Evidence map›Paper›PMID 25119520›Full record

ArticleACS nano2014

Self-titrating anticoagulant nanocomplexes that restore homeostatic regulation of the coagulation cascade.

Kevin Y Lin, Justin H Lo, Nikita Consul, Gabriel A Kwong, Sangeeta N Bhatia

Abstract read
In one paragraph

Article in ACS nano, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Progress of nanomaterials in the treatment of thrombus.Drug delivery and translational research · 2024
    Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Advances in bioresponsive closed-loop drug delivery systems.International journal of pharmaceutics · 2018
    Review
  11. Designing hydrogels for controlled drug delivery.Nature reviews. Materials · 2016
    Article
  12. Article
  13. Smart nanosystems: Bio-inspired technologies that interact with the host environment.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Kevin Y LinDepartment of Chemical Engineering and ‡Harvard-MIT Division of Health Sciences and Technology, Massachusetts Institute of Technology , Cambridge, Massachusetts 02139, United States.
Justin H Lo
Nikita Consul
Gabriel A Kwong
Sangeeta N Bhatia

Funding

VIRUS PRODUCTION COREP30CA014051 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI Jacqueline A. Lees · 1985 to 2026
$93.9M
Medical Scientist Training ProgramT32GM007753 · NIGMS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI WALENSKY, LOREN DAVID · 1985 to 2021
$50.0M
Tumor Therapy/Annihilation Using a Smart NanoPlatform (SNaP)U54CA119335 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ESENER, SADIK · 2005 to 2010
$21.2M
TREATMENT OF CANCER WITH siRNA DELVIERED BY NANOPARTICLESU54CA119349 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BELCHER, ANGELA M. · 2005 to 2009
$20.5M
The Development of Clinical Grade, Targeted Magnetic NanoparticlesU54CA151884 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI LANGER, ROBERT SAMUEL · 2010 to 2014
$11.3M
Engineering Multifunctional NanoparticlesR01CA124427 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BHATIA, SANGEETA N. · 2006 to 2010
$4.7M
Diagnostic peptide-nanoparticle probes for profiling tumor protease activityF32CA159496 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI KWONG, GABRIEL A · 2011 to 2012
$101k
Howard Hughes Medical InstituteNCI NIH HHS 5 U54 CA151884-03NCI NIH HHS F32 CA159496NCI NIH HHS F32CA159496-02NCI NIH HHS P30 CA014051NCI NIH HHS P30-CA14051NCI NIH HHS R01 CA124427NCI NIH HHS R01CA124427-01NCI NIH HHS U54 CA119335NCI NIH HHS U54CA119335NCI NIH HHS U54 CA119349NCI NIH HHS U54CA119349NCI NIH HHS U54 CA151884NCI NIH HHS U54CA151884NIGMS NIH HHS T32 GM007753NIGMS NIH HHS T32GM007753
6 · The paper itself

Abstract

Antithrombotic therapy is a critical portion of the treatment regime for a number of life-threatening conditions, including cardiovascular disease, stroke, and cancer; yet, proper clinical management of anticoagulation remains a challenge because existing agents increase the propensity for bleeding in patients. Here, we describe the development of a bioresponsive peptide-polysaccharide nanocomplex that utilizes a negative feedback mechanism to self-titrate the release of anticoagulant in response to varying levels of coagulation activity. This nanoscale self-titrating activatable therapeutic, or nanoSTAT, consists of a cationic thrombin-cleavable peptide and heparin, an anionic polysaccharide and widely used clinical anticoagulant. Under nonthrombotic conditions, nanoSTATs circulate inactively, neither releasing anticoagulant nor significantly prolonging bleeding time. However, in response to life-threatening pulmonary embolism, nanoSTATs locally release their drug payload and prevent thrombosis. This autonomous negative feedback regulator may improve antithrombotic therapy by increasing the therapeutic window and decreasing the bleeding risk of anticoagulants.

Indexed as

AnimalsAnticoagulantsBlood CoagulationCattleHeparinHomeostasisHumansHuman Umbilical Vein Endothelial CellsMiceNanostructuresPolyethylene GlycolsPulmonary EmbolismThrombosisAnticoagulantsHeparinPolyethylene Glycolsanticoagulationnanomedicineproteaseself-regulationstimuli-responsive

Identifiers

PMID25119520
PMCPMC4174090

What OpenQuestion holds

Textmetadata
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.