Evidence map›Paper›PMID 39598573›Full record

ArticlePharmaceutics2024

A Perspective on the Use of Hydroxyapatites to Improve the Dissolution Behavior of Poorly Water-Soluble Piretanide.

Valeria Friuli, Claudia Loi, Giovanna Bruni, Lauretta Maggi, Marcella Bini

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Article in Pharmaceutics, 2024. 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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2 · The registry

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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

5 authors.

Valeria FriuliDepartment of Drug Sciences, University of Pavia, viale Taramelli 12, 27100 Pavia, Italy.ORCID 0000-0002-2975-4362
Claudia LoiDepartment of Chemistry, University of Pavia, viale Taramelli 16, 27100 Pavia, Italy.
Giovanna BruniDepartment of Chemistry, University of Pavia, viale Taramelli 16, 27100 Pavia, Italy.ORCID 0000-0003-1958-2998
Lauretta MaggiDepartment of Drug Sciences, University of Pavia, viale Taramelli 12, 27100 Pavia, Italy.ORCID 0000-0002-1408-8846
Marcella BiniDepartment of Chemistry, University of Pavia, viale Taramelli 16, 27100 Pavia, Italy.ORCID 0000-0001-7099-0650

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

objectivesInterest in drug delivery systems (DDS) based on inorganic substrates has increased in parallel with the increase in the number of poorly water-soluble drugs. Hydroxyapatite is one of the ideal matrices for DDS due to its biocompatibility, low cost, and ease of preparation.

methodsWe propose two doped hydroxyapatites, one with Ba on Ca sites another with Si on P sites, with the aim of improving the dissolution rate of piretanide, a diuretic, poorly water-soluble drug. The hybrids were characterized by different physical-chemical techniques, and their formation was demonstrated by infrared spectroscopy, thermal analysis, and electron microanalysis, as well as by comparing the results with those obtained on physical mixtures of HAPs and properly prepared piretanide.

resultsBoth the hybrids improved the piretanide dissolution rate compared with the physical mixtures and the drug alone. The dose was completely solubilized from the Si-doped hybrid in about 5 min in the three fluids considered. This remarkable improvement can be explained by an increase in the wettability and solubility of the drug loaded in the drug-carrier systems.

conclusionsDifferent experimental techniques, in particular spectroscopy and electronic microanalysis, proved the successful loading of piretanide onto doped HAP. Pharmaceutical measurements demonstrated rapid drug release in different fluids simulating gastrointestinal conditions after oral administration. These hybrid systems could be a very promising platform for drug delivery.

Indexed as

dissolution ratedopingdrug deliveryhydroxyapatitepiretanidewettability

Identifiers

PMID39598573
PMCPMC11597431

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