Evidence map›Paper›PMID 26309493›Full record

ArticleInternational journal of clinical and experimental medicine2015

The preparation of core/shell structured microsphere of multi first-line anti-tuberculosis drugs and evaluation of biological safety.

Hao Zeng, Xiaoyang Pang, Shuo Wang, Zhengquan Xu, Wei Peng, Penghui Zhang, Yupeng Zhang, Zheng Liu, Chengke Luo, Xiyang Wang and 1 more

Abstract read
In one paragraph

Article in International journal of clinical and experimental medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 29% 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

1 citing paper in PubMed, 6 citations in OpenAlex.

  1. 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

11 authors at 2 institutions in 1 country.

Hao ZengDepartment of Spine Surgery, The Xiangya Hospital of Central South University 87# Xiangya Road, Changsha 410008, People's Republic of China.
Xiaoyang PangDepartment of Orthopedics Surgery, The Xiangya Hospital of Central South University 87# Xiangya Road, Changsha 410008, People's Republic of China.
Shuo WangDepartment of Biomedical Engineering, College of Biology, Hunan University Changsha 410082, People's Republic of China.
Zhengquan XuDepartment of Spine Surgery, The Xiangya Hospital of Central South University 87# Xiangya Road, Changsha 410008, People's Republic of China.
Wei PengDepartment of Spine Surgery, The Xiangya Hospital of Central South University 87# Xiangya Road, Changsha 410008, People's Republic of China.
Penghui ZhangDepartment of Spine Surgery, The Xiangya Hospital of Central South University 87# Xiangya Road, Changsha 410008, People's Republic of China.
Yupeng ZhangDepartment of Spine Surgery, The Xiangya Hospital of Central South University 87# Xiangya Road, Changsha 410008, People's Republic of China.
Zheng LiuDepartment of Spine Surgery, The Xiangya Hospital of Central South University 87# Xiangya Road, Changsha 410008, People's Republic of China.
Chengke LuoDepartment of Spine Surgery, The Xiangya Hospital of Central South University 87# Xiangya Road, Changsha 410008, People's Republic of China.
Xiyang WangDepartment of Spine Surgery, The Xiangya Hospital of Central South University 87# Xiangya Road, Changsha 410008, People's Republic of China.
Hemin NieDepartment of Biomedical Engineering, College of Biology, Hunan University Changsha 410082, People's Republic of China.
Central South University · CNHunan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To introduce a modified method, namely coaxial electrohydrodynamic atomization for the fabrication of distinct core/shell structured microspheres of four first-line ant-tuberculosis drugs with different characteristics in hydrophilic properties in one single step. In group B, we prepared microspheres in which the core and the shell contain hydrophobic and hydrophilic drugs, respectively. In contrast, in group C, the opposite is prepared. The detection of encapsulation efficiency and in vitro release test were performed to confirm the feasibility of the drug-loaded core/shell structured microspheres. Moreover, cell culture experiments and animal experiments have been carried out to evaluate the biological safety of different microspheres in cell growth, cell viability, osteogenesis and migration of BMSCs in vitro and the bone fusion in a bone deficits model in SD rat. Meanwhile, the distribution of drugs and liver and kidney toxicity were monitored. The release patterns of the two groups are significantly different. The release of drugs from Group B microspheres is rather sequential, whereas group C microspheres release drugs in a parallel (co-release) manner. And various concentrations of carrier materials produces core/shell structured microspheres with different appearance. Moreover, the biological safety of core/shell structured microspheres was testified to be satisfactory. These findings present the advantages and possible application of this kind of multi-drug release system in treating skeletal tuberculosis. Moreover, the characteristic sequential release of multi-drugs can be controlled and adjusted based on treatment need and used in treating other disorders.

Indexed as

ant-tuberculosis drugsco-releaseCore/shell structuremicrospheresmulti drugs

Identifiers

PMID26309493
PMCPMC4538136
OpenAlexW1482592880

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.