Evidence map›Paper›PMID 25948966›Full record

ArticleToxicology international

Rifapentine-proliposomes for inhalation: in vitro and in vivo toxicity.

Arpana A Patil-Gadhe, Abhay Y Kyadarkunte, Michael Pereira, Gauri Jejurikar, Milind S Patole, Arun Risbud, Varsha B Pokharkar

Abstract read
In one paragraph

Article in Toxicology international. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.4field-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

6 citing papers in PubMed, 34 citations in OpenAlex.

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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

7 authors at 2 institutions in 1 country.

Arpana A Patil-GadheDepartment of Pharmaceutics, Bharati Vidyapeeth University, Poona College of Pharmacy, Erandwane, Pune, India ; National Centre for Cell Sciences, University of Pune Campus, Ganeshkhind, Pune, India.
Abhay Y KyadarkunteDepartment of Pharmaceutics, Bharati Vidyapeeth University, Poona College of Pharmacy, Erandwane, Pune, India ; National Centre for Cell Sciences, University of Pune Campus, Ganeshkhind, Pune, India.
Michael PereiraDepartment of Microbiology, National Aids Research Centre, Bhosari, Pune, Maharashtra, India.
Gauri JejurikarDepartment of Microbiology, National Aids Research Centre, Bhosari, Pune, Maharashtra, India.
Milind S PatoleNational Centre for Cell Sciences, University of Pune Campus, Ganeshkhind, Pune, India.
Arun RisbudDepartment of Microbiology, National Aids Research Centre, Bhosari, Pune, Maharashtra, India.
Varsha B PokharkarDepartment of Pharmaceutics, Bharati Vidyapeeth University, Poona College of Pharmacy, Erandwane, Pune, India.
Bharati Vidyapeeth Deemed University · INNational Centre for Cell Science · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOral therapy for pulmonary tuberculosis (TB) treatment suffers from the limitation of hepatic metabolism leading insufficient concentration of antitubercular (anti-TB) drugs in alveolar macrophage which harbors Mycobacterium tuberculosis (MTB). Targeted aerosol delivery of antituberculous drug to lung is efficient for treating local lung TB infection.

objectiveThe present study was aimed to evaluate rifapentine (RPT) loaded proliposomal dry powder for inhalation (RLDPI) for anti-TBactivity and cytotoxicity in vitro. In vivo toxicity study was also undertaken in Wistar rats to determine safe concentration of RLDPI for administration. MATERIALS AND

methodsAnti-TB activity of developed RLDPI was assessed using drug susceptibility testing (DST) on Mycobacteria growth indicator tube (MGIT) method. In vitro cytotoxicity was performed in A549 cell lines and IC50 values were used to compare the cytotoxicity of formulation with pure RPT. In vivo repeated dose toxicity study was undertaken using Wistar rats at three different doses for 28-days by intratracheal insufflations method.

resultsThe results of DST study revealed sensitivity of tubercle bacteria to RLDPI at concentration equivalent to 10 μg/mL of RPT. This study confirmed anti-TB potential of RPT in spray-dried RLDPI, though the spray drying method is reported to reduce activity of drugs. Cytotoxicity study in A549 cells demonstrated that RPT when encapsulated in liposomes as RLDPI was safe to cells as compared to pure RPT. In vivo toxicity study revealed that RPT in the form of RLDPI was safe at 1 and 5 mg/kg dose. However, mortality was seen at higher dose (10 mg/kg), possibly because of liver and kidney damage.

conclusionThus, these studies demonstrated safety of RLDPI for the treatment of pulmonary TB.

Indexed as

A549 cell linedrug susceptibility testing on Mycobacteria growth indicator tubepulmonary tuberculosisrifapentinetoxicity

Identifiers

PMID25948966
PMCPMC4413410
OpenAlexW2009786324

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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.