Cargando…
Enhanced Solubility of Telmisartan Phthalic Acid Cocrystals within the pH Range of a Systemic Absorption Site
[Image: see text] Telmisartan (TLM), a nonpeptide angiotensin II antagonist, is widely prescribed for treating arterial hypertension and marketed by the innovator with the trade name of Micardis and Micardis plus. Telmisartan exhibits low aqueous solubility in the pH range of 3–7, which is the physi...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2018
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6644309/ https://www.ncbi.nlm.nih.gov/pubmed/31458196 http://dx.doi.org/10.1021/acsomega.8b02144 |
_version_ | 1783437227621089280 |
---|---|
author | Kundu, Sudeshna Kumari, Nimmy Soni, Saundray Raj Ranjan, Subham Kumar, Rajan Sharon, Ashoke Ghosh, Animesh |
author_facet | Kundu, Sudeshna Kumari, Nimmy Soni, Saundray Raj Ranjan, Subham Kumar, Rajan Sharon, Ashoke Ghosh, Animesh |
author_sort | Kundu, Sudeshna |
collection | PubMed |
description | [Image: see text] Telmisartan (TLM), a nonpeptide angiotensin II antagonist, is widely prescribed for treating arterial hypertension and marketed by the innovator with the trade name of Micardis and Micardis plus. Telmisartan exhibits low aqueous solubility in the pH range of 3–7, which is the physiological pH. For addressing the issue of poor solubility of TLM, its commercial form makes use of inorganic alkalinizers. The present work illustrates the attempt to improve the solubility of telmisartan via a crystal engineering approach. A novel solid form of telmisartan with phthalic acid was obtained through the solution crystallization method (TPS) and the reaction crystallization method (TPR). Both the forms (TPS and TPR) were thoroughly characterized by powder diffraction X-ray diffraction, differential scanning calorimetry, thermogravimetric analysis, Fourier transform infrared spectroscopy, and (1)H NMR and were identified to be two different crystalline forms. Solubility studies of TPS and TPR were conducted at varying pH of phosphate buffer, and they exhibited 11-fold and 22-fold increased solubility, respectively, when compared to that of the pure drug at pH 5, which is within the pH of small intestine at which telmisartan is best absorbed orally from the systemic circulation. |
format | Online Article Text |
id | pubmed-6644309 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-66443092019-08-27 Enhanced Solubility of Telmisartan Phthalic Acid Cocrystals within the pH Range of a Systemic Absorption Site Kundu, Sudeshna Kumari, Nimmy Soni, Saundray Raj Ranjan, Subham Kumar, Rajan Sharon, Ashoke Ghosh, Animesh ACS Omega [Image: see text] Telmisartan (TLM), a nonpeptide angiotensin II antagonist, is widely prescribed for treating arterial hypertension and marketed by the innovator with the trade name of Micardis and Micardis plus. Telmisartan exhibits low aqueous solubility in the pH range of 3–7, which is the physiological pH. For addressing the issue of poor solubility of TLM, its commercial form makes use of inorganic alkalinizers. The present work illustrates the attempt to improve the solubility of telmisartan via a crystal engineering approach. A novel solid form of telmisartan with phthalic acid was obtained through the solution crystallization method (TPS) and the reaction crystallization method (TPR). Both the forms (TPS and TPR) were thoroughly characterized by powder diffraction X-ray diffraction, differential scanning calorimetry, thermogravimetric analysis, Fourier transform infrared spectroscopy, and (1)H NMR and were identified to be two different crystalline forms. Solubility studies of TPS and TPR were conducted at varying pH of phosphate buffer, and they exhibited 11-fold and 22-fold increased solubility, respectively, when compared to that of the pure drug at pH 5, which is within the pH of small intestine at which telmisartan is best absorbed orally from the systemic circulation. American Chemical Society 2018-11-13 /pmc/articles/PMC6644309/ /pubmed/31458196 http://dx.doi.org/10.1021/acsomega.8b02144 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Kundu, Sudeshna Kumari, Nimmy Soni, Saundray Raj Ranjan, Subham Kumar, Rajan Sharon, Ashoke Ghosh, Animesh Enhanced Solubility of Telmisartan Phthalic Acid Cocrystals within the pH Range of a Systemic Absorption Site |
title | Enhanced Solubility of Telmisartan Phthalic Acid Cocrystals
within the pH Range of a Systemic Absorption Site |
title_full | Enhanced Solubility of Telmisartan Phthalic Acid Cocrystals
within the pH Range of a Systemic Absorption Site |
title_fullStr | Enhanced Solubility of Telmisartan Phthalic Acid Cocrystals
within the pH Range of a Systemic Absorption Site |
title_full_unstemmed | Enhanced Solubility of Telmisartan Phthalic Acid Cocrystals
within the pH Range of a Systemic Absorption Site |
title_short | Enhanced Solubility of Telmisartan Phthalic Acid Cocrystals
within the pH Range of a Systemic Absorption Site |
title_sort | enhanced solubility of telmisartan phthalic acid cocrystals
within the ph range of a systemic absorption site |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6644309/ https://www.ncbi.nlm.nih.gov/pubmed/31458196 http://dx.doi.org/10.1021/acsomega.8b02144 |
work_keys_str_mv | AT kundusudeshna enhancedsolubilityoftelmisartanphthalicacidcocrystalswithinthephrangeofasystemicabsorptionsite AT kumarinimmy enhancedsolubilityoftelmisartanphthalicacidcocrystalswithinthephrangeofasystemicabsorptionsite AT sonisaundrayraj enhancedsolubilityoftelmisartanphthalicacidcocrystalswithinthephrangeofasystemicabsorptionsite AT ranjansubham enhancedsolubilityoftelmisartanphthalicacidcocrystalswithinthephrangeofasystemicabsorptionsite AT kumarrajan enhancedsolubilityoftelmisartanphthalicacidcocrystalswithinthephrangeofasystemicabsorptionsite AT sharonashoke enhancedsolubilityoftelmisartanphthalicacidcocrystalswithinthephrangeofasystemicabsorptionsite AT ghoshanimesh enhancedsolubilityoftelmisartanphthalicacidcocrystalswithinthephrangeofasystemicabsorptionsite |