Evidence map›Paper›PMID 34407975›Full record

ArticleEuropean journal of hospital pharmacy : science and practice2023

Extemporaneous preparation of rifampicin granules from capsules to improve usability.

Yasunori Miyazaki, Tomonobu Uchino, Yoshiyuki Kagawa

Abstract read
In one paragraph

Article in European journal of hospital pharmacy : science and practice, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Yasunori MiyazakiDepartment of Clinical Pharmaceutics, University of Shizuoka, Shizuoka, Japan miyaza@u-shizuoka-ken.ac.jp.ORCID 0000-0002-4679-0058
Tomonobu UchinoDepartment of Clinical Pharmaceutics, University of Shizuoka, Shizuoka, Japan.
Yoshiyuki KagawaDepartment of Clinical Pharmaceutics, University of Shizuoka, Shizuoka, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesManipulation of tablets or capsules is frequently carried out in pharmacies to regulate doses for personalised therapy. We proposed the use of reconstructed granules as a suitable, flexible dosage form and developed an on-site granulation method using a compounding mixer. The aim of this study was to demonstrate the feasibility of small-scale preparation of granules in a pharmacy setting. Rifampicin capsules were used as a model medicine because of the associated need for drug desensitisation therapy.

methodsThe contents of a rifampicin capsule were granulated using a compounding mixer, and small ointment containers (12 mL) with filling rates of 4%, 8%, 12%, and 16% were used as granulation vessels. The obtained granules were examined for particle size distribution, yield, crystal transition, drug dissolution profile, storage stability, and weight loss during dosing.

resultsThe yields increased by >95%, and the span of the particle size distribution decreased to 1.0, as the filling rate increased. The smallest batch size was found to be 0.8 g in a 12 mL vessel. Examination of the resultant granules revealed that granulation did not affect the crystal polymorphism, dissolution profile, or storage stability of rifampicin. Furthermore, the weight loss of the granules during the dosing process was significantly lower than that of the capsule powder content.

conclusionsWe demonstrated that granules with sufficient quality for clinical use could be extemporaneously prepared using a compounding mixer in pharmacies. This improved the usability of the medicine, preventing weight loss, and making it a suitable alternative formulation for precise personalised pharmacotherapy.

Indexed as

RifampinTabletsRifampinTabletsdrug compoundinghospitalpediatricspharmaceutical preparationspharmacy administrationpharmacy service

Identifiers

PMID34407975
PMCPMC10086731

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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.