Evidence map›Paper›PMID 33116484›Full record

ArticleInternational journal of nanomedicine2020

Development of Rifapentine-Loaded PLGA-Based Nanoparticles: In vitro Characterisation and in vivo Study in Mice.

Qiuzhen Liang, Haibin Xiang, Xinyu Li, Chunxia Luo, Xuehong Ma, Wenhui Zhao, Jiangtao Chen, Zheng Tian, Xinxia Li, Xinghua Song

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

20 citing papers in PubMed, 45 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Mannosamine-Modified Poly(lactic-Bioconjugate chemistry · 2025
    Article
  7. Article
  8. Inhalational Delivery ofAdvanced therapeutics · 2025
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review
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

10 authors at 3 institutions in 1 country.

Qiuzhen Liang *Department of Orthopaedics, The First Affiliated Hospital of Xinjiang Medical University, Urumqi 830054, People's Republic of China.
Haibin Xiang *Department of Orthopaedics, The First Affiliated Hospital of Xinjiang Medical University, Urumqi 830054, People's Republic of China.
Xinyu LiSchool of Pharmacy, Xinjiang Medical University, Urumqi 830011, People's Republic of China.
Chunxia LuoSchool of Pharmacy, Xinjiang Medical University, Urumqi 830011, People's Republic of China.
Xuehong MaSchool of Pharmacy, Xinjiang Medical University, Urumqi 830011, People's Republic of China.
Wenhui ZhaoSchool of Pharmacy, Xinjiang Medical University, Urumqi 830011, People's Republic of China.
Jiangtao ChenDepartment of Orthopaedics, The First Affiliated Hospital of Xinjiang Medical University, Urumqi 830054, People's Republic of China.
Zheng TianDepartment of Orthopaedics, The First Affiliated Hospital of Xinjiang Medical University, Urumqi 830054, People's Republic of China.
Xinxia LiSchool of Pharmacy, Xinjiang Medical University, Urumqi 830011, People's Republic of China.
Xinghua SongDepartment of Orthopaedic, The First Affiliated Hospital of Jinan University, Guangzhou, Guangdong Province 510630, People's Republic of China.
Xinjiang Medical University · CNFirst Affiliated Hospital of Xinjiang Medical University · CNFirst Affiliated Hospital of Jinan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTuberculosis (TB) is a leading cause of death amongst infectious diseases. The poor response to antitubercular agents necessitates the long-term use of high drug doses, resulting in low patient compliance, which is the main reason for chemotherapy failure and contributes to the development of multidrug-resistant TB. Patient non-compliance has been a major obstacle in the successful management of TB. The aim of this work was to develop and characterise rifapentine (RPT)-loaded PLGA-based nanoparticles (NPs) for reducing dosing frequency.

methodsRPT-loaded PLGA and PLGA-PEG NPs were prepared using premix membrane homogenisation combined with solvent evaporation method. The resulting NPs were characterised in terms of physicochemical characteristics, toxicity, cellular uptake and antitubercular activity. NPs were further evaluated for pharmacokinetic and biodistribution studies in mice.

resultsThe resulting NPs showed suitable and safe physicochemical characteristics and could be taken up by macrophages. RPT-loaded NPs were more effective against

conclusionThe application of PLGA-based NPs as sustained-release delivery vehicles for RPT could prolong drug release, modify pharmacokinetics, increase antitubercular activity and diminish toxicity, thereby allowing low dosage and frequency.

Indexed as

Administration, OralAnimalsAntitubercular AgentsDrug CarriersDrug Delivery SystemsDrug LiberationHemolysisHumansMacrophagesMaleMice, Inbred BALB CMycobacterium tuberculosisNanoparticlesParticle SizePolyestersPolyethylene GlycolsAntitubercular AgentsDrug CarriersPolyesterspolyethylene glycol-poly(lactide-co-glycolide)Polyethylene GlycolsProstaglandins ARifampinrifapentinedrug delivery systemnanoparticlesrifapentinetuberculosis

Identifiers

PMID33116484
PMCPMC7547843
OpenAlexW3091742121

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.