薬品の溶解性改善に関する研究 : A study on agueous solubility improvement of poorly water-soluble drugs by fine particle formation.

Degree: 2003, Chiba University / 千葉大学

研究科: 千葉大学大学院薬学研究院

学位:千大院薬博乙第242号

Advisors/Committee Members: 千葉大学大学院薬学研究院.

Subjects/Keywords: poorly water-soluble drug; micro emulsion; solubilization; nanoparticle; 難水溶性医薬品; マイクロエマルジョン; 可溶化; ナノ粒子

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APA (6th Edition):

伊藤, . (2003). 微粒子形成による難水溶性医薬品の溶解性改善に関する研究 : A study on agueous solubility improvement of poorly water-soluble drugs by fine particle formation. (Thesis). Chiba University / 千葉大学. Retrieved from http://opac.ll.chiba-u.jp/da/curator/900022627/

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):

伊藤, 弘一. “微粒子形成による難水溶性医薬品の溶解性改善に関する研究 : A study on agueous solubility improvement of poorly water-soluble drugs by fine particle formation.” 2003. Thesis, Chiba University / 千葉大学. Accessed January 21, 2020. http://opac.ll.chiba-u.jp/da/curator/900022627/.

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

MLA Handbook (7th Edition):

伊藤, 弘一. “微粒子形成による難水溶性医薬品の溶解性改善に関する研究 : A study on agueous solubility improvement of poorly water-soluble drugs by fine particle formation.” 2003. Web. 21 Jan 2020.

Vancouver:

伊藤 . 微粒子形成による難水溶性医薬品の溶解性改善に関する研究 : A study on agueous solubility improvement of poorly water-soluble drugs by fine particle formation. [Internet] [Thesis]. Chiba University / 千葉大学; 2003. [cited 2020 Jan 21]. Available from: http://opac.ll.chiba-u.jp/da/curator/900022627/.

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

Council of Science Editors:

伊藤 . 微粒子形成による難水溶性医薬品の溶解性改善に関する研究 : A study on agueous solubility improvement of poorly water-soluble drugs by fine particle formation. [Thesis]. Chiba University / 千葉大学; 2003. Available from: http://opac.ll.chiba-u.jp/da/curator/900022627/

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

19. Setiawan, Nico. UNDERSTANDING THE THERMODYNAMICS AND ORAL ABSORPTION POTENTIAL OF PHARMACEUTICAL AMORPHOUS SOLID DISPERSIONS.

Degree: 2018, University of Kentucky

 Supersaturating drug delivery systems, such as amorphous solid dispersions (ASDs), have been used extensively to elevate the apparent solubility and oral bioavailability of poorly water-soluble(more)

Subjects/Keywords: supersaturation; crystallization; amorphous; poorly water-soluble drugs; excipients; absorption; Chemical Engineering; Pharmacy and Pharmaceutical Sciences

…70 Chapter 3 - What is the True Driving Force for Absorption of Poorly Water-Soluble Drugs… …NCEs have been identified as being poorly water-soluble, which is inextricably linked to the… …poorly soluble drugs with PVP and concluded that miscibility could be maintained with low ASD… …65 2.5.2 Impact of Water on the Activity Coefficient and Chemical Potential of the API in… …63 Table 3.1 Summary of E2 thermodynamic activity, free drug concentration, and number of… 

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APA (6th Edition):

Setiawan, N. (2018). UNDERSTANDING THE THERMODYNAMICS AND ORAL ABSORPTION POTENTIAL OF PHARMACEUTICAL AMORPHOUS SOLID DISPERSIONS. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/pharmacy_etds/85

Chicago Manual of Style (16th Edition):

Setiawan, Nico. “UNDERSTANDING THE THERMODYNAMICS AND ORAL ABSORPTION POTENTIAL OF PHARMACEUTICAL AMORPHOUS SOLID DISPERSIONS.” 2018. Doctoral Dissertation, University of Kentucky. Accessed January 21, 2020. https://uknowledge.uky.edu/pharmacy_etds/85.

MLA Handbook (7th Edition):

Setiawan, Nico. “UNDERSTANDING THE THERMODYNAMICS AND ORAL ABSORPTION POTENTIAL OF PHARMACEUTICAL AMORPHOUS SOLID DISPERSIONS.” 2018. Web. 21 Jan 2020.

