Evidence map›Paper›PMID 34890192›Full record

ArticleBiomacromolecules2022

Influence of Polymer Structure and Architecture on Drug Loading and Redox-Triggered Release.

Peidong Wu, Jingjing Gao, Priyaa Prasad, Kingshuk Dutta, Pintu Kanjilal, S Thayumanavan

Abstract read
In one paragraph

Article in Biomacromolecules, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
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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.

Peidong WuDepartment of Chemistry, University of Massachusetts Amherst, Amherst, Massachusetts 01003, United States.
Jingjing GaoDepartment of Chemistry, University of Massachusetts Amherst, Amherst, Massachusetts 01003, United States.
Priyaa PrasadDepartment of Chemistry, University of Massachusetts Amherst, Amherst, Massachusetts 01003, United States.
Kingshuk DuttaDepartment of Chemistry, University of Massachusetts Amherst, Amherst, Massachusetts 01003, United States.
Pintu KanjilalDepartment of Chemistry, University of Massachusetts Amherst, Amherst, Massachusetts 01003, United States.
S ThayumanavanDepartment of Chemistry, University of Massachusetts Amherst, Amherst, Massachusetts 01003, United States.ORCID 0000-0002-6475-6726

Funding

CHEMISTRY-BIOLOGY INTERFACE PREDOCTORAL TRAINING GRANTST32GM008515 · NIGMS · UNIVERSITY OF MASSACHUSETTS AMHERST · PI THOMPSON, LYNMARIE K. · 1995 to 2020
$4.3M
Protein-Induced Self-Assembly and Disassembly of Nanostructures Based on OligoR35GM136395 · NIGMS · UNIVERSITY OF MASSACHUSETTS AMHERST · PI Sankaran Thayumanavan · 2020 to 2026
$3.5M
Chemistry-Biology Interface Predoctoral Training GrantT32GM139789 · NIGMS · UNIVERSITY OF MASSACHUSETTS AMHERST · PI ERIC Robert STRIETER · 2021 to 2026
$3.4M
NIGMS NIH HHS R35 GM136395NIGMS NIH HHS T32 GM008515NIGMS NIH HHS T32 GM139789
6 · The paper itself

Abstract

Disulfide cross-linked nanoassemblies have attracted considerable attention as a drug delivery vehicle due to their responsiveness to the natural redox gradient in biology. Fundamentally understanding the factors that influence the drug loading capacity, encapsulation stability, and precise control of the liberation of encapsulated cargo would be profoundly beneficial to redox-responsive materials. Reported herein are block copolymer (BCP)-based self-cross-linked nanogels, which exhibit high drug loading capacity, high encapsulation stability, and controllable release kinetics. BCP nanogels show considerably higher loading capacity and better encapsulation stability than the random copolymer nanogels at micromolar glutathione concentrations. By partially substituting thiol-reactive pyridyl disulfide into the unreactive benzyl or butyl group, we observed opposite effects on the cross-linking process of BCP nanogels. We further studied the redox-responsive cytotoxicity of our drug-encapsulated nanogels in various cancer cell lines.

Indexed as

Polyethylene GlycolsPolymersDrug CarriersDrug LiberationNanogelsOxidation-ReductionPharmaceutical PreparationsDrug CarriersNanogelsPharmaceutical PreparationsPolyethylene GlycolsPolymers

Identifiers

PMID34890192
PMCPMC8757658

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Registered trials

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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.