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Exploring the use of modified in vitro digestion assays for the evaluation of ritonavir loaded solid lipid-based formulations

Andreadis, Ioannis I. (author)
Uppsala universitet,Institutionen för farmaci,Aristotle Univ Thessaloniki, Fac Hlth Sci, Dept Pharm, Lab Pharmaceut Technol, GR-54124 Thessaloniki, Greece.
Schulzen, Arne (author)
Heinrich Heine Univ, Inst Pharmaceut & Biopharmaceut, Univ str 1, D-40225 Dusseldorf, Germany.
Quodbach, Julian (author)
Univ Utrecht, Dept Pharmaceut, Univ weg 99, NL-3584 CG Utrecht, Netherlands.
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Bergström, Christel, 1973- (author)
Uppsala universitet,Institutionen för farmaci
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 (creator_code:org_t)
Elsevier BV, 2023
2023
English.
In: European Journal of Pharmaceutical Sciences. - : Elsevier BV. - 0928-0987 .- 1879-0720. ; 189
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Solid lipid-based formulations (sLBFs) have the potential to increase the oral bioavailability of drugs with poor solubility in water, while counteracting some of the disadvantages of liquid LBFs. The most common experimental set-up to study the performance of LBFs in vitro is the lipolysis assay, during which the LBFs are digested by lipases in an environment mimicking the human small intestine. However, this assay has failed in many cases to correctly predict the performance of LBFs in vivo, highlighting the need for new and improved in vitro assays to evaluate LBFs at the preclinical stage. In this study, the suitability of three different in vitro digestion assays for the evaluation of sLBFs was assessed; the classic one-step intestinal digestion assay, a two-step gastrointestinal digestion assay and a bicompartmental assay permitting the simultaneous monitoring of digestion and permeation of the active pharmaceutical ingredient (API) across an artificial membrane (Lecithin in Dodecane - LiDo). Three sLBFs (M1-M3) with varied composition and ritonavir as model drug were prepared and examined. When comparing the ability of these formulations to keep the drug solubilized in the aqueous phase, all three assays show that M1 performs better, while M3 presents poor performance. However, the classic in vitro intestinal digestion assay fails to provide a clear ranking of the three formulations, something that is more evident when using the two modified and more physiologically relevant assays. Also, the two modified assays provide additional information about the performance of the formulations including the performance in the gastric environment and intestinal flux of the drug. These modified in vitro digestion assays are valuable tools for the development and evaluation of sLBFs to make better informed decisions of which formulations to pursue for in vivo studies.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmaceutiska vetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmaceutical Sciences (hsv//eng)

Keyword

In vitro model
Lipid digestion
Solid lipid based formulation
Ritonavir
Oral drug delivery

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ref (subject category)
art (subject category)

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Andreadis, Ioann ...
Schulzen, Arne
Quodbach, Julian
Bergström, Chris ...
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MEDICAL AND HEALTH SCIENCES
MEDICAL AND HEAL ...
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