Optimization of aceclofenac proniosomes by using different carriers, Part 1 : development and characterization

In the contemporary medical model world, the proniosomal system has been serving as a new drug delivery system that is considered to significantly enhance the bioavailability of drugs with low water solubility. The application of this system can improve the bioavailability of aceclofenac that is use...

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Main Authors: Sammour, Rana M.F., Taher, Muhammad, Chatterjee, Bappaditya, Shahiwala, Aliasgar, Mahmood, Syed
Format: Article
Language:English
Published: MDPI 2019
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Online Access:http://umpir.ump.edu.my/id/eprint/26270/
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http://umpir.ump.edu.my/id/eprint/26270/1/Optimization%20of%20aceclofenac%20proniosomes%20by%20using%20different%20carriers.pdf
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spelling ump-262702019-12-09T01:29:43Z http://umpir.ump.edu.my/id/eprint/26270/ Optimization of aceclofenac proniosomes by using different carriers, Part 1 : development and characterization Sammour, Rana M.F. Taher, Muhammad Chatterjee, Bappaditya Shahiwala, Aliasgar Mahmood, Syed RS Pharmacy and materia medica TP Chemical technology In the contemporary medical model world, the proniosomal system has been serving as a new drug delivery system that is considered to significantly enhance the bioavailability of drugs with low water solubility. The application of this system can improve the bioavailability of aceclofenac that is used for the relief of pain and inflammation in osteoarthritis, rheumatoid arthritis, and ankylosing spondylitis. The present study is intended to develop an optimized proniosomal aceclofenac formula by the use of different carriers. Aceclofenac proniosomes have been prepared by slurry method, and different carriers such as maltodextrin, mannitol, and glucose were tried. Prepared proniosomes characterized by differential scanning calorimetry (DSC) analysis and Fourier transform infrared (FTIR) analysis revealed the compatibility of the drug chosen with the ingredient added, powder X-ray diffractometry (XRD) confirmed the amorphous phase of the prepared proniosomes, and finally, the surfactant layer was observed by scanning electron microscopy (SEM). Aceclofenac physical state transformations were confirmed with all formulas but maltodextrin proniosomes exhibited solubility more than other formulations. HPLC method has been used to analyze the niosomes derived from proniosomes in terms of their entrapment capability and drug content. The obtained results revealed that aceclofenac proniosomes can be successfully prepared by using different carriers. MDPI 2019-07-18 Article PeerReviewed pdf en cc_by_4 http://umpir.ump.edu.my/id/eprint/26270/1/Optimization%20of%20aceclofenac%20proniosomes%20by%20using%20different%20carriers.pdf Sammour, Rana M.F. and Taher, Muhammad and Chatterjee, Bappaditya and Shahiwala, Aliasgar and Mahmood, Syed (2019) Optimization of aceclofenac proniosomes by using different carriers, Part 1 : development and characterization. Pharmaceutics, 11 (7). pp. 1-19. ISSN 1999-4923 https://doi.org/10.3390/pharmaceutics11070350 https://doi.org/10.3390/pharmaceutics11070350
repository_type Digital Repository
institution_category Local University
institution Universiti Malaysia Pahang
building UMP Institutional Repository
collection Online Access
language English
topic RS Pharmacy and materia medica
TP Chemical technology
spellingShingle RS Pharmacy and materia medica
TP Chemical technology
Sammour, Rana M.F.
Taher, Muhammad
Chatterjee, Bappaditya
Shahiwala, Aliasgar
Mahmood, Syed
Optimization of aceclofenac proniosomes by using different carriers, Part 1 : development and characterization
description In the contemporary medical model world, the proniosomal system has been serving as a new drug delivery system that is considered to significantly enhance the bioavailability of drugs with low water solubility. The application of this system can improve the bioavailability of aceclofenac that is used for the relief of pain and inflammation in osteoarthritis, rheumatoid arthritis, and ankylosing spondylitis. The present study is intended to develop an optimized proniosomal aceclofenac formula by the use of different carriers. Aceclofenac proniosomes have been prepared by slurry method, and different carriers such as maltodextrin, mannitol, and glucose were tried. Prepared proniosomes characterized by differential scanning calorimetry (DSC) analysis and Fourier transform infrared (FTIR) analysis revealed the compatibility of the drug chosen with the ingredient added, powder X-ray diffractometry (XRD) confirmed the amorphous phase of the prepared proniosomes, and finally, the surfactant layer was observed by scanning electron microscopy (SEM). Aceclofenac physical state transformations were confirmed with all formulas but maltodextrin proniosomes exhibited solubility more than other formulations. HPLC method has been used to analyze the niosomes derived from proniosomes in terms of their entrapment capability and drug content. The obtained results revealed that aceclofenac proniosomes can be successfully prepared by using different carriers.
format Article
author Sammour, Rana M.F.
Taher, Muhammad
Chatterjee, Bappaditya
Shahiwala, Aliasgar
Mahmood, Syed
author_facet Sammour, Rana M.F.
Taher, Muhammad
Chatterjee, Bappaditya
Shahiwala, Aliasgar
Mahmood, Syed
author_sort Sammour, Rana M.F.
title Optimization of aceclofenac proniosomes by using different carriers, Part 1 : development and characterization
title_short Optimization of aceclofenac proniosomes by using different carriers, Part 1 : development and characterization
title_full Optimization of aceclofenac proniosomes by using different carriers, Part 1 : development and characterization
title_fullStr Optimization of aceclofenac proniosomes by using different carriers, Part 1 : development and characterization
title_full_unstemmed Optimization of aceclofenac proniosomes by using different carriers, Part 1 : development and characterization
title_sort optimization of aceclofenac proniosomes by using different carriers, part 1 : development and characterization
publisher MDPI
publishDate 2019
url http://umpir.ump.edu.my/id/eprint/26270/
http://umpir.ump.edu.my/id/eprint/26270/
http://umpir.ump.edu.my/id/eprint/26270/
http://umpir.ump.edu.my/id/eprint/26270/1/Optimization%20of%20aceclofenac%20proniosomes%20by%20using%20different%20carriers.pdf
first_indexed 2023-09-18T22:40:48Z
last_indexed 2023-09-18T22:40:48Z
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