ArticlePharmaceutical research2026
Fresh 3D Printing of Spanlastics Hydrogel for Drug Delivery Applications In Vitro.
Article in Pharmaceutical research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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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.
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Who cites it
1 citing paper in PubMed.
- From Technological Innovation to Clinical Translation: Progress and Challenges in 3D Bioprinting for the Development of Breast Cancer Bone Metastasis Models.Advanced healthcare materials · 2026Review
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Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
purposeTo develop a localized delivery implant by integrating doxorubicin loaded spanlastic vesicles within Freeform Reversible Embedding of Suspended Hydrogels (FRESH) printed alginate constructs.
methodsSpanlastics composed of Sorbitan Monostearate (Span60) and an edge activator, Polyethylene sorbitol ester (Tween 80), were prepared by ethanolic injection. Plain and drug-loaded spanlastics were characterized for their physicochemical properties. Vesicles were incorporated into 3D printed sodium alginate hydrogels in 'FRESH' bioprinting process to promote the sustained drug release of doxorubicin which was assessed using dialysis membrane for drug release. In vitro uptake and cytotoxicity were evaluated in MCF7 breast cancer cells.
resultsOptimized formulations produced vesicles of approximately 200 to 300 nm with moderate encapsulation efficiency (33 to 44%) and stability during hydrogel incorporation and printing. Printed depots provided sustained doxorubicin release relative to suspension and reduced MCF7 viability, with preferential intracellular and nuclear localization consistent with doxorubicin activity.
conclusionSpanlastic-loaded FRESH printed alginate implants combine vesicle-mediated cellular delivery with matrix-governed sustained release, supporting their potential as a localized chemotherapy depot for further in vivo validation.
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Registered trials
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