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Development and Optimization of Imiquimod-Loaded Nanostructured Lipid Carriers Using a Hybrid Design of Experiments Approach

BACKGROUND: Imiquimod (IMQ) is an immunomodulating drug that is approved for the treatment of superficial basal cell carcinoma, actinic keratosis, external genital warts and perianal warts. However, IMQ cream (Aldara(®)) has several drawbacks including poor skin permeation, local toxicity, and compr...

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Autores principales: Kim, Sangseo, Abdella, Sadikalmahdi, Abid, Fatima, Afinjuomo, Franklin, Youssef, Souha H, Holmes, Amy, Song, Yunmei, Vaidya, Sachin, Garg, Sanjay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9968428/
https://www.ncbi.nlm.nih.gov/pubmed/36855538
http://dx.doi.org/10.2147/IJN.S400610
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author Kim, Sangseo
Abdella, Sadikalmahdi
Abid, Fatima
Afinjuomo, Franklin
Youssef, Souha H
Holmes, Amy
Song, Yunmei
Vaidya, Sachin
Garg, Sanjay
author_facet Kim, Sangseo
Abdella, Sadikalmahdi
Abid, Fatima
Afinjuomo, Franklin
Youssef, Souha H
Holmes, Amy
Song, Yunmei
Vaidya, Sachin
Garg, Sanjay
author_sort Kim, Sangseo
collection PubMed
description BACKGROUND: Imiquimod (IMQ) is an immunomodulating drug that is approved for the treatment of superficial basal cell carcinoma, actinic keratosis, external genital warts and perianal warts. However, IMQ cream (Aldara(®)) has several drawbacks including poor skin permeation, local toxicity, and compromised patient compliance as a topical pharmacological option. METHODS: Our research aimed to develop and optimize nanostructured lipid carriers (NLCs) containing IMQ for the first time using a hybrid design of experiments approach. The optimized formulation was then incorporated into a matrix-type topical patch as an alternative dosage form for topical application and evaluated for IMQ deposition across different skin layers in comparison to the performance of the commercial product. Additionally, our work also attempted to highlight the possibility of implementing environment-friendly practices in our IMQ-NLCs formulation development by reviewing our analytical methods and experimental designs and reducing energy and solvent consumption where possible. RESULTS: In this study, stearyl alcohol, oleic acid, Tween(®) 80 (polysorbate 80), and Gelucire(®) 50/13 (Stearoyl polyoxyl-32 glycerides) were selected for formulation development. The formulation was optimized using a 2(k) factorial design and a central composite design. The optimized formulation achieved the average particle size, polydispersity index, and zeta potential of 75.6 nm, 0.235, and – 30.9 mV, respectively. Subsequently, a matrix-type patch containing IMQ-NLCs was developed and achieved a statistically significant improvement in IMQ deposition in the deeper skin layers. The IMQ deposition from the patch into the dermis layer and receptor chamber was 3.3 ± 0.9 µg/cm(2) and 12.3 ± 2.2 µg/cm(2), while the commercial cream only deposited 1.0 ± 0.8 µg/cm(2) and 1.5 ± 0.5 µg/cm(2) of IMQ, respectively. CONCLUSION: In summary, IMQ-NLC-loaded patches represent great potential as a topical treatment option for skin cancer with improved patient compliance.
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spelling pubmed-99684282023-02-27 Development and Optimization of Imiquimod-Loaded Nanostructured Lipid Carriers Using a Hybrid Design of Experiments Approach Kim, Sangseo Abdella, Sadikalmahdi Abid, Fatima Afinjuomo, Franklin Youssef, Souha H Holmes, Amy Song, Yunmei Vaidya, Sachin Garg, Sanjay Int J Nanomedicine Original Research BACKGROUND: Imiquimod (IMQ) is an immunomodulating drug that is approved for the treatment of superficial basal cell carcinoma, actinic keratosis, external genital warts and perianal warts. However, IMQ cream (Aldara(®)) has several drawbacks including poor skin permeation, local toxicity, and compromised patient compliance as a topical pharmacological option. METHODS: Our research aimed to develop and optimize nanostructured lipid carriers (NLCs) containing IMQ for the first time using a hybrid design of experiments approach. The optimized formulation was then incorporated into a matrix-type topical patch as an alternative dosage form for topical application and evaluated for IMQ deposition across different skin layers in comparison to the performance of the commercial product. Additionally, our work also attempted to highlight the possibility of implementing environment-friendly practices in our IMQ-NLCs formulation development by reviewing our analytical methods and experimental designs and reducing energy and solvent consumption where possible. RESULTS: In this study, stearyl alcohol, oleic acid, Tween(®) 80 (polysorbate 80), and Gelucire(®) 50/13 (Stearoyl polyoxyl-32 glycerides) were selected for formulation development. The formulation was optimized using a 2(k) factorial design and a central composite design. The optimized formulation achieved the average particle size, polydispersity index, and zeta potential of 75.6 nm, 0.235, and – 30.9 mV, respectively. Subsequently, a matrix-type patch containing IMQ-NLCs was developed and achieved a statistically significant improvement in IMQ deposition in the deeper skin layers. The IMQ deposition from the patch into the dermis layer and receptor chamber was 3.3 ± 0.9 µg/cm(2) and 12.3 ± 2.2 µg/cm(2), while the commercial cream only deposited 1.0 ± 0.8 µg/cm(2) and 1.5 ± 0.5 µg/cm(2) of IMQ, respectively. CONCLUSION: In summary, IMQ-NLC-loaded patches represent great potential as a topical treatment option for skin cancer with improved patient compliance. Dove 2023-02-22 /pmc/articles/PMC9968428/ /pubmed/36855538 http://dx.doi.org/10.2147/IJN.S400610 Text en © 2023 Kim et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Kim, Sangseo
Abdella, Sadikalmahdi
Abid, Fatima
Afinjuomo, Franklin
Youssef, Souha H
Holmes, Amy
Song, Yunmei
Vaidya, Sachin
Garg, Sanjay
Development and Optimization of Imiquimod-Loaded Nanostructured Lipid Carriers Using a Hybrid Design of Experiments Approach
title Development and Optimization of Imiquimod-Loaded Nanostructured Lipid Carriers Using a Hybrid Design of Experiments Approach
title_full Development and Optimization of Imiquimod-Loaded Nanostructured Lipid Carriers Using a Hybrid Design of Experiments Approach
title_fullStr Development and Optimization of Imiquimod-Loaded Nanostructured Lipid Carriers Using a Hybrid Design of Experiments Approach
title_full_unstemmed Development and Optimization of Imiquimod-Loaded Nanostructured Lipid Carriers Using a Hybrid Design of Experiments Approach
title_short Development and Optimization of Imiquimod-Loaded Nanostructured Lipid Carriers Using a Hybrid Design of Experiments Approach
title_sort development and optimization of imiquimod-loaded nanostructured lipid carriers using a hybrid design of experiments approach
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9968428/
https://www.ncbi.nlm.nih.gov/pubmed/36855538
http://dx.doi.org/10.2147/IJN.S400610
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