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Int J Pharm ; 658: 124204, 2024 Jun 10.
Article in English | MEDLINE | ID: mdl-38710297

ABSTRACT

Pulsatile drug delivery is hardly achieved by conventional gastro-retentive dosage forms. Artesunate as a typical anti-malaria medicine needs oral pulsatile release. Here, artesunate-loaded pulsatile-release multi-unit gastro-retentive tablets (APGTs) were prepared with a semi-solid extrusion three-dimensional (3D) printing method. An APGT was composed of three units: artesunate-loaded immediate and delayed release units and a block unit. The matrix of the immediate/delayed release units consisted of polyvinylpyrrolidone (PVP) K30 and croscarmellose sodium, which improved the rapid release of artesunate when contacting water. The block unit consisted of octadecanol, hydroxypropyl methyl cellulose K15M, PVP K30, and poloxamer F68. APGTs showed multi-phase release in simulated gastric liquids (SGLs). The first immediate release phase continued for 1 h followed by a long block phase for 7 h. The second rapid release phase was initiated when the eroded holes in the block unit extended to the inner delayed release unit, and this phase continued for about 14 h. Low-density APGTs could ensure their long-term floating in the stomach. Oral APGTs remained in the rabbit stomach for about 20 h. 3D printing provides a new strategy for the preparation of oral pulsatile-release tablets.


Subject(s)
Antimalarials , Artesunate , Delayed-Action Preparations , Drug Liberation , Povidone , Printing, Three-Dimensional , Tablets , Artesunate/administration & dosage , Artesunate/chemistry , Artesunate/pharmacokinetics , Animals , Rabbits , Antimalarials/administration & dosage , Antimalarials/chemistry , Antimalarials/pharmacokinetics , Povidone/chemistry , Hypromellose Derivatives/chemistry , Excipients/chemistry , Drug Delivery Systems , Administration, Oral , Carboxymethylcellulose Sodium/chemistry , Poloxamer/chemistry , Gastric Mucosa/metabolism
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