Vancouver:

Setiawan N. UNDERSTANDING THE THERMODYNAMICS AND ORAL ABSORPTION POTENTIAL OF PHARMACEUTICAL AMORPHOUS SOLID DISPERSIONS. [Internet] [Doctoral dissertation]. University of Kentucky; 2018. [cited 2020 Jan 21]. Available from: https://uknowledge.uky.edu/pharmacy_etds/85.

Council of Science Editors:

Setiawan N. UNDERSTANDING THE THERMODYNAMICS AND ORAL ABSORPTION POTENTIAL OF PHARMACEUTICAL AMORPHOUS SOLID DISPERSIONS. [Doctoral Dissertation]. University of Kentucky; 2018. Available from: https://uknowledge.uky.edu/pharmacy_etds/85

20. LOW QIAO JUN, ARIANA. DEVELOPMENT OF ORODISPERSIBLE FILMS PRODUCED BY HOT-MELT EXTRUSION FOR POORLY WATER SOLUBLE DRUGS.

Degree: 2015, National University of Singapore

Subjects/Keywords: hot-melt extrusion; amorphous solid dispersion; orodispersible films; poorly water soluble drugs; kollidon; soluplus

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APA (6th Edition):

LOW QIAO JUN, A. (2015). DEVELOPMENT OF ORODISPERSIBLE FILMS PRODUCED BY HOT-MELT EXTRUSION FOR POORLY WATER SOLUBLE DRUGS. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/122645

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):

LOW QIAO JUN, ARIANA. “DEVELOPMENT OF ORODISPERSIBLE FILMS PRODUCED BY HOT-MELT EXTRUSION FOR POORLY WATER SOLUBLE DRUGS.” 2015. Thesis, National University of Singapore. Accessed January 21, 2020. http://scholarbank.nus.edu.sg/handle/10635/122645.

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

MLA Handbook (7th Edition):

LOW QIAO JUN, ARIANA. “DEVELOPMENT OF ORODISPERSIBLE FILMS PRODUCED BY HOT-MELT EXTRUSION FOR POORLY WATER SOLUBLE DRUGS.” 2015. Web. 21 Jan 2020.

Vancouver:

LOW QIAO JUN A. DEVELOPMENT OF ORODISPERSIBLE FILMS PRODUCED BY HOT-MELT EXTRUSION FOR POORLY WATER SOLUBLE DRUGS. [Internet] [Thesis]. National University of Singapore; 2015. [cited 2020 Jan 21]. Available from: http://scholarbank.nus.edu.sg/handle/10635/122645.

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

Council of Science Editors:

LOW QIAO JUN A. DEVELOPMENT OF ORODISPERSIBLE FILMS PRODUCED BY HOT-MELT EXTRUSION FOR POORLY WATER SOLUBLE DRUGS. [Thesis]. National University of Singapore; 2015. Available from: http://scholarbank.nus.edu.sg/handle/10635/122645

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


Temple University

21. Thakare, Kalpana. THE EVALUATION OF LARCH ARABINOGALACTAN AS A NEW CARRIER IN THE FORMULATION OF SOLID DISPERSIONS OF POORLY WATER- SOLUBLE DRUGS.

Degree: PhD, 2013, Temple University

Pharmaceutical Sciences

Advanced drug discovery techniques have produced more lipophilic compounds. Formation of an amorphous solid dispersion of such poorly water-soluble drugs improves their solubility… (more)

Subjects/Keywords: Pharmaceutical sciences;

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APA (6th Edition):

Thakare, K. (2013). THE EVALUATION OF LARCH ARABINOGALACTAN AS A NEW CARRIER IN THE FORMULATION OF SOLID DISPERSIONS OF POORLY WATER- SOLUBLE DRUGS. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,232942

Chicago Manual of Style (16th Edition):

Thakare, Kalpana. “THE EVALUATION OF LARCH ARABINOGALACTAN AS A NEW CARRIER IN THE FORMULATION OF SOLID DISPERSIONS OF POORLY WATER- SOLUBLE DRUGS.” 2013. Doctoral Dissertation, Temple University. Accessed January 21, 2020. http://digital.library.temple.edu/u?/p245801coll10,232942.

