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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...

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Autores principales: Zaid, Abdel Naser, Zohud, Nihal, E’layan, Bushra, Aburadi, Tasneem, Jaradat, Nidal, Ali, Iyad, Hussein, Fatima, Ghanem, Mashhour, Qaddomi, Aiman, Abu Zaaror, Yara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
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.
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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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