Evidence map›Paper›PMID 40565328›Full record

ArticleInternational journal of molecular sciences2025

Self-Assembling Amphiphilic ABA Triblock Copolymers of Hyperbranched Polyglycerol with Poly(tetrahydrofuran) and Their Nanomicelles as Highly Efficient Solubilization and Delivery Systems of Curcumin.

Dóra Fecske, György Kasza, Gergő Gyulai, Kata Horváti, Márk Szabó, András Wacha, Zoltán Varga, Györgyi Szarka, Yi Thomann, Ralf Thomann and 6 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. 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. 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

16 authors.

Dóra FecskePolymer Chemistry and Physics Research Group, Institute of Materials and Environmental Chemistry, HUN-REN Research Centre for Natural Sciences, Magyar tudósok körútja 2, H-1117 Budapest, Hungary.
György KaszaPolymer Chemistry and Physics Research Group, Institute of Materials and Environmental Chemistry, HUN-REN Research Centre for Natural Sciences, Magyar tudósok körútja 2, H-1117 Budapest, Hungary.ORCID 0000-0003-3335-8730
Gergő GyulaiLaboratory of Interfaces and Nanostructures, Institute of Chemistry, Eötvös Loránd University, P.O. Box 32, H-1518 Budapest, Hungary.
Kata HorvátiMTA-HUN-REN "Momentum" Peptide-Based Vaccines Research Group, Institute of Materials and Environmental Chemistry, HUN-REN Research Centre for Natural Sciences, Magyar tudósok körútja 2, H-1117 Budapest, Hungary.ORCID 0000-0003-4092-6011
Márk SzabóNMR Research Laboratory, Centre for Structural Science, HUN-REN Research Centre for Natural Sciences, Magyar tudósok körútja 2, H-1117 Budapest, Hungary.
András WachaBiological Nanochemistry Research Group, Institute of Materials and Environmental Chemistry, HUN-REN Research Centre for Natural Sciences, Magyar tudósok körútja 2, H-1117 Budapest, Hungary.ORCID 0000-0002-9609-0893
Zoltán VargaBiological Nanochemistry Research Group, Institute of Materials and Environmental Chemistry, HUN-REN Research Centre for Natural Sciences, Magyar tudósok körútja 2, H-1117 Budapest, Hungary.ORCID 0000-0002-5741-2669
Györgyi SzarkaPolymer Chemistry and Physics Research Group, Institute of Materials and Environmental Chemistry, HUN-REN Research Centre for Natural Sciences, Magyar tudósok körútja 2, H-1117 Budapest, Hungary.
Yi ThomannFreiburg Materials Research Center, University of Freiburg, Stefan-Meier-Str. 21, D-79104 Freiburg, Germany.ORCID 0000-0001-6082-5061
Ralf ThomannFreiburg Materials Research Center, University of Freiburg, Stefan-Meier-Str. 21, D-79104 Freiburg, Germany.
Rolf MülhauptFreiburg Materials Research Center, University of Freiburg, Stefan-Meier-Str. 21, D-79104 Freiburg, Germany.
Éva KissLaboratory of Interfaces and Nanostructures, Institute of Chemistry, Eötvös Loránd University, P.O. Box 32, H-1518 Budapest, Hungary.
Attila DomjánNMR Research Laboratory, Centre for Structural Science, HUN-REN Research Centre for Natural Sciences, Magyar tudósok körútja 2, H-1117 Budapest, Hungary.
Szilvia BőszeHUN-REN-ELTE Research Group of Peptide Chemistry, Hungarian Research Network, Pázmány Péter sétány 1/A, H-1117 Budapest, Hungary.
Laura BereczkiChemical Crystallography Research Laboratory, Centre of Structural Science, HUN-REN Research Centre for Natural Sciences, Magyar tudósok körútja 2, H-1117 Budapest, Hungary.
Béla IvánPolymer Chemistry and Physics Research Group, Institute of Materials and Environmental Chemistry, HUN-REN Research Centre for Natural Sciences, Magyar tudósok körútja 2, H-1117 Budapest, Hungary.ORCID 0000-0003-2475-6841

Funding

National Research, Development and Innovation Office, Hungary PD139162, NN116252, NN129366, 115939, K135946, FK142754, FK146081, K142904, TKP2021-EGA-31
6 · The paper itself

Abstract

Delivering of hydrophobic drugs by polymeric nanoparticles is an intensively investigated research and development field worldwide due to the insufficient solubility of many existing and potential new drugs in aqueous media. Among polymeric nanoparticles, micelles of biocompatible amphiphilic block copolymers are among the most promising candidates for solubilization, encapsulation, and delivery of hydrophobic drugs to improve the water solubility and thus the bioavailability of such drugs. In this study, amphiphilic ABA triblock copolymers containing biocompatible hydrophilic hyperbranched (dendritic) polyglycerol (HbPG) outer and hydrophobic poly(tetrahydrofuran) (PTHF) inner segments were synthesized using amine-telechelic PTHF as a macroinitiator for glycidol polymerization. These hyperbranched-linear-hyperbranched block copolymers form nanosized micelles with 15-20 nm diameter above the critical micelle concentration. Coagulation experiments proved high colloidal stability of the aqueous micellar solutions of these block copolymers against temperature changes. The applicability of block copolymers as drug delivery systems was investigated using curcumin, a highly hydrophobic, water-insoluble, natural anti-cancer agent. High and efficient drug solubilization up to more than 3 orders of magnitude to that of the water solubility of curcumin (>1500-fold) is achieved with the HbPG-PTHF-HbPG block copolymer nanomicelles, locating the drug in amorphous form in the inner PTHF core. Outstanding stability of and sustained curcumin release from the drug-loaded block copolymer micelles were observed. The in vitro bioactivity of the curcumin-loaded nanomicelles was investigated on U-87 glioblastoma cell line, and an optimal triblock copolymer composition was found, which showed highly effective cellular uptake and no toxicity. These findings indicate that the HbPG-PTHF-HbPG triblock copolymers are promising candidates for advanced drug solubilization and delivery systems.

Indexed as

CurcuminDrug CarriersDrug Delivery SystemsFuransGlycerolMicellesNanoparticlesPolymersAntineoplastic AgentsCell Line, TumorDrug LiberationHumansHydrophobic and Hydrophilic InteractionsSolubilityAntineoplastic AgentsCurcuminDrug CarriersFuransGlycerolMicellespolyglycerolPolymerstetrahydrofuranamphiphilic ABA triblock copolymercell internalizationcurcumindrug deliverydrug solubilizationhyperbranched polyglycerol (HbPG)nanomicellar carriernanomicellepoly(tetrahydrofuran) (PTHF)self-assembly

Identifiers

PMID40565328
PMCPMC12192588

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.