Evidence map›Paper›PMID 30087562›Full record

ArticleInternational journal of nanomedicine2018

Antimycobacterial susceptibility evaluation of rifampicin and isoniazid benz-hydrazone in biodegradable polymeric nanoparticles against

Sushruta S Hakkimane, Vishnu Prasad Shenoy, Santosh L Gaonkar, Indira Bairy, Bharath Raja Guru

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2018. 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
2.5field-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

20 citing papers in PubMed, 74 citations in OpenAlex.

  1. Review
  2. Article
  3. Drug-loaded polymer-coated silver nanoparticles for lung cancer theranostics.Medical oncology (Northwood, London, England) · 2024
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  8. Potential Impact of Long-Acting Products on the Control of Tuberculosis: Preclinical Advancements and Translational Tools in Preventive Treatment.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2022
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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

5 authors at 1 institution in 1 country.

Sushruta S HakkimaneDepartment of Biotechnology, Manipal Institute of Technology, Manipal Academy of Higher Education, Manipal, India, bharath.guru@manipal.edu.
Vishnu Prasad ShenoyDepartment of Microbiology, Kasturba Medical College, Manipal Academy of Higher Education, Manipal, India.
Santosh L GaonkarDepartment of Chemistry, Manipal Institute of Technology, Manipal Academy of Higher Education, Manipal, India.
Indira BairyDepartment of Microbiology, Melaka Manipal Medical College, Manipal Academy of Higher Education, Manipal, India.
Bharath Raja GuruDepartment of Biotechnology, Manipal Institute of Technology, Manipal Academy of Higher Education, Manipal, India, bharath.guru@manipal.edu.
Manipal Academy of Higher Education · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionTuberculosis (TB) is the single largest infectious disease which requires a prolonged treatment regime with multiple drugs. The present treatment for TB includes frequent administration of a combination of four drugs for a duration of 6 months. This leads to patient's noncompliance, in addition to developing drug-resistant strains which makes treatment more difficult. The formulation of drugs with biodegradable polymeric nanoparticles (NPs) promises to overcome this problem. MATERIALS AND

methodsIn this study, we focus on two important drugs used for TB treatment - rifampicin (RIF) and isoniazid (INH) - and report a detailed study of RIF-loaded poly lactic-co-glycolic acid (PLGA) NPs and INH modified as INH benz-hydrazone (IH2) which gives the same therapeutic effect as INH but is more stable and enhances the drug loading in PLGA NPs by 15-fold compared to INH. The optimized formulation was characterized using particle size analyzer, scanning electron microscopy and transmission electron microscopy. The drug release from NPs and stability of drug were tested in different pH conditions.

resultsIt was found that RIF and IH2 loaded in NPs release in a slow and sustained manner over a period of 1 month and they are more stable in NPs formulation compared to the free form. RIF- and IH2-loaded NPs were tested for antimicrobial susceptibility against

conclusionThese results show that NP formulations will improve the efficacy of drug delivery for TB treatment.

Indexed as

A549 CellsAnimalsAntitubercular AgentsBiocompatible MaterialsCell DeathChromatography, High Pressure LiquidChromatography, Reverse-PhaseDrug CompoundingDrug Delivery SystemsDrug LiberationHumansIsoniazidLactic AcidMiceMicrobial Sensitivity TestsMycobacterium tuberculosisAntitubercular AgentsBiocompatible MaterialsIsoniazidLactic AcidPolyglycolic AcidPolylactic Acid-Polyglycolic Acid CopolymerPolymersRifampindrug susceptibilityisoniazid hydrazoneMycobacterium tuberculosisrifampicin nanoparticles

Identifiers

PMID30087562
PMCPMC6061404
OpenAlexW2884946551

What OpenQuestion holds

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LicenceCC BY-NC
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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.