Biogenic nanoparticles from liquid and solid matrices: biochemical and biophysical properties of Extracellular Vesicles-enriched samples from human plasma and skeletal muscle tissue. DOI Open Access
Valentina Mangolini, Annalisa Radeghieri, Simone Piva

et al.

bioRxiv (Cold Spring Harbor Laboratory), Journal Year: 2024, Volume and Issue: unknown

Published: Feb. 19, 2024

The majority of studies on extracellular vesicles (EVs) focused samples isolated from liquid matrices, such as cell culture media and blood, due to their accessibility. However, recent research highlights the emerging roles EVs derived solid tissues, including brain, muscles tumors. Investigating matrix tissues offers insights into microenvironment potential biological influences surrounding cells. This study presents a method for comparing EV-enriched (human skeletal muscle biopsy) (plasma) addressing technical challenges minimizing biases in separation techniques. By employing optimized protocols advanced analytical techniques, reveals differences biochemical composition, nanomechanical properties, particle yield, size distribution, colloidal stability between human plasma EVs. Understanding these distinctions may contribute development novel diagnostic assays muscular pathologies shed light EVs' diverse tissue environments.

Language: Английский

Insight into the Functional Dynamics and Challenges of Exosomes in Pharmaceutical Innovation and Precision Medicine DOI Creative Commons
Anu Sharma, Anita Yadav,

Aparajita Nandy

et al.

Pharmaceutics, Journal Year: 2024, Volume and Issue: 16(6), P. 709 - 709

Published: May 24, 2024

Of all the numerous nanosized extracellular vesicles released by a cell, endosomal-originated exosomes are increasingly recognized as potential therapeutics, owing to their inherent stability, low immunogenicity, and targeted delivery capabilities. This review critically evaluates transformative of exosome-based modalities across pharmaceutical precision medicine landscapes. Because precise biomolecular cargo delivery, posited ideal candidates in drug enhancing regenerative strategies, advancing diagnostic technologies. Despite significant market growth projections exosome therapy, its utilization is encumbered substantial scientific regulatory challenges. These include lack universally accepted protocols for isolation complexities associated with navigating environment, particularly guidelines set forth U.S. Food Drug Administration (FDA). presents comprehensive overview current research trajectories aimed at addressing these impediments discusses prospective advancements that could substantiate clinical translation exosomal therapies. By providing analysis both capabilities hurdles therapeutic applications, this article aims inform direct future paradigms, thereby fostering integration systems into mainstream practice.

Language: Английский

Citations

17

Label‐free discrimination of extracellular vesicles from large lipoproteins DOI Creative Commons
Anna D. Kashkanova, Martin Blessing,

Marie Reischke

et al.

Journal of Extracellular Vesicles, Journal Year: 2023, Volume and Issue: 12(8)

Published: July 25, 2023

Extracellular vesicles (EVs) are increasingly gaining interest as biomarkers and therapeutics. Accurate sizing quantification of EVs remain problematic, given their nanometre size range small scattering cross-sections. This is compounded by the fact that common EV isolation methods result in co-isolation particles with comparable features. Especially blood plasma, similarly-sized lipoproteins outnumber to a great extent. Recently, interferometric nanoparticle tracking analysis (iNTA) was introduced particle method enables determining refractive index nanoparticles high sensitivity precision. In this work, we apply iNTA differentiate between lipoproteins, compare its performance conventional (NTA). We show can accurately quantify artificial EV-lipoprotein mixtures plasma-derived samples varying complexity. Conventional NTA could not report on numbers, it able distinguish from lipoproteins. has potential become new standard for label-free characterization suspension.

Language: Английский

Citations

24

Particle profiling of EV‐lipoprotein mixtures by AFM nanomechanical imaging DOI Creative Commons
Andrea Ridolfi, Laura Conti, Marco Brucale

et al.

