Evidence map›Paper›PMID 30142268›Full record

ArticleMolecular pharmaceutics2018

Impact of Drug Physicochemical Properties on Lipolysis-Triggered Drug Supersaturation and Precipitation from Lipid-Based Formulations.

Linda C Alskär, Janneke Keemink, Jenny Johannesson, Christopher J H Porter, Christel A S Bergström

Open access · bronzeAbstract read
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Article in Molecular pharmaceutics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.4field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 61 citations in OpenAlex.

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  9. Acta pharmaceutica Sinica. B · 2021
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 2 countries.

Linda C AlskärDepartment of Pharmacy , Uppsala University , Uppsala Biomedical Center P.O. Box 580, SE-751 23 Uppsala , Sweden.ORCID 0000-0002-3905-4001
Janneke KeeminkDepartment of Pharmacy , Uppsala University , Uppsala Biomedical Center P.O. Box 580, SE-751 23 Uppsala , Sweden.
Jenny JohannessonDepartment of Pharmacy , Uppsala University , Uppsala Biomedical Center P.O. Box 580, SE-751 23 Uppsala , Sweden.
Christopher J H PorterDrug Delivery, Disposition and Dynamics , Monash Institute of Pharmaceutical Sciences, Monash University , 381 Royal Parade , Parkville , Victoria 3052 , Australia.ORCID 0000-0003-3474-7551
Christel A S BergströmDepartment of Pharmacy , Uppsala University , Uppsala Biomedical Center P.O. Box 580, SE-751 23 Uppsala , Sweden.
Uppsala University · SEMonash University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this study we investigated lipolysis-triggered supersaturation and precipitation of a set of model compounds formulated in lipid-based formulations (LBFs). The purpose was to explore the relationship between precipitated solid form and inherent physicochemical properties of the drug. Eight drugs were studied after formulation in three LBFs, representing lipid-rich (extensively digestible) to surfactant-rich (less digestible) formulations. In vitro lipolysis of drug-loaded LBFs were conducted, and the amount of dissolved and precipitated drug was quantified. Solid form of the precipitated drug was characterized with polarized light microscopy (PLM) and Raman spectroscopy. A significant solubility increase for the weak bases in the presence of digestion products was observed, in contrast to the neutral and acidic compounds for which the solubility decreased. The fold-increase in solubility was linked to the degree of ionization of the weak bases and thus their attraction to free fatty acids. A high level of supersaturation was needed to cause precipitation. For the weak bases, the dose number indicated that precipitation would not occur during lipolysis; hence, these compounds were not included in further studies. The solid state analysis proved that danazol and griseofulvin precipitated in a crystalline form, while niclosamide precipitated as a hydrate. Felodipine and indomethacin crystals were visible in the PLM, whereas the Raman spectra showed presence of amorphous drug, indicating amorphous precipitation that quickly crystallized. The solid state analysis was combined with literature data to allow analysis of the relationship between solid form and the physicochemical properties of the drug. It was found that low molecular weight and high melting temperature increases the probability of crystalline precipitation, whereas precipitation in an amorphous form was favored by high molecular weight, low melting temperature, and positive charge.

Indexed as

Drug CompoundingFelodipineIndomethacinLipolysisMicroscopySolubilitySpectrum Analysis, RamanFelodipineIndomethacinlipid digestionphysicochemical propertiesPoorly water-soluble drugsprecipitationsolid statesupersaturation

Identifiers

PMID30142268
PMCPMC6209313
OpenAlexW2888154372

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.