MLA Handbook (7th Edition):

Thakare, Kalpana. “THE EVALUATION OF LARCH ARABINOGALACTAN AS A NEW CARRIER IN THE FORMULATION OF SOLID DISPERSIONS OF POORLY WATER- SOLUBLE DRUGS.” 2013. Web. 21 Jan 2020.

Vancouver:

Thakare K. THE EVALUATION OF LARCH ARABINOGALACTAN AS A NEW CARRIER IN THE FORMULATION OF SOLID DISPERSIONS OF POORLY WATER- SOLUBLE DRUGS. [Internet] [Doctoral dissertation]. Temple University; 2013. [cited 2020 Jan 21]. Available from: http://digital.library.temple.edu/u?/p245801coll10,232942.

Council of Science Editors:

Thakare K. THE EVALUATION OF LARCH ARABINOGALACTAN AS A NEW CARRIER IN THE FORMULATION OF SOLID DISPERSIONS OF POORLY WATER- SOLUBLE DRUGS. [Doctoral Dissertation]. Temple University; 2013. Available from: http://digital.library.temple.edu/u?/p245801coll10,232942


Temple University

22. Puppolo, Michael McBride. BIOMIMETIC DISSOLUTION: A TOOL TO EVALUATE AMORPHOUS SOLID DISPERSION PERFORMANCE.

Degree: PhD, 2017, Temple University

Chemistry

The pharmaceutical industry is at a critical juncture. With little remnants of the “Golden Age of the Pharmaceuticals” and applied pressure from large companies… (more)

Subjects/Keywords: Analytical chemistry;

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APA (6th Edition):

Puppolo, M. M. (2017). BIOMIMETIC DISSOLUTION: A TOOL TO EVALUATE AMORPHOUS SOLID DISPERSION PERFORMANCE. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,452599

Chicago Manual of Style (16th Edition):

Puppolo, Michael McBride. “BIOMIMETIC DISSOLUTION: A TOOL TO EVALUATE AMORPHOUS SOLID DISPERSION PERFORMANCE.” 2017. Doctoral Dissertation, Temple University. Accessed January 21, 2020. http://digital.library.temple.edu/u?/p245801coll10,452599.

MLA Handbook (7th Edition):

Puppolo, Michael McBride. “BIOMIMETIC DISSOLUTION: A TOOL TO EVALUATE AMORPHOUS SOLID DISPERSION PERFORMANCE.” 2017. Web. 21 Jan 2020.

Vancouver:

Puppolo MM. BIOMIMETIC DISSOLUTION: A TOOL TO EVALUATE AMORPHOUS SOLID DISPERSION PERFORMANCE. [Internet] [Doctoral dissertation]. Temple University; 2017. [cited 2020 Jan 21]. Available from: http://digital.library.temple.edu/u?/p245801coll10,452599.

Council of Science Editors:

Puppolo MM. BIOMIMETIC DISSOLUTION: A TOOL TO EVALUATE AMORPHOUS SOLID DISPERSION PERFORMANCE. [Doctoral Dissertation]. Temple University; 2017. Available from: http://digital.library.temple.edu/u?/p245801coll10,452599

23. Resende de Azevedo, Jacqueline. Etude de la cristallisation d’une nouvelle molécule à efficacité cardiotonique dans un mélange liquide ionique - eau : Crystallization study of a new cardiotonic drug in an ionic liquid–water mixture.

Degree: Docteur es, Génie des Procédés et de l'Environnement, 2014, Ecole nationale des Mines d'Albi-Carmaux

La cristallisation par effet anti-solvant, comme technique de production de micro/nanoparticules, présente certains inconvénients. En effet, pour des molécules nouvellement synthétisées ou découvertes, comme le… (more)

Subjects/Keywords: Molécule hydrophobe; Cristallisation; Liquide ionique; Solubilité; Atomisation; Poorly water-soluble drug; Crystallization; Ionic liquid; Solubility; Spray drying; 660.2

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APA (6th Edition):

Resende de Azevedo, J. (2014). Etude de la cristallisation d’une nouvelle molécule à efficacité cardiotonique dans un mélange liquide ionique - eau : Crystallization study of a new cardiotonic drug in an ionic liquid–water mixture. (Doctoral Dissertation). Ecole nationale des Mines d'Albi-Carmaux. Retrieved from http://www.theses.fr/2014EMAC0009

Chicago Manual of Style (16th Edition):

Resende de Azevedo, Jacqueline. “Etude de la cristallisation d’une nouvelle molécule à efficacité cardiotonique dans un mélange liquide ionique - eau : Crystallization study of a new cardiotonic drug in an ionic liquid–water mixture.” 2014. Doctoral Dissertation, Ecole nationale des Mines d'Albi-Carmaux. Accessed January 21, 2020. http://www.theses.fr/2014EMAC0009.

