Evidence map›Paper›PMID 31012249›Full record

ArticleJournal of biomedical materials research. Part A2019

Sustained-release of sclerostin single-chain antibody fragments using poly(lactic-co-glycolic acid) microspheres for osteoporotic fracture repair.

Ming Li, Shifei Li, Jianheng Liu, Xiang Cui, Shudong Zhang, Jian Zhou, Xiumei Wang, Qi Yao

Open access · hybridAbstract read
In one paragraph

Article in Journal of biomedical materials research. Part A, 2019. 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
0.5field-weighted citation impact, top 28% 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

3 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Review
  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 at 4 institutions in 1 country.

Ming LiDepartment of Orthopaedics, Chinese PLA General Hospital, Beijing, China.
Shifei LiDepartment of Orthopedics, Beijing Shijitan Hospital Affiliated to Capital Medical University, Peking University Ninth School of Clinical Medicine, Beijing, China.
Jianheng LiuDepartment of Orthopaedics, Chinese PLA General Hospital, Beijing, China.
Xiang CuiDepartment of Orthopaedics, Chinese PLA General Hospital, Beijing, China.
Shudong ZhangDepartment of Orthopedics, Beijing Shijitan Hospital Affiliated to Capital Medical University, Peking University Ninth School of Clinical Medicine, Beijing, China.
Jian ZhouDepartment of Orthopedics, Beijing Shijitan Hospital Affiliated to Capital Medical University, Peking University Ninth School of Clinical Medicine, Beijing, China.
Xiumei WangState Key Laboratory of New Ceramics and Fine Processing, School of Materials Science and Engineering, Tsinghua University, Beijing, China.
Qi YaoDepartment of Orthopedics, Beijing Shijitan Hospital Affiliated to Capital Medical University, Peking University Ninth School of Clinical Medicine, Beijing, China.
Beijing Shijitan Hospital · CNChinese PLA General Hospital · CNPeking University · CNTsinghua University · CN

Funding

Beijing Council of Science and Technology Z151100003915094Clinical Research Support Fund of PLA General Hospital 2017FC-TSYS-2006National Natural Science Foundation of China 81702121National Natural Science Foundation of China 81702153Scientific Research Project of Capital Health Development 2018-4-5014Subsidiary of PLA Major Project AWS17J004
6 · The paper itself

Abstract

Osteoporotic fracture is one of the most common bone diseases in middle and old age, as the most serious consequence of osteoporosis. Sclerostin single-chain antibody fragments (SCL-scFv) have been proven to promote bone formation by binding to scleroprotein, a natural antagonist of the Wnt pathway, but it is difficult to rule alone due to the weak permeability and immunogenicity. Herein, we prepared poly(lactic-co-glycolic acid) microspheres as a sustained-release vehicle to prolong the activity of SCL-scFv. The morphology of microspheres were uniform and nearly sphere, loading efficiency and encapsulation efficiency of SCL-scFv microspheres were 6.28 ± 1.04% and 48.37 ± 8.11%, respectively. Approximately 90% of the SCL-scFvs were released from the microspheres over 28 days with initial burst releasing (38%) in the first 4 days. Sustained-release of active SCL-scFv from microspheres promoted bone marrow mesenchymal stem cells osteogenic differentiation in vitro and enhanced fracture healing in ovariectomized rats by improving bone mass and bone formation in the fracture region. All these findings demonstrate that the microspheres are able to simultaneously achieve localized long-term SCL-scFv controlled release and effectively promote bone formation, which provides a promising approach for osteoporotic fracture.

Indexed as

Fracture HealingMicrospheresAdaptor Proteins, Signal TransducingAlkaline PhosphataseAnimalsCell DifferentiationCell ProliferationDelayed-Action PreparationsFemaleFemoral FracturesGene Expression RegulationMesenchymal Stem CellsOsteogenesisOsteoporotic FracturesPolylactic Acid-Polyglycolic Acid CopolymerRats, Sprague-DawleyAdaptor Proteins, Signal TransducingAlkaline PhosphataseDelayed-Action PreparationsPolylactic Acid-Polyglycolic Acid CopolymerSingle-Chain Antibodiesfracture healingmicrospheresosteoporosisprotein releasesclerostin-scFv

Identifiers

PMID31012249
PMCPMC6618085
OpenAlexW2940679497

What OpenQuestion holds

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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.