Evidence map›Paper›PMID 42807438›Full record

ArticleNanotechnology, science and applications2026

Functionalized Colloidal Hydroxyapatite for Combined Delivery of Cannabidiol and Epirubicin: Characterization, Biomimetic Membrane Interaction, and Cytotoxicity Studies.

Paulina Końska, Magdalena Osial, Daria Paulina Kępińska, Jan Taudul, Sławomir Wilczewski, Emilia Świątek, Agnieszka Majkowska-Pilip, Kinga Żelechowska-Matysiak, Thu Phuong Nguyen, Paweł Krysiński and 1 more

Abstract read
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Article in Nanotechnology, science and applications, 2026. 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

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Paulina KońskaFaculty of Chemistry, University of Warsaw, Warsaw, Poland.
Magdalena OsialInstitute of Fundamental Technological Research, Polish Academy of Sciences, Warsaw, Poland.
Daria Paulina KępińskaBiotech Evolution, Łomianki, Poland.
Jan TaudulFaculty of Chemistry, University of Warsaw, Warsaw, Poland.ORCID 0009-0006-5686-490X
Sławomir WilczewskiFaculty of Chemical Technology and Engineering, Bydgoszcz University of Science and Technology, Bydgoszcz, Poland.
Emilia ŚwiątekFaculty of Chemistry, University of Warsaw, Warsaw, Poland.ORCID 0009-0008-8607-4735
Agnieszka Majkowska-PilipInstitute of Nuclear Chemistry and Technology, Warsaw, Poland.ORCID 0000-0001-9449-6411
Kinga Żelechowska-MatysiakInstitute of Nuclear Chemistry and Technology, Warsaw, Poland.
Thu Phuong NguyenUniversity of Science and Technology of Hanoi, Vietnam Academy of Science and Technology, Hanoi, Vietnam.
Paweł KrysińskiFaculty of Chemistry, University of Warsaw, Warsaw, Poland.
Dorota NiecieckaFaculty of Chemistry, University of Warsaw, Warsaw, Poland.ORCID 0000-0001-7155-7197

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: A stable colloidal hydroxyapatite (cHAp) platform was successfully developed for the co-delivery of cannabidiol (CBD), a natural bioactive compound, and epirubicin (EPI), a chemotherapeutic agent, to enhance cytotoxicity against ovarian cancer cells. Methods: Colloidal cHAp was synthesized and functionalized with CBD and EPI to obtain a multifunctional drug delivery system. The resulting composite was characterized using high-performance liquid chromatography, UV-Vis spectrometry, transmission and scanning electron microscopies, Fourier-transform infrared spectroscopy, Turbiscan analysis, and differential scanning calorimetry. Drug release in phosphate-buffered saline (PBS, pH 7) was evaluated by differential pulse voltammetry. Interactions with model lipid monolayers mimicking healthy and cancerous cell membranes were investigated using the Langmuir technique, and cytotoxicity was assessed by MTS assays. Results: The successful incorporation of both biologically active compounds into the cHAp carrier and its excellent colloidal stability were confirmed. The epirubicin loading content was 0.0605 mg per 1 mg of cHAp. Drug release followed a time-dependent profile, reaching approximately 2 μg mL Conclusion: The developed cHAp platform provides a stable and multifunctional carrier for the co-delivery of CBD and epirubicin. Its favorable physicochemical properties, enhanced membrane interactions, and improved anticancer activity highlight its potential as a promising nanocarrier for targeted ovarian cancer therapy.

Indexed as

cannabinoidsdrug deliveryepirubicinhydroxyapatite

Identifiers

PMID42807438
PMCPMC13617019

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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.