MLA Handbook (7th Edition):

Resende de Azevedo, Jacqueline. “Etude de la cristallisation d’une nouvelle molécule à efficacité cardiotonique dans un mélange liquide ionique - eau : Crystallization study of a new cardiotonic drug in an ionic liquid–water mixture.” 2014. Web. 21 Jan 2020.

Vancouver:

Resende de Azevedo J. Etude de la cristallisation d’une nouvelle molécule à efficacité cardiotonique dans un mélange liquide ionique - eau : Crystallization study of a new cardiotonic drug in an ionic liquid–water mixture. [Internet] [Doctoral dissertation]. Ecole nationale des Mines d'Albi-Carmaux; 2014. [cited 2020 Jan 21]. Available from: http://www.theses.fr/2014EMAC0009.

Council of Science Editors:

Resende de Azevedo J. Etude de la cristallisation d’une nouvelle molécule à efficacité cardiotonique dans un mélange liquide ionique - eau : Crystallization study of a new cardiotonic drug in an ionic liquid–water mixture. [Doctoral Dissertation]. Ecole nationale des Mines d'Albi-Carmaux; 2014. Available from: http://www.theses.fr/2014EMAC0009


University of Kentucky

24. Hollis, Christin P. NANOCRYSTALS OF CHEMOTHERAPEUTIC AGENTS FOR CANCER THERANOSTICS: DEVELOPMENT AND IN VITRO AND IN VIVO EVALUATION.

Degree: 2012, University of Kentucky

 The majority of pharmacologically active chemotherapeutics are poorly water soluble. Solubilization enhancement by the utilization of organic solvents often leads to adverse side effects. Nanoparticle-based… (more)

Subjects/Keywords: nanocrystals; theranostics; poorly water soluble; drug delivery; fluorescence; Nanoscience and Nanotechnology; Other Pharmacy and Pharmaceutical Sciences; Therapeutics

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APA (6th Edition):

Hollis, C. P. (2012). NANOCRYSTALS OF CHEMOTHERAPEUTIC AGENTS FOR CANCER THERANOSTICS: DEVELOPMENT AND IN VITRO AND IN VIVO EVALUATION. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/pharmacy_etds/17

Chicago Manual of Style (16th Edition):

Hollis, Christin P. “NANOCRYSTALS OF CHEMOTHERAPEUTIC AGENTS FOR CANCER THERANOSTICS: DEVELOPMENT AND IN VITRO AND IN VIVO EVALUATION.” 2012. Doctoral Dissertation, University of Kentucky. Accessed January 21, 2020. https://uknowledge.uky.edu/pharmacy_etds/17.

MLA Handbook (7th Edition):

Hollis, Christin P. “NANOCRYSTALS OF CHEMOTHERAPEUTIC AGENTS FOR CANCER THERANOSTICS: DEVELOPMENT AND IN VITRO AND IN VIVO EVALUATION.” 2012. Web. 21 Jan 2020.

Vancouver:

Hollis CP. NANOCRYSTALS OF CHEMOTHERAPEUTIC AGENTS FOR CANCER THERANOSTICS: DEVELOPMENT AND IN VITRO AND IN VIVO EVALUATION. [Internet] [Doctoral dissertation]. University of Kentucky; 2012. [cited 2020 Jan 21]. Available from: https://uknowledge.uky.edu/pharmacy_etds/17.

Council of Science Editors:

Hollis CP. NANOCRYSTALS OF CHEMOTHERAPEUTIC AGENTS FOR CANCER THERANOSTICS: DEVELOPMENT AND IN VITRO AND IN VIVO EVALUATION. [Doctoral Dissertation]. University of Kentucky; 2012. Available from: https://uknowledge.uky.edu/pharmacy_etds/17


New Jersey Institute of Technology

25. Vizzotti, Emanuel Joseph. Production of stable bcs class ii drug suspensions by melt emulsification and subsequent incorporation into polymer strip films.

