Evidence map›Paper›PMID 32228620›Full record

ArticleJournal of nanobiotechnology2020

Drug affinity and targeted delivery: double functionalization of silk spheres for controlled doxorubicin delivery into Her2-positive cancer cells.

Kamil Kucharczyk, Anna Florczak, Tomasz Deptuch, Karolina Penderecka, Katarzyna Jastrzebska, Andrzej Mackiewicz, Hanna Dams-Kozlowska

Open access · goldAbstract read
In one paragraph

Article in Journal of nanobiotechnology, 2020. 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
2.1field-weighted citation impact, top 13% 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, 39 citations in OpenAlex.

  1. Article
  2. Review
  3. Nanostructured Protein Surfaces Inspired by Spider Silk.Advanced materials (Deerfield Beach, Fla.) · 2025
    Review
  4. Article
  5. Article
  6. Unveiling the Rational Development of Stimuli-Responsive Silk Fibroin-Based Ionogel Formulations.Chemistry of materials : a publication of the American Chemical Society · 2023
    Article
  7. Review
  8. Facile Synthesis of FeMolecules (Basel, Switzerland) · 2022
    Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. 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 at 1 institution in 1 country.

Kamil KucharczykChair of Medical Biotechnology, Poznan University of Medical Sciences, 61-688, Poznan, Poland.
Anna FlorczakChair of Medical Biotechnology, Poznan University of Medical Sciences, 61-688, Poznan, Poland.
Tomasz DeptuchChair of Medical Biotechnology, Poznan University of Medical Sciences, 61-688, Poznan, Poland.
Karolina PendereckaChair of Medical Biotechnology, Poznan University of Medical Sciences, 61-688, Poznan, Poland.
Katarzyna JastrzebskaChair of Medical Biotechnology, Poznan University of Medical Sciences, 61-688, Poznan, Poland.
Andrzej MackiewiczChair of Medical Biotechnology, Poznan University of Medical Sciences, 61-688, Poznan, Poland.
Hanna Dams-KozlowskaChair of Medical Biotechnology, Poznan University of Medical Sciences, 61-688, Poznan, Poland. hanna.dams-kozlowska@wco.pl.ORCID http://orcid.org/0000-0003-2349-419X
Poznan University of Medical Sciences · PL

Funding

Narodowym Centrum Nauki (PL) 2014/15/B/NZ7/00903
6 · The paper itself

Abstract

backgroundThe optimal drug delivery system should be biocompatible, biodegradable, and allow the sustained release of the drug only after it reaches the target cells. Silk, as a natural polymer, is a great candidate for building drug carriers. Genetically engineered silks offer the possibility of functionalization. Previously, we characterized bioengineered silk spheres that were functionalized with H2.1 peptide that selectively delivered a drug to Her2-positive cancer cells. However, drug leakage from the silk spheres showed the need for improved control.

resultsTo control the drug loading and release, we designed and produced functional silk (DOXMS2) that contains a DOX peptide with an affinity for doxorubicin. The DOXMS2 spheres showed the decreased release of doxorubicin compared with MS2 particles. Next, the DOXMS2 silk was blended with the H2.1MS1 polymer to improve the control of doxorubicin binding and release into Her2-positive cancer cells. The H2.1MS1:DOXMS2 particles showed the highest doxorubicin-loading capacity and binding per cell, which resulted in the highest cytotoxic effect compared with that of other sphere variants. Since drug release at a pH of 7.4 from the blended H2.1MS1:DOXMS2 particles was significantly lower than from blended spheres without DOXMS2 silk, this indicated that such particles could control the release of the drug into the circulatory system before the carrier reached the tumor site.

conclusionsThis strategy, which is based on the blending of silks, allows for the generation of particles that deliver drugs in a controlled manner.

Indexed as

Antineoplastic AgentsDoxorubicinDrug CarriersDrug Delivery SystemsDrug LiberationErb-b2 Receptor Tyrosine KinasesGenetic EngineeringHumansPeptidesSilkAntineoplastic AgentsDoxorubicinDrug CarriersERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesPeptidesSilkCancerDoxorubicinDrug carrierGenetic engineeringSilkSpheres

Identifiers

PMID32228620
PMCPMC7106823
OpenAlexW3013838466

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.