Evidence map›Paper›PMID 32382838›Full record

ArticlePharmaceutical research2020

Designing Biodegradable Wafers Based on Poly(L-lactide-co-glycolide) and Poly(glycolide-co-ε-caprolactone) for the Prolonged and Local Release of Idarubicin for the Therapy of Glioblastoma Multiforme.

Artur Turek, Katarzyna Stoklosa, Aleksandra Borecka, Monika Paul-Samojedny, Bożena Kaczmarczyk, Andrzej Marcinkowski, Janusz Kasperczyk

Abstract read
In one paragraph

Article in Pharmaceutical research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
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

7 authors.

Artur TurekFaculty of Pharmaceutical Sciences in Sosnowiec, Medical University of Silesia, Katowice, Chair and Department of Biopharmacy, Jedności 8, 41-200, Katowice, Poland. a.turek75@gmail.com.
Katarzyna StoklosaFaculty of Pharmaceutical Sciences in Sosnowiec, Medical University of Silesia, Katowice, Chair and Department of Biopharmacy, Jedności 8, 41-200, Katowice, Poland.
Aleksandra BoreckaCentre of Polymer and Carbon Materials, Polish Academy of Sciences, M. Curie-Sklodowskiej 43, 41-819, Zabrze, Poland.
Monika Paul-SamojednyFaculty of Pharmaceutical Sciences in Sosnowiec, Medical University of Silesia, Katowice, Chair and Department of Medical Genetics, Jedności 8, 41-200, Sosnowiec, Poland.
Bożena KaczmarczykCentre of Polymer and Carbon Materials, Polish Academy of Sciences, M. Curie-Sklodowskiej 43, 41-819, Zabrze, Poland.
Andrzej MarcinkowskiCentre of Polymer and Carbon Materials, Polish Academy of Sciences, M. Curie-Sklodowskiej 43, 41-819, Zabrze, Poland.
Janusz KasperczykFaculty of Pharmaceutical Sciences in Sosnowiec, Medical University of Silesia, Katowice, Chair and Department of Biopharmacy, Jedności 8, 41-200, Katowice, Poland.

Funding

Śląski Uniwersytet Medyczny KNW-1-040/N/9/O
6 · The paper itself

Abstract

purposeThe blood-brain barrier limits the application of idarubicin in the therapy of glioblastoma multiforme. Biodegradable, intracranial wafers with prolonged release may increase therapy efficiency.

methodsBlank wafers, wafers containing 5% w/w and 10% w/w of idarubicin were formulated by solution casting from poly(L-lactide-co-glycolide) and poly(glycolide-co-ε-caprolactone). The following methods were used: NMR, GPC, DSC, FTIR, AFM, UV-VIS, and a viability and proliferation assay for idarubicin action (U87MG cell line).

resultsWafers showed a surface with numerous immersions and hills. A lack of interactions between idarubicin and the copolymers was observed. The substance was entrapped in the matrix and released in two phases for all wafers with the appropriate bolus and maintenance dose. The burst effect was observed for all wafers, however, the biggest bolus for poly(L-lactide-co-glycolide) wafers containing 5% w/w of idarubicin was noted. The stable and steady degradation of poly(glycolide-co-ε-caprolactone) wafers containing 5% w/w of idarubicin ensures the most optimal release profile and high inhibition of proliferation.

conclusionsCopolymer wafers with idarubicin are an interesting proposition with great potential for the local treatment of glioblastoma multiforme. The release rate and dose may be regulated by the amount and kind of wafers for various effects.

Indexed as

Cell Line, TumorCell SurvivalDrug CarriersDrug LiberationGlioblastomaHumansIdarubicinPolylactic Acid-Polyglycolic Acid CopolymerPolymersTechnology, PharmaceuticalDrug CarriersIdarubicinPolylactic Acid-Polyglycolic Acid CopolymerPolymersglioblastoma multiformeidarubicinpoly(glycolide-co-ε-caprolactone)poly(L-lactide-co-glycolide)wafer

Identifiers

PMID32382838
PMCPMC7205781

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.