Evidence map›Paper›PMID 35890597›Full record

ArticlePolymers2022

Chitosan and Sodium Alginate Implementation as Pharmaceutical Excipients in Multiple-Unit Particulate Systems.

Martina Čierna, Pavel Mučaji, Miroslava Špaglová, Mária Čuchorová, Oliver Macho

Open access · goldAbstract read
In one paragraph

Article in Polymers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 40% 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

2 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. 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

5 authors at 2 institutions in 1 country.

Martina ČiernaDepartment of Galenic Pharmacy, Faculty of Pharmacy, Comenius University Bratislava, 832 32 Bratislava, Slovakia.
Pavel MučajiDepartment of Pharmacognosy and Botany, Faculty of Pharmacy, Comenius University Bratislava, 832 32 Bratislava, Slovakia.ORCID 0000-0003-4490-2615
Miroslava ŠpaglováDepartment of Galenic Pharmacy, Faculty of Pharmacy, Comenius University Bratislava, 832 32 Bratislava, Slovakia.ORCID 0000-0002-8462-2565
Mária ČuchorováDepartment of Galenic Pharmacy, Faculty of Pharmacy, Comenius University Bratislava, 832 32 Bratislava, Slovakia.
Oliver MachoInstitute of Process Enginering, Faculty of Mechanical Engineering, Slovak University of Technology in Bratislava, 812 31 Bratislava, Slovakia.ORCID 0000-0002-2387-6991
Comenius University Bratislava · SKSlovak University of Technology in Bratislava · SK

Funding

Faculty of Pharmacy, Comenius University Bratislava, Slovakia FaF UK/35/2018Ministry of Education, Science, Research and Sport of the Slovak Republic KEGA 021 STU-4/2022Ministry of Education, Science, Research and Sport of the Slovak Republic VEGA 1/0226/22
6 · The paper itself

Abstract

This study aimed to prepare and evaluate pellets containing acyclovir as a model drug. Pellets were prepared by the extrusion-spheronization process. Aqueous solutions of natural marine polymers (sodium alginate, chitosan) were compared to semi-synthetic hydroxypropyl methylcellulose (HPMC) in the role of binders. The study focused on the characterization of the pellet properties that are crucial for the formulation of the final dosage form, such as in multi-unit pellet system (MUPS) tablets or hard gelatin capsules filled with the pellets. Finally, the mentioned dosage forms were tested for drug dissolution. The morphology of pellets observed by scanning electron microscopy correlated with the shape evaluation performed by dynamic image analysis. Sodium alginate pellets exhibited the lowest value of sphericity (0.93), and many elongated rods and dumbbells were observed in this batch. Chitosan pellets had the highest value of sphericity (0.97) and were also less rough on the surface. The pellets maintained a constant surface geometry during the dissolution studies; they only reduced in size. The most significant reduction in size and weight was assessed after 2 h of dissolution testing. This fact was in line with the drug release from pellets in capsules or MUPS tablets, which was massive during the first hour, in both cases. The dissolution profiles of all of the batches were comparable.

Indexed as

acyclovirchitosanhydroxypropyl methylcellulosemulti-unit pellet systempelletssodium alginate

Identifiers

PMID35890597
PMCPMC9316923
OpenAlexW4285095018

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.