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Published on: August 10, 2020
Optimization of Aceclofenac Proniosomes by Using Different Carriers, Part 1: Development and Characterization
Rana M F Sammour1,2, Muhammad Taher3, Bappaditya Chatterjee1
1Pharmaceutical Technology Department, Kulliyyah of Pharmacy, International Islamic University Malaysia, Kuantan 25200, Pahang, Malaysia.
This study optimized proniosomal aceclofenac formulations using various carriers. Maltodextrin-based proniosomes showed enhanced solubility, indicating potential for improved drug delivery.
Area of Science:
- Pharmaceutical Sciences
- Drug Delivery Systems
Background:
- Proniosomal systems enhance bioavailability for poorly water-soluble drugs.
- Aceclofenac is used for pain and inflammation in conditions like osteoarthritis and rheumatoid arthritis.
Purpose of the Study:
- To develop and optimize proniosomal aceclofenac formulations using different carriers.
- To evaluate the physical characteristics and drug compatibility of the prepared proniosomes.
Main Methods:
- Proniosomes prepared using the slurry method with carriers: maltodextrin, mannitol, and glucose.
- Characterization included DSC, FTIR, XRD, and SEM.
- Drug content and entrapment efficiency analyzed using HPLC.
Main Results:
- Compatibility of aceclofenac with carriers confirmed by DSC and FTIR.
- XRD confirmed the amorphous nature of proniosomes.
- Maltodextrin-based proniosomes demonstrated superior solubility compared to other formulations.
Conclusions:
- Proniosomal aceclofenac formulations can be successfully prepared using various carriers.
- Maltodextrin shows promise as a carrier for enhancing aceclofenac solubility in proniosomal systems.
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