Evidence map›Paper›PMID 39679250›Full record

ArticleInternational journal of nanomedicine2024

Fabrication of Biomimetic Hybrid Liposomes via Microfluidic Technology: Homotypic Targeting and Antitumor Efficacy Studies in Glioma Cells.

Ilaria Arduino, Roberta Di Fonte, Federica Sommonte, Angela Assunta Lopedota, Letizia Porcelli, Jiachen Li, Simona Serrati, Raquel Bártolo, Hélder A Santos, Rosa Maria Iacobazzi and 2 more

Abstract read
In one paragraph

Article in International journal of nanomedicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

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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

12 authors.

Ilaria ArduinoDepartment of Pharmacy-Pharmaceutical Sciences, University of Bari, Bari, 70125, Italy.
Roberta Di FonteIRCCS Istituto Tumori "Giovanni Paolo II", Bari, 70124, Italy.
Federica SommonteIRCCS Istituto Tumori "Giovanni Paolo II", Bari, 70124, Italy.
Angela Assunta LopedotaDepartment of Pharmacy-Pharmaceutical Sciences, University of Bari, Bari, 70125, Italy.
Letizia PorcelliIRCCS Istituto Tumori "Giovanni Paolo II", Bari, 70124, Italy.
Jiachen LiDepartment of Biomaterials and Biomedical Technology, University Medical Center Groningen (UMCG), The Personalized Medicine Research Institute (PRECISION), University of Groningen, Groningen, AV, 9713, Netherlands.
Simona SerratiIRCCS Istituto Tumori "Giovanni Paolo II", Bari, 70124, Italy.
Raquel BártoloDepartment of Biomaterials and Biomedical Technology, University Medical Center Groningen (UMCG), The Personalized Medicine Research Institute (PRECISION), University of Groningen, Groningen, AV, 9713, Netherlands.
Hélder A SantosDepartment of Biomaterials and Biomedical Technology, University Medical Center Groningen (UMCG), The Personalized Medicine Research Institute (PRECISION), University of Groningen, Groningen, AV, 9713, Netherlands.ORCID 0000-0001-7850-6309
Rosa Maria IacobazziDepartment of Pharmacy-Pharmaceutical Sciences, University of Bari, Bari, 70125, Italy.
Amalia Azzariti *IRCCS Istituto Tumori "Giovanni Paolo II", Bari, 70124, Italy.
Nunzio Denora *Department of Pharmacy-Pharmaceutical Sciences, University of Bari, Bari, 70125, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The treatment of glioblastoma is hindered by the blood-brain barrier (BBB) and rapid drug clearance by the immune system. To address these challenges, we propose a novel drug delivery system using liposomes modified with cell membrane fragments. These modified liposomes can evade the immune system, cross the BBB, and accumulate in tumor tissue through homotypic targeting, thereby delivering drugs like paclitaxel and carboplatin more effectively. Methods: In this work, the hybrid liposomes were synthesized using microfluidics and integrating 3D printing to produce the microfluidic devices. In vitro, we explored the homotypic targeting capability, BBB passing ability, and therapeutic efficacy of paclitaxel and carboplatin. Results: The production of hybrid liposomes by microfluidics has been key to creating high-quality biomimetic nanoparticles, and the integration of 3D printing has simplified the production of microfluidic devices, making the process more efficient and economical. In vitro experiments have shown that these drug-loaded biomimetic hybrid liposomes are able to reach the homotypic target, cross the BBB, and maintain the efficacy of paclitaxel and carboplatin. Conclusions: The development of biomimetic hybrid liposomes represents a promising approach for the treatment of glioblastoma. By combining the advantages of liposomal drug delivery with the stealth properties and targeting capabilities of cell membrane fragments, these nanoparticles can potentially overcome the challenges associated with traditional therapies.

Indexed as

Biomimetic MaterialsBlood-Brain BarrierBrain NeoplasmsCarboplatinLiposomesPaclitaxelAntineoplastic AgentsBiomimeticsCell Line, TumorDrug Delivery SystemsGlioblastomaGliomaHumansLab-On-A-Chip DevicesMicrofluidicsNanoparticlesAntineoplastic AgentsCarboplatinLiposomesPaclitaxelbioinspired materialsbiomimetic nanoparticlesdrug delivery systememerging technologyglioblastoma cellsmicrofluidics

Identifiers

PMID39679250
PMCPMC11638480

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Registered trials

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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.