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Itraconazole-hydroxypropyl-β-cyclodextrin loaded deformable liposomes: In vitro skin penetration studies and antifungal efficacy using Candida albicans as model
Abstract
The study aimed to develop novel ITZ-loaded deformable liposomes (DL) in presence of hydroxypropyl-β-cyclodextrin (HPβCD) (DL-CD) to enhance antifungal activity. These formulations have been reported as conceivable vesicles to deliver drug molecules to the skin layers. The efficiency of the prepared systems was compared with conventional liposomes (CL) and ITZ solution. The developed liposomes were characterized for particle size, entrapment efficiency (EE %), deformability, stability, and morphology of the vesicles. In addition, ex vivo penetration and antifungal activity were evaluated. It was found that the presence of HPβCD played a significant role in reducing the vesicle size to nano range. The deformability study and TEM images revealed that membrane deformability of DL and DL-CD was much higher than that of CL. Moreover, DL-CD enhanced the amount of ITZ in SC and deeper skin layers compared to DL and CL. The antifungal activity of ITZ-loaded deformable liposomes remained intact compared to ITZ solution. It can be concluded that deformable liposomes in the presence of HPβCD may be a promising carrier for effective cutaneous delivery of ITZ.
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“This reduction in size was attributed to the action of the edge activator (tween 80) on the membrane of liposomes to reduce the surface tension of the media, leading to phospholipid arrangement in small vesicles (Alomrani et al., 2015).”
From The use of chitosan-coated flexible liposomes as a remarkable carrier to enhance the antitumor efficacy of 5-fluorouracil against colorectal cancer (2019) · cites this paper as Alomrani et al., 2015
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“These results demonstrate that the presence of tween 80 (F2) enhanced EE% and DL% of liposomes, aligning with the results found by El Zaafarany et al., 2010, Alomrani et al., 2015.”
From The use of chitosan-coated flexible liposomes as a remarkable carrier to enhance the antitumor efficacy of 5-fluorouracil against colorectal cancer (2019) · cites this paper as Alomrani et al., 2015
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Cited by
Sorted by citations
Alomrani, A., Badran, M., Harisa, G. I., ALshehry, M., Alhariri, M., Alshamsan, A., & Alkholief, M. (2019) · Saudi Pharmaceutical Journal · doi:10.1016/j.jsps.2019.02.008 · Cited by 143
Self-citationLamie, C., Elmowafy, E., Attia, D. A., Elmazar, M. M., & Mortada, N. D. (2022) · Nanomedicine: Nanotechnology, Biology and Medicine · doi:10.1016/j.nano.2022.102561 · Cited by 29
Metadata
- Authors
- Alomrani, A. H., Shazly, G. A., Amara, A. A., & Badran, M. M.
- Venue
- Colloids and Surfaces B: Biointerfaces
- Publisher
- Elsevier BV
- Published
- 2014-09
- Volume
- 121
- Pages
- 74-81
- ISSN
- 0927-7765
- Cited by
- 79
- References
- 0
- Language
- en
- Funders
- King Saud University (RGP-VPP-287)
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- Alomrani, A. H., Shazly, G. A., Amara, A. A., & Badran, M. M. (2014). Itraconazole-hydroxypropyl-β-cyclodextrin loaded deformable liposomes: In vitro skin penetration studies and antifungal efficacy using Candida albicans as model. Colloids and Surfaces B: Biointerfaces. https://doi.org/10.1016/j.colsurfb.2014.05.030