Abstract
Objective: Currently, there is a clear lack of effective topical treatments for psoriasis. In light of this unaddressed requirement, the work intends to develop, enhance, and assess the effectiveness of a curcumin transethosomal gel for managing psoriasis. This work signifies the delivery of a potential solution to fill the gap in topical psoriasis treatment.
Materials and Methods: Curcumin-loaded transethosomes were prepared using a mechanical dispersion method. An initial study was conducted to determine the ideal concentrations of Lipoid S100 and Isopropyl Myristate (IPM). To refine the ultimate transethosomal formulation, a full factorial design (32) was employed, incorporating different levels of Lipoid S100 and IPM. Drug release investigations and pharmacokinetics assessments of curcumin concentrations were performed using a specialized dissolution apparatus and an animal model, respectively.
Results: The characterization profile and analytical examinations have affirmed the stability of the formulation throughout the study duration. Our findings indicate that the drug release mechanism conforms to a diffusion pattern akin to Fickian transport. Furthermore, In-vivo investigations revealed that the curcumin concentration in the bloodstream after oral administration was significantly superior to that of the conventional formulation.
Conclusion: Using curcumin-loaded transethosomes extends drug contact time and facilitates controlled drug release, leading to enhanced bioavailability, decreased dosage needs, and heightened patient safety.
Graphical Abstract
[http://dx.doi.org/10.18632/oncotarget.20585] [PMID: 29312556]
[http://dx.doi.org/10.1016/j.drudis.2011.09.009]
[http://dx.doi.org/10.1016/j.canlet.2004.09.041] [PMID: 15896452]
[http://dx.doi.org/10.1016/j.intimp.2014.03.009] [PMID: 24675438]
[http://dx.doi.org/10.1016/j.colsurfb.2014.05.005] [PMID: 24984268]
[http://dx.doi.org/10.1016/j.colsurfb.2013.06.032]
[http://dx.doi.org/10.2147/IJN.S59779]
[http://dx.doi.org/10.1016/j.biomaterials.2010.08.112] [PMID: 20933280]
[http://dx.doi.org/10.1021/mp700113r]
[http://dx.doi.org/10.1016/j.hermed.2015.03.001]
[http://dx.doi.org/10.1016/j.biomaterials.2013.12.090] [PMID: 24439402]
[http://dx.doi.org/10.1208/s12248-015-9811-z] [PMID: 26335307]
[http://dx.doi.org/10.2174/1567201813666160520114436]
[http://dx.doi.org/10.2174/1381612825666190716095826]
[http://dx.doi.org/10.3390/pharmaceutics13122129] [PMID: 34959410]
[http://dx.doi.org/10.1016/j.ijpharm.2013.11.017]
[http://dx.doi.org/10.1208/pt0804111] [PMID: 18181532]
[http://dx.doi.org/10.1049/nbt2.12069]
[http://dx.doi.org/10.2174/2211738506666180813122102] [PMID: 30101725]
[http://dx.doi.org/10.1016/j.ejps.2016.12.026] [PMID: 28039091]
[http://dx.doi.org/10.2147/IJN.S196771]
[http://dx.doi.org/10.3390/pharmaceutics13081124] [PMID: 34452085]
[http://dx.doi.org/10.3390/pharmaceutics14112268] [PMID: 36365087]
[http://dx.doi.org/10.1055/a-1924-7818] [PMID: 36138545]
[http://dx.doi.org/10.3390/pharmaceutics14050991] [PMID: 35631577]
[http://dx.doi.org/10.1080/10837450.2023.2229104]
[http://dx.doi.org/10.34172/apb.2021.015] [PMID: 33747861]
[http://dx.doi.org/10.1016/j.chemphyslip.2020.105028] [PMID: 33309940]
[http://dx.doi.org/10.3390/gels9080626] [PMID: 37623081]
[http://dx.doi.org/10.1080/08982104.2023.2221354]
[http://dx.doi.org/10.1007/s13346-022-01172-z] [PMID: 35622235]
[http://dx.doi.org/10.3390/pharmaceutics16020267] [PMID: 38399321]
[http://dx.doi.org/10.3390/ph15060657] [PMID: 35745575]
[http://dx.doi.org/10.37319/iqnjm.5.2.4]