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Efficacy and safety of a novel topical agent for gallstone dissolution: 2-methoxy-6-methylpyridine
BACKGROUND: Although methyl-tertiary butyl ether (MTBE) is the only clinical topical agent for gallstone dissolution, its use is limited by its side effects mostly arising from a relatively low boiling point (55 °C). In this study, we developed the gallstone-dissolving compound containing an aromati...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6558798/ https://www.ncbi.nlm.nih.gov/pubmed/31182117 http://dx.doi.org/10.1186/s12967-019-1943-y |
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author | Choi, Ho Joong Cho, Suk Joon Kim, Ok-Hee Song, Jin Sook Hong, Ha-Eun Lee, Sang Chul Kim, Kee-Hwan Lee, Sang Kuon You, Young Kyoung Hong, Tae Ho Kim, Eun Young Park, Jung Hyun Na, Gun Hyung Do You, Dong Han, Jae Hyun Park, Jae Woo Kwak, Bong Jun Lee, Tae Yun Ahn, Joseph Lee, Hwan Hee Kang, Seung Kyu Hwang, Kyu-Seok Jung, Jae-Kyung Jung, Kwan-Young Kim, Say-June |
author_facet | Choi, Ho Joong Cho, Suk Joon Kim, Ok-Hee Song, Jin Sook Hong, Ha-Eun Lee, Sang Chul Kim, Kee-Hwan Lee, Sang Kuon You, Young Kyoung Hong, Tae Ho Kim, Eun Young Park, Jung Hyun Na, Gun Hyung Do You, Dong Han, Jae Hyun Park, Jae Woo Kwak, Bong Jun Lee, Tae Yun Ahn, Joseph Lee, Hwan Hee Kang, Seung Kyu Hwang, Kyu-Seok Jung, Jae-Kyung Jung, Kwan-Young Kim, Say-June |
author_sort | Choi, Ho Joong |
collection | PubMed |
description | BACKGROUND: Although methyl-tertiary butyl ether (MTBE) is the only clinical topical agent for gallstone dissolution, its use is limited by its side effects mostly arising from a relatively low boiling point (55 °C). In this study, we developed the gallstone-dissolving compound containing an aromatic moiety, named 2-methoxy-6-methylpyridine (MMP) with higher boiling point (156 °C), and compared its effectiveness and toxicities with MTBE. METHODS: The dissolubility of MTBE and MMP in vitro was determined by placing human gallstones in glass containers with either solvent and, then, measuring their dry weights. Their dissolubility in vivo was determined by comparing the weights of solvent-treated gallstones and control (dimethyl sulfoxide)-treated gallstones, after directly injecting each solvent into the gallbladder in hamster models with cholesterol and pigmented gallstones. RESULTS: In the in vitro dissolution test, MMP demonstrated statistically higher dissolubility than did MTBE for cholesterol and pigmented gallstones (88.2% vs. 65.7%, 50.8% vs. 29.0%, respectively; P < 0.05). In the in vivo experiments, MMP exhibited 59.0% and 54.3% dissolubility for cholesterol and pigmented gallstones, respectively, which were significantly higher than those of MTBE (50.0% and 32.0%, respectively; P < 0.05). The immunohistochemical stains of gallbladder specimens obtained from the MMP-treated hamsters demonstrated that MMP did not significantly increase the expression of cleaved caspase 9 or significantly decrease the expression of proliferation cell nuclear antigen. CONCLUSIONS: This study demonstrated that MMP has better potential than does MTBE in dissolving gallstones, especially pigmented gallstones, while resulting in lesser toxicities. