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Pharmacodynamic testing and new validated HPLC method to assess the interchangeability between multi-source orlistat capsules
BACKGROUND: Orlistat is an irreversible inhibitor of the lipase enzyme that prevents trigylcerides from being digested, thereby inhibiting triglyceride hydrolysis and absorption. The resultant reduced calorie uptake enables a positive effect on weight control. Systemic absorption of the drug is, the...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5701567/ https://www.ncbi.nlm.nih.gov/pubmed/29200824 http://dx.doi.org/10.2147/DDDT.S138926 |
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author | Zaid, Abdel Naser Zohud, Nihal E’layan, Bushra Aburadi, Tasneem Jaradat, Nidal Ali, Iyad Hussein, Fatima Ghanem, Mashhour Qaddomi, Aiman Abu Zaaror, Yara |
author_facet | Zaid, Abdel Naser Zohud, Nihal E’layan, Bushra Aburadi, Tasneem Jaradat, Nidal Ali, Iyad Hussein, Fatima Ghanem, Mashhour Qaddomi, Aiman Abu Zaaror, Yara |
author_sort | Zaid, Abdel Naser |
collection | PubMed |
description | BACKGROUND: Orlistat is an irreversible inhibitor of the lipase enzyme that prevents trigylcerides from being digested, thereby inhibiting triglyceride hydrolysis and absorption. The resultant reduced calorie uptake enables a positive effect on weight control. Systemic absorption of the drug is, therefore, not necessary for its mode of action. An alternative in vitro study (pharmacodynamic) has been introduced for this drug, as in vivo bioavailability studies are irrelevant with regard to the achievement of the product’s intended purposes. OBJECTIVES: To develop a new validated high-performance liquid chromatography (HPLC) method for the analysis of orlistat and to assess the potency and equivalence of three orlistat formulations using the pharmacodynamic method as a surrogate indicator of pharmaceutical interchangeability. METHODS: A new HPLC method was developed for the analysis and for the dissolution studies of orlistat in capsules. Pancreatic lipase activity was measured for three different capsule products: Orlislim(®), Slimcare(®), and Xenical(®), G1, G2, and the brand, respectively. Porcine pancreatic lipase and p-nitrophenyl butyrate (PNPB) were placed in a pH 7.4 reaction buffer at 37°C, and substrate hydrolysis was monitored by measuring absorbance changes at 410 nm; this was repeated on six capsules of each product. The inhibition was expressed by the concentration of product, which inhibited 50% of the activity of pancreatic lipase (IC(50)). RESULTS: The new analytical method was suitable for orlistat analysis. Values of IC(50) from regression lines and equations were 6.14, 8.43, and 7.80 μg/mL for Orlislim(®), Xenical(®), and Slimcare(®), respectively. CONCLUSION: Pharmacodynamic studies of lipase inhibition could be used to support in vitro dissolution, which demonstrates interchangeability between generic and branded orlistat capsules. Moreover, it could be suggested as an alternative tool to bioequivalence studies for orlistat oral products. |
format | Online Article Text |
id | pubmed-5701567 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-57015672017-11-30 Pharmacodynamic testing and new validated HPLC method to assess the interchangeability between multi-source orlistat capsules Zaid, Abdel Naser Zohud, Nihal E’layan, Bushra Aburadi, Tasneem Jaradat, Nidal Ali, Iyad Hussein, Fatima Ghanem, Mashhour Qaddomi, Aiman Abu Zaaror, Yara Drug Des Devel Ther Original Research BACKGROUND: Orlistat is an irreversible inhibitor of the lipase enzyme that prevents trigylcerides from being digested, thereby inhibiting triglyceride hydrolysis and absorption. The resultant reduced calorie uptake enables a positive effect on weight control. Systemic absorption of the drug is, therefore, not necessary for its mode of action. An alternative in vitro study (pharmacodynamic) has been introduced for this drug, as in vivo bioavailability studies are irrelevant with regard to the achievement of the product’s intended purposes. OBJECTIVES: To develop a new validated high-performance liquid chromatography (HPLC) method for the analysis of orlistat and to assess the potency and equivalence of three orlistat formulations using the pharmacodynamic method as a surrogate indicator of pharmaceutical interchangeability. METHODS: A new HPLC method was developed for the analysis and for the dissolution studies of orlistat in capsules. Pancreatic lipase activity was measured for three different capsule products: Orlislim(®), Slimcare(®), and Xenical(®), G1, G2, and the brand, respectively. Porcine pancreatic lipase and p-nitrophenyl butyrate (PNPB) were placed in a pH 7.4 reaction buffer at 37°C, and substrate hydrolysis was monitored by measuring absorbance changes at 410 nm; this was repeated on six capsules of each product. The inhibition was expressed by the concentration of product, which inhibited 50% of the activity of pancreatic lipase (IC(50)). RESULTS: The new analytical method was suitable for orlistat analysis. Values of IC(50) from regression lines and equations were 6.14, 8.43, and 7.80 μg/mL for Orlislim(®), Xenical(®), and Slimcare(®), respectively. CONCLUSION: Pharmacodynamic studies of lipase inhibition could be used to support in vitro dissolution, which demonstrates interchangeability between generic and branded orlistat capsules. Moreover, it could be suggested as an alternative tool to bioequivalence studies for orlistat oral products. Dove Medical Press 2017-11-21 /pmc/articles/PMC5701567/ /pubmed/29200824 http://dx.doi.org/10.2147/DDDT.S138926 Text en © 2017 Zaid et al. 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/). 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. |
spellingShingle | Original Research Zaid, Abdel Naser Zohud, Nihal E’layan, Bushra Aburadi, Tasneem Jaradat, Nidal Ali, Iyad Hussein, Fatima Ghanem, Mashhour Qaddomi, Aiman Abu Zaaror, Yara Pharmacodynamic testing and new validated HPLC method to assess the interchangeability between multi-source orlistat capsules |
title | Pharmacodynamic testing and new validated HPLC method to assess the interchangeability between multi-source orlistat capsules |
title_full | Pharmacodynamic testing and new validated HPLC method to assess the interchangeability between multi-source orlistat capsules |
title_fullStr | Pharmacodynamic testing and new validated HPLC method to assess the interchangeability between multi-source orlistat capsules |
title_full_unstemmed | Pharmacodynamic testing and new validated HPLC method to assess the interchangeability between multi-source orlistat capsules |
title_short | Pharmacodynamic testing and new validated HPLC method to assess the interchangeability between multi-source orlistat capsules |
title_sort | pharmacodynamic testing and new validated hplc method to assess the interchangeability between multi-source orlistat capsules |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5701567/ https://www.ncbi.nlm.nih.gov/pubmed/29200824 http://dx.doi.org/10.2147/DDDT.S138926 |
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