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

  One of the ways to improve the dissolution rate of poorly water-soluble drugs is to produce fine drug particles with increased surface area. This… (more)

Subjects/Keywords: Water-soluble drugs; Dissolution rate; Melt emulsification technique; Chemical Engineering

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APA (6th Edition):

Vizzotti, E. J. (2013). Production of stable bcs class ii drug suspensions by melt emulsification and subsequent incorporation into polymer strip films. (Thesis). New Jersey Institute of Technology. Retrieved from https://digitalcommons.njit.edu/theses/151

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):

Vizzotti, Emanuel Joseph. “Production of stable bcs class ii drug suspensions by melt emulsification and subsequent incorporation into polymer strip films.” 2013. Thesis, New Jersey Institute of Technology. Accessed January 21, 2020. https://digitalcommons.njit.edu/theses/151.

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

MLA Handbook (7th Edition):

Vizzotti, Emanuel Joseph. “Production of stable bcs class ii drug suspensions by melt emulsification and subsequent incorporation into polymer strip films.” 2013. Web. 21 Jan 2020.

Vancouver:

Vizzotti EJ. Production of stable bcs class ii drug suspensions by melt emulsification and subsequent incorporation into polymer strip films. [Internet] [Thesis]. New Jersey Institute of Technology; 2013. [cited 2020 Jan 21]. Available from: https://digitalcommons.njit.edu/theses/151.

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

Council of Science Editors:

Vizzotti EJ. Production of stable bcs class ii drug suspensions by melt emulsification and subsequent incorporation into polymer strip films. [Thesis]. New Jersey Institute of Technology; 2013. Available from: https://digitalcommons.njit.edu/theses/151

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

26. Ramu anne. Design and evaluation of solid dispersions of poorly soluble drugs for improving bioavailability;.

Degree: Pharmaceutical Sciences, 2015, Jawaharlal Nehru Technological University, Anantapuram

No newline

conclusion - 211-224, references- 225-241

Advisors/Committee Members: Dr. S. Vidyadhara and Dr. N. Devanna.

Subjects/Keywords: Pharmaceutical Sciences; Poorly Soluble Drugs for Improving Bioavailabilty; Solid Dispersions

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

APA (6th Edition):

anne, R. (2015). Design and evaluation of solid dispersions of poorly soluble drugs for improving bioavailability;. (Thesis). Jawaharlal Nehru Technological University, Anantapuram. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/35702

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):

anne, Ramu. “Design and evaluation of solid dispersions of poorly soluble drugs for improving bioavailability;.” 2015. Thesis, Jawaharlal Nehru Technological University, Anantapuram. Accessed January 21, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/35702.

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

MLA Handbook (7th Edition):

anne, Ramu. “Design and evaluation of solid dispersions of poorly soluble drugs for improving bioavailability;.” 2015. Web. 21 Jan 2020.

Vancouver:

anne R. Design and evaluation of solid dispersions of poorly soluble drugs for improving bioavailability;. [Internet] [Thesis]. Jawaharlal Nehru Technological University, Anantapuram; 2015. [cited 2020 Jan 21]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/35702.

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

Council of Science Editors:

anne R. Design and evaluation of solid dispersions of poorly soluble drugs for improving bioavailability;. [Thesis]. Jawaharlal Nehru Technological University, Anantapuram; 2015. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/35702

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


Freie Universität Berlin

27. Salazar, Jaime. Kombinatorische Partikelgrößenreduktion-Technologien für die Formulierung schwerlöslicher Wirkstoffe.

