Evidence map›Paper›PMID 23665448›Full record

ReviewEuropean journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V2013

Application of in vitro biopharmaceutical methods in development of immediate release oral dosage forms intended for paediatric patients.

Hannah K Batchelor, Richard Kendall, Sabine Desset-Brethes, Rainer Alex, Terry B Ernest, European Paediatric Formulation Initiative

Abstract readReview
PubMed Publisher
In one paragraph

Review in European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Article
  2. State of the art in pediatric nanomedicines.Drug delivery and translational research · 2024
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
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  11. Article
  12. UnderstandingActa pharmaceutica Sinica. B · 2017
    Review
  13. Review
  14. Article
  15. Article
  16. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Hannah K BatchelorPharmacy, Pharmacology and Therapeutics Section, University of Birmingham, Birmingham, UK. Electronic address: h.k.batchelor@bham.ac.uk.
Richard Kendall
Sabine Desset-Brethes
Rainer Alex
Terry B Ernest
European Paediatric Formulation Initiative

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Biopharmaceutics is routinely used in the design and development of medicines to generate science based evidence to predict in vivo performance; the application of this knowledge specifically to paediatric medicines development is yet to be explored. The aim of this review is to present the current status of available biopharmaceutical tools and tests including solubility, permeability and dissolution that may be appropriate for use in the development of immediate release oral paediatric medicines. The existing tools used in adults are discussed together with any limitations for their use within paediatric populations. The results of this review highlight several knowledge gaps in current methodologies in paediatric biopharmaceutics. The authors provide recommendations based on existing knowledge to adapt tests to better represent paediatric patient populations and also provide suggestions for future research that may lead to better tools to evaluate paediatric medicines.

Indexed as

AbsorptionAdministration, OralAdultBiopharmaceuticsChemistry, PharmaceuticalChildComputer SimulationDrug Delivery SystemsFood-Drug InteractionsHumansHydrogen-Ion ConcentrationIntestinal AbsorptionPediatricsPermeabilityPharmaceutical PreparationsSolubilityPharmaceutical PreparationsAbsorptionBCSBioavailabilityBiopharmaceuticsBiopharmaceutics classification systemDissolutionEMAEuropean Medicines AgencyFaSSIFFasted state simulated intestinal fluidFDAFed state simulated intestinal fluidFeSSIFGastrointestinalGIIn vitro in vivo relationshipIVIVRMADMaximum absorbable dosePaediatricPBPKPermeabilityP-GlycoproteinP-gpPharmacokineticPhysiologically based pharmacokineticPKSGFSimulated gastric fluidSolubility(United States) Food and Drug AdministrationUnited States pharmacopoeiaUSP

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.