Journal of Extracellular Vesicles, Journal Year: 2023, Volume and Issue: 12(10)

Published: Oct. 1, 2023

The widely overlapping physicochemical properties of lipoproteins (LPs) and extracellular vesicles (EVs) represents one the main obstacles for isolation characterization these pervasive biogenic lipid nanoparticles. We herein present application an atomic force microscopy (AFM)-based quantitative morphometry assay to rapid nanomechanical screening mixed LPs EVs samples. method can determine diameter mechanical stiffness hundreds individual nanometric objects within few hours. obtained diameters are in accord with those measured via cryo-electron (cryo-EM); assignment specific readout each object enables simultaneous discrimination co-isolated even if they have size distributions. all classes shown be characterised by combinations stiffness, thus making it possible estimate their relative abundance EV/LP samples terms stoichiometric ratio, surface area volume. As a side finding, we show how behaviour LP is correlated distinctive structural features revealed cryo-EM. described approach label-free, single-step relatively quick perform. Importantly, used analyse which prove very challenging assess several established techniques due ensemble-averaging, low sensibility small particles, or both, providing useful tool quickly assessing purity isolates including plasma- serum-derived preparations.

Language: Английский

Citations

24

Addressing Heterogeneity in Direct Analysis of Extracellular Vesicles and Their Analogs by Membrane Sensing Peptides as Pan‐Vesicular Affinity Probes DOI Creative Commons
Alessandro Gori, Roberto Frigerio, Paola Gagni

et al.

Advanced Science, Journal Year: 2024, Volume and Issue: 11(29)

Published: May 31, 2024

Abstract Extracellular vesicles (EVs), crucial mediators of cell‐to‐cell communication, hold significant diagnostic potential due to their ability concentrate protein biomarkers in bodily fluids. However, challenges isolating EVs from biological specimens hinder widespread use. The preferred strategy involves direct analysis, integrating isolation and analysis solutions, with immunoaffinity methods currently dominating. Yet, the heterogeneous nature poses challenges, as proposed markers may not be universally present thought, raising concerns about biomarker screening reliability. This issue extends EV‐mimics, where conventional lack applicability. Addressing these study reports on Membrane Sensing Peptides (MSP) pan‐vesicular affinity ligands for both non‐canonical analogs, streamlining capture phenotyping through Single Molecule Array (SiMoA). MSP enable circulating EVs, eliminating need prior isolation. Demonstrating clinical translation, technology detects an EV‐associated epitope signature serum plasma, distinguishing myocardial infarction stable angina. Additionally, allow tetraspanin‐lacking Red Blood Cell‐derived overcoming limitations associated antibody‐based methods. Overall, work underlines value complementary tools antibodies, advancing EV diagnostics beyond, marking first‐ever peptide‐based application SiMoA technology.

Language: Английский

Citations

7

Azithromycin-loaded liposomes and niosomes for the treatment of skin infections: Influence of excipients and preparative methods on the functional properties DOI Creative Commons
Angela Abruzzo, Rejane Loose Pucci, Provvidenza Maria Abruzzo

et al.

European Journal of Pharmaceutics and Biopharmaceutics, Journal Year: 2024, Volume and Issue: 197, P. 114233 - 114233

Published: Feb. 20, 2024

Language: Английский

Citations

5

Toward Clarity in Single Extracellular Vesicle Research: Defining the Field and Correcting Missteps DOI Creative Commons
Yun Su,

Wanzhuo He,

Lei Zheng

et al.

ACS Nano, Journal Year: 2025, Volume and Issue: unknown

Published: April 24, 2025

Single extracellular vesicle (EV) research holds the potential to revolutionize our understanding of cellular communication and enable breakthroughs in diagnostics therapeutics. However, lack a clear, consensus-driven definition single EV has led methodological inconsistencies, overgeneralized interpretations, and, some cases, misleading claims. In this perspective, we propose framework for defining research, critique current challenges misconceptions field, discuss its implications biomedical applications. We argue that precise experimental design, rigorous validation, interdisciplinary collaboration approaches are needed establish as cornerstone precision medicine.