Degree: 2013, Freie Universität Berlin

 Eine schlechte Wasserlöslichkeit von neuen Arzneistoffen stellt ein zunehmendes Problem für die Pharmaindustrie dar. Schwerlösliche Arzneistoffe zeigen häufig Nachteile, wie z.B. schlechte orale Bioverfügbarkeit. Partikelgrößenreduktion,… (more)

Subjects/Keywords: poorly soluble drugs; particle size reduction, drug nanocrystals; high pressure homogenization; freeze-drying; spray-drying; 500 Naturwissenschaften und Mathematik::540 Chemie; 600 Technik, Medizin, angewandte Wissenschaften

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

APA (6th Edition):

Salazar, J. (2013). Kombinatorische Partikelgrößenreduktion-Technologien für die Formulierung schwerlöslicher Wirkstoffe. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-14404

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):

Salazar, Jaime. “Kombinatorische Partikelgrößenreduktion-Technologien für die Formulierung schwerlöslicher Wirkstoffe.” 2013. Thesis, Freie Universität Berlin. Accessed January 21, 2020. http://dx.doi.org/10.17169/refubium-14404.

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

MLA Handbook (7th Edition):

Salazar, Jaime. “Kombinatorische Partikelgrößenreduktion-Technologien für die Formulierung schwerlöslicher Wirkstoffe.” 2013. Web. 21 Jan 2020.

Vancouver:

Salazar J. Kombinatorische Partikelgrößenreduktion-Technologien für die Formulierung schwerlöslicher Wirkstoffe. [Internet] [Thesis]. Freie Universität Berlin; 2013. [cited 2020 Jan 21]. Available from: http://dx.doi.org/10.17169/refubium-14404.

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

Council of Science Editors:

Salazar J. Kombinatorische Partikelgrößenreduktion-Technologien für die Formulierung schwerlöslicher Wirkstoffe. [Thesis]. Freie Universität Berlin; 2013. Available from: http://dx.doi.org/10.17169/refubium-14404

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


University of Michigan

28. Ping, Haili. Bridging in vitro Dissolution Tests to in vivo Dissolution for Poorly Soluable Acidic Drugs.

Degree: PhD, Pharmaceutical Sciences, 2010, University of Michigan

 Developing meaningful in vitro dissolution methods is critical for evaluating the drug in vivo performance and providing a better standard for biowaiver tests. For Biopharmaceutical… (more)

Subjects/Keywords: In Vitro Dissolution; Biopharmaceutical Classification System; In Vitro-in Vivo Correlation; Biorelevant Dissolution Method; Bioequivalence and Biowaiver; Poorly Soluble Drugs; Pharmacy and Pharmacology; Health Sciences

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

APA (6th Edition):

Ping, H. (2010). Bridging in vitro Dissolution Tests to in vivo Dissolution for Poorly Soluable Acidic Drugs. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/75973

Chicago Manual of Style (16th Edition):

Ping, Haili. “Bridging in vitro Dissolution Tests to in vivo Dissolution for Poorly Soluable Acidic Drugs.” 2010. Doctoral Dissertation, University of Michigan. Accessed January 21, 2020. http://hdl.handle.net/2027.42/75973.

MLA Handbook (7th Edition):

Ping, Haili. “Bridging in vitro Dissolution Tests to in vivo Dissolution for Poorly Soluable Acidic Drugs.” 2010. Web. 21 Jan 2020.

Vancouver:

Ping H. Bridging in vitro Dissolution Tests to in vivo Dissolution for Poorly Soluable Acidic Drugs. [Internet] [Doctoral dissertation]. University of Michigan; 2010. [cited 2020 Jan 21]. Available from: http://hdl.handle.net/2027.42/75973.

Council of Science Editors:

Ping H. Bridging in vitro Dissolution Tests to in vivo Dissolution for Poorly Soluable Acidic Drugs. [Doctoral Dissertation]. University of Michigan; 2010. Available from: http://hdl.handle.net/2027.42/75973

29. Adchara, Pongpeerapat. Nanoparticle formation of poorly water-soluble drug by co-grinding with polymer and solubilizing agent : 高分子、可溶化剤との混合粉砕による難水溶性医薬品のナノ微粒子化.

