Evidence map›Paper›PMID 26367020›Full record

ArticleBiomacromolecules2015

Polyamide Nanogels from Generally Recognized as Safe Components and Their Toxicity in Mouse Preimplantation Embryos.

Priyaa Prasad, Mijanur Rahaman Molla, Wei Cui, Mine Canakci, Barbara Osborne, Jesse Mager, S Thayumanavan

Open access · greenAbstract read
In one paragraph

Article in Biomacromolecules, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 36% 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

2 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. A Nonsurgical Embryo Transfer Technique for Fresh and Cultured Blastocysts in Rats.Journal of the American Association for Laboratory Animal Science : JAALAS · 2020
    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

7 authors at 1 institution in 1 country.

Priyaa PrasadDepartment of Chemistry, ‡Department of Veterinary and Animal Science, and §Molecular and Cellular Biology Program, University of Massachusetts , Amherst, Massachusetts 01003, United States.
Mijanur Rahaman MollaDepartment of Chemistry, ‡Department of Veterinary and Animal Science, and §Molecular and Cellular Biology Program, University of Massachusetts , Amherst, Massachusetts 01003, United States.
Wei CuiDepartment of Chemistry, ‡Department of Veterinary and Animal Science, and §Molecular and Cellular Biology Program, University of Massachusetts , Amherst, Massachusetts 01003, United States.
Mine CanakciDepartment of Chemistry, ‡Department of Veterinary and Animal Science, and §Molecular and Cellular Biology Program, University of Massachusetts , Amherst, Massachusetts 01003, United States.
Barbara OsborneDepartment of Chemistry, ‡Department of Veterinary and Animal Science, and §Molecular and Cellular Biology Program, University of Massachusetts , Amherst, Massachusetts 01003, United States.
Jesse MagerDepartment of Chemistry, ‡Department of Veterinary and Animal Science, and §Molecular and Cellular Biology Program, University of Massachusetts , Amherst, Massachusetts 01003, United States.
S ThayumanavanDepartment of Chemistry, ‡Department of Veterinary and Animal Science, and §Molecular and Cellular Biology Program, University of Massachusetts , Amherst, Massachusetts 01003, United States.
University of Massachusetts Amherst · US

Funding

Targeting TGF-b Inhibitors and PPAR-y Agonists To Enhance IPF TherapyP01HL119165 · NHLBI · PROTEOGENOMICS RESEARCH INSTIT/SYS/ MED · PI BOROK, ZEA · 2015 to 2019
$13.6M
Targeting y-secretase in GVHDP01CA166009 · NCI · UNIVERSITY OF MASSACHUSETTS AMHERST · PI OSBORNE, BARBARA A · 2013 to 2017
$4.9M
Functional Annotation of the Preimplantation TranscriptomeR21HD078942 · NICHD · UNIVERSITY OF MASSACHUSETTS AMHERST · PI MAGER, JESSE · 2014 to 2015
$420k
NCI NIH HHS P01 CA166009NHLBI NIH HHS HL-119165NHLBI NIH HHS P01 HL119165NICHD NIH HHS HD078942
6 · The paper itself

Abstract

Safe delivery systems that can not only encapsulate hydrophobic drug molecules, but also release them in response to specific triggers are important in several therapeutic and biomedical applications. In this paper, we have designed a nanogel based on molecules that are generally recognized as safe (GRAS). We have shown that the resultant polymeric nanogels exhibit responsive molecular release and also show high in vitro cellular viability on HEK 293T, HeLa, MCF 7, and A549 cell lines. The toxicity of these nanogels was further evaluated with a highly sensitive assay using mouse preimplantation embryo development, where blastocysts were formed after 4 days of in vitro culture, and live pups were born when morulae/early blastocysts were transferred to the uteri of surrogate recipients. Our results indicate that these nanogels are nontoxic during mammalian development and do not alter normal growth or early embryo success rate.

Indexed as

AnimalsBlastocystCell SurvivalFemaleHEK293 CellsHeLa CellsHumansHydrophobic and Hydrophilic InteractionsMCF-7 CellsMiceNanogelsNylonsPolyethylene GlycolsPolyethyleneimineNanogelsNylonspolyethylene glycol polyethyleneimine nanogelPolyethylene GlycolsPolyethyleneimine

Identifiers

PMID26367020
PMCPMC4970214
OpenAlexW2427197806

What OpenQuestion holds

Textmetadata
LicenceTDM
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.