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12967-019-1943-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6558798 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-65587982019-06-13 Efficacy and safety of a novel topical agent for gallstone dissolution: 2-methoxy-6-methylpyridine Choi, Ho Joong Cho, Suk Joon Kim, Ok-Hee Song, Jin Sook Hong, Ha-Eun Lee, Sang Chul Kim, Kee-Hwan Lee, Sang Kuon You, Young Kyoung Hong, Tae Ho Kim, Eun Young Park, Jung Hyun Na, Gun Hyung Do You, Dong Han, Jae Hyun Park, Jae Woo Kwak, Bong Jun Lee, Tae Yun Ahn, Joseph Lee, Hwan Hee Kang, Seung Kyu Hwang, Kyu-Seok Jung, Jae-Kyung Jung, Kwan-Young Kim, Say-June J Transl Med Research BACKGROUND: Although methyl-tertiary butyl ether (MTBE) is the only clinical topical agent for gallstone dissolution, its use is limited by its side effects mostly arising from a relatively low boiling point (55 °C). In this study, we developed the gallstone-dissolving compound containing an aromatic moiety, named 2-methoxy-6-methylpyridine (MMP) with higher boiling point (156 °C), and compared its effectiveness and toxicities with MTBE. METHODS: The dissolubility of MTBE and MMP in vitro was determined by placing human gallstones in glass containers with either solvent and, then, measuring their dry weights. Their dissolubility in vivo was determined by comparing the weights of solvent-treated gallstones and control (dimethyl sulfoxide)-treated gallstones, after directly injecting each solvent into the gallbladder in hamster models with cholesterol and pigmented gallstones. RESULTS: In the in vitro dissolution test, MMP demonstrated statistically higher dissolubility than did MTBE for cholesterol and pigmented gallstones (88.2% vs. 65.7%, 50.8% vs. 29.0%, respectively; P < 0.05). In the in vivo experiments, MMP exhibited 59.0% and 54.3% dissolubility for cholesterol and pigmented gallstones, respectively, which were significantly higher than those of MTBE (50.0% and 32.0%, respectively; P < 0.05). The immunohistochemical stains of gallbladder specimens obtained from the MMP-treated hamsters demonstrated that MMP did not significantly increase the expression of cleaved caspase 9 or significantly decrease the expression of proliferation cell nuclear antigen. CONCLUSIONS: This study demonstrated that MMP has better potential than does MTBE in dissolving gallstones, especially pigmented gallstones, while resulting in lesser toxicities. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12967-019-1943-y) contains supplementary material, which is available to authorized users. BioMed Central 2019-06-10 /pmc/articles/PMC6558798/ /pubmed/31182117 http://dx.doi.org/10.1186/s12967-019-1943-y Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Choi, Ho Joong Cho, Suk Joon Kim, Ok-Hee Song, Jin Sook Hong, Ha-Eun Lee, Sang Chul Kim, Kee-Hwan Lee, Sang Kuon You, Young Kyoung Hong, Tae Ho Kim, Eun Young Park, Jung Hyun Na, Gun Hyung Do You, Dong Han, Jae Hyun Park, Jae Woo Kwak, Bong Jun Lee, Tae Yun Ahn, Joseph Lee, Hwan Hee Kang, Seung Kyu Hwang, Kyu-Seok Jung, Jae-Kyung Jung, Kwan-Young Kim, Say-June Efficacy and safety of a novel topical agent for gallstone dissolution: 2-methoxy-6-methylpyridine |
title | Efficacy and safety of a novel topical agent for gallstone dissolution: 2-methoxy-6-methylpyridine |
title_full | Efficacy and safety of a novel topical agent for gallstone dissolution: 2-methoxy-6-methylpyridine |
title_fullStr | Efficacy and safety of a novel topical agent for gallstone dissolution: 2-methoxy-6-methylpyridine |
title_full_unstemmed | Efficacy and safety of a novel topical agent for gallstone dissolution: 2-methoxy-6-methylpyridine |
title_short | Efficacy and safety of a novel topical agent for gallstone dissolution: 2-methoxy-6-methylpyridine |
title_sort | efficacy and safety of a novel topical agent for gallstone dissolution: 2-methoxy-6-methylpyridine |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6558798/ https://www.ncbi.nlm.nih.gov/pubmed/31182117 http://dx.doi.org/10.1186/s12967-019-1943-y |
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