Degree: 2006, Chiba University / 千葉大学

研究科: 千葉大学大学院薬学研究院

修了年:2006

千大院医薬甲博第33号

Ternary ground mixtures (GMs) of drug/PVP K17/SDS were prepared with seventeen poorly water-soluble drugs. Most of the poorly water-soluble drugs provided… (more)

Subjects/Keywords: NANOPARTICLE; GRINDING; POORLY WATER-SOLUBLE DRUG; POLYVINYLPYRROLIDONE; SODIUM DODECYL SULFATE

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

APA (6th Edition):

Adchara, P. (2006). Nanoparticle formation of poorly water-soluble drug by co-grinding with polymer and solubilizing agent : 高分子、可溶化剤との混合粉砕による難水溶性医薬品のナノ微粒子化. (Thesis). Chiba University / 千葉大学. Retrieved from http://opac.ll.chiba-u.jp/da/curator/900034430/

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):

Adchara, Pongpeerapat. “Nanoparticle formation of poorly water-soluble drug by co-grinding with polymer and solubilizing agent : 高分子、可溶化剤との混合粉砕による難水溶性医薬品のナノ微粒子化.” 2006. Thesis, Chiba University / 千葉大学. Accessed January 21, 2020. http://opac.ll.chiba-u.jp/da/curator/900034430/.

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

MLA Handbook (7th Edition):

Adchara, Pongpeerapat. “Nanoparticle formation of poorly water-soluble drug by co-grinding with polymer and solubilizing agent : 高分子、可溶化剤との混合粉砕による難水溶性医薬品のナノ微粒子化.” 2006. Web. 21 Jan 2020.

Vancouver:

Adchara P. Nanoparticle formation of poorly water-soluble drug by co-grinding with polymer and solubilizing agent : 高分子、可溶化剤との混合粉砕による難水溶性医薬品のナノ微粒子化. [Internet] [Thesis]. Chiba University / 千葉大学; 2006. [cited 2020 Jan 21]. Available from: http://opac.ll.chiba-u.jp/da/curator/900034430/.

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

Council of Science Editors:

Adchara P. Nanoparticle formation of poorly water-soluble drug by co-grinding with polymer and solubilizing agent : 高分子、可溶化剤との混合粉砕による難水溶性医薬品のナノ微粒子化. [Thesis]. Chiba University / 千葉大学; 2006. Available from: http://opac.ll.chiba-u.jp/da/curator/900034430/

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


Univerzitet u Beogradu

30. Savić, Sanela M., 1987-. Parenteralne nanoemulzije sa slabo rastvorljivim psihofarmakološkim lekovima: formulacija, optimizacija i in vivo procena.

Degree: Farmaceutski fakultet, 2018, Univerzitet u Beogradu

Farmacija - Farmaceutska tehnologija / Pharmacy - Pharmaceutical Technology

Da bi se obezbedila brza/kontrolisana isporuka lekovite supstance u mozak i poboljšala njena biološka raspoloživost na… (more)

Subjects/Keywords: parenteral nanoemulsion; poorly water-soluble drug; brain targeting; experimental design; atomic force microscopy; drug–vehicle interaction; stability; reverse dialysis bag technique; pharmacokinetics; antipsychotic efficiency

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

APA (6th Edition):

Savić, Sanela M., 1. (2018). Parenteralne nanoemulzije sa slabo rastvorljivim psihofarmakološkim lekovima: formulacija, optimizacija i in vivo procena. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:17263/bdef:Content/get

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):

Savić, Sanela M., 1987-. “Parenteralne nanoemulzije sa slabo rastvorljivim psihofarmakološkim lekovima: formulacija, optimizacija i in vivo procena.” 2018. Thesis, Univerzitet u Beogradu. Accessed January 21, 2020. https://fedorabg.bg.ac.rs/fedora/get/o:17263/bdef:Content/get.

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

MLA Handbook (7th Edition):

Savić, Sanela M., 1987-. “Parenteralne nanoemulzije sa slabo rastvorljivim psihofarmakološkim lekovima: formulacija, optimizacija i in vivo procena.” 2018. Web. 21 Jan 2020.

Vancouver:

Savić, Sanela M. 1. Parenteralne nanoemulzije sa slabo rastvorljivim psihofarmakološkim lekovima: formulacija, optimizacija i in vivo procena. [Internet] [Thesis]. Univerzitet u Beogradu; 2018. [cited 2020 Jan 21]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:17263/bdef:Content/get.

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

Council of Science Editors:

Savić, Sanela M. 1. Parenteralne nanoemulzije sa slabo rastvorljivim psihofarmakološkim lekovima: formulacija, optimizacija i in vivo procena. [Thesis]. Univerzitet u Beogradu; 2018. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:17263/bdef:Content/get

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

[1] [2] [3] [4] [5] … [5356]

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