Evidence map›Paper›PMID 26485440›Full record

ArticleMolecular pharmaceutics2015

Polymeric Micelles as Carriers for Nerve-Highlighting Fluorescent Probe Delivery.

Kayla M Hackman, Bhuvana Shyam Doddapaneni, Connor W Barth, Igor H Wierzbicki, Adam W G Alani, Summer L Gibbs

Open access · greenAbstract read
In one paragraph

Article in Molecular pharmaceutics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.7field-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

15 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. A targeted combinatorial therapy for Ewing's sarcoma.Nanomedicine : nanotechnology, biology, and medicine · 2021
    Article
  6. Article
  7. Article
  8. Diagnostic Performance of Receptor-Specific Surgical Specimen Staining Correlate with Receptor Expression Level.Proceedings of SPIE--the International Society for Optical Engineering · 2019
    Article
  9. Article
  10. Investigation of Oxazine and Rhodamine Derivatives as Peripheral Nerve Tissue Targeting Contrast Agent forProceedings of SPIE--the International Society for Optical Engineering · 2019
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Visualizing Oxazine 4 nerve-specific fluorescenceProceedings of SPIE--the International Society for Optical Engineering · 2016
    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 2 institutions in 1 country.

Kayla M Hackman
Bhuvana Shyam DoddapaneniPharmaceutical Sciences Division, College of Pharmacy, Oregon State University , 2730 SW Moody Avenue, CL5CP Portland, Oregon 97201, United States.
Connor W Barth
Igor H WierzbickiPharmaceutical Sciences Division, College of Pharmacy, Oregon State University , 2730 SW Moody Avenue, CL5CP Portland, Oregon 97201, United States.
Adam W G AlaniPharmaceutical Sciences Division, College of Pharmacy, Oregon State University , 2730 SW Moody Avenue, CL5CP Portland, Oregon 97201, United States.
Summer L Gibbs
Oregon State University · USOregon Health & Science University · US

Funding

Nerve-Specific Near-Infrared Fluorescent Contrast Agents for Image-Guided SurgeryK01EB010201 · NIBIB · OREGON HEALTH & SCIENCE UNIVERSITY · PI GIBBS, SUMMER LYNNE · 2010 to 2014
$727k
NIBIB NIH HHS K01 EB010201NIBIB NIH HHS NIBIB K01EB010201
6 · The paper itself

Abstract

Nerve damage during surgery is a common morbidity experienced by patients that leaves them with chronic pain and/or loss of function. Currently, no clinically approved imaging technique exists to enhance nerve visualization in the operating room. Fluorescence image-guided surgery has gained in popularity and clinical acceptance over the past decade with a handful of imaging systems approved for clinical use. However, contrast agent development to complement these fluorescence-imaging systems has lagged behind with all currently approved fluorescent agents providing untargeted blood pool information. Nerve-specific fluorophores are known, however translations of these agents to the clinic has been complicated by their lipophilic nature, which necessitates specialized formulation strategies for successful systemic administration. To date the known nerve-specific fluorophores have only been demonstrated preclinically due to the necessity of a dimethyl sulfoxide containing formulation for solubilization. In the current study, a polymeric micellar (PM) formulation strategy was developed for a representative nerve-specific fluorophore from the distyrylbenzene family, BMB. The PM formulation strategy was able to solubilize BMB and demonstrated improved nerve-specific accumulation and fluorescence intensity when the same fluorophore dose was administered to mice utilizing the previous formulation strategy. The success of the PM formulation strategy will be important for moving toward clinical translation of these novel nerve-specific probes as it is nontoxic and biodegradable and has the potential to decrease the necessary dose for imaging while also improving the safety profile.

Indexed as

AnimalsCell LineCell Line, TumorChemistry, PharmaceuticalContrast MediaDimethyl SulfoxideDrug CarriersDrug Delivery SystemsFluorescent DyesHumansMaleMiceMicellesPolymersStyrenesContrast MediaDimethyl SulfoxidedistyrylbenzeneDrug CarriersFluorescent DyesMicellesPolymersStyrenesimage-guided surgerynerve-specific fluorescencepolymeric micellesmall molecule formulation

Identifiers

PMID26485440
PMCPMC4674818
OpenAlexW1750595029

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.