Evidence map›Paper›PMID 36987222›Full record

ArticlePolymers2023

Application of Amyloid-Based Hybrid Membranes in Drug Delivery.

You-Ren Lai, Steven S-S Wang, Ti-Lun Hsu, Szu-Hui Chou, Su-Chun How, Ta-Hsien Lin

Open access · goldAbstract read
In one paragraph

Article in Polymers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

9 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Catalytic Amyloids: Turning Fibrils Into Biocatalysts.Chemistry (Weinheim an der Bergstrasse, Germany) · 2026
    Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Novel Ultrasound-Responsive Amyloid Formulation.Pharmaceuticals (Basel, Switzerland) · 2024
    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

6 authors at 3 institutions in 1 country.

You-Ren LaiDepartment of Chemical Engineering, National Taiwan University, Taipei 10617, Taiwan.ORCID 0000-0002-0493-4922
Steven S-S WangDepartment of Chemical Engineering, National Taiwan University, Taipei 10617, Taiwan.ORCID 0000-0001-5432-3268
Ti-Lun HsuDepartment of Chemical Engineering, National Taiwan University, Taipei 10617, Taiwan.
Szu-Hui ChouDepartment of Chemical Engineering, National Taiwan University, Taipei 10617, Taiwan.ORCID 0009-0006-0557-0784
Su-Chun HowDepartment of Chemical Engineering and Biotechnology, Tatung University, Taipei 104, Taiwan.
Ta-Hsien LinLaboratory of Nuclear Magnetic Resonance, Department of Medical Research, Taipei Veterans General Hospital, Taipei 11217, Taiwan.
National Taiwan University · TWNational Yang Ming Chiao Tung University · TWTatung University · TW

Funding

National Science and Technology Council MOST 110-2113-M-A49A-502-National Science and Technology Council MOST 111-2221-E-002-020-MY3National Science and Technology Council NSTC 111-2222-E-036-001 -
6 · The paper itself

Abstract

The properties of amyloid fibrils, e.g., unique structural characteristics and superior biocompatibility, make them a promising vehicle for drug delivery. Here, carboxymethyl cellulose (CMC) and whey protein isolate amyloid fibril (WPI-AF) were used to synthesize amyloid-based hybrid membranes as vehicles for the delivery of cationic and hydrophobic drugs (e.g., methylene blue (MB) and riboflavin (RF)). The CMC/WPI-AF membranes were synthesized via chemical crosslinking coupled with phase inversion. The zeta potential and scanning electron microscopy results revealed a negative charge and a pleated surface microstructure with a high content of WPI-AF. FTIR analysis showed that the CMC and WPI-AF were cross-linked via glutaraldehyde and the interacting forces between membrane and MB or RF was found to be electrostatic interaction and hydrogen bonding, respectively. Next, the in vitro drug release from membranes was monitored using UV-vis spectrophotometry. Additionally, two empirical models were used to analyze the drug release data and relevant rate constant and parameters were determined accordingly. Moreover, our results indicated that in vitro drug release rates depended on the drug-matrix interactions and transport mechanism, which could be controlled by altering the WPI-AF content in membrane. This research provides an excellent example of utilizing two-dimensional amyloid-based materials for drug delivery.

Indexed as

amyloidcarboxymethyl cellulosedrug deliverymembranewhey protein isolate

Identifiers

PMID36987222
PMCPMC10052896
OpenAlexW4324143050

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.