Stability of Methylphenidate under Various pH Conditions in the Presence or Absence of Gut Microbiota
Methylphenidate is one of the most widely used oral treatments for attention-deficit/hyperactivity disorder (ADHD). The drug is mainly absorbed in the small intestine and has low bioavailability. Accordingly, a high interindividual variability in terms of response to the treatment is known among ADH...
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doaj-41adeb2eb219436d86d6c272c6bd5c662021-08-26T14:12:10ZengMDPI AGPharmaceuticals1424-82472021-07-011473373310.3390/ph14080733Stability of Methylphenidate under Various pH Conditions in the Presence or Absence of Gut MicrobiotaJulia Aresti-Sanz0Markus Schwalbe1Rob Rodrigues Pereira2Hjalmar Permentier3Sahar El Aidy4Host-Microbe Interactions, Groningen Biomolecular Sciences and Biotechnology Institute (GBB), University of Groningen, 9747 AG Groningen, The NetherlandsHost-Microbe Interactions, Groningen Biomolecular Sciences and Biotechnology Institute (GBB), University of Groningen, 9747 AG Groningen, The NetherlandsMedical Center Kinderplein, 3083 BB Rotterdam, The NetherlandsInterfaculty Mass Spectrometry Center, Department of Analytical Biochemistry, Groningen Research Institute of Pharmacy (GRIP), 9713 AV Groningen, The NetherlandsHost-Microbe Interactions, Groningen Biomolecular Sciences and Biotechnology Institute (GBB), University of Groningen, 9747 AG Groningen, The NetherlandsMethylphenidate is one of the most widely used oral treatments for attention-deficit/hyperactivity disorder (ADHD). The drug is mainly absorbed in the small intestine and has low bioavailability. Accordingly, a high interindividual variability in terms of response to the treatment is known among ADHD patients treated with methylphenidate. Nonetheless, very little is known about the factors that influence the drug’s absorption and bioavailability. Gut microbiota has been shown to reduce the bioavailability of a wide variety of orally administered drugs. Here, we tested the ability of small intestinal bacteria to metabolize methylphenidate. In silico analysis identified several small intestinal bacteria to harbor homologues of the human carboxylesterase 1 enzyme responsible for the hydrolysis of methylphenidate in the liver into the inactive form, ritalinic acid. Despite our initial results hinting towards possible bacterial hydrolysis of the drug, up to 60% of methylphenidate is spontaneously hydrolyzed in the absence of bacteria and this hydrolysis is pH-dependent. Overall, our results indicate that the stability of methylphenidate is compromised under certain pH conditions in the presence or absence of gut microbiota.https://www.mdpi.com/1424-8247/14/8/733Retalinmetabolismavailabilityintestinal pHgut bacteria |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Julia Aresti-Sanz Markus Schwalbe Rob Rodrigues Pereira Hjalmar Permentier Sahar El Aidy |
spellingShingle |
Julia Aresti-Sanz Markus Schwalbe Rob Rodrigues Pereira Hjalmar Permentier Sahar El Aidy Stability of Methylphenidate under Various pH Conditions in the Presence or Absence of Gut Microbiota Pharmaceuticals Retalin metabolism availability intestinal pH gut bacteria |
author_facet |
Julia Aresti-Sanz Markus Schwalbe Rob Rodrigues Pereira Hjalmar Permentier Sahar El Aidy |
author_sort |
Julia Aresti-Sanz |
title |
Stability of Methylphenidate under Various pH Conditions in the Presence or Absence of Gut Microbiota |
title_short |
Stability of Methylphenidate under Various pH Conditions in the Presence or Absence of Gut Microbiota |
title_full |
Stability of Methylphenidate under Various pH Conditions in the Presence or Absence of Gut Microbiota |
title_fullStr |
Stability of Methylphenidate under Various pH Conditions in the Presence or Absence of Gut Microbiota |
title_full_unstemmed |
Stability of Methylphenidate under Various pH Conditions in the Presence or Absence of Gut Microbiota |
title_sort |
stability of methylphenidate under various ph conditions in the presence or absence of gut microbiota |
publisher |
MDPI AG |
series |
Pharmaceuticals |
issn |
1424-8247 |
publishDate |
2021-07-01 |
description |
Methylphenidate is one of the most widely used oral treatments for attention-deficit/hyperactivity disorder (ADHD). The drug is mainly absorbed in the small intestine and has low bioavailability. Accordingly, a high interindividual variability in terms of response to the treatment is known among ADHD patients treated with methylphenidate. Nonetheless, very little is known about the factors that influence the drug’s absorption and bioavailability. Gut microbiota has been shown to reduce the bioavailability of a wide variety of orally administered drugs. Here, we tested the ability of small intestinal bacteria to metabolize methylphenidate. In silico analysis identified several small intestinal bacteria to harbor homologues of the human carboxylesterase 1 enzyme responsible for the hydrolysis of methylphenidate in the liver into the inactive form, ritalinic acid. Despite our initial results hinting towards possible bacterial hydrolysis of the drug, up to 60% of methylphenidate is spontaneously hydrolyzed in the absence of bacteria and this hydrolysis is pH-dependent. Overall, our results indicate that the stability of methylphenidate is compromised under certain pH conditions in the presence or absence of gut microbiota. |
topic |
Retalin metabolism availability intestinal pH gut bacteria |
url |
https://www.mdpi.com/1424-8247/14/8/733 |
work_keys_str_mv |
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