Formulation And Evaluation Of Self-Emulsifying Drug Delivery Systems Of Azithromycin To Enhance Its Penetration Through The Epithelial Tight Junctions
Azithromycin (AZM) is a macrolide antibiotic used for the treatment of a number of bacterial infections. It is known to have a low oral bioavailability (37 %) due to its relatively high molecular weight, incomplete solubility and/or poor intestinal permeability, which is potentially restricting its...
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my-usm-ep.442592019-05-06T01:39:00Z Formulation And Evaluation Of Self-Emulsifying Drug Delivery Systems Of Azithromycin To Enhance Its Penetration Through The Epithelial Tight Junctions 2018-03 Assi, Reem Abou RS1-441 Pharmacy and materia medica Azithromycin (AZM) is a macrolide antibiotic used for the treatment of a number of bacterial infections. It is known to have a low oral bioavailability (37 %) due to its relatively high molecular weight, incomplete solubility and/or poor intestinal permeability, which is potentially restricting its intestinal absorption. To overcome these drawbacks liquid and solid self-emulsifying drug delivery systems (L-SEDDs and S-SEDDs) of AZM were prepared in an attempt to enhance its solubility, and altering its cellular penetration, which might improve its oral bioavailability. 2018-03 Thesis http://eprints.usm.my/44259/ http://eprints.usm.my/44259/1/REEM%20ABOU%20ASSI.pdf application/pdf en public masters Universiti Sains Malaysia Pusat Pengajian Sains Farmasi |
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Universiti Sains Malaysia |
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English |
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RS1-441 Pharmacy and materia medica |
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RS1-441 Pharmacy and materia medica Assi, Reem Abou Formulation And Evaluation Of Self-Emulsifying Drug Delivery Systems Of Azithromycin To Enhance Its Penetration Through The Epithelial Tight Junctions |
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Azithromycin (AZM) is a macrolide antibiotic used for the treatment of a number of bacterial infections. It is known to have a low oral bioavailability (37 %) due to its relatively high molecular weight, incomplete solubility and/or poor intestinal permeability, which is potentially restricting its intestinal absorption. To overcome these drawbacks liquid and solid self-emulsifying drug delivery systems (L-SEDDs and S-SEDDs) of AZM were prepared in an attempt to enhance its solubility, and altering its cellular penetration, which might improve its oral bioavailability. |
format |
Thesis |
qualification_level |
Master's degree |
author |
Assi, Reem Abou |
author_facet |
Assi, Reem Abou |
author_sort |
Assi, Reem Abou |
title |
Formulation And Evaluation Of Self-Emulsifying Drug Delivery Systems Of Azithromycin To Enhance Its Penetration Through The Epithelial Tight Junctions |
title_short |
Formulation And Evaluation Of Self-Emulsifying Drug Delivery Systems Of Azithromycin To Enhance Its Penetration Through The Epithelial Tight Junctions |
title_full |
Formulation And Evaluation Of Self-Emulsifying Drug Delivery Systems Of Azithromycin To Enhance Its Penetration Through The Epithelial Tight Junctions |
title_fullStr |
Formulation And Evaluation Of Self-Emulsifying Drug Delivery Systems Of Azithromycin To Enhance Its Penetration Through The Epithelial Tight Junctions |
title_full_unstemmed |
Formulation And Evaluation Of Self-Emulsifying Drug Delivery Systems Of Azithromycin To Enhance Its Penetration Through The Epithelial Tight Junctions |
title_sort |
formulation and evaluation of self-emulsifying drug delivery systems of azithromycin to enhance its penetration through the epithelial tight junctions |
granting_institution |
Universiti Sains Malaysia |
granting_department |
Pusat Pengajian Sains Farmasi |
publishDate |
2018 |
url |
http://eprints.usm.my/44259/1/REEM%20ABOU%20ASSI.pdf |
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1747821349459460096 |