Evidence map›Paper›PMID 30974523›Full record

ArticlePolymers2016

An Osteoconductive Antibiotic Bone Eluting Putty with a Custom Polymer Matrix.

John Curley, Mohammad Raquibul Hasan, Jacob Larson, Benjamin D Brooks, Qianhui Liu, Tanmay Jain, Abraham Joy, Amanda E Brooks

Abstract read
In one paragraph

Article in Polymers, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

8 authors.

John CurleyDepartment of Pharmaceutical Sciences, North Dakota State University, Fargo, ND 58105, USA. john.curley@ndsu.edu.
Mohammad Raquibul HasanDepartment of Pharmaceutical Sciences, North Dakota State University, Fargo, ND 58105, USA. raquib.hasan@ndsu.edu.ORCID 0000-0001-7706-0106
Jacob LarsonDepartment of Industrial and Manufacturing Engineering, North Dakota State University, Fargo, ND 58105, USA. jacob.s.larson@ndsu.edu.
Benjamin D BrooksDepartment of Electrical and Computer Engineering, North Dakota State University, Fargo, ND 58105, USA. ben@brooks.nu.
Qianhui LiuDepartment of Polymer Science, University of Akron, Akron, OH 44325, USA. ql17@zips.uakron.edu.
Tanmay JainDepartment of Polymer Science, University of Akron, Akron, OH 44325, USA. tpj13@zips.uakron.edu.
Abraham JoyDepartment of Polymer Science, University of Akron, Akron, OH 44325, USA. abraham@uakron.edu.
Amanda E BrooksDepartment of Pharmaceutical Sciences, North Dakota State University, Fargo, ND 58105, USA. amanda.e.brooks@ndsu.edu.

Funding

Engbretson Family FoundationNational Science Foundation 0619098National Science Foundation 092334National Science Foundation 1229417North Dakota State University Start up funds
6 · The paper itself

Abstract

With the rising tide of antibiotic resistant bacteria, extending the longevity of the current antibiotic arsenal is becoming a necessity. Developing local, controlled release antibiotic strategies, particularly for difficult to penetrate tissues such as bone, may prove to be a better alternative. Previous efforts to develop an osteoconductive local antibiotic release device for bone were created as solid molded composites; however, intimate contact with host bone was found to be critical to support host bone regrowth; thus, an osteocondconductive antibiotic releasing bone void filling putty was developed. Furthermore, a controlled releasing polymer matrix was refined using pendant-functionalized diols to provide tailorable pharmacokinetics. In vitro pharmacokinetic and bioactivity profiles were compared for a putty formulation with an analogous composition as its molded counterpart as well as four new pendant-functionalized polymers. A best-fit analysis of polymer composition in either small cylindrical disks or larger spheres revealed that the new pendant-functionalized polymers appear to release vancomycin via both diffusion and erosion regardless of the geometry of the putty. In silico simulations, a valuable technique for diffusion mediated controlled release models, will be used to confirm and optimize this property.

Indexed as

bone void fillercontrolled drug releaseosteomyelitispendant-functionalized diolpharmacokineticsputty

Identifiers

PMID30974523
PMCPMC6432247

What OpenQuestion holds

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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.