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Human Serum Albumin Conjugates of 7-Ethyl-10-hydroxycamptothecin (SN38) for Cancer Treatment
SN38 (7-ethyl-10-hydroxy-comptothecin) is a potent metabolite of irinotecan, which has been approved for treatment of metastatic colorectal cancer. Considering the notable potency of SN38, it has been introduced as an anticancer candidate. In this study, human serum albumin (HSA) conjugates of SN38...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4033423/ https://www.ncbi.nlm.nih.gov/pubmed/24895635 http://dx.doi.org/10.1155/2014/963507 |
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author | Sepehri, Nima Rouhani, Hasti Ghanbarpour, Ahmad Reza Gharghabi, Mehdi Tavassolian, Faranak Amini, Mohsen Ostad, Seyed Nasser Ghahremani, Mohammad Hossein Dinarvand, Rassoul |
author_facet | Sepehri, Nima Rouhani, Hasti Ghanbarpour, Ahmad Reza Gharghabi, Mehdi Tavassolian, Faranak Amini, Mohsen Ostad, Seyed Nasser Ghahremani, Mohammad Hossein Dinarvand, Rassoul |
author_sort | Sepehri, Nima |
collection | PubMed |
description | SN38 (7-ethyl-10-hydroxy-comptothecin) is a potent metabolite of irinotecan, which has been approved for treatment of metastatic colorectal cancer. Considering the notable potency of SN38, it has been introduced as an anticancer candidate. In this study, human serum albumin (HSA) conjugates of SN38 were formulated to overcome the solubility problem beside improving the active form stability and tumor tissue targeting. In this target, two different molar ratios of conjugates (SN38 : HSA 15 : 1 and 60 : 1) were prepared by derivatization of 20-hydroxyl group of SN38 with glycine, followed by addition of succinyl group to glycine through which HSA was covalently attached. The conjugates with particle size of about 100 nm revealed enhanced water solubility and were relatively stable in neutral and acidic solutions. For SN38-HSA-15 and SN38-HSA-60 IC(50) values were compared with irinotecan in HT-29 human colon cancer cells. Furthermore, biodistribution studies of SN38-HSA conjugate resulted in proper blood concentration level within 4 h. Moreover, blood cytotoxicity assay revealed no toxicity effect on liver and spleen. Collectively, our present investigation offers a water-soluble form of SN38 attached to HSA and suggests using favorable properties as a promising anticancer agent for further preclinical and clinical investigations. |
format | Online Article Text |
id | pubmed-4033423 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-40334232014-06-03 Human Serum Albumin Conjugates of 7-Ethyl-10-hydroxycamptothecin (SN38) for Cancer Treatment Sepehri, Nima Rouhani, Hasti Ghanbarpour, Ahmad Reza Gharghabi, Mehdi Tavassolian, Faranak Amini, Mohsen Ostad, Seyed Nasser Ghahremani, Mohammad Hossein Dinarvand, Rassoul Biomed Res Int Research Article SN38 (7-ethyl-10-hydroxy-comptothecin) is a potent metabolite of irinotecan, which has been approved for treatment of metastatic colorectal cancer. Considering the notable potency of SN38, it has been introduced as an anticancer candidate. In this study, human serum albumin (HSA) conjugates of SN38 were formulated to overcome the solubility problem beside improving the active form stability and tumor tissue targeting. In this target, two different molar ratios of conjugates (SN38 : HSA 15 : 1 and 60 : 1) were prepared by derivatization of 20-hydroxyl group of SN38 with glycine, followed by addition of succinyl group to glycine through which HSA was covalently attached. The conjugates with particle size of about 100 nm revealed enhanced water solubility and were relatively stable in neutral and acidic solutions. For SN38-HSA-15 and SN38-HSA-60 IC(50) values were compared with irinotecan in HT-29 human colon cancer cells. Furthermore, biodistribution studies of SN38-HSA conjugate resulted in proper blood concentration level within 4 h. Moreover, blood cytotoxicity assay revealed no toxicity effect on liver and spleen. Collectively, our present investigation offers a water-soluble form of SN38 attached to HSA and suggests using favorable properties as a promising anticancer agent for further preclinical and clinical investigations. Hindawi Publishing Corporation 2014 2014-05-07 /pmc/articles/PMC4033423/ /pubmed/24895635 http://dx.doi.org/10.1155/2014/963507 Text en Copyright © 2014 Nima Sepehri et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Sepehri, Nima Rouhani, Hasti Ghanbarpour, Ahmad Reza Gharghabi, Mehdi Tavassolian, Faranak Amini, Mohsen Ostad, Seyed Nasser Ghahremani, Mohammad Hossein Dinarvand, Rassoul Human Serum Albumin Conjugates of 7-Ethyl-10-hydroxycamptothecin (SN38) for Cancer Treatment |
title | Human Serum Albumin Conjugates of 7-Ethyl-10-hydroxycamptothecin (SN38) for Cancer Treatment |
title_full | Human Serum Albumin Conjugates of 7-Ethyl-10-hydroxycamptothecin (SN38) for Cancer Treatment |
title_fullStr | Human Serum Albumin Conjugates of 7-Ethyl-10-hydroxycamptothecin (SN38) for Cancer Treatment |
title_full_unstemmed | Human Serum Albumin Conjugates of 7-Ethyl-10-hydroxycamptothecin (SN38) for Cancer Treatment |
title_short | Human Serum Albumin Conjugates of 7-Ethyl-10-hydroxycamptothecin (SN38) for Cancer Treatment |
title_sort | human serum albumin conjugates of 7-ethyl-10-hydroxycamptothecin (sn38) for cancer treatment |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4033423/ https://www.ncbi.nlm.nih.gov/pubmed/24895635 http://dx.doi.org/10.1155/2014/963507 |
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