Evidence map›Paper›PMID 32048079›Full record

ArticleThe AAPS journal2020

Biopharmaceutical Understanding of Excipient Variability on Drug Apparent Solubility Based on Drug Physicochemical Properties. Case Study: Superdisintegrants.

Panagiota Zarmpi, Talia Flanagan, Elizabeth Meehan, James Mann, Nikoletta Fotaki

Abstract readComparative Study
In one paragraph

Article in The AAPS journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Variations of Major Glucosinolates in Diverse Chinese Cabbage (International journal of molecular sciences · 2024
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
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.

Panagiota ZarmpiDepartment of Pharmacy and Pharmacology, University of Bath, Bath, BA2 7AY, UK.
Talia FlanaganPharmaceutical Technology & Development, AstraZeneca, Macclesfield, UK.
Elizabeth MeehanPharmaceutical Technology & Development, AstraZeneca, Macclesfield, UK.
James MannPharmaceutical Technology & Development, AstraZeneca, Macclesfield, UK.
Nikoletta FotakiDepartment of Pharmacy and Pharmacology, University of Bath, Bath, BA2 7AY, UK. n.fotaki@bath.ac.uk.ORCID http://orcid.org/0000-0003-1826-7363

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The presence of different excipient types/brands in solid oral dosage forms may affect product performance and drug bioavailability. Understanding the biopharmaceutical implications of superdisintegrant variability (changes in material properties), variation (changes in excipient amount) and interchangeability (use of different excipient types with the same intended functionality) in oral drug performance would be beneficial for the development of robust final dosage forms. The current study investigated the impact of superdisintegrants (sodium starch glycolate, croscarmellose sodium, crospovidone) on the apparent solubility of drugs with different physicochemical properties (drug ionisation, drug lipophilicity, drug aqueous solubility). Compendial and biorelevant media were used to assess the impact of gastrointestinal conditions on the effects of excipient on drug apparent solubility. For the majority of compounds, changes in drug apparent solubility were not observed in superdisintegrant presence, apart from the cases of highly ionised compounds (significant decrease in drug solubility) and/or compounds that aggregate/precipitate in solution (significant increase in drug solubility). Excipient variability did not greatly affect the impact of excipients on drug apparent solubility. The use of multivariate data analysis identified the biopharmaceutical factors affecting excipient performance. The construction of roadmaps revealed that superdisintegrants may be of low risk for the impact of excipients on oral drug performance based on drug solubility alone; superdisintegrants activity could still be a risk for oral bioavailability due to their effects on tablet disintegration.

Indexed as

Carboxymethylcellulose SodiumDrug CompoundingExcipientsHydrogen-Ion ConcentrationModels, ChemicalPharmaceutical PreparationsPovidoneSolubilityStarchViscosityCarboxymethylcellulose SodiumExcipientsPharmaceutical PreparationsPovidonesodium starch glycolateStarchcroscarmellose sodiumcrospovidonedrug solubilityexcipient variabilitysodium starch glycolate

Identifiers

PMID32048079
PMCPMC7012964

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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.