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A novel folate-modified self-microemulsifying drug delivery system of curcumin for colon targeting
BACKGROUND: The objective of this study was to prepare, characterize, and evaluate a folate-modified self-microemulsifying drug delivery system (FSMEDDS) with the aim to improve the solubility of curcumin and its delivery to the colon, facilitating endocytosis of FSMEDDS mediated by folate receptors...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3263408/ https://www.ncbi.nlm.nih.gov/pubmed/22275831 http://dx.doi.org/10.2147/IJN.S27639 |
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author | Zhang, Lin Zhu, Weiwei Yang, Chunfen Guo, Hongxia Yu, Aihua Ji, Jianbo Gao, Yan Sun, Min Zhai, Guangxi |
author_facet | Zhang, Lin Zhu, Weiwei Yang, Chunfen Guo, Hongxia Yu, Aihua Ji, Jianbo Gao, Yan Sun, Min Zhai, Guangxi |
author_sort | Zhang, Lin |
collection | PubMed |
description | BACKGROUND: The objective of this study was to prepare, characterize, and evaluate a folate-modified self-microemulsifying drug delivery system (FSMEDDS) with the aim to improve the solubility of curcumin and its delivery to the colon, facilitating endocytosis of FSMEDDS mediated by folate receptors on colon cancer cells. METHODS: Ternary phase diagrams were constructed in order to obtain the most efficient self-emulsification region, and the formulation of curcumin-loaded SMEDDS was optimized by a simplex lattice experiment design. Then, three lipophilic folate derivatives (folate-polyethylene glycol-distearoylphosphatidylethanolamine, folate-polyethylene glycol-cholesteryl hemisuccinate, and folate-polyethylene glycol-cholesterol) used as a surfactant were added to curcumin-loaded SMEDDS formulations. An in situ colon perfusion method in rats was used to optimize the formulation of FSMEDDS. Curcumin-loaded FSMEDDS was then filled into colon-targeted capsules and the in vitro release was investigated. Cytotoxicity studies and cellular uptake studies was used in this research. RESULTS: The optimal formulation of FSMEDDS obtained with the established in situ colon perfusion method in rats was comprised of 57.5% Cremophor(®) EL, 32.5% Transcutol(®) HP, 10% Capryol™ 90, and a small amount of folate-polyethylene glycol-cholesteryl hemisuccinate (the weight ratio of folate materials to Cremophor EL was 1:100). The in vitro release results indicated that the obtained formulation of curcumin could reach the colon efficiently and release the drug immediately. Cellular uptake studies analyzed with fluorescence microscopy and flow cytometry indicated that the FSMEDDS formulation could efficiently bind with the folate receptors on the surface of positive folate receptors cell lines. In addition, FSMEDDS showed greater cytotoxicity than SMEDDS in the above two cells. CONCLUSION: FSMEDDS-filled colon-targeted capsules are a potential carrier for colon delivery of curcumin. |
format | Online Article Text |
id | pubmed-3263408 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-32634082012-01-24 A novel folate-modified self-microemulsifying drug delivery system of curcumin for colon targeting Zhang, Lin Zhu, Weiwei Yang, Chunfen Guo, Hongxia Yu, Aihua Ji, Jianbo Gao, Yan Sun, Min Zhai, Guangxi Int J Nanomedicine Original Research BACKGROUND: The objective of this study was to prepare, characterize, and evaluate a folate-modified self-microemulsifying drug delivery system (FSMEDDS) with the aim to improve the solubility of curcumin and its delivery to the colon, facilitating endocytosis of FSMEDDS mediated by folate receptors on colon cancer cells. METHODS: Ternary phase diagrams were constructed in order to obtain the most efficient self-emulsification region, and the formulation of curcumin-loaded SMEDDS was optimized by a simplex lattice experiment design. Then, three lipophilic folate derivatives (folate-polyethylene glycol-distearoylphosphatidylethanolamine, folate-polyethylene glycol-cholesteryl hemisuccinate, and folate-polyethylene glycol-cholesterol) used as a surfactant were added to curcumin-loaded SMEDDS formulations. An in situ colon perfusion method in rats was used to optimize the formulation of FSMEDDS. Curcumin-loaded FSMEDDS was then filled into colon-targeted capsules and the in vitro release was investigated. Cytotoxicity studies and cellular uptake studies was used in this research. RESULTS: The optimal formulation of FSMEDDS obtained with the established in situ colon perfusion method in rats was comprised of 57.5% Cremophor(®) EL, 32.5% Transcutol(®) HP, 10% Capryol™ 90, and a small amount of folate-polyethylene glycol-cholesteryl hemisuccinate (the weight ratio of folate materials to Cremophor EL was 1:100). The in vitro release results indicated that the obtained formulation of curcumin could reach the colon efficiently and release the drug immediately. Cellular uptake studies analyzed with fluorescence microscopy and flow cytometry indicated that the FSMEDDS formulation could efficiently bind with the folate receptors on the surface of positive folate receptors cell lines. In addition, FSMEDDS showed greater cytotoxicity than SMEDDS in the above two cells. CONCLUSION: FSMEDDS-filled colon-targeted capsules are a potential carrier for colon delivery of curcumin. Dove Medical Press 2012 2012-01-09 /pmc/articles/PMC3263408/ /pubmed/22275831 http://dx.doi.org/10.2147/IJN.S27639 Text en © 2012 Zhang et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited. |
spellingShingle | Original Research Zhang, Lin Zhu, Weiwei Yang, Chunfen Guo, Hongxia Yu, Aihua Ji, Jianbo Gao, Yan Sun, Min Zhai, Guangxi A novel folate-modified self-microemulsifying drug delivery system of curcumin for colon targeting |
title | A novel folate-modified self-microemulsifying drug delivery system of curcumin for colon targeting |
title_full | A novel folate-modified self-microemulsifying drug delivery system of curcumin for colon targeting |
title_fullStr | A novel folate-modified self-microemulsifying drug delivery system of curcumin for colon targeting |
title_full_unstemmed | A novel folate-modified self-microemulsifying drug delivery system of curcumin for colon targeting |
title_short | A novel folate-modified self-microemulsifying drug delivery system of curcumin for colon targeting |
title_sort | novel folate-modified self-microemulsifying drug delivery system of curcumin for colon targeting |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3263408/ https://www.ncbi.nlm.nih.gov/pubmed/22275831 http://dx.doi.org/10.2147/IJN.S27639 |
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