Language: Английский

Citations

0

Mucoadhesive polymer-coated liposomes as a promising approach to counteract bacteria responsible for aerobic vaginitis DOI Creative Commons

Sara Lugli,

Angela Abruzzo, Carola Parolin

et al.

International Journal of Pharmaceutics, Journal Year: 2025, Volume and Issue: unknown, P. 125667 - 125667

Published: April 1, 2025

Aerobic vaginitis is an infectious disease characterized by the overgrowth of abnormal vaginal microflora. Conventional local dosage forms are not always effective, due to their inadequate drug release and residence time within cavity. Therefore, this study aimed develop azithromycin (AZT)-loaded liposomes, coated with two mucoadhesive polymers, chitosan (CS) sodium hyaluronate (HYA), increase thedrug's stay at site infection control its release. Liposomes were developed through thin film hydration method followed extrusion subsequently added polymer solution. Later, they size, surface charge, morphology, encapsulation efficiency. Furthermore, properties behavior investigated different pH values, e.g., 4.5 7.4, mimicking physiological pathological conditions, respectively. Finally, antimicrobial tests in vitro permeation studies carried out. Results showed size charge variations LP respect uncoated ones, confirming success coating process. possessed a good capacity encapsulate drug. Among all formulations, CS-LP demonstrated superior greatest both tested pHs, as well highest accumulation inside tissue, maintaining same AZT effect. Overall, could be proposed promising nanocarrier for delivery, virtue ability achieve locally sustained drug, helping lower administration frequency, consequently improving treatment efficacy.

Language: Английский

Citations

0

The physico-chemical landscape of extracellular vesicles DOI
Mauro Manno, Antonella Bongiovanni, Leonid Margolis

et al.

Nature Reviews Bioengineering, Journal Year: 2024, Volume and Issue: unknown

Published: Nov. 12, 2024

Language: Английский

Citations

3

Extracellular vesicles deliver functional extrachromosomal DNA in FGFR2-amplified cancer of unknown primary DOI Creative Commons
Irene Salamon, Giulia Gallerani, Gianluca Storci

et al.

Research Square (Research Square), Journal Year: 2025, Volume and Issue: unknown

Published: Feb. 27, 2025

Abstract Background The extracellular vesicle (EV) pathway plays a critical role in cell-to-cell communication. Cancer cells release EVs into the space, where they interact with both cancerous and noncancerous cells, activating signaling pathways remodeling tumor microenvironment (TME). In this study, we investigated functional of released by FGFR2-amplified cancers unknown primary (CUPs), which generate extrachromosomal circular DNA (ecDNA) to enhance oncogenic amplification.Methods FGFR2 copy number was quantified using droplet digital PCR (ddPCR) visualized fluorescent situ hybridization (FISH). were isolated via ultracentrifugation, nature ecDNA assessed Plasmid-Safe ATP-dependent DNase treatment atomic force microscopy (AFM). Oncogene transfer through evaluated administering CUP-derived recipient NCI-N87 or coculture system that facilitated EV THP-1, HUVEC, fibroblast cell lines.Results FGFR2-containing ecDNA, is partially circular, packaged within exhibited activity upon delivery TME cells. When cancer (NCI-N87, THP-1) noncancer (HUVECs, fibroblasts) exposed EVs—either direct administration coculture—they internalized DNA, subsequently transcribed, leading altered morphology increased proliferation, depending on type. induced THP-1 polarization toward M2 macrophage subtype promoted HUVEC proliferation.Conclusion This mechanism oncogene can contribute remodeling, potentially explaining early metastatic potential CUP.

Language: Английский

Citations

0

Quantifying the Shape and Stiffness of Single Extracellular Vesicles in Aqueous Solution via Membrane Diffusivity Measurements DOI Creative Commons
Yihan Wang,

Huihui Gao,

Chu Han

et al.

Chemical & Biomedical Imaging, Journal Year: 2025, Volume and Issue: unknown

Published: April 9, 2025

Language: Английский

Citations

0