Evidence map›Paper›PMID 34435280›Full record

ArticleAAPS PharmSciTech2021

Salts and Polymorph Screens for Bedaquiline.

Mercy Okezue, Susan Bogdanowich-Knipp, Daniel Smith, Matthias Zeller, Stephen Byrn, Pamela Smith, Dale K Purcell, Kari Clase

Open access · hybridAbstract read
In one paragraph

Article in AAPS PharmSciTech, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 32% 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

8 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
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  7. Article
  8. Comparison of pharmacokinetics and bioavailability of bedaquiline fumarate, benzoate and maleate in dogs.The international journal of tuberculosis and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease · 2023
    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 2 institutions in 1 country.

Mercy OkezueBiotechnology Innovation and Regulatory Science Center, ABE, Purdue University, 225 S. University Street, Indiana, 47906, West Lafayette, USA. mokezue@purdue.edu.
Susan Bogdanowich-KnippRavine Pharmaceuticals, LLC, 3425 DuBois St., Indiana, West Lafayette, USA.
Daniel SmithIndustrial and Physical Pharmacy, Purdue University, 575 Stadium Mall, Indiana, 47907, West Lafayette, USA.
Matthias ZellerChemistry, Purdue University, 560 Oval Dr, Indiana, 47907-2084, West Lafayette, USA.
Stephen ByrnIndustrial and Physical Pharmacy, Purdue University, 575 Stadium Mall, Indiana, 47907, West Lafayette, USA.
Pamela SmithImproved Pharma LLC, 1281 Win Hentschel Blvd, Indiana, 47906, West Lafayette, USA.
Dale K PurcellChemical Microscopy LLC, 1281 Win Hentschel Blvd, Indiana, 47906, West Lafayette, USA.
Kari ClaseBiotechnology Innovation and Regulatory Science Center, ABE, Purdue University, 225 S. University Street, Indiana, 47906, West Lafayette, USA.
Purdue University West Lafayette · USImproved Pharma (United States)

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bedaquiline is used to treat multi-resistant tuberculosis in adults. The fumarate salt is commercially available and used in the product Sirturo. To provide open access to bedaquiline molecule once the patent on the chemical substance expires, new salts were screened. This work offers additional information on the bedaquiline system, as new salts may present better pharmacokinetic properties. The current studies focus on the attempted isolation of the acetate, benzoate, benzenesulfonate, hydrobromide, succinate, hydrochloride, tartrate, lactate, maleate, malate, and mesylate salts of bedaquiline. Potential salts were screened using a unique combination of conventional screening, and small-scale experiments supplemented by crystallographic analysis and infrared microspectroscopy. Salts were prepared on a larger scale by dissolving 1:1 ratios of the individual salt formers and bedaquiline base (30 mg, 0.055 mmol) in different solvents and allowing the solutions to evaporate or crystallize. X-ray diffraction (XRD) techniques and spectroscopic and thermal analyses were employed to characterize the salts. The benzoate and maleate salts were selected as lead candidates after reviewing preliminary characterization data. To determine the most stable forms for the leads, a polymorph screen was conducted using solvents of various polarities. These salt screens successfully generated five new salts of bedaquiline, namely, benzoate, maleate, hydrochloride, besylate, and mesylate. The existence of these salts was confirmed by powder XRD, proton NMR, and IR spectroscopies. TGA and DSC thermal analysis along with hot-stage optical microscopy were further used to characterize the salts. The polymorph screen conducted on the salts suggested the absence of additional polymorphs at 1 g scale.

Indexed as

DiarylquinolinesSaltsPowdersSolubilityX-Ray DiffractionbedaquilineDiarylquinolinesPowdersSaltsBedaquilinePolymorph screenSalt screenX-ray diffraction and Tuberculosis

Identifiers

PMID34435280
PMCPMC8387259
OpenAlexW3194237592

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.